Job ID = 2007729 sra ファイルのダウンロード中... Read layout: PAIRED fastq に変換中... spots read : 55,313 reads read : 110,626 reads written : 110,626 rm: cannot remove ‘[DSE]RR*’: No such file or directory fastq に変換しました。 bowtie でマッピング中... Time loading reference: 00:00:00 Time loading forward index: 00:00:00 Time loading mirror index: 00:00:00 Multiseed full-index search: 00:00:02 55313 reads; of these: 55313 (100.00%) were paired; of these: 5229 (9.45%) aligned concordantly 0 times 46103 (83.35%) aligned concordantly exactly 1 time 3981 (7.20%) aligned concordantly >1 times ---- 5229 pairs aligned concordantly 0 times; of these: 2962 (56.65%) aligned discordantly 1 time ---- 2267 pairs aligned 0 times concordantly or discordantly; of these: 4534 mates make up the pairs; of these: 2702 (59.59%) aligned 0 times 1140 (25.14%) aligned exactly 1 time 692 (15.26%) aligned >1 times 97.56% overall alignment rate Time searching: 00:00:02 Overall time: 00:00:02 マッピングが完了しました。 samtools でBAM に変換中... [samopen] SAM header is present: 17 sequences. [bam_rmdup_core] processing reference chrI... [bam_rmdup_core] processing reference chrII... [bam_rmdup_core] processing reference chrIII... [bam_rmdup_core] processing reference chrIV... [bam_rmdup_core] processing reference chrIX... [bam_rmdup_core] processing reference chrM... [bam_rmdup_core] processing reference chrV... [bam_rmdup_core] processing reference chrVI... [bam_rmdup_core] processing reference chrVII... [bam_rmdup_core] processing reference chrVIII... [bam_rmdup_core] processing reference chrX... [bam_rmdup_core] processing reference chrXI... [bam_rmdup_core] processing reference chrXII... [bam_rmdup_core] processing reference chrXIII... [bam_rmdup_core] processing reference chrXIV... [bam_rmdup_core] processing reference chrXV... [bam_rmdup_core] processing reference chrXVI... [bam_rmdup_core] 63 / 52066 = 0.0012 in library ' ' BAM に変換しました。 Bed ファイルを作成中... BedGraph に変換中... INFO @ Fri, 05 Jul 2019 16:24:13: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/ERX433677/ERX433677.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/ERX433677/ERX433677.05 -q 1e-05 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/ERX433677/ERX433677.05 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/ERX433677/ERX433677.bam'] # control file = None # effective genome size = 1.21e+07 # band width = 300 # model fold = [5, 50] # qvalue cutoff = 1.00e-05 # Larger dataset will be scaled towards smaller dataset. # Range for calculating regional lambda is: 10000 bps # Broad region calling is off # Paired-End mode is off INFO @ Fri, 05 Jul 2019 16:24:13: #1 read tag files... INFO @ Fri, 05 Jul 2019 16:24:13: #1 read treatment tags... INFO @ Fri, 05 Jul 2019 16:24:14: #1 tag size is determined as 25 bps INFO @ Fri, 05 Jul 2019 16:24:14: #1 tag size = 25 INFO @ Fri, 05 Jul 2019 16:24:14: #1 total tags in treatment: 50023 INFO @ Fri, 05 Jul 2019 16:24:14: #1 user defined the maximum tags... INFO @ Fri, 05 Jul 2019 16:24:14: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Fri, 05 Jul 2019 16:24:14: #1 tags after filtering in treatment: 49843 INFO @ Fri, 05 Jul 2019 16:24:14: #1 Redundant rate of treatment: 0.00 INFO @ Fri, 05 Jul 2019 16:24:14: #1 finished! INFO @ Fri, 05 Jul 2019 16:24:14: #2 Build Peak Model... INFO @ Fri, 05 Jul 2019 16:24:14: #2 looking for paired plus/minus strand peaks... INFO @ Fri, 05 Jul 2019 16:24:14: #2 number of paired peaks: 384 WARNING @ Fri, 05 Jul 2019 16:24:14: Fewer paired peaks (384) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 384 pairs to build model! INFO @ Fri, 05 Jul 2019 16:24:14: start