Job ID = 14520280 SRX = SRX8421776 Genome = sacCer3 sra ファイルのダウンロード中... Read layout: SINGLE fastq に変換中... Read 6657792 spots for SRR11872069/SRR11872069.sra Written 6657792 spots for SRR11872069/SRR11872069.sra 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: 00:01:52 6657792 reads; of these: 6657792 (100.00%) were unpaired; of these: 235757 (3.54%) aligned 0 times 4269605 (64.13%) aligned exactly 1 time 2152430 (32.33%) aligned >1 times 96.46% overall alignment rate Time searching: 00:01:52 Overall time: 00:01:52 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_rmdupse_core] 3173355 / 6422035 = 0.4941 in library ' ' BAM に変換しました。 Bed ファイルを作成中... WARNING: Skipping mount /opt/pkg/singularity/3.8.3/var/singularity/mnt/session/etc/resolv.conf [files]: /etc/resolv.conf doesn't exist in container INFO @ Sat, 15 Jan 2022 18:53:58: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/SRX8421776/SRX8421776.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/SRX8421776/SRX8421776.05 -q 1e-05 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/SRX8421776/SRX8421776.05 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/SRX8421776/SRX8421776.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 @ Sat, 15 Jan 2022 18:53:58: #1 read tag files... INFO @ Sat, 15 Jan 2022 18:53:58: #1 read treatment tags... INFO @ Sat, 15 Jan 2022 18:54:06: 1000000 INFO @ Sat, 15 Jan 2022 18:54:13: 2000000 INFO @ Sat, 15 Jan 2022 18:54:20: 3000000 INFO @ Sat, 15 Jan 2022 18:54:22: #1 tag size is determined as 101 bps INFO @ Sat, 15 Jan 2022 18:54:22: #1 tag size = 101 INFO @ Sat, 15 Jan 2022 18:54:22: #1 total tags in treatment: 3248680 INFO @ Sat, 15 Jan 2022 18:54:22: #1 user defined the maximum tags... INFO @ Sat, 15 Jan 2022 18:54:22: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Sat, 15 Jan 2022 18:54:22: #1 tags after filtering in treatment: 3248680 INFO @ Sat, 15 Jan 2022 18:54:22: #1 Redundant rate of treatment: 0.00 INFO @ Sat, 15 Jan 2022 18:54:22: #1 finished! INFO @ Sat, 15 Jan 2022 18:54:22: #2 Build Peak Model... INFO @ Sat, 15 Jan 2022 18:54:22: #2 looking for paired plus/minus strand peaks... INFO @ Sat, 15 Jan 2022 18:54:22: #2 number of paired peaks: 154 WARNING @ Sat, 15 Jan 2022 18:54:22: Fewer paired peaks (154) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 154 pairs to build model! INFO @ Sat, 15 Jan 2022 18:54:22: start model_add_line... INFO @ Sat, 15 Jan 2022 18:54:22: start X-correlation... INFO @ Sat, 15 Jan 2022 18:54:22: end of X-cor INFO @ Sat, 15 Jan 2022 18:54:22: #2 finished! INFO @ Sat, 15 Jan 2022 18:54:22: #2 predicted fragment length is 1 bps INFO @ Sat, 15 Jan 2022 18:54:22: #2 alternative fragment length(s) may be 1,16,23,54,83,125,155,175,179,200,224,293 bps INFO @ Sat, 15 Jan 2022 18:54:22: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/sacCer3/SRX8421776/SRX8421776.05_model.r WARNING @ Sat, 15 Jan 2022 18:54:22: #2 Since the d (1) calculated from paired-peaks are smaller than 2*tag length, it may be influenced by unknown sequencing problem! WARNING @ Sat, 15 Jan 2022 18:54:22: #2 You may need to consider one of the other alternative d(s): 1,16,23,54,83,125,155,175,179,200,224,293 WARNING @ Sat, 15 Jan 2022 18:54:22: #2 You can restart the process with --nomodel --extsize XXX with your choice or an arbitrary number. Nontheless, MACS will continute computing. INFO @ Sat, 15 Jan 2022 18:54:22: #3 Call peaks... INFO @ Sat, 15 Jan 2022 18:54:22: #3 Pre-compute pvalue-qvalue table... WARNING: Skipping mount /opt/pkg/singularity/3.8.3/var/singularity/mnt/session/etc/resolv.conf [files]: /etc/resolv.conf doesn't exist in container INFO @ Sat, 15 Jan 2022 18:54:26: #3 Call peaks for each chromosome... INFO @ Sat, 15 Jan 2022 18:54:28: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/SRX8421776/SRX8421776.