SRA SRX MGI old new predict judge 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX076077 N2|Whole worm, young, control, H3K27me3 ChIP|whole body Adl@ Adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX076078 N2|Whole worm, old, control, H3K27me3 ChIP|whole body Adl@ Adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX076079 N2|Whole worm, old, Utx-1 RNAi, H3K27me3 ChIP|whole body Adl@ Adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX113608 nrde-2(gg091)|adult C. elegans|adult Adl@ Adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX113609 rrf-3 (pk1426)|adult C. elegans|adult Adl@ Adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX113610 rde-1(ne300)|adult C. elegans|adult Adl@ Adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX113611 MAGO (ppw-1(tm914), sago-1(tm1195), sago-2(tm894), F58G1.1(tm1019), C06A1.4(tm887), and M03D4.6(tm1144)|adult C. elegans|adult Adl@ Adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX148637 YY158, nrde-3(gg066)|adult C. elegans|adult Adl@ Adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX148638 YY453, nrde-4(gg129)|adult C. elegans|adult Adl@ Adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX148639 SS104, glp-4(bn2)|adult C. elegans|adult Adl@ Adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX5073498 DLS422|Whole animals|Day 1 adults Adl@ Adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX5073500 DLS435|Whole animals|Day 1 adults Adl@ Adult?0 1 2 https://www.ncbi.nlm.nih.gov/sra?term=SRX1030169 whole worm WT gDNA|WT (N2) mixed stage worms Adl@ Adult?0 1 2 https://www.ncbi.nlm.nih.gov/sra?term=SRX113600 eri-1(mg366)|adult C. elegans|adult Adl@ Adult?0 1 2 https://www.ncbi.nlm.nih.gov/sra?term=SRX3923761 DLS396|Whole animals|Day 1 adults Adl@ Adult?0 1 2 https://www.ncbi.nlm.nih.gov/sra?term=SRX4419811 FAS107|Adult total nuclei (enriched for germ cell nuclei)|adult Adl@ Adult?0 1 2 https://www.ncbi.nlm.nih.gov/sra?term=SRX4419813 FAS119|Adult total nuclei (enriched for germ cell nuclei)|adult Adl@ Adult?0 1 2 https://www.ncbi.nlm.nih.gov/sra?term=SRX4419821 FAS100|Adult total nuclei (enriched for germ cell nuclei)|adult Adl@ Adult?0 1 2 https://www.ncbi.nlm.nih.gov/sra?term=SRX4419823 FAS104|Adult total nuclei (enriched for germ cell nuclei)|adult Adl@ Adult?0 1 2 https://www.ncbi.nlm.nih.gov/sra?term=SRX4419827 CGC42|Adult total nuclei (enriched for germ cell nuclei)|adult Adl@ Adult?0 1 2 https://www.ncbi.nlm.nih.gov/sra?term=SRX4419829 FAS93|Adult total nuclei (enriched for germ cell nuclei)|adult Adl@ Adult?0 1 2 https://www.ncbi.nlm.nih.gov/sra?term=SRX5073496 OP201|Whole animals|Day 1 adults Adl@ Adult?0 1 4 https://www.ncbi.nlm.nih.gov/sra?term=SRX3923758 DLS395|Whole animals|Day 1 adults Adl@ Adult?0 1 4 https://www.ncbi.nlm.nih.gov/sra?term=SRX4419807 N2|Adult total nuclei (enriched for germ cell nuclei)|adult Adl@ Adult?0 1 4 https://www.ncbi.nlm.nih.gov/sra?term=SRX4419809 FAS58|Adult total nuclei (enriched for germ cell nuclei)|adult Adl@ Adult?0 1 5 https://www.ncbi.nlm.nih.gov/sra?term=SRX958294 whole animal|whole animal|adult Adl@ Adult?0 1 6 https://www.ncbi.nlm.nih.gov/sra?term=SRX5709759 N2; Ispvha-6::klf-1-yfp|Whole organism|Whole body|First day of adulthood Adl@ Adult?0 1 6 https://www.ncbi.nlm.nih.gov/sra?term=SRX5709765 isp-1(qm150); ctb-1(qm189); Ispvha-6::klf-1-yfp|Whole organism|Whole body|First day of adulthood Adl@ Adult?0 1 7 https://www.ncbi.nlm.nih.gov/sra?term=SRX113605 wild type|adult C. elegans|adult Adl@ Adult?0 1 7 https://www.ncbi.nlm.nih.gov/sra?term=SRX3942553 Whole body adult stage Adl@ Adult?0 1 2 https://www.ncbi.nlm.nih.gov/sra?term=SRX8392413 dve-1p::dve-1::gfp; glp-4(bn2)|DVE-1_input (hda-1)|Day1 of adulthood Adl@ Adult body?0 1 2 https://www.ncbi.nlm.nih.gov/sra?term=SRX8392415 dve-1p::dve-1::gfp; glp-4(bn2)|DVE-1_input (hda-1+atp-2)|Day1 of adulthood Adl@ Adult body?0 1 2 https://www.ncbi.nlm.nih.gov/sra?term=SRX8392417 dve-1p::dve-1::gfp; glp-4(bn2)|DVE-1_ChIP (hda-1)|Day1 of adulthood Adl@ Adult body?0 1 2 https://www.ncbi.nlm.nih.gov/sra?term=SRX8392419 dve-1p::dve-1::gfp; glp-4(bn2)|DVE-1_ChIP (hda-1+atp-2)|Day1 of adulthood Adl@ Adult body?0 1 3 https://www.ncbi.nlm.nih.gov/sra?term=SRX8392421 hda-1p::hda-1::gfp; glp-4(bn2)|HDA-1_input (dve-1)|Day1 of adulthood Adl@ Adult body?0 1 3 https://www.ncbi.nlm.nih.gov/sra?term=SRX8392424 hda-1p::hda-1::gfp; glp-4(bn2)|HDA-1_input (dve-1+atp-2)|Day1 of adulthood Adl@ Adult body?0 1 3 https://www.ncbi.nlm.nih.gov/sra?term=SRX8392427 hda-1p::hda-1::gfp; glp-4(bn2)|HDA-1_ChIP (dve-1)|Day1 of adulthood Adl@ Adult body?0 1 3 https://www.ncbi.nlm.nih.gov/sra?term=SRX8392430 hda-1p::hda-1::gfp; glp-4(bn2)|HDA-1_ChIP (dve-1+atp-2)|Day1 of adulthood Adl@ Adult body?0 1 8 https://www.ncbi.nlm.nih.gov/sra?term=SRX7217778 hda-1p::hda-1::gfp; glp-4(bn2)|the whole organism|Day1 of adulthood Adl@ Adult body?0 1 8 https://www.ncbi.nlm.nih.gov/sra?term=SRX7217786 dve-1p::dve-1::gfp; glp-4(bn2)|the whole organism|Day1 of adulthood Adl@ Adult body?0 1 6 https://www.ncbi.nlm.nih.gov/sra?term=SRX7971790 N2|Isolated germ nuclei from wild-type adults|Isolated germ nuclei|Young adult Adl@ Germline cells?0 1 6 https://www.ncbi.nlm.nih.gov/sra?term=SRX7971794 YL585|Isolated germ nuclei from oef-1(vr25) mutant adults|Isolated germ nuclei|Young adult Adl@ Germline cells?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331337 fem-2(b245)|seq-Ab2621_H3K79me3_FEM2_AD_Input_Rep1|Germline containing young adult Adl@ Germline containing young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331338 fem-2(b245)|seq-Ab2621_H3K79me3_FEM2_AD_Input_Rep2|Germline containing young adult Adl@ Germline containing young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331340 fem-2(b245)|seq-Ab2621_H3K79me3_FEM2_AD_ChIP_Rep2|Germline containing young adult Adl@ Germline containing young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331349 fem-2(b245)|seq-HK72A9_H4K8ac_FEM2_AD_Input_Rep1|Germline containing young adult Adl@ Germline containing young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331350 fem-2(b245)|seq-HK72A9_H4K8ac_FEM2_AD_Input_Rep2|Germline containing young adult Adl@ Germline containing young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331351 fem-2(b245)|seq-HK72A9_H4K8ac_FEM2_AD_ChIP_Rep1|Germline containing young adult Adl@ Germline containing young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331352 fem-2(b245)|seq-HK72A9_H4K8ac_FEM2_AD_ChIP_Rep2|Germline containing young adult Adl@ Germline containing young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX466563 fem-2(b245)|seq-SDQ0812_COH1_FEM2_AD_Input_Rep1|Germline containing young adult Adl@ Germline containing young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX466564 fem-2(b245)|seq-SDQ0812_COH1_FEM2_AD_Input_Rep2|Germline containing young adult Adl@ Germline containing young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX466565 fem-2(b245)|seq-SDQ0812_COH1_FEM2_AD_ChIP_Rep1|Germline containing young adult Adl@ Germline containing young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX466566 fem-2(b245)|seq-SDQ0812_COH1_FEM2_AD_ChIP_Rep2|Germline containing young adult Adl@ Germline containing young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX466567 fem-2(b245)|seq-SDQ0821_SCC1_FEM2_AD_Input_Rep1|Germline containing young adult Adl@ Germline containing young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX466568 fem-2(b245)|seq-SDQ0821_SCC1_FEM2_AD_ChIP_Rep1|Germline containing young adult Adl@ Germline containing young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX466569 fem-2(b245)|seq-SDQ1665_1666_MRG1_FEM2_AD_Input_Rep1|Germline containing young adult Adl@ Germline containing young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX466570 fem-2(b245)|seq-SDQ1665_1666_MRG1_FEM2_AD_Input_Rep2|Germline containing young adult Adl@ Germline containing young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX466571 fem-2(b245)|seq-SDQ1665_1666_MRG1_FEM2_AD_ChIP_Rep1|Germline containing young adult Adl@ Germline containing young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX466572 fem-2(b245)|seq-SDQ1665_1666_MRG1_FEM2_AD_ChIP_Rep2|Germline containing young adult Adl@ Germline containing young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX466575 fem-2(b245)|seq-SDQ2972_HIM8_FEM2_AD_ChIP_Rep1|Germline containing young adult Adl@ Germline containing young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX466576 fem-2(b245)|seq-SDQ2972_HIM8_FEM2_AD_ChIP_Rep2|Germline containing young adult Adl@ Germline containing young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX466581 fem-2(b245)|seq-SDQ3898_KLE2_FEM2_AD_Input_Rep1|Germline containing young adult Adl@ Germline containing young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX466582 fem-2(b245)|seq-SDQ3898_KLE2_FEM2_AD_Input_Rep2|Germline containing young adult Adl@ Germline containing young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX466583 fem-2(b245)|seq-SDQ3898_KLE2_FEM2_AD_ChIP_Rep1|Germline containing young adult Adl@ Germline containing young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX466584 fem-2(b245)|seq-SDQ3898_KLE2_FEM2_AD_ChIP_Rep2|Germline containing young adult Adl@ Germline containing young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX494823 fem-2(b245)|seq-SDQ0801_HIM17_FEM2_AD_Input_Rep1|Germline containing young adult Adl@ Germline containing young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX494824 fem-2(b245)|seq-SDQ0801_HIM17_FEM2_AD_Input_Rep2|Germline containing young adult Adl@ Germline containing young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX494825 fem-2(b245)|seq-SDQ0801_HIM17_FEM2_AD_ChIP_Rep1|Germline containing young adult Adl@ Germline containing young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX494826 fem-2(b245)|seq-SDQ0801_HIM17_FEM2_AD_ChIP_Rep2|Germline containing young adult Adl@ Germline containing young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX494827 fem-2(b245)|seq-SDQ0811_RAD51_FEM2_AD_Input_Rep1|Germline containing young adult Adl@ Germline containing young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX494856 fem-2(b245)|seq-Ab52946_H3K14ac_FEM2_AD_Input_Rep1|Germline containing young adult Adl@ Germline containing young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX494857 fem-2(b245)|seq-Ab52946_H3K14ac_FEM2_AD_Input_Rep2|Germline containing young adult Adl@ Germline containing young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX494858 fem-2(b245)|seq-Ab52946_H3K14ac_FEM2_AD_ChIP_Rep1|Germline containing young adult Adl@ Germline containing young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX494859 fem-2(b245)|seq-Ab52946_H3K14ac_FEM2_AD_ChIP_Rep2|Germline containing young adult Adl@ Germline containing young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX494860 fem-2(b245)|seq-SDQ0835_SCC1_FEM2_AD_Input_Rep1|Germline containing young adult Adl@ Germline containing young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX494861 fem-2(b245)|seq-SDQ0835_SCC1_FEM2_AD_ChIP_Rep1|Germline containing young adult Adl@ Germline containing young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX494862 fem-2(b245)|seq-SDQ2356_MRE11_FEM2_AD_Input_Rep1|Germline containing young adult Adl@ Germline containing young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX494863 fem-2(b245)|seq-SDQ2356_MRE11_FEM2_AD_Input_Rep2|Germline containing young adult Adl@ Germline containing young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX494864 fem-2(b245)|seq-SDQ2356_MRE11_FEM2_AD_ChIP_Rep2|Germline containing young adult Adl@ Germline containing young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX494865 fem-2(b245)|seq-SDQ2366_MRE11_FEM2_AD_Input_Rep1|Germline containing young adult Adl@ Germline containing young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX494866 fem-2(b245)|seq-SDQ2366_MRE11_FEM2_AD_Input_Rep2|Germline containing young adult Adl@ Germline containing young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX494867 fem-2(b245)|seq-SDQ2366_MRE11_FEM2_AD_ChIP_Rep1|Germline containing young adult Adl@ Germline containing young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX494868 fem-2(b245)|seq-SDQ2366_MRE11_FEM2_AD_ChIP_Rep2|Germline containing young adult Adl@ Germline containing young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX494869 fem-2(b245)|seq-SDQ3849_CHD3_FEM2_AD_Input_Rep2|Germline containing young adult Adl@ Germline containing young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX494870 fem-2(b245)|seq-SDQ3849_CHD3_FEM2_AD_ChIP_Rep2|Germline containing young adult Adl@ Germline containing young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX494871 fem-2(b245)|seq-SDQ3853_MSH5_FEM2_AD_Input_Rep1|Germline containing young adult Adl@ Germline containing young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX494872 fem-2(b245)|seq-SDQ3853_MSH5_FEM2_AD_Input_Rep2|Germline containing young adult Adl@ Germline containing young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX494873 fem-2(b245)|seq-SDQ3853_MSH5_FEM2_AD_ChIP_Rep1|Germline containing young adult Adl@ Germline containing young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX494874 fem-2(b245)|seq-SDQ3853_MSH5_FEM2_AD_ChIP_Rep2|Germline containing young adult Adl@ Germline containing young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX494875 fem-2(b245)|seq-SDQ3866_MRE11_FEM2_AD_Input_Rep1|Germline containing young adult Adl@ Germline containing young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX494876 fem-2(b245)|seq-SDQ3866_MRE11_FEM2_AD_Input_Rep2|Germline containing young adult Adl@ Germline containing young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX494877 fem-2(b245)|seq-SDQ3866_MRE11_FEM2_AD_ChIP_Rep2|Germline containing young adult Adl@ Germline containing young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX494878 fem-2(b245)|seq-SDQ3907_CHD3_FEM2_AD_Input_Rep1|Germline containing young adult Adl@ Germline containing young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX494879 fem-2(b245)|seq-SDQ3907_CHD3_FEM2_AD_Input_Rep2|Germline containing young adult Adl@ Germline containing young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX494880 fem-2(b245)|seq-SDQ3907_CHD3_FEM2_AD_ChIP_Rep1|Germline containing young adult Adl@ Germline containing young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX494881 fem-2(b245)|seq-SDQ3907_CHD3_FEM2_AD_ChIP_Rep2|Germline containing young adult Adl@ Germline containing young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX494882 fem-2(b245)|seq-SDQ3925_ZHP3_FEM2_AD_Input_Rep1|Germline containing young adult Adl@ Germline containing young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX494883 fem-2(b245)|seq-SDQ3925_ZHP3_FEM2_AD_Input_Rep2|Germline containing young adult Adl@ Germline containing young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX494884 fem-2(b245)|seq-SDQ3925_ZHP3_FEM2_AD_ChIP_Rep1|Germline containing young adult Adl@ Germline containing young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX494889 fem-2(b245)|seq-SDQ3942_KLE2_FEM2_AD_ChIP_Rep1|Germline containing young adult Adl@ Germline containing young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX494890 fem-2(b245)|seq-SDQ3948_COH3_FEM2_AD_Input_Rep1|Germline containing young adult Adl@ Germline containing young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX494891 fem-2(b245)|seq-SDQ3948_COH3_FEM2_AD_Input_Rep2|Germline containing young adult Adl@ Germline containing young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX494892 fem-2(b245)|seq-SDQ3948_COH3_FEM2_AD_ChIP_Rep1|Germline containing young adult Adl@ Germline containing young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX494893 fem-2(b245)|seq-SDQ3948_COH3_FEM2_AD_ChIP_Rep2|Germline containing young adult Adl@ Germline containing young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX494894 fem-2(b245)|seq-SDQ3949_ZIM3_FEM2_AD_Input_Rep1|Germline containing young adult Adl@ Germline containing young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX494895 fem-2(b245)|seq-SDQ3949_ZIM3_FEM2_AD_Input_Rep2|Germline containing young adult Adl@ Germline containing young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX494896 fem-2(b245)|seq-SDQ3949_ZIM3_FEM2_AD_ChIP_Rep1|Germline containing young adult Adl@ Germline containing young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX494897 fem-2(b245)|seq-SDQ3949_ZIM3_FEM2_AD_ChIP_Rep2|Germline containing young adult Adl@ Germline containing young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX494898 fem-2(b245)|seq-SDQ3953_REC8_FEM2_AD_Input_Rep1|Germline containing young adult Adl@ Germline containing young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX494899 fem-2(b245)|seq-SDQ3953_REC8_FEM2_AD_Input_Rep2|Germline containing young adult Adl@ Germline containing young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX494900 fem-2(b245)|seq-SDQ3953_REC8_FEM2_AD_ChIP_Rep1|Germline containing young adult Adl@ Germline containing young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX494901 fem-2(b245)|seq-SDQ3953_REC8_FEM2_AD_ChIP_Rep2|Germline containing young adult Adl@ Germline containing young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX494902 fem-2(b245)|seq-SDQ3956_ZHP3_FEM2_AD_Input_Rep1|Germline containing young adult Adl@ Germline containing young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX494903 fem-2(b245)|seq-SDQ3956_ZHP3_FEM2_AD_Input_Rep2|Germline containing young adult Adl@ Germline containing young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX494904 fem-2(b245)|seq-SDQ3956_ZHP3_FEM2_AD_ChIP_Rep1|Germline containing young adult Adl@ Germline containing young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX494905 fem-2(b245)|seq-SDQ3956_ZHP3_FEM2_AD_ChIP_Rep2|Germline containing young adult Adl@ Germline containing young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX494906 fem-2(b245)|seq-SDQ3965_ZIM1_FEM2_AD_Input_Rep1|Germline containing young adult Adl@ Germline containing young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX494907 fem-2(b245)|seq-SDQ3965_ZIM1_FEM2_AD_Input_Rep2|Germline containing young adult Adl@ Germline containing young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX494908 fem-2(b245)|seq-SDQ3965_ZIM1_FEM2_AD_ChIP_Rep1|Germline containing young adult Adl@ Germline containing young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX494909 fem-2(b245)|seq-SDQ3965_ZIM1_FEM2_AD_ChIP_Rep2|Germline containing young adult Adl@ Germline containing young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX494910 fem-2(b245)|seq-SDQ3972_COH3_FEM2_AD_Input_Rep1|Germline containing young adult Adl@ Germline containing young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX494911 fem-2(b245)|seq-SDQ3972_COH3_FEM2_AD_Input_Rep2|Germline containing young adult Adl@ Germline containing young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX494912 fem-2(b245)|seq-SDQ3972_COH3_FEM2_AD_ChIP_Rep1|Germline containing young adult Adl@ Germline containing young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX494913 fem-2(b245)|seq-SDQ3972_COH3_FEM2_AD_ChIP_Rep2|Germline containing young adult Adl@ Germline containing young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX494914 fem-2(b245)|seq-SDQ3989_ASH2_FEM2_AD_Input_Rep1|Germline containing young adult Adl@ Germline containing young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX494915 fem-2(b245)|seq-SDQ3989_ASH2_FEM2_AD_Input_Rep2|Germline containing young adult Adl@ Germline containing young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX494916 fem-2(b245)|seq-SDQ3989_ASH2_FEM2_AD_ChIP_Rep1|Germline containing young adult Adl@ Germline containing young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX494917 fem-2(b245)|seq-SDQ3989_ASH2_FEM2_AD_ChIP_Rep2|Germline containing young adult Adl@ Germline containing young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX494918 fem-2(b245)|seq-SDQ4068_MRG1_FEM2_AD_Input_Rep1|Germline containing young adult Adl@ Germline containing young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX494919 fem-2(b245)|seq-SDQ4068_MRG1_FEM2_AD_Input_Rep2|Germline containing young adult Adl@ Germline containing young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX494920 fem-2(b245)|seq-SDQ4068_MRG1_FEM2_AD_ChIP_Rep1|Germline containing young adult Adl@ Germline containing young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX494921 fem-2(b245)|seq-SDQ4068_MRG1_FEM2_AD_ChIP_Rep2|Germline containing young adult Adl@ Germline containing young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX494922 fem-2(b245)|seq-SDQ4498_HIM3_FEM2_AD_Input_Rep1|Germline containing young adult Adl@ Germline containing young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX494923 fem-2(b245)|seq-SDQ4498_HIM3_FEM2_AD_ChIP_Rep1|Germline containing young adult Adl@ Germline containing young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX494924 fem-2(b245)|seq-SDQ4713_HIM3_FEM2_AD_Input_Rep1|Germline containing young adult Adl@ Germline containing young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX494925 fem-2(b245)|seq-SDQ4713_HIM3_FEM2_AD_Input_Rep2|Germline containing young adult Adl@ Germline containing young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX494927 fem-2(b245)|seq-WA30335199_H3Ser10_FEM2_AD_Input_Rep1|Germline containing young adult Adl@ Germline containing young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX494928 fem-2(b245)|seq-WA30335199_H3Ser10_FEM2_AD_Input_Rep2|Germline containing young adult Adl@ Germline containing young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX494929 fem-2(b245)|seq-WA30335199_H3Ser10_FEM2_AD_ChIP_Rep1|Germline containing young adult Adl@ Germline containing young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX494930 fem-2(b245)|seq-WA30335199_H3Ser10_FEM2_AD_ChIP_Rep2|Germline containing young adult Adl@ Germline containing young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX494931 fem-2(b245)|seq-WA30534799_H3K4me1_FEM2_AD_Input_Rep1|Germline containing young adult Adl@ Germline containing young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX494932 fem-2(b245)|seq-WA30534799_H3K4me1_FEM2_AD_Input_Rep2|Germline containing young adult Adl@ Germline containing young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX494933 fem-2(b245)|seq-WA30534799_H3K4me1_FEM2_AD_ChIP_Rep1|Germline containing young adult Adl@ Germline containing young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX494934 fem-2(b245)|seq-WA30534799_H3K4me1_FEM2_AD_ChIP_Rep2|Germline containing young adult Adl@ Germline containing young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX494935 WH223|seq-ab45142_H2AK5ac_ojIs9_YA_germline_Input_Rep1|Germline containing young adult Adl@ Germline containing young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX494936 WH223|seq-ab45142_H2AK5ac_ojIs9_YA_germline_Input_Rep2|Germline containing young adult Adl@ Germline containing young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX494937 WH223|seq-ab45142_H2AK5ac_ojIs9_YA_germline_ChIP_Rep1|Germline containing young adult Adl@ Germline containing young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX494938 WH223|seq-ab45142_H2AK5ac_ojIs9_YA_germline_ChIP_Rep2|Germline containing young adult Adl@ Germline containing young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX494939 fem-2(b245)|seq-ab45142_H2AK5ac_FEM2_YA_Input_Rep1|Germline containing young adult Adl@ Germline containing young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX494940 fem-2(b245)|seq-ab45142_H2AK5ac_FEM2_YA_Input_Rep2|Germline containing young adult Adl@ Germline containing young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX494941 fem-2(b245)|seq-ab45142_H2AK5ac_FEM2_YA_ChIP_Rep1|Germline containing young adult Adl@ Germline containing young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX494942 fem-2(b245)|seq-ab45142_H2AK5ac_FEM2_YA_ChIP_Rep2|Germline containing young adult Adl@ Germline containing young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX494943 WH223|seq-WA30834809_H3K4me2_ojIs9_YA_germline_Input_Rep1|Germline containing young adult Adl@ Germline containing young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX494944 WH223|seq-WA30834809_H3K4me2_ojIs9_YA_germline_Input_Rep2|Germline containing young adult Adl@ Germline containing young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX494945 WH223|seq-WA30834809_H3K4me2_ojIs9_YA_germline_ChIP_Rep1|Germline containing young adult Adl@ Germline containing young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX494946 WH223|seq-WA30834809_H3K4me2_ojIs9_YA_germline_ChIP_Rep2|Germline containing young adult Adl@ Germline containing young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX494978 fem-2(b245)|seq-SDQ4625_T09A5.8_FEM2_AD_Input_Rep1|Germline containing young adult Adl@ Germline containing young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX494979 fem-2(b245)|seq-SDQ4625_T09A5.8_FEM2_AD_Input_Rep2|Germline containing young adult Adl@ Germline containing young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX494980 fem-2(b245)|seq-SDQ4625_T09A5.8_FEM2_AD_ChIP_Rep1|Germline containing young adult Adl@ Germline containing young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX494981 fem-2(b245)|seq-SDQ4625_T09A5.8_FEM2_AD_ChIP_Rep2|Germline containing young adult Adl@ Germline containing young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX495025 fem-2(b245)|seq-Ab9048_H3K36me1_fem2_AD_Input_Rep1|Germline containing young adult Adl@ Germline containing young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX495026 fem-2(b245)|seq-Ab9048_H3K36me1_fem2_AD_Input_Rep2|Germline containing young adult Adl@ Germline containing young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX495027 fem-2(b245)|seq-Ab9048_H3K36me1_fem2_AD_ChIP_Rep1|Germline containing young adult Adl@ Germline containing young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX495028 fem-2(b245)|seq-Ab9048_H3K36me1_fem2_AD_ChIP_Rep2|Germline containing young adult Adl@ Germline containing young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX495029 fem-2(b245)|seq-Ab8895_H3K4me1_fem2_AD_Input_Rep1|Germline containing young adult Adl@ Germline containing young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX495030 fem-2(b245)|seq-Ab8895_H3K4me1_fem2_AD_Input_Rep2|Germline containing young adult Adl@ Germline containing young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX495031 fem-2(b245)|seq-Ab8895_H3K4me1_fem2_AD_ChIP_Rep1|Germline containing young adult Adl@ Germline containing young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX495032 fem-2(b245)|seq-Ab8895_H3K4me1_fem2_AD_ChIP_Rep2|Germline containing young adult Adl@ Germline containing young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX495037 fem-2(b245)|seq-Ab6002_H3K27me3_fem2_AD_Input_Rep1|Germline containing young adult Adl@ Germline containing young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX495038 fem-2(b245)|seq-Ab6002_H3K27me3_fem2_AD_Input_Rep2|Germline containing young adult Adl@ Germline containing young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX495039 fem-2(b245)|seq-Ab6002_H3K27me3_fem2_AD_ChIP_Rep1|Germline containing young adult Adl@ Germline containing young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX495040 fem-2(b245)|seq-Ab6002_H3K27me3_fem2_AD_ChIP_Rep2|Germline containing young adult Adl@ Germline containing young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX495041 fem-2(b245)|seq-HK00001-H3K36me3_13C9_fem2_AD_Input_Rep1|Germline containing young adult Adl@ Germline containing young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX495042 fem-2(b245)|seq-HK00001-H3K36me3_13C9_fem2_AD_Input_Rep2|Germline containing young adult Adl@ Germline containing young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX495043 fem-2(b245)|seq-HK00001-H3K36me3_13C9_fem2_AD_ChIP_Rep1|Germline containing young adult Adl@ Germline containing young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX495044 fem-2(b245)|seq-HK00001-H3K36me3_13C9_fem2_AD_ChIP_Rep2|Germline containing young adult Adl@ Germline containing young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX495061 fem-2(b245)|seq-G0655G0656_HTP3_fem2_AD_Input_Rep1|Germline containing young adult Adl@ Germline containing young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX495062 fem-2(b245)|seq-G0655G0656_HTP3_fem2_AD_Input_Rep2|Germline containing young adult Adl@ Germline containing young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX495063 fem-2(b245)|seq-G0655G0656_HTP3_fem2_AD_ChIP_Rep1|Germline containing young adult Adl@ Germline containing young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX495064 fem-2(b245)|seq-G0655G0656_HTP3_fem2_AD_ChIP_Rep2|Germline containing young adult Adl@ Germline containing young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX495065 fem-2(b245)|seq-SDQ0802_REC8_fem2_AD_Input_Rep1|Germline containing young adult Adl@ Germline containing young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX495066 fem-2(b245)|seq-SDQ0802_REC8_fem2_AD_Input_Rep2|Germline containing young adult Adl@ Germline containing young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX495067 fem-2(b245)|seq-SDQ0802_REC8_fem2_AD_ChIP_Rep1|Germline containing young adult Adl@ Germline containing young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX495068 fem-2(b245)|seq-SDQ0802_REC8_fem2_AD_ChIP_Rep2|Germline containing young adult Adl@ Germline containing young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX495069 fem-2(b245)|seq-SDQ3914_REC8_fem2_AD_Input_Rep1|Germline containing young adult Adl@ Germline containing young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX495070 fem-2(b245)|seq-SDQ3914_REC8_fem2_AD_Input_Rep2|Germline containing young adult Adl@ Germline containing young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX495071 fem-2(b245)|seq-SDQ3914_REC8_fem2_AD_ChIP_Rep1|Germline containing young adult Adl@ Germline containing young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX495072 fem-2(b245)|seq-SDQ3914_REC8_fem2_AD_ChIP_Rep2|Germline containing young adult Adl@ Germline containing young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX495077 fem-2(b245)|seq-SDQ0809_COH1_fem2_AD_Input_Rep1|Germline containing young adult Adl@ Germline containing young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX495078 fem-2(b245)|seq-SDQ0809_COH1_fem2_AD_Input_Rep2|Germline containing young adult Adl@ Germline containing young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX495079 fem-2(b245)|seq-SDQ0809_COH1_fem2_AD_ChIP_Rep1|Germline containing young adult Adl@ Germline containing young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX495080 fem-2(b245)|seq-SDQ0809_COH1_fem2_AD_ChIP_Rep2|Germline containing young adult Adl@ Germline containing young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX495101 fem-2(b245)|seq-SDQ2382_him5_fem2_AD_Input_Rep1|Germline containing young adult Adl@ Germline containing young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX495102 fem-2(b245)|seq-SDQ2382_him5_fem2_AD_Input_Rep2|Germline containing young adult Adl@ Germline containing young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX495103 fem-2(b245)|seq-SDQ2382_him5_fem2_AD_ChIP_Rep1|Germline containing young adult Adl@ Germline containing young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX495104 fem-2(b245)|seq-SDQ2382_him5_fem2_AD_ChIP_Rep2|Germline containing young adult Adl@ Germline containing young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX495105 WH223|seq-302-32369_H3K9me2_ojIs9_YA_germline_Input_Rep1|Germline containing young adult Adl@ Germline containing young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX495106 WH223|seq-302-32369_H3K9me2_ojIs9_YA_germline_Input_Rep2|Germline containing young adult Adl@ Germline containing young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX495107 WH223|seq-302-32369_H3K9me2_ojIs9_YA_germline_ChIP_Rep1|Germline containing young adult Adl@ Germline containing young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX495108 WH223|seq-302-32369_H3K9me2_ojIs9_YA_germline_ChIP_Rep2|Germline containing young adult Adl@ Germline containing young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX495121 fem-2(b245)|seq-SDQ5413_CEC7_fem2_AD_Input_Rep2|Germline containing young adult Adl@ Germline containing young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX495122 fem-2(b245)|seq-SDQ5413_CEC7_fem2_AD_ChIP_Rep2|Germline containing young adult Adl@ Germline containing young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX495123 fem-2(b245)|seq-SDQ5421_CEC7_fem2_AD_Input_Rep1|Germline containing young adult Adl@ Germline containing young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX495124 fem-2(b245)|seq-SDQ5421_CEC7_fem2_AD_ChIP_Rep1|Germline containing young adult Adl@ Germline containing young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX529214 fem-2(b245)|seq-SDQ4501_T09A5.8_FEM2_AD_Input_Rep1|Germline containing young adult Adl@ Germline containing young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX529215 fem-2(b245)|seq-SDQ4501_T09A5.8_FEM2_AD_Input_Rep2|Germline containing young adult Adl@ Germline containing young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX529216 fem-2(b245)|seq-SDQ4501_T09A5.8_FEM2_AD_ChIP_Rep1|Germline containing young adult Adl@ Germline containing young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX529217 fem-2(b245)|seq-SDQ4501_T09A5.8_FEM2_AD_ChIP_Rep2|Germline containing young adult Adl@ Germline containing young adult?0 1 8 https://www.ncbi.nlm.nih.gov/sra?term=SRX4200528 Ovulated but unfertilized oocytes collected from feminized worms Adl@ Oocytes?0 1 8 https://www.ncbi.nlm.nih.gov/sra?term=SRX4200530 Mature sperm isolated from adult males Adl@ Sperm?0 1 3 https://www.ncbi.nlm.nih.gov/sra?term=SRX4029333 whole worms|whole worms Adl@ Whole body?0 1 12 https://www.ncbi.nlm.nih.gov/sra?term=SRX3008761 frozen whole worms|whole worms Adl@ Whole worm?0 1 12 https://www.ncbi.nlm.nih.gov/sra?term=SRX743640 glp-1(e2141)|whole animal Adl@ Whole worm?0 1 14 https://www.ncbi.nlm.nih.gov/sra?term=SRX4626826 whole animal|whole animal Adl@ Whole worm?0 1 16 https://www.ncbi.nlm.nih.gov/sra?term=SRX6619530 baz2(tm0235)|The whole worm Adl@ Whole worm?0 1 16 https://www.ncbi.nlm.nih.gov/sra?term=SRX6619538 set6(ok2195)|The whole worm Adl@ Whole worm?0 1 16 https://www.ncbi.nlm.nih.gov/sra?term=SRX6619546 baz2(tm0235)set6(ok2195)|The whole worm Adl@ Whole worm?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX2035135 WT_AA_Input|whole body|L3-L4 mix Adl@ Whole worm?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX2035138 WT_NT_Input|whole body|L3-L4 mix Adl@ Whole worm?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX4344417 RIE470_4|whole animal Adl@ Whole worm?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX4344426 RIE470_2|whole animal Adl@ Whole worm?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX4344456 RIE328_2|whole animal Adl@ Whole worm?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX4344458 RIE328_4|whole animal Adl@ Whole worm?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX4344460 RIE531_2|whole animal Adl@ Whole worm?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX6720161 CB1370_4|whole animal Adl@ Whole worm?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX6720163 GR1895_2|whole animal Adl@ Whole worm?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX6720165 GR1895_4|whole animal Adl@ Whole worm?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX6720167 RIE384_2|whole animal Adl@ Whole worm?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX6720169 RIE500_4|whole animal Adl@ Whole worm?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX6720171 RIE500_6|whole animal Adl@ Whole worm?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX6720173 CB1370_8|whole animal Adl@ Whole worm?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX6720175 RIE500_2|whole animal Adl@ Whole worm?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX6720177 RIE500_8|whole animal Adl@ Whole worm?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX6720188 CB1370_6|whole animal Adl@ Whole worm?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX6720190 CB1370_2|whole animal Adl@ Whole worm?0 1 20 https://www.ncbi.nlm.nih.gov/sra?term=SRX6619542 Bristol N2|The whole worm Adl@ Whole worm?0 1 24 https://www.ncbi.nlm.nih.gov/sra?term=SRX3043399 glp-1(e2141)|whole animal|whole animal Adl@ Whole worm?0 1 2 https://www.ncbi.nlm.nih.gov/sra?term=SRX1844113 C. elegans whole worm lysate Adl@ Whole worm?0 1 2 https://www.ncbi.nlm.nih.gov/sra?term=SRX2035133 WT_AA_H3K4me3|whole body|L3-L4 mix Adl@ Whole worm?0 1 2 https://www.ncbi.nlm.nih.gov/sra?term=SRX2035136 WT_NT_H3K4me3|whole body|L3-L4 mix Adl@ Whole worm?0 1 2 https://www.ncbi.nlm.nih.gov/sra?term=SRX5702594 mixed|mixed stage populations|whole animal|mixed Adl@ Whole worm?0 1 2 https://www.ncbi.nlm.nih.gov/sra?term=SRX5702597 jhdm-1 (ok2364)|mixed stage populations|whole animal|mixed Adl@ Whole worm?0 1 3 https://www.ncbi.nlm.nih.gov/sra?term=SRX2370184 nematode whole body Adl@ Whole worm?0 1 3 https://www.ncbi.nlm.nih.gov/sra?term=SRX5702591 wdr-5 (ok1417)|mixed stage populations|whole animal|mixed Adl@ Whole worm?0 1 4 https://www.ncbi.nlm.nih.gov/sra?term=SRX2582951 SX2966|whole animal,mixed population Adl@ Whole worm?0 1 4 https://www.ncbi.nlm.nih.gov/sra?term=SRX7627594 Bristol|whole animal|whole animal Adl@ Whole worm?0 1 5 https://www.ncbi.nlm.nih.gov/sra?term=SRX5702588 N2|mixed stage populations|whole animal|mixed Adl@ Whole worm?0 1 6 https://www.ncbi.nlm.nih.gov/sra?term=SRX7971802 SS104|Staged young adults from glp-4(bn2) strain|Whole animal|Young adult Adl@ Whole worm?0 1 6 https://www.ncbi.nlm.nih.gov/sra?term=SRX7971806 YL679|Staged young adults from glp-4(bn2); oef-1(vr25) strain|Whole animal|Young adult Adl@ Whole worm?0 1 10 https://www.ncbi.nlm.nih.gov/sra?term=SRX2350718 N2|Whole animal, young adult Adl@ Young adult?0 1 10 https://www.ncbi.nlm.nih.gov/sra?term=SRX2350720 morc-1(tm6048)|Whole animal, young adult Adl@ Young adult?0 1 11 https://www.ncbi.nlm.nih.gov/sra?term=SRX4456922 C. elegans young adults|young adult Adl@ Young adult?0 1 12 https://www.ncbi.nlm.nih.gov/sra?term=SRX554715 whole adult animals|young adult Adl@ Young adult?0 1 14 https://www.ncbi.nlm.nih.gov/sra?term=SRX373265 whole young adult worm lysates|young adult Adl@ Young adult?0 1 18 https://www.ncbi.nlm.nih.gov/sra?term=SRX1674086 Young adults Adl@ Young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX043963 N2(genotype : wild type genotype : DR subclone of DB original (Tc1 pattern I) official name : N2 )|Snyder_N2_POLII_YA_rep1 extraction1_seq1 channel_1|Young Adult Adl@ Young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX043964 N2(genotype : wild type genotype : DR subclone of DB original (Tc1 pattern I) official name : N2 )|Snyder_N2_POLII_YA_rep1 extraction1_seq1 channel_2|Young Adult Adl@ Young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX043965 N2(genotype : wild type genotype : DR subclone of DB original (Tc1 pattern I) official name : N2 )|Snyder_N2_POLII_YA_rep2 extraction2_seq1 channel_1|Young Adult Adl@ Young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX043966 N2(genotype : wild type genotype : DR subclone of DB original (Tc1 pattern I) official name : N2 )|Snyder_N2_POLII_YA_rep2 extraction2_seq1 channel_2|Young Adult Adl@ Young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX054205 OP37(official name : OP37 genotype : unc-119(ed3) III; wgIs37 unc-119(+) pha-4::TY1::EGFP::3xFLAG outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The PHA-4::EGFP fusion protein is expressed in the correct pha-4 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the PHA-4 transcription factor. made_by : R. Waterston and S. Kim )|Snyder_PHA-4_GFP_YA_rep2 extraction1_seq1 channel_1|Young Adult Adl@ Young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX054206 OP37(official name : OP37 genotype : unc-119(ed3) III; wgIs37 unc-119(+) pha-4::TY1::EGFP::3xFLAG outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The PHA-4::EGFP fusion protein is expressed in the correct pha-4 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the PHA-4 transcription factor. made_by : R. Waterston and S. Kim )|Snyder_PHA-4_GFP_YA_rep2 extraction2_seq2 channel_1|Young Adult Adl@ Young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX054207 OP37(official name : OP37 genotype : unc-119(ed3) III; wgIs37 unc-119(+) pha-4::TY1::EGFP::3xFLAG outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The PHA-4::EGFP fusion protein is expressed in the correct pha-4 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the PHA-4 transcription factor. made_by : R. Waterston and S. Kim )|Snyder_PHA-4_GFP_YA_rep2 extraction3_seq3 channel_1|Young Adult Adl@ Young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX054208 OP37(official name : OP37 genotype : unc-119(ed3) III; wgIs37 unc-119(+) pha-4::TY1::EGFP::3xFLAG outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The PHA-4::EGFP fusion protein is expressed in the correct pha-4 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the PHA-4 transcription factor. made_by : R. Waterston and S. Kim )|Snyder_PHA-4_GFP_YA_rep2 extraction4_seq4 channel_1|Young Adult Adl@ Young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX054209 OP37(official name : OP37 genotype : unc-119(ed3) III; wgIs37 unc-119(+) pha-4::TY1::EGFP::3xFLAG outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The PHA-4::EGFP fusion protein is expressed in the correct pha-4 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the PHA-4 transcription factor. made_by : R. Waterston and S. Kim )|Snyder_PHA-4_GFP_YA_rep2 extraction5_seq5 channel_1|Young Adult Adl@ Young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX054210 OP37(official name : OP37 genotype : unc-119(ed3) III; wgIs37 unc-119(+) pha-4::TY1::EGFP::3xFLAG outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The PHA-4::EGFP fusion protein is expressed in the correct pha-4 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the PHA-4 transcription factor. made_by : R. Waterston and S. Kim )|Snyder_PHA-4_GFP_YA_rep1 extraction6_seq6 channel_1|Young Adult Adl@ Young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX054211 OP37(official name : OP37 genotype : unc-119(ed3) III; wgIs37 unc-119(+) pha-4::TY1::EGFP::3xFLAG outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The PHA-4::EGFP fusion protein is expressed in the correct pha-4 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the PHA-4 transcription factor. made_by : R. Waterston and S. Kim )|Snyder_PHA-4_GFP_YA_rep1 extraction7_seq7 channel_1|Young Adult Adl@ Young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX065630 OP215(official name : OP215 genotype : unc119(ed3); wgIs215(W03F9.2::TY1 EGFP FLAG; unc119) outcross : 0 mutagen : None tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for bombardment transformation of an unc-119(ed3) strain. The W03F9.2::EGFP fusion protein is mainly expressed in germline cells. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the W03F9.2 transcription factor. made_by : Tony Hyman's lab from MPI-CBG )|Snyder_W03F9.2_Input_YA extraction1_seq1 channel_1|L4-Young Adult Adl@ Young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX065631 OP215(official name : OP215 genotype : unc119(ed3); wgIs215(W03F9.2::TY1 EGFP FLAG; unc119) outcross : 0 mutagen : None tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for bombardment transformation of an unc-119(ed3) strain. The W03F9.2::EGFP fusion protein is mainly expressed in germline cells. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the W03F9.2 transcription factor. made_by : Tony Hyman's lab from MPI-CBG )|Snyder_W03F9.2_Input_YA extraction2_seq2 channel_1|L4-Young Adult Adl@ Young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX065632 OP215(official name : OP215 genotype : unc119(ed3); wgIs215(W03F9.2::TY1 EGFP FLAG; unc119) outcross : 0 mutagen : None tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for bombardment transformation of an unc-119(ed3) strain. The W03F9.2::EGFP fusion protein is mainly expressed in germline cells. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the W03F9.2 transcription factor. made_by : Tony Hyman's lab from MPI-CBG )|Snyder_W03F9.2_GFP_YA_rep1 extraction3_seq3 channel_1|L4-Young Adult Adl@ Young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX065633 OP215(official name : OP215 genotype : unc119(ed3); wgIs215(W03F9.2::TY1 EGFP FLAG; unc119) outcross : 0 mutagen : None tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for bombardment transformation of an unc-119(ed3) strain. The W03F9.2::EGFP fusion protein is mainly expressed in germline cells. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the W03F9.2 transcription factor. made_by : Tony Hyman's lab from MPI-CBG )|Snyder_W03F9.2_GFP_YA_rep2 extraction4_seq4 channel_1|L4-Young Adult Adl@ Young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX146417 YL445(official name : YL445 genotype : unc119(ed3); vrIs81 pPIE-1::EFL-1::GFP FLAG: EFL-1 3?UTR genotype : unc-119 (+) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : made_by : )|Snyder_Ppie1_EFL1_Input_YA_rep1|Young Adult Adl@ Young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX146418 YL445(official name : YL445 genotype : unc119(ed3); vrIs81 pPIE-1::EFL-1::GFP FLAG: EFL-1 3?UTR genotype : unc-119 (+) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : made_by : )|Snyder_Ppie1_EFL1_Input_YA_rep2 extraction1_seq1|Young Adult Adl@ Young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX146419 YL445(official name : YL445 genotype : unc119(ed3); vrIs81 pPIE-1::EFL-1::GFP FLAG: EFL-1 3?UTR genotype : unc-119 (+) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : made_by : )|Snyder_Ppie1_EFL1_GFP_YA_rep1|Young Adult Adl@ Young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX146420 YL445(official name : YL445 genotype : unc119(ed3); vrIs81 pPIE-1::EFL-1::GFP FLAG: EFL-1 3?UTR genotype : unc-119 (+) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : made_by : )|Snyder_Ppie1_EFL1_GFP_YA_rep2|Young Adult Adl@ Young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX146421 YL390(official name : YL390 genotype : unc119(ed3); vrIs48 pPIE-1::DPL-1::GFP FLAG: DPL-1 3?UTR genotype : unc-119 (+) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : made_by : )|Snyder_Ppie1_DPL1_Input_YA_rep1|Young Adult Adl@ Young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX146422 YL390(official name : YL390 genotype : unc119(ed3); vrIs48 pPIE-1::DPL-1::GFP FLAG: DPL-1 3?UTR genotype : unc-119 (+) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : made_by : )|Snyder_Ppie1_DPL1_Input_YA_rep2|Young Adult Adl@ Young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX146423 YL390(official name : YL390 genotype : unc119(ed3); vrIs48 pPIE-1::DPL-1::GFP FLAG: DPL-1 3?UTR genotype : unc-119 (+) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : made_by : )|Snyder_Ppie1_DPL1_GFP_YA_rep1|Young Adult Adl@ Young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX146424 YL390(official name : YL390 genotype : unc119(ed3); vrIs48 pPIE-1::DPL-1::GFP FLAG: DPL-1 3?UTR genotype : unc-119 (+) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : made_by : )|Snyder_Ppie1_DPL1_GFP_YA_rep2|Young Adult Adl@ Young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX151400 OP600(official name : OP600 genotype : unc119(ed3); wgIs600(unc-62::TY1 EGFP FLAG; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The UNC-62::EGFP fusion protein is expressed in the correct unc-62 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the UNC-62 transcription factor. made_by : S Kim )|Snyder_UNC-62_Input_D4YA_rep1|Day Four Young Adult Adl@ Young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX151401 OP600(official name : OP600 genotype : unc119(ed3); wgIs600(unc-62::TY1 EGFP FLAG; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The UNC-62::EGFP fusion protein is expressed in the correct unc-62 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the UNC-62 transcription factor. made_by : S Kim )|Snyder_UNC-62_Input_D4YA_rep2|Day Four Young Adult Adl@ Young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX151402 OP600(official name : OP600 genotype : unc119(ed3); wgIs600(unc-62::TY1 EGFP FLAG; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The UNC-62::EGFP fusion protein is expressed in the correct unc-62 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the UNC-62 transcription factor. made_by : S Kim )|Snyder_UNC-62_GFP_D4YA_rep1|Day Four Young Adult Adl@ Young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX151403 OP600(official name : OP600 genotype : unc119(ed3); wgIs600(unc-62::TY1 EGFP FLAG; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The UNC-62::EGFP fusion protein is expressed in the correct unc-62 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the UNC-62 transcription factor. made_by : S Kim )|Snyder_UNC-62_GFP_D4YA_rep2|Day Four Young Adult Adl@ Young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX2202789 young adults, input EGS|whole body Adl@ Young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX2202790 young adults, input FRM|whole body Adl@ Young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX235166 YL402(official name : YL402 genotype : unc-119(ed3) III; vrIs56pPIE-1::LIN-35::GFP FLAG: LIN-35 3'-UTR genotype : unc-119 (+) outcross : 0 mutagen : None tags : GFP::3xFlag description : The LIN-35::GFP fusion protein is driven by the pie-1 promoter. made_by : Michelle Kudron in Reinke lab )|Snyder_LIN-35_GFP_yA_rep1_Input_TGCT|Young adult Adl@ Young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX235167 YL402(official name : YL402 genotype : unc-119(ed3) III; vrIs56pPIE-1::LIN-35::GFP FLAG: LIN-35 3'-UTR genotype : unc-119 (+) outcross : 0 mutagen : None tags : GFP::3xFlag description : The LIN-35::GFP fusion protein is driven by the pie-1 promoter. made_by : Michelle Kudron in Reinke lab )|Snyder_LIN-35_GFP_yA_rep2_Input_TGCT|Young adult Adl@ Young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX235168 YL402(official name : YL402 genotype : unc-119(ed3) III; vrIs56pPIE-1::LIN-35::GFP FLAG: LIN-35 3'-UTR genotype : unc-119 (+) outcross : 0 mutagen : None tags : GFP::3xFlag description : The LIN-35::GFP fusion protein is driven by the pie-1 promoter. made_by : Michelle Kudron in Reinke lab )|Snyder_LIN-35_GFP_yA_rep1_GFP_TGCT|Young adult Adl@ Young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX235169 YL402(official name : YL402 genotype : unc-119(ed3) III; vrIs56pPIE-1::LIN-35::GFP FLAG: LIN-35 3'-UTR genotype : unc-119 (+) outcross : 0 mutagen : None tags : GFP::3xFlag description : The LIN-35::GFP fusion protein is driven by the pie-1 promoter. made_by : Michelle Kudron in Reinke lab )|Snyder_LIN-35_GFP_yA_rep2_GFP_TGCT|Young adult Adl@ Young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331061 OP179(official name : OP179 genotype : unc-119(ed3) III; wgIs179 unc-119(+) gei-11::TY1::EGFP::3xFLAG outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The GEI-11::EGFP fusion protein is expressed in the correct gei-11 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the GEI-11 transcription factor. made_by : R. Waterston )|GEI-11_GFP_YA_Input_Rep1|Young Adult Adl@ Young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331062 OP179(official name : OP179 genotype : unc-119(ed3) III; wgIs179 unc-119(+) gei-11::TY1::EGFP::3xFLAG outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The GEI-11::EGFP fusion protein is expressed in the correct gei-11 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the GEI-11 transcription factor. made_by : R. Waterston )|GEI-11_GFP_YA_ChIP_Rep1|Young Adult Adl@ Young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331063 OP179(official name : OP179 genotype : unc-119(ed3) III; wgIs179 unc-119(+) gei-11::TY1::EGFP::3xFLAG outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The GEI-11::EGFP fusion protein is expressed in the correct gei-11 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the GEI-11 transcription factor. made_by : R. Waterston )|GEI-11_GFP_YA_Input_Rep2|Young Adult Adl@ Young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331064 OP179(official name : OP179 genotype : unc-119(ed3) III; wgIs179 unc-119(+) gei-11::TY1::EGFP::3xFLAG outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The GEI-11::EGFP fusion protein is expressed in the correct gei-11 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the GEI-11 transcription factor. made_by : R. Waterston )|GEI-11_GFP_YA_ChIP_Rep2|Young Adult Adl@ Young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331113 YL468(official name : YL468 genotype : unc-119(ed3) III; vrIs93 pMEX-5::LIN-35:GFP:FLAG::LIN-35 3-UTR genotype : unc-119 (+)) outcross : 0 mutagen : None tags : GFP::3xFlag description : LIN-35 expressed under the germline-specific promoter MEX-5. made_by : Michelle Kudron in Reinke lab )|Pmex-5_LIN-35_YL468_yAd_Input_Rep1|Young adult Adl@ Young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331114 YL468(official name : YL468 genotype : unc-119(ed3) III; vrIs93 pMEX-5::LIN-35:GFP:FLAG::LIN-35 3-UTR genotype : unc-119 (+)) outcross : 0 mutagen : None tags : GFP::3xFlag description : LIN-35 expressed under the germline-specific promoter MEX-5. made_by : Michelle Kudron in Reinke lab )|Pmex-5_LIN-35_YL468_yAd_ChIP_Rep1|Young adult Adl@ Young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331115 YL468(official name : YL468 genotype : unc-119(ed3) III; vrIs93 pMEX-5::LIN-35:GFP:FLAG::LIN-35 3-UTR genotype : unc-119 (+)) outcross : 0 mutagen : None tags : GFP::3xFlag description : LIN-35 expressed under the germline-specific promoter MEX-5. made_by : Michelle Kudron in Reinke lab )|Pmex-5_LIN-35_YL468_yAd_Input_Rep2|Young adult Adl@ Young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331116 YL468(official name : YL468 genotype : unc-119(ed3) III; vrIs93 pMEX-5::LIN-35:GFP:FLAG::LIN-35 3-UTR genotype : unc-119 (+)) outcross : 0 mutagen : None tags : GFP::3xFlag description : LIN-35 expressed under the germline-specific promoter MEX-5. made_by : Michelle Kudron in Reinke lab )|Pmex-5_LIN-35_YL468_yAd_ChIP_Rep2|Young adult Adl@ Young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331267 N2(official name : N2 genotype : wild type genotype : DR subclone of DB original (Tc1 pattern I) )|N2_POLIII_YA_Input_Rep1|Young adult Adl@ Young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331268 N2(official name : N2 genotype : wild type genotype : DR subclone of DB original (Tc1 pattern I) )|N2_POLIII_YA_ChIP_Rep1|Young adult Adl@ Young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331269 N2(official name : N2 genotype : wild type genotype : DR subclone of DB original (Tc1 pattern I) )|N2_POLIII_YA_Input_Rep2|Young adult Adl@ Young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331270 N2(official name : N2 genotype : wild type genotype : DR subclone of DB original (Tc1 pattern I) )|N2_POLIII_YA_ChIP_Rep2|Young adult Adl@ Young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331305 OP429(official name : OP429 genotype : unc-119(ed3) III; wgIs429(F23B12.7::TY1GFP-3xFLA; unc-119(+)) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology and Genetics in Dresden description : using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The F23B12.7::EGFP fusion protein is expressed in the correct F23B12.7 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the F23B12.7 transcription factor. made_by : Unknown )|F23B12.7_GFP_YA_Input_Rep1|Young adult Adl@ Young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331306 OP429(official name : OP429 genotype : unc-119(ed3) III; wgIs429(F23B12.7::TY1GFP-3xFLA; unc-119(+)) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology and Genetics in Dresden description : using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The F23B12.7::EGFP fusion protein is expressed in the correct F23B12.7 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the F23B12.7 transcription factor. made_by : Unknown )|F23B12.7_GFP_YA_ChIP_Rep1|Young adult Adl@ Young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331307 OP429(official name : OP429 genotype : unc-119(ed3) III; wgIs429(F23B12.7::TY1GFP-3xFLA; unc-119(+)) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology and Genetics in Dresden description : using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The F23B12.7::EGFP fusion protein is expressed in the correct F23B12.7 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the F23B12.7 transcription factor. made_by : Unknown )|F23B12.7_GFP_YA_Input_Rep2|Young adult Adl@ Young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331308 OP429(official name : OP429 genotype : unc-119(ed3) III; wgIs429(F23B12.7::TY1GFP-3xFLA; unc-119(+)) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology and Genetics in Dresden description : using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The F23B12.7::EGFP fusion protein is expressed in the correct F23B12.7 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the F23B12.7 transcription factor. made_by : Unknown )|F23B12.7_GFP_YA_ChIP_Rep2|Young adult Adl@ Young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331329 OP404(official name : OP404 genotype : unc-119(ed3) III; wgIs404(nfya-1::TY1-GFP-3xFLA; unc-119(+)) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology and Genetics in Dresden description : using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The NFYA-1::EGFP fusion protein is expressed in the correct nfya-1 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the NFYA-1 transcription factor. made_by : Unknown )|NFYA-1_GFP_YA_Input_Rep1|Young adult Adl@ Young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331330 OP404(official name : OP404 genotype : unc-119(ed3) III; wgIs404(nfya-1::TY1-GFP-3xFLA; unc-119(+)) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology and Genetics in Dresden description : using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The NFYA-1::EGFP fusion protein is expressed in the correct nfya-1 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the NFYA-1 transcription factor. made_by : Unknown )|NFYA-1_GFP_YA_ChIP_Rep1|Young adult Adl@ Young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331331 OP404(official name : OP404 genotype : unc-119(ed3) III; wgIs404(nfya-1::TY1-GFP-3xFLA; unc-119(+)) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology and Genetics in Dresden description : using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The NFYA-1::EGFP fusion protein is expressed in the correct nfya-1 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the NFYA-1 transcription factor. made_by : Unknown )|NFYA-1_GFP_YA_Input_Rep2|Young adult Adl@ Young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331332 OP404(official name : OP404 genotype : unc-119(ed3) III; wgIs404(nfya-1::TY1-GFP-3xFLA; unc-119(+)) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology and Genetics in Dresden description : using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The NFYA-1::EGFP fusion protein is expressed in the correct nfya-1 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the NFYA-1 transcription factor. made_by : Unknown )|NFYA-1_GFP_YA_ChIP_Rep2|Young adult Adl@ Young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX467091 YL472(official name : YL472 genotype : unc-119(ed3) III; vrEx66 pMEX-5::HPL-2:GFP:FLAG::HPL-2 3?UTR genotype : unc-119 (+)) outcross : 0 mutagen : None tags : GFP::3xFlag description : It is actually extrachromosomal line by bombardment. made_by : Michelle Kudron in Reinke lab )|Snyder Pmex-5 HPL-2 eGFP YL472 yAd Input Rep.1|Young adult Adl@ Young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX467092 YL472(official name : YL472 genotype : unc-119(ed3) III; vrEx66 pMEX-5::HPL-2:GFP:FLAG::HPL-2 3?UTR genotype : unc-119 (+)) outcross : 0 mutagen : None tags : GFP::3xFlag description : It is actually extrachromosomal line by bombardment. made_by : Michelle Kudron in Reinke lab )|Snyder Pmex-5 HPL-2 eGFP YL472 yAd ChIP Rep.1|Young adult Adl@ Young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX467093 YL472(official name : YL472 genotype : unc-119(ed3) III; vrEx66 pMEX-5::HPL-2:GFP:FLAG::HPL-2 3?UTR genotype : unc-119 (+)) outcross : 0 mutagen : None tags : GFP::3xFlag description : It is actually extrachromosomal line by bombardment. made_by : Michelle Kudron in Reinke lab )|Snyder Pmex-5 HPL-2 eGFP YL472 yAd Input Rep.2|Young adult Adl@ Young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX467094 YL472(official name : YL472 genotype : unc-119(ed3) III; vrEx66 pMEX-5::HPL-2:GFP:FLAG::HPL-2 3?UTR genotype : unc-119 (+)) outcross : 0 mutagen : None tags : GFP::3xFlag description : It is actually extrachromosomal line by bombardment. made_by : Michelle Kudron in Reinke lab )|Snyder Pmex-5 HPL-2 eGFP YL472 yAd ChIP Rep.2|Young adult Adl@ Young adult?0 1 2 https://www.ncbi.nlm.nih.gov/sra?term=SRX012299 zim-2(tm574)|synchronized young adult population of mutant strain zim-2(tm574)|young adult Adl@ Young adult?0 1 2 https://www.ncbi.nlm.nih.gov/sra?term=SRX2202775 young adults, H3K9me2 ChIP|whole body Adl@ Young adult?0 1 2 https://www.ncbi.nlm.nih.gov/sra?term=SRX2202779 young adults, HPL-2 ChIP|whole body Adl@ Young adult?0 1 2 https://www.ncbi.nlm.nih.gov/sra?term=SRX2202781 young adults, LET-418 ChIP|whole body Adl@ Young adult?0 1 2 https://www.ncbi.nlm.nih.gov/sra?term=SRX2202783 young adults, LIN-13 ChIP|whole body Adl@ Young adult?0 1 2 https://www.ncbi.nlm.nih.gov/sra?term=SRX2202785 young adults, LIN-61 ChIP|whole body Adl@ Young adult?0 1 2 https://www.ncbi.nlm.nih.gov/sra?term=SRX2202787 young adults, MET-2 ChIP|whole body Adl@ Young adult?0 1 2 https://www.ncbi.nlm.nih.gov/sra?term=SRX2599461 young adults|whole body Adl@ Young adult?0 1 2 https://www.ncbi.nlm.nih.gov/sra?term=SRX395527 YL457|staged young adults from YL457 (germline-specific SNPC-4-GFP transgenic strain)|germline|YA Adl@ Young adult?0 1 2 https://www.ncbi.nlm.nih.gov/sra?term=SRX395529 YL524|staged young adults from YL524 glp-1;OP179 (germ cell-deficient SNPC-4-GFP transgenic strain)|soma|YA Adl@ Young adult?0 1 2 https://www.ncbi.nlm.nih.gov/sra?term=SRX395531 N2|staged young adults (N2)|whole animal|YA Adl@ Young adult?0 1 3 https://www.ncbi.nlm.nih.gov/sra?term=SRX012296 N2|synchronized young adult population of wild type strain N2|young adult Adl@ Young adult?0 1 3 https://www.ncbi.nlm.nih.gov/sra?term=SRX1949396 YL529|staged young adult (YA) from YL529 (LET-607-GFP transgenic strain)|whole animal|YA Adl@ Young adult?0 1 3 https://www.ncbi.nlm.nih.gov/sra?term=SRX2985927 N2 (Bristol)|whole worm|young adult Adl@ Young adult?0 1 3 https://www.ncbi.nlm.nih.gov/sra?term=SRX2985929 tdp-1(ok803)|whole worm|young adult Adl@ Young adult?0 1 3 https://www.ncbi.nlm.nih.gov/sra?term=SRX323683 N2|glp-4 (bn2) yound adult Adl@ Young adult?0 1 3 https://www.ncbi.nlm.nih.gov/sra?term=SRX323686 N2|spe-11(hc77) yound adult Adl@ Young adult?0 1 3 https://www.ncbi.nlm.nih.gov/sra?term=SRX3411419 OP383|staged young adult (YA) from OP383 (OEF-1:GFP transgenic strain)|whole animal|YA Adl@ Young adult?0 1 3 https://www.ncbi.nlm.nih.gov/sra?term=SRX707297 tdp-1(ok803)|CHIP from whole worm extract|young adult Adl@ Young adult?0 1 3 https://www.ncbi.nlm.nih.gov/sra?term=SRX982067 N2|whole worms|YA Adl@ Young adult?0 1 4 https://www.ncbi.nlm.nih.gov/sra?term=SRX080059 YL445|Ppie-1 EFL-1:GFP:FLAG whole animal|Young adult Adl@ Young adult?0 1 4 https://www.ncbi.nlm.nih.gov/sra?term=SRX080063 YL390|Ppie-1_DPL-1:GFP:FLAG whole animal|Young adult Adl@ Young adult?0 1 4 https://www.ncbi.nlm.nih.gov/sra?term=SRX080072 YL468|Pmex-5 LIN-35:GFP:FLAG whole animal|Young adult Adl@ Young adult?0 1 4 https://www.ncbi.nlm.nih.gov/sra?term=SRX395523 OP179|staged young adults from OP179 (SNPC-4-GFP transgenic strain)|whole animal|YA Adl@ Young adult?0 1 5 https://www.ncbi.nlm.nih.gov/sra?term=SRX080067 YL402|Ppie-1 LIN-35:GFP:FLAG whole animal|Young adult Adl@ Young adult?0 1 5 https://www.ncbi.nlm.nih.gov/sra?term=SRX2350736 met-1(xk4); hrde(tm1200)|Whole animal, young adult Adl@ Young adult?0 1 5 https://www.ncbi.nlm.nih.gov/sra?term=SRX3883435 Young adults|whole animal extract|Young adults Adl@ Young adult?0 1 6 https://www.ncbi.nlm.nih.gov/sra?term=SRX005625 OP34|L4/young adult Adl@ Young adult?0 1 6 https://www.ncbi.nlm.nih.gov/sra?term=SRX005631 TJ356|L4/Young adult Adl@ Young adult?0 1 8 https://www.ncbi.nlm.nih.gov/sra?term=SRX2350723 hrde-1(tm1200)|Whole animal, young adult Adl@ Young adult?0 1 8 https://www.ncbi.nlm.nih.gov/sra?term=SRX4082344 N2|young adults Adl@ Young adult?0 1 8 https://www.ncbi.nlm.nih.gov/sra?term=SRX5985664 VC2010|Isolated germ nuclei from 2% formaldehyde pre-fixed VC2010 wild type young adult animals|Isolated germ nuclei|young adult (YA) Adl@ Young adult?0 1 8 https://www.ncbi.nlm.nih.gov/sra?term=SRX5985668 JK1107|2% formaldehyde pre-fixed glp-1(q224) young adult animals|Soma|young adult (YA) Adl@ Young adult?0 1 9 https://www.ncbi.nlm.nih.gov/sra?term=SRX1769990 AM1061|young adults|whole animal|young adults Adl@ Young adult?0 1 9 https://www.ncbi.nlm.nih.gov/sra?term=SRX2350732 met-1(xk4)|Whole animal, young adult Adl@ Young adult?0 1 9 https://www.ncbi.nlm.nih.gov/sra?term=SRX2350734 met-1(xk4); morc-1(tm6048)|Whole animal, young adult Adl@ Young adult?0 2 19 https://www.ncbi.nlm.nih.gov/sra?term=SRX4085427 wild-type N2|young adults Adl@ Young adult?0 3 118 https://www.ncbi.nlm.nih.gov/sra?term=SRX7262192 Young adult whole animal Adl@ Young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=ERX1485062 ERS1162600|mixed stage, early embryos Emb@ Early embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=ERX1485063 ERS1162601|mixed stage, early embryos Emb@ Early embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX043863 N2(genotype : wild type genotype : DR subclone of DB original (Tc1 pattern I) official name : N2 )|Snyder_N2_POLII_eemb_rep1 extraction1_seq1 channel_1|early embryo Emb@ Early embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX043864 N2(genotype : wild type genotype : DR subclone of DB original (Tc1 pattern I) official name : N2 )|Snyder_N2_POLII_eemb_rep1 extraction1_seq1 channel_2|early embryo Emb@ Early embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX043865 N2(genotype : wild type genotype : DR subclone of DB original (Tc1 pattern I) official name : N2 )|Snyder_N2_POLII_eemb_rep2 extraction2_seq1 channel_1|early embryo Emb@ Early embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX043866 N2(genotype : wild type genotype : DR subclone of DB original (Tc1 pattern I) official name : N2 )|Snyder_N2_POLII_eemb_rep2 extraction2_seq1 channel_2|early embryo Emb@ Early embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331333 N2|seq-HK00009_H3K9me3_2F3_N2_Eemb_Input_Rep1|Early Embryo Emb@ Early embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331334 N2|seq-HK00009_H3K9me3_2F3_N2_Eemb_Input_Rep2|Early Embryo Emb@ Early embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331335 N2|seq-HK00009_H3K9me3_2F3_N2_Eemb_ChIP_Rep1|Early Embryo Emb@ Early embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331336 N2|seq-HK00009_H3K9me3_2F3_N2_Eemb_ChIP_Rep2|Early Embryo Emb@ Early embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX466499 N2|seq-ab12181_H3K9acS10ph_873968_N2_Eemb_Input_Rep1|Early Embryo Emb@ Early embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX466500 N2|seq-ab12181_H3K9acS10ph_873968_N2_Eemb_Input_Rep2|Early Embryo Emb@ Early embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX466501 N2|seq-ab12181_H3K9acS10ph_873968_N2_Eemb_ChIP_Rep1|Early Embryo Emb@ Early embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX466502 N2|seq-ab12181_H3K9acS10ph_873968_N2_Eemb_ChIP_Rep2|Early Embryo Emb@ Early embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX466503 N2|seq-MP07355_H3K23ac_27133_N2_Eemb_Input_Rep1|Early Embryo Emb@ Early embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX466504 N2|seq-MP07355_H3K23ac_27133_N2_Eemb_Input_Rep2|Early Embryo Emb@ Early embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX466505 N2|seq-MP07355_H3K23ac_27133_N2_Eemb_ChIP_Rep1|Early Embryo Emb@ Early embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX466516 N2|seq-WA30834809_H3K4me2_8002_N2_Eemb_Input_Rep2|Early Embryo Emb@ Early embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX466517 N2|seq-WA30834809_H3K4me2_8002_N2_Eemb_ChIP_Rep1|Early Embryo Emb@ Early embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX466518 N2|seq-WA30834809_H3K4me2_8002_N2_Eemb_ChIP_Rep2|Early Embryo Emb@ Early embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX466519 N2|seq-WA30634849_H3K27ac_8002_N2_Eemb_Input_Rep1|Early Embryo Emb@ Early embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX466520 N2|seq-WA30634849_H3K27ac_8002_N2_Eemb_Input_Rep2|Early Embryo Emb@ Early embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX466521 N2|seq-WA30634849_H3K27ac_8002_N2_Eemb_ChIP_Rep1|Early Embryo Emb@ Early embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX466522 N2|seq-WA30634849_H3K27ac_8002_N2_Eemb_ChIP_Rep2|Early Embryo Emb@ Early embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX466523 N2|seq-UP07448_H3K27me1_24439_N2_Eemb_Input_Rep1|Early Embryo Emb@ Early embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX466524 N2|seq-UP07448_H3K27me1_24439_N2_Eemb_Input_Rep2|Early Embryo Emb@ Early embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX466525 N2|seq-UP07448_H3K27me1_24439_N2_Eemb_ChIP_Rep1|Early Embryo Emb@ Early embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX466526 N2|seq-UP07448_H3K27me1_24439_N2_Eemb_ChIP_Rep2|Early Embryo Emb@ Early embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX466527 N2|seq-HK00008_H3K9me2_6D11_N2_Eemb_Input_Rep1|Early Embryo Emb@ Early embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX466528 N2|seq-HK00008_H3K9me2_6D11_N2_Eemb_Input_Rep2|Early Embryo Emb@ Early embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX466529 N2|seq-HK00008_H3K9me2_6D11_N2_Eemb_ChIP_Rep1|Early Embryo Emb@ Early embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX466530 N2|seq-HK00008_H3K9me2_6D11_N2_Eemb_ChIP_Rep2|Early Embryo Emb@ Early embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX466531 N2|seq-ab15823_H4K8ac_487128_N2_Eemb_Input_Rep1|Early Embryo Emb@ Early embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX466532 N2|seq-ab15823_H4K8ac_487128_N2_Eemb_Input_Rep2|Early Embryo Emb@ Early embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX466533 N2|seq-ab15823_H4K8ac_487128_N2_Eemb_ChIP_Rep1|Early Embryo Emb@ Early embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX466534 N2|seq-ab15823_H4K8ac_487128_N2_Eemb_ChIP_Rep2|Early Embryo Emb@ Early embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX466535 N2|seq-HK00013_H3K27me3_1E7_N2_Eemb_Input_Rep1|Early Embryo Emb@ Early embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX466536 N2|seq-HK00013_H3K27me3_1E7_N2_Eemb_Input_Rep2|Early Embryo Emb@ Early embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX466537 N2|seq-HK00013_H3K27me3_1E7_N2_Eemb_ChIP_Rep1|Early Embryo Emb@ Early embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX466538 N2|seq-HK00013_H3K27me3_1E7_N2_Eemb_ChIP_Rep2|Early Embryo Emb@ Early embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX466539 N2|seq-WA30532379_H3K4me3_10001_N2_Eemb_Input_Rep1|Early Embryo Emb@ Early embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX466540 N2|seq-WA30532379_H3K4me3_10001_N2_Eemb_Input_Rep2|Early Embryo Emb@ Early embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX466541 N2|seq-WA30532379_H3K4me3_10001_N2_Eemb_ChIP_Rep1|Early Embryo Emb@ Early embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX466542 N2|seq-WA30532379_H3K4me3_10001_N2_Eemb_ChIP_Rep2|Early Embryo Emb@ Early embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX466543 N2|seq-ab9048_H3K36me1_206009_N2_Eemb_Input_Rep1|Early Embryo Emb@ Early embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX466544 N2|seq-ab9048_H3K36me1_206009_N2_Eemb_Input_Rep2|Early Embryo Emb@ Early embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX466545 N2|seq-ab9048_H3K36me1_206009_N2_Eemb_ChIP_Rep1|Early Embryo Emb@ Early embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX466546 N2|seq-ab9048_H3K36me1_206009_N2_Eemb_ChIP_Rep2|Early Embryo Emb@ Early embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX466547 N2|seq-ab2886_H3K79me1_361912_N2_Eemb_Input_Rep1|Early Embryo Emb@ Early embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX466548 N2|seq-ab2886_H3K79me1_361912_N2_Eemb_Input_Rep2|Early Embryo Emb@ Early embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX466549 N2|seq-ab2886_H3K79me1_361912_N2_Eemb_ChIP_Rep1|Early Embryo Emb@ Early embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX466550 N2|seq-ab2886_H3K79me1_361912_N2_Eemb_ChIP_Rep2|Early Embryo Emb@ Early embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX466551 N2|seq-ab3594_H3K79me2_346021_N2_Eemb_Input_Rep1|Early Embryo Emb@ Early embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX466552 N2|seq-ab3594_H3K79me2_346021_N2_Eemb_Input_Rep2|Early Embryo Emb@ Early embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX466553 N2|seq-ab3594_H3K79me2_346021_N2_Eemb_ChIP_Rep1|Early Embryo Emb@ Early embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX466554 N2|seq-ab3594_H3K79me2_346021_N2_Eemb_ChIP_Rep2|Early Embryo Emb@ Early embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX466555 N2|seq-ab2621_H3K79me3_361576_N2_Eemb_Input_Rep1|Early Embryo Emb@ Early embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX466556 N2|seq-ab2621_H3K79me3_361576_N2_Eemb_Input_Rep2|Early Embryo Emb@ Early embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX466557 N2|seq-ab2621_H3K79me3_361576_N2_Eemb_ChIP_Rep1|Early Embryo Emb@ Early embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX466558 N2|seq-ab2621_H3K79me3_361576_N2_Eemb_ChIP_Rep2|Early Embryo Emb@ Early embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX466559 N2|seq-ab8896_H3K9me1_104560_N2_Eemb_Input_Rep1|Early Embryo Emb@ Early embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX466560 N2|seq-ab8896_H3K9me1_104560_N2_Eemb_Input_Rep2|Early Embryo Emb@ Early embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX466561 N2|seq-ab8896_H3K9me1_104560_N2_Eemb_ChIP_Rep1|Early Embryo Emb@ Early embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX466562 N2|seq-ab8896_H3K9me1_104560_N2_Eemb_ChIP_Rep2|Early Embryo Emb@ Early embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX494832 N2|seq-ab1791_H3_377098_N2_Eemb_Input_Rep1|Early Embryo Emb@ Early embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX494833 N2|seq-ab1791_H3_377098_N2_Eemb_Input_Rep2|Early Embryo Emb@ Early embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX494834 N2|seq-ab1791_H3_377098_N2_Eemb_ChIP_Rep1|Early Embryo Emb@ Early embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX494835 N2|seq-ab1791_H3_377098_N2_Eemb_ChIP_Rep2|Early Embryo Emb@ Early embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX494840 N2|seq-UP07442_H3K9me3_DAM1411287_N2_Eemb_Input_Rep1|Early Embryo Emb@ Early embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX494841 N2|seq-UP07442_H3K9me3_DAM1411287_N2_Eemb_Input_Rep2|Early Embryo Emb@ Early embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX494842 N2|seq-UP07442_H3K9me3_DAM1411287_N2_Eemb_ChIP_Rep1|Early Embryo Emb@ Early embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX494843 N2|seq-UP07442_H3K9me3_DAM1411287_N2_Eemb_ChIP_Rep2|Early Embryo Emb@ Early embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX494844 N2|seq-ab8895_H3K4me1_733246_N2_Eemb_Input_Rep1|Early Embryo Emb@ Early embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX494845 N2|seq-ab8895_H3K4me1_733246_N2_Eemb_Input_Rep2|Early Embryo Emb@ Early embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX494846 N2|seq-ab8895_H3K4me1_733246_N2_Eemb_ChIP_Rep1|Early Embryo Emb@ Early embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX494847 N2|seq-ab8895_H3K4me1_733246_N2_Eemb_ChIP_Rep2|Early Embryo Emb@ Early embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX494848 N2|seq-HK00012_H3K36me2_2C3_N2_Eemb_Input_Rep1|Early Embryo Emb@ Early embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX494849 N2|seq-HK00012_H3K36me2_2C3_N2_Eemb_Input_Rep2|Early Embryo Emb@ Early embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX494850 N2|seq-HK00012_H3K36me2_2C3_N2_Eemb_ChIP_Rep1|Early Embryo Emb@ Early embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX494851 N2|seq-HK00012_H3K36me2_2C3_N2_Eemb_ChIP_Rep2|Early Embryo Emb@ Early embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX494852 N2|seq-HK00001_H3K36me3_13C9_N2_Eemb_Input_Rep1|Early Embryo Emb@ Early embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX494853 N2|seq-HK00001_H3K36me3_13C9_N2_Eemb_Input_Rep2|Early Embryo Emb@ Early embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX494854 N2|seq-HK00001_H3K36me3_13C9_N2_Eemb_ChIP_Rep1|Early Embryo Emb@ Early embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX494855 N2|seq-HK00001_H3K36me3_13C9_N2_Eemb_ChIP_Rep2|Early Embryo Emb@ Early embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX495109 N2|seq-SDQ3838_T26A5.5_N2_Eemb_Input_Rep1|Early Embryo Emb@ Early embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX495110 N2|seq-SDQ3838_T26A5.5_N2_Eemb_Input_Rep2|Early Embryo Emb@ Early embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX495111 N2|seq-SDQ3838_T26A5.5_N2_Eemb_ChIP_Rep1|Early Embryo Emb@ Early embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX495112 N2|seq-SDQ3838_T26A5.5_N2_Eemb_ChIP_Rep2|Early Embryo Emb@ Early embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX495113 N2|seq-SDQ3927_MRG1_N2_Eemb_Input_Rep1|Early Embryo Emb@ Early embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX495114 N2|seq-SDQ3927_MRG1_N2_Eemb_Input_Rep2|Early Embryo Emb@ Early embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX495115 N2|seq-SDQ3927_MRG1_N2_Eemb_ChIP_Rep1|Early Embryo Emb@ Early embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX495116 N2|seq-SDQ3927_MRG1_N2_Eemb_ChIP_Rep2|Early Embryo Emb@ Early embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX495117 N2|seq-ab817_8WG16_639746_N2_Eemb_Input_Rep1|Early Embryo Emb@ Early embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX495118 N2|seq-ab817_8WG16_639746_N2_Eemb_Input_Rep2|Early Embryo Emb@ Early embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX495119 N2|seq-ab817_8WG16_639746_N2_Eemb_ChIP_Rep1|Early Embryo Emb@ Early embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX495120 N2|seq-ab817_8WG16_639746_N2_Eemb_ChIP_Rep2|Early Embryo Emb@ Early embryo?0 1 2 https://www.ncbi.nlm.nih.gov/sra?term=SRX514727 N2|early embryos H4K16ac ChIP seq|whole embryo|early embryos Emb@ Early embryo?0 1 2 https://www.ncbi.nlm.nih.gov/sra?term=SRX514728 N2|early embryos Input DNA seq|whole embryo|early embryos Emb@ Early embryo?0 1 4 https://www.ncbi.nlm.nih.gov/sra?term=SRX1353657 GW1|Early embryo extracts|early embryo Emb@ Early embryo?0 1 4 https://www.ncbi.nlm.nih.gov/sra?term=SRX1353659 GW638|Early embryo extracts|early embryo Emb@ Early embryo?0 1 4 https://www.ncbi.nlm.nih.gov/sra?term=SRX1353661 GW828|Early embryo extracts|early embryo Emb@ Early embryo?0 1 6 https://www.ncbi.nlm.nih.gov/sra?term=SRX4996803 N2 (Bristol)|early embryo Emb@ Early embryo?0 1 6 https://www.ncbi.nlm.nih.gov/sra?term=SRX4996806 met-2(n4256) III|early embryo Emb@ Early embryo?0 1 6 https://www.ncbi.nlm.nih.gov/sra?term=SRX4996809 set-25(n5021) III|early embryo Emb@ Early embryo?0 1 8 https://www.ncbi.nlm.nih.gov/sra?term=SRX1995023 N2|embryo|early embryo Emb@ Early embryo?0 1 8 https://www.ncbi.nlm.nih.gov/sra?term=SRX2978695 met-2(n4256) III|early embryo|early embryo Emb@ Early embryo?0 1 8 https://www.ncbi.nlm.nih.gov/sra?term=SRX2978699 set-25(n5021) III|early embryo|early embryo Emb@ Early embryo?0 1 12 https://www.ncbi.nlm.nih.gov/sra?term=SRX257655 TY1072|whole worms|embryo Emb@ Embryos?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX002673 OP37|embyro Emb@ Embryos?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX043855 OP64(made_by : R. Waterston description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The HLH-1::EGFP fusion protein is expressed in the correct hlh-1 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the HLH-1 transcription factor. tags : GFP::3xFlag mutagen : Bombard outcross : 3 genotype : unc-119(ed3) III; wgIs64 unc-119(+) hlh-1::TY1::EGFP::3xFLAG official name : OP64 )|Snyder_HLH-1_GFP_emb_rep1 extraction1_seq1 channel_1|embryo Emb@ Embryos?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX043856 OP64(made_by : R. Waterston description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The HLH-1::EGFP fusion protein is expressed in the correct hlh-1 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the HLH-1 transcription factor. tags : GFP::3xFlag mutagen : Bombard outcross : 3 genotype : unc-119(ed3) III; wgIs64 unc-119(+) hlh-1::TY1::EGFP::3xFLAG official name : OP64 )|Snyder_HLH-1_GFP_emb_rep1 extraction1_seq1 channel_2|embryo Emb@ Embryos?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX043857 OP64(made_by : R. Waterston description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The HLH-1::EGFP fusion protein is expressed in the correct hlh-1 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the HLH-1 transcription factor. tags : GFP::3xFlag mutagen : Bombard outcross : 3 genotype : unc-119(ed3) III; wgIs64 unc-119(+) hlh-1::TY1::EGFP::3xFLAG official name : OP64 )|Snyder_HLH-1_GFP_emb_rep2 extraction2_seq1 channel_1|embryo Emb@ Embryos?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX043858 OP64(made_by : R. Waterston description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The HLH-1::EGFP fusion protein is expressed in the correct hlh-1 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the HLH-1 transcription factor. tags : GFP::3xFlag mutagen : Bombard outcross : 3 genotype : unc-119(ed3) III; wgIs64 unc-119(+) hlh-1::TY1::EGFP::3xFLAG official name : OP64 )|Snyder_HLH-1_GFP_emb_rep2 extraction2_seq1 channel_2|embryo Emb@ Embryos?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX043975 OP37(made_by : R. Waterston and S. Kim description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The PHA-4::EGFP fusion protein is expressed in the correct pha-4 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the PHA-4 transcription factor. tags : GFP::3xFlag mutagen : Bombard outcross : 3 genotype : unc-119(ed3) III; wgIs37 unc-119(+) pha-4::TY1::EGFP::3xFLAG official name : OP37 )|Snyder_PHA4_GFP_lemb_rep1 extraction1_seq1 channel_1|late embryo Emb@ Embryos?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX043976 OP37(made_by : R. Waterston and S. Kim description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The PHA-4::EGFP fusion protein is expressed in the correct pha-4 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the PHA-4 transcription factor. tags : GFP::3xFlag mutagen : Bombard outcross : 3 genotype : unc-119(ed3) III; wgIs37 unc-119(+) pha-4::TY1::EGFP::3xFLAG official name : OP37 )|Snyder_PHA4_GFP_lemb_rep1 extraction1_seq1 channel_2|late embryo Emb@ Embryos?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX043977 OP37(made_by : R. Waterston and S. Kim description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The PHA-4::EGFP fusion protein is expressed in the correct pha-4 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the PHA-4 transcription factor. tags : GFP::3xFlag mutagen : Bombard outcross : 3 genotype : unc-119(ed3) III; wgIs37 unc-119(+) pha-4::TY1::EGFP::3xFLAG official name : OP37 )|Snyder_PHA4_GFP_lemb_rep2 extraction2_seq1 channel_1|late embryo Emb@ Embryos?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX043978 OP37(made_by : R. Waterston and S. Kim description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The PHA-4::EGFP fusion protein is expressed in the correct pha-4 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the PHA-4 transcription factor. tags : GFP::3xFlag mutagen : Bombard outcross : 3 genotype : unc-119(ed3) III; wgIs37 unc-119(+) pha-4::TY1::EGFP::3xFLAG official name : OP37 )|Snyder_PHA4_GFP_lemb_rep2 extraction2_seq1 channel_2|late embryo Emb@ Embryos?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX043979 OP70(made_by : R Waterston tags : GFP::3xFlag mutagen : Bombard genotype : unc119(ed3); wgIs70(mep-1::TY1 EGFP FLAG C; unc119) official name : WBGene00003218 )|Snyder_MEP-1_GFP_emb_rep1 extraction1_seq1 channel_1|embryo Emb@ Embryos?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX043980 OP70(made_by : R Waterston tags : GFP::3xFlag mutagen : Bombard genotype : unc119(ed3); wgIs70(mep-1::TY1 EGFP FLAG C; unc119) official name : WBGene00003218 )|Snyder_MEP-1_GFP_emb_rep1 extraction1_seq1 channel_2|embryo Emb@ Embryos?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX043981 OP70(made_by : R Waterston tags : GFP::3xFlag mutagen : Bombard genotype : unc119(ed3); wgIs70(mep-1::TY1 EGFP FLAG C; unc119) official name : WBGene00003218 )|Snyder_MEP-1_GFP_emb_rep2 extraction2_seq1 channel_1|embryo Emb@ Embryos?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX043982 OP70(made_by : R Waterston tags : GFP::3xFlag mutagen : Bombard genotype : unc119(ed3); wgIs70(mep-1::TY1 EGFP FLAG C; unc119) official name : WBGene00003218 )|Snyder_MEP-1_GFP_emb_rep2 extraction2_seq1 channel_2|embryo Emb@ Embryos?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX043995 OP51(made_by : R Waterston description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The LIN-13::EGFP fusion protein is expressed in the correct LIN-13 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the LIN-13 transcription factor. tags : GFP::3xFlag mutagen : Bombard outcross : 3 genotype : unc-119 (ed3) III; wgIs73 lin-13::TY1::EGFP::FLAG; unc-119 (+) official name : OP51 )|Snyder_LIN-13_GFP_emb_rep1 extraction1_seq1 channel_1|embryo Emb@ Embryos?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX043996 OP51(made_by : R Waterston description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The LIN-13::EGFP fusion protein is expressed in the correct LIN-13 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the LIN-13 transcription factor. tags : GFP::3xFlag mutagen : Bombard outcross : 3 genotype : unc-119 (ed3) III; wgIs73 lin-13::TY1::EGFP::FLAG; unc-119 (+) official name : OP51 )|Snyder_LIN-13_GFP_emb_rep1 extraction1_seq1 channel_2|embryo Emb@ Embryos?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX043997 OP51(made_by : R Waterston description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The LIN-13::EGFP fusion protein is expressed in the correct LIN-13 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the LIN-13 transcription factor. tags : GFP::3xFlag mutagen : Bombard outcross : 3 genotype : unc-119 (ed3) III; wgIs73 lin-13::TY1::EGFP::FLAG; unc-119 (+) official name : OP51 )|Snyder_LIN-13_GFP_emb_rep2 extraction2_seq1 channel_1|embryo Emb@ Embryos?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX043998 OP51(made_by : R Waterston description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The LIN-13::EGFP fusion protein is expressed in the correct LIN-13 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the LIN-13 transcription factor. tags : GFP::3xFlag mutagen : Bombard outcross : 3 genotype : unc-119 (ed3) III; wgIs73 lin-13::TY1::EGFP::FLAG; unc-119 (+) official name : OP51 )|Snyder_LIN-13_GFP_emb_rep2 extraction2_seq1 channel_2|embryo Emb@ Embryos?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX044003 OP120(made_by : R Waterston description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The CEH-30::EGFP fusion protein is expressed in the correct ceh-30 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the CEH-30 transcription factor. tags : GFP::3xFlag mutagen : Bombard outcross : 3 genotype : unc119(ed3); wgIs120(ceh-30::TY1 EGFP FLAG; unc119) official name : OP120 )|Snyder_CEH-30_GFP_lemb_rep1 extraction1_seq1 channel_1|late embryo Emb@ Embryos?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX044004 OP120(made_by : R Waterston description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The CEH-30::EGFP fusion protein is expressed in the correct ceh-30 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the CEH-30 transcription factor. tags : GFP::3xFlag mutagen : Bombard outcross : 3 genotype : unc119(ed3); wgIs120(ceh-30::TY1 EGFP FLAG; unc119) official name : OP120 )|Snyder_CEH-30_GFP_lemb_rep1 extraction1_seq1 channel_2|late embryo Emb@ Embryos?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX044005 OP120(made_by : R Waterston description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The CEH-30::EGFP fusion protein is expressed in the correct ceh-30 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the CEH-30 transcription factor. tags : GFP::3xFlag mutagen : Bombard outcross : 3 genotype : unc119(ed3); wgIs120(ceh-30::TY1 EGFP FLAG; unc119) official name : OP120 )|Snyder_CEH-30_GFP_lemb_rep2 extraction2_seq1 channel_1|late embryo Emb@ Embryos?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX044006 OP120(made_by : R Waterston description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The CEH-30::EGFP fusion protein is expressed in the correct ceh-30 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the CEH-30 transcription factor. tags : GFP::3xFlag mutagen : Bombard outcross : 3 genotype : unc119(ed3); wgIs120(ceh-30::TY1 EGFP FLAG; unc119) official name : OP120 )|Snyder_CEH-30_GFP_lemb_rep2 extraction2_seq1 channel_2|late embryo Emb@ Embryos?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX146413 OP500(official name : OP500 genotype : unc119(ed3); wgIs500(ceh-26::TY1 EGFP FLAG; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Dresden using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The CEH-26::EGFP fusion protein is expressed in the correct ceh-26 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the CEH-26 transcription factor. made_by : R. Waterston )|Snyder_CEH-26_Input_LE_rep1|late embryo Emb@ Embryos?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX146414 OP500(official name : OP500 genotype : unc119(ed3); wgIs500(ceh-26::TY1 EGFP FLAG; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Dresden using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The CEH-26::EGFP fusion protein is expressed in the correct ceh-26 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the CEH-26 transcription factor. made_by : R. Waterston )|Snyder_CEH-26_Input_LE_rep2|late embryo Emb@ Embryos?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX146415 OP500(official name : OP500 genotype : unc119(ed3); wgIs500(ceh-26::TY1 EGFP FLAG; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Dresden using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The CEH-26::EGFP fusion protein is expressed in the correct ceh-26 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the CEH-26 transcription factor. made_by : R. Waterston )|Snyder_CEH-26_GFP_LE_rep1|late embryo Emb@ Embryos?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX146416 OP500(official name : OP500 genotype : unc119(ed3); wgIs500(ceh-26::TY1 EGFP FLAG; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Dresden using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The CEH-26::EGFP fusion protein is expressed in the correct ceh-26 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the CEH-26 transcription factor. made_by : R. Waterston )|Snyder_CEH-26_GFP_LE_rep2|late embryo Emb@ Embryos?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX246029 crosslinked ChIPed chromatin|embryo Emb@ Embryos?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX277041 OP186(official name : OP186 genotype : unc119(ed3); wgIs186(unc39::TY1 EGFP FLAG C; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The UNC-39::EGFP fusion protein is expressed in the correct unc-39 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the UNC-39 transcription factor. made_by : Unknown )|UNC-39 EMB InputRep1|embryo Emb@ Embryos?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX277042 OP186(official name : OP186 genotype : unc119(ed3); wgIs186(unc39::TY1 EGFP FLAG C; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The UNC-39::EGFP fusion protein is expressed in the correct unc-39 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the UNC-39 transcription factor. made_by : Unknown )|UNC-39 EMB InputRep2|embryo Emb@ Embryos?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX277043 OP186(official name : OP186 genotype : unc119(ed3); wgIs186(unc39::TY1 EGFP FLAG C; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The UNC-39::EGFP fusion protein is expressed in the correct unc-39 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the UNC-39 transcription factor. made_by : Unknown )|UNC-39 EMB ChIPRep1|embryo Emb@ Embryos?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX277044 OP186(official name : OP186 genotype : unc119(ed3); wgIs186(unc39::TY1 EGFP FLAG C; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The UNC-39::EGFP fusion protein is expressed in the correct unc-39 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the UNC-39 transcription factor. made_by : Unknown )|UNC-39 EMB ChIPRep2|embryo Emb@ Embryos?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX277049 OP75(official name : OP75 genotype : unc-119 (ed3) III; wgIs75 elt-3::TY1::EGFP::FLAG; unc-119 (+) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The ELT-3::EGFP fusion protein is expressed in the correct elt-3 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the ELT-3 transcription factor. made_by : R Waterston )|ELT-3 EMB InputRep1|embryo Emb@ Embryos?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX277050 OP75(official name : OP75 genotype : unc-119 (ed3) III; wgIs75 elt-3::TY1::EGFP::FLAG; unc-119 (+) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The ELT-3::EGFP fusion protein is expressed in the correct elt-3 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the ELT-3 transcription factor. made_by : R Waterston )|ELT-3 EMB InputRep2|embryo Emb@ Embryos?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX277051 OP75(official name : OP75 genotype : unc-119 (ed3) III; wgIs75 elt-3::TY1::EGFP::FLAG; unc-119 (+) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The ELT-3::EGFP fusion protein is expressed in the correct elt-3 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the ELT-3 transcription factor. made_by : R Waterston )|ELT-3 EMB ChIPRep1|embryo Emb@ Embryos?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX277052 OP75(official name : OP75 genotype : unc-119 (ed3) III; wgIs75 elt-3::TY1::EGFP::FLAG; unc-119 (+) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The ELT-3::EGFP fusion protein is expressed in the correct elt-3 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the ELT-3 transcription factor. made_by : R Waterston )|ELT-3 EMB ChIPRep2|embryo Emb@ Embryos?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX277082 OP318(official name : OP318 genotype : unc-119(ed3); wgIs318(nhr-12::TY1 EGFP FLAG; unc-119(+)) outcross : 3 mutagen : None tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Dresden using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The spatio-temporal expression pattern of NHR-12::EGFP fusion protein was examined through in vivo microscopy. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the NHR-12 transcription factor. made_by : Bob Waterston's lab from UW )|NHR-12 EMB InputRep1|embryo Emb@ Embryos?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX277083 OP318(official name : OP318 genotype : unc-119(ed3); wgIs318(nhr-12::TY1 EGFP FLAG; unc-119(+)) outcross : 3 mutagen : None tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Dresden using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The spatio-temporal expression pattern of NHR-12::EGFP fusion protein was examined through in vivo microscopy. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the NHR-12 transcription factor. made_by : Bob Waterston's lab from UW )|NHR-12 EMB InputRep2|embryo Emb@ Embryos?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX277084 OP318(official name : OP318 genotype : unc-119(ed3); wgIs318(nhr-12::TY1 EGFP FLAG; unc-119(+)) outcross : 3 mutagen : None tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Dresden using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The spatio-temporal expression pattern of NHR-12::EGFP fusion protein was examined through in vivo microscopy. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the NHR-12 transcription factor. made_by : Bob Waterston's lab from UW )|NHR-12 EMB ChIPRep1|embryo Emb@ Embryos?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX277085 OP318(official name : OP318 genotype : unc-119(ed3); wgIs318(nhr-12::TY1 EGFP FLAG; unc-119(+)) outcross : 3 mutagen : None tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Dresden using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The spatio-temporal expression pattern of NHR-12::EGFP fusion protein was examined through in vivo microscopy. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the NHR-12 transcription factor. made_by : Bob Waterston's lab from UW )|NHR-12 EMB ChIPRep2|embryo Emb@ Embryos?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331139 OP327(official name : OP327 genotype : unc327(ed3); wgIs102(F23F12.::TY1 EGFP FLAG; unc119) outcross : 0 mutagen : None tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for bombardment transformation of an unc-119(ed3) strain. made_by : Bob Waterston's lab from UW )|F23F12.9_GFP_Emb_Input_Rep1|embryo Emb@ Embryos?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331140 OP327(official name : OP327 genotype : unc327(ed3); wgIs102(F23F12.::TY1 EGFP FLAG; unc119) outcross : 0 mutagen : None tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for bombardment transformation of an unc-119(ed3) strain. made_by : Bob Waterston's lab from UW )|F23F12.9_GFP_Emb_ChIP_Rep1|embryo Emb@ Embryos?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331141 OP327(official name : OP327 genotype : unc327(ed3); wgIs102(F23F12.::TY1 EGFP FLAG; unc119) outcross : 0 mutagen : None tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for bombardment transformation of an unc-119(ed3) strain. made_by : Bob Waterston's lab from UW )|F23F12.9_GFP_Emb_Input_Rep2|embryo Emb@ Embryos?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331142 OP327(official name : OP327 genotype : unc327(ed3); wgIs102(F23F12.::TY1 EGFP FLAG; unc119) outcross : 0 mutagen : None tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for bombardment transformation of an unc-119(ed3) strain. made_by : Bob Waterston's lab from UW )|F23F12.9_GFP_Emb_ChIP_Rep2|embryo Emb@ Embryos?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331153 OP27(official name : OP27 genotype : unc-119(ed3); wgIs27(mab-5::TY1 EGFP FLAG; unc-119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology and Genetics in Dresden using Tony Hyman's recombineering pipeline. The resulting plasmid was used for bombardment transformation of an unc-119(ed3) strain. The MAB-5::EGFP fusion protein is expressed in the correct mab-5 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the MAB-5 transcription factor. made_by : Bob Waterston's lab from UW )|MAB-5_GFP_Embryo_Input_Rep1|embryo Emb@ Embryos?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331154 OP27(official name : OP27 genotype : unc-119(ed3); wgIs27(mab-5::TY1 EGFP FLAG; unc-119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology and Genetics in Dresden using Tony Hyman's recombineering pipeline. The resulting plasmid was used for bombardment transformation of an unc-119(ed3) strain. The MAB-5::EGFP fusion protein is expressed in the correct mab-5 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the MAB-5 transcription factor. made_by : Bob Waterston's lab from UW )|MAB-5_GFP_Embryo_ChIP_Rep1|embryo Emb@ Embryos?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331155 OP27(official name : OP27 genotype : unc-119(ed3); wgIs27(mab-5::TY1 EGFP FLAG; unc-119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology and Genetics in Dresden using Tony Hyman's recombineering pipeline. The resulting plasmid was used for bombardment transformation of an unc-119(ed3) strain. The MAB-5::EGFP fusion protein is expressed in the correct mab-5 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the MAB-5 transcription factor. made_by : Bob Waterston's lab from UW )|MAB-5_GFP_Embryo_Input_Rep2|embryo Emb@ Embryos?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331156 OP27(official name : OP27 genotype : unc-119(ed3); wgIs27(mab-5::TY1 EGFP FLAG; unc-119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology and Genetics in Dresden using Tony Hyman's recombineering pipeline. The resulting plasmid was used for bombardment transformation of an unc-119(ed3) strain. The MAB-5::EGFP fusion protein is expressed in the correct mab-5 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the MAB-5 transcription factor. made_by : Bob Waterston's lab from UW )|MAB-5_GFP_Embryo_ChIP_Rep2|embryo Emb@ Embryos?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331161 OP367(official name : OP367 genotype : unc-119(ed3); wgIs367(lsy-2::TY1 EGFP FLAG; unc-119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology and Genetics in Dresden using Tony Hyman's recombineering pipeline. The resulting plasmid was used for bombardment transformation of an unc-119(ed3) strain. The LSY-2::EGFP fusion protein is expressed in the correct lsy-2 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the LSY-2 transcription factor. made_by : Bob Waterston's lab from UW )|LSY-2_GFP_Embryo_Input_Rep1|embryo Emb@ Embryos?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331162 OP367(official name : OP367 genotype : unc-119(ed3); wgIs367(lsy-2::TY1 EGFP FLAG; unc-119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology and Genetics in Dresden using Tony Hyman's recombineering pipeline. The resulting plasmid was used for bombardment transformation of an unc-119(ed3) strain. The LSY-2::EGFP fusion protein is expressed in the correct lsy-2 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the LSY-2 transcription factor. made_by : Bob Waterston's lab from UW )|LSY-2_GFP_Embryo_ChIP_Rep1|embryo Emb@ Embryos?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331163 OP367(official name : OP367 genotype : unc-119(ed3); wgIs367(lsy-2::TY1 EGFP FLAG; unc-119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology and Genetics in Dresden using Tony Hyman's recombineering pipeline. The resulting plasmid was used for bombardment transformation of an unc-119(ed3) strain. The LSY-2::EGFP fusion protein is expressed in the correct lsy-2 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the LSY-2 transcription factor. made_by : Bob Waterston's lab from UW )|LSY-2_GFP_Embryo_Input_Rep2|embryo Emb@ Embryos?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331164 OP367(official name : OP367 genotype : unc-119(ed3); wgIs367(lsy-2::TY1 EGFP FLAG; unc-119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology and Genetics in Dresden using Tony Hyman's recombineering pipeline. The resulting plasmid was used for bombardment transformation of an unc-119(ed3) strain. The LSY-2::EGFP fusion protein is expressed in the correct lsy-2 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the LSY-2 transcription factor. made_by : Bob Waterston's lab from UW )|LSY-2_GFP_Embryo_ChIP_Rep2|embryo Emb@ Embryos?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331185 OP228(official name : OP228 genotype : unc119(ed3); wgIs228(nhr-237:TY1 EGFP FLAG; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The NHR-237::EGFP fusion protein is expressed in the correct nhr-237 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the NHR-237 transcription factor. made_by : Unknown )|NHR-237_GFP_EMB_Input_Rep1|embryo Emb@ Embryos?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331186 OP228(official name : OP228 genotype : unc119(ed3); wgIs228(nhr-237:TY1 EGFP FLAG; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The NHR-237::EGFP fusion protein is expressed in the correct nhr-237 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the NHR-237 transcription factor. made_by : Unknown )|NHR-237_GFP_EMB_ChIP_Rep1|embryo Emb@ Embryos?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331187 OP228(official name : OP228 genotype : unc119(ed3); wgIs228(nhr-237:TY1 EGFP FLAG; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The NHR-237::EGFP fusion protein is expressed in the correct nhr-237 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the NHR-237 transcription factor. made_by : Unknown )|NHR-237_GFP_EMB_Input_Rep2|embryo Emb@ Embryos?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331188 OP228(official name : OP228 genotype : unc119(ed3); wgIs228(nhr-237:TY1 EGFP FLAG; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The NHR-237::EGFP fusion protein is expressed in the correct nhr-237 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the NHR-237 transcription factor. made_by : Unknown )|NHR-237_GFP_EMB_ChIP_Rep2|embryo Emb@ Embryos?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331189 OP117(official name : OP117 genotype : unc119(ed3); wgIs117(pax-1::TY1 EGFP FLAG; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The PAX-1::EGFP fusion protein is expressed in the correct pax-1 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the PAX-1 transcription factor. made_by : Unknown )|PAX-1_GFP_EMB_Input_Rep1|embryo Emb@ Embryos?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331190 OP117(official name : OP117 genotype : unc119(ed3); wgIs117(pax-1::TY1 EGFP FLAG; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The PAX-1::EGFP fusion protein is expressed in the correct pax-1 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the PAX-1 transcription factor. made_by : Unknown )|PAX-1_GFP_EMB_ChIP_Rep1|embryo Emb@ Embryos?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331191 OP117(official name : OP117 genotype : unc119(ed3); wgIs117(pax-1::TY1 EGFP FLAG; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The PAX-1::EGFP fusion protein is expressed in the correct pax-1 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the PAX-1 transcription factor. made_by : Unknown )|PAX-1_GFP_EMB_Input_Rep2|embryo Emb@ Embryos?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331192 OP117(official name : OP117 genotype : unc119(ed3); wgIs117(pax-1::TY1 EGFP FLAG; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The PAX-1::EGFP fusion protein is expressed in the correct pax-1 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the PAX-1 transcription factor. made_by : Unknown )|PAX-1_GFP_EMB_ChIP_Rep2|embryo Emb@ Embryos?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331193 OP174(official name : OP174 genotype : unc-119(ed3); wgIs174(ces-1::TY1 EGFP FLAG; unc-119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The CES-1::EGFP fusion protein is expressed in the correct ces-1 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the CES-1 transcription factor. made_by : S. Kim )|CES-1_GFP_EMB_Input_Rep1|embryo Emb@ Embryos?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331194 OP174(official name : OP174 genotype : unc-119(ed3); wgIs174(ces-1::TY1 EGFP FLAG; unc-119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The CES-1::EGFP fusion protein is expressed in the correct ces-1 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the CES-1 transcription factor. made_by : S. Kim )|CES-1_GFP_EMB_ChIP_Rep1|embryo Emb@ Embryos?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331195 OP174(official name : OP174 genotype : unc-119(ed3); wgIs174(ces-1::TY1 EGFP FLAG; unc-119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The CES-1::EGFP fusion protein is expressed in the correct ces-1 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the CES-1 transcription factor. made_by : S. Kim )|CES-1_GFP_EMB_Input_Rep2|embryo Emb@ Embryos?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331196 OP174(official name : OP174 genotype : unc-119(ed3); wgIs174(ces-1::TY1 EGFP FLAG; unc-119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The CES-1::EGFP fusion protein is expressed in the correct ces-1 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the CES-1 transcription factor. made_by : S. Kim )|CES-1_GFP_EMB_ChIP_Rep2|embryo Emb@ Embryos?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331197 OP169(official name : OP169 genotype : unc119(ed3); wgIs169(ceh-39::TY1 EGFP FLAG; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The CEH-39::EGFP fusion protein is expressed in the correct ceh-39 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the CEH-39 transcription factor. made_by : Unknown )|CEH-39_GFP_EMB_Input_Rep1|embryo Emb@ Embryos?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331198 OP169(official name : OP169 genotype : unc119(ed3); wgIs169(ceh-39::TY1 EGFP FLAG; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The CEH-39::EGFP fusion protein is expressed in the correct ceh-39 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the CEH-39 transcription factor. made_by : Unknown )|CEH-39_GFP_EMB_ChIP_Rep1|embryo Emb@ Embryos?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331199 OP169(official name : OP169 genotype : unc119(ed3); wgIs169(ceh-39::TY1 EGFP FLAG; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The CEH-39::EGFP fusion protein is expressed in the correct ceh-39 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the CEH-39 transcription factor. made_by : Unknown )|CEH-39_GFP_EMB_Input_Rep2|embryo Emb@ Embryos?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331200 OP169(official name : OP169 genotype : unc119(ed3); wgIs169(ceh-39::TY1 EGFP FLAG; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The CEH-39::EGFP fusion protein is expressed in the correct ceh-39 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the CEH-39 transcription factor. made_by : Unknown )|CEH-39_GFP_EMB_ChIP_Rep2|embryo Emb@ Embryos?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331221 OP600(official name : OP600 genotype : unc119(ed3); wgIs600(unc-62::TY1 EGFP FLAG; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The UNC-62::EGFP fusion protein is expressed in the correct unc-62 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the UNC-62 transcription factor. made_by : S Kim )|UNC_62_GFP_EMB_Input_Rep1|embryo Emb@ Embryos?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331222 OP600(official name : OP600 genotype : unc119(ed3); wgIs600(unc-62::TY1 EGFP FLAG; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The UNC-62::EGFP fusion protein is expressed in the correct unc-62 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the UNC-62 transcription factor. made_by : S Kim )|UNC_62_GFP_EMB_ChIP_Rep1|embryo Emb@ Embryos?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331223 OP600(official name : OP600 genotype : unc119(ed3); wgIs600(unc-62::TY1 EGFP FLAG; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The UNC-62::EGFP fusion protein is expressed in the correct unc-62 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the UNC-62 transcription factor. made_by : S Kim )|UNC_62_GFP_EMB_Input_Rep2|embryo Emb@ Embryos?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331224 OP600(official name : OP600 genotype : unc119(ed3); wgIs600(unc-62::TY1 EGFP FLAG; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The UNC-62::EGFP fusion protein is expressed in the correct unc-62 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the UNC-62 transcription factor. made_by : S Kim )|UNC_62_GFP_EMB_ChIP_Rep2|embryo Emb@ Embryos?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331225 OP317(official name : OP317 genotype : unc119(ed3); wgIs317(nhr-28::TY1 EGFP FLAG; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The NHR-28::EGFP fusion protein is expressed in the correct nhr-28 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the NHR-28 transcription factor. made_by : R Waterston )|NHR-28_GFP_EMB_Input_Rep1|embryo Emb@ Embryos?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331226 OP317(official name : OP317 genotype : unc119(ed3); wgIs317(nhr-28::TY1 EGFP FLAG; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The NHR-28::EGFP fusion protein is expressed in the correct nhr-28 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the NHR-28 transcription factor. made_by : R Waterston )|NHR-28_GFP_EMB_ChIP_Rep1|embryo Emb@ Embryos?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331227 OP317(official name : OP317 genotype : unc119(ed3); wgIs317(nhr-28::TY1 EGFP FLAG; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The NHR-28::EGFP fusion protein is expressed in the correct nhr-28 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the NHR-28 transcription factor. made_by : R Waterston )|NHR-28_GFP_EMB_Input_Rep2|embryo Emb@ Embryos?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331228 OP317(official name : OP317 genotype : unc119(ed3); wgIs317(nhr-28::TY1 EGFP FLAG; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The NHR-28::EGFP fusion protein is expressed in the correct nhr-28 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the NHR-28 transcription factor. made_by : R Waterston )|NHR-28_GFP_EMB_ChIP_Rep2|embryo Emb@ Embryos?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331241 OP99(official name : OP99 genotype : unc119(ed3); wgIs99(nhr-2::TY1 EGFP FLAG; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Dresden using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The NHR-2::EGFP fusion protein is expressed in the correct nhr-2 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the NHR-2 transcription factor. made_by : Unknown )|NHR-2_GFP_EMB_Input_Rep1|embryo Emb@ Embryos?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331242 OP99(official name : OP99 genotype : unc119(ed3); wgIs99(nhr-2::TY1 EGFP FLAG; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Dresden using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The NHR-2::EGFP fusion protein is expressed in the correct nhr-2 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the NHR-2 transcription factor. made_by : Unknown )|NHR-2_GFP_EMB_ChIP_Rep1|embryo Emb@ Embryos?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331243 OP99(official name : OP99 genotype : unc119(ed3); wgIs99(nhr-2::TY1 EGFP FLAG; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Dresden using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The NHR-2::EGFP fusion protein is expressed in the correct nhr-2 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the NHR-2 transcription factor. made_by : Unknown )|NHR-2_GFP_EMB_Input_Rep2|embryo Emb@ Embryos?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331244 OP99(official name : OP99 genotype : unc119(ed3); wgIs99(nhr-2::TY1 EGFP FLAG; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Dresden using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The NHR-2::EGFP fusion protein is expressed in the correct nhr-2 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the NHR-2 transcription factor. made_by : Unknown )|NHR-2_GFP_EMB_ChIP_Rep2|embryo Emb@ Embryos?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331277 OP109(official name : OP109 genotype : unc-119 (ed3) III; wgIs109 blmp-1::TY1::EGFP::FLAG; unc-119 (+) outcross : 0 mutagen : None tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The BLMP-1::EGFP fusion protein is expressed in the correct blmp-1 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the BLMP-1 transcription factor. made_by : R Waterston )|BLMP-1_GFP_Emb_Input_Rep1|embryo Emb@ Embryos?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331278 OP109(official name : OP109 genotype : unc-119 (ed3) III; wgIs109 blmp-1::TY1::EGFP::FLAG; unc-119 (+) outcross : 0 mutagen : None tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The BLMP-1::EGFP fusion protein is expressed in the correct blmp-1 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the BLMP-1 transcription factor. made_by : R Waterston )|BLMP-1_GFP_Emb_ChIP_Rep1|embryo Emb@ Embryos?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331279 OP109(official name : OP109 genotype : unc-119 (ed3) III; wgIs109 blmp-1::TY1::EGFP::FLAG; unc-119 (+) outcross : 0 mutagen : None tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The BLMP-1::EGFP fusion protein is expressed in the correct blmp-1 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the BLMP-1 transcription factor. made_by : R Waterston )|BLMP-1_GFP_Emb_Input_Rep2|embryo Emb@ Embryos?