model_add_line... INFO @ Fri, 05 Jul 2019 16:24:14: start X-correlation... INFO @ Fri, 05 Jul 2019 16:24:14: end of X-cor INFO @ Fri, 05 Jul 2019 16:24:14: #2 finished! INFO @ Fri, 05 Jul 2019 16:24:14: #2 predicted fragment length is 284 bps INFO @ Fri, 05 Jul 2019 16:24:14: #2 alternative fragment length(s) may be 11,71,213,228,255,284,309,358,445,534 bps INFO @ Fri, 05 Jul 2019 16:24:14: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/sacCer3/ERX433677/ERX433677.05_model.r INFO @ Fri, 05 Jul 2019 16:24:14: #3 Call peaks... INFO @ Fri, 05 Jul 2019 16:24:14: #3 Pre-compute pvalue-qvalue table... INFO @ Fri, 05 Jul 2019 16:24:14: #3 Call peaks for each chromosome... INFO @ Fri, 05 Jul 2019 16:24:14: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/ERX433677/ERX433677.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/ERX433677/ERX433677.10 -q 1e-10 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/ERX433677/ERX433677.10 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/ERX433677/ERX433677.bam'] # control file = None # effective genome size = 1.21e+07 # band width = 300 # model fold = [5, 50] # qvalue cutoff = 1.00e-10 # Larger dataset will be scaled towards smaller dataset. # Range for calculating regional lambda is: 10000 bps # Broad region calling is off # Paired-End mode is off INFO @ Fri, 05 Jul 2019 16:24:14: #1 read tag files... INFO @ Fri, 05 Jul 2019 16:24:14: #1 read treatment tags... INFO @ Fri, 05 Jul 2019 16:24:14: #4 Write output xls file... /home/okishinya/chipatlas/results/sacCer3/ERX433677/ERX433677.05_peaks.xls INFO @ Fri, 05 Jul 2019 16:24:14: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/sacCer3/ERX433677/ERX433677.05_peaks.narrowPeak INFO @ Fri, 05 Jul 2019 16:24:14: #4 Write summits bed file... /home/okishinya/chipatlas/results/sacCer3/ERX433677/ERX433677.05_summits.bed INFO @ Fri, 05 Jul 2019 16:24:14: Done! pass1 - making usageList (12 chroms): 1 millis pass2 - checking and writing primary data (26 records, 4 fields): 2 millis BedGraph に変換しました。 BigWig に変換中... BigWig に変換しました。 INFO @ Fri, 05 Jul 2019 16:24:15: #1 tag size is determined as 25 bps INFO @ Fri, 05 Jul 2019 16:24:15: #1 tag size = 25 INFO @ Fri, 05 Jul 2019 16:24:15: #1 total tags in treatment: 50023 INFO @ Fri, 05 Jul 2019 16:24:15: #1 user defined the maximum tags... INFO @ Fri, 05 Jul 2019 16:24:15: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Fri, 05 Jul 2019 16:24:15: #1 tags after filtering in treatment: 49843 INFO @ Fri, 05 Jul 2019 16:24:15: #1 Redundant rate of treatment: 0.00 INFO @ Fri, 05 Jul 2019 16:24:15: #1 finished! INFO @ Fri, 05 Jul 2019 16:24:15: #2 Build Peak Model... INFO @ Fri, 05 Jul 2019 16:24:15: #2 looking for paired plus/minus strand peaks... INFO @ Fri, 05 Jul 2019 16:24:15: #2 number of paired peaks: 384 WARNING @ Fri, 05 Jul 2019 16:24:15: Fewer paired peaks (384) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 384 pairs to build model! INFO @ Fri, 05 Jul 2019 16:24:15: start model_add_line... INFO @ Fri, 05 Jul 2019 16:24:15: start X-correlation... INFO @ Fri, 05 Jul 2019 16:24:15: end of X-cor INFO @ Fri, 05 Jul 2019 16:24:15: #2 finished! INFO @ Fri, 05 Jul 2019 16:24:15: #2 predicted fragment length is 284 bps INFO @ Fri, 05 Jul 2019 16:24:15: #2 alternative fragment length(s) may be 11,71,213,228,255,284,309,358,445,534 bps INFO @ Fri, 05 Jul 2019 16:24:15: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/sacCer3/ERX433677/ERX433677.10_model.r INFO @ Fri, 05 Jul 2019 16:24:15: #3 Call peaks... INFO @ Fri, 05 Jul 2019 16:24:15: #3 Pre-compute pvalue-qvalue table... INFO @ Fri, 05 Jul 2019 16:24:15: #3 Call peaks for each chromosome... INFO @ Fri, 05 Jul 2019 16:24:15: #4 Write output xls file... /home/okishinya/chipatlas/results/sacCer3/ERX433677/ERX433677.10_peaks.xls INFO @ Fri, 05 Jul 2019 16:24:15: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/sacCer3/ERX433677/ERX433677.10_peaks.narrowPeak INFO @ Fri, 05 Jul 2019 16:24:15: #4 Write summits bed file... /home/okishinya/chipatlas/results/sacCer3/ERX433677/ERX433677.10_summits.bed INFO @ Fri, 05 Jul 2019 16:24:15: Done! INFO @ Fri, 05 Jul 2019 16:24:15: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/ERX433677/ERX433677.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/ERX433677/ERX433677.20 -q 1e-20 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/ERX433677/ERX433677.20 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/ERX433677/ERX433677.bam'] # control file = None # effective genome size = 1.21e+07 # band width = 300 # model fold = [5, 50] # qvalue cutoff = 1.00e-20 # Larger dataset will be scaled towards smaller dataset. # Range for calculating regional lambda is: 10000 bps # Broad region calling is off # Paired-End mode is off INFO @ Fri, 05 Jul 2019 16:24:15: #1 read tag files... INFO @ Fri, 05 Jul 2019 16:24:15: #1 read treatment tags... pass1 - making usageList (5 chroms): 1 millis pass2 - checking and writing primary data (5 records, 4 fields): 2 millis INFO @ Fri, 05 Jul 2019 16:24:16: #1 tag size is determined as 25 bps INFO @ Fri, 05 Jul 2019 16:24:16: #1 tag size = 25 INFO @ Fri, 05 Jul 2019 16:24:16: #1 total tags in treatment: 50023 INFO @ Fri, 05 Jul 2019 16:24:16: #1 user defined the maximum tags... INFO @ Fri, 05 Jul 2019 16:24:16: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Fri, 05 Jul 2019 16:24:16: #1 tags after filtering in treatment: 49843 INFO @ Fri, 05 Jul 2019 16:24:16: #1 Redundant rate of treatment: 0.00 INFO @ Fri, 05 Jul 2019 16:24:16: #1 finished! INFO @ Fri, 05 Jul 2019 16:24:16: #2 Build Peak Model... INFO @ Fri, 05 Jul 2019 16:24:16: #2 looking for paired plus/minus strand peaks... INFO @ Fri, 05 Jul 2019 16:24:16: #2 number of paired peaks: 384 WARNING @ Fri, 05 Jul 2019 16:24:16: Fewer paired peaks (384) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 384 pairs to build model! INFO @ Fri, 05 Jul 2019 16:24:16: start model_add_line... INFO @ Fri, 05 Jul 2019 16:24:16: start X-correlation... INFO @ Fri, 05 Jul 2019 16:24:16: end of X-cor INFO @ Fri, 05 Jul 2019 16:24:16: #2 finished! INFO @ Fri, 05 Jul 2019 16:24:16: #2 predicted fragment length is 284 bps INFO @ Fri, 05 Jul 2019 16:24:16: #2 alternative fragment length(s) may be 11,71,213,228,255,284,309,358,445,534 bps INFO @ Fri, 05 Jul 2019 16:24:16: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/sacCer3/ERX433677/ERX433677.20_model.r INFO @ Fri, 05 Jul 2019 16:24:16: #3 Call peaks... INFO @ Fri, 05 Jul 2019 16:24:16: #3 Pre-compute pvalue-qvalue table... INFO @ Fri, 05 Jul 2019 16:24:16: #3 Call peaks for each chromosome... INFO @ Fri, 05 Jul 2019 16:24:16: #4 Write output xls file... /home/okishinya/chipatlas/results/sacCer3/ERX433677/ERX433677.20_peaks.xls INFO @ Fri, 05 Jul 2019 16:24:16: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/sacCer3/ERX433677/ERX433677.20_peaks.narrowPeak INFO @ Fri, 05 Jul 2019 16:24:16: #4 Write summits bed file... /home/okishinya/chipatlas/results/sacCer3/ERX433677/ERX433677.20_summits.bed INFO @ Fri, 05 Jul 2019 16:24:16: Done! pass1 - making usageList (1 chroms): 1 millis pass2 - checking and writing primary data (1 records, 4 fields): 1 millis CompletedMACS2peakCalling CompletedMACS2peakCalling CompletedMACS2peakCalling