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/SRX8421776/SRX8421776.10 -q 1e-10 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/SRX8421776/SRX8421776.10 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/SRX8421776/SRX8421776.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 @ Sat, 15 Jan 2022 18:54:28: #1 read tag files... INFO @ Sat, 15 Jan 2022 18:54:28: #1 read treatment tags... INFO @ Sat, 15 Jan 2022 18:54:28: #4 Write output xls file... /home/okishinya/chipatlas/results/sacCer3/SRX8421776/SRX8421776.05_peaks.xls INFO @ Sat, 15 Jan 2022 18:54:28: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/sacCer3/SRX8421776/SRX8421776.05_peaks.narrowPeak INFO @ Sat, 15 Jan 2022 18:54:28: #4 Write summits bed file... /home/okishinya/chipatlas/results/sacCer3/SRX8421776/SRX8421776.05_summits.bed INFO @ Sat, 15 Jan 2022 18:54:28: Done! pass1 - making usageList (0 chroms): 1 millis needLargeMem: trying to allocate 0 bytes (limit: 17179869184) CompletedMACS2peakCalling INFO @ Sat, 15 Jan 2022 18:54:36: 1000000 INFO @ Sat, 15 Jan 2022 18:54:44: 2000000 INFO @ Sat, 15 Jan 2022 18:54:50: 3000000 INFO @ Sat, 15 Jan 2022 18:54:51: #1 tag size is determined as 101 bps INFO @ Sat, 15 Jan 2022 18:54:51: #1 tag size = 101 INFO @ Sat, 15 Jan 2022 18:54:51: #1 total tags in treatment: 3248680 INFO @ Sat, 15 Jan 2022 18:54:51: #1 user defined the maximum tags... INFO @ Sat, 15 Jan 2022 18:54:51: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Sat, 15 Jan 2022 18:54:52: #1 tags after filtering in treatment: 3248680 INFO @ Sat, 15 Jan 2022 18:54:52: #1 Redundant rate of treatment: 0.00 INFO @ Sat, 15 Jan 2022 18:54:52: #1 finished! INFO @ Sat, 15 Jan 2022 18:54:52: #2 Build Peak Model... INFO @ Sat, 15 Jan 2022 18:54:52: #2 looking for paired plus/minus strand peaks... INFO @ Sat, 15 Jan 2022 18:54:52: #2 number of paired peaks: 154 WARNING @ Sat, 15 Jan 2022 18:54:52: Fewer paired peaks (154) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 154 pairs to build model! INFO @ Sat, 15 Jan 2022 18:54:52: start model_add_line... INFO @ Sat, 15 Jan 2022 18:54:52: start X-correlation... INFO @ Sat, 15 Jan 2022 18:54:52: end of X-cor INFO @ Sat, 15 Jan 2022 18:54:52: #2 finished! INFO @ Sat, 15 Jan 2022 18:54:52: #2 predicted fragment length is 1 bps INFO @ Sat, 15 Jan 2022 18:54:52: #2 alternative fragment length(s) may be 1,16,23,54,83,125,155,175,179,200,224,293 bps INFO @ Sat, 15 Jan 2022 18:54:52: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/sacCer3/SRX8421776/SRX8421776.10_model.r WARNING @ Sat, 15 Jan 2022 18:54:52: #2 Since the d (1) calculated from paired-peaks are smaller than 2*tag length, it may be influenced by unknown sequencing problem! WARNING @ Sat, 15 Jan 2022 18:54:52: #2 You may need to consider one of the other alternative d(s): 1,16,23,54,83,125,155,175,179,200,224,293 WARNING @ Sat, 15 Jan 2022 18:54:52: #2 You can restart the process with --nomodel --extsize XXX with your choice or an arbitrary number. Nontheless, MACS will continute computing. INFO @ Sat, 15 Jan 2022 18:54:52: #3 Call peaks... INFO @ Sat, 15 Jan 2022 18:54:52: #3 Pre-compute pvalue-qvalue table... INFO @ Sat, 15 Jan 2022 18:54:56: #3 Call peaks for each chromosome... BedGraph に変換中... WARNING: Skipping mount /opt/pkg/singularity/3.8.3/var/singularity/mnt/session/etc/resolv.conf [files]: /etc/resolv.conf doesn't exist in container INFO @ Sat, 15 Jan 2022 18:54:58: #4 Write output xls file... /home/okishinya/chipatlas/results/sacCer3/SRX8421776/SRX8421776.10_peaks.xls INFO @ Sat, 15 Jan 2022 18:54:58: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/sacCer3/SRX8421776/SRX8421776.10_peaks.narrowPeak INFO @ Sat, 15 Jan 2022 18:54:58: #4 Write summits bed file... /home/okishinya/chipatlas/results/sacCer3/SRX8421776/SRX8421776.10_summits.bed INFO @ Sat, 15 Jan 2022 18:54:58: Done! INFO @ Sat, 15 Jan 2022 18:54:58: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/SRX8421776/SRX8421776.