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331280 OP109(official name : OP109 genotype : unc-119 (ed3) III; wgIs109 blmp-1::TY1::EGFP::FLAG; unc-119 (+) outcross : 0 mutagen : None tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The BLMP-1::EGFP fusion protein is expressed in the correct blmp-1 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the BLMP-1 transcription factor. made_by : R Waterston )|BLMP-1_GFP_Emb_ChIP_Rep2|embryo Emb@ Embryos?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331281 OP179(official name : OP179 genotype : unc-119(ed3) III; wgIs179 unc-119(+) gei-11::TY1::EGFP::3xFLAG outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The GEI-11::EGFP fusion protein is expressed in the correct gei-11 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the GEI-11 transcription factor. made_by : R. Waterston )|GEI-11_GFP_Emb_Input_Rep1|embryo Emb@ Embryos?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331282 OP179(official name : OP179 genotype : unc-119(ed3) III; wgIs179 unc-119(+) gei-11::TY1::EGFP::3xFLAG outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The GEI-11::EGFP fusion protein is expressed in the correct gei-11 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the GEI-11 transcription factor. made_by : R. Waterston )|GEI-11_GFP_Emb_ChIP_Rep1|embryo Emb@ Embryos?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331283 OP179(official name : OP179 genotype : unc-119(ed3) III; wgIs179 unc-119(+) gei-11::TY1::EGFP::3xFLAG outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The GEI-11::EGFP fusion protein is expressed in the correct gei-11 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the GEI-11 transcription factor. made_by : R. Waterston )|GEI-11_GFP_Emb_Input_Rep2|embryo Emb@ Embryos?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331284 OP179(official name : OP179 genotype : unc-119(ed3) III; wgIs179 unc-119(+) gei-11::TY1::EGFP::3xFLAG outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The GEI-11::EGFP fusion protein is expressed in the correct gei-11 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the GEI-11 transcription factor. made_by : R. Waterston )|GEI-11_GFP_Emb_ChIP_Rep2|embryo Emb@ Embryos?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331289 OP236(official name : OP236 genotype : unc-119(ed3) III; wgIs236(ekl-2::TY1 EGFP FLAG; unc-119(+)) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology and Genetics in Dresden description : using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The ZTF-11::EGFP fusion protein is expressed in the correct ztf-11 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the ZTF-11 transcription factor. made_by : Unknown )|ZTF-11_GFP_EMB_Input_Rep1|embryo Emb@ Embryos?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331290 OP236(official name : OP236 genotype : unc-119(ed3) III; wgIs236(ekl-2::TY1 EGFP FLAG; unc-119(+)) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology and Genetics in Dresden description : using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The ZTF-11::EGFP fusion protein is expressed in the correct ztf-11 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the ZTF-11 transcription factor. made_by : Unknown )|ZTF-11_GFP_EMB_ChIP_Rep1|embryo Emb@ Embryos?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331291 OP236(official name : OP236 genotype : unc-119(ed3) III; wgIs236(ekl-2::TY1 EGFP FLAG; unc-119(+)) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology and Genetics in Dresden description : using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The ZTF-11::EGFP fusion protein is expressed in the correct ztf-11 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the ZTF-11 transcription factor. made_by : Unknown )|ZTF-11_GFP_EMB_Input_Rep2|embryo Emb@ Embryos?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331292 OP236(official name : OP236 genotype : unc-119(ed3) III; wgIs236(ekl-2::TY1 EGFP FLAG; unc-119(+)) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology and Genetics in Dresden description : using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The ZTF-11::EGFP fusion protein is expressed in the correct ztf-11 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the ZTF-11 transcription factor. made_by : Unknown )|ZTF-11_GFP_EMB_ChIP_Rep2|embryo Emb@ Embryos?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331317 OP391(official name : OP391 genotype : unc-119(ed3) III; wgIs391(med-1::TY1 EGFP FLAG C; unc-119(+)) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology and Genetics in Dresden description : using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The MED-1::EGFP fusion protein is expressed in the correct med-1 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the MED-1 transcription factor. made_by : Unknown )|MED-1_GFP_MIDEMB_Input_Rep1|embryo Emb@ Embryos?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331318 OP391(official name : OP391 genotype : unc-119(ed3) III; wgIs391(med-1::TY1 EGFP FLAG C; unc-119(+)) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology and Genetics in Dresden description : using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The MED-1::EGFP fusion protein is expressed in the correct med-1 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the MED-1 transcription factor. made_by : Unknown )|MED-1_GFP_MIDEMB_ChIP_Rep1|embryo Emb@ Embryos?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331319 OP391(official name : OP391 genotype : unc-119(ed3) III; wgIs391(med-1::TY1 EGFP FLAG C; unc-119(+)) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology and Genetics in Dresden description : using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The MED-1::EGFP fusion protein is expressed in the correct med-1 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the MED-1 transcription factor. made_by : Unknown )|MED-1_GFP_MIDEMB_Input_Rep2|embryo Emb@ Embryos?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331320 OP391(official name : OP391 genotype : unc-119(ed3) III; wgIs391(med-1::TY1 EGFP FLAG C; unc-119(+)) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology and Genetics in Dresden description : using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The MED-1::EGFP fusion protein is expressed in the correct med-1 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the MED-1 transcription factor. made_by : Unknown )|MED-1_GFP_MIDEMB_ChIP_Rep2|embryo Emb@ Embryos?0 1 2 https://www.ncbi.nlm.nih.gov/sra?term=SRX005648 OP37|embryo Emb@ Embryos?0 1 2 https://www.ncbi.nlm.nih.gov/sra?term=SRX212235 Wild-type embryos|Embryo Emb@ Embryos?0 1 2 https://www.ncbi.nlm.nih.gov/sra?term=SRX657410 sdc-2(y93) with RNAi against sdc-2|mixed stage embryos|embryo Emb@ Embryos?0 1 3 https://www.ncbi.nlm.nih.gov/sra?term=SRX1099840 SET4|whole worms|embryo Emb@ Embryos?0 1 3 https://www.ncbi.nlm.nih.gov/sra?term=SRX113602 eri-1(mg366)|embryonic C. elegans|embryo Emb@ Embryos?0 1 4 https://www.ncbi.nlm.nih.gov/sra?term=SRX003830 OP32|embryo Emb@ Embryos?0 1 4 https://www.ncbi.nlm.nih.gov/sra?term=SRX2543050 late C. elegans embryos N2|whole embryo Emb@ Embryos?0 1 4 https://www.ncbi.nlm.nih.gov/sra?term=SRX2543054 late C. elegans embryos wdr-5(-)|whole embryo Emb@ Embryos?0 1 4 https://www.ncbi.nlm.nih.gov/sra?term=SRX2543058 late C. elegans embryos rbbp-5(-)|whole embryo Emb@ Embryos?0 1 6 https://www.ncbi.nlm.nih.gov/sra?term=SRX246024 ChIPed chromatin|embryo Emb@ Embryos?0 1 6 https://www.ncbi.nlm.nih.gov/sra?term=SRX7202519 CG21 egl-30(tg26) I; him-5(e1490) V|Embryonic cells Emb@ Embryos?0 1 6 https://www.ncbi.nlm.nih.gov/sra?term=SRX982063 MT14911|whole worms|embryo Emb@ Embryos?0 1 8 https://www.ncbi.nlm.nih.gov/sra?term=SRX4012473 embryonic lysate Emb@ Embryos?0 1 9 https://www.ncbi.nlm.nih.gov/sra?term=SRX1099837 CB428|whole worms|embryo Emb@ Embryos?0 2 2 https://www.ncbi.nlm.nih.gov/sra?term=SRX013986 OP37|pha-4 transgenic worm OP37|emrbyo Emb@ Embryos?0 3 69 https://www.ncbi.nlm.nih.gov/sra?term=SRX982069 N2|whole worms|embryo Emb@ Embryos?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX043867 N2(genotype : wild type genotype : DR subclone of DB original (Tc1 pattern I) official name : N2 )|Snyder_N2_POLII_lemb_rep1 extraction1_seq1 channel_1|late embryo 20dC 4.5 hrs post-early embryo Emb@ Late embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX043868 N2(genotype : wild type genotype : DR subclone of DB original (Tc1 pattern I) official name : N2 )|Snyder_N2_POLII_lemb_rep1 extraction1_seq1 channel_2|late embryo 20dC 4.5 hrs post-early embryo Emb@ Late embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX043869 N2(genotype : wild type genotype : DR subclone of DB original (Tc1 pattern I) official name : N2 )|Snyder_N2_POLII_lemb_rep2 extraction2_seq1 channel_1|late embryo 20dC 4.5 hrs post-early embryo Emb@ Late embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX043870 N2(genotype : wild type genotype : DR subclone of DB original (Tc1 pattern I) official name : N2 )|Snyder_N2_POLII_lemb_rep2 extraction2_seq1 channel_2|late embryo 20dC 4.5 hrs post-early embryo Emb@ Late embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX2576642 LIN-37 ChIP-seq in wild-type late embryos|late embryo Emb@ Late embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331229 OP305(official name : OP305 genotype : unc119(ed3); wgIs305(nhr-11::TY1 EGFP FLAG; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The NHR-11::EGFP fusion protein is expressed in the correct nhr-11 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the NHR-11 transcription factor. made_by : R Waterston )|NHR-11_GFP_LEMB_Input_Rep1|Late Embryo Emb@ Late embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331230 OP305(official name : OP305 genotype : unc119(ed3); wgIs305(nhr-11::TY1 EGFP FLAG; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The NHR-11::EGFP fusion protein is expressed in the correct nhr-11 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the NHR-11 transcription factor. made_by : R Waterston )|NHR-11_GFP_LEMB_ChIP_Rep1|Late Embryo Emb@ Late embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331231 OP305(official name : OP305 genotype : unc119(ed3); wgIs305(nhr-11::TY1 EGFP FLAG; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The NHR-11::EGFP fusion protein is expressed in the correct nhr-11 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the NHR-11 transcription factor. made_by : R Waterston )|NHR-11_GFP_LEMB_Input_Rep2|Late Embryo Emb@ Late embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331232 OP305(official name : OP305 genotype : unc119(ed3); wgIs305(nhr-11::TY1 EGFP FLAG; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The NHR-11::EGFP fusion protein is expressed in the correct nhr-11 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the NHR-11 transcription factor. made_by : R Waterston )|NHR-11_GFP_LEMB_ChIP_Rep2|Late Embryo Emb@ Late embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331245 OP337(official name : OP337 genotype : unc119(ed3); wgIs377(fkh-10::TY1 EGFP FLAG; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The FKH-10::EGFP fusion protein is expressed in the correct fkh-10 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the FKH-10 transcription factor. made_by : Unknown )|FKH-10_GFP_LEMB_Input_Rep1|Late Embryo Emb@ Late embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331246 OP337(official name : OP337 genotype : unc119(ed3); wgIs377(fkh-10::TY1 EGFP FLAG; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The FKH-10::EGFP fusion protein is expressed in the correct fkh-10 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the FKH-10 transcription factor. made_by : Unknown )|FKH-10_GFP_LEMB_ChIP_Rep1|Late Embryo Emb@ Late embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331247 OP337(official name : OP337 genotype : unc119(ed3); wgIs377(fkh-10::TY1 EGFP FLAG; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The FKH-10::EGFP fusion protein is expressed in the correct fkh-10 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the FKH-10 transcription factor. made_by : Unknown )|FKH-10_GFP_LEMB_Input_Rep2|Late Embryo Emb@ Late embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331248 OP337(official name : OP337 genotype : unc119(ed3); wgIs377(fkh-10::TY1 EGFP FLAG; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The FKH-10::EGFP fusion protein is expressed in the correct fkh-10 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the FKH-10 transcription factor. made_by : Unknown )|FKH-10_GFP_LEMB_ChIP_Rep2|Late Embryo Emb@ Late embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331301 OP398(official name : OP398 genotype : unc-119(ed3) III; wgIs398(dve-1::TY1EGFPFLAG C; unc-119(+)) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology and Genetics in Dresden description : using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The DVE-1::EGFP fusion protein is expressed in the correct dve-1 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the DVE-1 transcription factor. made_by : Unknown )|DVE-1_GFP_LateEMB_Input_Rep1|Late Embryo Emb@ Late embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331302 OP398(official name : OP398 genotype : unc-119(ed3) III; wgIs398(dve-1::TY1EGFPFLAG C; unc-119(+)) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology and Genetics in Dresden description : using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The DVE-1::EGFP fusion protein is expressed in the correct dve-1 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the DVE-1 transcription factor. made_by : Unknown )|DVE-1_GFP_LateEMB_ChIP_Rep1|Late Embryo Emb@ Late embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331303 OP398(official name : OP398 genotype : unc-119(ed3) III; wgIs398(dve-1::TY1EGFPFLAG C; unc-119(+)) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology and Genetics in Dresden description : using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The DVE-1::EGFP fusion protein is expressed in the correct dve-1 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the DVE-1 transcription factor. made_by : Unknown )|DVE-1_GFP_LateEMB_Input_Rep2|Late Embryo Emb@ Late embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331304 OP398(official name : OP398 genotype : unc-119(ed3) III; wgIs398(dve-1::TY1EGFPFLAG C; unc-119(+)) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology and Genetics in Dresden description : using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The DVE-1::EGFP fusion protein is expressed in the correct dve-1 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the DVE-1 transcription factor. made_by : Unknown )|DVE-1_GFP_LateEMB_ChIP_Rep2|Late Embryo Emb@ Late embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331313 OP433(official name : OP433 genotype : unc-119(ed3) III; wgIs433(hlh-30::TY1 EGFP FLAG; unc-119(+)) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology and Genetics in Dresden description : using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The HLH-30::EGFP fusion protein is expressed in the correct hlh-30 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the HLH-30 transcription factor. made_by : Unknown )|HLH-30_GFP_LateEMB_Input_Rep1|Late Embryo Emb@ Late embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331314 OP433(official name : OP433 genotype : unc-119(ed3) III; wgIs433(hlh-30::TY1 EGFP FLAG; unc-119(+)) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology and Genetics in Dresden description : using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The HLH-30::EGFP fusion protein is expressed in the correct hlh-30 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the HLH-30 transcription factor. made_by : Unknown )|HLH-30_GFP_LateEMB_ChIP_Rep1|Late Embryo Emb@ Late embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331315 OP433(official name : OP433 genotype : unc-119(ed3) III; wgIs433(hlh-30::TY1 EGFP FLAG; unc-119(+)) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology and Genetics in Dresden description : using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The HLH-30::EGFP fusion protein is expressed in the correct hlh-30 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the HLH-30 transcription factor. made_by : Unknown )|HLH-30_GFP_LateEMB_Input_Rep2|Late Embryo Emb@ Late embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331316 OP433(official name : OP433 genotype : unc-119(ed3) III; wgIs433(hlh-30::TY1 EGFP FLAG; unc-119(+)) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology and Genetics in Dresden description : using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The HLH-30::EGFP fusion protein is expressed in the correct hlh-30 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the HLH-30 transcription factor. made_by : Unknown )|HLH-30_GFP_LateEMB_ChIP_Rep2|Late Embryo Emb@ Late embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331325 OP404(official name : OP404 genotype : unc-119(ed3) III; wgIs404(nfya-1::TY1-GFP-3xFLA; unc-119(+)) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology and Genetics in Dresden description : using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The NFYA-1::EGFP fusion protein is expressed in the correct nfya-1 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the NFYA-1 transcription factor. made_by : Unknown )|NFYA-1_GFP_LateEMB_Input_Rep1|Late Embryo Emb@ Late embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331326 OP404(official name : OP404 genotype : unc-119(ed3) III; wgIs404(nfya-1::TY1-GFP-3xFLA; unc-119(+)) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology and Genetics in Dresden description : using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The NFYA-1::EGFP fusion protein is expressed in the correct nfya-1 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the NFYA-1 transcription factor. made_by : Unknown )|NFYA-1_GFP_LateEMB_ChIP_Rep1|Late Embryo Emb@ Late embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331327 OP404(official name : OP404 genotype : unc-119(ed3) III; wgIs404(nfya-1::TY1-GFP-3xFLA; unc-119(+)) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology and Genetics in Dresden description : using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The NFYA-1::EGFP fusion protein is expressed in the correct nfya-1 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the NFYA-1 transcription factor. made_by : Unknown )|NFYA-1_GFP_LateEMB_Input_Rep2|Late Embryo Emb@ Late embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331328 OP404(official name : OP404 genotype : unc-119(ed3) III; wgIs404(nfya-1::TY1-GFP-3xFLA; unc-119(+)) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology and Genetics in Dresden description : using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The NFYA-1::EGFP fusion protein is expressed in the correct nfya-1 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the NFYA-1 transcription factor. made_by : Unknown )|NFYA-1_GFP_LateEMB_ChIP_Rep2|Late Embryo Emb@ Late embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX494828 N2|seq-SDQ2370_LIN53_N2_LTemb_Input_Rep1|Late Embryos Emb@ Late embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX494829 N2|seq-SDQ2370_LIN53_N2_LTemb_Input_Rep2|Late Embryos Emb@ Late embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX494830 N2|seq-SDQ2370_LIN53_N2_LTemb_ChIP_Rep1|Late Embryos Emb@ Late embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX494831 N2|seq-SDQ2370_LIN53_N2_LTemb_ChIP_Rep2|Late Embryos Emb@ Late embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX529218 N2|seq-SDQ3166_LIN37_N2_LTemb_Input_Rep1|Late Embryos Emb@ Late embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX529219 N2|seq-SDQ3166_LIN37_N2_LTemb_Input_Rep2|Late Embryos Emb@ Late embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX529220 N2|seq-SDQ3166_LIN37_N2_LTemb_ChIP_Rep1|Late Embryos Emb@ Late embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX529221 N2|seq-SDQ3166_LIN37_N2_LTemb_ChIP_Rep2|Late Embryos Emb@ Late embryo?0 1 2 https://www.ncbi.nlm.nih.gov/sra?term=SRX2576632 LIN-35 ChIP-seq in wild-type late embryos|late embryo Emb@ Late embryo?0 1 2 https://www.ncbi.nlm.nih.gov/sra?term=SRX2576634 LIN-35 ChIP-seq in lin-35(n745) late embryos|late embryo Emb@ Late embryo?0 1 2 https://www.ncbi.nlm.nih.gov/sra?term=SRX335101 JA1597|late embryos_CFP-1::GFP ChIP seq|whole embryo|Late embryo Emb@ Late embryo?0 1 2 https://www.ncbi.nlm.nih.gov/sra?term=SRX335103 JA1597|late embryos_H3K4me3 ChIP seq|whole embryo|Late embryo Emb@ Late embryo?0 1 3 https://www.ncbi.nlm.nih.gov/sra?term=SRX2576620 DPL-1 ChIP-seq in wild-type late embryos|late embryo Emb@ Late embryo?0 1 3 https://www.ncbi.nlm.nih.gov/sra?term=SRX2576623 DPL-1 ChIP-seq in lin-35(n745) late embryos|late embryo Emb@ Late embryo?0 1 3 https://www.ncbi.nlm.nih.gov/sra?term=SRX2576626 EFL-1 ChIP-seq in wild-type late embryos|late embryo Emb@ Late embryo?0 1 3 https://www.ncbi.nlm.nih.gov/sra?term=SRX2576629 EFL-1 ChIP-seq in lin-35(n745) late embryos|late embryo Emb@ Late embryo?0 1 3 https://www.ncbi.nlm.nih.gov/sra?term=SRX2576636 LIN-9 ChIP-seq in wild-type late embryos|late embryo Emb@ Late embryo?0 1 3 https://www.ncbi.nlm.nih.gov/sra?term=SRX2576639 LIN-9 ChIP-seq in lin-35(n745) late embryos|late embryo Emb@ Late embryo?0 1 3 https://www.ncbi.nlm.nih.gov/sra?term=SRX2576643 LIN-37 ChIP-seq in lin-35(n745) late embryos|late embryo Emb@ Late embryo?0 1 3 https://www.ncbi.nlm.nih.gov/sra?term=SRX2576646 LIN-52 ChIP-seq in wild-type late embryos|late embryo Emb@ Late embryo?0 1 3 https://www.ncbi.nlm.nih.gov/sra?term=SRX2576649 LIN-52 ChIP-seq in lin-35(n745) late embryos|late embryo Emb@ Late embryo?0 1 3 https://www.ncbi.nlm.nih.gov/sra?term=SRX2576652 LIN-54 ChIP-seq in wild-type late embryos|late embryo Emb@ Late embryo?0 1 3 https://www.ncbi.nlm.nih.gov/sra?term=SRX2576655 LIN-54 ChIP-seq in lin-35(n745) late embryos|late embryo Emb@ Late embryo?0 1 3 https://www.ncbi.nlm.nih.gov/sra?term=SRX2576663 Input for ChIP-seq, lin-35(n745) extract|late embryo Emb@ Late embryo?0 1 5 https://www.ncbi.nlm.nih.gov/sra?term=SRX2576658 Input for ChIP-seq, wildtype extract|late embryo Emb@ Late embryo?0 1 4 https://www.ncbi.nlm.nih.gov/sra?term=SRX2710279 N2|N2 Embryo|Mid-Embryogenesis (roughly 40 cell stage) Emb@ Mid embryo?0 1 10 https://www.ncbi.nlm.nih.gov/sra?term=SRX2228878 ERC38|whole worms|mixed embryo Emb@ Mixed embryo?0 1 10 https://www.ncbi.nlm.nih.gov/sra?term=SRX5020784 OP37|whole worms|mixed embryo Emb@ Mixed embryo?0 1 11 https://www.ncbi.nlm.nih.gov/sra?term=SRX5545237 mixed-stage embryos Emb@ Mixed embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=ERX1485064 Input_DNA|ERS1162602|mixed stage, early embryos Emb@ Mixed embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX059266 N2|Control sample from mixed embryo N2 worms, whole body|whole body|mixed stages Emb@ Mixed embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX2958247 N2|mixed stage embryos Emb@ Mixed embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX2958248 dpy-21(y607)|mixed stage embryos Emb@ Mixed embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX2958249 dpy-21(e428)|mixed stage embryos Emb@ Mixed embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331353 N2|seq-SDQ2966_MIS12_N2_Mxemb_Input_Rep1|Mixed Embryo Emb@ Mixed embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331354 N2|seq-SDQ2966_MIS12_N2_Mxemb_Input_Rep2|Mixed Embryo Emb@ Mixed embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331355 N2|seq-SDQ2966_MIS12_N2_Mxemb_ChIP_Rep1|Mixed Embryo Emb@ Mixed embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331356 N2|seq-SDQ2966_MIS12_N2_Mxemb_ChIP_Rep2|Mixed Embryo Emb@ Mixed embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331357 N2|seq-AB46540_NIgG_N2_Mxemb_Input_Rep1|Mixed Embryo Emb@ Mixed embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331358 N2|seq-AB46540_NIgG_N2_Mxemb_Input_Rep2|Mixed Embryo Emb@ Mixed embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331359 N2|seq-AB46540_NIgG_N2_Mxemb_ChIP_Rep1|Mixed Embryo Emb@ Mixed embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331360 N2|seq-AB46540_NIgG_N2_Mxemb_ChIP_Rep2|Mixed Embryo Emb@ Mixed embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331361 N2|seq-ab9051_H4K20me1_N2_Mxemb_Input_Rep1|Mixed Embryo Emb@ Mixed embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331362 N2|seq-ab9051_H4K20me1_N2_Mxemb_Input_Rep2|Mixed Embryo Emb@ Mixed embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331363 N2|seq-ab9051_H4K20me1_N2_Mxemb_ChIP_Rep1|Mixed Embryo Emb@ Mixed embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331364 N2|seq-ab9051_H4K20me1_N2_Mxemb_ChIP_Rep2|Mixed Embryo Emb@ Mixed embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX466585 N2|seq-SDQ2946_HCP4_N2_Mxemb_Input_Rep1|Mixed Embryo Emb@ Mixed embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX466586 N2|seq-SDQ2946_HCP4_N2_Mxemb_Input_Rep2|Mixed Embryo Emb@ Mixed embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX466587 N2|seq-SDQ2946_HCP4_N2_Mxemb_ChIP_Rep1|Mixed Embryo Emb@ Mixed embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX466588 N2|seq-SDQ2946_HCP4_N2_Mxemb_ChIP_Rep2|Mixed Embryo Emb@ Mixed embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX494982 TY1072|seq-ab9051_H4K20me1_TY1072_Mxemb_Input_Rep1|Mixed Embryo Emb@ Mixed embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX494983 TY1072|seq-ab9051_H4K20me1_TY1072_Mxemb_Input_Rep2|Mixed Embryo Emb@ Mixed embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX494984 TY1072|seq-ab9051_H4K20me1_TY1072_Mxemb_ChIP_Rep1|Mixed Embryo Emb@ Mixed embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX494985 TY1072|seq-ab9051_H4K20me1_TY1072_Mxemb_ChIP_Rep2|Mixed Embryo Emb@ Mixed embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX494990 N2|seq-NBP170893_HTZ1_N2_Mxemb_Input_Rep1|Mixed Embryo Emb@ Mixed embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX494991 N2|seq-NBP170893_HTZ1_N2_Mxemb_Input_Rep2|Mixed Embryo Emb@ Mixed embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX494992 N2|seq-NBP170893_HTZ1_N2_Mxemb_ChIP_Rep1|Mixed Embryo Emb@ Mixed embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX494993 N2|seq-NBP170893_HTZ1_N2_Mxemb_ChIP_Rep2|Mixed Embryo Emb@ Mixed embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX494994 N2|seq-OD0039_SMC4_N2_Mxemb_Input_Rep1|Mixed Embryo Emb@ Mixed embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX494995 N2|seq-OD0039_SMC4_N2_Mxemb_Input_Rep2|Mixed Embryo Emb@ Mixed embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX494996 N2|seq-OD0039_SMC4_N2_Mxemb_ChIP_Rep2|Mixed Embryo Emb@ Mixed embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX494997 N2|seq-SDQ0839_TBP1_N2_Mxemb_EE_Input_Rep1|Mixed Embryo Emb@ Mixed embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX494998 N2|seq-SDQ0839_TBP1_N2_Mxemb_EE_Input_Rep2|Mixed Embryo Emb@ Mixed embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX494999 N2|seq-SDQ0839_TBP1_N2_Mxemb_EE_ChIP_Rep1|Mixed Embryo Emb@ Mixed embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX495000 N2|seq-SDQ0839_TBP1_N2_Mxemb_EE_ChIP_Rep2|Mixed Embryo Emb@ Mixed embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX495001 N2|seq-SDQ2357Q2358_AMA1_N2_Mxemb_EE_Input_Rep1|Mixed Embryo Emb@ Mixed embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX495002 N2|seq-SDQ2357Q2358_AMA1_N2_Mxemb_EE_Input_Rep2|Mixed Embryo Emb@ Mixed embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX495003 N2|seq-SDQ2357Q2358_AMA1_N2_Mxemb_EE_ChIP_Rep1|Mixed Embryo Emb@ Mixed embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX495004 N2|seq-SDQ2357Q2358_AMA1_N2_Mxemb_EE_ChIP_Rep2|Mixed Embryo Emb@ Mixed embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX495005 N2|seq-SDQ2357Q2358_AMA1_N2_Mxemb_RiIMB1_Input_Rep1|Mixed Embryo Emb@ Mixed embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX495006 N2|seq-SDQ2357Q2358_AMA1_N2_Mxemb_RiIMB1_Input_Rep2|Mixed Embryo Emb@ Mixed embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX495007 N2|seq-SDQ2357Q2358_AMA1_N2_Mxemb_RiIMB1_ChIP_Rep1|Mixed Embryo Emb@ Mixed embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX495008 N2|seq-SDQ2357Q2358_AMA1_N2_Mxemb_RiIMB1_ChIP_Rep2|Mixed Embryo Emb@ Mixed embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX495009 N2|seq-SDQ3499_DPY30_N2_Mxemb_Input_Rep1|Mixed Embryo Emb@ Mixed embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX495010 N2|seq-SDQ3499_DPY30_N2_Mxemb_Input_Rep2|Mixed Embryo Emb@ Mixed embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX495011 N2|seq-SDQ3499_DPY30_N2_Mxemb_ChIP_Rep1|Mixed Embryo Emb@ Mixed embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX495012 N2|seq-SDQ3499_DPY30_N2_Mxemb_ChIP_Rep2|Mixed Embryo Emb@ Mixed embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX495013 N2|seq-SDQ3582_CBP1_N2_Mxemb_Input_Rep1|Mixed Embryo Emb@ Mixed embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX495014 N2|seq-SDQ3582_CBP1_N2_Mxemb_Input_Rep2|Mixed Embryo Emb@ Mixed embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX495015 N2|seq-SDQ3582_CBP1_N2_Mxemb_ChIP_Rep1|Mixed Embryo Emb@ Mixed embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX495016 N2|seq-SDQ3582_CBP1_N2_Mxemb_ChIP_Rep2|Mixed Embryo Emb@ Mixed embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX495017 N2|seq-SDQ3856_SDC1_N2_Mxemb_Input_Rep1|Mixed Embryo Emb@ Mixed embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX495018 N2|seq-SDQ3856_SDC1_N2_Mxemb_Input_Rep2|Mixed Embryo Emb@ Mixed embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX495019 N2|seq-SDQ3856_SDC1_N2_Mxemb_ChIP_Rep1|Mixed Embryo Emb@ Mixed embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX495020 N2|seq-SDQ3856_SDC1_N2_Mxemb_ChIP_Rep2|Mixed Embryo Emb@ Mixed embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX495021 N2|seq-SDQ3892_MIX1_N2_Mxemb_Input_Rep1|Mixed Embryo Emb@ Mixed embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX495022 N2|seq-SDQ3892_MIX1_N2_Mxemb_Input_Rep2|Mixed Embryo Emb@ Mixed embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX495023 N2|seq-SDQ3892_MIX1_N2_Mxemb_ChIP_Rep1|Mixed Embryo Emb@ Mixed embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX495024 N2|seq-SDQ3892_MIX1_N2_Mxemb_ChIP_Rep2|Mixed Embryo Emb@ Mixed embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX495033 N2|seq-SDQ4109_TAF1_N2_Mxemb_Input_Rep1|Mixed Embryo Emb@ Mixed embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX495034 N2|seq-SDQ4109_TAF1_N2_Mxemb_Input_Rep2|Mixed Embryo Emb@ Mixed embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX495035 N2|seq-SDQ4109_TAF1_N2_Mxemb_ChIP_Rep1|Mixed Embryo Emb@ Mixed embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX495036 N2|seq-SDQ4109_TAF1_N2_Mxemb_ChIP_Rep2|Mixed Embryo Emb@ Mixed embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX495045 N2|seq-SDQ4154_IMB1_N2_Mxemb_Input_Rep1|Mixed Embryo Emb@ Mixed embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX495046 N2|seq-SDQ4154_IMB1_N2_Mxemb_Input_Rep2|Mixed Embryo Emb@ Mixed embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX495047 N2|seq-SDQ4154_IMB1_N2_Mxemb_ChIP_Rep1|Mixed Embryo Emb@ Mixed embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX495048 N2|seq-SDQ4154_IMB1_N2_Mxemb_ChIP_Rep2|Mixed Embryo Emb@ Mixed embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX495049 N2|seq-SDQ4481_PQN85_N2_Mxemb_Input_Rep1|Mixed Embryo Emb@ Mixed embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX495050 N2|seq-SDQ4481_PQN85_N2_Mxemb_Input_Rep2|Mixed Embryo Emb@ Mixed embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX495051 N2|seq-SDQ4481_PQN85_N2_Mxemb_ChIP_Rep1|Mixed Embryo Emb@ Mixed embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX495052 N2|seq-SDQ4481_PQN85_N2_Mxemb_ChIP_Rep2|Mixed Embryo Emb@ Mixed embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX495053 N2|seq-SDQ4493_MAU2_N2_Mxemb_Input_Rep1|Mixed Embryo Emb@ Mixed embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX495054 N2|seq-SDQ4493_MAU2_N2_Mxemb_Input_Rep2|Mixed Embryo Emb@ Mixed embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX495055 N2|seq-SDQ4493_MAU2_N2_Mxemb_ChIP_Rep1|Mixed Embryo Emb@ Mixed embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX495056 N2|seq-SDQ4493_MAU2_N2_Mxemb_ChIP_Rep2|Mixed Embryo Emb@ Mixed embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX495057 N2|seq-SDQ4496_DPY26_N2_Mxemb_Input_Rep1|Mixed Embryo Emb@ Mixed embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX495058 N2|seq-SDQ4496_DPY26_N2_Mxemb_Input_Rep2|Mixed Embryo Emb@ Mixed embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX495059 N2|seq-SDQ4496_DPY26_N2_Mxemb_ChIP_Rep1|Mixed Embryo Emb@ Mixed embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX495060 N2|seq-SDQ4496_DPY26_N2_Mxemb_ChIP_Rep2|Mixed Embryo Emb@ Mixed embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX495073 N2|seq-SDQ4561_DPY26_N2_Mxemb_Input_Rep1|Mixed Embryo Emb@ Mixed embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX495074 N2|seq-SDQ4561_DPY26_N2_Mxemb_Input_Rep2|Mixed Embryo Emb@ Mixed embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX495075 N2|seq-SDQ4561_DPY26_N2_Mxemb_ChIP_Rep1|Mixed Embryo Emb@ Mixed embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX495076 N2|seq-SDQ4561_DPY26_N2_Mxemb_ChIP_Rep2|Mixed Embryo Emb@ Mixed embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX495081 N2|seq-SDQ4562_SMC6_N2_Mxemb_Input_Rep1|Mixed Embryo Emb@ Mixed embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX495082 N2|seq-SDQ4562_SMC6_N2_Mxemb_Input_Rep2|Mixed Embryo Emb@ Mixed embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX495083 N2|seq-SDQ4562_SMC6_N2_Mxemb_ChIP_Rep1|Mixed Embryo Emb@ Mixed embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX495084 N2|seq-SDQ4562_SMC6_N2_Mxemb_ChIP_Rep2|Mixed Embryo Emb@ Mixed embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX495085 N2|seq-SDQ4564_DPY28_N2_Mxemb_Input_Rep1|Mixed Embryo Emb@ Mixed embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX495086 N2|seq-SDQ4564_DPY28_N2_Mxemb_Input_Rep2|Mixed Embryo Emb@ Mixed embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX495087 N2|seq-SDQ4564_DPY28_N2_Mxemb_ChIP_Rep1|Mixed Embryo Emb@ Mixed embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX495088 N2|seq-SDQ4564_DPY28_N2_Mxemb_ChIP_Rep2|Mixed Embryo Emb@ Mixed embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX495089 N2|seq-SDQ4585_ASH2_N2_Mxemb_Input_Rep1|Mixed Embryo Emb@ Mixed embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX495090 N2|seq-SDQ4585_ASH2_N2_Mxemb_Input_Rep2|Mixed Embryo Emb@ Mixed embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX495091 N2|seq-SDQ4585_ASH2_N2_Mxemb_ChIP_Rep1|Mixed Embryo Emb@ Mixed embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX495092 N2|seq-SDQ4585_ASH2_N2_Mxemb_ChIP_Rep2|Mixed Embryo Emb@ Mixed embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX495093 N2|seq-SDQ4640_SWD3_N2_Mxemb_Input_Rep1|Mixed Embryo Emb@ Mixed embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX495094 N2|seq-SDQ4640_SWD3_N2_Mxemb_Input_Rep2|Mixed Embryo Emb@ Mixed embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX495095 N2|seq-SDQ4640_SWD3_N2_Mxemb_ChIP_Rep1|Mixed Embryo Emb@ Mixed embryo?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX495096 N2|seq-SDQ4640_SWD3_N2_Mxemb_ChIP_Rep2|Mixed Embryo Emb@ Mixed embryo?0 1 2 https://www.ncbi.nlm.nih.gov/sra?term=SRX4107866 set-2(bn129)|Mixed Embryos|whole larvae|MxE Emb@ Mixed embryo?0 1 2 https://www.ncbi.nlm.nih.gov/sra?term=SRX657408 N2|mixed stage embryos|embryo Emb@ Mixed embryo?0 1 2 https://www.ncbi.nlm.nih.gov/sra?term=SRX7630548 RB2301|mixed-stage embryos|mixed-stage embryos Emb@ Mixed embryo?0 1 3 https://www.ncbi.nlm.nih.gov/sra?term=SRX4200536 Mixed stage early embryos Emb@ Mixed embryo?0 1 4 https://www.ncbi.nlm.nih.gov/sra?term=SRX2228873 TY2205|whole worms|mixed embryo Emb@ Mixed embryo?0 1 4 https://www.ncbi.nlm.nih.gov/sra?term=SRX2228885 ERC54|whole worms|mixed embryo Emb@ Mixed embryo?0 1 4 https://www.ncbi.nlm.nih.gov/sra?term=SRX2228887 ERC64|whole worms|mixed embryo Emb@ Mixed embryo?0 1 4 https://www.ncbi.nlm.nih.gov/sra?term=SRX2249332 Bristol N2|whole embryo|mixed stage (embryonic) Emb@ Mixed embryo?0 1 4 https://www.ncbi.nlm.nih.gov/sra?term=SRX5729148 N2|whole worms|whole worms|mixed embryo Emb@ Mixed embryo?0 1 4 https://www.ncbi.nlm.nih.gov/sra?term=SRX7630544 GW0638|mixed-stage embryos|mixed-stage embryos Emb@ Mixed embryo?0 1 4 https://www.ncbi.nlm.nih.gov/sra?term=SRX982085 MT14911|whole worms|mixed embryo Emb@ Mixed embryo?0 1 6 https://www.ncbi.nlm.nih.gov/sra?term=SRX2228890 ERC51|whole worms|mixed embryo Emb@ Mixed embryo?0 1 6 https://www.ncbi.nlm.nih.gov/sra?term=SRX4107864 cfp-1(tm6369)|Mixed Embryos|whole larvae|MxE Emb@ Mixed embryo?0 1 8 https://www.ncbi.nlm.nih.gov/sra?term=SRX2011718 KW2309|mixed stage early embryos Emb@ Mixed embryo?0 1 8 https://www.ncbi.nlm.nih.gov/sra?term=SRX2228871 TY1072|whole worms|mixed embryo Emb@ Mixed embryo?0 1 8 https://www.ncbi.nlm.nih.gov/sra?term=SRX4082334 N2|mixed embryos Emb@ Mixed embryo?0 1 8 https://www.ncbi.nlm.nih.gov/sra?term=SRX4107862 N2|Mixed Embryos|whole larvae|MxE Emb@ Mixed embryo?0 1 8 https://www.ncbi.nlm.nih.gov/sra?term=SRX5020759 GW638|whole worms|mixed embryo Emb@ Mixed embryo?0 2 20 https://www.ncbi.nlm.nih.gov/sra?term=SRX4085338 wild-type N2|mixed embryos Emb@ Mixed embryo?0 2 24 https://www.ncbi.nlm.nih.gov/sra?term=SRX341784 N2|Mixed-stage embryos Emb@ Mixed embryo?0 2 30 https://www.ncbi.nlm.nih.gov/sra?term=SRX982089 CB428|whole worms|mixed embryo Emb@ Mixed embryo?0 2 4 https://www.ncbi.nlm.nih.gov/sra?term=SRX027210 N2|Caenorhabditis elegans_N2_MXemb|MXemb Emb@ Mixed embryo?0 3 134 https://www.ncbi.nlm.nih.gov/sra?term=SRX982084 N2|whole worms|mixed embryo Emb@ Mixed embryo?0 1 2 https://www.ncbi.nlm.nih.gov/sra?term=SRX4082402 glp-1(e2144)|day 13 adults Adl@ Adult?0 Unc@ Unclassified 1 2 https://www.ncbi.nlm.nih.gov/sra?term=SRX4082394 glp-1(e2144)|day 1 / young adults Adl@ Young adult?0 Adl@ Young adult?0 1 2 https://www.ncbi.nlm.nih.gov/sra?term=SRX4082396 glp-1(e2144)|day 2 adults Adl@ Adult?0 Adl@ Young adult?0 1 2 https://www.ncbi.nlm.nih.gov/sra?term=SRX4082398 glp-1(e2144)|day 6 adults Adl@ Adult?0 Adl@ Young adult?0 1 2 https://www.ncbi.nlm.nih.gov/sra?term=SRX4082400 glp-1(e2144)|day 9 adults Adl@ Adult?0 Adl@ Young adult?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX7246275 JA1585|Muscle nuclei|fed L1 Lar@ Muscle?0 Lar@ L1?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX7246276 JA1585|Muscle nuclei|L3 Lar@ Muscle?0 Lar@ L3?0 1 4 https://www.ncbi.nlm.nih.gov/sra?term=SRX7246257 JA1585|Muscle nuclei|YA Adl@ Muscle?0 Unc@ Unclassified 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX7246277 JA1616|Germline nuclei|L3 Lar@ Germline cells?0 Lar@ L3?0 1 4 https://www.ncbi.nlm.nih.gov/sra?term=SRX7246255 JA1616|Germline nuclei|YA Adl@ Germline?0 Unc@ Unclassified 1 4 https://www.ncbi.nlm.nih.gov/sra?term=SRX7246258 JA1815|Hypodermis nuclei|YA Adl@ Hypodermis?0 Unc@ Unclassified 1 4 https://www.ncbi.nlm.nih.gov/sra?term=SRX7246256 JA1816|Neurons nuclei|YA Adl@ Neurons?0 Unc@ Unclassified 1 4 https://www.ncbi.nlm.nih.gov/sra?term=SRX7246259 JA1817|Intestine nuclei|YA Adl@ Intestine?0 Unc@ Unclassified 1 4 https://www.ncbi.nlm.nih.gov/sra?term=SRX7627551 Bristol|germline|germline Lar@ Germline cells?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX002675 OP37|L1 Lar@ L1?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX043851 OP77(made_by : R. Waterston description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The UNC-130::EGFP fusion protein is expressed in the correct unc-130 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the UNC-130 transcription factor. tags : GFP::3xFlag mutagen : Bombard outcross : 3 genotype : unc-119(ed3) III; wgIs77 unc-119(+) unc-130::TY1::EGFP::3xFLAG official name : OP77 )|Snyder_UNC-130_GFP_L1_rep1 extraction1_seq1 channel_1|fed L1 Lar@ L1?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX043852 OP77(made_by : R. Waterston description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The UNC-130::EGFP fusion protein is expressed in the correct unc-130 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the UNC-130 transcription factor. tags : GFP::3xFlag mutagen : Bombard outcross : 3 genotype : unc-119(ed3) III; wgIs77 unc-119(+) unc-130::TY1::EGFP::3xFLAG official name : OP77 )|Snyder_UNC-130_GFP_L1_rep1 extraction1_seq1 channel_2|fed L1 Lar@ L1?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX043853 OP77(made_by : R. Waterston description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The UNC-130::EGFP fusion protein is expressed in the correct unc-130 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the UNC-130 transcription factor. tags : GFP::3xFlag mutagen : Bombard outcross : 3 genotype : unc-119(ed3) III; wgIs77 unc-119(+) unc-130::TY1::EGFP::3xFLAG official name : OP77 )|Snyder_UNC-130_GFP_L1_rep2 extraction2_seq1 channel_1|fed L1 Lar@ L1?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX043854 OP77(made_by : R. Waterston description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The UNC-130::EGFP fusion protein is expressed in the correct unc-130 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the UNC-130 transcription factor. tags : GFP::3xFlag mutagen : Bombard outcross : 3 genotype : unc-119(ed3) III; wgIs77 unc-119(+) unc-130::TY1::EGFP::3xFLAG official name : OP77 )|Snyder_UNC-130_GFP_L1_rep2 extraction2_seq1 channel_2|fed L1 Lar@ L1?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX043871 N2(genotype : wild type genotype : DR subclone of DB original (Tc1 pattern I) official name : N2 )|Snyder_N2_POLII_L1_rep1 extraction1_seq1 channel_1|fed L1 Lar@ L1?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX043872 N2(genotype : wild type genotype : DR subclone of DB original (Tc1 pattern I) official name : N2 )|Snyder_N2_POLII_L1_rep1 extraction1_seq1 channel_2|fed L1 Lar@ L1?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX043873 N2(genotype : wild type genotype : DR subclone of DB original (Tc1 pattern I) official name : N2 )|Snyder_N2_POLII_L1_rep2 extraction2_seq1 channel_1|fed L1 Lar@ L1?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX043874 N2(genotype : wild type genotype : DR subclone of DB original (Tc1 pattern I) official name : N2 )|Snyder_N2_POLII_L1_rep2 extraction2_seq1 channel_2|fed L1 Lar@ L1?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX043983 OP106(made_by : R Waterston description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The MDL-1::EGFP fusion protein is expressed in the correct mdl-1 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the MDL-1 transcription factor. tags : GFP::3xFlag mutagen : Bombard outcross : 3 genotype : unc-119 (ed3) III; wgIs106 mdl-1::TY1::EGFP::FLAG; unc-119(+)) official name : OP106 )|Snyder_MDL-1_GFP_L1_rep1 extraction1_seq1 channel_1|fed L1 Lar@ L1?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX043984 OP106(made_by : R Waterston description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The MDL-1::EGFP fusion protein is expressed in the correct mdl-1 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the MDL-1 transcription factor. tags : GFP::3xFlag mutagen : Bombard outcross : 3 genotype : unc-119 (ed3) III; wgIs106 mdl-1::TY1::EGFP::FLAG; unc-119(+)) official name : OP106 )|Snyder_MDL-1_GFP_L1_rep1 extraction1_seq1 channel_2|fed L1 Lar@ L1?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX043985 OP106(made_by : R Waterston description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The MDL-1::EGFP fusion protein is expressed in the correct mdl-1 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the MDL-1 transcription factor. tags : GFP::3xFlag mutagen : Bombard outcross : 3 genotype : unc-119 (ed3) III; wgIs106 mdl-1::TY1::EGFP::FLAG; unc-119(+)) official name : OP106 )|Snyder_MDL-1_GFP_L1_rep2 extraction2_seq1 channel_1|fed L1 Lar@ L1?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX043986 OP106(made_by : R Waterston description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The MDL-1::EGFP fusion protein is expressed in the correct mdl-1 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the MDL-1 transcription factor. tags : GFP::3xFlag mutagen : Bombard outcross : 3 genotype : unc-119 (ed3) III; wgIs106 mdl-1::TY1::EGFP::FLAG; unc-119(+)) official name : OP106 )|Snyder_MDL-1_GFP_L1_rep2 extraction2_seq1 channel_2|fed L1 Lar@ L1?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX043991 OP109(made_by : R Waterston description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The BLMP-1::EGFP fusion protein is expressed in the correct blmp-1 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the BLMP-1 transcription factor. tags : GFP::3xFlag mutagen : Bombard outcross : 3 genotype : unc-119 (ed3) III; wgIs109 blmp-1::TY1::EGFP::FLAG; unc-119 (+) official name : OP109 )|Snyder_BLMP-1_GFP_L1_rep1 extraction1_seq1 channel_1|fed L1 Lar@ L1?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX043992 OP109(made_by : R Waterston description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The BLMP-1::EGFP fusion protein is expressed in the correct blmp-1 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the BLMP-1 transcription factor. tags : GFP::3xFlag mutagen : Bombard outcross : 3 genotype : unc-119 (ed3) III; wgIs109 blmp-1::TY1::EGFP::FLAG; unc-119 (+) official name : OP109 )|Snyder_BLMP-1_GFP_L1_rep1 extraction1_seq1 channel_2|fed L1 Lar@ L1?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX043993 OP109(made_by : R Waterston description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The BLMP-1::EGFP fusion protein is expressed in the correct blmp-1 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the BLMP-1 transcription factor. tags : GFP::3xFlag mutagen : Bombard outcross : 3 genotype : unc-119 (ed3) III; wgIs109 blmp-1::TY1::EGFP::FLAG; unc-119 (+) official name : OP109 )|Snyder_BLMP-1_GFP_L1_rep2 extraction2_seq1 channel_1|fed L1 Lar@ L1?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX043994 OP109(made_by : R Waterston description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The BLMP-1::EGFP fusion protein is expressed in the correct blmp-1 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the BLMP-1 transcription factor. tags : GFP::3xFlag mutagen : Bombard outcross : 3 genotype : unc-119 (ed3) III; wgIs109 blmp-1::TY1::EGFP::FLAG; unc-119 (+) official name : OP109 )|Snyder_BLMP-1_GFP_L1_rep2 extraction2_seq1 channel_2|fed L1 Lar@ L1?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX043999 OP75(made_by : R Waterston description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The ELT-3::EGFP fusion protein is expressed in the correct elt-3 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the ELT-3 transcription factor. tags : GFP::3xFlag mutagen : Bombard outcross : 3 genotype : unc-119 (ed3) III; wgIs75 elt-3::TY1::EGFP::FLAG; unc-119 (+) official name : OP75 )|Snyder_ELT-3_GFP_L1_rep1 extraction1_seq1 channel_1|fed L1 Lar@ L1?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX044000 OP75(made_by : R Waterston description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The ELT-3::EGFP fusion protein is expressed in the correct elt-3 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the ELT-3 transcription factor. tags : GFP::3xFlag mutagen : Bombard outcross : 3 genotype : unc-119 (ed3) III; wgIs75 elt-3::TY1::EGFP::FLAG; unc-119 (+) official name : OP75 )|Snyder_ELT-3_GFP_L1_rep1 extraction1_seq1 channel_2|fed L1 Lar@ L1?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX044001 OP75(made_by : R Waterston description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The ELT-3::EGFP fusion protein is expressed in the correct elt-3 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the ELT-3 transcription factor. tags : GFP::3xFlag mutagen : Bombard outcross : 3 genotype : unc-119 (ed3) III; wgIs75 elt-3::TY1::EGFP::FLAG; unc-119 (+) official name : OP75 )|Snyder_ELT-3_GFP_L1_rep2 extraction2_seq1 channel_1|fed L1 Lar@ L1?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX044002 OP75(made_by : R Waterston description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The ELT-3::EGFP fusion protein is expressed in the correct elt-3 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the ELT-3 transcription factor. tags : GFP::3xFlag mutagen : Bombard outcross : 3 genotype : unc-119 (ed3) III; wgIs75 elt-3::TY1::EGFP::FLAG; unc-119 (+) official name : OP75 )|Snyder_ELT-3_GFP_L1_rep2 extraction2_seq1 channel_2|fed L1 Lar@ L1?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX044007 OP177(made_by : S Kim description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The EGL-27::EGFP fusion protein is expressed in the correct egl-27 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the EGL-27 transcription factor. tags : GFP::3xFlag mutagen : Bombard outcross : 3 genotype : unc119(ed3); wgIs177(egl-27::TY1 EGFP FLAG; unc119) official name : OP177 )|Snyder_EGL-27_GFP_L1_rep1 extraction1_seq1 channel_1|fed L1 Lar@ L1?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX044008 OP177(made_by : S Kim description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The EGL-27::EGFP fusion protein is expressed in the correct egl-27 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the EGL-27 transcription factor. tags : GFP::3xFlag mutagen : Bombard outcross : 3 genotype : unc119(ed3); wgIs177(egl-27::TY1 EGFP FLAG; unc119) official name : OP177 )|Snyder_EGL-27_GFP_L1_rep1 extraction1_seq1 channel_2|fed L1 Lar@ L1?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX044009 OP177(made_by : S Kim description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The EGL-27::EGFP fusion protein is expressed in the correct egl-27 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the EGL-27 transcription factor. tags : GFP::3xFlag mutagen : Bombard outcross : 3 genotype : unc119(ed3); wgIs177(egl-27::TY1 EGFP FLAG; unc119) official name : OP177 )|Snyder_EGL-27_GFP_L1_rep2 extraction2_seq1 channel_1|fed L1 Lar@ L1?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX044010 OP177(made_by : S Kim description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The EGL-27::EGFP fusion protein is expressed in the correct egl-27 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the EGL-27 transcription factor. tags : GFP::3xFlag mutagen : Bombard outcross : 3 genotype : unc119(ed3); wgIs177(egl-27::TY1 EGFP FLAG; unc119) official name : OP177 )|Snyder_EGL-27_GFP_L1_rep2 extraction2_seq1 channel_2|fed L1 Lar@ L1?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX044011 OP178(made_by : S Kim tags : GFP::3xFlag mutagen : Bombard outcross : 3 genotype : unc119(ed3); wgIs178(skn-1::TY1 EGFP FLAG; unc119) official name : WBGene00004804 )|Snyder_SKN-1_GFP_L1_rep1 extraction1_seq1 channel_1|fed L1 Lar@ L1?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX044012 OP178(made_by : S Kim tags : GFP::3xFlag mutagen : Bombard outcross : 3 genotype : unc119(ed3); wgIs178(skn-1::TY1 EGFP FLAG; unc119) official name : WBGene00004804 )|Snyder_SKN-1_GFP_L1_rep1 extraction1_seq1 channel_2|fed L1 Lar@ L1?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX044013 OP178(made_by : S Kim tags : GFP::3xFlag mutagen : Bombard outcross : 3 genotype : unc119(ed3); wgIs178(skn-1::TY1 EGFP FLAG; unc119) official name : WBGene00004804 )|Snyder_SKN-1_GFP_L1_rep2 extraction2_seq1 channel_1|fed L1 Lar@ L1?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX044014 OP178(made_by : S Kim tags : GFP::3xFlag mutagen : Bombard outcross : 3 genotype : unc119(ed3); wgIs178(skn-1::TY1 EGFP FLAG; unc119) official name : WBGene00004804 )|Snyder_SKN-1_GFP_L1_rep2 extraction2_seq1 channel_2|fed L1 Lar@ L1?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX065622 OP321(official name : TLP-1 genotype : unc119(ed3); wgIs321(tlp-1::TY1 EGFP FLAG; unc119) outcross : 0 mutagen : None tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The spatio-temporal expression pattern of TLP-1::EGFP fusion protein was examined through in vivo microscopy. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the TLP-1 transcription factor. made_by : Bob Waterston's lab from UW )|Snyder_TLP-1_Input_L1 extraction1_seq1 channel_1|fed L1 Lar@ L1?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX065623 OP321(official name : TLP-1 genotype : unc119(ed3); wgIs321(tlp-1::TY1 EGFP FLAG; unc119) outcross : 0 mutagen : None tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The spatio-temporal expression pattern of TLP-1::EGFP fusion protein was examined through in vivo microscopy. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the TLP-1 transcription factor. made_by : Bob Waterston's lab from UW )|Snyder_TLP-1_Input_L1 extraction2_seq2 channel_1|fed L1 Lar@ L1?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX065624 OP321(official name : TLP-1 genotype : unc119(ed3); wgIs321(tlp-1::TY1 EGFP FLAG; unc119) outcross : 0 mutagen : None tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The spatio-temporal expression pattern of TLP-1::EGFP fusion protein was examined through in vivo microscopy. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the TLP-1 transcription factor. made_by : Bob Waterston's lab from UW )|Snyder_TLP-1_GFP_L1_rep1 extraction3_seq3 channel_1|fed L1 Lar@ L1?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX065625 OP321(official name : TLP-1 genotype : unc119(ed3); wgIs321(tlp-1::TY1 EGFP FLAG; unc119) outcross : 0 mutagen : None tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The spatio-temporal expression pattern of TLP-1::EGFP fusion protein was examined through in vivo microscopy. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the TLP-1 transcription factor. made_by : Bob Waterston's lab from UW )|Snyder_TLP-1_GFP_L1_rep2 extraction4_seq4 channel_1|fed L1 Lar@ L1?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX065683 OP600(official name : OP600 genotype : unc119(ed3); wgIs600(unc-62::TY1 EGFP FLAG; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The UNC-62::EGFP fusion protein is expressed in the correct unc-62 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the UNC-62 transcription factor. made_by : S Kim )|Snyder_UNC-62_Input_L1 extraction1_seq1 channel_1|fed L1 Lar@ L1?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX065684 OP600(official name : OP600 genotype : unc119(ed3); wgIs600(unc-62::TY1 EGFP FLAG; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The UNC-62::EGFP fusion protein is expressed in the correct unc-62 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the UNC-62 transcription factor. made_by : S Kim )|Snyder_UNC-62_Input_L1 extraction2_seq2 channel_1|fed L1 Lar@ L1?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX065685 OP600(official name : OP600 genotype : unc119(ed3); wgIs600(unc-62::TY1 EGFP FLAG; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The UNC-62::EGFP fusion protein is expressed in the correct unc-62 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the UNC-62 transcription factor. made_by : S Kim )|Snyder_UNC-62_GFP_L1_rep1 extraction3_seq3 channel_1|fed L1 Lar@ L1?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX065686 OP600(official name : OP600 genotype : unc119(ed3); wgIs600(unc-62::TY1 EGFP FLAG; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The UNC-62::EGFP fusion protein is expressed in the correct unc-62 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the UNC-62 transcription factor. made_by : S Kim )|Snyder_UNC-62_GFP_L1_rep2 extraction4_seq4 channel_1|fed L1 Lar@ L1?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX065695 OP83(official name : OP83 genotype : unc119(ed3); wgIs83(zag-1::TY1 EGFP FLAG; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The ZAG-1::EGFP fusion protein is expressed in the correct zag-1 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the ZAG-1 transcription factor. made_by : R Waterston )|Snyder_ZAG-1_Input_L1 extraction1_seq1 channel_1|fed L1 Lar@ L1?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX065696 OP83(official name : OP83 genotype : unc119(ed3); wgIs83(zag-1::TY1 EGFP FLAG; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The ZAG-1::EGFP fusion protein is expressed in the correct zag-1 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the ZAG-1 transcription factor. made_by : R Waterston )|Snyder_ZAG-1_Input_L1 extraction2_seq2 channel_1|fed L1 Lar@ L1?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX065697 OP83(official name : OP83 genotype : unc119(ed3); wgIs83(zag-1::TY1 EGFP FLAG; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The ZAG-1::EGFP fusion protein is expressed in the correct zag-1 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the ZAG-1 transcription factor. made_by : R Waterston )|Snyder_ZAG-1_GFP_L1_rep1 extraction3_seq3 channel_1|fed L1 Lar@ L1?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX065698 OP83(official name : OP83 genotype : unc119(ed3); wgIs83(zag-1::TY1 EGFP FLAG; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The ZAG-1::EGFP fusion protein is expressed in the correct zag-1 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the ZAG-1 transcription factor. made_by : R Waterston )|Snyder_ZAG-1_GFP_L1_rep2 extraction4_seq4 channel_1|fed L1 Lar@ L1?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX065707 OP217(official name : OP217 genotype : unc119(ed3); wgIs217(aly-2:TY1 EGFP FLAG; unc119) outcross : 3 transgene : aly-2 tags : Bombard tag : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The ALY-2::EGFP fusion protein is expressed in the correct aly-2 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the ALY-2 transcription factor. made_by : Mihail Sarov )|Snyder_ALY-2_Input_L1 extraction1_seq1 channel_1|fed L1 Lar@ L1?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX065708 OP217(official name : OP217 genotype : unc119(ed3); wgIs217(aly-2:TY1 EGFP FLAG; unc119) outcross : 3 transgene : aly-2 tags : Bombard tag : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The ALY-2::EGFP fusion protein is expressed in the correct aly-2 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the ALY-2 transcription factor. made_by : Mihail Sarov )|Snyder_ALY-2_Input_L1 extraction2_seq2 channel_1|fed L1 Lar@ L1?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX065709 OP217(official name : OP217 genotype : unc119(ed3); wgIs217(aly-2:TY1 EGFP FLAG; unc119) outcross : 3 transgene : aly-2 tags : Bombard tag : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The ALY-2::EGFP fusion protein is expressed in the correct aly-2 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the ALY-2 transcription factor. made_by : Mihail Sarov )|Snyder_ALY-2_GFP_L1_rep1 extraction3_seq3 channel_1|fed L1 Lar@ L1?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX065710 OP217(official name : OP217 genotype : unc119(ed3); wgIs217(aly-2:TY1 EGFP FLAG; unc119) outcross : 3 transgene : aly-2 tags : Bombard tag : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The ALY-2::EGFP fusion protein is expressed in the correct aly-2 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the ALY-2 transcription factor. made_by : Mihail Sarov )|Snyder_ALY-2_GFP_L1_rep2 extraction4_seq4 channel_1|fed L1 Lar@ L1?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX120284 OP304(official name : OP304 genotype : unc119(ed3); wgIs304(fos-1::TY1 EGFP FLAG; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The FOS-1::EGFP fusion protein is expressed in the correct fos-1 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the FOS-1 transcription factor. made_by : R Waterston )|Snyder_FOS-1_Input_L1_rep1 extraction1_seq1|fed L1 Lar@ L1?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX120285 OP304(official name : OP304 genotype : unc119(ed3); wgIs304(fos-1::TY1 EGFP FLAG; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The FOS-1::EGFP fusion protein is expressed in the correct fos-1 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the FOS-1 transcription factor. made_by : R Waterston )|Snyder_FOS-1_Input_L1_rep2 extraction1_seq1|fed L1 Lar@ L1?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX120286 OP304(official name : OP304 genotype : unc119(ed3); wgIs304(fos-1::TY1 EGFP FLAG; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The FOS-1::EGFP fusion protein is expressed in the correct fos-1 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the FOS-1 transcription factor. made_by : R Waterston )|Snyder_FOS-1_GFP_L1_rep1 extraction1_seq1|fed L1 Lar@ L1?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX120287 OP304(official name : OP304 genotype : unc119(ed3); wgIs304(fos-1::TY1 EGFP FLAG; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The FOS-1::EGFP fusion protein is expressed in the correct fos-1 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the FOS-1 transcription factor. made_by : R Waterston )|Snyder_FOS-1_GFP_L1_rep2 extraction1_seq1|fed L1 Lar@ L1?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX146458 YL424(official name : YL424 genotype : unc-119(ed3); vrIs68pEFL-1::EFL-1::GFP FLAG: EFL-1 3?UTR genotype : unc-119 (+) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : made_by : )|Snyder_Pefl1_EFL1_Input_L1_rep1|fed L1 Lar@ L1?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX146459 YL424(official name : YL424 genotype : unc-119(ed3); vrIs68pEFL-1::EFL-1::GFP FLAG: EFL-1 3?UTR genotype : unc-119 (+) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : made_by : )|Snyder_Pefl1_EFL1_Input_L1_rep2|fed L1 Lar@ L1?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX146460 YL424(official name : YL424 genotype : unc-119(ed3); vrIs68pEFL-1::EFL-1::GFP FLAG: EFL-1 3?UTR genotype : unc-119 (+) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : made_by : )|Snyder_Pefl1_EFL1_GFP_L1_rep1|fed L1 Lar@ L1?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX146461 YL424(official name : YL424 genotype : unc-119(ed3); vrIs68pEFL-1::EFL-1::GFP FLAG: EFL-1 3?UTR genotype : unc-119 (+) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : made_by : )|Snyder_Pefl1_EFL1_GFP_L1_rep2|fed L1 Lar@ L1?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX146462 YL425(official name : YL425 genotype : unc-119(ed3) III; vrIs69pDPL-1::DPL-1::GFP FLAG: DPL-1 3?UTR genotype : unc-119 (+) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : made_by : )|Snyder_Pdpl1_DPL1_Input_L1_rep1|fed L1 Lar@ L1?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX146463 YL425(official name : YL425 genotype : unc-119(ed3) III; vrIs69pDPL-1::DPL-1::GFP FLAG: DPL-1 3?UTR genotype : unc-119 (+) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : made_by : )|Snyder_Pdpl1_DPL1_Input_L1_rep2|fed L1 Lar@ L1?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX146464 YL425(official name : YL425 genotype : unc-119(ed3) III; vrIs69pDPL-1::DPL-1::GFP FLAG: DPL-1 3?UTR genotype : unc-119 (+) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : made_by : )|Snyder_Pdpl1_DPL1_GFP_L1_rep1|fed L1 Lar@ L1?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX146465 YL425(official name : YL425 genotype : unc-119(ed3) III; vrIs69pDPL-1::DPL-1::GFP FLAG: DPL-1 3?UTR genotype : unc-119 (+) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : made_by : )|Snyder_Pdpl1_DPL1_GFP_L1_rep2|fed L1 Lar@ L1?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX146466 OP174(official name : OP174 genotype : unc-119(ed3); wgIs174(ces-1::TY1 EGFP FLAG; unc-119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The CES-1::EGFP fusion protein is expressed in the correct ces-1 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the CES-1 transcription factor. made_by : S. Kim )|Snyder_CES1_Input_L1_rep1|fed L1 Lar@ L1?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX146467 OP174(official name : OP174 genotype : unc-119(ed3); wgIs174(ces-1::TY1 EGFP FLAG; unc-119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The CES-1::EGFP fusion protein is expressed in the correct ces-1 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the CES-1 transcription factor. made_by : S. Kim )|Snyder_CES1_Input_L1_rep2|fed L1 Lar@ L1?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX146468 OP174(official name : OP174 genotype : unc-119(ed3); wgIs174(ces-1::TY1 EGFP FLAG; unc-119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The CES-1::EGFP fusion protein is expressed in the correct ces-1 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the CES-1 transcription factor. made_by : S. Kim )|Snyder_CES1_GFP_L1_rep1|fed L1 Lar@ L1?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX146469 OP174(official name : OP174 genotype : unc-119(ed3); wgIs174(ces-1::TY1 EGFP FLAG; unc-119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The CES-1::EGFP fusion protein is expressed in the correct ces-1 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the CES-1 transcription factor. made_by : S. Kim )|Snyder_CES1_GFP_L1_rep2|fed L1 Lar@ L1?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX146514 OP114(official name : OP114 genotype : unc119(ed3); wgIs114(F16B12.6::TY1 EGFP FLAG; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The F16B12.6::EGFP fusion protein is expressed in the correct F16B12.6 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the F16B12.6 transcription factor. made_by : R Waterston )|Snyder_F16B12.6_Input_L1_rep1|fed L1 Lar@ L1?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX146515 OP114(official name : OP114 genotype : unc119(ed3); wgIs114(F16B12.6::TY1 EGFP FLAG; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The F16B12.6::EGFP fusion protein is expressed in the correct F16B12.6 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the F16B12.6 transcription factor. made_by : R Waterston )|Snyder_F16B12.6_Input_L1_rep2|fed L1 Lar@ L1?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX146516 OP114(official name : OP114 genotype : unc119(ed3); wgIs114(F16B12.6::TY1 EGFP FLAG; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The F16B12.6::EGFP fusion protein is expressed in the correct F16B12.6 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the F16B12.6 transcription factor. made_by : R Waterston )|Snyder_F16B12.6_GFP_L1_rep1|fed L1 Lar@ L1?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX146517 OP114(official name : OP114 genotype : unc119(ed3); wgIs114(F16B12.6::TY1 EGFP FLAG; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The F16B12.6::EGFP fusion protein is expressed in the correct F16B12.6 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the F16B12.6 transcription factor. made_by : R Waterston )|Snyder_F16B12.6_GFP_L1_rep2|fed L1 Lar@ L1?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX147611 OP301(official name : OP301 genotype : unc119(ed3); wgIs301(mef-2::TY1 EGFP FLAG; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The MEF-2::EGFP fusion protein is expressed in the correct mef-2 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the MEF-2 transcription factor. made_by : R Waterston )|Snyder_MEF-2_Input_L1_rep1|fed L1 Lar@ L1?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX147612 OP301(official name : OP301 genotype : unc119(ed3); wgIs301(mef-2::TY1 EGFP FLAG; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The MEF-2::EGFP fusion protein is expressed in the correct mef-2 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the MEF-2 transcription factor. made_by : R Waterston )|Snyder_MEF-2_Input_L1_rep2|fed L1 Lar@ L1?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX147613 OP301(official name : OP301 genotype : unc119(ed3); wgIs301(mef-2::TY1 EGFP FLAG; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The MEF-2::EGFP fusion protein is expressed in the correct mef-2 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the MEF-2 transcription factor. made_by : R Waterston )|Snyder_MEF-2_GFP_L1_rep1|fed L1 Lar@ L1?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX147614 OP301(official name : OP301 genotype : unc119(ed3); wgIs301(mef-2::TY1 EGFP FLAG; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The MEF-2::EGFP fusion protein is expressed in the correct mef-2 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the MEF-2 transcription factor. made_by : R Waterston )|Snyder_MEF-2_GFP_L1_rep2|fed L1 Lar@ L1?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX147643 OP212(official name : OP212 genotype : unc-119(ed3); wgIs212(F45C12.2:TY1 EGFP FLAG; unc-119(+)) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Dresden using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The F45C12.2::EGFP fusion protein is expressed in the correct F45C12.2 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the F45C12.2 transcription factor. made_by : Mihail Sarov )|Snyder_F45C12.2_Input_L1_rep1|fed L1 Lar@ L1?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX147644 OP212(official name : OP212 genotype : unc-119(ed3); wgIs212(F45C12.2:TY1 EGFP FLAG; unc-119(+)) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Dresden using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The F45C12.2::EGFP fusion protein is expressed in the correct F45C12.2 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the F45C12.2 transcription factor. made_by : Mihail Sarov )|Snyder_F45C12.2_Input_L1_rep2|fed L1 Lar@ L1?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX147645 OP212(official name : OP212 genotype : unc-119(ed3); wgIs212(F45C12.2:TY1 EGFP FLAG; unc-119(+)) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Dresden using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The F45C12.2::EGFP fusion protein is expressed in the correct F45C12.2 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the F45C12.2 transcription factor. made_by : Mihail Sarov )|Snyder_F45C12.2_GFP_L1_rep1|fed L1 Lar@ L1?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX147646 OP212(official name : OP212 genotype : unc-119(ed3); wgIs212(F45C12.2:TY1 EGFP FLAG; unc-119(+)) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Dresden using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The F45C12.2::EGFP fusion protein is expressed in the correct F45C12.2 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the F45C12.2 transcription factor. made_by : Mihail Sarov )|Snyder_F45C12.2_GFP_L1_rep2|fed L1 Lar@ L1?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX222636 OP345(official name : OP345 genotype : unc119(ed3); wgIs345(C16A3.4::TY1 EGFP FLAG; unc119) outcross : 0 mutagen : None tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for bombardment transformation of an unc-119(ed3) strain. The C16A3.4::EGFP fusion protein has broad expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the C16A3.4 transcription factor. made_by : Bob Waterston's lab from UW )|Snyder_C16A3.4_Input_L1_rep1_GTAT|fed L1 Lar@ L1?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX222637 OP345(official name : OP345 genotype : unc119(ed3); wgIs345(C16A3.4::TY1 EGFP FLAG; unc119) outcross : 0 mutagen : None tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for bombardment transformation of an unc-119(ed3) strain. The C16A3.4::EGFP fusion protein has broad expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the C16A3.4 transcription factor. made_by : Bob Waterston's lab from UW )|Snyder_C16A3.4_Input_L1_rep2_CATT|fed L1 Lar@ L1?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX222638 OP345(official name : OP345 genotype : unc119(ed3); wgIs345(C16A3.4::TY1 EGFP FLAG; unc119) outcross : 0 mutagen : None tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for bombardment transformation of an unc-119(ed3) strain. The C16A3.4::EGFP fusion protein has broad expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the C16A3.4 transcription factor. made_by : Bob Waterston's lab from UW )|Snyder_C16A3.4_GFP_L1_rep1_GTAT|fed L1 Lar@ L1?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX222639 OP345(official name : OP345 genotype : unc119(ed3); wgIs345(C16A3.4::TY1 EGFP FLAG; unc119) outcross : 0 mutagen : None tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for bombardment transformation of an unc-119(ed3) strain. The C16A3.4::EGFP fusion protein has broad expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the C16A3.4 transcription factor. made_by : Bob Waterston's lab from UW )|Snyder_C16A3.4_GFP_L1_rep2_CATT|fed L1 Lar@ L1?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX233415 OP105(official name : OP105 genotype : unc119(ed3); wgIs105(dpl-1::TY1 EGFP FLAG; unc119) outcross : 0 mutagen : None tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for bombardment transformation of an unc-119(ed3) strain. The DPL-1::EGFP fusion protein has broad expression pattern description : but silence in germline cells. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the DPL-1 transcription factor. made_by : Bob Waterston's lab from UW )|Snyder_DPL-1_GFP_L1v2_rep1_Input_GTAT|fed L1 Lar@ L1?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX233416 OP105(official name : OP105 genotype : unc119(ed3); wgIs105(dpl-1::TY1 EGFP FLAG; unc119) outcross : 0 mutagen : None tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for bombardment transformation of an unc-119(ed3) strain. The DPL-1::EGFP fusion protein has broad expression pattern description : but silence in germline cells. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the DPL-1 transcription factor. made_by : Bob Waterston's lab from UW )|Snyder_DPL-1_GFP_L1v2_rep2_Input_CATT|fed L1 Lar@ L1?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX233417 OP105(official name : OP105 genotype : unc119(ed3); wgIs105(dpl-1::TY1 EGFP FLAG; unc119) outcross : 0 mutagen : None tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for bombardment transformation of an unc-119(ed3) strain. The DPL-1::EGFP fusion protein has broad expression pattern description : but silence in germline cells. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the DPL-1 transcription factor. made_by : Bob Waterston's lab from UW )|Snyder_DPL-1_GFP_L1v2_rep1_GFP_GTAT|fed L1 Lar@ L1?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX233418 OP105(official name : OP105 genotype : unc119(ed3); wgIs105(dpl-1::TY1 EGFP FLAG; unc119) outcross : 0 mutagen : None tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for bombardment transformation of an unc-119(ed3) strain. The DPL-1::EGFP fusion protein has broad expression pattern description : but silence in germline cells. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the DPL-1 transcription factor. made_by : Bob Waterston's lab from UW )|Snyder_DPL-1_GFP_L1v2_rep2_GFP_CATT|fed L1 Lar@ L1?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX233451 OP184(official name : OP184 genotype : unc119(ed3); wgIs184(lin-15B::TY1 EGFP FLAG; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The LIN-15B::EGFP fusion protein is expressed in the correct lin-15B spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the LIN-15B transcription factor. made_by : S Kim )|Snyder_LIN-15B_GFP_L1_rep1_Input_CATT|fed L1 Lar@ L1?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX233452 OP184(official name : OP184 genotype : unc119(ed3); wgIs184(lin-15B::TY1 EGFP FLAG; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The LIN-15B::EGFP fusion protein is expressed in the correct lin-15B spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the LIN-15B transcription factor. made_by : S Kim )|Snyder_LIN-15B_GFP_L1_rep2_Input_GTAT|fed L1 Lar@ L1?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX233453 OP184(official name : OP184 genotype : unc119(ed3); wgIs184(lin-15B::TY1 EGFP FLAG; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The LIN-15B::EGFP fusion protein is expressed in the correct lin-15B spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the LIN-15B transcription factor. made_by : S Kim )|Snyder_LIN-15B_GFP_L1_rep1_GFP_GTAT|fed L1 Lar@ L1?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX233454 OP184(official name : OP184 genotype : unc119(ed3); wgIs184(lin-15B::TY1 EGFP FLAG; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The LIN-15B::EGFP fusion protein is expressed in the correct lin-15B spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the LIN-15B transcription factor. made_by : S Kim )|Snyder_LIN-15B_GFP_L1_rep2_GFP_CATT|fed L1 Lar@ L1?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX233455 OP353(official name : OP353 genotype : unc119(ed3); wgIs353(nhr-77::TY1 EGFP FLAG; unc119) outcross : 3 transgene : nhr-77 tags : Bombard tag : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The NHR-77::EGFP fusion protein is expressed in the correct nhr-77 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the NHR-77 transcription factor. made_by : R Waterston )|Snyder_NHR-77_GFP_L1_rep1_Input_GTAT|fed L1 Lar@ L1?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX233456 OP353(official name : OP353 genotype : unc119(ed3); wgIs353(nhr-77::TY1 EGFP FLAG; unc119) outcross : 3 transgene : nhr-77 tags : Bombard tag : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The NHR-77::EGFP fusion protein is expressed in the correct nhr-77 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the NHR-77 transcription factor. made_by : R Waterston )|Snyder_NHR-77_GFP_L1_rep2_Input_CATT|fed L1 Lar@ L1?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX233457 OP353(official name : OP353 genotype : unc119(ed3); wgIs353(nhr-77::TY1 EGFP FLAG; unc119) outcross : 3 transgene : nhr-77 tags : Bombard tag : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The NHR-77::EGFP fusion protein is expressed in the correct nhr-77 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the NHR-77 transcription factor. made_by : R Waterston )|Snyder_NHR-77_GFP_L1_rep1_GFP_ACGT|fed L1 Lar@ L1?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX233458 OP353(official name : OP353 genotype : unc119(ed3); wgIs353(nhr-77::TY1 EGFP FLAG; unc119) outcross : 3 transgene : nhr-77 tags : Bombard tag : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The NHR-77::EGFP fusion protein is expressed in the correct nhr-77 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the NHR-77 transcription factor. made_by : R Waterston )|Snyder_NHR-77_GFP_L1_rep2_GFP_TGCT|fed L1 Lar@ L1?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX233459 YL398(official name : YL398 genotype : unc-119(ed3) III; vrIs55pGES-1::LIN-35::GFP FLAG: LIN-35 3'-UTR genotype : unc-119 (+) outcross : 0 mutagen : None tags : GFP::3xFlag description : The LIN-35::GFP fusion protein is driven by the ges-1 promoter and is expressed in the intestine. made_by : Michelle Kudron in Reinke lab )|Snyder_Pges-1_LIN-35_YL398_L1_rep1_Input_GTAT|fed L1 Lar@ L1?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX233460 YL398(official name : YL398 genotype : unc-119(ed3) III; vrIs55pGES-1::LIN-35::GFP FLAG: LIN-35 3'-UTR genotype : unc-119 (+) outcross : 0 mutagen : None tags : GFP::3xFlag description : The LIN-35::GFP fusion protein is driven by the ges-1 promoter and is expressed in the intestine. made_by : Michelle Kudron in Reinke lab )|Snyder_Pges-1_LIN-35_YL398_L1_rep2_Input_CATT|fed L1 Lar@ L1?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX233461 YL398(official name : YL398 genotype : unc-119(ed3) III; vrIs55pGES-1::LIN-35::GFP FLAG: LIN-35 3'-UTR genotype : unc-119 (+) outcross : 0 mutagen : None tags : GFP::3xFlag description : The LIN-35::GFP fusion protein is driven by the ges-1 promoter and is expressed in the intestine. made_by : Michelle Kudron in Reinke lab )|Snyder_Pges-1_LIN-35_YL398_L1_rep1_GFP_GTAT|fed L1 Lar@ L1?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX233462 YL398(official name : YL398 genotype : unc-119(ed3) III; vrIs55pGES-1::LIN-35::GFP FLAG: LIN-35 3'-UTR genotype : unc-119 (+) outcross : 0 mutagen : None tags : GFP::3xFlag description : The LIN-35::GFP fusion protein is driven by the ges-1 promoter and is expressed in the intestine. made_by : Michelle Kudron in Reinke lab )|Snyder_Pges-1_LIN-35_YL398_L1_rep2_GFP_GTAT|fed L1 Lar@ L1?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX234910 OP355(official name : OP355 genotype : unc-119(ed3) III; wgIs355(ZK377.2::TY1 EGFP FLAG; unc-119(+)) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Dresden using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The sax-3::EGFP fusion protein is expressed in the correct sax-3 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the sax-3 transcription factor. The sax-3 gene is encoded by the ZK377.2 CDS. made_by : R Waterston )|Snyder_ZK377.2_GFP_L1_rep1_Input_GTAT|fed L1 Lar@ L1?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX234911 OP355(official name : OP355 genotype : unc-119(ed3) III; wgIs355(ZK377.2::TY1 EGFP FLAG; unc-119(+)) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Dresden using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The sax-3::EGFP fusion protein is expressed in the correct sax-3 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the sax-3 transcription factor. The sax-3 gene is encoded by the ZK377.2 CDS. made_by : R Waterston )|Snyder_ZK377.2_GFP_L1_rep2_Input_CATT|fed L1 Lar@ L1?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX234912 OP355(official name : OP355 genotype : unc-119(ed3) III; wgIs355(ZK377.2::TY1 EGFP FLAG; unc-119(+)) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Dresden using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The sax-3::EGFP fusion protein is expressed in the correct sax-3 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the sax-3 transcription factor. The sax-3 gene is encoded by the ZK377.2 CDS. made_by : R Waterston )|Snyder_ZK377.2_GFP_L1_rep1_GFP_GTAT|fed L1 Lar@ L1?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX234913 OP355(official name : OP355 genotype : unc-119(ed3) III; wgIs355(ZK377.2::TY1 EGFP FLAG; unc-119(+)) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Dresden using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The sax-3::EGFP fusion protein is expressed in the correct sax-3 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the sax-3 transcription factor. The sax-3 gene is encoded by the ZK377.2 CDS. made_by : R Waterston )|Snyder_ZK377.2_GFP_L1_rep2_GFP_CATT|fed L1 Lar@ L1?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX234922 YL416(official name : YL416 genotype : unc-119(ed3) III; vrIs64pGES-1::HPL-2::GFP FLAG: HPL-2 3'-UTR genotype : unc-119 (+) outcross : 0 mutagen : None tags : GFP::3xFlag description : The HPL-2::GFP fusion protein is driven by the ges-1 promoter and is expressed in the intestine. made_by : Michelle Kudron in Reinke lab )|Snyder_Pges-1_HPL-2_YL416_L1_rep1_Input_ACGT|fed L1 Lar@ L1?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX234923 YL416(official name : YL416 genotype : unc-119(ed3) III; vrIs64pGES-1::HPL-2::GFP FLAG: HPL-2 3'-UTR genotype : unc-119 (+) outcross : 0 mutagen : None tags : GFP::3xFlag description : The HPL-2::GFP fusion protein is driven by the ges-1 promoter and is expressed in the intestine. made_by : Michelle Kudron in Reinke lab )|Snyder_Pges-1_HPL-2_YL416_L1_rep2_Input_ACGT|fed L1 Lar@ L1?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX234924 YL416(official name : YL416 genotype : unc-119(ed3) III; vrIs64pGES-1::HPL-2::GFP FLAG: HPL-2 3'-UTR genotype : unc-119 (+) outcross : 0 mutagen : None tags : GFP::3xFlag description : The HPL-2::GFP fusion protein is driven by the ges-1 promoter and is expressed in the intestine. made_by : Michelle Kudron in Reinke lab )|Snyder_Pges-1_HPL-2_YL416_L1_rep1_GFP_ACGT|fed L1 Lar@ L1?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX234925 YL416(official name : YL416 genotype : unc-119(ed3) III; vrIs64pGES-1::HPL-2::GFP FLAG: HPL-2 3'-UTR genotype : unc-119 (+) outcross : 0 mutagen : None tags : GFP::3xFlag description : The HPL-2::GFP fusion protein is driven by the ges-1 promoter and is expressed in the intestine. made_by : Michelle Kudron in Reinke lab )|Snyder_Pges-1_HPL-2_YL416_L1_rep2_GFP_ACGT|fed L1 Lar@ L1?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX235170 OP196(official name : OP196 genotype : unc119(ed3); wgIs196(sptf1::TY1 EGFP FLAG C; unc119) outcross : 3 transgene : sptf-1 tags : Bombard tag : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The SPTF-1::EGFP fusion protein is expressed in the correct sptf-1 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the SPTF-1 transcription factor. made_by : S Kim )|Snyder_SPTF-1_GFP_L1_rep1_Input_GTAT|fed L1 Lar@ L1?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX235171 OP196(official name : OP196 genotype : unc119(ed3); wgIs196(sptf1::TY1 EGFP FLAG C; unc119) outcross : 3 transgene : sptf-1 tags : Bombard tag : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The SPTF-1::EGFP fusion protein is expressed in the correct sptf-1 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the SPTF-1 transcription factor. made_by : S Kim )|Snyder_SPTF-1_GFP_L1_rep2_Input_CATT|fed L1 Lar@ L1?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX235172 OP196(official name : OP196 genotype : unc119(ed3); wgIs196(sptf1::TY1 EGFP FLAG C; unc119) outcross : 3 transgene : sptf-1 tags : Bombard tag : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The SPTF-1::EGFP fusion protein is expressed in the correct sptf-1 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the SPTF-1 transcription factor. made_by : S Kim )|Snyder_SPTF-1_GFP_L1_rep1_GFP_GTAT|fed L1 Lar@ L1?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX235173 OP196(official name : OP196 genotype : unc119(ed3); wgIs196(sptf1::TY1 EGFP FLAG C; unc119) outcross : 3 transgene : sptf-1 tags : Bombard tag : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The SPTF-1::EGFP fusion protein is expressed in the correct sptf-1 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the SPTF-1 transcription factor. made_by : S Kim )|Snyder_SPTF-1_GFP_L1_rep2_GFP_CATT|fed L1 Lar@ L1?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX277020 OP234(official name : OP234 genotype : unc119(ed3); wgIs234(T24H10.7:TY1 EGFP FLAG; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The JUN-1::EGFP fusion protein is expressed in the correct jun-1 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the JUN-1 transcription factor. made_by : Unknown )|JUN-1 L1 InputRep1|L1 26dC Lar@ L1?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX277021 OP234(official name : OP234 genotype : unc119(ed3); wgIs234(T24H10.7:TY1 EGFP FLAG; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The JUN-1::EGFP fusion protein is expressed in the correct jun-1 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the JUN-1 transcription factor. made_by : Unknown )|JUN-1 L1 InputRep2|L1 26dC Lar@ L1?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX277022 OP234(official name : OP234 genotype : unc119(ed3); wgIs234(T24H10.7:TY1 EGFP FLAG; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The JUN-1::EGFP fusion protein is expressed in the correct jun-1 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the JUN-1 transcription factor. made_by : Unknown )|JUN-1 L1 ChIPRep1|L1 26dC Lar@ L1?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX277023 OP234(official name : OP234 genotype : unc119(ed3); wgIs234(T24H10.7:TY1 EGFP FLAG; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The JUN-1::EGFP fusion protein is expressed in the correct jun-1 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the JUN-1 transcription factor. made_by : Unknown )|JUN-1 L1 ChIPRep2|L1 26dC Lar@ L1?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX277057 OP322(official name : OP322 genotype : unc-119(ed3); wgIs322(ztf-4::TY1 EGFP FLAG; unc119(+)) outcross : 0 mutagen : None tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Dresden using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The spatio-temporal expression pattern of ZTF-4::EGFP fusion protein was examined through in vivo microscopy. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the ZTF-4 transcription factor. made_by : Bob Waterston's lab from UW )|ZTF-4 L1 InputRep1|L1 26dC Lar@ L1?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX277058 OP322(official name : OP322 genotype : unc-119(ed3); wgIs322(ztf-4::TY1 EGFP FLAG; unc119(+)) outcross : 0 mutagen : None tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Dresden using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The spatio-temporal expression pattern of ZTF-4::EGFP fusion protein was examined through in vivo microscopy. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the ZTF-4 transcription factor. made_by : Bob Waterston's lab from UW )|ZTF-4 L1 InputRep2|L1 26dC Lar@ L1?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX277059 OP322(official name : OP322 genotype : unc-119(ed3); wgIs322(ztf-4::TY1 EGFP FLAG; unc119(+)) outcross : 0 mutagen : None tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Dresden using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The spatio-temporal expression pattern of ZTF-4::EGFP fusion protein was examined through in vivo microscopy. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the ZTF-4 transcription factor. made_by : Bob Waterston's lab from UW )|ZTF-4 L1 ChIPRep1|L1 26dC Lar@ L1?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX277060 OP322(official name : OP322 genotype : unc-119(ed3); wgIs322(ztf-4::TY1 EGFP FLAG; unc119(+)) outcross : 0 mutagen : None tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Dresden using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The spatio-temporal expression pattern of ZTF-4::EGFP fusion protein was examined through in vivo microscopy. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the ZTF-4 transcription factor. made_by : Bob Waterston's lab from UW )|ZTF-4 L1 ChIPRep2|L1 26dC Lar@ L1?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX277086 OP49(official name : OP49 genotype : unc119(ed3); wgIs49(lin-13::TY1 EGFP FLAG; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The LIN-13::EGFP fusion protein is expressed in the correct lin-13 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the LIN-13 transcription factor. made_by : Unknown )|LIN-13 L1 InputRep1|L1 26dC Lar@ L1?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX277087 OP49(official name : OP49 genotype : unc119(ed3); wgIs49(lin-13::TY1 EGFP FLAG; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The LIN-13::EGFP fusion protein is expressed in the correct lin-13 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the LIN-13 transcription factor. made_by : Unknown )|LIN-13 L1 InputRep2|L1 26dC Lar@ L1?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX277088 OP49(official name : OP49 genotype : unc119(ed3); wgIs49(lin-13::TY1 EGFP FLAG; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The LIN-13::EGFP fusion protein is expressed in the correct lin-13 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the LIN-13 transcription factor. made_by : Unknown )|LIN-13 L1 ChIPRep1|L1 26dC Lar@ L1?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX277089 OP49(official name : OP49 genotype : unc119(ed3); wgIs49(lin-13::TY1 EGFP FLAG; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The LIN-13::EGFP fusion protein is expressed in the correct lin-13 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the LIN-13 transcription factor. made_by : Unknown )|LIN-13 L1 ChIPRep2|L1 26dC Lar@ L1?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331041 OP124(official name : OP124 genotype : unc-119(ed3); wgIs124(aha-1::TY1 EGFP FLAG; unc-119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The AHA-1::EGFP fusion protein is expressed in the correct aha-1 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the AHA-1 transcription factor. made_by : R. Waterston and S. Kim )|AHA-1_GFP_L1_Input_Rep1|fed L1 Lar@ L1?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331042 OP124(official name : OP124 genotype : unc-119(ed3); wgIs124(aha-1::TY1 EGFP FLAG; unc-119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The AHA-1::EGFP fusion protein is expressed in the correct aha-1 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the AHA-1 transcription factor. made_by : R. Waterston and S. Kim )|AHA-1_GFP_L1_ChIP_Rep1|fed L1 Lar@ L1?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331043 OP124(official name : OP124 genotype : unc-119(ed3); wgIs124(aha-1::TY1 EGFP FLAG; unc-119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The AHA-1::EGFP fusion protein is expressed in the correct aha-1 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the AHA-1 transcription factor. made_by : R. Waterston and S. Kim )|AHA-1_GFP_L1_Input_Rep2|fed L1 Lar@ L1?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331044 OP124(official name : OP124 genotype : unc-119(ed3); wgIs124(aha-1::TY1 EGFP FLAG; unc-119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The AHA-1::EGFP fusion protein is expressed in the correct aha-1 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the AHA-1 transcription factor. made_by : R. Waterston and S. Kim )|AHA-1_GFP_L1_ChIP_Rep2|fed L1 Lar@ L1?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331069 OP102(official name : OP102 genotype : unc-119 (ed3); wgIs102 (ham-1::TY1 EGFP FLAG; unc-119(+)) outcross : 0 mutagen : None tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The HAM-1::EGFP fusion protein is expressed in the correct ham-1 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the HAM-1 transcription factor. made_by : R Waterston )|HAM-1_GFP_L1_Input_Rep1|fed L1 Lar@ L1?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331070 OP102(official name : OP102 genotype : unc-119 (ed3); wgIs102 (ham-1::TY1 EGFP FLAG; unc-119(+)) outcross : 0 mutagen : None tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The HAM-1::EGFP fusion protein is expressed in the correct ham-1 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the HAM-1 transcription factor. made_by : R Waterston )|HAM-1_GFP_L1_ChIP_Rep1|fed L1 Lar@ L1?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331071 OP102(official name : OP102 genotype : unc-119 (ed3); wgIs102 (ham-1::TY1 EGFP FLAG; unc-119(+)) outcross : 0 mutagen : None tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The HAM-1::EGFP fusion protein is expressed in the correct ham-1 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the HAM-1 transcription factor. made_by : R Waterston )|HAM-1_GFP_L1_Input_Rep2|fed L1 Lar@ L1?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331072 OP102(official name : OP102 genotype : unc-119 (ed3); wgIs102 (ham-1::TY1 EGFP FLAG; unc-119(+)) outcross : 0 mutagen : None tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The HAM-1::EGFP fusion protein is expressed in the correct ham-1 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the HAM-1 transcription factor. made_by : R Waterston )|HAM-1_GFP_L1_ChIP_Rep2|fed L1 Lar@ L1?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331081 YL448(official name : YL448 genotype : unc-119(ed3) III; vrIs83 pGES-1::DPL-1::GFP FLAG: DPL-1 3'UTR genotype : unc-119 (+) outcross : 0 mutagen : None tags : GFP::3xFlag made_by : Michelle Kudron (Valerie Reinke's lab) )|DPL-1_GFP_L1_Input_Rep1|fed L1 Lar@ L1?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331082 YL448(official name : YL448 genotype : unc-119(ed3) III; vrIs83 pGES-1::DPL-1::GFP FLAG: DPL-1 3'UTR genotype : unc-119 (+) outcross : 0 mutagen : None tags : GFP::3xFlag made_by : Michelle Kudron (Valerie Reinke's lab) )|DPL-1_GFP_L1_ChIP_Rep1|fed L1 Lar@ L1?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331083 YL448(official name : YL448 genotype : unc-119(ed3) III; vrIs83 pGES-1::DPL-1::GFP FLAG: DPL-1 3'UTR genotype : unc-119 (+) outcross : 0 mutagen : None tags : GFP::3xFlag made_by : Michelle Kudron (Valerie Reinke's lab) )|DPL-1_GFP_L1_Input_Rep2|fed L1 Lar@ L1?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331084 YL448(official name : YL448 genotype : unc-119(ed3) III; vrIs83 pGES-1::DPL-1::GFP FLAG: DPL-1 3'UTR genotype : unc-119 (+) outcross : 0 mutagen : None tags : GFP::3xFlag made_by : Michelle Kudron (Valerie Reinke's lab) )|DPL-1_GFP_L1_ChIP_Rep2|fed L1 Lar@ L1?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331085 YL409(official name : YL409 genotype : unc-119(ed3) III; vrIs60 pLIN-35::LIN-35:GFP:FLAG::DPL-1 3'-UTR genotype : unc-119 (+)) outcross : 0 mutagen : None tags : GFP::3xFlag description : The LIN-35::GFP fusion protein is driven by its own lin-35 promoter. made_by : Michelle Kudron (Valerie Reinke's lab) )|LIN-35_GFP_L1_Input_Rep1|fed L1 Lar@ L1?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331086 YL409(official name : YL409 genotype : unc-119(ed3) III; vrIs60 pLIN-35::LIN-35:GFP:FLAG::DPL-1 3'-UTR genotype : unc-119 (+)) outcross : 0 mutagen : None tags : GFP::3xFlag description : The LIN-35::GFP fusion protein is driven by its own lin-35 promoter. made_by : Michelle Kudron (Valerie Reinke's lab) )|LIN-35_GFP_L1_ChIP_Rep1|fed L1 Lar@ L1?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331087 YL409(official name : YL409 genotype : unc-119(ed3) III; vrIs60 pLIN-35::LIN-35:GFP:FLAG::DPL-1 3'-UTR genotype : unc-119 (+)) outcross : 0 mutagen : None tags : GFP::3xFlag description : The LIN-35::GFP fusion protein is driven by its own lin-35 promoter. made_by : Michelle Kudron (Valerie Reinke's lab) )|LIN-35_GFP_L1_Input_Rep2|fed L1 Lar@ L1?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331088 YL409(official name : YL409 genotype : unc-119(ed3) III; vrIs60 pLIN-35::LIN-35:GFP:FLAG::DPL-1 3'-UTR genotype : unc-119 (+)) outcross : 0 mutagen : None tags : GFP::3xFlag description : The LIN-35::GFP fusion protein is driven by its own lin-35 promoter. made_by : Michelle Kudron (Valerie Reinke's lab) )|LIN-35_GFP_L1_ChIP_Rep2|fed L1 Lar@ L1?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331101 OP179(official name : OP179 genotype : unc-119(ed3) III; wgIs179 unc-119(+) gei-11::TY1::EGFP::3xFLAG outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The GEI-11::EGFP fusion protein is expressed in the correct gei-11 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the GEI-11 transcription factor. made_by : R. Waterston )|GEI-11_GFP_L1_Input_Rep1|fed L1 Lar@ L1?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331102 OP179(official name : OP179 genotype : unc-119(ed3) III; wgIs179 unc-119(+) gei-11::TY1::EGFP::3xFLAG outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The GEI-11::EGFP fusion protein is expressed in the correct gei-11 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the GEI-11 transcription factor. made_by : R. Waterston )|GEI-11_GFP_L1_ChIP_Rep1|fed L1 Lar@ L1?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331103 OP179(official name : OP179 genotype : unc-119(ed3) III; wgIs179 unc-119(+) gei-11::TY1::EGFP::3xFLAG outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The GEI-11::EGFP fusion protein is expressed in the correct gei-11 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the GEI-11 transcription factor. made_by : R. Waterston )|GEI-11_GFP_L1_Input_Rep2|fed L1 Lar@ L1?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331104 OP179(official name : OP179 genotype : unc-119(ed3) III; wgIs179 unc-119(+) gei-11::TY1::EGFP::3xFLAG outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The GEI-11::EGFP fusion protein is expressed in the correct gei-11 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the GEI-11 transcription factor. made_by : R. Waterston )|GEI-11_GFP_L1_ChIP_Rep2|fed L1 Lar@ L1?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331105 DevStageWorm:L1 26dC:MS:1(official name : L1 26dC )|N2_EFL-1_Ab_Input_Rep1|L1 larva Lar@ L1?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331106 DevStageWorm:L1 26dC:MS:1(official name : L1 26dC )|N2_EFL-1_Ab_ChIP_Rep1|L1 larva Lar@ L1?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331107 DevStageWorm:L1 26dC:MS:1(official name : L1 26dC )|N2_EFL-1_Ab_Input_Rep2|L1 larva Lar@ L1?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331108 DevStageWorm:L1 26dC:MS:1(official name : L1 26dC )|N2_EFL-1_Ab_ChIP_Rep2|L1 larva Lar@ L1?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331117 YL474(official name : YL474 genotype : lin-35(n745) I; unc-119(ed3) III; vrIs64pGES-1::HPL-2::GFP FLAG: HPL-2 3-UTR genotype : unc-119 (+) outcross : 0 mutagen : None tags : GFP::3xFlag description : The HPL-2::GFP fusion protein is driven by the ges-1 promoter and expressed in the intestine. The original transgene was subsequently crossed into a lin-35 mutant. made_by : Michelle Kudron in Reinke lab )|pGES_HPL-2_lin-35_YL474_L1_Input_Rep1|starved L1 Lar@ L1?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331118 YL474(official name : YL474 genotype : lin-35(n745) I; unc-119(ed3) III; vrIs64pGES-1::HPL-2::GFP FLAG: HPL-2 3-UTR genotype : unc-119 (+) outcross : 0 mutagen : None tags : GFP::3xFlag description : The HPL-2::GFP fusion protein is driven by the ges-1 promoter and expressed in the intestine. The original transgene was subsequently crossed into a lin-35 mutant. made_by : Michelle Kudron in Reinke lab )|pGES_HPL-2_lin-35_YL474_L1_ChIP_Rep1|starved L1 Lar@ L1?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331119 YL474(official name : YL474 genotype : lin-35(n745) I; unc-119(ed3) III; vrIs64pGES-1::HPL-2::GFP FLAG: HPL-2 3-UTR genotype : unc-119 (+) outcross : 0 mutagen : None tags : GFP::3xFlag description : The HPL-2::GFP fusion protein is driven by the ges-1 promoter and expressed in the intestine. The original transgene was subsequently crossed into a lin-35 mutant. made_by : Michelle Kudron in Reinke lab )|pGES_HPL-2_lin-35_YL474_L1_Input_Rep2|starved L1 Lar@ L1?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331120 YL474(official name : YL474 genotype : lin-35(n745) I; unc-119(ed3) III; vrIs64pGES-1::HPL-2::GFP FLAG: HPL-2 3-UTR genotype : unc-119 (+) outcross : 0 mutagen : None tags : GFP::3xFlag description : The HPL-2::GFP fusion protein is driven by the ges-1 promoter and expressed in the intestine. The original transgene was subsequently crossed into a lin-35 mutant. made_by : Michelle Kudron in Reinke lab )|pGES_HPL-2_lin-35_YL474_L1_ChIP_Rep2|starved L1 Lar@ L1?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331165 OP367(official name : OP367 genotype : unc-119(ed3); wgIs367(lsy-2::TY1 EGFP FLAG; unc-119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology and Genetics in Dresden using Tony Hyman's recombineering pipeline. The resulting plasmid was used for bombardment transformation of an unc-119(ed3) strain. The LSY-2::EGFP fusion protein is expressed in the correct lsy-2 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the LSY-2 transcription factor. made_by : Bob Waterston's lab from UW )|LSY-2_GFP_L1_Input_Rep1|fed L1 Lar@ L1?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331166 OP367(official name : OP367 genotype : unc-119(ed3); wgIs367(lsy-2::TY1 EGFP FLAG; unc-119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology and Genetics in Dresden using Tony Hyman's recombineering pipeline. The resulting plasmid was used for bombardment transformation of an unc-119(ed3) strain. The LSY-2::EGFP fusion protein is expressed in the correct lsy-2 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the LSY-2 transcription factor. made_by : Bob Waterston's lab from UW )|LSY-2_GFP_L1_ChIP_Rep1|fed L1 Lar@ L1?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331168 OP367(official name : OP367 genotype : unc-119(ed3); wgIs367(lsy-2::TY1 EGFP FLAG; unc-119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology and Genetics in Dresden using Tony Hyman's recombineering pipeline. The resulting plasmid was used for bombardment transformation of an unc-119(ed3) strain. The LSY-2::EGFP fusion protein is expressed in the correct lsy-2 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the LSY-2 transcription factor. made_by : Bob Waterston's lab from UW )|LSY-2_GFP_L1_ChIP_Rep2|fed L1 Lar@ L1?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331169 DevStageWorm:starved L1:MS:1(official name : starved L1 )|LSY-2_GFP_Starved_Input_Rep1|L1 larva Lar@ L1?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331170 DevStageWorm:starved L1:MS:1(official name : starved L1 )|LSY-2_GFP_Starved_ChIP_Rep1|L1 larva Lar@ L1?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331171 DevStageWorm:starved L1:MS:1(official name : starved L1 )|LSY-2_GFP_Starved_Input_Rep2|L1 larva Lar@ L1?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331172 DevStageWorm:starved L1:MS:1(official name : starved L1 )|LSY-2_GFP_Starved_ChIP_Rep2|L1 larva Lar@ L1?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331181 OP228(official name : OP228 genotype : unc119(ed3); wgIs228(nhr-237:TY1 EGFP FLAG; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The NHR-237::EGFP fusion protein is expressed in the correct nhr-237 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the NHR-237 transcription factor. made_by : Unknown )|nhr-237_GFP_L1_Input_Rep1|L1 26dC Lar@ L1?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331182 OP228(official name : OP228 genotype : unc119(ed3); wgIs228(nhr-237:TY1 EGFP FLAG; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The NHR-237::EGFP fusion protein is expressed in the correct nhr-237 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the NHR-237 transcription factor. made_by : Unknown )|nhr-237_GFP_L1_ChIP_Rep1|L1 26dC Lar@ L1?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331183 OP228(official name : OP228 genotype : unc119(ed3); wgIs228(nhr-237:TY1 EGFP FLAG; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The NHR-237::EGFP fusion protein is expressed in the correct nhr-237 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the NHR-237 transcription factor. made_by : Unknown )|nhr-237_GFP_L1_Input_Rep2|L1 26dC Lar@ L1?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331184 OP228(official name : OP228 genotype : unc119(ed3); wgIs228(nhr-237:TY1 EGFP FLAG; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The NHR-237::EGFP fusion protein is expressed in the correct nhr-237 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the NHR-237 transcription factor. made_by : Unknown )|nhr-237_GFP_L1_ChIP_Rep2|L1 26dC Lar@ L1?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331233 OP305(official name : OP305 genotype : unc119(ed3); wgIs305(nhr-11::TY1 EGFP FLAG; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The NHR-11::EGFP fusion protein is expressed in the correct nhr-11 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the NHR-11 transcription factor. made_by : R Waterston )|NHR-11_GFP_L1_Input_Rep1|L1 26dC Lar@ L1?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331234 OP305(official name : OP305 genotype : unc119(ed3); wgIs305(nhr-11::TY1 EGFP FLAG; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The NHR-11::EGFP fusion protein is expressed in the correct nhr-11 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the NHR-11 transcription factor. made_by : R Waterston )|NHR-11_GFP_L1_ChIP_Rep1|L1 26dC Lar@ L1?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331235 OP305(official name : OP305 genotype : unc119(ed3); wgIs305(nhr-11::TY1 EGFP FLAG; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The NHR-11::EGFP fusion protein is expressed in the correct nhr-11 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the NHR-11 transcription factor. made_by : R Waterston )|NHR-11_GFP_L1_Input_Rep2|L1 26dC Lar@ L1?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331236 OP305(official name : OP305 genotype : unc119(ed3); wgIs305(nhr-11::TY1 EGFP FLAG; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The NHR-11::EGFP fusion protein is expressed in the correct nhr-11 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the NHR-11 transcription factor. made_by : R Waterston )|NHR-11_GFP_L1_ChIP_Rep2|L1 26dC Lar@ L1?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331237 OP317(official name : OP317 genotype : unc119(ed3); wgIs317(nhr-28::TY1 EGFP FLAG; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The NHR-28::EGFP fusion protein is expressed in the correct nhr-28 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the NHR-28 transcription factor. made_by : R Waterston )|NHR-28_GFP_L1_Input_Rep1|L1 26dC Lar@ L1?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331238 OP317(official name : OP317 genotype : unc119(ed3); wgIs317(nhr-28::TY1 EGFP FLAG; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The NHR-28::EGFP fusion protein is expressed in the correct nhr-28 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the NHR-28 transcription factor. made_by : R Waterston )|NHR-28_GFP_L1_ChIP_Rep1|L1 26dC Lar@ L1?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331239 OP317(official name : OP317 genotype : unc119(ed3); wgIs317(nhr-28::TY1 EGFP FLAG; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The NHR-28::EGFP fusion protein is expressed in the correct nhr-28 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the NHR-28 transcription factor. made_by : R Waterston )|NHR-28_GFP_L1_Input_Rep2|L1 26dC Lar@ L1?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331240 OP317(official name : OP317 genotype : unc119(ed3); wgIs317(nhr-28::TY1 EGFP FLAG; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The NHR-28::EGFP fusion protein is expressed in the correct nhr-28 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the NHR-28 transcription factor. made_by : R Waterston )|NHR-28_GFP_L1_ChIP_Rep2|L1 26dC Lar@ L1?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331257 OP18(official name : OP18 genotype : unc-119(ed3) III; wgIs18 unc-119(+) lin-39::TY1::EGFP::3xFLAG outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The LIN-39::EGFP fusion protein is expressed in the correct lin-39 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the LIN-39 transcription factor. made_by : R. Waterston and S. Kim )|LIN-39_GFP_L1_Input_Rep1|fed L1 Lar@ L1?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331258 OP18(official name : OP18 genotype : unc-119(ed3) III; wgIs18 unc-119(+) lin-39::TY1::EGFP::3xFLAG outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The LIN-39::EGFP fusion protein is expressed in the correct lin-39 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the LIN-39 transcription factor. made_by : R. Waterston and S. Kim )|LIN-39_GFP_L1_ChIP_Rep1|fed L1 Lar@ L1?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331259 OP18(official name : OP18 genotype : unc-119(ed3) III; wgIs18 unc-119(+) lin-39::TY1::EGFP::3xFLAG outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The LIN-39::EGFP fusion protein is expressed in the correct lin-39 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the LIN-39 transcription factor. made_by : R. Waterston and S. Kim )|LIN-39_GFP_L1_Input_Rep2|fed L1 Lar@ L1?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331260 OP18(official name : OP18 genotype : unc-119(ed3) III; wgIs18 unc-119(+) lin-39::TY1::EGFP::3xFLAG outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The LIN-39::EGFP fusion protein is expressed in the correct lin-39 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the LIN-39 transcription factor. made_by : R. Waterston and S. Kim )|LIN-39_GFP_L1_ChIP_Rep2|fed L1 Lar@ L1?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX467177 MT10430(official name : MT10430 genotype : lin-35(n745) I. )|Snyder lin-35 n745 EFL-1 Ab L1 ChIP Rep.1|L1 26dC Lar@ L1?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX467178 MT10430(official name : MT10430 genotype : lin-35(n745) I. )|Snyder lin-35 n745 EFL-1 Ab L1 Input Rep.1|L1 26dC Lar@ L1?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX467179 MT10430(official name : MT10430 genotype : lin-35(n745) I. )|Snyder lin-35 n745 EFL-1 Ab L1 ChIP Rep.2|L1 26dC Lar@ L1?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX467180 MT10430(official name : MT10430 genotype : lin-35(n745) I. )|Snyder lin-35 n745 EFL-1 Ab L1 Input Rep.2|L1 26dC Lar@ L1?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX515118 YL418(official name : YL418 genotype : unc-119(ed3) III; vrIs65pGES-1::EFL-1::GFP FLAG:EFL-1 3'-UTR genotype : unc-119 (+) outcross : 0 mutagen : None tags : GFP::3xFlag description : The EFL-1::GFP fusion protein is driven by the ges-1 promoter and expressed in the instestine. made_by : Michelle Kudron (Valerie Reinke's lab) )|EFL-1_GFP_L1 Input Rep.2 extraction4_seq4|fed L1 Lar@ L1?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX5402697 H3K27me3 N2 20C|L1 Lar@ L1?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX5402698 H3K27me3 N2 26C|L1 Lar@ L1?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX5402699 H3K27me3 lin15B 20C|L1 Lar@ L1?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX5402700 H3K27me3 lin15B 26C|L1 Lar@ L1?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX5402701 H3K27me3 lin35 20C|L1 Lar@ L1?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX5402702 H3K27me3 lin35 26C|L1 Lar@ L1?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX5402703 H3K27me3 lin37 20C|L1 Lar@ L1?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX5402704 H3K27me3 lin37 26C|L1 Lar@ L1?0 1 2 https://www.ncbi.nlm.nih.gov/sra?term=SRX005650 OP37|starved L1 Lar@ L1?0 1 2 https://www.ncbi.nlm.nih.gov/sra?term=SRX1010108 N2|bean syncrhonized embryos Lar@ L1?0 1 2 https://www.ncbi.nlm.nih.gov/sra?term=SRX5402705 H3K36me3 N2 20C|L1 Lar@ L1?0 1 2 https://www.ncbi.nlm.nih.gov/sra?term=SRX5402707 H3K36me3 N2 26C|L1 Lar@ L1?0 1 2 https://www.ncbi.nlm.nih.gov/sra?term=SRX5402709 H3K36me3 lin15B 20C|L1 Lar@ L1?0 1 2 https://www.ncbi.nlm.nih.gov/sra?term=SRX5402711 H3K36me3 lin15B 26C|L1 Lar@ L1?0 1 2 https://www.ncbi.nlm.nih.gov/sra?term=SRX5402713 H3K36me3 lin35 20C|L1 Lar@ L1?0 1 2 https://www.ncbi.nlm.nih.gov/sra?term=SRX5402715 H3K36me3 lin35 26C|L1 Lar@ L1?0 1 2 https://www.ncbi.nlm.nih.gov/sra?term=SRX5402723 H3K4me3 N2 20C|L1 Lar@ L1?0 1 2 https://www.ncbi.nlm.nih.gov/sra?term=SRX5402725 H3K4me3 N2 26C|L1 Lar@ L1?0 1 2 https://www.ncbi.nlm.nih.gov/sra?term=SRX5402727 H3K4me3 lin15B 20C|L1 Lar@ L1?0 1 2 https://www.ncbi.nlm.nih.gov/sra?term=SRX5402729 H3K4me3 lin15B 26C|L1 Lar@ L1?0 1 2 https://www.ncbi.nlm.nih.gov/sra?term=SRX5402731 H3K4me3 lin35 20C|L1 Lar@ L1?0 1 2 https://www.ncbi.nlm.nih.gov/sra?term=SRX5402733 H3K4me3 lin35 26C|L1 Lar@ L1?0 1 2 https://www.ncbi.nlm.nih.gov/sra?term=SRX5402735 H3K4me3 lin37 20C|L1 Lar@ L1?0 1 2 https://www.ncbi.nlm.nih.gov/sra?term=SRX5402737 H3K4me3 lin37 26C|L1 Lar@ L1?0 1 2 https://www.ncbi.nlm.nih.gov/sra?term=SRX5402739 H3K9me2 N2 20C|L1 Lar@ L1?0 1 2 https://www.ncbi.nlm.nih.gov/sra?term=SRX5402741 H3K9me2 N2 26C|L1 Lar@ L1?0 1 2 https://www.ncbi.nlm.nih.gov/sra?term=SRX5402743 H3K9me2 lin15B 20C|L1 Lar@ L1?0 1 2 https://www.ncbi.nlm.nih.gov/sra?term=SRX5402745 H3K9me2 lin15B 26C|L1 Lar@ L1?0 1 2 https://www.ncbi.nlm.nih.gov/sra?term=SRX5402747 H3K9me2 lin35 20C|L1 Lar@ L1?0 1 2 https://www.ncbi.nlm.nih.gov/sra?term=SRX5402749 H3K9me2 lin35 26C|L1 Lar@ L1?0 1 2 https://www.ncbi.nlm.nih.gov/sra?term=SRX5402751 H3K9me2 lin37 20C|L1 Lar@ L1?0 1 2 https://www.ncbi.nlm.nih.gov/sra?term=SRX5402753 H3K9me2 lin37 26C|L1 Lar@ L1?0 1 2 https://www.ncbi.nlm.nih.gov/sra?term=SRX5402755 Input N2 20C|L1 Lar@ L1?0 1 2 https://www.ncbi.nlm.nih.gov/sra?term=SRX5402757 Input N2 26C|L1 Lar@ L1?0 1 2 https://www.ncbi.nlm.nih.gov/sra?term=SRX5402759 Input lin15B 20C|L1 Lar@ L1?0 1 2 https://www.ncbi.nlm.nih.gov/sra?term=SRX5402767 Input lin35 26C|L1 Lar@ L1?0 1 2 https://www.ncbi.nlm.nih.gov/sra?term=SRX7574650 spr-5 (by101)(I); met-2 (n4256)(III)|L1 larvae|whole animal|L1 larvae Lar@ L1?0 1 3 https://www.ncbi.nlm.nih.gov/sra?term=SRX1010104 N2|8E syncrhonized embryos Lar@ L1?0 1 3 https://www.ncbi.nlm.nih.gov/sra?term=SRX5402717 H3K36me3 lin37 20C|L1 Lar@ L1?0 1 3 https://www.ncbi.nlm.nih.gov/sra?term=SRX5402720 H3K36me3 lin37 26C|L1 Lar@ L1?0 1 3 https://www.ncbi.nlm.nih.gov/sra?term=SRX5402761 Input lin15B 26C|L1 Lar@ L1?0 1 3 https://www.ncbi.nlm.nih.gov/sra?term=SRX5402764 Input lin35 20C|L1 Lar@ L1?0 1 3 https://www.ncbi.nlm.nih.gov/sra?term=SRX5402769 Input lin37 20C|L1 Lar@ L1?0 1 3 https://www.ncbi.nlm.nih.gov/sra?term=SRX5402772 Input lin37 26C|L1 Lar@ L1?0 1 3 https://www.ncbi.nlm.nih.gov/sra?term=SRX7574649 N2|L1 larvae|whole animal|L1 larvae Lar@ L1?0 1 4 https://www.ncbi.nlm.nih.gov/sra?term=SRX080076 YL424|Pefl-1 EFL-1:GFP:FLAG whole animal|L1 Lar@ L1?0 1 4 https://www.ncbi.nlm.nih.gov/sra?term=SRX080080 YL425|Pdpl-1_DPL-1:GFP:FLAG whole animal|L1 Lar@ L1?0 1 4 https://www.ncbi.nlm.nih.gov/sra?term=SRX080090 YL418|pGES-1 EFL-1:GFP:FLAG whole animal|L1 Lar@ L1?0 1 4 https://www.ncbi.nlm.nih.gov/sra?term=SRX080094 YL448|pGES-1 DPL-1:GFP:FLAG whole animal|L1 Lar@ L1?0 1 4 https://www.ncbi.nlm.nih.gov/sra?term=SRX080098 YL398|pGES-1 LIN-35:GFP:FLAG whole animal|L1 Lar@ L1?0 1 5 https://www.ncbi.nlm.nih.gov/sra?term=SRX080102 YL416|pGES-1 HPL-2:GFP:FLAG whole animal|L1 Lar@ L1?0 1 6 https://www.ncbi.nlm.nih.gov/sra?term=SRX080084 YL409|Plin-35_LIN-35:GFP:FLAG whole animal|L1 Lar@ L1?0 1 6 https://www.ncbi.nlm.nih.gov/sra?term=SRX245912 N2|embryonic stage|Fed L1 Lar@ L1?0 1 8 https://www.ncbi.nlm.nih.gov/sra?term=SRX4082336 N2|L1 larvae Lar@ L1?0 2 20 https://www.ncbi.nlm.nih.gov/sra?term=SRX4085356 wild-type N2|L1 larvae Lar@ L1?0 2 2 https://www.ncbi.nlm.nih.gov/sra?term=SRX013987 OP37|pha-4 transgenic worm OP37|L1 Lar@ L1?