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/SRX8421776/SRX8421776.20 -q 1e-20 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/SRX8421776/SRX8421776.20 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/SRX8421776/SRX8421776.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 @ Sat, 15 Jan 2022 18:54:58: #1 read tag files... INFO @ Sat, 15 Jan 2022 18:54:58: #1 read treatment tags... pass1 - making usageList (0 chroms): 1 millis needLargeMem: trying to allocate 0 bytes (limit: 17179869184) CompletedMACS2peakCalling INFO @ Sat, 15 Jan 2022 18:55:06: 1000000 INFO @ Sat, 15 Jan 2022 18:55:13: 2000000 BedGraph に変換しました。 BigWig に変換中... INFO @ Sat, 15 Jan 2022 18:55:21: 3000000 INFO @ Sat, 15 Jan 2022 18:55:23: #1 tag size is determined as 101 bps INFO @ Sat, 15 Jan 2022 18:55:23: #1 tag size = 101 INFO @ Sat, 15 Jan 2022 18:55:23: #1 total tags in treatment: 3248680 INFO @ Sat, 15 Jan 2022 18:55:23: #1 user defined the maximum tags... INFO @ Sat, 15 Jan 2022 18:55:23: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Sat, 15 Jan 2022 18:55:23: #1 tags after filtering in treatment: 3248680 INFO @ Sat, 15 Jan 2022 18:55:23: #1 Redundant rate of treatment: 0.00 INFO @ Sat, 15 Jan 2022 18:55:23: #1 finished! INFO @ Sat, 15 Jan 2022 18:55:23: #2 Build Peak Model... INFO @ Sat, 15 Jan 2022 18:55:23: #2 looking for paired plus/minus strand peaks... INFO @ Sat, 15 Jan 2022 18:55:23: #2 number of paired peaks: 154 WARNING @ Sat, 15 Jan 2022 18:55:23: Fewer paired peaks (154) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 154 pairs to build model! INFO @ Sat, 15 Jan 2022 18:55:23: start model_add_line... INFO @ Sat, 15 Jan 2022 18:55:23: start X-correlation... INFO @ Sat, 15 Jan 2022 18:55:23: end of X-cor INFO @ Sat, 15 Jan 2022 18:55:23: #2 finished! INFO @ Sat, 15 Jan 2022 18:55:23: #2 predicted fragment length is 1 bps INFO @ Sat, 15 Jan 2022 18:55:23: #2 alternative fragment length(s) may be 1,16,23,54,83,125,155,175,179,200,224,293 bps INFO @ Sat, 15 Jan 2022 18:55:23: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/sacCer3/SRX8421776/SRX8421776.20_model.r WARNING @ Sat, 15 Jan 2022 18:55:23: #2 Since the d (1) calculated from paired-peaks are smaller than 2*tag length, it may be influenced by unknown sequencing problem! WARNING @ Sat, 15 Jan 2022 18:55:23: #2 You may need to consider one of the other alternative d(s): 1,16,23,54,83,125,155,175,179,200,224,293 WARNING @ Sat, 15 Jan 2022 18:55:23: #2 You can restart the process with --nomodel --extsize XXX with your choice or an arbitrary number. Nontheless, MACS will continute computing. INFO @ Sat, 15 Jan 2022 18:55:23: #3 Call peaks... INFO @ Sat, 15 Jan 2022 18:55:23: #3 Pre-compute pvalue-qvalue table... BigWig に変換しました。 INFO @ Sat, 15 Jan 2022 18:55:27: #3 Call peaks for each chromosome... INFO @ Sat, 15 Jan 2022 18:55:29: #4 Write output xls file... /home/okishinya/chipatlas/results/sacCer3/SRX8421776/SRX8421776.20_peaks.xls INFO @ Sat, 15 Jan 2022 18:55:29: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/sacCer3/SRX8421776/SRX8421776.20_peaks.narrowPeak INFO @ Sat, 15 Jan 2022 18:55:29: #4 Write summits bed file... /home/okishinya/chipatlas/results/sacCer3/SRX8421776/SRX8421776.20_summits.bed INFO @ Sat, 15 Jan 2022 18:55:29: Done! pass1 - making usageList (0 chroms): 1 millis needLargeMem: trying to allocate 0 bytes (limit: 17179869184) CompletedMACS2peakCalling