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX1007132 sydn-1(0)|sydn-1(0) worms|L1-L2 Lar@ L1-L2?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX1007133 ssup-72(0); sydn-1(0)|ssup-72(0); sydn-1(0) worms|L1-L2 Lar@ L1-L2?0 1 2 https://www.ncbi.nlm.nih.gov/sra?term=SRX1007130 N2|wild type worms|L1-L2 Lar@ L1-L2?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX043847 OP62(made_by : R Waterston description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The LIN-11::EGFP fusion protein is expressed in the correct lin-11 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the LIN-11 transcription factor. tags : GFP::3xFlag mutagen : Bombard outcross : 3 genotype : unc-119(ed3) III; wgIs62 unc-119(+) lin-11::TY1::EGFP::3xFLAG official name : OP62 )|Snyder_LIN-11_GFP_L2_rep1 extraction1_seq1 channel_1|L2 Lar@ L2?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX043848 OP62(made_by : R Waterston description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The LIN-11::EGFP fusion protein is expressed in the correct lin-11 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the LIN-11 transcription factor. tags : GFP::3xFlag mutagen : Bombard outcross : 3 genotype : unc-119(ed3) III; wgIs62 unc-119(+) lin-11::TY1::EGFP::3xFLAG official name : OP62 )|Snyder_LIN-11_GFP_L2_rep1 extraction1_seq1 channel_2|L2 Lar@ L2?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX043849 OP62(made_by : R Waterston description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The LIN-11::EGFP fusion protein is expressed in the correct lin-11 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the LIN-11 transcription factor. tags : GFP::3xFlag mutagen : Bombard outcross : 3 genotype : unc-119(ed3) III; wgIs62 unc-119(+) lin-11::TY1::EGFP::3xFLAG official name : OP62 )|Snyder_LIN-11_GFP_L2_rep2 extraction2_seq1 channel_1|L2 Lar@ L2?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX043850 OP62(made_by : R Waterston description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The LIN-11::EGFP fusion protein is expressed in the correct lin-11 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the LIN-11 transcription factor. tags : GFP::3xFlag mutagen : Bombard outcross : 3 genotype : unc-119(ed3) III; wgIs62 unc-119(+) lin-11::TY1::EGFP::3xFLAG official name : OP62 )|Snyder_LIN-11_GFP_L2_rep2 extraction2_seq1 channel_2|L2 Lar@ L2?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX043859 OP90(made_by : R. Waterston description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The NHR-6::EGFP fusion protein is expressed in the correct nhr-6 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the NHR-6 transcription factor. tags : GFP::3xFlag mutagen : Bombard outcross : 3 genotype : unc-119(ed3) III; wgIs90 unc-119(+) nhr-6::TY1::EGFP::3xFLAG official name : OP90 )|Snyder_NHR-6_GFP_L2_rep1 extraction1_seq1 channel_1|L2 Lar@ L2?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX043860 OP90(made_by : R. Waterston description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The NHR-6::EGFP fusion protein is expressed in the correct nhr-6 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the NHR-6 transcription factor. tags : GFP::3xFlag mutagen : Bombard outcross : 3 genotype : unc-119(ed3) III; wgIs90 unc-119(+) nhr-6::TY1::EGFP::3xFLAG official name : OP90 )|Snyder_NHR-6_GFP_L2_rep1 extraction1_seq1 channel_2|L2 Lar@ L2?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX043861 OP90(made_by : R. Waterston description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The NHR-6::EGFP fusion protein is expressed in the correct nhr-6 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the NHR-6 transcription factor. tags : GFP::3xFlag mutagen : Bombard outcross : 3 genotype : unc-119(ed3) III; wgIs90 unc-119(+) nhr-6::TY1::EGFP::3xFLAG official name : OP90 )|Snyder_NHR-6_GFP_L2_rep2 extraction2_seq1 channel_1|L2 Lar@ L2?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX043862 OP90(made_by : R. Waterston description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The NHR-6::EGFP fusion protein is expressed in the correct nhr-6 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the NHR-6 transcription factor. tags : GFP::3xFlag mutagen : Bombard outcross : 3 genotype : unc-119(ed3) III; wgIs90 unc-119(+) nhr-6::TY1::EGFP::3xFLAG official name : OP90 )|Snyder_NHR-6_GFP_L2_rep2 extraction2_seq1 channel_2|L2 Lar@ L2?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX043875 N2(genotype : wild type genotype : DR subclone of DB original (Tc1 pattern I) official name : N2 )|Snyder_N2_POLII_L2_rep1 extraction1_seq1 channel_1|L2 Lar@ L2?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX043876 N2(genotype : wild type genotype : DR subclone of DB original (Tc1 pattern I) official name : N2 )|Snyder_N2_POLII_L2_rep1 extraction1_seq1 channel_2|L2 Lar@ L2?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX043877 N2(genotype : wild type genotype : DR subclone of DB original (Tc1 pattern I) official name : N2 )|Snyder_N2_POLII_L2_rep2 extraction2_seq1 channel_1|L2 Lar@ L2?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX043878 N2(genotype : wild type genotype : DR subclone of DB original (Tc1 pattern I) official name : N2 )|Snyder_N2_POLII_L2_rep2 extraction2_seq1 channel_2|L2 Lar@ L2?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX054248 OP200(official name : OP200 genotype : unc119(ed3); wgIs200(alr-1::TY1 EGFP FLAG C; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : his strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The ALR-1::EGFP fusion protein is expressed in the correct alr-1 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the ALR-1 transcription factor. made_by : R. Waterston )|Snyder_ALR-1_GFP_L2_rep2 extraction1_seq1 channel_1|L2 Lar@ L2?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX054249 OP200(official name : OP200 genotype : unc119(ed3); wgIs200(alr-1::TY1 EGFP FLAG C; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : his strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The ALR-1::EGFP fusion protein is expressed in the correct alr-1 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the ALR-1 transcription factor. made_by : R. Waterston )|Snyder_ALR-1_GFP_L2_rep1 extraction2_seq2 channel_1|L2 Lar@ L2?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX054250 OP200(official name : OP200 genotype : unc119(ed3); wgIs200(alr-1::TY1 EGFP FLAG C; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : his strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The ALR-1::EGFP fusion protein is expressed in the correct alr-1 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the ALR-1 transcription factor. made_by : R. Waterston )|Snyder_ALR-1_GFP_L2_rep1 extraction3_seq3 channel_1|L2 Lar@ L2?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX054251 OP200(official name : OP200 genotype : unc119(ed3); wgIs200(alr-1::TY1 EGFP FLAG C; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : his strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The ALR-1::EGFP fusion protein is expressed in the correct alr-1 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the ALR-1 transcription factor. made_by : R. Waterston )|Snyder_ALR-1_GFP_L2_rep1 extraction4_seq4 channel_1|L2 Lar@ L2?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX054252 OP200(official name : OP200 genotype : unc119(ed3); wgIs200(alr-1::TY1 EGFP FLAG C; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : his strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The ALR-1::EGFP fusion protein is expressed in the correct alr-1 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the ALR-1 transcription factor. made_by : R. Waterston )|Snyder_ALR-1_GFP_L2_rep1 extraction5_seq5 channel_1|L2 Lar@ L2?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX054253 OP37(official name : OP37 genotype : unc-119(ed3) III; wgIs37 unc-119(+) pha-4::TY1::EGFP::3xFLAG outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The PHA-4::EGFP fusion protein is expressed in the correct pha-4 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the PHA-4 transcription factor. made_by : R. Waterston and S. Kim )|Snyder_PHA-4_GFP_L2_rep2 extraction1_seq1 channel_1|L2 Lar@ L2?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX054254 OP37(official name : OP37 genotype : unc-119(ed3) III; wgIs37 unc-119(+) pha-4::TY1::EGFP::3xFLAG outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The PHA-4::EGFP fusion protein is expressed in the correct pha-4 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the PHA-4 transcription factor. made_by : R. Waterston and S. Kim )|Snyder_PHA-4_GFP_L2_rep2 extraction2_seq2 channel_1|L2 Lar@ L2?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX054255 OP37(official name : OP37 genotype : unc-119(ed3) III; wgIs37 unc-119(+) pha-4::TY1::EGFP::3xFLAG outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The PHA-4::EGFP fusion protein is expressed in the correct pha-4 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the PHA-4 transcription factor. made_by : R. Waterston and S. Kim )|Snyder_PHA-4_GFP_L2_rep1 extraction3_seq3 channel_1|L2 Lar@ L2?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX054256 OP37(official name : OP37 genotype : unc-119(ed3) III; wgIs37 unc-119(+) pha-4::TY1::EGFP::3xFLAG outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The PHA-4::EGFP fusion protein is expressed in the correct pha-4 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the PHA-4 transcription factor. made_by : R. Waterston and S. Kim )|Snyder_PHA-4_GFP_L2_rep1 extraction4_seq4 channel_1|L2 Lar@ L2?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX054257 OP37(official name : OP37 genotype : unc-119(ed3) III; wgIs37 unc-119(+) pha-4::TY1::EGFP::3xFLAG outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The PHA-4::EGFP fusion protein is expressed in the correct pha-4 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the PHA-4 transcription factor. made_by : R. Waterston and S. Kim )|Snyder_PHA-4_GFP_L2_rep1 extraction5_seq5 channel_1|L2 Lar@ L2?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX065642 OP83(official name : OP83 genotype : unc119(ed3); wgIs83(zag-1::TY1 EGFP FLAG; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The ZAG-1::EGFP fusion protein is expressed in the correct zag-1 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the ZAG-1 transcription factor. made_by : R Waterston )|Snyder_ZAG-1_Input_L2 extraction1_seq1 channel_1|L2 Lar@ L2?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX065643 OP83(official name : OP83 genotype : unc119(ed3); wgIs83(zag-1::TY1 EGFP FLAG; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The ZAG-1::EGFP fusion protein is expressed in the correct zag-1 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the ZAG-1 transcription factor. made_by : R Waterston )|Snyder_ZAG-1_Input_L2 extraction2_seq2 channel_1|L2 Lar@ L2?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX065644 OP83(official name : OP83 genotype : unc119(ed3); wgIs83(zag-1::TY1 EGFP FLAG; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The ZAG-1::EGFP fusion protein is expressed in the correct zag-1 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the ZAG-1 transcription factor. made_by : R Waterston )|Snyder_ZAG-1_GFP_L2_rep1 extraction3_seq3 channel_1|L2 Lar@ L2?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX065645 OP83(official name : OP83 genotype : unc119(ed3); wgIs83(zag-1::TY1 EGFP FLAG; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The ZAG-1::EGFP fusion protein is expressed in the correct zag-1 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the ZAG-1 transcription factor. made_by : R Waterston )|Snyder_ZAG-1_GFP_L2_rep2 extraction4_seq4 channel_1|L2 Lar@ L2?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX065658 OP304(official name : OP304 genotype : unc119(ed3); wgIs304(fos-1::TY1 EGFP FLAG; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The FOS-1::EGFP fusion protein is expressed in the correct fos-1 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the FOS-1 transcription factor. made_by : R Waterston )|Snyder_FOS-1_Input_L2 extraction1_seq1 channel_1|L2 Lar@ L2?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX065659 OP304(official name : OP304 genotype : unc119(ed3); wgIs304(fos-1::TY1 EGFP FLAG; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The FOS-1::EGFP fusion protein is expressed in the correct fos-1 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the FOS-1 transcription factor. made_by : R Waterston )|Snyder_FOS-1_Input_L2 extraction2_seq2 channel_1|L2 Lar@ L2?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX065660 OP304(official name : OP304 genotype : unc119(ed3); wgIs304(fos-1::TY1 EGFP FLAG; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The FOS-1::EGFP fusion protein is expressed in the correct fos-1 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the FOS-1 transcription factor. made_by : R Waterston )|Snyder_FOS-1_GFP_L2_rep1 extraction3_seq3 channel_1|L2 Lar@ L2?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX065661 OP304(official name : OP304 genotype : unc119(ed3); wgIs304(fos-1::TY1 EGFP FLAG; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The FOS-1::EGFP fusion protein is expressed in the correct fos-1 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the FOS-1 transcription factor. made_by : R Waterston )|Snyder_FOS-1_GFP_L2_rep2 extraction4_seq4 channel_1|L2 Lar@ L2?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX065662 OP600(official name : OP600 genotype : unc119(ed3); wgIs600(unc-62::TY1 EGFP FLAG; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The UNC-62::EGFP fusion protein is expressed in the correct unc-62 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the UNC-62 transcription factor. made_by : S Kim )|Snyder_UNC-62_Input_L2 extraction1_seq1 channel_1|L2 Lar@ L2?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX065663 OP600(official name : OP600 genotype : unc119(ed3); wgIs600(unc-62::TY1 EGFP FLAG; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The UNC-62::EGFP fusion protein is expressed in the correct unc-62 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the UNC-62 transcription factor. made_by : S Kim )|Snyder_UNC-62_Input_L2 extraction2_seq2 channel_1|L2 Lar@ L2?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX065664 OP600(official name : OP600 genotype : unc119(ed3); wgIs600(unc-62::TY1 EGFP FLAG; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The UNC-62::EGFP fusion protein is expressed in the correct unc-62 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the UNC-62 transcription factor. made_by : S Kim )|Snyder_UNC-62_GFP_L2_rep1 extraction3_seq3 channel_1|L2 Lar@ L2?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX065665 OP600(official name : OP600 genotype : unc119(ed3); wgIs600(unc-62::TY1 EGFP FLAG; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The UNC-62::EGFP fusion protein is expressed in the correct unc-62 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the UNC-62 transcription factor. made_by : S Kim )|Snyder_UNC-62_GFP_L2_rep2 extraction4_seq4 channel_1|L2 Lar@ L2?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX065675 OP343(official name : OP343 genotype : unc119(ed3); wgIs343(C01B12.2:TY1 EGFP FLAG; unc119) outcross : 0 mutagen : None tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for bombardment transformation of an unc-119(ed3) strain. The C01B12.2::EGFP fusion protein has broad expression pattern at L2 stage. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the DPL-1 transcription factor. made_by : Bob Waterston's lab from UW )|Snyder_C01B12.2_Input_L2 extraction1_seq1 channel_1|L2 Lar@ L2?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX065676 OP343(official name : OP343 genotype : unc119(ed3); wgIs343(C01B12.2:TY1 EGFP FLAG; unc119) outcross : 0 mutagen : None tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for bombardment transformation of an unc-119(ed3) strain. The C01B12.2::EGFP fusion protein has broad expression pattern at L2 stage. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the DPL-1 transcription factor. made_by : Bob Waterston's lab from UW )|Snyder_C01B12.2_Input_L2 extraction2_seq2 channel_1|L2 Lar@ L2?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX065677 OP343(official name : OP343 genotype : unc119(ed3); wgIs343(C01B12.2:TY1 EGFP FLAG; unc119) outcross : 0 mutagen : None tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for bombardment transformation of an unc-119(ed3) strain. The C01B12.2::EGFP fusion protein has broad expression pattern at L2 stage. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the DPL-1 transcription factor. made_by : Bob Waterston's lab from UW )|Snyder_C01B12.2_GFP_L2_rep1 extraction3_seq3 channel_1|L2 Lar@ L2?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX065678 OP343(official name : OP343 genotype : unc119(ed3); wgIs343(C01B12.2:TY1 EGFP FLAG; unc119) outcross : 0 mutagen : None tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for bombardment transformation of an unc-119(ed3) strain. The C01B12.2::EGFP fusion protein has broad expression pattern at L2 stage. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the DPL-1 transcription factor. made_by : Bob Waterston's lab from UW )|Snyder_C01B12.2_GFP_L2_rep2 extraction4_seq4 channel_1|L2 Lar@ L2?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX065687 OP90(official name : OP90 genotype : unc-119(ed3) III; wgIs90 unc-119(+) nhr-6::TY1::EGFP::3xFLAG outcross : 0 mutagen : None tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The NHR-6::EGFP fusion protein is expressed in neurons surrounding pharynx at L2 stage. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the NHR-6 transcription factor. made_by : R. Waterston )|Snyder_NHR-6v2_Input_L2 extraction1_seq1 channel_1|L2 Lar@ L2?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX065688 OP90(official name : OP90 genotype : unc-119(ed3) III; wgIs90 unc-119(+) nhr-6::TY1::EGFP::3xFLAG outcross : 0 mutagen : None tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The NHR-6::EGFP fusion protein is expressed in neurons surrounding pharynx at L2 stage. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the NHR-6 transcription factor. made_by : R. Waterston )|Snyder_NHR-6v2_Input_L2 extraction2_seq2 channel_1|L2 Lar@ L2?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX065689 OP90(official name : OP90 genotype : unc-119(ed3) III; wgIs90 unc-119(+) nhr-6::TY1::EGFP::3xFLAG outcross : 0 mutagen : None tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The NHR-6::EGFP fusion protein is expressed in neurons surrounding pharynx at L2 stage. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the NHR-6 transcription factor. made_by : R. Waterston )|Snyder_NHR-6v2_GFP_L2_rep1 extraction3_seq3 channel_1|L2 Lar@ L2?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX065690 OP90(official name : OP90 genotype : unc-119(ed3) III; wgIs90 unc-119(+) nhr-6::TY1::EGFP::3xFLAG outcross : 0 mutagen : None tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The NHR-6::EGFP fusion protein is expressed in neurons surrounding pharynx at L2 stage. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the NHR-6 transcription factor. made_by : R. Waterston )|Snyder_NHR-6v2_GFP_L2_rep2 extraction4_seq4 channel_1|L2 Lar@ L2?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX065719 OP218(official name : OP218 genotype : unc-119(ed3); wgIs218(R02D3.7:TY1 EGFP FLAG; unc-119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The R02D3.7::EGFP fusion protein is expressed in the correct R02D3.7 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the RO2D3.7 transcription factor. made_by : )|Snyder_R02D3.7_Input_L2 extraction1_seq1 channel_1|L2 Lar@ L2?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX065720 OP218(official name : OP218 genotype : unc-119(ed3); wgIs218(R02D3.7:TY1 EGFP FLAG; unc-119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The R02D3.7::EGFP fusion protein is expressed in the correct R02D3.7 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the RO2D3.7 transcription factor. made_by : )|Snyder_R02D3.7_Input_L2 extraction2_seq2 channel_1|L2 Lar@ L2?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX065721 OP218(official name : OP218 genotype : unc-119(ed3); wgIs218(R02D3.7:TY1 EGFP FLAG; unc-119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The R02D3.7::EGFP fusion protein is expressed in the correct R02D3.7 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the RO2D3.7 transcription factor. made_by : )|Snyder_R02D3.7_GFP_L2_rep1 extraction3_seq3 channel_1|L2 Lar@ L2?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX065722 OP218(official name : OP218 genotype : unc-119(ed3); wgIs218(R02D3.7:TY1 EGFP FLAG; unc-119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The R02D3.7::EGFP fusion protein is expressed in the correct R02D3.7 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the RO2D3.7 transcription factor. made_by : )|Snyder_R02D3.7_GFP_L2_rep2 extraction4_seq4 channel_1|L2 Lar@ L2?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX146502 OP305(official name : OP305 genotype : unc119(ed3); wgIs305(nhr-11::TY1 EGFP FLAG; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The NHR-11::EGFP fusion protein is expressed in the correct nhr-11 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the NHR-11 transcription factor. made_by : R Waterston )|Snyder_NHR11_Input_L2_rep1|L2 Lar@ L2?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX146503 OP305(official name : OP305 genotype : unc119(ed3); wgIs305(nhr-11::TY1 EGFP FLAG; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The NHR-11::EGFP fusion protein is expressed in the correct nhr-11 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the NHR-11 transcription factor. made_by : R Waterston )|Snyder_NHR11_Input_L2_rep2|L2 Lar@ L2?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX146504 OP305(official name : OP305 genotype : unc119(ed3); wgIs305(nhr-11::TY1 EGFP FLAG; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The NHR-11::EGFP fusion protein is expressed in the correct nhr-11 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the NHR-11 transcription factor. made_by : R Waterston )|Snyder_NHR11_GFP_L2_rep1|L2 Lar@ L2?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX146505 OP305(official name : OP305 genotype : unc119(ed3); wgIs305(nhr-11::TY1 EGFP FLAG; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The NHR-11::EGFP fusion protein is expressed in the correct nhr-11 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the NHR-11 transcription factor. made_by : R Waterston )|Snyder_NHR11_GFP_L2_rep2|L2 Lar@ L2?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX146518 OP179(official name : OP179 genotype : unc-119(ed3) III; wgIs179 unc-119(+) gei-11::TY1::EGFP::3xFLAG outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The GEI-11::EGFP fusion protein is expressed in the correct gei-11 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the GEI-11 transcription factor. made_by : R. Waterston )|Snyder_GEI-11_Input_L2_rep1|L2 Lar@ L2?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX146519 OP179(official name : OP179 genotype : unc-119(ed3) III; wgIs179 unc-119(+) gei-11::TY1::EGFP::3xFLAG outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The GEI-11::EGFP fusion protein is expressed in the correct gei-11 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the GEI-11 transcription factor. made_by : R. Waterston )|Snyder_GEI-11_Input_L2_rep2|L2 Lar@ L2?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX146520 OP179(official name : OP179 genotype : unc-119(ed3) III; wgIs179 unc-119(+) gei-11::TY1::EGFP::3xFLAG outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The GEI-11::EGFP fusion protein is expressed in the correct gei-11 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the GEI-11 transcription factor. made_by : R. Waterston )|Snyder_GEI-11_GFP_L2_rep1|L2 Lar@ L2?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX146521 OP179(official name : OP179 genotype : unc-119(ed3) III; wgIs179 unc-119(+) gei-11::TY1::EGFP::3xFLAG outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The GEI-11::EGFP fusion protein is expressed in the correct gei-11 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the GEI-11 transcription factor. made_by : R. Waterston )|Snyder_GEI-11_GFP_L2_rep2|L2 Lar@ L2?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX147623 OP355(official name : OP355 genotype : unc-119(ed3) III; wgIs355(ZK377.2::TY1 EGFP FLAG; unc-119(+)) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Dresden using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The sax-3::EGFP fusion protein is expressed in the correct sax-3 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the sax-3 transcription factor. The sax-3 gene is encoded by the ZK377.2 CDS. made_by : R Waterston )|Snyder_ZK377.2_Input_L2_rep1|L2 Lar@ L2?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX147624 OP355(official name : OP355 genotype : unc-119(ed3) III; wgIs355(ZK377.2::TY1 EGFP FLAG; unc-119(+)) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Dresden using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The sax-3::EGFP fusion protein is expressed in the correct sax-3 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the sax-3 transcription factor. The sax-3 gene is encoded by the ZK377.2 CDS. made_by : R Waterston )|Snyder_ZK377.2_Input_L2_rep2|L2 Lar@ L2?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX147625 OP355(official name : OP355 genotype : unc-119(ed3) III; wgIs355(ZK377.2::TY1 EGFP FLAG; unc-119(+)) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Dresden using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The sax-3::EGFP fusion protein is expressed in the correct sax-3 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the sax-3 transcription factor. The sax-3 gene is encoded by the ZK377.2 CDS. made_by : R Waterston )|Snyder_ZK377.2_GFP_L2_rep1|L2 Lar@ L2?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX147626 OP355(official name : OP355 genotype : unc-119(ed3) III; wgIs355(ZK377.2::TY1 EGFP FLAG; unc-119(+)) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Dresden using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The sax-3::EGFP fusion protein is expressed in the correct sax-3 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the sax-3 transcription factor. The sax-3 gene is encoded by the ZK377.2 CDS. made_by : R Waterston )|Snyder_ZK377.2_GFP_L2_rep2|L2 Lar@ L2?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX147627 OP353(official name : OP353 genotype : unc119(ed3); wgIs353(nhr-77::TY1 EGFP FLAG; unc119) outcross : 3 transgene : nhr-77 tags : Bombard tag : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The NHR-77::EGFP fusion protein is expressed in the correct nhr-77 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the NHR-77 transcription factor. made_by : R Waterston )|Snyder_NHR-77_Input_L2_rep1|L2 Lar@ L2?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX147628 OP353(official name : OP353 genotype : unc119(ed3); wgIs353(nhr-77::TY1 EGFP FLAG; unc119) outcross : 3 transgene : nhr-77 tags : Bombard tag : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The NHR-77::EGFP fusion protein is expressed in the correct nhr-77 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the NHR-77 transcription factor. made_by : R Waterston )|Snyder_NHR-77_Input_L2_rep2|L2 Lar@ L2?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX147629 OP353(official name : OP353 genotype : unc119(ed3); wgIs353(nhr-77::TY1 EGFP FLAG; unc119) outcross : 3 transgene : nhr-77 tags : Bombard tag : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The NHR-77::EGFP fusion protein is expressed in the correct nhr-77 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the NHR-77 transcription factor. made_by : R Waterston )|Snyder_NHR-77_GFP_L2_rep1|L2 Lar@ L2?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX147630 OP353(official name : OP353 genotype : unc119(ed3); wgIs353(nhr-77::TY1 EGFP FLAG; unc119) outcross : 3 transgene : nhr-77 tags : Bombard tag : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The NHR-77::EGFP fusion protein is expressed in the correct nhr-77 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the NHR-77 transcription factor. made_by : R Waterston )|Snyder_NHR-77_GFP_L2_rep2|L2 Lar@ L2?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX147639 OP226(official name : OP226 genotype : unc119(ed3); wgIs226(nhr-116::TY1 EGFP FLAG; unc119) outcross : 3 transgene : nhr-116 tags : Bombard tag : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The NHR-116::EGFP fusion protein is expressed in the correct nhr-116 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the NHR-116 transcription factor. made_by : M Sarov )|Snyder_NHR-116_Input_L2_rep1|L2 Lar@ L2?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX147640 OP226(official name : OP226 genotype : unc119(ed3); wgIs226(nhr-116::TY1 EGFP FLAG; unc119) outcross : 3 transgene : nhr-116 tags : Bombard tag : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The NHR-116::EGFP fusion protein is expressed in the correct nhr-116 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the NHR-116 transcription factor. made_by : M Sarov )|Snyder_NHR-116_Input_L2_rep2|L2 Lar@ L2?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX147641 OP226(official name : OP226 genotype : unc119(ed3); wgIs226(nhr-116::TY1 EGFP FLAG; unc119) outcross : 3 transgene : nhr-116 tags : Bombard tag : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The NHR-116::EGFP fusion protein is expressed in the correct nhr-116 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the NHR-116 transcription factor. made_by : M Sarov )|Snyder_NHR-116_GFP_L2_rep1|L2 Lar@ L2?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX147642 OP226(official name : OP226 genotype : unc119(ed3); wgIs226(nhr-116::TY1 EGFP FLAG; unc119) outcross : 3 transgene : nhr-116 tags : Bombard tag : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The NHR-116::EGFP fusion protein is expressed in the correct nhr-116 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the NHR-116 transcription factor. made_by : M Sarov )|Snyder_NHR-116_GFP_L2_rep2|L2 Lar@ L2?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX233439 OP212(official name : OP212 genotype : unc119(ed3); wgIs212(F45C12.2:TY1 EGFP FLAG; unc119) outcross : 3 transgene : F45C12.2 tags : Bombard tag : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The F45C12.2::EGFP fusion protein is expressed in the correct F45C12.2 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the F45C12.2 transcription factor. made_by : Mihail Sarov )|Snyder_F45C12.2_Input_L2_rep1_ACGT|L2 Lar@ L2?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX233440 OP212(official name : OP212 genotype : unc119(ed3); wgIs212(F45C12.2:TY1 EGFP FLAG; unc119) outcross : 3 transgene : F45C12.2 tags : Bombard tag : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The F45C12.2::EGFP fusion protein is expressed in the correct F45C12.2 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the F45C12.2 transcription factor. made_by : Mihail Sarov )|Snyder_F45C12.2_Input_L2_rep2_TGCT|L2 Lar@ L2?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX233441 OP212(official name : OP212 genotype : unc119(ed3); wgIs212(F45C12.2:TY1 EGFP FLAG; unc119) outcross : 3 transgene : F45C12.2 tags : Bombard tag : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The F45C12.2::EGFP fusion protein is expressed in the correct F45C12.2 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the F45C12.2 transcription factor. made_by : Mihail Sarov )|Snyder_F45C12.2_GFP_L2_rep1_ACGT|L2 Lar@ L2?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX233442 OP212(official name : OP212 genotype : unc119(ed3); wgIs212(F45C12.2:TY1 EGFP FLAG; unc119) outcross : 3 transgene : F45C12.2 tags : Bombard tag : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The F45C12.2::EGFP fusion protein is expressed in the correct F45C12.2 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the F45C12.2 transcription factor. made_by : Mihail Sarov )|Snyder_F45C12.2_GFP_L2_rep2_TGCT|L2 Lar@ L2?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX233443 OP217(official name : OP217 genotype : unc-119(ed3); wgIs217(aly-2:TY1 EGFP FLAG; unc-119(+)) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Dresden using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The ALY-2::EGFP fusion protein is expressed in the correct aly-2 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the ALY-2 transcription factor. made_by : Mihail Sarov )|Snyder_ALY-2_Input_L2_rep1_GTAT|L2 Lar@ L2?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX233444 OP217(official name : OP217 genotype : unc-119(ed3); wgIs217(aly-2:TY1 EGFP FLAG; unc-119(+)) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Dresden using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The ALY-2::EGFP fusion protein is expressed in the correct aly-2 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the ALY-2 transcription factor. made_by : Mihail Sarov )|Snyder_ALY-2_Input_L2_rep2_CATT|L2 Lar@ L2?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX233445 OP217(official name : OP217 genotype : unc-119(ed3); wgIs217(aly-2:TY1 EGFP FLAG; unc-119(+)) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Dresden using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The ALY-2::EGFP fusion protein is expressed in the correct aly-2 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the ALY-2 transcription factor. made_by : Mihail Sarov )|Snyder_ALY-2_GFP_L2_rep1_GTAT|L2 Lar@ L2?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX233446 OP217(official name : OP217 genotype : unc-119(ed3); wgIs217(aly-2:TY1 EGFP FLAG; unc-119(+)) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Dresden using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The ALY-2::EGFP fusion protein is expressed in the correct aly-2 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the ALY-2 transcription factor. made_by : Mihail Sarov )|Snyder_ALY-2_GFP_L2_rep2_CATT|L2 Lar@ L2?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX277033 OP354(official name : OP354 genotype : unc119(ed3); wgIs354(elt-1::TY1 EGFP FLAG; unc119) outcross : 0 mutagen : None tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for bombardment transformation of an unc-119(ed3) strain. made_by : Bob Waterston's lab from UW )|ELT-1 L2 InputRep1|L2 Lar@ L2?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX277034 OP354(official name : OP354 genotype : unc119(ed3); wgIs354(elt-1::TY1 EGFP FLAG; unc119) outcross : 0 mutagen : None tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for bombardment transformation of an unc-119(ed3) strain. made_by : Bob Waterston's lab from UW )|ELT-1 L2 InputRep2|L2 Lar@ L2?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX277035 OP354(official name : OP354 genotype : unc119(ed3); wgIs354(elt-1::TY1 EGFP FLAG; unc119) outcross : 0 mutagen : None tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for bombardment transformation of an unc-119(ed3) strain. made_by : Bob Waterston's lab from UW )|ELT-1 L2 ChIPRep1|L2 Lar@ L2?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX277036 OP354(official name : OP354 genotype : unc119(ed3); wgIs354(elt-1::TY1 EGFP FLAG; unc119) outcross : 0 mutagen : None tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for bombardment transformation of an unc-119(ed3) strain. made_by : Bob Waterston's lab from UW )|ELT-1 L2 ChIPRep2|L2 Lar@ L2?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX277037 OP43(official name : OP43 genotype : unc-119(ed3); wgIs43(nhr-23::TY1 EGFP FLAG; unc-119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology and Genetics in Dresden using Tony Hyman's recombineering pipeline. The resulting plasmid was used for bombardment transformation of an unc-119(ed3) strain. The NHR-23::EGFP fusion protein is expressed in the correct nhr-23 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the NHR-223 transcription factor. made_by : Bob Waterston's lab from UW )|nhr-23 L2 InputRep1|L2 Lar@ L2?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX277038 OP43(official name : OP43 genotype : unc-119(ed3); wgIs43(nhr-23::TY1 EGFP FLAG; unc-119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology and Genetics in Dresden using Tony Hyman's recombineering pipeline. The resulting plasmid was used for bombardment transformation of an unc-119(ed3) strain. The NHR-23::EGFP fusion protein is expressed in the correct nhr-23 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the NHR-223 transcription factor. made_by : Bob Waterston's lab from UW )|nhr-23 L2 InputRep2|L2 Lar@ L2?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX277039 OP43(official name : OP43 genotype : unc-119(ed3); wgIs43(nhr-23::TY1 EGFP FLAG; unc-119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology and Genetics in Dresden using Tony Hyman's recombineering pipeline. The resulting plasmid was used for bombardment transformation of an unc-119(ed3) strain. The NHR-23::EGFP fusion protein is expressed in the correct nhr-23 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the NHR-223 transcription factor. made_by : Bob Waterston's lab from UW )|nhr-23 L2 ChIPRep1|L2 Lar@ L2?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX277040 OP43(official name : OP43 genotype : unc-119(ed3); wgIs43(nhr-23::TY1 EGFP FLAG; unc-119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology and Genetics in Dresden using Tony Hyman's recombineering pipeline. The resulting plasmid was used for bombardment transformation of an unc-119(ed3) strain. The NHR-23::EGFP fusion protein is expressed in the correct nhr-23 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the NHR-223 transcription factor. made_by : Bob Waterston's lab from UW )|nhr-23 L2 ChIPRep2|L2 Lar@ L2?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX277045 OP186(official name : OP186 genotype : unc119(ed3); wgIs186(unc39::TY1 EGFP FLAG C; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The UNC-39::EGFP fusion protein is expressed in the correct unc-39 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the UNC-39 transcription factor. made_by : Unknown )|UNC-39 L2 InputRep1|L2 Lar@ L2?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX277046 OP186(official name : OP186 genotype : unc119(ed3); wgIs186(unc39::TY1 EGFP FLAG C; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The UNC-39::EGFP fusion protein is expressed in the correct unc-39 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the UNC-39 transcription factor. made_by : Unknown )|UNC-39 L2 InputRep2|L2 Lar@ L2?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX277047 OP186(official name : OP186 genotype : unc119(ed3); wgIs186(unc39::TY1 EGFP FLAG C; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The UNC-39::EGFP fusion protein is expressed in the correct unc-39 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the UNC-39 transcription factor. made_by : Unknown )|UNC-39 L2 ChIPRep1|L2 Lar@ L2?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX277048 OP186(official name : OP186 genotype : unc119(ed3); wgIs186(unc39::TY1 EGFP FLAG C; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The UNC-39::EGFP fusion protein is expressed in the correct unc-39 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the UNC-39 transcription factor. made_by : Unknown )|UNC-39 L2 ChIPRep2|L2 Lar@ L2?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX277073 OP240(official name : OP240 genotype : unc119(ed3); wgIs240(lsy-2::TY1 EGFP FLAG; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The LSY-2::EGFP fusion protein is expressed in the correct lsy-2 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the LSY-2 transcription factor. made_by : Unknown )|LSY-2 L2 v2 InputRep1|L2 Lar@ L2?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX277074 OP240(official name : OP240 genotype : unc119(ed3); wgIs240(lsy-2::TY1 EGFP FLAG; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The LSY-2::EGFP fusion protein is expressed in the correct lsy-2 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the LSY-2 transcription factor. made_by : Unknown )|LSY-2 L2 v2 InputRep2|L2 Lar@ L2?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX277075 OP240(official name : OP240 genotype : unc119(ed3); wgIs240(lsy-2::TY1 EGFP FLAG; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The LSY-2::EGFP fusion protein is expressed in the correct lsy-2 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the LSY-2 transcription factor. made_by : Unknown )|LSY-2 L2 v2 ChIPRep1|L2 Lar@ L2?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX277076 OP240(official name : OP240 genotype : unc119(ed3); wgIs240(lsy-2::TY1 EGFP FLAG; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The LSY-2::EGFP fusion protein is expressed in the correct lsy-2 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the LSY-2 transcription factor. made_by : Unknown )|LSY-2 L2 v2 ChIPRep2|L2 Lar@ L2?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX277090 OP49(official name : OP49 genotype : unc119(ed3); wgIs49(lin-13::TY1 EGFP FLAG; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The LIN-13::EGFP fusion protein is expressed in the correct lin-13 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the LIN-13 transcription factor. made_by : Unknown )|LIN-13 L2 InputRep1|L2 Lar@ L2?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX277091 OP49(official name : OP49 genotype : unc119(ed3); wgIs49(lin-13::TY1 EGFP FLAG; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The LIN-13::EGFP fusion protein is expressed in the correct lin-13 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the LIN-13 transcription factor. made_by : Unknown )|LIN-13 L2 InputRep2|L2 Lar@ L2?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX277092 OP49(official name : OP49 genotype : unc119(ed3); wgIs49(lin-13::TY1 EGFP FLAG; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The LIN-13::EGFP fusion protein is expressed in the correct lin-13 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the LIN-13 transcription factor. made_by : Unknown )|LIN-13 L2 ChIPRep1|L2 Lar@ L2?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX277093 OP49(official name : OP49 genotype : unc119(ed3); wgIs49(lin-13::TY1 EGFP FLAG; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The LIN-13::EGFP fusion protein is expressed in the correct lin-13 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the LIN-13 transcription factor. made_by : Unknown )|LIN-13 L2 ChIPRep2|L2 Lar@ L2?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX277098 OP322(official name : OP322 genotype : unc-119(ed3); wgIs322(ztf-4::TY1 EGFP FLAG; unc119(+)) outcross : 0 mutagen : None tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Dresden using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The spatio-temporal expression pattern of ZTF-4::EGFP fusion protein was examined through in vivo microscopy. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the ZTF-4 transcription factor. made_by : Bob Waterston's lab from UW )|ZTF-4 L2 InputRep1|L2 Lar@ L2?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX277099 OP322(official name : OP322 genotype : unc-119(ed3); wgIs322(ztf-4::TY1 EGFP FLAG; unc119(+)) outcross : 0 mutagen : None tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Dresden using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The spatio-temporal expression pattern of ZTF-4::EGFP fusion protein was examined through in vivo microscopy. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the ZTF-4 transcription factor. made_by : Bob Waterston's lab from UW )|ZTF-4 L2 InputRep2|L2 Lar@ L2?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX277100 OP322(official name : OP322 genotype : unc-119(ed3); wgIs322(ztf-4::TY1 EGFP FLAG; unc119(+)) outcross : 0 mutagen : None tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Dresden using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The spatio-temporal expression pattern of ZTF-4::EGFP fusion protein was examined through in vivo microscopy. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the ZTF-4 transcription factor. made_by : Bob Waterston's lab from UW )|ZTF-4 L2 ChIPRep1|L2 Lar@ L2?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX277101 OP322(official name : OP322 genotype : unc-119(ed3); wgIs322(ztf-4::TY1 EGFP FLAG; unc119(+)) outcross : 0 mutagen : None tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Dresden using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The spatio-temporal expression pattern of ZTF-4::EGFP fusion protein was examined through in vivo microscopy. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the ZTF-4 transcription factor. made_by : Bob Waterston's lab from UW )|ZTF-4 L2 ChIPRep2|L2 Lar@ L2?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX277102 OP361(official name : OP361 genotype : unc119(ed3); wgIs361(nhr-21::TY1-GFP-3xFLAG; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The NHR-21::EGFP fusion protein is expressed in the correct nhr-21 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the NHR-21 transcription factor. made_by : Unknown )|NHR-21 L2 InputRep1|L2 Lar@ L2?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX277103 OP361(official name : OP361 genotype : unc119(ed3); wgIs361(nhr-21::TY1-GFP-3xFLAG; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The NHR-21::EGFP fusion protein is expressed in the correct nhr-21 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the NHR-21 transcription factor. made_by : Unknown )|NHR-21 L2 InputRep2|L2 Lar@ L2?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX277104 OP361(official name : OP361 genotype : unc119(ed3); wgIs361(nhr-21::TY1-GFP-3xFLAG; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The NHR-21::EGFP fusion protein is expressed in the correct nhr-21 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the NHR-21 transcription factor. made_by : Unknown )|NHR-21 L2 ChIPRep1|L2 Lar@ L2?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX277105 OP361(official name : OP361 genotype : unc119(ed3); wgIs361(nhr-21::TY1-GFP-3xFLAG; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The NHR-21::EGFP fusion protein is expressed in the correct nhr-21 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the NHR-21 transcription factor. made_by : Unknown )|NHR-21 L2 ChIPRep2|L2 Lar@ L2?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331073 OP324(official name : OP324 genotype : unc119(ed3); wgIs324(C34F6.9::TY1 EGFP FLAG; unc119) outcross : 0 mutagen : None tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The spatio-temporal expression pattern of C34F6.9::EGFP fusion protein was examined through in vivo microscopy. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the C34F6.9 transcription factor. made_by : Bob Waterston's lab from UW )|C34F6.9_GFP_L2_Input_Rep1|L2 Lar@ L2?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331074 OP324(official name : OP324 genotype : unc119(ed3); wgIs324(C34F6.9::TY1 EGFP FLAG; unc119) outcross : 0 mutagen : None tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The spatio-temporal expression pattern of C34F6.9::EGFP fusion protein was examined through in vivo microscopy. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the C34F6.9 transcription factor. made_by : Bob Waterston's lab from UW )|C34F6.9_GFP_L2_ChIP_Rep1|L2 Lar@ L2?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331075 OP324(official name : OP324 genotype : unc119(ed3); wgIs324(C34F6.9::TY1 EGFP FLAG; unc119) outcross : 0 mutagen : None tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The spatio-temporal expression pattern of C34F6.9::EGFP fusion protein was examined through in vivo microscopy. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the C34F6.9 transcription factor. made_by : Bob Waterston's lab from UW )|C34F6.9_GFP_L2_Input_Rep2|L2 Lar@ L2?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331076 OP324(official name : OP324 genotype : unc119(ed3); wgIs324(C34F6.9::TY1 EGFP FLAG; unc119) outcross : 0 mutagen : None tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The spatio-temporal expression pattern of C34F6.9::EGFP fusion protein was examined through in vivo microscopy. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the C34F6.9 transcription factor. made_by : Bob Waterston's lab from UW )|C34F6.9_GFP_L2_ChIP_Rep2|L2 Lar@ L2?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331077 OP82(official name : OP82 genotype : unc119(ed3); wgIs82(ceh-16::TY1 EGFP FLAG; unc119) outcross : 0 mutagen : None tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The CEH-16::EGFP fusion protein is expressed in the correct CEH-16 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the CEH-16 transcription factor. made_by : Bob Waterston's lab from UW )|CEH-16_GFP_L2_Input_Rep1|L2 Lar@ L2?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331078 OP82(official name : OP82 genotype : unc119(ed3); wgIs82(ceh-16::TY1 EGFP FLAG; unc119) outcross : 0 mutagen : None tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The CEH-16::EGFP fusion protein is expressed in the correct CEH-16 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the CEH-16 transcription factor. made_by : Bob Waterston's lab from UW )|CEH-16_GFP_L2_ChIP_Rep1|L2 Lar@ L2?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331079 OP82(official name : OP82 genotype : unc119(ed3); wgIs82(ceh-16::TY1 EGFP FLAG; unc119) outcross : 0 mutagen : None tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The CEH-16::EGFP fusion protein is expressed in the correct CEH-16 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the CEH-16 transcription factor. made_by : Bob Waterston's lab from UW )|CEH-16_GFP_L2_Input_Rep2|L2 Lar@ L2?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331080 OP82(official name : OP82 genotype : unc119(ed3); wgIs82(ceh-16::TY1 EGFP FLAG; unc119) outcross : 0 mutagen : None tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The CEH-16::EGFP fusion protein is expressed in the correct CEH-16 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the CEH-16 transcription factor. made_by : Bob Waterston's lab from UW )|CEH-16_GFP_L2_ChIP_Rep2|L2 Lar@ L2?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331089 OP318(official name : OP318 genotype : unc-119(ed3); wgIs318(nhr-12::TY1 EGFP FLAG; unc-119(+)) outcross : 3 mutagen : None tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Dresden using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The spatio-temporal expression pattern of NHR-12::EGFP fusion protein was examined through in vivo microscopy. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the NHR-12 transcription factor. made_by : Bob Waterston's lab from UW )|NHR-12_GFP_L2_Input_Rep1|L2 Lar@ L2?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331090 OP318(official name : OP318 genotype : unc-119(ed3); wgIs318(nhr-12::TY1 EGFP FLAG; unc-119(+)) outcross : 3 mutagen : None tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Dresden using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The spatio-temporal expression pattern of NHR-12::EGFP fusion protein was examined through in vivo microscopy. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the NHR-12 transcription factor. made_by : Bob Waterston's lab from UW )|NHR-12_GFP_L2_ChIP_Rep1|L2 Lar@ L2?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331091 OP318(official name : OP318 genotype : unc-119(ed3); wgIs318(nhr-12::TY1 EGFP FLAG; unc-119(+)) outcross : 3 mutagen : None tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Dresden using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The spatio-temporal expression pattern of NHR-12::EGFP fusion protein was examined through in vivo microscopy. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the NHR-12 transcription factor. made_by : Bob Waterston's lab from UW )|NHR-12_GFP_L2_Input_Rep2|L2 Lar@ L2?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331092 OP318(official name : OP318 genotype : unc-119(ed3); wgIs318(nhr-12::TY1 EGFP FLAG; unc-119(+)) outcross : 3 mutagen : None tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Dresden using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The spatio-temporal expression pattern of NHR-12::EGFP fusion protein was examined through in vivo microscopy. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the NHR-12 transcription factor. made_by : Bob Waterston's lab from UW )|NHR-12_GFP_L2_ChIP_Rep2|L2 Lar@ L2?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331093 OP130(official name : OP130 genotype : unc119(ed3); wgIs130(sma-9::TY1 EGFP FLAG C; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The SMA-9::EGFP fusion protein is expressed in the correct sma-9 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the SMA-9 transcription factor. made_by : S Kim )|SMA-9_GFP_L2_Input_Rep1|L2 Lar@ L2?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331094 OP130(official name : OP130 genotype : unc119(ed3); wgIs130(sma-9::TY1 EGFP FLAG C; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The SMA-9::EGFP fusion protein is expressed in the correct sma-9 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the SMA-9 transcription factor. made_by : S Kim )|SMA-9_GFP_L2_ChIP_Rep1|L2 Lar@ L2?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331095 OP130(official name : OP130 genotype : unc119(ed3); wgIs130(sma-9::TY1 EGFP FLAG C; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The SMA-9::EGFP fusion protein is expressed in the correct sma-9 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the SMA-9 transcription factor. made_by : S Kim )|SMA-9_GFP_L2_Input_Rep2|L2 Lar@ L2?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331096 OP130(official name : OP130 genotype : unc119(ed3); wgIs130(sma-9::TY1 EGFP FLAG C; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The SMA-9::EGFP fusion protein is expressed in the correct sma-9 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the SMA-9 transcription factor. made_by : S Kim )|SMA-9_GFP_L2_ChIP_Rep2|L2 Lar@ L2?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331097 OP339(official name : OP339 genotype : unc119(ed3); wgIs339(nhr-129::TY1 EGFP FLAG; unc119) outcross : 0 mutagen : None tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for bombardment transformation of an unc-119(ed3) strain. The NHR-129::EGFP fusion protein was expressed in seam cells description : pharynx description : head neurons at L2 stage. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the NHR-129 transcription factor. made_by : Bob Waterston's lab from UW )|NHR-129_GFP_L2_Input_Rep1|L2 Lar@ L2?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331098 OP339(official name : OP339 genotype : unc119(ed3); wgIs339(nhr-129::TY1 EGFP FLAG; unc119) outcross : 0 mutagen : None tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for bombardment transformation of an unc-119(ed3) strain. The NHR-129::EGFP fusion protein was expressed in seam cells description : pharynx description : head neurons at L2 stage. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the NHR-129 transcription factor. made_by : Bob Waterston's lab from UW )|NHR-129_GFP_L2_ChIP_Rep1|L2 Lar@ L2?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331099 OP339(official name : OP339 genotype : unc119(ed3); wgIs339(nhr-129::TY1 EGFP FLAG; unc119) outcross : 0 mutagen : None tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for bombardment transformation of an unc-119(ed3) strain. The NHR-129::EGFP fusion protein was expressed in seam cells description : pharynx description : head neurons at L2 stage. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the NHR-129 transcription factor. made_by : Bob Waterston's lab from UW )|NHR-129_GFP_L2_Input_Rep2|L2 Lar@ L2?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331100 OP339(official name : OP339 genotype : unc119(ed3); wgIs339(nhr-129::TY1 EGFP FLAG; unc119) outcross : 0 mutagen : None tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for bombardment transformation of an unc-119(ed3) strain. The NHR-129::EGFP fusion protein was expressed in seam cells description : pharynx description : head neurons at L2 stage. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the NHR-129 transcription factor. made_by : Bob Waterston's lab from UW )|NHR-129_GFP_L2_ChIP_Rep2|L2 Lar@ L2?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331109 OP57(official name : OP57 genotype : unc-119(ed3); wgIs57(sem-4::TY1 EGFP FLAG; unc-119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology and Genetics in Dresden using Tony Hyman's recombineering pipeline. The resulting plasmid was used for bombardment transformation of an unc-119(ed3) strain. The SEM-4::EGFP fusion protein is expressed in the correct sem-4 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the sem-4 transcription factor. made_by : Bob Waterston's lab from UW )|SEM-4_GFP_L2_Input_Rep1|L2 Lar@ L2?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331110 OP57(official name : OP57 genotype : unc-119(ed3); wgIs57(sem-4::TY1 EGFP FLAG; unc-119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology and Genetics in Dresden using Tony Hyman's recombineering pipeline. The resulting plasmid was used for bombardment transformation of an unc-119(ed3) strain. The SEM-4::EGFP fusion protein is expressed in the correct sem-4 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the sem-4 transcription factor. made_by : Bob Waterston's lab from UW )|SEM-4_GFP_L2_ChIP_Rep1|L2 Lar@ L2?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331111 OP57(official name : OP57 genotype : unc-119(ed3); wgIs57(sem-4::TY1 EGFP FLAG; unc-119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology and Genetics in Dresden using Tony Hyman's recombineering pipeline. The resulting plasmid was used for bombardment transformation of an unc-119(ed3) strain. The SEM-4::EGFP fusion protein is expressed in the correct sem-4 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the sem-4 transcription factor. made_by : Bob Waterston's lab from UW )|SEM-4_GFP_L2_Input_Rep2|L2 Lar@ L2?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331112 OP57(official name : OP57 genotype : unc-119(ed3); wgIs57(sem-4::TY1 EGFP FLAG; unc-119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology and Genetics in Dresden using Tony Hyman's recombineering pipeline. The resulting plasmid was used for bombardment transformation of an unc-119(ed3) strain. The SEM-4::EGFP fusion protein is expressed in the correct sem-4 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the sem-4 transcription factor. made_by : Bob Waterston's lab from UW )|SEM-4_GFP_L2_ChIP_Rep2|L2 Lar@ L2?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331121 OP33(official name : OP33 genotype : unc119(ed3); wgIs33(nhr-25::TY1 EGFP FLAG; unc119) outcross : 0 mutagen : None tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for bombardment transformation of an unc-119(ed3) strain. made_by : Bob Waterston's lab from UW )|NHR-25_GFP_L2_Input_Rep1|L2 Lar@ L2?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331122 OP33(official name : OP33 genotype : unc119(ed3); wgIs33(nhr-25::TY1 EGFP FLAG; unc119) outcross : 0 mutagen : None tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for bombardment transformation of an unc-119(ed3) strain. made_by : Bob Waterston's lab from UW )|NHR-25_GFP_L2_ChIP_Rep1|L2 Lar@ L2?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331123 OP33(official name : OP33 genotype : unc119(ed3); wgIs33(nhr-25::TY1 EGFP FLAG; unc119) outcross : 0 mutagen : None tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for bombardment transformation of an unc-119(ed3) strain. made_by : Bob Waterston's lab from UW )|NHR-25_GFP_L2_Input_Rep2|L2 Lar@ L2?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331124 OP33(official name : OP33 genotype : unc119(ed3); wgIs33(nhr-25::TY1 EGFP FLAG; unc119) outcross : 0 mutagen : None tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for bombardment transformation of an unc-119(ed3) strain. made_by : Bob Waterston's lab from UW )|NHR-25_GFP_L2_ChIP_Rep2|L2 Lar@ L2?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331125 OP33(official name : OP33 genotype : unc119(ed3); wgIs33(nhr-25::TY1 EGFP FLAG; unc119) outcross : 0 mutagen : None tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for bombardment transformation of an unc-119(ed3) strain. made_by : Bob Waterston's lab from UW )|NHR-25_GFP_L2_Input_Rep3|L2 Lar@ L2?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331126 OP33(official name : OP33 genotype : unc119(ed3); wgIs33(nhr-25::TY1 EGFP FLAG; unc119) outcross : 0 mutagen : None tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for bombardment transformation of an unc-119(ed3) strain. made_by : Bob Waterston's lab from UW )|NHR-25_GFP_L2_ChIP_Rep3|L2 Lar@ L2?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331143 OP86(official name : OP86 genotype : unc119(ed3); wgIs86(peb-1::TY1 EGFP FLAG; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The PEB-1::EGFP fusion protein is expressed in the correct peb-1 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the PEB-1 transcription factor. made_by : R Waterston )|PEB-1_GFP_L2_Input_Rep1|L2 Lar@ L2?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331144 OP86(official name : OP86 genotype : unc119(ed3); wgIs86(peb-1::TY1 EGFP FLAG; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The PEB-1::EGFP fusion protein is expressed in the correct peb-1 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the PEB-1 transcription factor. made_by : R Waterston )|PEB-1_GFP_L2_ChIP_Rep1|L2 Lar@ L2?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331145 OP86(official name : OP86 genotype : unc119(ed3); wgIs86(peb-1::TY1 EGFP FLAG; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The PEB-1::EGFP fusion protein is expressed in the correct peb-1 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the PEB-1 transcription factor. made_by : R Waterston )|PEB-1_GFP_L2_Input_Rep2|L2 Lar@ L2?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331146 OP86(official name : OP86 genotype : unc119(ed3); wgIs86(peb-1::TY1 EGFP FLAG; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The PEB-1::EGFP fusion protein is expressed in the correct peb-1 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the PEB-1 transcription factor. made_by : R Waterston )|PEB-1_GFP_L2_ChIP_Rep2|L2 Lar@ L2?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331173 OP228(official name : OP228 genotype : unc119(ed3); wgIs228(nhr-237:TY1 EGFP FLAG; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The NHR-237::EGFP fusion protein is expressed in the correct nhr-237 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the NHR-237 transcription factor. made_by : Unknown )|NHR-237_GFP_L2_Input_Rep1|L2 Lar@ L2?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331174 OP228(official name : OP228 genotype : unc119(ed3); wgIs228(nhr-237:TY1 EGFP FLAG; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The NHR-237::EGFP fusion protein is expressed in the correct nhr-237 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the NHR-237 transcription factor. made_by : Unknown )|NHR-237_GFP_L2_ChIP_Rep1|L2 Lar@ L2?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331175 OP228(official name : OP228 genotype : unc119(ed3); wgIs228(nhr-237:TY1 EGFP FLAG; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The NHR-237::EGFP fusion protein is expressed in the correct nhr-237 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the NHR-237 transcription factor. made_by : Unknown )|NHR-237_GFP_L2_Input_Rep2|L2 Lar@ L2?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331176 OP228(official name : OP228 genotype : unc119(ed3); wgIs228(nhr-237:TY1 EGFP FLAG; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The NHR-237::EGFP fusion protein is expressed in the correct nhr-237 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the NHR-237 transcription factor. made_by : Unknown )|NHR-237_GFP_L2_ChIP_Rep2|L2 Lar@ L2?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331209 OP18(official name : OP18 genotype : unc-119(ed3) III; wgIs18 unc-119(+) lin-39::TY1::EGFP::3xFLAG outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The LIN-39::EGFP fusion protein is expressed in the correct lin-39 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the LIN-39 transcription factor. made_by : R. Waterston and S. Kim )|LIN-39_GFP_L2_Input_Rep1|L2 Lar@ L2?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331210 OP18(official name : OP18 genotype : unc-119(ed3) III; wgIs18 unc-119(+) lin-39::TY1::EGFP::3xFLAG outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The LIN-39::EGFP fusion protein is expressed in the correct lin-39 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the LIN-39 transcription factor. made_by : R. Waterston and S. Kim )|LIN-39_GFP_L2_ChIP_Rep1|L2 Lar@ L2?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331211 OP18(official name : OP18 genotype : unc-119(ed3) III; wgIs18 unc-119(+) lin-39::TY1::EGFP::3xFLAG outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The LIN-39::EGFP fusion protein is expressed in the correct lin-39 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the LIN-39 transcription factor. made_by : R. Waterston and S. Kim )|LIN-39_GFP_L2_Input_Rep2|L2 Lar@ L2?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331212 OP18(official name : OP18 genotype : unc-119(ed3) III; wgIs18 unc-119(+) lin-39::TY1::EGFP::3xFLAG outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The LIN-39::EGFP fusion protein is expressed in the correct lin-39 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the LIN-39 transcription factor. made_by : R. Waterston and S. Kim )|LIN-39_GFP_L2_ChIP_Rep2|L2 Lar@ L2?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331271 NC1639(official name : NC1639 genotype : wdIs49 (pttr39::UNC-55a::GFP; dpy-20+) III outcross : 0 mutagen : None tags : GFP description : Expresses functional *GFP-tagged UNC-55* (COUP-TF) in ventral cord GABA motor neurons (also some ectopic expression in other cells). This line is integrated and shows strong GFP expression. made_by : David Miller lab )|UNC-55_GFP_L2_Input_Rep1|L2 Lar@ L2?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331272 NC1639(official name : NC1639 genotype : wdIs49 (pttr39::UNC-55a::GFP; dpy-20+) III outcross : 0 mutagen : None tags : GFP description : Expresses functional *GFP-tagged UNC-55* (COUP-TF) in ventral cord GABA motor neurons (also some ectopic expression in other cells). This line is integrated and shows strong GFP expression. made_by : David Miller lab )|UNC-55_GFP_L2_ChIP_Rep1|L2 Lar@ L2?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331273 NC1639(official name : NC1639 genotype : wdIs49 (pttr39::UNC-55a::GFP; dpy-20+) III outcross : 0 mutagen : None tags : GFP description : Expresses functional *GFP-tagged UNC-55* (COUP-TF) in ventral cord GABA motor neurons (also some ectopic expression in other cells). This line is integrated and shows strong GFP expression. made_by : David Miller lab )|UNC-55_GFP_L2_Input_Rep2|L2 Lar@ L2?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331274 NC1639(official name : NC1639 genotype : wdIs49 (pttr39::UNC-55a::GFP; dpy-20+) III outcross : 0 mutagen : None tags : GFP description : Expresses functional *GFP-tagged UNC-55* (COUP-TF) in ventral cord GABA motor neurons (also some ectopic expression in other cells). This line is integrated and shows strong GFP expression. made_by : David Miller lab )|UNC-55_GFP_L2_ChIP_Rep2|L2 Lar@ L2?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331275 NC1639(official name : NC1639 genotype : wdIs49 (pttr39::UNC-55a::GFP; dpy-20+) III outcross : 0 mutagen : None tags : GFP description : Expresses functional *GFP-tagged UNC-55* (COUP-TF) in ventral cord GABA motor neurons (also some ectopic expression in other cells). This line is integrated and shows strong GFP expression. made_by : David Miller lab )|UNC-55_GFP_L2_Input_Rep3|L2 Lar@ L2?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331276 NC1639(official name : NC1639 genotype : wdIs49 (pttr39::UNC-55a::GFP; dpy-20+) III outcross : 0 mutagen : None tags : GFP description : Expresses functional *GFP-tagged UNC-55* (COUP-TF) in ventral cord GABA motor neurons (also some ectopic expression in other cells). This line is integrated and shows strong GFP expression. made_by : David Miller lab )|UNC-55_GFP_L2_ChIP_Rep3|L2 Lar@ L2?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331285 OP27(official name : OP27 genotype : unc-119(ed3); wgIs27(mab-5::TY1 EGFP FLAG; unc-119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology and Genetics in Dresden using Tony Hyman's recombineering pipeline. The resulting plasmid was used for bombardment transformation of an unc-119(ed3) strain. The MAB-5::EGFP fusion protein is expressed in the correct mab-5 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the MAB-5 transcription factor. made_by : Bob Waterston's lab from UW )|MAB-5_GFP_L2_Input_Rep1|L2 Lar@ L2?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331286 OP27(official name : OP27 genotype : unc-119(ed3); wgIs27(mab-5::TY1 EGFP FLAG; unc-119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology and Genetics in Dresden using Tony Hyman's recombineering pipeline. The resulting plasmid was used for bombardment transformation of an unc-119(ed3) strain. The MAB-5::EGFP fusion protein is expressed in the correct mab-5 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the MAB-5 transcription factor. made_by : Bob Waterston's lab from UW )|MAB-5_GFP_L2_ChIP_Rep1|L2 Lar@ L2?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331287 OP27(official name : OP27 genotype : unc-119(ed3); wgIs27(mab-5::TY1 EGFP FLAG; unc-119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology and Genetics in Dresden using Tony Hyman's recombineering pipeline. The resulting plasmid was used for bombardment transformation of an unc-119(ed3) strain. The MAB-5::EGFP fusion protein is expressed in the correct mab-5 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the MAB-5 transcription factor. made_by : Bob Waterston's lab from UW )|MAB-5_GFP_L2_Input_Rep2|L2 Lar@ L2?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331288 OP27(official name : OP27 genotype : unc-119(ed3); wgIs27(mab-5::TY1 EGFP FLAG; unc-119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology and Genetics in Dresden using Tony Hyman's recombineering pipeline. The resulting plasmid was used for bombardment transformation of an unc-119(ed3) strain. The MAB-5::EGFP fusion protein is expressed in the correct mab-5 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the MAB-5 transcription factor. made_by : Bob Waterston's lab from UW )|MAB-5_GFP_L2_ChIP_Rep2|L2 Lar@ L2?0 1 3 https://www.ncbi.nlm.nih.gov/sra?term=SRX015093 OP73|OP73, CEH-14:GFP:3xFLAG animals|L2 Lar@ L2?0 1 3 https://www.ncbi.nlm.nih.gov/sra?term=SRX323677 N2|N2 strain, L2 stage Lar@ L2?0 1 4 https://www.ncbi.nlm.nih.gov/sra?term=SRX3058057 GSH100|whole worms|whole worms|L2 Lar@ L2?0 1 8 https://www.ncbi.nlm.nih.gov/sra?term=SRX4082338 N2|L2 larvae Lar@ L2?0 1 9 https://www.ncbi.nlm.nih.gov/sra?term=SRX1769982 AM1061|L2 larvae|whole animal|L2 larvae Lar@ L2?0 2 20 https://www.ncbi.nlm.nih.gov/sra?term=SRX4085374 wild-type N2|L2 larvae Lar@ L2?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX1007136 sydn-1(0)|sydn-1(0) worms|L2-L3 Lar@ L2-L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX1007137 ssup-72(0)|ssup-72(0) worms|L2-L3 Lar@ L2-L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX1007138 ssup-72(0); sydn-1(0)|ssup-72(0); sydn-1(0) worms|L2-L3 Lar@ L2-L3?0 1 2 https://www.ncbi.nlm.nih.gov/sra?term=SRX1007134 N2|wild type worms|L2-L3 Lar@ L2-L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX043843 OP26(made_by : R. Waterston and S. Kim description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The MAB-5::EGFP fusion protein is expressed in the correct mab-5 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the MAB-5 transcription factor. tags : GFP::3xFlag mutagen : Bombard outcross : 3 genotype : unc-119(ed3) III; wgIs26 unc-119(+) mab-5::TY1::EGFP::3xFLAG official name : OP26 )|Snyder_MAB5_POLII_L3_rep1 extraction1_seq1 channel_1|L3 Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX043844 OP26(made_by : R. Waterston and S. Kim description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The MAB-5::EGFP fusion protein is expressed in the correct mab-5 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the MAB-5 transcription factor. tags : GFP::3xFlag mutagen : Bombard outcross : 3 genotype : unc-119(ed3) III; wgIs26 unc-119(+) mab-5::TY1::EGFP::3xFLAG official name : OP26 )|Snyder_MAB5_POLII_L3_rep1 extraction1_seq1 channel_2|L3 Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX043845 OP26(made_by : R. Waterston and S. Kim description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The MAB-5::EGFP fusion protein is expressed in the correct mab-5 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the MAB-5 transcription factor. tags : GFP::3xFlag mutagen : Bombard outcross : 3 genotype : unc-119(ed3) III; wgIs26 unc-119(+) mab-5::TY1::EGFP::3xFLAG official name : OP26 )|Snyder_MAB5_POLII_L3_rep2 extraction2_seq1 channel_1|L3 Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX043846 OP26(made_by : R. Waterston and S. Kim description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The MAB-5::EGFP fusion protein is expressed in the correct mab-5 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the MAB-5 transcription factor. tags : GFP::3xFlag mutagen : Bombard outcross : 3 genotype : unc-119(ed3) III; wgIs26 unc-119(+) mab-5::TY1::EGFP::3xFLAG official name : OP26 )|Snyder_MAB5_POLII_L3_rep2 extraction2_seq1 channel_2|L3 Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX043879 N2(genotype : wild type genotype : DR subclone of DB original (Tc1 pattern I) official name : N2 )|Snyder_N2_POLII_L3_rep1 extraction1_seq1 channel_1|L3 Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX043880 N2(genotype : wild type genotype : DR subclone of DB original (Tc1 pattern I) official name : N2 )|Snyder_N2_POLII_L3_rep1 extraction1_seq1 channel_2|L3 Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX043881 N2(genotype : wild type genotype : DR subclone of DB original (Tc1 pattern I) official name : N2 )|Snyder_N2_POLII_L3_rep2 extraction2_seq1 channel_1|L3 Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX043882 N2(genotype : wild type genotype : DR subclone of DB original (Tc1 pattern I) official name : N2 )|Snyder_N2_POLII_L3_rep2 extraction2_seq1 channel_2|L3 Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX043987 OP184(made_by : S Kim description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The LIN-15B::EGFP fusion protein is expressed in the correct lin-15B spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the LIN-15B transcription factor. tags : GFP::3xFlag mutagen : Bombard outcross : 3 genotype : unc119(ed3); wgIs184(lin-15B::TY1 EGFP FLAG; unc119) official name : OP184 )|Snyder_LIN-15B_GFP_L3_rep1 extraction1_seq1 channel_1|L3 Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX043988 OP184(made_by : S Kim description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The LIN-15B::EGFP fusion protein is expressed in the correct lin-15B spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the LIN-15B transcription factor. tags : GFP::3xFlag mutagen : Bombard outcross : 3 genotype : unc119(ed3); wgIs184(lin-15B::TY1 EGFP FLAG; unc119) official name : OP184 )|Snyder_LIN-15B_GFP_L3_rep1 extraction1_seq1 channel_2|L3 Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX043989 OP184(made_by : S Kim description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The LIN-15B::EGFP fusion protein is expressed in the correct lin-15B spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the LIN-15B transcription factor. tags : GFP::3xFlag mutagen : Bombard outcross : 3 genotype : unc119(ed3); wgIs184(lin-15B::TY1 EGFP FLAG; unc119) official name : OP184 )|Snyder_LIN-15B_GFP_L3_rep2 extraction2_seq1 channel_1|L3 Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX043990 OP184(made_by : S Kim description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The LIN-15B::EGFP fusion protein is expressed in the correct lin-15B spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the LIN-15B transcription factor. tags : GFP::3xFlag mutagen : Bombard outcross : 3 genotype : unc119(ed3); wgIs184(lin-15B::TY1 EGFP FLAG; unc119) official name : OP184 )|Snyder_LIN-15B_GFP_L3_rep2 extraction2_seq1 channel_2|L3 Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX044015 OP201(made_by : S Kim description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The PQM-1::EGFP fusion protein is expressed in the correct pqm-1 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the PQM-1 transcription factor. tags : GFP::3xFlag mutagen : Bombard outcross : 3 genotype : unc119(ed3); wgIs201(pqm-1::TY1 EGFP FLAG C; unc119) official name : OP201 )|Snyder_PQM-1_GFP_L3_rep1 extraction1_seq1 channel_1|L3 Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX044016 OP201(made_by : S Kim description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The PQM-1::EGFP fusion protein is expressed in the correct pqm-1 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the PQM-1 transcription factor. tags : GFP::3xFlag mutagen : Bombard outcross : 3 genotype : unc119(ed3); wgIs201(pqm-1::TY1 EGFP FLAG C; unc119) official name : OP201 )|Snyder_PQM-1_GFP_L3_rep1 extraction1_seq1 channel_2|L3 Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX044017 OP201(made_by : S Kim description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The PQM-1::EGFP fusion protein is expressed in the correct pqm-1 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the PQM-1 transcription factor. tags : GFP::3xFlag mutagen : Bombard outcross : 3 genotype : unc119(ed3); wgIs201(pqm-1::TY1 EGFP FLAG C; unc119) official name : OP201 )|Snyder_PQM-1_GFP_L3_rep2 extraction2_seq1 channel_1|L3 Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX044018 OP201(made_by : S Kim description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The PQM-1::EGFP fusion protein is expressed in the correct pqm-1 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the PQM-1 transcription factor. tags : GFP::3xFlag mutagen : Bombard outcross : 3 genotype : unc119(ed3); wgIs201(pqm-1::TY1 EGFP FLAG C; unc119) official name : OP201 )|Snyder_PQM-1_GFP_L3_rep2 extraction2_seq1 channel_2|L3 Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX044021 OP18(made_by : R. Waterston and S. Kim description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The LIN-39::EGFP fusion protein is expressed in the correct lin-39 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the LIN-39 transcription factor. tags : GFP::3xFlag mutagen : Bombard outcross : 3 genotype : unc-119(ed3) III; wgIs18 unc-119(+) lin-39::TY1::EGFP::3xFLAG official name : OP18 )|Snyder_LIN-39-GFP_L3_rep1 extraction1_seq1 channel_1|L3 Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX044022 OP18(made_by : R. Waterston and S. Kim description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The LIN-39::EGFP fusion protein is expressed in the correct lin-39 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the LIN-39 transcription factor. tags : GFP::3xFlag mutagen : Bombard outcross : 3 genotype : unc-119(ed3) III; wgIs18 unc-119(+) lin-39::TY1::EGFP::3xFLAG official name : OP18 )|Snyder_LIN-39-GFP_L3_rep1 extraction1_seq1 channel_2|L3 Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX044023 OP18(made_by : R. Waterston and S. Kim description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The LIN-39::EGFP fusion protein is expressed in the correct lin-39 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the LIN-39 transcription factor. tags : GFP::3xFlag mutagen : Bombard outcross : 3 genotype : unc-119(ed3) III; wgIs18 unc-119(+) lin-39::TY1::EGFP::3xFLAG official name : OP18 )|Snyder_LIN-39-GFP_L3_rep2 extraction2_seq1 channel_1|L3 Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX044024 OP18(made_by : R. Waterston and S. Kim description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The LIN-39::EGFP fusion protein is expressed in the correct lin-39 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the LIN-39 transcription factor. tags : GFP::3xFlag mutagen : Bombard outcross : 3 genotype : unc-119(ed3) III; wgIs18 unc-119(+) lin-39::TY1::EGFP::3xFLAG official name : OP18 )|Snyder_LIN-39-GFP_L3_rep2 extraction2_seq1 channel_2|L3 Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX054303 OP54(official name : OP54 genotype : unc-119(ed3) III; wgIs54 unc-119(+) egl-5::TY1::EGFP::3xFLAG outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The EGL-5::EGFP fusion protein is expressed in the correct egl-5 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the EGL-5 transcription factor. made_by : R. Waterston and S. Kim )|Snyder_EGL-5_GFP_L3_rep2 extraction1_seq1 channel_1|L3 Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX054304 OP54(official name : OP54 genotype : unc-119(ed3) III; wgIs54 unc-119(+) egl-5::TY1::EGFP::3xFLAG outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The EGL-5::EGFP fusion protein is expressed in the correct egl-5 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the EGL-5 transcription factor. made_by : R. Waterston and S. Kim )|Snyder_EGL-5_GFP_L3_rep2 extraction2_seq2 channel_1|L3 Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX054305 OP54(official name : OP54 genotype : unc-119(ed3) III; wgIs54 unc-119(+) egl-5::TY1::EGFP::3xFLAG outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The EGL-5::EGFP fusion protein is expressed in the correct egl-5 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the EGL-5 transcription factor. made_by : R. Waterston and S. Kim )|Snyder_EGL-5_GFP_L3_rep2 extraction3_seq3 channel_1|L3 Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX054306 OP54(official name : OP54 genotype : unc-119(ed3) III; wgIs54 unc-119(+) egl-5::TY1::EGFP::3xFLAG outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The EGL-5::EGFP fusion protein is expressed in the correct egl-5 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the EGL-5 transcription factor. made_by : R. Waterston and S. Kim )|Snyder_EGL-5_GFP_L3_rep2 extraction4_seq4 channel_1|L3 Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX054307 OP54(official name : OP54 genotype : unc-119(ed3) III; wgIs54 unc-119(+) egl-5::TY1::EGFP::3xFLAG outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The EGL-5::EGFP fusion protein is expressed in the correct egl-5 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the EGL-5 transcription factor. made_by : R. Waterston and S. Kim )|Snyder_EGL-5_GFP_L3_rep2 extraction5_seq5 channel_1|L3 Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX054308 OP54(official name : OP54 genotype : unc-119(ed3) III; wgIs54 unc-119(+) egl-5::TY1::EGFP::3xFLAG outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The EGL-5::EGFP fusion protein is expressed in the correct egl-5 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the EGL-5 transcription factor. made_by : R. Waterston and S. Kim )|Snyder_EGL-5_GFP_L3_rep1 extraction6_seq6 channel_1|L3 Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX054309 OP54(official name : OP54 genotype : unc-119(ed3) III; wgIs54 unc-119(+) egl-5::TY1::EGFP::3xFLAG outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The EGL-5::EGFP fusion protein is expressed in the correct egl-5 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the EGL-5 transcription factor. made_by : R. Waterston and S. Kim )|Snyder_EGL-5_GFP_L3_rep1 extraction7_seq7 channel_1|L3 Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX054310 OP54(official name : OP54 genotype : unc-119(ed3) III; wgIs54 unc-119(+) egl-5::TY1::EGFP::3xFLAG outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The EGL-5::EGFP fusion protein is expressed in the correct egl-5 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the EGL-5 transcription factor. made_by : R. Waterston and S. Kim )|Snyder_EGL-5_GFP_L3_rep2 extraction8_seq8 channel_1|L3 Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX054311 OP54(official name : OP54 genotype : unc-119(ed3) III; wgIs54 unc-119(+) egl-5::TY1::EGFP::3xFLAG outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The EGL-5::EGFP fusion protein is expressed in the correct egl-5 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the EGL-5 transcription factor. made_by : R. Waterston and S. Kim )|Snyder_EGL-5_GFP_L3_rep2 extraction9_seq9 channel_1|L3 Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX065626 OP37(official name : OP37 genotype : unc-119(ed3) III; wgIs37 unc-119(+) pha-4::TY1::EGFP::3xFLAG outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The PHA-4::EGFP fusion protein is expressed in the correct pha-4 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the PHA-4 transcription factor. made_by : R. Waterston and S. Kim )|Snyder_PHA-4_Input_L3 extraction1_seq1 channel_1|L3 Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX065627 OP37(official name : OP37 genotype : unc-119(ed3) III; wgIs37 unc-119(+) pha-4::TY1::EGFP::3xFLAG outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The PHA-4::EGFP fusion protein is expressed in the correct pha-4 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the PHA-4 transcription factor. made_by : R. Waterston and S. Kim )|Snyder_PHA-4_Input_L3 extraction2_seq2 channel_1|L3 Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX065628 OP37(official name : OP37 genotype : unc-119(ed3) III; wgIs37 unc-119(+) pha-4::TY1::EGFP::3xFLAG outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The PHA-4::EGFP fusion protein is expressed in the correct pha-4 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the PHA-4 transcription factor. made_by : R. Waterston and S. Kim )|Snyder_PHA-4_GFP_L3_rep1 extraction3_seq3 channel_1|L3 Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX065629 OP37(official name : OP37 genotype : unc-119(ed3) III; wgIs37 unc-119(+) pha-4::TY1::EGFP::3xFLAG outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The PHA-4::EGFP fusion protein is expressed in the correct pha-4 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the PHA-4 transcription factor. made_by : R. Waterston and S. Kim )|Snyder_PHA-4_GFP_L3_rep2 extraction4_seq4 channel_1|L3 Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX065634 OP322(official name : ZTF-4 genotype : unc119(ed3); wgIs322(ztf-4::TY1 EGFP FLAG; unc119) outcross : 0 mutagen : None tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The spatio-temporal expression pattern of ZTF-4::EGFP fusion protein was examined through in vivo microscopy. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the ZTF-4 transcription factor. made_by : Bob Waterston's lab from UW )|Snyder_ZTF-4_Input_L3 extraction1_seq1 channel_1|L3 Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX065635 OP322(official name : ZTF-4 genotype : unc119(ed3); wgIs322(ztf-4::TY1 EGFP FLAG; unc119) outcross : 0 mutagen : None tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The spatio-temporal expression pattern of ZTF-4::EGFP fusion protein was examined through in vivo microscopy. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the ZTF-4 transcription factor. made_by : Bob Waterston's lab from UW )|Snyder_ZTF-4_Input_L3 extraction2_seq2 channel_1|L3 Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX065636 OP322(official name : ZTF-4 genotype : unc119(ed3); wgIs322(ztf-4::TY1 EGFP FLAG; unc119) outcross : 0 mutagen : None tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The spatio-temporal expression pattern of ZTF-4::EGFP fusion protein was examined through in vivo microscopy. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the ZTF-4 transcription factor. made_by : Bob Waterston's lab from UW )|Snyder_ZTF-4_GFP_L3_rep1 extraction3_seq3 channel_1|L3 Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX065637 OP322(official name : ZTF-4 genotype : unc119(ed3); wgIs322(ztf-4::TY1 EGFP FLAG; unc119) outcross : 0 mutagen : None tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The spatio-temporal expression pattern of ZTF-4::EGFP fusion protein was examined through in vivo microscopy. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the ZTF-4 transcription factor. made_by : Bob Waterston's lab from UW )|Snyder_ZTF-4_GFP_L3_rep2 extraction4_seq4 channel_1|L3 Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX065650 OP600(official name : OP600 genotype : unc119(ed3); wgIs600(unc-62::TY1 EGFP FLAG; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The UNC-62::EGFP fusion protein is expressed in the correct unc-62 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the UNC-62 transcription factor. made_by : S Kim )|Snyder_UNC-62_Input_L3 extraction1_seq1 channel_1|L3 Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX065651 OP600(official name : OP600 genotype : unc119(ed3); wgIs600(unc-62::TY1 EGFP FLAG; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The UNC-62::EGFP fusion protein is expressed in the correct unc-62 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the UNC-62 transcription factor. made_by : S Kim )|Snyder_UNC-62_Input_L3 extraction2_seq2 channel_1|L3 Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX065652 OP600(official name : OP600 genotype : unc119(ed3); wgIs600(unc-62::TY1 EGFP FLAG; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The UNC-62::EGFP fusion protein is expressed in the correct unc-62 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the UNC-62 transcription factor. made_by : S Kim )|Snyder_UNC-62_GFP_L3_rep1 extraction3_seq3 channel_1|L3 Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX065653 OP600(official name : OP600 genotype : unc119(ed3); wgIs600(unc-62::TY1 EGFP FLAG; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The UNC-62::EGFP fusion protein is expressed in the correct unc-62 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the UNC-62 transcription factor. made_by : S Kim )|Snyder_UNC-62_GFP_L3_rep2 extraction4_seq4 channel_1|L3 Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX065679 OP81(official name : OP81 genotype : unc-119(ed3) III; wgIs81 unc-119(+) eor-1::TY1::EGFP::3xFLAG outcross : 0 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The EOR-1::EGFP fusion protein is expressed in the correct eor-1 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the EOR-1 transcription factor. made_by : R. Waterston and S. Kim )|Snyder_EOR-1_Input_L3 extraction1_seq1 channel_1|L3 Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX065680 OP81(official name : OP81 genotype : unc-119(ed3) III; wgIs81 unc-119(+) eor-1::TY1::EGFP::3xFLAG outcross : 0 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The EOR-1::EGFP fusion protein is expressed in the correct eor-1 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the EOR-1 transcription factor. made_by : R. Waterston and S. Kim )|Snyder_EOR-1_Input_L3 extraction2_seq2 channel_1|L3 Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX065681 OP81(official name : OP81 genotype : unc-119(ed3) III; wgIs81 unc-119(+) eor-1::TY1::EGFP::3xFLAG outcross : 0 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The EOR-1::EGFP fusion protein is expressed in the correct eor-1 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the EOR-1 transcription factor. made_by : R. Waterston and S. Kim )|Snyder_EOR-1_GFP_L3_rep1 extraction3_seq3 channel_1|L3 Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX065682 OP81(official name : OP81 genotype : unc-119(ed3) III; wgIs81 unc-119(+) eor-1::TY1::EGFP::3xFLAG outcross : 0 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The EOR-1::EGFP fusion protein is expressed in the correct eor-1 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the EOR-1 transcription factor. made_by : R. Waterston and S. Kim )|Snyder_EOR-1_GFP_L3_rep2 extraction4_seq4 channel_1|L3 Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX065691 OP83(official name : OP83 genotype : unc119(ed3); wgIs83(zag-1::TY1 EGFP FLAG; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The ZAG-1::EGFP fusion protein is expressed in the correct zag-1 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the ZAG-1 transcription factor. made_by : R Waterston )|Snyder_ZAG-1_Input_L3 extraction1_seq1 channel_1|L3 Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX065692 OP83(official name : OP83 genotype : unc119(ed3); wgIs83(zag-1::TY1 EGFP FLAG; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The ZAG-1::EGFP fusion protein is expressed in the correct zag-1 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the ZAG-1 transcription factor. made_by : R Waterston )|Snyder_ZAG-1_Input_L3 extraction2_seq2 channel_1|L3 Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX065693 OP83(official name : OP83 genotype : unc119(ed3); wgIs83(zag-1::TY1 EGFP FLAG; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The ZAG-1::EGFP fusion protein is expressed in the correct zag-1 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the ZAG-1 transcription factor. made_by : R Waterston )|Snyder_ZAG-1_GFP_L3_rep1 extraction3_seq3 channel_1|L3 Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX065694 OP83(official name : OP83 genotype : unc119(ed3); wgIs83(zag-1::TY1 EGFP FLAG; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The ZAG-1::EGFP fusion protein is expressed in the correct zag-1 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the ZAG-1 transcription factor. made_by : R Waterston )|Snyder_ZAG-1_GFP_L3_rep2 extraction4_seq4 channel_1|L3 Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX065699 OP212(official name : OP212 genotype : unc119(ed3); wgIs212(F45C12.2:TY1 EGFP FLAG; unc119) outcross : 3 transgene : F45C12.2 tags : Bombard tag : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The F45C12.2::EGFP fusion protein is expressed in the correct F45C12.2 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the F45C12.2 transcription factor. made_by : Mihail Sarov )|Snyder_F45C12.2_Input_L3 extraction1_seq1 channel_1|L3 Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX065700 OP212(official name : OP212 genotype : unc119(ed3); wgIs212(F45C12.2:TY1 EGFP FLAG; unc119) outcross : 3 transgene : F45C12.2 tags : Bombard tag : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The F45C12.2::EGFP fusion protein is expressed in the correct F45C12.2 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the F45C12.2 transcription factor. made_by : Mihail Sarov )|Snyder_F45C12.2_Input_L3 extraction2_seq2 channel_1|L3 Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX065701 OP212(official name : OP212 genotype : unc119(ed3); wgIs212(F45C12.2:TY1 EGFP FLAG; unc119) outcross : 3 transgene : F45C12.2 tags : Bombard tag : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The F45C12.2::EGFP fusion protein is expressed in the correct F45C12.2 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the F45C12.2 transcription factor. made_by : Mihail Sarov )|Snyder_F45C12.2_GFP_L3_rep1 extraction3_seq3 channel_1|L3 Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX065702 OP212(official name : OP212 genotype : unc119(ed3); wgIs212(F45C12.2:TY1 EGFP FLAG; unc119) outcross : 3 transgene : F45C12.2 tags : Bombard tag : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The F45C12.2::EGFP fusion protein is expressed in the correct F45C12.2 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the F45C12.2 transcription factor. made_by : Mihail Sarov )|Snyder_F45C12.2_GFP_L3_rep2 extraction4_seq4 channel_1|L3 Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX065703 OP222(official name : OP222 genotype : unc119(ed3); wgIs222(daf-12:TY1 EGFP FLAG; unc119) outcross : 3 transgene : daf-12 tags : Bombard tag : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The DAF-12::EGFP fusion protein is expressed in the correct daf-12 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the DAF-12 transcription factor. made_by : Mihail Sarov )|Snyder_DAF-12_Input_L3 extraction1_seq1 channel_1|L3 Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX065704 OP222(official name : OP222 genotype : unc119(ed3); wgIs222(daf-12:TY1 EGFP FLAG; unc119) outcross : 3 transgene : daf-12 tags : Bombard tag : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The DAF-12::EGFP fusion protein is expressed in the correct daf-12 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the DAF-12 transcription factor. made_by : Mihail Sarov )|Snyder_DAF-12_Input_L3 extraction2_seq2 channel_1|L3 Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX065705 OP222(official name : OP222 genotype : unc119(ed3); wgIs222(daf-12:TY1 EGFP FLAG; unc119) outcross : 3 transgene : daf-12 tags : Bombard tag : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The DAF-12::EGFP fusion protein is expressed in the correct daf-12 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the DAF-12 transcription factor. made_by : Mihail Sarov )|Snyder_DAF-12_GFP_L3_rep1 extraction3_seq3 channel_1|L3 Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX065706 OP222(official name : OP222 genotype : unc119(ed3); wgIs222(daf-12:TY1 EGFP FLAG; unc119) outcross : 3 transgene : daf-12 tags : Bombard tag : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The DAF-12::EGFP fusion protein is expressed in the correct daf-12 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the DAF-12 transcription factor. made_by : Mihail Sarov )|Snyder_DAF-12_GFP_L3_rep2 extraction4_seq4 channel_1|L3 Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX065715 OP217(official name : OP217 genotype : unc119(ed3); wgIs217(aly-2:TY1 EGFP FLAG; unc119) outcross : 3 transgene : aly-2 tags : Bombard tag : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The ALY-2::EGFP fusion protein is expressed in the correct aly-2 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the ALY-2 transcription factor. made_by : Mihail Sarov )|Snyder_ALY-2_Input_L3 extraction1_seq1 channel_1|L3 Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX065716 OP217(official name : OP217 genotype : unc119(ed3); wgIs217(aly-2:TY1 EGFP FLAG; unc119) outcross : 3 transgene : aly-2 tags : Bombard tag : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The ALY-2::EGFP fusion protein is expressed in the correct aly-2 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the ALY-2 transcription factor. made_by : Mihail Sarov )|Snyder_ALY-2_Input_L3 extraction2_seq2 channel_1|L3 Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX065717 OP217(official name : OP217 genotype : unc119(ed3); wgIs217(aly-2:TY1 EGFP FLAG; unc119) outcross : 3 transgene : aly-2 tags : Bombard tag : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The ALY-2::EGFP fusion protein is expressed in the correct aly-2 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the ALY-2 transcription factor. made_by : Mihail Sarov )|Snyder_ALY-2_GFP_L3_rep1 extraction3_seq3 channel_1|L3 Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX065718 OP217(official name : OP217 genotype : unc119(ed3); wgIs217(aly-2:TY1 EGFP FLAG; unc119) outcross : 3 transgene : aly-2 tags : Bombard tag : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The ALY-2::EGFP fusion protein is expressed in the correct aly-2 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the ALY-2 transcription factor. made_by : Mihail Sarov )|Snyder_ALY-2_GFP_L3_rep2 extraction4_seq4 channel_1|L3 Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX065723 OP317(official name : OP317 genotype : unc119(ed3); wgIs317(nhr-28::TY1 EGFP FLAG; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The NHR-28::EGFP fusion protein is expressed in the correct nhr-28 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the NHR-28 transcription factor. made_by : R Waterston )|Snyder_NHR-28_Input_L3 extraction1_seq1 channel_1|L3 Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX065724 OP317(official name : OP317 genotype : unc119(ed3); wgIs317(nhr-28::TY1 EGFP FLAG; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The NHR-28::EGFP fusion protein is expressed in the correct nhr-28 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the NHR-28 transcription factor. made_by : R Waterston )|Snyder_NHR-28_Input_L3 extraction2_seq2 channel_1|L3 Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX065725 OP317(official name : OP317 genotype : unc119(ed3); wgIs317(nhr-28::TY1 EGFP FLAG; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The NHR-28::EGFP fusion protein is expressed in the correct nhr-28 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the NHR-28 transcription factor. made_by : R Waterston )|Snyder_NHR-28_GFP_L3_rep1 extraction3_seq3 channel_1|L3 Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX065726 OP317(official name : OP317 genotype : unc119(ed3); wgIs317(nhr-28::TY1 EGFP FLAG; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The NHR-28::EGFP fusion protein is expressed in the correct nhr-28 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the NHR-28 transcription factor. made_by : R Waterston )|Snyder_NHR-28_GFP_L3_rep2 extraction4_seq4 channel_1|L3 Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX118219 OP179(official name : OP179 genotype : unc-119(ed3) III; wgIs179 unc-119(+) gei-11::TY1::EGFP::3xFLAG outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The GEI-11::EGFP fusion protein is expressed in the correct gei-11 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the GEI-11 transcription factor. made_by : R. Waterston )|Snyder_GEI-11_Input_L3_rep1|L3 Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX118220 OP179(official name : OP179 genotype : unc-119(ed3) III; wgIs179 unc-119(+) gei-11::TY1::EGFP::3xFLAG outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The GEI-11::EGFP fusion protein is expressed in the correct gei-11 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the GEI-11 transcription factor. made_by : R. Waterston )|Snyder_GEI-11_Input_L3_rep2|L3 Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX118221 OP179(official name : OP179 genotype : unc-119(ed3) III; wgIs179 unc-119(+) gei-11::TY1::EGFP::3xFLAG outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The GEI-11::EGFP fusion protein is expressed in the correct gei-11 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the GEI-11 transcription factor. made_by : R. Waterston )|Snyder_GEI-11_GFP_L3_rep1|L3 Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX118222 OP179(official name : OP179 genotype : unc-119(ed3) III; wgIs179 unc-119(+) gei-11::TY1::EGFP::3xFLAG outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The GEI-11::EGFP fusion protein is expressed in the correct gei-11 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the GEI-11 transcription factor. made_by : R. Waterston )|Snyder_GEI-11_GFP_L3_rep2|L3 Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX118224 OP174(official name : OP174 genotype : unc-119(ed3); wgIs174(ces-1::TY1 EGFP FLAG; unc-119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The CES-1::EGFP fusion protein is expressed in the correct ces-1 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the CES-1 transcription factor. made_by : S. Kim )|Snyder_CES1_Input_L3_rep1|L3 Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX118225 OP174(official name : OP174 genotype : unc-119(ed3); wgIs174(ces-1::TY1 EGFP FLAG; unc-119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The CES-1::EGFP fusion protein is expressed in the correct ces-1 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the CES-1 transcription factor. made_by : S. Kim )|Snyder_CES1_Input_L3_rep2|L3 Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX118226 OP174(official name : OP174 genotype : unc-119(ed3); wgIs174(ces-1::TY1 EGFP FLAG; unc-119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The CES-1::EGFP fusion protein is expressed in the correct ces-1 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the CES-1 transcription factor. made_by : S. Kim )|Snyder_CES1_GFP_L3_rep1|L3 Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX118227 OP174(official name : OP174 genotype : unc-119(ed3); wgIs174(ces-1::TY1 EGFP FLAG; unc-119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The CES-1::EGFP fusion protein is expressed in the correct ces-1 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the CES-1 transcription factor. made_by : S. Kim )|Snyder_CES1_GFP_L3_rep2|L3 Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX146498 OP81(official name : OP81 genotype : unc-119(ed3) III; wgIs81 unc-119(+) eor-1::TY1::EGFP::3xFLAG outcross : 0 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The EOR-1::EGFP fusion protein is expressed in the correct eor-1 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the EOR-1 transcription factor. made_by : R. Waterston and S. Kim )|Snyder_EOR-1_Input_L3_rep1|L3 Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX146499 OP81(official name : OP81 genotype : unc-119(ed3) III; wgIs81 unc-119(+) eor-1::TY1::EGFP::3xFLAG outcross : 0 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The EOR-1::EGFP fusion protein is expressed in the correct eor-1 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the EOR-1 transcription factor. made_by : R. Waterston and S. Kim )|Snyder_EOR-1_Input_L3_rep2|L3 Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX146500 OP81(official name : OP81 genotype : unc-119(ed3) III; wgIs81 unc-119(+) eor-1::TY1::EGFP::3xFLAG outcross : 0 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The EOR-1::EGFP fusion protein is expressed in the correct eor-1 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the EOR-1 transcription factor. made_by : R. Waterston and S. Kim )|Snyder_EOR-1_GFP_L3_rep1|L3 Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX146501 OP81(official name : OP81 genotype : unc-119(ed3) III; wgIs81 unc-119(+) eor-1::TY1::EGFP::3xFLAG outcross : 0 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The EOR-1::EGFP fusion protein is expressed in the correct eor-1 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the EOR-1 transcription factor. made_by : R. Waterston and S. Kim )|Snyder_EOR-1_GFP_L3_rep2|L3 Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX146506 OP193(official name : OP193 genotype : unc-119(ed3); wgIs193(sea-2::TY1 EGFP FLAG C; unc-119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The SEA-2::EGFP fusion protein is expressed in the correct sea-2 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the SEA-2 transcription factor. made_by : )|Snyder_SEA2_GFP_L3_rep1|L3 Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX146507 OP193(official name : OP193 genotype : unc-119(ed3); wgIs193(sea-2::TY1 EGFP FLAG C; unc-119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The SEA-2::EGFP fusion protein is expressed in the correct sea-2 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the SEA-2 transcription factor. made_by : )|Snyder_SEA2_GFP_L3_rep2|L3 Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX146508 OP193(official name : OP193 genotype : unc-119(ed3); wgIs193(sea-2::TY1 EGFP FLAG C; unc-119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The SEA-2::EGFP fusion protein is expressed in the correct sea-2 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the SEA-2 transcription factor. made_by : )|Snyder_SEA2_Input_L3_rep1|L3 Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX146509 OP193(official name : OP193 genotype : unc-119(ed3); wgIs193(sea-2::TY1 EGFP FLAG C; unc-119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The SEA-2::EGFP fusion protein is expressed in the correct sea-2 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the SEA-2 transcription factor. made_by : )|Snyder_SEA2_Input_L3_rep2|L3 Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX146510 OP167(official name : OP167 genotype : unc119(ed3); wgIs167(daf-12::TY1 EGFP FLAG; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The DAF-12::EGFP fusion protein is expressed in the correct daf-12 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the DAF-12 transcription factor. made_by : S Kim )|Snyder_DAF12_Input_L3_rep1|L3 Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX146511 OP167(official name : OP167 genotype : unc119(ed3); wgIs167(daf-12::TY1 EGFP FLAG; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The DAF-12::EGFP fusion protein is expressed in the correct daf-12 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the DAF-12 transcription factor. made_by : S Kim )|Snyder_DAF12_Input_L3_rep2|L3 Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX146512 OP167(official name : OP167 genotype : unc119(ed3); wgIs167(daf-12::TY1 EGFP FLAG; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The DAF-12::EGFP fusion protein is expressed in the correct daf-12 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the DAF-12 transcription factor. made_by : S Kim )|Snyder_DAF12_GFP_L3_rep1|L3 Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX146513 OP167(official name : OP167 genotype : unc119(ed3); wgIs167(daf-12::TY1 EGFP FLAG; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The DAF-12::EGFP fusion protein is expressed in the correct daf-12 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the DAF-12 transcription factor. made_by : S Kim )|Snyder_DAF12_GFP_L3_rep2|L3 Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX147615 OP304(official name : OP304 genotype : unc119(ed3); wgIs304(fos-1::TY1 EGFP FLAG; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The FOS-1::EGFP fusion protein is expressed in the correct fos-1 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the FOS-1 transcription factor. made_by : R Waterston )|Snyder_FOS-1_Input_L3_rep1|L3 Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX147616 OP304(official name : OP304 genotype : unc119(ed3); wgIs304(fos-1::TY1 EGFP FLAG; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The FOS-1::EGFP fusion protein is expressed in the correct fos-1 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the FOS-1 transcription factor. made_by : R Waterston )|Snyder_FOS-1_Input_L3_rep2|L3 Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX147617 OP304(official name : OP304 genotype : unc119(ed3); wgIs304(fos-1::TY1 EGFP FLAG; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The FOS-1::EGFP fusion protein is expressed in the correct fos-1 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the FOS-1 transcription factor. made_by : R Waterston )|Snyder_FOS-1_GFP_L3_rep1|L3 Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX147618 OP304(official name : OP304 genotype : unc119(ed3); wgIs304(fos-1::TY1 EGFP FLAG; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The FOS-1::EGFP fusion protein is expressed in the correct fos-1 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the FOS-1 transcription factor. made_by : R Waterston )|Snyder_FOS-1_GFP_L3_rep2|L3 Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX147635 OP353(official name : OP353 genotype : unc119(ed3); wgIs353(nhr-77::TY1 EGFP FLAG; unc119) outcross : 3 transgene : nhr-77 tags : Bombard tag : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The NHR-77::EGFP fusion protein is expressed in the correct nhr-77 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the NHR-77 transcription factor. made_by : R Waterston )|Snyder_NHR-77_Input_L3_rep1|L3 Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX147636 OP353(official name : OP353 genotype : unc119(ed3); wgIs353(nhr-77::TY1 EGFP FLAG; unc119) outcross : 3 transgene : nhr-77 tags : Bombard tag : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The NHR-77::EGFP fusion protein is expressed in the correct nhr-77 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the NHR-77 transcription factor. made_by : R Waterston )|Snyder_NHR-77_Input_L3_rep2|L3 Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX147637 OP353(official name : OP353 genotype : unc119(ed3); wgIs353(nhr-77::TY1 EGFP FLAG; unc119) outcross : 3 transgene : nhr-77 tags : Bombard tag : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The NHR-77::EGFP fusion protein is expressed in the correct nhr-77 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the NHR-77 transcription factor. made_by : R Waterston )|Snyder_NHR-77_GFP_L3_rep1|L3 Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX147638 OP353(official name : OP353 genotype : unc119(ed3); wgIs353(nhr-77::TY1 EGFP FLAG; unc119) outcross : 3 transgene : nhr-77 tags : Bombard tag : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The NHR-77::EGFP fusion protein is expressed in the correct nhr-77 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the NHR-77 transcription factor. made_by : R Waterston )|Snyder_NHR-77_GFP_L3_rep2|L3 Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX172525 N2|L3 larvae, wild-type, H4K20me1 ChIP|whole body|L3 larvae Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX188613 OP54(official name : OP54 genotype : unc-119(ed3) III; wgIs54 unc-119(+) egl-5::TY1::EGFP::3xFLAG outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The EOR-1::EGFP fusion protein is expressed in the correct egl-5 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the EOR-1 transcription factor. made_by : R. Waterston and S. Kim )|Snyder_EOR-1_POL-2_L3_rep1|L3 Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX188614 OP54(official name : OP54 genotype : unc-119(ed3) III; wgIs54 unc-119(+) egl-5::TY1::EGFP::3xFLAG outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The EOR-1::EGFP fusion protein is expressed in the correct egl-5 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the EOR-1 transcription factor. made_by : R. Waterston and S. Kim )|Snyder_EOR-1_POL-2_L3_rep2|L3 Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX188615 OP54(official name : OP54 genotype : unc-119(ed3) III; wgIs54 unc-119(+) egl-5::TY1::EGFP::3xFLAG outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The EOR-1::EGFP fusion protein is expressed in the correct egl-5 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the EOR-1 transcription factor. made_by : R. Waterston and S. Kim )|Snyder_EOR-1_Input_L3_rep1|L3 Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX188616 OP54(official name : OP54 genotype : unc-119(ed3) III; wgIs54 unc-119(+) egl-5::TY1::EGFP::3xFLAG outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The EOR-1::EGFP fusion protein is expressed in the correct egl-5 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the EOR-1 transcription factor. made_by : R. Waterston and S. Kim )|Snyder_EOR-1_Input_L3_rep2|L3 Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX188617 OP54(official name : OP54 genotype : unc-119(ed3) III; wgIs54 unc-119(+) egl-5::TY1::EGFP::3xFLAG outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The EGL-5::EGFP fusion protein is expressed in the correct egl-5 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the EGL-5 transcription factor. made_by : R. Waterston and S. Kim )|Snyder_EGL-5_POL-2_L3_rep1|L3 Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX188618 OP54(official name : OP54 genotype : unc-119(ed3) III; wgIs54 unc-119(+) egl-5::TY1::EGFP::3xFLAG outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The EGL-5::EGFP fusion protein is expressed in the correct egl-5 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the EGL-5 transcription factor. made_by : R. Waterston and S. Kim )|Snyder_EGL-5_POL-2_L3_rep2|L3 Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX188619 OP54(official name : OP54 genotype : unc-119(ed3) III; wgIs54 unc-119(+) egl-5::TY1::EGFP::3xFLAG outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The EGL-5::EGFP fusion protein is expressed in the correct egl-5 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the EGL-5 transcription factor. made_by : R. Waterston and S. Kim )|Snyder_EGL-5_Input_L3_rep1|L3 Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX188620 OP54(official name : OP54 genotype : unc-119(ed3) III; wgIs54 unc-119(+) egl-5::TY1::EGFP::3xFLAG outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The EGL-5::EGFP fusion protein is expressed in the correct egl-5 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the EGL-5 transcription factor. made_by : R. Waterston and S. Kim )|Snyder_EGL-5_Input_L3_rep2|L3 Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX233447 OP218(official name : OP218 genotype : unc-119(ed3); wgIs218(R02D3.7:TY1 EGFP FLAG; unc-119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The R02D3.7::EGFP fusion protein is expressed in the correct R02D3.7 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the RO2D3.7 transcription factor. made_by : Mihail Sarov )|Snyder_R02D3.7_GFP_L3_rep1_Input_ACGT|L3 Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX233448 OP218(official name : OP218 genotype : unc-119(ed3); wgIs218(R02D3.7:TY1 EGFP FLAG; unc-119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The R02D3.7::EGFP fusion protein is expressed in the correct R02D3.7 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the RO2D3.7 transcription factor. made_by : Mihail Sarov )|Snyder_R02D3.7_GFP_L3_rep2_Input_TGCT|L3 Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX233449 OP218(official name : OP218 genotype : unc-119(ed3); wgIs218(R02D3.7:TY1 EGFP FLAG; unc-119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The R02D3.7::EGFP fusion protein is expressed in the correct R02D3.7 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the RO2D3.7 transcription factor. made_by : Mihail Sarov )|Snyder_R02D3.7_GFP_L3_rep1_GFP_CATT|L3 Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX233450 OP218(official name : OP218 genotype : unc-119(ed3); wgIs218(R02D3.7:TY1 EGFP FLAG; unc-119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The R02D3.7::EGFP fusion protein is expressed in the correct R02D3.7 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the RO2D3.7 transcription factor. made_by : Mihail Sarov )|Snyder_R02D3.7_GFP_L3_rep2_GFP_ACGT|L3 Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX234914 OP355(official name : OP355 genotype : unc-119(ed3) III; wgIs355(ZK377.2::TY1 EGFP FLAG; unc-119(+)) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Dresden using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The sax-3::EGFP fusion protein is expressed in the correct sax-3 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the sax-3 transcription factor. The sax-3 gene is encoded by the ZK377.2 CDS. made_by : R Waterston )|Snyder_ZK377.2_GFP_L3_rep1_Input_GTAT|L3 Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX234915 OP355(official name : OP355 genotype : unc-119(ed3) III; wgIs355(ZK377.2::TY1 EGFP FLAG; unc-119(+)) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Dresden using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The sax-3::EGFP fusion protein is expressed in the correct sax-3 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the sax-3 transcription factor. The sax-3 gene is encoded by the ZK377.2 CDS. made_by : R Waterston )|Snyder_ZK377.2_GFP_L3_rep2_Input_CATT|L3 Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX234916 OP355(official name : OP355 genotype : unc-119(ed3) III; wgIs355(ZK377.2::TY1 EGFP FLAG; unc-119(+)) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Dresden using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The sax-3::EGFP fusion protein is expressed in the correct sax-3 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the sax-3 transcription factor. The sax-3 gene is encoded by the ZK377.2 CDS. made_by : R Waterston )|Snyder_ZK377.2_GFP_L3_rep1_GFP_ACGT|L3 Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX234917 OP355(official name : OP355 genotype : unc-119(ed3) III; wgIs355(ZK377.2::TY1 EGFP FLAG; unc-119(+)) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Dresden using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The sax-3::EGFP fusion protein is expressed in the correct sax-3 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the sax-3 transcription factor. The sax-3 gene is encoded by the ZK377.2 CDS. made_by : R Waterston )|Snyder_ZK377.2_GFP_L3_rep2_GFP_TGCT|L3 Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX276909 OP236(official name : OP236 genotype : unc119(ed3); wgIs236(elk-2::TY1 EGFP FLAG; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The ZTF-11::EGFP fusion protein is expressed in the correct ztf-11 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the ZTF-11 transcription factor. made_by : Unknown )|ZTF-11 L3 InputRep1|L3 Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX276910 OP236(official name : OP236 genotype : unc119(ed3); wgIs236(elk-2::TY1 EGFP FLAG; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The ZTF-11::EGFP fusion protein is expressed in the correct ztf-11 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the ZTF-11 transcription factor. made_by : Unknown )|ZTF-11 L3 InputRep2|L3 Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX276911 OP236(official name : OP236 genotype : unc119(ed3); wgIs236(elk-2::TY1 EGFP FLAG; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The ZTF-11::EGFP fusion protein is expressed in the correct ztf-11 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the ZTF-11 transcription factor. made_by : Unknown )|ZTF-11 L3 ChIPRep1|L3 Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX276912 OP236(official name : OP236 genotype : unc119(ed3); wgIs236(elk-2::TY1 EGFP FLAG; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The ZTF-11::EGFP fusion protein is expressed in the correct ztf-11 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the ZTF-11 transcription factor. made_by : Unknown )|ZTF-11 L3 ChIPRep2|L3 Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX277024 OP234(official name : OP234 genotype : unc119(ed3); wgIs234(T24H10.7:TY1 EGFP FLAG; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The JUN-1::EGFP fusion protein is expressed in the correct jun-1 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the JUN-1 transcription factor. made_by : Unknown )|JUN-1 L3 InputRep1|L3 Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX277025 OP234(official name : OP234 genotype : unc119(ed3); wgIs234(T24H10.7:TY1 EGFP FLAG; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The JUN-1::EGFP fusion protein is expressed in the correct jun-1 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the JUN-1 transcription factor. made_by : Unknown )|JUN-1 L3 InputRep2|L3 Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX277026 OP234(official name : OP234 genotype : unc119(ed3); wgIs234(T24H10.7:TY1 EGFP FLAG; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The JUN-1::EGFP fusion protein is expressed in the correct jun-1 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the JUN-1 transcription factor. made_by : Unknown )|JUN-1 L3 ChIPRep1|L3 Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX277027 OP234(official name : OP234 genotype : unc119(ed3); wgIs234(T24H10.7:TY1 EGFP FLAG; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The JUN-1::EGFP fusion protein is expressed in the correct jun-1 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the JUN-1 transcription factor. made_by : Unknown )|JUN-1 L3 ChIPRep2|L3 Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX277053 OP318(official name : OP318 genotype : unc-119(ed3); wgIs318(nhr-12::TY1 EGFP FLAG; unc-119(+)) outcross : 3 mutagen : None tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Dresden using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The spatio-temporal expression pattern of NHR-12::EGFP fusion protein was examined through in vivo microscopy. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the NHR-12 transcription factor. made_by : Bob Waterston's lab from UW )|NHR-12 L3 InputRep1|L3 Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX277054 OP318(official name : OP318 genotype : unc-119(ed3); wgIs318(nhr-12::TY1 EGFP FLAG; unc-119(+)) outcross : 3 mutagen : None tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Dresden using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The spatio-temporal expression pattern of NHR-12::EGFP fusion protein was examined through in vivo microscopy. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the NHR-12 transcription factor. made_by : Bob Waterston's lab from UW )|NHR-12 L3 InputRep2|L3 Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX277055 OP318(official name : OP318 genotype : unc-119(ed3); wgIs318(nhr-12::TY1 EGFP FLAG; unc-119(+)) outcross : 3 mutagen : None tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Dresden using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The spatio-temporal expression pattern of NHR-12::EGFP fusion protein was examined through in vivo microscopy. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the NHR-12 transcription factor. made_by : Bob Waterston's lab from UW )|NHR-12 L3 ChIPRep1|L3 Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX277056 OP318(official name : OP318 genotype : unc-119(ed3); wgIs318(nhr-12::TY1 EGFP FLAG; unc-119(+)) outcross : 3 mutagen : None tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Dresden using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The spatio-temporal expression pattern of NHR-12::EGFP fusion protein was examined through in vivo microscopy. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the NHR-12 transcription factor. made_by : Bob Waterston's lab from UW )|NHR-12 L3 ChIPRep2|L3 Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX277069 OP241(official name : OP241 genotype : unc119(ed3); wgIs241(ceh-38::TY1 EGFP FLAG; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The CEH-38::EGFP fusion protein is expressed in the correct ceh-38 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the CEH-38 transcription factor. made_by : Unknwon )|CEH-28 L3 InputRep1|L3 Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX277070 OP241(official name : OP241 genotype : unc119(ed3); wgIs241(ceh-38::TY1 EGFP FLAG; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The CEH-38::EGFP fusion protein is expressed in the correct ceh-38 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the CEH-38 transcription factor. made_by : Unknwon )|CEH-28 L3 InputRep2|L3 Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX277071 OP241(official name : OP241 genotype : unc119(ed3); wgIs241(ceh-38::TY1 EGFP FLAG; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The CEH-38::EGFP fusion protein is expressed in the correct ceh-38 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the CEH-38 transcription factor. made_by : Unknwon )|CEH-28 L3 ChIPRep1|L3 Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX277072 OP241(official name : OP241 genotype : unc119(ed3); wgIs241(ceh-38::TY1 EGFP FLAG; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The CEH-38::EGFP fusion protein is expressed in the correct ceh-38 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the CEH-38 transcription factor. made_by : Unknwon )|CEH-28 L3 ChIPRep2|L3 Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331045 OP185(official name : OP185 genotype : unc-119(ed3); wgIs185(fkh-2::TY1 EGFP FLAG C; unc-119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The FKH-1::EGFP fusion protein is expressed in the correct fkh-2 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the FKH-2 transcription factor. made_by : R Waterston )|FKH-2_GFP_L3_Input_Rep1|L3 Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331046 OP185(official name : OP185 genotype : unc-119(ed3); wgIs185(fkh-2::TY1 EGFP FLAG C; unc-119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The FKH-1::EGFP fusion protein is expressed in the correct fkh-2 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the FKH-2 transcription factor. made_by : R Waterston )|FKH-2_GFP_L3_ChIP_Rep1|L3 Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331047 OP185(official name : OP185 genotype : unc-119(ed3); wgIs185(fkh-2::TY1 EGFP FLAG C; unc-119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The FKH-1::EGFP fusion protein is expressed in the correct fkh-2 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the FKH-2 transcription factor. made_by : R Waterston )|FKH-2_GFP_L3_Input_Rep2|L3 Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331048 OP185(official name : OP185 genotype : unc-119(ed3); wgIs185(fkh-2::TY1 EGFP FLAG C; unc-119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The FKH-1::EGFP fusion protein is expressed in the correct fkh-2 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the FKH-2 transcription factor. made_by : R Waterston )|FKH-2_GFP_L3_ChIP_Rep2|L3 Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331049 OP198(official name : OP198 genotype : unc-119(ed3); wgIs198(mml-1::TY1 EGFP FLAG C; unc-119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The MML-1::EGFP fusion protein is expressed in the correct mml-1 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the MML-1 transcription factor. made_by : R Waterston )|MML-1_GFP_L3_Input_Rep1|L3 Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331050 OP198(official name : OP198 genotype : unc-119(ed3); wgIs198(mml-1::TY1 EGFP FLAG C; unc-119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The MML-1::EGFP fusion protein is expressed in the correct mml-1 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the MML-1 transcription factor. made_by : R Waterston )|MML-1_GFP_L3_ChIP_Rep1|L3 Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331051 OP198(official name : OP198 genotype : unc-119(ed3); wgIs198(mml-1::TY1 EGFP FLAG C; unc-119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The MML-1::EGFP fusion protein is expressed in the correct mml-1 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the MML-1 transcription factor. made_by : R Waterston )|MML-1_GFP_L3_Input_Rep2|L3 Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331052 OP198(official name : OP198 genotype : unc-119(ed3); wgIs198(mml-1::TY1 EGFP FLAG C; unc-119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The MML-1::EGFP fusion protein is expressed in the correct mml-1 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the MML-1 transcription factor. made_by : R Waterston )|MML-1_GFP_L3_ChIP_Rep2|L3 Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331053 OP203(official name : OP203 genotype : unc-119(ed3); wgIs203(nhr-76::TY1 EGFP FLAG; unc-119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The NHR-76::EGFP fusion protein is expressed in the correct nhr-76 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the NHR-76 transcription factor. made_by : R. Waterston )|NHR-76_GFP_L3_Input_Rep1|L3 Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331054 OP203(official name : OP203 genotype : unc-119(ed3); wgIs203(nhr-76::TY1 EGFP FLAG; unc-119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The NHR-76::EGFP fusion protein is expressed in the correct nhr-76 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the NHR-76 transcription factor. made_by : R. Waterston )|NHR-76_GFP_L3_ChIP_Rep1|L3 Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331055 OP203(official name : OP203 genotype : unc-119(ed3); wgIs203(nhr-76::TY1 EGFP FLAG; unc-119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The NHR-76::EGFP fusion protein is expressed in the correct nhr-76 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the NHR-76 transcription factor. made_by : R. Waterston )|NHR-76_GFP_L3_Input_Rep2|L3 Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331056 OP203(official name : OP203 genotype : unc-119(ed3); wgIs203(nhr-76::TY1 EGFP FLAG; unc-119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The NHR-76::EGFP fusion protein is expressed in the correct nhr-76 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the NHR-76 transcription factor. made_by : R. Waterston )|NHR-76_GFP_L3_ChIP_Rep2|L3 Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331131 OP43(official name : OP43 genotype : unc-119(ed3); wgIs43(nhr-23::TY1 EGFP FLAG; unc-119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology and Genetics in Dresden using Tony Hyman's recombineering pipeline. The resulting plasmid was used for bombardment transformation of an unc-119(ed3) strain. The NHR-23::EGFP fusion protein is expressed in the correct nhr-23 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the NHR-223 transcription factor. made_by : Bob Waterston's lab from UW )|NHR-23_GFP_L3_Input_Rep1|L3 Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331132 OP43(official name : OP43 genotype : unc-119(ed3); wgIs43(nhr-23::TY1 EGFP FLAG; unc-119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology and Genetics in Dresden using Tony Hyman's recombineering pipeline. The resulting plasmid was used for bombardment transformation of an unc-119(ed3) strain. The NHR-23::EGFP fusion protein is expressed in the correct nhr-23 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the NHR-223 transcription factor. made_by : Bob Waterston's lab from UW )|NHR-23_GFP_L3_ChIP_Rep1|L3 Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331133 OP43(official name : OP43 genotype : unc-119(ed3); wgIs43(nhr-23::TY1 EGFP FLAG; unc-119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology and Genetics in Dresden using Tony Hyman's recombineering pipeline. The resulting plasmid was used for bombardment transformation of an unc-119(ed3) strain. The NHR-23::EGFP fusion protein is expressed in the correct nhr-23 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the NHR-223 transcription factor. made_by : Bob Waterston's lab from UW )|NHR-23_GFP_L3_Input_Rep2|L3 Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331134 OP43(official name : OP43 genotype : unc-119(ed3); wgIs43(nhr-23::TY1 EGFP FLAG; unc-119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology and Genetics in Dresden using Tony Hyman's recombineering pipeline. The resulting plasmid was used for bombardment transformation of an unc-119(ed3) strain. The NHR-23::EGFP fusion protein is expressed in the correct nhr-23 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the NHR-223 transcription factor. made_by : Bob Waterston's lab from UW )|NHR-23_GFP_L3_ChIP_Rep2|L3 Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331135 OP342(official name : OP342 genotype : unc119(ed3); wgIs341(skn-1::TY1 EGFP FLAG; unc119) outcross : 0 mutagen : None tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for bombardment transformation of an unc-119(ed3) strain. made_by : Bob Waterston's lab from UW )|SKN-1_GFP_L3_Input_Rep1|L3 Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331136 OP342(official name : OP342 genotype : unc119(ed3); wgIs341(skn-1::TY1 EGFP FLAG; unc119) outcross : 0 mutagen : None tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for bombardment transformation of an unc-119(ed3) strain. made_by : Bob Waterston's lab from UW )|SKN-1_GFP_L3_ChIP_Rep1|L3 Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331137 OP342(official name : OP342 genotype : unc119(ed3); wgIs341(skn-1::TY1 EGFP FLAG; unc119) outcross : 0 mutagen : None tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for bombardment transformation of an unc-119(ed3) strain. made_by : Bob Waterston's lab from UW )|SKN-1_GFP_L3_Input_Rep2|L3 Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331138 OP342(official name : OP342 genotype : unc119(ed3); wgIs341(skn-1::TY1 EGFP FLAG; unc119) outcross : 0 mutagen : None tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for bombardment transformation of an unc-119(ed3) strain. made_by : Bob Waterston's lab from UW )|SKN-1_GFP_L3_ChIP_Rep2|L3 Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331157 OP354(official name : OP354 genotype : unc119(ed3); wgIs354(elt-1::TY1 EGFP FLAG; unc119) outcross : 0 mutagen : None tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for bombardment transformation of an unc-119(ed3) strain. made_by : Bob Waterston's lab from UW )|ELT-1_GFP_L3_Input_Rep1|L3 Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331158 OP354(official name : OP354 genotype : unc119(ed3); wgIs354(elt-1::TY1 EGFP FLAG; unc119) outcross : 0 mutagen : None tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for bombardment transformation of an unc-119(ed3) strain. made_by : Bob Waterston's lab from UW )|ELT-1_GFP_L3_ChIP_Rep1|L3 Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331159 OP354(official name : OP354 genotype : unc119(ed3); wgIs354(elt-1::TY1 EGFP FLAG; unc119) outcross : 0 mutagen : None tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for bombardment transformation of an unc-119(ed3) strain. made_by : Bob Waterston's lab from UW )|ELT-1_GFP_L3_Input_Rep2|L3 Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331160 OP354(official name : OP354 genotype : unc119(ed3); wgIs354(elt-1::TY1 EGFP FLAG; unc119) outcross : 0 mutagen : None tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for bombardment transformation of an unc-119(ed3) strain. made_by : Bob Waterston's lab from UW )|ELT-1_GFP_L3_ChIP_Rep2|L3 Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331177 OP228(official name : OP228 genotype : unc119(ed3); wgIs228(nhr-237:TY1 EGFP FLAG; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The NHR-237::EGFP fusion protein is expressed in the correct nhr-237 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the NHR-237 transcription factor. made_by : Unknown )|nhr-237_GFP_L3_Input_Rep1|L3 Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331178 OP228(official name : OP228 genotype : unc119(ed3); wgIs228(nhr-237:TY1 EGFP FLAG; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The NHR-237::EGFP fusion protein is expressed in the correct nhr-237 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the NHR-237 transcription factor. made_by : Unknown )|nhr-237_GFP_L3_ChIP_Rep1|L3 Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331179 OP228(official name : OP228 genotype : unc119(ed3); wgIs228(nhr-237:TY1 EGFP FLAG; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The NHR-237::EGFP fusion protein is expressed in the correct nhr-237 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the NHR-237 transcription factor. made_by : Unknown )|nhr-237_GFP_L3_Input_Rep2|L3 Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331180 OP228(official name : OP228 genotype : unc119(ed3); wgIs228(nhr-237:TY1 EGFP FLAG; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The NHR-237::EGFP fusion protein is expressed in the correct nhr-237 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the NHR-237 transcription factor. made_by : Unknown )|nhr-237_GFP_L3_ChIP_Rep2|L3 Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331201 OP305(official name : OP305 genotype : unc119(ed3); wgIs305(nhr-11::TY1 EGFP FLAG; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The NHR-11::EGFP fusion protein is expressed in the correct nhr-11 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the NHR-11 transcription factor. made_by : R Waterston )|NHR-11_GFP_L3_Input_Rep1|L3 Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331202 OP305(official name : OP305 genotype : unc119(ed3); wgIs305(nhr-11::TY1 EGFP FLAG; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The NHR-11::EGFP fusion protein is expressed in the correct nhr-11 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the NHR-11 transcription factor. made_by : R Waterston )|NHR-11_GFP_L3_ChIP_Rep1|L3 Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331203 OP305(official name : OP305 genotype : unc119(ed3); wgIs305(nhr-11::TY1 EGFP FLAG; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The NHR-11::EGFP fusion protein is expressed in the correct nhr-11 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the NHR-11 transcription factor. made_by : R Waterston )|NHR-11_GFP_L3_Input_Rep2|L3 Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331204 OP305(official name : OP305 genotype : unc119(ed3); wgIs305(nhr-11::TY1 EGFP FLAG; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The NHR-11::EGFP fusion protein is expressed in the correct nhr-11 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the NHR-11 transcription factor. made_by : R Waterston )|NHR-11_GFP_L3_ChIP_Rep2|L3 Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331253 OP373(official name : OP373 genotype : unc119(ed3); wgIs373(nhr-67::TY1 EGFP FLAG; unc119 outcross : 0 mutagen : None tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Dresden using Tony Hyman's recombineering pipeline. The resulting plasmid was used for bombardment transformation of an unc-119(ed3) strain. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the NHR-67 transcription factor. made_by : Bob Waterston's lab from UW )|NHR-67_GFP_L3_Input_Rep1|L3 Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331254 OP373(official name : OP373 genotype : unc119(ed3); wgIs373(nhr-67::TY1 EGFP FLAG; unc119 outcross : 0 mutagen : None tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Dresden using Tony Hyman's recombineering pipeline. The resulting plasmid was used for bombardment transformation of an unc-119(ed3) strain. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the NHR-67 transcription factor. made_by : Bob Waterston's lab from UW )|NHR-67_GFP_L3_ChIP_Rep1|L3 Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331255 OP373(official name : OP373 genotype : unc119(ed3); wgIs373(nhr-67::TY1 EGFP FLAG; unc119 outcross : 0 mutagen : None tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Dresden using Tony Hyman's recombineering pipeline. The resulting plasmid was used for bombardment transformation of an unc-119(ed3) strain. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the NHR-67 transcription factor. made_by : Bob Waterston's lab from UW )|NHR-67_GFP_L3_Input_Rep2|L3 Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331256 OP373(official name : OP373 genotype : unc119(ed3); wgIs373(nhr-67::TY1 EGFP FLAG; unc119 outcross : 0 mutagen : None tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Dresden using Tony Hyman's recombineering pipeline. The resulting plasmid was used for bombardment transformation of an unc-119(ed3) strain. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the NHR-67 transcription factor. made_by : Bob Waterston's lab from UW )|NHR-67_GFP_L3_ChIP_Rep2|L3 Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331321 OP404(official name : OP404 genotype : unc-119(ed3) III; wgIs404(nfya-1::TY1-GFP-3xFLA; unc-119(+)) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology and Genetics in Dresden description : using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The NFYA-1::EGFP fusion protein is expressed in the correct nfya-1 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the NFYA-1 transcription factor. made_by : Unknown )|NFYA-1_GFP_L3_Input_Rep1|L3 Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331322 OP404(official name : OP404 genotype : unc-119(ed3) III; wgIs404(nfya-1::TY1-GFP-3xFLA; unc-119(+)) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology and Genetics in Dresden description : using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The NFYA-1::EGFP fusion protein is expressed in the correct nfya-1 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the NFYA-1 transcription factor. made_by : Unknown )|NFYA-1_GFP_L3_ChIP_Rep1|L3 Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331323 OP404(official name : OP404 genotype : unc-119(ed3) III; wgIs404(nfya-1::TY1-GFP-3xFLA; unc-119(+)) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology and Genetics in Dresden description : using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The NFYA-1::EGFP fusion protein is expressed in the correct nfya-1 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the NFYA-1 transcription factor. made_by : Unknown )|NFYA-1_GFP_L3_Input_Rep2|L3 Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331324 OP404(official name : OP404 genotype : unc-119(ed3) III; wgIs404(nfya-1::TY1-GFP-3xFLA; unc-119(+)) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology and Genetics in Dresden description : using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The NFYA-1::EGFP fusion protein is expressed in the correct nfya-1 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the NFYA-1 transcription factor. made_by : Unknown )|NFYA-1_GFP_L3_ChIP_Rep2|L3 Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331341 N2|seq-SDQ3520_LIN61_N2_L3_Input_Rep1|L3 Larva Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331342 N2|seq-SDQ3520_LIN61_N2_L3_Input_Rep2|L3 Larva Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331343 N2|seq-SDQ3520_LIN61_N2_L3_ChIP_Rep1|L3 Larva Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331344 N2|seq-SDQ3520_LIN61_N2_L3_ChIP_Rep2|L3 Larva Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331345 N2|seq-ab12181_H3K9acS10_873968_N2_L3_Input_Rep1|L3 Larva Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331346 N2|seq-ab12181_H3K9acS10_873968_N2_L3_Input_Rep2|L3 Larva Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331347 N2|seq-ab12181_H3K9acS10_873968_N2_L3_ChIP_Rep1|L3 Larva Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331348 N2|seq-ab12181_H3K9acS10_873968_N2_L3_ChIP_Rep2|L3 Larva Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX463080 N2|seq-JA00001_HTZ1_N2_L3_Input_Rep1|L3 Larva Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX463081 N2|seq-JA00001_HTZ1_N2_L3_Input_Rep2|L3 Larva Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX463082 N2|seq-JA00001_HTZ1_N2_L3_ChIP_Rep1|L3 Larva Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX463083 N2|seq-JA00001_HTZ1_N2_L3_ChIP_Rep2|L3 Larva Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX466455 N2|seq-AB2621_H3K79me3:361576_N2_L3_Input_Rep1|L3 Larva Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX466456 N2|seq-AB2621_H3K79me3:361576_N2_L3_Input_Rep2|L3 Larva Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX466457 N2|seq-AB2621_H3K79me3:361576_N2_L3_ChIP_Rep1|L3 Larva Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX466458 N2|seq-AB2621_H3K79me3:361576_N2_L3_ChIP_Rep2|L3 Larva Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX466459 N2|seq-AB8898_H3K9me3:33990_N2_L3_Input_Rep1|L3 Larva Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX466460 N2|seq-AB8898_H3K9me3:33990_N2_L3_Input_Rep2|L3 Larva Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX466461 N2|seq-AB8898_H3K9me3:33990_N2_L3_ChIP_Rep1|L3 Larva Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX466462 N2|seq-AB8898_H3K9me3:33990_N2_L3_ChIP_Rep2|L3 Larva Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX466463 N2|seq-HK00009_H3K9me3:2F3_N2_L3_Input_Rep1|L3 Larva Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX466464 N2|seq-HK00009_H3K9me3:2F3_N2_L3_Input_Rep2|L3 Larva Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX466465 N2|seq-HK00009_H3K9me3:2F3_N2_L3_ChIP_Rep1|L3 Larva Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX466466 N2|seq-HK00009_H3K9me3:2F3_N2_L3_ChIP_Rep2|L3 Larva Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX466467 N2|seq-HK00012_H3K36me2:2C3_N2_L3_Input_Rep1|L3 Larva Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX466468 N2|seq-HK00012_H3K36me2:2C3_N2_L3_Input_Rep2|L3 Larva Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX466469 N2|seq-HK00012_H3K36me2:2C3_N2_L3_ChIP_Rep1|L3 Larva Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX466470 N2|seq-HK00012_H3K36me2:2C3_N2_L3_ChIP_Rep2|L3 Larva Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX466471 N2|seq-NB211254_H3K36ac_N2_L3_Input_Rep1|L3 Larva Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX466472 N2|seq-NB211254_H3K36ac_N2_L3_Input_Rep2|L3 Larva Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX466473 N2|seq-NB211254_H3K36ac_N2_L3_ChIP_Rep1|L3 Larva Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX466474 N2|seq-NB211254_H3K36ac_N2_L3_ChIP_Rep2|L3 Larva Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX466475 N2|seq-UP07448_H3K27me1:24439_N2_L3_Input_Rep1|L3 Larva Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX466476 N2|seq-UP07448_H3K27me1:24439_N2_L3_Input_Rep2|L3 Larva Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX466477 N2|seq-UP07448_H3K27me1:24439_N2_L3_ChIP_Rep1|L3 Larva Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX466478 N2|seq-UP07448_H3K27me1:24439_N2_L3_ChIP_Rep2|L3 Larva Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX466479 N2|seq-UP07449_H3K27me3:24440_N2_L3_Input_Rep1|L3 Larva Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX466480 N2|seq-UP07449_H3K27me3:24440_N2_L3_Input_Rep2|L3 Larva Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX466481 N2|seq-UP07449_H3K27me3:24440_N2_L3_ChIP_Rep1|L3 Larva Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX466482 N2|seq-UP07449_H3K27me3:24440_N2_L3_ChIP_Rep2|L3 Larva Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX466483 N2|seq-AB1191_H3K18ac_GR311521_N2_L3_Input_Rep1|L3 Larva Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX466484 N2|seq-AB1191_H3K18ac_GR311521_N2_L3_Input_Rep2|L3 Larva Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX466485 N2|seq-AB1191_H3K18ac_GR311521_N2_L3_ChIP_Rep1|L3 Larva Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX466486 N2|seq-AB1191_H3K18ac_GR311521_N2_L3_ChIP_Rep2|L3 Larva Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX466487 N2|seq-AB3594_H3K79me2:346021_N2_L3_Input_Rep1|L3 Larva Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX466488 N2|seq-AB3594_H3K79me2:346021_N2_L3_Input_Rep2|L3 Larva Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX466489 N2|seq-AB3594_H3K79me2:346021_N2_L3_ChIP_Rep1|L3 Larva Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX466490 N2|seq-AB3594_H3K79me2:346021_N2_L3_ChIP_Rep2|L3 Larva Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX466491 N2|seq-ab9048_H3K36me1:206009_N2_L3_Input_Rep1|L3 Larva Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX466492 N2|seq-ab9048_H3K36me1:206009_N2_L3_Input_Rep2|L3 Larva Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX466493 N2|seq-ab9048_H3K36me1:206009_N2_L3_ChIP_Rep1|L3 Larva Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX466494 N2|seq-ab9048_H3K36me1:206009_N2_L3_ChIP_Rep2|L3 Larva Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX466495 N2|seq-HK00008_H3K9me2:6D11_N2_L3_Input_Rep1|L3 Larva Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX466496 N2|seq-HK00008_H3K9me2:6D11_N2_L3_Input_Rep2|L3 Larva Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX466497 N2|seq-HK00008_H3K9me2:6D11_N2_L3_ChIP_Rep1|L3 Larva Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX466498 N2|seq-HK00008_H3K9me2:6D11_N2_L3_ChIP_Rep2|L3 Larva Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX466577 N2|seq-SDQ2340_HPL2_N2_L3_Input_Rep1|L3 Larva Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX466578 N2|seq-SDQ2340_HPL2_N2_L3_Input_Rep2|L3 Larva Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX466579 N2|seq-SDQ2340_HPL2_N2_L3_ChIP_Rep1|L3 Larva Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX466580 N2|seq-SDQ2340_HPL2_N2_L3_ChIP_Rep2|L3 Larva Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX494819 N2|seq-SDQ2370_LIN53_N2_L3_Input_Rep1|L3 Larva Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX494820 N2|seq-SDQ2370_LIN53_N2_L3_Input_Rep2|L3 Larva Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX494821 N2|seq-SDQ2370_LIN53_N2_L3_ChIP_Rep1|L3 Larva Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX494822 N2|seq-SDQ2370_LIN53_N2_L3_ChIP_Rep2|L3 Larva Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX494836 N2|seq-SN147_H4K20me1_N2_L3_Input_Rep1|L3 Larva Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX494837 N2|seq-SN147_H4K20me1_N2_L3_Input_Rep2|L3 Larva Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX494838 N2|seq-SN147_H4K20me1_N2_L3_ChIP_Rep1|L3 Larva Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX494839 N2|seq-SN147_H4K20me1_N2_L3_ChIP_Rep2|L3 Larva Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX494947 N2|seq-SDQ2354_HDA1_N2_L3_Input_Rep1|L3 Larva Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX494948 N2|seq-SDQ2354_HDA1_N2_L3_Input_Rep2|L3 Larva Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX494949 N2|seq-SDQ2354_HDA1_N2_L3_ChIP_Rep1|L3 Larva Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX494950 N2|seq-SDQ2354_HDA1_N2_L3_ChIP_Rep2|L3 Larva Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX494951 N2|seq-SDQ3861_LET418_N2_L3_Input_Rep1|L3 Larva Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX494952 N2|seq-SDQ3861_LET418_N2_L3_ChIP_Rep1|L3 Larva Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX494954 N2|seq-SDQ2342_LET418_N2_L3_Input_Rep1|L3 Larva Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX494955 N2|seq-SDQ2342_LET418_N2_L3_Input_Rep2|L3 Larva Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX494956 N2|seq-SDQ2342_LET418_N2_L3_ChIP_Rep1|L3 Larva Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX494957 N2|seq-SDQ2342_LET418_N2_L3_ChIP_Rep2|L3 Larva Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX494958 N2|seq-HM4077_LIN61_N2_L3_Input_Rep1|L3 Larva Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX494959 N2|seq-HM4077_LIN61_N2_L3_Input_Rep2|L3 Larva Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX494960 N2|seq-HM4077_LIN61_N2_L3_ChIP_Rep1|L3 Larva Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX494961 N2|seq-HM4077_LIN61_N2_L3_ChIP_Rep2|L3 Larva Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX494962 N2|seq-SDQ2940_NURF1_N2_L3_Input_Rep1|L3 Larva Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX494963 N2|seq-SDQ2940_NURF1_N2_L3_Input_Rep2|L3 Larva Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX494964 N2|seq-SDQ2940_NURF1_N2_L3_ChIP_Rep1|L3 Larva Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX494965 N2|seq-SDQ2940_NURF1_N2_L3_ChIP_Rep2|L3 Larva Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX494966 N2|seq-SDQ3525_NURF1_N2_L3_Input_Rep1|L3 Larva Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX494967 N2|seq-SDQ3525_NURF1_N2_L3_Input_Rep2|L3 Larva Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX494968 N2|seq-SDQ3525_NURF1_N2_L3_ChIP_Rep1|L3 Larva Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX494969 N2|seq-SDQ3525_NURF1_N2_L3_ChIP_Rep2|L3 Larva Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX494970 N2|seq-SDQ3528_NURF1_N2_L3_Input_Rep1|L3 Larva Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX494971 N2|seq-SDQ3528_NURF1_N2_L3_Input_Rep2|L3 Larva Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX494972 N2|seq-SDQ3528_NURF1_N2_L3_ChIP_Rep1|L3 Larva Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX494973 N2|seq-SDQ3528_NURF1_N2_L3_ChIP_Rep2|L3 Larva Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX494974 N2|seq-ab15823_H4K8ac_487128_N2_L3_Input_Rep1|L3 Larva Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX494975 N2|seq-ab15823_H4K8ac_487128_N2_L3_Input_Rep2|L3 Larva Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX494976 N2|seq-ab15823_H4K8ac_487128_N2_L3_ChIP_Rep1|L3 Larva Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX494977 N2|seq-ab15823_H4K8ac_487128_N2_L3_ChIP_Rep2|L3 Larva Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX494986 N2|seq-JL00006_ZFP1_N2_L3_Input_Rep1|L3 Larva Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX494987 N2|seq-JL00006_ZFP1_N2_L3_Input_Rep2|L3 Larva Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX494988 N2|seq-JL00006_ZFP1_N2_L3_ChIP_Rep1|L3 Larva Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX494989 N2|seq-JL00006_ZFP1_N2_L3_ChIP_Rep2|L3 Larva Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX495097 N2|seq-SDQ4663_RPC1_N2_L3_Input_Rep1|L3 Larva Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX495098 N2|seq-SDQ4663_RPC1_N2_L3_Input_Rep2|L3 Larva Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX495099 N2|seq-SDQ4663_RPC1_N2_L3_ChIP_Rep1|L3 Larva Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX495100 N2|seq-SDQ4663_RPC1_N2_L3_ChIP_Rep2|L3 Larva Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX529206 N2|seq-AR0144_H3_144_N2_L3_Input_Rep1|L3 Larva Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX529207 N2|seq-AR0144_H3_144_N2_L3_Input_Rep2|L3 Larva Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX529208 N2|seq-AR0144_H3_144_N2_L3_ChIP_Rep1|L3 Larva Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX529209 N2|seq-AR0144_H3_144_N2_L3_ChIP_Rep2|L3 Larva Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX529210 N2|seq-WA30932379_H3K9ac_N2_L3_Input_Rep1|L3 Larva Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX529211 N2|seq-WA30932379_H3K9ac_N2_L3_Input_Rep2|L3 Larva Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX529212 N2|seq-WA30932379_H3K9ac_N2_L3_ChIP_Rep1|L3 Larva Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX529213 N2|seq-WA30932379_H3K9ac_N2_L3_ChIP_Rep2|L3 Larva Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX529222 N2|seq-ab8896_H3K9me1_104560_N2_L3_Input_Rep1|L3 Larva Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX529223 N2|seq-ab8896_H3K9me1_104560_N2_L3_Input_Rep2|L3 Larva Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX529224 N2|seq-ab8896_H3K9me1_104560_N2_L3_ChIP_Rep1|L3 Larva Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX529225 N2|seq-ab8896_H3K9me1_104560_N2_L3_ChIP_Rep2|L3 Larva Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX529226 N2|seq-ab8895_H3K4me1:733246_N2_L3_Input_Rep1|L3 Larva Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX529227 N2|seq-ab8895_H3K4me1:733246_N2_L3_Input_Rep2|L3 Larva Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX529228 N2|seq-ab8895_H3K4me1:733246_N2_L3_ChIP_Rep1|L3 Larva Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX529229 N2|seq-ab8895_H3K4me1:733246_N2_L3_ChIP_Rep2|L3 Larva Lar@ L3?0 1 2 https://www.ncbi.nlm.nih.gov/sra?term=SRX1132913 N2|L3 staged worms_IgG_ChIP-seq|L3 staged worms Lar@ L3?0 1 2 https://www.ncbi.nlm.nih.gov/sra?term=SRX1132915 N2|L3 staged worms_H3K4me3_ChIP-seq|L3 staged worms Lar@ L3?0 1 2 https://www.ncbi.nlm.nih.gov/sra?term=SRX172526 L3 larvae, set-4 mutant, H4K20me1 ChIP|whole body|L3 larvae Lar@ L3?0 1 2 https://www.ncbi.nlm.nih.gov/sra?term=SRX323676 N2|tra-1(e1834) heterozygote L3 stage Lar@ L3?0 1 2 https://www.ncbi.nlm.nih.gov/sra?term=SRX323690 N2|tra-1(e1834) homozygote L3 stage Lar@ L3?0 1 2 https://www.ncbi.nlm.nih.gov/sra?term=SRX514567 L3 larvae, H4K16ac ChIP|whole body|L3 Lar@ L3?0 1 2 https://www.ncbi.nlm.nih.gov/sra?term=SRX514569 L3 larvae, input|whole body|L3 Lar@ L3?0 1 2 https://www.ncbi.nlm.nih.gov/sra?term=SRX7635313 egl43-gfp|L3|larvae|L3 Lar@ L3?0 1 3 https://www.ncbi.nlm.nih.gov/sra?term=SRX1132912 N2|L3 staged worms_ELT2_ChIP-seq|L3 staged worms Lar@ L3?0 1 3 https://www.ncbi.nlm.nih.gov/sra?term=SRX1132914 N2|L3 staged worms_input|L3 staged worms Lar@ L3?0 1 3 https://www.ncbi.nlm.nih.gov/sra?term=SRX323680 N2|N2 strain, L3 stage Lar@ L3?0 1 4 https://www.ncbi.nlm.nih.gov/sra?term=SRX005637 OP26|L3 Lar@ L3?0 1 4 https://www.ncbi.nlm.nih.gov/sra?term=SRX015096 OP81|OP81, EOR-1:GFP:3xFLAG animals|L3 Lar@ L3?0 1 4 https://www.ncbi.nlm.nih.gov/sra?term=SRX015100 OP74|OP74, HLH-8:GFP:3xFLAG animals|L3 Lar@ L3?0 1 4 https://www.ncbi.nlm.nih.gov/sra?term=SRX747295 N2|L3 larvae|whole larvae|L3 Lar@ L3?0 1 4 https://www.ncbi.nlm.nih.gov/sra?term=SRX982080 CB428|whole worms|L3 Lar@ L3?0 1 5 https://www.ncbi.nlm.nih.gov/sra?term=SRX105309 N2|whole body|L3 Lar@ L3?0 1 6 https://www.ncbi.nlm.nih.gov/sra?term=SRX063957 N2|L3 embyros|L3 Lar@ L3?0 1 6 https://www.ncbi.nlm.nih.gov/sra?term=SRX1936233 N2|L3 worms|L3 Lar@ L3?0 1 6 https://www.ncbi.nlm.nih.gov/sra?term=SRX1936239 TY1072|L3 worms|L3 Lar@ L3?0 1 7 https://www.ncbi.nlm.nih.gov/sra?term=SRX747299 JA1507|L3 larvae|whole larvae|L3 Lar@ L3?0 1 8 https://www.ncbi.nlm.nih.gov/sra?term=SRX4082340 N2|L3 larvae Lar@ L3?0 1 8 https://www.ncbi.nlm.nih.gov/sra?term=SRX4194184 N2 (Bristol)|L3 larvae Lar@ L3?0 1 8 https://www.ncbi.nlm.nih.gov/sra?term=SRX4194186 WM193 (csr-1, partial lof)|L3 larvae Lar@ L3?0 1 8 https://www.ncbi.nlm.nih.gov/sra?term=SRX4194190 drh-3(ne4253)|L3 larvae Lar@ L3?0 1 8 https://www.ncbi.nlm.nih.gov/sra?term=SRX982082 MT14911|whole worms|L3 Lar@ L3?0 1 9 https://www.ncbi.nlm.nih.gov/sra?term=SRX5020790 15eh1|whole worms|L3 Lar@ L3?0 2 19 https://www.ncbi.nlm.nih.gov/sra?term=SRX4085392 wild-type N2|L3 larvae Lar@ L3?0 22 48 https://www.ncbi.nlm.nih.gov/sra?term=SRX094514 N2|whole body|whole body|L3 Lar@ L3?0 4 22 https://www.ncbi.nlm.nih.gov/sra?term=SRX982065 N2|whole worms|L3 Lar@ L3?0 5 8 https://www.ncbi.nlm.nih.gov/sra?term=SRX094474 N2|Control sample from L3 stage N2 worms, whole body|whole body|L3 Lar@ L3?0 1 11 https://www.ncbi.nlm.nih.gov/sra?term=SRX3862408 Whole worm|L4 Lar@ L4?0 1 12 https://www.ncbi.nlm.nih.gov/sra?term=SRX1078705 pJK1728|Whole animal|L4 larva Lar@ L4?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX043967 N2(genotype : wild type genotype : DR subclone of DB original (Tc1 pattern I) official name : N2 )|Snyder_N2_POLII_L4_rep1 extraction1_seq1 channel_1|L4 Lar@ L4?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX043968 N2(genotype : wild type genotype : DR subclone of DB original (Tc1 pattern I) official name : N2 )|Snyder_N2_POLII_L4_rep1 extraction1_seq1 channel_2|L4 Lar@ L4?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX043969 N2(genotype : wild type genotype : DR subclone of DB original (Tc1 pattern I) official name : N2 )|Snyder_N2_POLII_L4_rep2 extraction2_seq1 channel_1|L4 Lar@ L4?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX043970 N2(genotype : wild type genotype : DR subclone of DB original (Tc1 pattern I) official name : N2 )|Snyder_N2_POLII_L4_rep2 extraction2_seq1 channel_2|L4 Lar@ L4?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX043971 OP179(made_by : R. Waterston description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The GEI-11::EGFP fusion protein is expressed in the correct gei-11 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the GEI-11 transcription factor. tags : GFP::3xFlag mutagen : Bombard outcross : 3 genotype : unc-119(ed3) III; wgIs179 unc-119(+) gei-11::TY1::EGFP::3xFLAG official name : OP179 )|Snyder_GEI11_GFP_L4_rep1 extraction1_seq1 channel_1|L4 Lar@ L4?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX043972 OP179(made_by : R. Waterston description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The GEI-11::EGFP fusion protein is expressed in the correct gei-11 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the GEI-11 transcription factor. tags : GFP::3xFlag mutagen : Bombard outcross : 3 genotype : unc-119(ed3) III; wgIs179 unc-119(+) gei-11::TY1::EGFP::3xFLAG official name : OP179 )|Snyder_GEI11_GFP_L4_rep1 extraction1_seq1 channel_2|L4 Lar@ L4?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX043973 OP179(made_by : R. Waterston description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The GEI-11::EGFP fusion protein is expressed in the correct gei-11 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the GEI-11 transcription factor. tags : GFP::3xFlag mutagen : Bombard outcross : 3 genotype : unc-119(ed3) III; wgIs179 unc-119(+) gei-11::TY1::EGFP::3xFLAG official name : OP179 )|Snyder_GEI11_GFP_L4_rep2 extraction2_seq1 channel_1|L4 Lar@ L4?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX043974 OP179(made_by : R. Waterston description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The GEI-11::EGFP fusion protein is expressed in the correct gei-11 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the GEI-11 transcription factor. tags : GFP::3xFlag mutagen : Bombard outcross : 3 genotype : unc-119(ed3) III; wgIs179 unc-119(+) gei-11::TY1::EGFP::3xFLAG official name : OP179 )|Snyder_GEI11_GFP_L4_rep2 extraction2_seq1 channel_2|L4 Lar@ L4?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX054258 OP87(official name : OP87 genotype : unc-119(ed3) III; wgIs87 unc-119(+) pes-1::TY1::EGFP::3xFLAG outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The PES-1::EGFP fusion protein is expressed in the correct pes-1 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the PES-1 transcription factor. made_by : R. Waterston )|Snyder_PES-1_GFP_L4_rep1 extraction1_seq1 channel_1|L4 Lar@ L4?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX054259 OP87(official name : OP87 genotype : unc-119(ed3) III; wgIs87 unc-119(+) pes-1::TY1::EGFP::3xFLAG outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The PES-1::EGFP fusion protein is expressed in the correct pes-1 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the PES-1 transcription factor. made_by : R. Waterston )|Snyder_PES-1_GFP_L4_rep1 extraction2_seq2 channel_1|L4 Lar@ L4?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX054260 OP87(official name : OP87 genotype : unc-119(ed3) III; wgIs87 unc-119(+) pes-1::TY1::EGFP::3xFLAG outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The PES-1::EGFP fusion protein is expressed in the correct pes-1 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the PES-1 transcription factor. made_by : R. Waterston )|Snyder_PES-1_GFP_L4_rep1 extraction3_seq3 channel_1|L4 Lar@ L4?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX054261 OP87(official name : OP87 genotype : unc-119(ed3) III; wgIs87 unc-119(+) pes-1::TY1::EGFP::3xFLAG outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The PES-1::EGFP fusion protein is expressed in the correct pes-1 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the PES-1 transcription factor. made_by : R. Waterston )|Snyder_PES-1_GFP_L4_rep1 extraction4_seq4 channel_1|L4 Lar@ L4?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX054262 OP87(official name : OP87 genotype : unc-119(ed3) III; wgIs87 unc-119(+) pes-1::TY1::EGFP::3xFLAG outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The PES-1::EGFP fusion protein is expressed in the correct pes-1 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the PES-1 transcription factor. made_by : R. Waterston )|Snyder_PES-1_GFP_L4_rep1 extraction5_seq5 channel_1|L4 Lar@ L4?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX054263 OP87(official name : OP87 genotype : unc-119(ed3) III; wgIs87 unc-119(+) pes-1::TY1::EGFP::3xFLAG outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The PES-1::EGFP fusion protein is expressed in the correct pes-1 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the PES-1 transcription factor. made_by : R. Waterston )|Snyder_PES-1_GFP_L4_rep1 extraction6_seq6 channel_1|L4 Lar@ L4?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX054264 OP87(official name : OP87 genotype : unc-119(ed3) III; wgIs87 unc-119(+) pes-1::TY1::EGFP::3xFLAG outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The PES-1::EGFP fusion protein is expressed in the correct pes-1 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the PES-1 transcription factor. made_by : R. Waterston )|Snyder_PES-1_GFP_L4_rep2 extraction7_seq7 channel_1|L4 Lar@ L4?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX054265 OP87(official name : OP87 genotype : unc-119(ed3) III; wgIs87 unc-119(+) pes-1::TY1::EGFP::3xFLAG outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The PES-1::EGFP fusion protein is expressed in the correct pes-1 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the PES-1 transcription factor. made_by : R. Waterston )|Snyder_PES-1_GFP_L4_rep2 extraction8_seq8 channel_1|L4 Lar@ L4?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX054266 OP87(official name : OP87 genotype : unc-119(ed3) III; wgIs87 unc-119(+) pes-1::TY1::EGFP::3xFLAG outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The PES-1::EGFP fusion protein is expressed in the correct pes-1 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the PES-1 transcription factor. made_by : R. Waterston )|Snyder_PES-1_GFP_L4_rep2 extraction9_seq9 channel_1|L4 Lar@ L4?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX065638 OP332(official name : ZTF-7 genotype : unc119(ed3); wgIs332(ztf-71::TY1 EGFP FLAG; unc119) outcross : 0 mutagen : None tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The spatio-temporal expression pattern of ZTF-7::EGFP fusion protein was examined through in vivo microscopy. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the ZTF-7 transcription factor. made_by : Bob Waterston's lab from UW )|Snyder_ZTF-7_Input_L4 extraction1_seq1 channel_1|L4 Lar@ L4?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX065639 OP332(official name : ZTF-7 genotype : unc119(ed3); wgIs332(ztf-71::TY1 EGFP FLAG; unc119) outcross : 0 mutagen : None tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The spatio-temporal expression pattern of ZTF-7::EGFP fusion protein was examined through in vivo microscopy. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the ZTF-7 transcription factor. made_by : Bob Waterston's lab from UW )|Snyder_ZTF-7_Input_L4 extraction2_seq2 channel_1|L4 Lar@ L4?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX065640 OP332(official name : ZTF-7 genotype : unc119(ed3); wgIs332(ztf-71::TY1 EGFP FLAG; unc119) outcross : 0 mutagen : None tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The spatio-temporal expression pattern of ZTF-7::EGFP fusion protein was examined through in vivo microscopy. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the ZTF-7 transcription factor. made_by : Bob Waterston's lab from UW )|Snyder_ZTF-7_GFP_L4_rep1 extraction3_seq3 channel_1|L4 Lar@ L4?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX065641 OP332(official name : ZTF-7 genotype : unc119(ed3); wgIs332(ztf-71::TY1 EGFP FLAG; unc119) outcross : 0 mutagen : None tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The spatio-temporal expression pattern of ZTF-7::EGFP fusion protein was examined through in vivo microscopy. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the ZTF-7 transcription factor. made_by : Bob Waterston's lab from UW )|Snyder_ZTF-7_GFP_L4_rep2 extraction4_seq4 channel_1|L4 Lar@ L4?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX065646 OP174(official name : OP174 genotype : unc-119(ed3); wgIs174(ces-1::TY1 EGFP FLAG; unc-119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The CES-1::EGFP fusion protein is expressed in the correct ces-1 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the CES-1 transcription factor. made_by : S. Kim )|Snyder_CES-1_Input_L4 extraction1_seq1 channel_1|L4 Lar@ L4?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX065647 OP174(official name : OP174 genotype : unc-119(ed3); wgIs174(ces-1::TY1 EGFP FLAG; unc-119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The CES-1::EGFP fusion protein is expressed in the correct ces-1 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the CES-1 transcription factor. made_by : S. Kim )|Snyder_CES-1_Input_L4 extraction2_seq2 channel_1|L4 Lar@ L4?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX065648 OP174(official name : OP174 genotype : unc-119(ed3); wgIs174(ces-1::TY1 EGFP FLAG; unc-119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The CES-1::EGFP fusion protein is expressed in the correct ces-1 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the CES-1 transcription factor. made_by : S. Kim )|Snyder_CES-1_GFP_L4_rep1 extraction3_seq3 channel_1|L4 Lar@ L4?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX065649 OP174(official name : OP174 genotype : unc-119(ed3); wgIs174(ces-1::TY1 EGFP FLAG; unc-119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The CES-1::EGFP fusion protein is expressed in the correct ces-1 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the CES-1 transcription factor. made_by : S. Kim )|Snyder_CES-1_GFP_L4_rep2 extraction4_seq4 channel_1|L4 Lar@ L4?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX065654 OP317(official name : OP317 genotype : unc119(ed3); wgIs317(nhr-28::TY1 EGFP FLAG; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The NHR-28::EGFP fusion protein is expressed in the correct nhr-28 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the NHR-28 transcription factor. made_by : R Waterston )|Snyder_NHR-28_Input_L4 extraction1_seq1 channel_1|L4 Lar@ L4?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX065655 OP317(official name : OP317 genotype : unc119(ed3); wgIs317(nhr-28::TY1 EGFP FLAG; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The NHR-28::EGFP fusion protein is expressed in the correct nhr-28 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the NHR-28 transcription factor. made_by : R Waterston )|Snyder_NHR-28_Input_L4 extraction2_seq2 channel_1|L4 Lar@ L4?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX065656 OP317(official name : OP317 genotype : unc119(ed3); wgIs317(nhr-28::TY1 EGFP FLAG; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The NHR-28::EGFP fusion protein is expressed in the correct nhr-28 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the NHR-28 transcription factor. made_by : R Waterston )|Snyder_NHR-28_GFP_L4_rep1 extraction3_seq3 channel_1|L4 Lar@ L4?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX065657 OP317(official name : OP317 genotype : unc119(ed3); wgIs317(nhr-28::TY1 EGFP FLAG; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The NHR-28::EGFP fusion protein is expressed in the correct nhr-28 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the NHR-28 transcription factor. made_by : R Waterston )|Snyder_NHR-28_GFP_L4_rep2 extraction4_seq4 channel_1|L4 Lar@ L4?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX065711 OP222(official name : OP222 genotype : unc119(ed3); wgIs222(daf-12:TY1 EGFP FLAG; unc119) outcross : 3 transgene : daf-12 tags : Bombard tag : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The DAF-12::EGFP fusion protein is expressed in the correct daf-12 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the DAF-12 transcription factor. made_by : Mihail Sarov )|Snyder_DAF-12_Input_L4 extraction1_seq1 channel_1|L4 Lar@ L4?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX065712 OP222(official name : OP222 genotype : unc119(ed3); wgIs222(daf-12:TY1 EGFP FLAG; unc119) outcross : 3 transgene : daf-12 tags : Bombard tag : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The DAF-12::EGFP fusion protein is expressed in the correct daf-12 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the DAF-12 transcription factor. made_by : Mihail Sarov )|Snyder_DAF-12_Input_L4 extraction2_seq2 channel_1|L4 Lar@ L4?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX065713 OP222(official name : OP222 genotype : unc119(ed3); wgIs222(daf-12:TY1 EGFP FLAG; unc119) outcross : 3 transgene : daf-12 tags : Bombard tag : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The DAF-12::EGFP fusion protein is expressed in the correct daf-12 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the DAF-12 transcription factor. made_by : Mihail Sarov )|Snyder_DAF-12_GFP_L4_rep1 extraction3_seq3 channel_1|L4 Lar@ L4?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX065714 OP222(official name : OP222 genotype : unc119(ed3); wgIs222(daf-12:TY1 EGFP FLAG; unc119) outcross : 3 transgene : daf-12 tags : Bombard tag : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The DAF-12::EGFP fusion protein is expressed in the correct daf-12 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the DAF-12 transcription factor. made_by : Mihail Sarov )|Snyder_DAF-12_GFP_L4_rep2 extraction4_seq4 channel_1|L4 Lar@ L4?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX146487 OP184(official name : OP184 genotype : unc119(ed3); wgIs184(lin-15B::TY1 EGFP FLAG; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The LIN-15B::EGFP fusion protein is expressed in the correct lin-15B spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the LIN-15B transcription factor. made_by : S Kim )|Snyder_LIN15B_Input_L4_rep1|L4 Lar@ L4?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX146488 OP184(official name : OP184 genotype : unc119(ed3); wgIs184(lin-15B::TY1 EGFP FLAG; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The LIN-15B::EGFP fusion protein is expressed in the correct lin-15B spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the LIN-15B transcription factor. made_by : S Kim )|Snyder_LIN15B_Input_L4_rep2|L4 Lar@ L4?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX146489 OP184(official name : OP184 genotype : unc119(ed3); wgIs184(lin-15B::TY1 EGFP FLAG; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The LIN-15B::EGFP fusion protein is expressed in the correct lin-15B spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the LIN-15B transcription factor. made_by : S Kim )|Snyder_LIN15B_GFP_L4_rep1|L4 Lar@ L4?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX146490 OP184(official name : OP184 genotype : unc119(ed3); wgIs184(lin-15B::TY1 EGFP FLAG; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The LIN-15B::EGFP fusion protein is expressed in the correct lin-15B spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the LIN-15B transcription factor. made_by : S Kim )|Snyder_LIN15B_GFP_L4_rep2|L4 Lar@ L4?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX147619 OP304(official name : OP304 genotype : unc119(ed3); wgIs304(fos-1::TY1 EGFP FLAG; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The FOS-1::EGFP fusion protein is expressed in the correct fos-1 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the FOS-1 transcription factor. made_by : R Waterston )|Snyder_FOS-1_Input_L4_rep1|L4 Lar@ L4?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX147620 OP304(official name : OP304 genotype : unc119(ed3); wgIs304(fos-1::TY1 EGFP FLAG; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The FOS-1::EGFP fusion protein is expressed in the correct fos-1 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the FOS-1 transcription factor. made_by : R Waterston )|Snyder_FOS-1_Input_L4_rep2|L4 Lar@ L4?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX147621 OP304(official name : OP304 genotype : unc119(ed3); wgIs304(fos-1::TY1 EGFP FLAG; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The FOS-1::EGFP fusion protein is expressed in the correct fos-1 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the FOS-1 transcription factor. made_by : R Waterston )|Snyder_FOS-1_GFP_L4_rep1|L4 Lar@ L4?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX147622 OP304(official name : OP304 genotype : unc119(ed3); wgIs304(fos-1::TY1 EGFP FLAG; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The FOS-1::EGFP fusion protein is expressed in the correct fos-1 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the FOS-1 transcription factor. made_by : R Waterston )|Snyder_FOS-1_GFP_L4_rep2|L4 Lar@ L4?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX147631 OP353(official name : OP353 genotype : unc119(ed3); wgIs353(nhr-77::TY1 EGFP FLAG; unc119) outcross : 3 transgene : nhr-77 tags : Bombard tag : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The NHR-77::EGFP fusion protein is expressed in the correct nhr-77 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the NHR-77 transcription factor. made_by : R Waterston )|Snyder_NHR-77_Input_L4_rep1|L4 Lar@ L4?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX147632 OP353(official name : OP353 genotype : unc119(ed3); wgIs353(nhr-77::TY1 EGFP FLAG; unc119) outcross : 3 transgene : nhr-77 tags : Bombard tag : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The NHR-77::EGFP fusion protein is expressed in the correct nhr-77 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the NHR-77 transcription factor. made_by : R Waterston )|Snyder_NHR-77_Input_L4_rep2|L4 Lar@ L4?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX147633 OP353(official name : OP353 genotype : unc119(ed3); wgIs353(nhr-77::TY1 EGFP FLAG; unc119) outcross : 3 transgene : nhr-77 tags : Bombard tag : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The NHR-77::EGFP fusion protein is expressed in the correct nhr-77 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the NHR-77 transcription factor. made_by : R Waterston )|Snyder_NHR-77_GFP_L4_rep1|L4 Lar@ L4?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX147634 OP353(official name : OP353 genotype : unc119(ed3); wgIs353(nhr-77::TY1 EGFP FLAG; unc119) outcross : 3 transgene : nhr-77 tags : Bombard tag : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The NHR-77::EGFP fusion protein is expressed in the correct nhr-77 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the NHR-77 transcription factor. made_by : R Waterston )|Snyder_NHR-77_GFP_L4_rep2|L4 Lar@ L4?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX151404 OP83(official name : OP83 genotype : unc119(ed3); wgIs83(zag-1::TY1 EGFP FLAG; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The ZAG-1::EGFP fusion protein is expressed in the correct zag-1 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the ZAG-1 transcription factor. made_by : R Waterston )|Snyder_ZAG-1_Input_L4_rep1|L4 Lar@ L4?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX151405 OP83(official name : OP83 genotype : unc119(ed3); wgIs83(zag-1::TY1 EGFP FLAG; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The ZAG-1::EGFP fusion protein is expressed in the correct zag-1 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the ZAG-1 transcription factor. made_by : R Waterston )|Snyder_ZAG-1_Input_L4_rep2|L4 Lar@ L4?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX151406 OP83(official name : OP83 genotype : unc119(ed3); wgIs83(zag-1::TY1 EGFP FLAG; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The ZAG-1::EGFP fusion protein is expressed in the correct zag-1 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the ZAG-1 transcription factor. made_by : R Waterston )|Snyder_ZAG-1_GFP_L4_rep1|L4 Lar@ L4?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX151407 OP83(official name : OP83 genotype : unc119(ed3); wgIs83(zag-1::TY1 EGFP FLAG; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The ZAG-1::EGFP fusion protein is expressed in the correct zag-1 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the ZAG-1 transcription factor. made_by : R Waterston )|Snyder_ZAG-1_GFP_L4_rep2|L4 Lar@ L4?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX222632 OP124(official name : OP124 genotype : unc-119(ed3); wgIs124(aha-1::TY1 EGFP FLAG; unc-119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The AHA-1::EGFP fusion protein is expressed in the correct aha-1 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the AHA-1 transcription factor. made_by : R. Waterston and S. Kim )|Snyder_AHA-1_Input_L4_rep1|L4 Lar@ L4?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX222633 OP124(official name : OP124 genotype : unc-119(ed3); wgIs124(aha-1::TY1 EGFP FLAG; unc-119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The AHA-1::EGFP fusion protein is expressed in the correct aha-1 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the AHA-1 transcription factor. made_by : R. Waterston and S. Kim )|Snyder_AHA-1_Input_L4_rep2|L4 Lar@ L4?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX222634 OP124(official name : OP124 genotype : unc-119(ed3); wgIs124(aha-1::TY1 EGFP FLAG; unc-119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The AHA-1::EGFP fusion protein is expressed in the correct aha-1 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the AHA-1 transcription factor. made_by : R. Waterston and S. Kim )|Snyder_AHA-1_GFP_L4_rep1|L4 Lar@ L4?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX222635 OP124(official name : OP124 genotype : unc-119(ed3); wgIs124(aha-1::TY1 EGFP FLAG; unc-119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The AHA-1::EGFP fusion protein is expressed in the correct aha-1 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the AHA-1 transcription factor. made_by : R. Waterston and S. Kim )|Snyder_AHA-1_GFP_L4_rep2|L4 Lar@ L4?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX222640 OP105(official name : OP105 genotype : unc119(ed3); wgIs105(dpl-1::TY1 EGFP FLAG; unc119) outcross : 0 mutagen : None tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for bombardment transformation of an unc-119(ed3) strain. The DPL-1::EGFP fusion protein has broad expression pattern description : but silence in germline cells. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the DPL-1 transcription factor. made_by : Bob Waterston's lab from UW )|Snyder_DPL-1_Input_L4_rep1_GTAT|L4 Lar@ L4?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX222641 OP105(official name : OP105 genotype : unc119(ed3); wgIs105(dpl-1::TY1 EGFP FLAG; unc119) outcross : 0 mutagen : None tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for bombardment transformation of an unc-119(ed3) strain. The DPL-1::EGFP fusion protein has broad expression pattern description : but silence in germline cells. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the DPL-1 transcription factor. made_by : Bob Waterston's lab from UW )|Snyder_DPL-1_Input_L4_rep2_ACGT|L4 Lar@ L4?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX222642 OP105(official name : OP105 genotype : unc119(ed3); wgIs105(dpl-1::TY1 EGFP FLAG; unc119) outcross : 0 mutagen : None tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for bombardment transformation of an unc-119(ed3) strain. The DPL-1::EGFP fusion protein has broad expression pattern description : but silence in germline cells. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the DPL-1 transcription factor. made_by : Bob Waterston's lab from UW )|Snyder_DPL-1_GFP_L4_rep1_TGCT|L4 Lar@ L4?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX222643 OP105(official name : OP105 genotype : unc119(ed3); wgIs105(dpl-1::TY1 EGFP FLAG; unc119) outcross : 0 mutagen : None tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for bombardment transformation of an unc-119(ed3) strain. The DPL-1::EGFP fusion protein has broad expression pattern description : but silence in germline cells. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the DPL-1 transcription factor. made_by : Bob Waterston's lab from UW )|Snyder_DPL-1_GFP_L4_rep2_ACGT|L4 Lar@ L4?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX233693 OP355(official name : OP355 genotype : unc-119(ed3) III; wgIs355(ZK377.2::TY1 EGFP FLAG; unc-119(+)) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Dresden using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The sax-3::EGFP fusion protein is expressed in the correct sax-3 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the sax-3 transcription factor. The sax-3 gene is encoded by the ZK377.2 CDS. made_by : R Waterston )|Snyder_ZK377.2_GFP_L4_rep1_Input_ACGT|L4 Lar@ L4?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX233694 OP355(official name : OP355 genotype : unc-119(ed3) III; wgIs355(ZK377.2::TY1 EGFP FLAG; unc-119(+)) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Dresden using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The sax-3::EGFP fusion protein is expressed in the correct sax-3 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the sax-3 transcription factor. The sax-3 gene is encoded by the ZK377.2 CDS. made_by : R Waterston )|Snyder_ZK377.2_GFP_L4_rep2_Input_TGCT|L4 Lar@ L4?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX233695 OP355(official name : OP355 genotype : unc-119(ed3) III; wgIs355(ZK377.2::TY1 EGFP FLAG; unc-119(+)) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Dresden using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The sax-3::EGFP fusion protein is expressed in the correct sax-3 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the sax-3 transcription factor. The sax-3 gene is encoded by the ZK377.2 CDS. made_by : R Waterston )|Snyder_ZK377.2_GFP_L4_rep1_GFP_ACGT|L4 Lar@ L4?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX233696 OP355(official name : OP355 genotype : unc-119(ed3) III; wgIs355(ZK377.2::TY1 EGFP FLAG; unc-119(+)) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Dresden using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The sax-3::EGFP fusion protein is expressed in the correct sax-3 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the sax-3 transcription factor. The sax-3 gene is encoded by the ZK377.2 CDS. made_by : R Waterston )|Snyder_ZK377.2_GFP_L4_rep2_GFP_TGCT|L4 Lar@ L4?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX234918 OP226(official name : OP226 genotype : unc119(ed3); wgIs226(nhr-116::TY1 EGFP FLAG; unc119) outcross : 3 transgene : nhr-116 tags : Bombard tag : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The NHR-116::EGFP fusion protein is expressed in the correct nhr-116 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the NHR-116 transcription factor. made_by : M Sarov )|Snyder_NHR-116_GFP_L4_rep1_Input_ACGT|L4 Lar@ L4?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX234919 OP226(official name : OP226 genotype : unc119(ed3); wgIs226(nhr-116::TY1 EGFP FLAG; unc119) outcross : 3 transgene : nhr-116 tags : Bombard tag : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The NHR-116::EGFP fusion protein is expressed in the correct nhr-116 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the NHR-116 transcription factor. made_by : M Sarov )|Snyder_NHR-116_GFP_L4_rep2_Input_TGCT|L4 Lar@ L4?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX234920 OP226(official name : OP226 genotype : unc119(ed3); wgIs226(nhr-116::TY1 EGFP FLAG; unc119) outcross : 3 transgene : nhr-116 tags : Bombard tag : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The NHR-116::EGFP fusion protein is expressed in the correct nhr-116 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the NHR-116 transcription factor. made_by : M Sarov )|Snyder_NHR-116_GFP_L4_rep1_GFP_ACGT|L4 Lar@ L4?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX234921 OP226(official name : OP226 genotype : unc119(ed3); wgIs226(nhr-116::TY1 EGFP FLAG; unc119) outcross : 3 transgene : nhr-116 tags : Bombard tag : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The NHR-116::EGFP fusion protein is expressed in the correct nhr-116 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the NHR-116 transcription factor. made_by : M Sarov )|Snyder_NHR-116_GFP_L4_rep2_GFP_TGCT|L4 Lar@ L4?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX276905 OP234(official name : OP234 genotype : unc119(ed3); wgIs234(T24H10.7:TY1 EGFP FLAG; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The JUN-1::EGFP fusion protein is expressed in the correct jun-1 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the JUN-1 transcription factor. made_by : Unknown )|JUN-1 L4 InputRep1|L4 Lar@ L4?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX276906 OP234(official name : OP234 genotype : unc119(ed3); wgIs234(T24H10.7:TY1 EGFP FLAG; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The JUN-1::EGFP fusion protein is expressed in the correct jun-1 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the JUN-1 transcription factor. made_by : Unknown )|JUN-1 L4 InputRep2|L4 Lar@ L4?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX276907 OP234(official name : OP234 genotype : unc119(ed3); wgIs234(T24H10.7:TY1 EGFP FLAG; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The JUN-1::EGFP fusion protein is expressed in the correct jun-1 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the JUN-1 transcription factor. made_by : Unknown )|JUN-1 L4 ChIPRep1|L4 Lar@ L4?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX276908 OP234(official name : OP234 genotype : unc119(ed3); wgIs234(T24H10.7:TY1 EGFP FLAG; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The JUN-1::EGFP fusion protein is expressed in the correct jun-1 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the JUN-1 transcription factor. made_by : Unknown )|JUN-1 L4 ChIPRep2|L4 Lar@ L4?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX276913 OP236(official name : OP236 genotype : unc119(ed3); wgIs236(elk-2::TY1 EGFP FLAG; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The ZTF-11::EGFP fusion protein is expressed in the correct ztf-11 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the ZTF-11 transcription factor. made_by : Unknown )|ZTF-11 L4 InputRep1|L4 Lar@ L4?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX276914 OP236(official name : OP236 genotype : unc119(ed3); wgIs236(elk-2::TY1 EGFP FLAG; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The ZTF-11::EGFP fusion protein is expressed in the correct ztf-11 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the ZTF-11 transcription factor. made_by : Unknown )|ZTF-11 L4 InputRep2|L4 Lar@ L4?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX276915 OP236(official name : OP236 genotype : unc119(ed3); wgIs236(elk-2::TY1 EGFP FLAG; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The ZTF-11::EGFP fusion protein is expressed in the correct ztf-11 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the ZTF-11 transcription factor. made_by : Unknown )|ZTF-11 L4 ChIPRep1|L4 Lar@ L4?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX276916 OP236(official name : OP236 genotype : unc119(ed3); wgIs236(elk-2::TY1 EGFP FLAG; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The ZTF-11::EGFP fusion protein is expressed in the correct ztf-11 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the ZTF-11 transcription factor. made_by : Unknown )|ZTF-11 L4 ChIPRep2|L4 Lar@ L4?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX276917 OP203(official name : OP203 genotype : unc-119(ed3); wgIs203(nhr-76::TY1 EGFP FLAG; unc-119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The NHR-76::EGFP fusion protein is expressed in the correct nhr-76 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the NHR-76 transcription factor. made_by : R. Waterston )|NHR-76 L4 InputRep1|L4 Lar@ L4?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX276918 OP203(official name : OP203 genotype : unc-119(ed3); wgIs203(nhr-76::TY1 EGFP FLAG; unc-119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The NHR-76::EGFP fusion protein is expressed in the correct nhr-76 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the NHR-76 transcription factor. made_by : R. Waterston )|NHR-76 L4 InputRep2|L4 Lar@ L4?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX276919 OP203(official name : OP203 genotype : unc-119(ed3); wgIs203(nhr-76::TY1 EGFP FLAG; unc-119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The NHR-76::EGFP fusion protein is expressed in the correct nhr-76 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the NHR-76 transcription factor. made_by : R. Waterston )|NHR-76 L4 ChIPRep1|L4 Lar@ L4?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX276920 OP203(official name : OP203 genotype : unc-119(ed3); wgIs203(nhr-76::TY1 EGFP FLAG; unc-119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The NHR-76::EGFP fusion protein is expressed in the correct nhr-76 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the NHR-76 transcription factor. made_by : R. Waterston )|NHR-76 L4 ChIPRep2|L4 Lar@ L4?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX277028 OP342(official name : OP342 genotype : unc119(ed3); wgIs341(skn-1::TY1 EGFP FLAG; unc119) outcross : 0 mutagen : None tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for bombardment transformation of an unc-119(ed3) strain. made_by : Bob Waterston's lab from UW )|SKN-1 L4 InputRep1|L4 Lar@ L4?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX277029 OP342(official name : OP342 genotype : unc119(ed3); wgIs341(skn-1::TY1 EGFP FLAG; unc119) outcross : 0 mutagen : None tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for bombardment transformation of an unc-119(ed3) strain. made_by : Bob Waterston's lab from UW )|SKN-1 L4 InputRep2|L4 Lar@ L4?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX277030 OP342(official name : OP342 genotype : unc119(ed3); wgIs341(skn-1::TY1 EGFP FLAG; unc119) outcross : 0 mutagen : None tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for bombardment transformation of an unc-119(ed3) strain. made_by : Bob Waterston's lab from UW )|SKN-1 L4 ChIPRep1|L4 Lar@ L4?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX277031 OP342(official name : OP342 genotype : unc119(ed3); wgIs341(skn-1::TY1 EGFP FLAG; unc119) outcross : 0 mutagen : None tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for bombardment transformation of an unc-119(ed3) strain. made_by : Bob Waterston's lab from UW )|SKN-1 L4 ChIPRep2|L4 Lar@ L4?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX277061 OP239(official name : OP239 genotype : unc119(ed3); wgIs239(nhr-10::TY1 EGFP FLAG; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The NHR-10::EGFP fusion protein is expressed in the correct nhr-10 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the NHR-10 transcription factor. made_by : Unknown )|NHR-10 L4 InputRep1|L4 Lar@ L4?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX277062 OP239(official name : OP239 genotype : unc119(ed3); wgIs239(nhr-10::TY1 EGFP FLAG; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The NHR-10::EGFP fusion protein is expressed in the correct nhr-10 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the NHR-10 transcription factor. made_by : Unknown )|NHR-10 L4 InputRep2|L4 Lar@ L4?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX277063 OP239(official name : OP239 genotype : unc119(ed3); wgIs239(nhr-10::TY1 EGFP FLAG; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The NHR-10::EGFP fusion protein is expressed in the correct nhr-10 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the NHR-10 transcription factor. made_by : Unknown )|NHR-10 L4 ChIPRep1|L4 Lar@ L4?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX277064 OP239(official name : OP239 genotype : unc119(ed3); wgIs239(nhr-10::TY1 EGFP FLAG; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The NHR-10::EGFP fusion protein is expressed in the correct nhr-10 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the NHR-10 transcription factor. made_by : Unknown )|NHR-10 L4 ChIPRep2|L4 Lar@ L4?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX277065 OP241(official name : OP241 genotype : unc119(ed3); wgIs241(ceh-38::TY1 EGFP FLAG; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The CEH-38::EGFP fusion protein is expressed in the correct ceh-38 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the CEH-38 transcription factor. made_by : Unknwon )|CEH-28 L4 InputRep1|L4 Lar@ L4?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX277066 OP241(official name : OP241 genotype : unc119(ed3); wgIs241(ceh-38::TY1 EGFP FLAG; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The CEH-38::EGFP fusion protein is expressed in the correct ceh-38 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the CEH-38 transcription factor. made_by : Unknwon )|CEH-28 L4 InputRep2|L4 Lar@ L4?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX277067 OP241(official name : OP241 genotype : unc119(ed3); wgIs241(ceh-38::TY1 EGFP FLAG; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The CEH-38::EGFP fusion protein is expressed in the correct ceh-38 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the CEH-38 transcription factor. made_by : Unknwon )|CEH-28 L4 ChIPRep1|L4 Lar@ L4?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX277068 OP241(official name : OP241 genotype : unc119(ed3); wgIs241(ceh-38::TY1 EGFP FLAG; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The CEH-38::EGFP fusion protein is expressed in the correct ceh-38 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the CEH-38 transcription factor. made_by : Unknwon )|CEH-28 L4 ChIPRep2|L4 Lar@ L4?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX277077 OP240(official name : OP240 genotype : unc119(ed3); wgIs240(lsy-2::TY1 EGFP FLAG; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The LSY-2::EGFP fusion protein is expressed in the correct lsy-2 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the LSY-2 transcription factor. made_by : Unknown )|LSY-2 L4 v2 InputRep1|L4 Lar@ L4?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX277078 OP240(official name : OP240 genotype : unc119(ed3); wgIs240(lsy-2::TY1 EGFP FLAG; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The LSY-2::EGFP fusion protein is expressed in the correct lsy-2 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the LSY-2 transcription factor. made_by : Unknown )|LSY-2 L4 v2 InputRep2|L4 Lar@ L4?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX277079 OP240(official name : OP240 genotype : unc119(ed3); wgIs240(lsy-2::TY1 EGFP FLAG; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The LSY-2::EGFP fusion protein is expressed in the correct lsy-2 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the LSY-2 transcription factor. made_by : Unknown )|LSY-2 L4 v2 ChIPRep1|L4 Lar@ L4?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX277080 OP240(official name : OP240 genotype : unc119(ed3); wgIs240(lsy-2::TY1 EGFP FLAG; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The LSY-2::EGFP fusion protein is expressed in the correct lsy-2 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the LSY-2 transcription factor. made_by : Unknown )|LSY-2 L4 v2 ChIPRep2|L4 Lar@ L4?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX277094 OP49(official name : OP49 genotype : unc119(ed3); wgIs49(lin-13::TY1 EGFP FLAG; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The LIN-13::EGFP fusion protein is expressed in the correct lin-13 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the LIN-13 transcription factor. made_by : Unknown )|LIN-13 L4 InputRep1|L4 Lar@ L4?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX277095 OP49(official name : OP49 genotype : unc119(ed3); wgIs49(lin-13::TY1 EGFP FLAG; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The LIN-13::EGFP fusion protein is expressed in the correct lin-13 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the LIN-13 transcription factor. made_by : Unknown )|LIN-13 L4 InputRep2|L4 Lar@ L4?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX277096 OP49(official name : OP49 genotype : unc119(ed3); wgIs49(lin-13::TY1 EGFP FLAG; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The LIN-13::EGFP fusion protein is expressed in the correct lin-13 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the LIN-13 transcription factor. made_by : Unknown )|LIN-13 L4 ChIPRep1|L4 Lar@ L4?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX277097 OP49(official name : OP49 genotype : unc119(ed3); wgIs49(lin-13::TY1 EGFP FLAG; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The LIN-13::EGFP fusion protein is expressed in the correct lin-13 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the LIN-13 transcription factor. made_by : Unknown )|LIN-13 L4 ChIPRep2|L4 Lar@ L4?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331057 OP37(official name : OP37 genotype : unc-119(ed3) III; wgIs37 unc-119(+) pha-4::TY1::EGFP::3xFLAG outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The PHA-4::EGFP fusion protein is expressed in the correct pha-4 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the PHA-4 transcription factor. made_by : R. Waterston and S. Kim )|PHA-4_GFP_L4_Input_Rep1|L4 Lar@ L4?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331065 OP218(official name : OP218 genotype : unc-119(ed3); wgIs218(R02D3.7:TY1 EGFP FLAG; unc-119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The R02D3.7::EGFP fusion protein is expressed in the correct R02D3.7 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the RO2D3.7 transcription factor. made_by : )|R02D3.7_GFP_L4_Input_Rep1|L4 Lar@ L4?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331066 OP218(official name : OP218 genotype : unc-119(ed3); wgIs218(R02D3.7:TY1 EGFP FLAG; unc-119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The R02D3.7::EGFP fusion protein is expressed in the correct R02D3.7 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the RO2D3.7 transcription factor. made_by : )|R02D3.7_GFP_L4_ChIP_Rep1|L4 Lar@ L4?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331067 OP218(official name : OP218 genotype : unc-119(ed3); wgIs218(R02D3.7:TY1 EGFP FLAG; unc-119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The R02D3.7::EGFP fusion protein is expressed in the correct R02D3.7 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the RO2D3.7 transcription factor. made_by : )|R02D3.7_GFP_L4_Input_Rep2|L4 Lar@ L4?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331068 OP218(official name : OP218 genotype : unc-119(ed3); wgIs218(R02D3.7:TY1 EGFP FLAG; unc-119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The R02D3.7::EGFP fusion protein is expressed in the correct R02D3.7 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the RO2D3.7 transcription factor. made_by : )|R02D3.7_GFP_L4_ChIP_Rep2|L4 Lar@ L4?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331127 OP90(official name : OP90 genotype : unc-119(ed3) III; wgIs90 unc-119(+) nhr-6::TY1::EGFP::3xFLAG outcross : 0 mutagen : None tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The NHR-6::EGFP fusion protein is expressed in neurons surrounding pharynx at L2 stage. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the NHR-6 transcription factor. made_by : R. Waterston )|NHR-6_GFP_L4_Input_Rep1|L4 Lar@ L4?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331128 OP90(official name : OP90 genotype : unc-119(ed3) III; wgIs90 unc-119(+) nhr-6::TY1::EGFP::3xFLAG outcross : 0 mutagen : None tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The NHR-6::EGFP fusion protein is expressed in neurons surrounding pharynx at L2 stage. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the NHR-6 transcription factor. made_by : R. Waterston )|NHR-6_GFP_L4_ChIP_Rep1|L4 Lar@ L4?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331129 OP90(official name : OP90 genotype : unc-119(ed3) III; wgIs90 unc-119(+) nhr-6::TY1::EGFP::3xFLAG outcross : 0 mutagen : None tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The NHR-6::EGFP fusion protein is expressed in neurons surrounding pharynx at L2 stage. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the NHR-6 transcription factor. made_by : R. Waterston )|NHR-6_GFP_L4_Input_Rep2|L4 Lar@ L4?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331130 OP90(official name : OP90 genotype : unc-119(ed3) III; wgIs90 unc-119(+) nhr-6::TY1::EGFP::3xFLAG outcross : 0 mutagen : None tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The NHR-6::EGFP fusion protein is expressed in neurons surrounding pharynx at L2 stage. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the NHR-6 transcription factor. made_by : R. Waterston )|NHR-6_GFP_L4_ChIP_Rep2|L4 Lar@ L4?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331147 OP102(official name : OP102 genotype : unc-119 (ed3); wgIs102 (ham-1::TY1 EGFP FLAG; unc-119(+)) outcross : 0 mutagen : None tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The HAM-1::EGFP fusion protein is expressed in the correct ham-1 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the HAM-1 transcription factor. made_by : R Waterston )|HAM-1_GFP_L4_Input_Rep1|L4 Lar@ L4?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331148 OP102(official name : OP102 genotype : unc-119 (ed3); wgIs102 (ham-1::TY1 EGFP FLAG; unc-119(+)) outcross : 0 mutagen : None tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The HAM-1::EGFP fusion protein is expressed in the correct ham-1 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the HAM-1 transcription factor. made_by : R Waterston )|HAM-1_GFP_L4_ChIP_Rep1|L4 Lar@ L4?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331149 OP102(official name : OP102 genotype : unc-119 (ed3); wgIs102 (ham-1::TY1 EGFP FLAG; unc-119(+)) outcross : 0 mutagen : None tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The HAM-1::EGFP fusion protein is expressed in the correct ham-1 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the HAM-1 transcription factor. made_by : R Waterston )|HAM-1_GFP_L4_Input_Rep2|L4 Lar@ L4?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331150 OP102(official name : OP102 genotype : unc-119 (ed3); wgIs102 (ham-1::TY1 EGFP FLAG; unc-119(+)) outcross : 0 mutagen : None tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The HAM-1::EGFP fusion protein is expressed in the correct ham-1 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the HAM-1 transcription factor. made_by : R Waterston )|HAM-1_GFP_L4_ChIP_Rep2|L4 Lar@ L4?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331151 OP102(official name : OP102 genotype : unc-119 (ed3); wgIs102 (ham-1::TY1 EGFP FLAG; unc-119(+)) outcross : 0 mutagen : None tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The HAM-1::EGFP fusion protein is expressed in the correct ham-1 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the HAM-1 transcription factor. made_by : R Waterston )|HAM-1_GFP_L4_Input_Rep3|L4 Lar@ L4?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331152 OP102(official name : OP102 genotype : unc-119 (ed3); wgIs102 (ham-1::TY1 EGFP FLAG; unc-119(+)) outcross : 0 mutagen : None tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The HAM-1::EGFP fusion protein is expressed in the correct ham-1 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the HAM-1 transcription factor. made_by : R Waterston )|HAM-1_GFP_L4_ChIP_Rep3|L4 Lar@ L4?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331205 OP305(official name : OP305 genotype : unc119(ed3); wgIs305(nhr-11::TY1 EGFP FLAG; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The NHR-11::EGFP fusion protein is expressed in the correct nhr-11 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the NHR-11 transcription factor. made_by : R Waterston )|NHR-11_GFP_L4_Input_Rep1|L4 Lar@ L4?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331206 OP305(official name : OP305 genotype : unc119(ed3); wgIs305(nhr-11::TY1 EGFP FLAG; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The NHR-11::EGFP fusion protein is expressed in the correct nhr-11 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the NHR-11 transcription factor. made_by : R Waterston )|NHR-11_GFP_L4_ChIP_Rep1|L4 Lar@ L4?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331207 OP305(official name : OP305 genotype : unc119(ed3); wgIs305(nhr-11::TY1 EGFP FLAG; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The NHR-11::EGFP fusion protein is expressed in the correct nhr-11 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the NHR-11 transcription factor. made_by : R Waterston )|NHR-11_GFP_L4_Input_Rep2|L4 Lar@ L4?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331208 OP305(official name : OP305 genotype : unc119(ed3); wgIs305(nhr-11::TY1 EGFP FLAG; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The NHR-11::EGFP fusion protein is expressed in the correct nhr-11 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the NHR-11 transcription factor. made_by : R Waterston )|NHR-11_GFP_L4_ChIP_Rep2|L4 Lar@ L4?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331213 OP18(official name : OP18 genotype : unc-119(ed3) III; wgIs18 unc-119(+) lin-39::TY1::EGFP::3xFLAG outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The LIN-39::EGFP fusion protein is expressed in the correct lin-39 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the LIN-39 transcription factor. made_by : R. Waterston and S. Kim )|LIN-39_GFP_L4_Input_Rep1|L4 Lar@ L4?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331214 OP18(official name : OP18 genotype : unc-119(ed3) III; wgIs18 unc-119(+) lin-39::TY1::EGFP::3xFLAG outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The LIN-39::EGFP fusion protein is expressed in the correct lin-39 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the LIN-39 transcription factor. made_by : R. Waterston and S. Kim )|LIN-39_GFP_L4_ChIP_Rep1|L4 Lar@ L4?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331215 OP18(official name : OP18 genotype : unc-119(ed3) III; wgIs18 unc-119(+) lin-39::TY1::EGFP::3xFLAG outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The LIN-39::EGFP fusion protein is expressed in the correct lin-39 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the LIN-39 transcription factor. made_by : R. Waterston and S. Kim )|LIN-39_GFP_L4_Input_Rep2|L4 Lar@ L4?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331216 OP18(official name : OP18 genotype : unc-119(ed3) III; wgIs18 unc-119(+) lin-39::TY1::EGFP::3xFLAG outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The LIN-39::EGFP fusion protein is expressed in the correct lin-39 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the LIN-39 transcription factor. made_by : R. Waterston and S. Kim )|LIN-39_GFP_L4_ChIP_Rep2|L4 Lar@ L4?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331217 OP600(official name : OP600 genotype : unc119(ed3); wgIs600(unc-62::TY1 EGFP FLAG; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The UNC-62::EGFP fusion protein is expressed in the correct unc-62 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the UNC-62 transcription factor. made_by : S Kim )|UNC_62_GFP_L4_Input_Rep1|L4 Lar@ L4?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331218 OP600(official name : OP600 genotype : unc119(ed3); wgIs600(unc-62::TY1 EGFP FLAG; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The UNC-62::EGFP fusion protein is expressed in the correct unc-62 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the UNC-62 transcription factor. made_by : S Kim )|UNC_62_GFP_L4_ChIP_Rep1|L4 Lar@ L4?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331219 OP600(official name : OP600 genotype : unc119(ed3); wgIs600(unc-62::TY1 EGFP FLAG; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The UNC-62::EGFP fusion protein is expressed in the correct unc-62 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the UNC-62 transcription factor. made_by : S Kim )|UNC_62_GFP_L4_Input_Rep2|L4 Lar@ L4?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331220 OP600(official name : OP600 genotype : unc119(ed3); wgIs600(unc-62::TY1 EGFP FLAG; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The UNC-62::EGFP fusion protein is expressed in the correct unc-62 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the UNC-62 transcription factor. made_by : S Kim )|UNC_62_GFP_L4_ChIP_Rep2|L4 Lar@ L4?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331249 OP337(official name : OP337 genotype : unc119(ed3); wgIs377(fkh-10::TY1 EGFP FLAG; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The FKH-10::EGFP fusion protein is expressed in the correct fkh-10 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the FKH-10 transcription factor. made_by : Unknown )|FKH-10_GFP_L4_Input_Rep1|L4 Lar@ L4?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331250 OP337(official name : OP337 genotype : unc119(ed3); wgIs377(fkh-10::TY1 EGFP FLAG; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The FKH-10::EGFP fusion protein is expressed in the correct fkh-10 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the FKH-10 transcription factor. made_by : Unknown )|FKH-10_GFP_L4_ChIP_Rep1|L4 Lar@ L4?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331251 OP337(official name : OP337 genotype : unc119(ed3); wgIs377(fkh-10::TY1 EGFP FLAG; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The FKH-10::EGFP fusion protein is expressed in the correct fkh-10 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the FKH-10 transcription factor. made_by : Unknown )|FKH-10_GFP_L4_Input_Rep2|L4 Lar@ L4?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331252 OP337(official name : OP337 genotype : unc119(ed3); wgIs377(fkh-10::TY1 EGFP FLAG; unc119) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The FKH-10::EGFP fusion protein is expressed in the correct fkh-10 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the FKH-10 transcription factor. made_by : Unknown )|FKH-10_GFP_L4_ChIP_Rep2|L4 Lar@ L4?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331261 OP37(official name : OP37 genotype : unc-119(ed3) III; wgIs37 unc-119(+) pha-4::TY1::EGFP::3xFLAG outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The PHA-4::EGFP fusion protein is expressed in the correct pha-4 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the PHA-4 transcription factor. made_by : R. Waterston and S. Kim )|PHA-4_Male_L4_Input_Rep1|L4 Lar@ L4?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331262 OP37(official name : OP37 genotype : unc-119(ed3) III; wgIs37 unc-119(+) pha-4::TY1::EGFP::3xFLAG outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The PHA-4::EGFP fusion protein is expressed in the correct pha-4 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the PHA-4 transcription factor. made_by : R. Waterston and S. Kim )|PHA-4_Male_L4_ChIP_Rep1|L4 Lar@ L4?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331263 OP37(official name : OP37 genotype : unc-119(ed3) III; wgIs37 unc-119(+) pha-4::TY1::EGFP::3xFLAG outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The PHA-4::EGFP fusion protein is expressed in the correct pha-4 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the PHA-4 transcription factor. made_by : R. Waterston and S. Kim )|PHA-4_Male_L4_Input_Rep2|L4 Lar@ L4?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331264 OP37(official name : OP37 genotype : unc-119(ed3) III; wgIs37 unc-119(+) pha-4::TY1::EGFP::3xFLAG outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The PHA-4::EGFP fusion protein is expressed in the correct pha-4 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the PHA-4 transcription factor. made_by : R. Waterston and S. Kim )|PHA-4_Male_L4_ChIP_Rep2|L4 Lar@ L4?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331265 OP37(official name : OP37 genotype : unc-119(ed3) III; wgIs37 unc-119(+) pha-4::TY1::EGFP::3xFLAG outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The PHA-4::EGFP fusion protein is expressed in the correct pha-4 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the PHA-4 transcription factor. made_by : R. Waterston and S. Kim )|PHA-4_Male_L4_Input_Rep3|L4 Lar@ L4?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331266 OP37(official name : OP37 genotype : unc-119(ed3) III; wgIs37 unc-119(+) pha-4::TY1::EGFP::3xFLAG outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology in Tubiginen using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The PHA-4::EGFP fusion protein is expressed in the correct pha-4 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the PHA-4 transcription factor. made_by : R. Waterston and S. Kim )|PHA-4_Male_L4_ChIP_Rep3|L4 Lar@ L4?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331293 OP432(official name : OP432 genotype : unc-119(ed3) III; wgIs432(zip-2::TY1-GFP-3xFLA; unc-119(+)) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology and Genetics in Dresden description : using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The ZIP-2::EGFP fusion protein is expressed in the correct zip-2 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the ZIP-2 transcription factor. made_by : Unknown )|ZIP-2_GFP_L4_Input_Rep1|L4 Lar@ L4?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331294 OP432(official name : OP432 genotype : unc-119(ed3) III; wgIs432(zip-2::TY1-GFP-3xFLA; unc-119(+)) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology and Genetics in Dresden description : using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The ZIP-2::EGFP fusion protein is expressed in the correct zip-2 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the ZIP-2 transcription factor. made_by : Unknown )|ZIP-2_GFP_L4_ChIP_Rep1|L4 Lar@ L4?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331295 OP432(official name : OP432 genotype : unc-119(ed3) III; wgIs432(zip-2::TY1-GFP-3xFLA; unc-119(+)) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology and Genetics in Dresden description : using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The ZIP-2::EGFP fusion protein is expressed in the correct zip-2 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the ZIP-2 transcription factor. made_by : Unknown )|ZIP-2_GFP_L4_Input_Rep2|L4 Lar@ L4?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331296 OP432(official name : OP432 genotype : unc-119(ed3) III; wgIs432(zip-2::TY1-GFP-3xFLA; unc-119(+)) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology and Genetics in Dresden description : using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The ZIP-2::EGFP fusion protein is expressed in the correct zip-2 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the ZIP-2 transcription factor. made_by : Unknown )|ZIP-2_GFP_L4_ChIP_Rep2|L4 Lar@ L4?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331297 OP398(official name : OP398 genotype : unc-119(ed3) III; wgIs398(dve-1::TY1EGFPFLAG C; unc-119(+)) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology and Genetics in Dresden description : using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The DVE-1::EGFP fusion protein is expressed in the correct dve-1 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the DVE-1 transcription factor. made_by : Unknown )|DVE-1_GFP_L4_Input_Rep1|L4 Lar@ L4?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331298 OP398(official name : OP398 genotype : unc-119(ed3) III; wgIs398(dve-1::TY1EGFPFLAG C; unc-119(+)) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology and Genetics in Dresden description : using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The DVE-1::EGFP fusion protein is expressed in the correct dve-1 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the DVE-1 transcription factor. made_by : Unknown )|DVE-1_GFP_L4_ChIP_Rep1|L4 Lar@ L4?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331299 OP398(official name : OP398 genotype : unc-119(ed3) III; wgIs398(dve-1::TY1EGFPFLAG C; unc-119(+)) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology and Genetics in Dresden description : using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The DVE-1::EGFP fusion protein is expressed in the correct dve-1 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the DVE-1 transcription factor. made_by : Unknown )|DVE-1_GFP_L4_Input_Rep2|L4 Lar@ L4?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331300 OP398(official name : OP398 genotype : unc-119(ed3) III; wgIs398(dve-1::TY1EGFPFLAG C; unc-119(+)) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology and Genetics in Dresden description : using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The DVE-1::EGFP fusion protein is expressed in the correct dve-1 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the DVE-1 transcription factor. made_by : Unknown )|DVE-1_GFP_L4_ChIP_Rep2|L4 Lar@ L4?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331309 OP433(official name : OP433 genotype : unc-119(ed3) III; wgIs433(hlh-30::TY1 EGFP FLAG; unc-119(+)) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology and Genetics in Dresden description : using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The HLH-30::EGFP fusion protein is expressed in the correct hlh-30 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the HLH-30 transcription factor. made_by : Unknown )|HLH-30_GFP_L4_Input_Rep1|L4 Lar@ L4?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331310 OP433(official name : OP433 genotype : unc-119(ed3) III; wgIs433(hlh-30::TY1 EGFP FLAG; unc-119(+)) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology and Genetics in Dresden description : using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The HLH-30::EGFP fusion protein is expressed in the correct hlh-30 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the HLH-30 transcription factor. made_by : Unknown )|HLH-30_GFP_L4_ChIP_Rep1|L4 Lar@ L4?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331311 OP433(official name : OP433 genotype : unc-119(ed3) III; wgIs433(hlh-30::TY1 EGFP FLAG; unc-119(+)) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology and Genetics in Dresden description : using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The HLH-30::EGFP fusion protein is expressed in the correct hlh-30 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the HLH-30 transcription factor. made_by : Unknown )|HLH-30_GFP_L4_Input_Rep2|L4 Lar@ L4?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX331312 OP433(official name : OP433 genotype : unc-119(ed3) III; wgIs433(hlh-30::TY1 EGFP FLAG; unc-119(+)) outcross : 3 mutagen : Bombard tags : GFP::3xFlag description : This strain's transgene was constructed by Mihail Sarov at the Max Planck Institute for Cell Biology and Genetics in Dresden description : using Tony Hyman's recombineering pipeline. The resulting plasmid was used for biolistic transformation of an unc-119(ed3) strain. The HLH-30::EGFP fusion protein is expressed in the correct hlh-30 spatio-temporal expression pattern. This strain was used for ChIP-seq experiments to map the in vivo binding sites for the HLH-30 transcription factor. made_by : Unknown )|HLH-30_GFP_L4_ChIP_Rep2|L4 Lar@ L4?0 1 2 https://www.ncbi.nlm.nih.gov/sra?term=SRX113620 wild type|larval L4 stage C. elegans|larval L4 stage C. elegans Lar@ L4?0 1 2 https://www.ncbi.nlm.nih.gov/sra?term=SRX2163949 wild type Bristol N2|whole organism|L4 Lar@ L4?0 1 2 https://www.ncbi.nlm.nih.gov/sra?term=SRX2163950 rbr-2(tm3141)|whole organism|L4 Lar@ L4?0 1 2 https://www.ncbi.nlm.nih.gov/sra?term=SRX2965733 set-9::gfp_whole_worm|L4 Lar@ L4?0 1 2 https://www.ncbi.nlm.nih.gov/sra?term=SRX2965735 set-26::gfp_whole_worm|L4 Lar@ L4?0 1 2 https://www.ncbi.nlm.nih.gov/sra?term=SRX2965737 set-9::gfpset-26::gfp_whole_worm|L4 Lar@ L4?0 1 2 https://www.ncbi.nlm.nih.gov/sra?term=SRX2965739 mix_of_set-9::gfp/set-26::gfp_whole_worm|L4 Lar@ L4?0 1 2 https://www.ncbi.nlm.nih.gov/sra?term=SRX2973381 pooled_inputDNA|whole_worm|L4 Lar@ L4?0 1 2 https://www.ncbi.nlm.nih.gov/sra?term=SRX2973385 SET-26::GFP|whole_worm|L4 Lar@ L4?0 1 2 https://www.ncbi.nlm.nih.gov/sra?term=SRX2973387 SET-9::GFP SET-26::GFP|whole_worm|L4 Lar@ L4?0 1 2 https://www.ncbi.nlm.nih.gov/sra?term=SRX2973398 SET-9::GFP|whole_worm|L4 Lar@ L4?0 1 2 https://www.ncbi.nlm.nih.gov/sra?term=SRX395521 OP179|staged L4 larvae from OP179 (SNPC-4-GFP transgenic strain)|whole animal|L4 Lar@ L4?0 1 2 https://www.ncbi.nlm.nih.gov/sra?term=SRX7175088 whole worm|L4 stage hermaphrodite worms Lar@ L4?0 1 4 https://www.ncbi.nlm.nih.gov/sra?term=SRX2965743 set-9set-26_whole_worm|L4 Lar@ L4?0 1 4 https://www.ncbi.nlm.nih.gov/sra?term=SRX2973383 N2|whole_worm|L4 Lar@ L4?0 1 4 https://www.ncbi.nlm.nih.gov/sra?term=SRX2973389 set-9set-26|whole_worm|L4 Lar@ L4?0 1 4 https://www.ncbi.nlm.nih.gov/sra?term=SRX3583336 F1set9set26_whole_worm|L4 Lar@ L4?0 1 4 https://www.ncbi.nlm.nih.gov/sra?term=SRX3583338 F3set9set26_whole_worm|L4 Lar@ L4?0 1 4 https://www.ncbi.nlm.nih.gov/sra?term=SRX3583340 glp-1_whole_worm|L4 Lar@ L4?0 1 4 https://www.ncbi.nlm.nih.gov/sra?term=SRX3583342 glp-1; set-26_whole_worm|L4 Lar@ L4?0 1 4 https://www.ncbi.nlm.nih.gov/sra?term=SRX5064640 N2|whole worms|L4 Lar@ L4?0 1 6 https://www.ncbi.nlm.nih.gov/sra?term=SRX3733151 SS104 glp-4(bn2) I.|whole worm|L4 Lar@ L4?0 1 6 https://www.ncbi.nlm.nih.gov/sra?term=SRX3733157 N2|whole worm|L4 Lar@ L4?0 1 8 https://www.ncbi.nlm.nih.gov/sra?term=SRX1078711 pJK1689|Whole animal|L4 larva Lar@ L4?0 1 8 https://www.ncbi.nlm.nih.gov/sra?term=SRX1078725 pJK1662|Whole animal|L4 larva Lar@ L4?0 1 8 https://www.ncbi.nlm.nih.gov/sra?term=SRX2737086 N2 (wild-type)|whole body|L4 Lar@ L4?0 1 8 https://www.ncbi.nlm.nih.gov/sra?term=SRX3104605 Whole worms|L4 Lar@ L4?0 1 8 https://www.ncbi.nlm.nih.gov/sra?term=SRX4082342 N2|L4 larvae Lar@ L4?0 2 20 https://www.ncbi.nlm.nih.gov/sra?term=SRX4085409 wild-type N2|L4 larvae Lar@ L4?0 2 8 https://www.ncbi.nlm.nih.gov/sra?term=SRX3583334 N2_whole_worm|L4 Lar@ L4?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX2170085 N2|whole L4 stage wildtype C. elegans gDNA|L4 Lar@ L4?0 Lar@ L4?0 1 3 https://www.ncbi.nlm.nih.gov/sra?term=SRX2332995 N2|whole organisms|early embryo Emb@ Early embryo?0 Emb@ Early embryo?0 1 3 https://www.ncbi.nlm.nih.gov/sra?term=SRX2332996 N2|whole organisms|larval stage 3 Lar@ L3?0 Lar@ L3?0 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX2333004 N2|whole organisms|NA Unc@ Unclassified Adl@ Young adult?0 1 3 https://www.ncbi.nlm.nih.gov/sra?term=SRX2332997 N2|whole organisms|young adult Adl@ Young adult?0 Adl@ Young adult?0 1 6 https://www.ncbi.nlm.nih.gov/sra?term=SRX7687144 N2 - wild-type|isolated germline nuclei|Day 1 Adult Adl@ Germline cells?0 ? 1 6 https://www.ncbi.nlm.nih.gov/sra?term=SRX7687147 NL1810 - mut-16(pk710) I.|isolated germline nuclei|Day 1 Adult Adl@ Germline cells?0 ? 1 4 https://www.ncbi.nlm.nih.gov/sra?term=SRX2969570 Sorted L1 PGCs|Starved L1 Lar@ Germline cells?0 Lar@ L1?0 1 2 https://www.ncbi.nlm.nih.gov/sra?term=SRX3141082 stage L3|whole worms Lar@ L3?0 Lar@ L3?0 1 14 https://www.ncbi.nlm.nih.gov/sra?term=SRX003816 wild-type N2 Unc@ Unclassified 1 1 https://www.ncbi.nlm.nih.gov/sra?term=ERX1270342 ERS1026566 Unc@ Unclassified 1 1 https://www.ncbi.nlm.nih.gov/sra?term=ERX1270343 ERS1026567 Unc@ Unclassified 1 1 https://www.ncbi.nlm.nih.gov/sra?term=ERX1270344 ERS1026568 Unc@ Unclassified 1 1 https://www.ncbi.nlm.nih.gov/sra?term=ERX1999196 SX1316-ChIP-1|ERS1671236 Unc@ Unclassified 1 1 https://www.ncbi.nlm.nih.gov/sra?term=ERX1999197 SX1316-ChIP-2|ERS1671237 Unc@ Unclassified 1 1 https://www.ncbi.nlm.nih.gov/sra?term=ERX1999198 SX1316-ChIP-3|ERS1671238 Unc@ Unclassified 1 1 https://www.ncbi.nlm.nih.gov/sra?term=ERX1999199 ERS1671239 Unc@ Unclassified 1 1 https://www.ncbi.nlm.nih.gov/sra?term=ERX1999200 ERS1671240 Unc@ Unclassified 1 1 https://www.ncbi.nlm.nih.gov/sra?term=ERX1999201 ERS1671241 Unc@ Unclassified 1 1 https://www.ncbi.nlm.nih.gov/sra?term=ERX1999202 ERS1671242 Unc@ Unclassified 1 1 https://www.ncbi.nlm.nih.gov/sra?term=ERX1999203 ERS1671243 Unc@ Unclassified 1 1 https://www.ncbi.nlm.nih.gov/sra?term=ERX1999204 ERS1671244 Unc@ Unclassified 1 1 https://www.ncbi.nlm.nih.gov/sra?term=ERX1999205 ERS1671245 Unc@ Unclassified 1 1 https://www.ncbi.nlm.nih.gov/sra?term=ERX1999206 ERS1671246 Unc@ Unclassified 1 1 https://www.ncbi.nlm.nih.gov/sra?term=ERX1999207 SX2000-input-2|ERS1671247 Unc@ Unclassified 1 1 https://www.ncbi.nlm.nih.gov/sra?term=ERX1999208 SX2000-input-3|ERS1671248 Unc@ Unclassified 1 1 https://www.ncbi.nlm.nih.gov/sra?term=ERX1999209 SX2000-input-4|ERS1671249 Unc@ Unclassified 1 1 https://www.ncbi.nlm.nih.gov/sra?term=ERX1999210 ERS1671250 Unc@ Unclassified 1 1 https://www.ncbi.nlm.nih.gov/sra?term=ERX1999211 ERS1671251 Unc@ Unclassified 1 1 https://www.ncbi.nlm.nih.gov/sra?term=ERX1999212 ERS1671252 Unc@ Unclassified 1 1 https://www.ncbi.nlm.nih.gov/sra?term=ERX1999213 ERS1671253 Unc@ Unclassified 1 1 https://www.ncbi.nlm.nih.gov/sra?term=ERX1999214 ERS1671254 Unc@ Unclassified 1 1 https://www.ncbi.nlm.nih.gov/sra?term=ERX1999215 ERS1671255 Unc@ Unclassified 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX216728 GR1895|daf-2_DAF-16::GFP_IN Unc@ Unclassified 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX216729 GR1900|daf-2_SWSN-1::GFP_IN Unc@ Unclassified 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX216753 GR1895|daf-2_DAF-16::GFP_IP Unc@ Unclassified 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX216754 GR1907|daf-2_swsn-1_DAF-16::GFP_IN Unc@ Unclassified 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX216755 GR1907|daf-2_swsn-1_DAF-16::GFP_IP Unc@ Unclassified 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX216757 GR1900|daf-2_SWSN-1::GFP_IP Unc@ Unclassified 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX216758 GR1909|daf-2_daf-16_SWSN-1::GFP_IN Unc@ Unclassified 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX216759 GR1909|daf-2_daf-16_SWSN-1::GFP_IP Unc@ Unclassified 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX216761 GR1908|daf-2_SWSN-4::GFP_IN Unc@ Unclassified 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX216762 GR1908|daf-2_SWSN-4::GFP_IP Unc@ Unclassified 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX216763 GR1910|daf-2_daf-16_SWSN-4::GFP_IN Unc@ Unclassified 1 1 https://www.ncbi.nlm.nih.gov/sra?term=SRX216764 GR1910|daf-2_daf-16_SWSN-4::GFP_IP Unc@ Unclassified 1 2 https://www.ncbi.nlm.nih.gov/sra?term=SRX796306 daf-2 (e1370)|mix stage culture|Mix Culture Unc@ Unclassified 1 3 https://www.ncbi.nlm.nih.gov/sra?term=SRX278065 missing Unc@ Unclassified 1 5 https://www.ncbi.nlm.nih.gov/sra?term=SRX2710283 N2|N2 L1 Arrest|L1 Arrest Unc@ Unclassified 1 5 https://www.ncbi.nlm.nih.gov/sra?term=SRX278067 N2 Unc@ Unclassified 1 5 https://www.ncbi.nlm.nih.gov/sra?term=SRX560679 HML214|Whoel animal extract|GFP Unc@ Unclassified 1 6 https://www.ncbi.nlm.nih.gov/sra?term=SRX997747 mix stage culture|Mix Culture Unc@ Unclassified 1 14 https://www.ncbi.nlm.nih.gov/sra?term=SRX3029121 whole worms|whole body|L4 Lar@ L4?0 Adl@ Whole worm?0 1 3 https://www.ncbi.nlm.nih.gov/sra?term=SRX4029336 worm gonads|worm gonads Lar@ Gonads?0 ?