Job ID = 6626423 SRX = SRX7630545 Genome = ce10 sra ファイルのダウンロード中... Read layout: SINGLE fastq に変換中... Read 25067172 spots for SRR10964907/SRR10964907.sra Written 25067172 spots for SRR10964907/SRR10964907.sra fastq に変換しました。 bowtie でマッピング中... Your job 6626568 ("srTce11") has been submitted Time loading reference: 00:00:00 Time loading forward index: 00:00:00 Time loading mirror index: 00:00:00 Multiseed full-index search: 00:01:53 25067172 reads; of these: 25067172 (100.00%) were unpaired; of these: 23561955 (94.00%) aligned 0 times 1256804 (5.01%) aligned exactly 1 time 248413 (0.99%) aligned >1 times 6.00% overall alignment rate Time searching: 00:01:53 Overall time: 00:01:53 マッピングが完了しました。 samtools でBAM に変換中... [samopen] SAM header is present: 7 sequences. [bam_rmdupse_core] 385546 / 1505217 = 0.2561 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/3.5.2/var/singularity/mnt/session/etc/resolv.conf [files]: /etc/resolv.conf doesn't exist in container INFO @ Tue, 14 Jul 2020 07:04:22: # Command line: callpeak -t /home/okishinya/chipatlas/results/ce10/SRX7630545/SRX7630545.bam -f BAM -g ce -n /home/okishinya/chipatlas/results/ce10/SRX7630545/SRX7630545.05 -q 1e-05 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/ce10/SRX7630545/SRX7630545.05 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/ce10/SRX7630545/SRX7630545.bam'] # control file = None # effective genome size = 9.00e+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 @ Tue, 14 Jul 2020 07:04:22: #1 read tag files... INFO @ Tue, 14 Jul 2020 07:04:22: #1 read treatment tags... INFO @ Tue, 14 Jul 2020 07:04:27: 1000000 INFO @ Tue, 14 Jul 2020 07:04:28: #1 tag size is determined as 51 bps INFO @ Tue, 14 Jul 2020 07:04:28: #1 tag size = 51 INFO @ Tue, 14 Jul 2020 07:04:28: #1 total tags in treatment: 1119671 INFO @ Tue, 14 Jul 2020 07:04:28: #1 user defined the maximum tags... INFO @ Tue, 14 Jul 2020 07:04:28: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Tue, 14 Jul 2020 07:04:28: #1 tags after filtering in treatment: 1119671 INFO @ Tue, 14 Jul 2020 07:04:28: #1 Redundant rate of treatment: 0.00 INFO @ Tue, 14 Jul 2020 07:04:28: #1 finished! INFO @ Tue, 14 Jul 2020 07:04:28: #2 Build Peak Model... INFO @ Tue, 14 Jul 2020 07:04:28: #2 looking for paired plus/minus strand peaks... INFO @ Tue, 14 Jul 2020 07:04:28: #2 number of paired peaks: 411 WARNING @ Tue, 14 Jul 2020 07:04:28: Fewer paired peaks (411) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 411 pairs to build model! INFO @ Tue, 14 Jul 2020 07:04:28: start model_add_line... INFO @ Tue, 14 Jul 2020 07:04:28: start X-correlation... INFO @ Tue, 14 Jul 2020 07:04:28: end of X-cor INFO @ Tue, 14 Jul 2020 07:04:28: #2 finished! INFO @ Tue, 14 Jul 2020 07:04:28: #2 predicted fragment length is 52 bps INFO @ Tue, 14 Jul 2020 07:04:28: #2 alternative fragment length(s) may be 52,240,423,456,474,538 bps INFO @ Tue, 14 Jul 2020 07:04:28: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/ce10/SRX7630545/SRX7630545.05_model.r WARNING @ Tue, 14 Jul 2020 07:04:28: #2 Since the d (52) calculated from paired-peaks are smaller than 2*tag length, it may be influenced by unknown sequencing problem! WARNING @ Tue, 14 Jul 2020 07:04:28: #2 You may need to consider one of the other alternative d(s): 52,240,423,456,474,538 WARNING @ Tue, 14 Jul 2020 07:04:28: #2 You can restart the process with --nomodel --extsize XXX with your choice or an arbitrary number. Nontheless, MACS will continute computing. INFO @ Tue, 14 Jul 2020 07:04:28: #3 Call peaks... INFO @ Tue, 14 Jul 2020 07:04:28: #3 Pre-compute pvalue-qvalue table... INFO @ Tue, 14 Jul 2020 07:04:31: #3 Call peaks for each chromosome... INFO @ Tue, 14 Jul 2020 07:04:32: #4 Write output xls file... /home/okishinya/chipatlas/results/ce10/SRX7630545/SRX7630545.05_peaks.xls INFO @ Tue, 14 Jul 2020 07:04:32: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/ce10/SRX7630545/SRX7630545.05_peaks.narrowPeak INFO @ Tue, 14 Jul 2020 07:04:32: #4 Write summits bed file... /home/okishinya/chipatlas/results/ce10/SRX7630545/SRX7630545.05_summits.bed INFO @ Tue, 14 Jul 2020 07:04:32: Done! pass1 - making usageList (6 chroms): 1 millis pass2 - checking and writing primary data (248 records, 4 fields): 53 millis CompletedMACS2peakCalling WARNING: Skipping mount /opt/pkg/singularity/3.5.2/var/singularity/mnt/session/etc/resolv.conf [files]: /etc/resolv.conf doesn't exist in container INFO @ Tue, 14 Jul 2020 07:04:51: # Command line: callpeak -t /home/okishinya/chipatlas/results/ce10/SRX7630545/SRX7630545.bam -f BAM -g ce -n /home/okishinya/chipatlas/results/ce10/SRX7630545/SRX7630545.10 -q 1e-10 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/ce10/SRX7630545/SRX7630545.10 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/ce10/SRX7630545/SRX7630545.bam'] # control file = None # effective genome size = 9.00e+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 @ Tue, 14 Jul 2020 07:04:51: #1 read tag files... INFO @ Tue, 14 Jul 2020 07:04:51: #1 read treatment tags... INFO @ Tue, 14 Jul 2020 07:04:57: 1000000 INFO @ Tue, 14 Jul 2020 07:04:58: #1 tag size is determined as 51 bps INFO @ Tue, 14 Jul 2020 07:04:58: #1 tag size = 51 INFO @ Tue, 14 Jul 2020 07:04:58: #1 total tags in treatment: 1119671 INFO @ Tue, 14 Jul 2020 07:04:58: #1 user defined the maximum tags... INFO @ Tue, 14 Jul 2020 07:04:58: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Tue, 14 Jul 2020 07:04:58: #1 tags after filtering in treatment: 1119671 INFO @ Tue, 14 Jul 2020 07:04:58: #1 Redundant rate of treatment: 0.00 INFO @ Tue, 14 Jul 2020 07:04:58: #1 finished! INFO @ Tue, 14 Jul 2020 07:04:58: #2 Build Peak Model... INFO @ Tue, 14 Jul 2020 07:04:58: #2 looking for paired plus/minus strand peaks... INFO @ Tue, 14 Jul 2020 07:04:58: #2 number of paired peaks: 411 WARNING @ Tue, 14 Jul 2020 07:04:58: Fewer paired peaks (411) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 411 pairs to build model! INFO @ Tue, 14 Jul 2020 07:04:58: start model_add_line... INFO @ Tue, 14 Jul 2020 07:04:58: start X-correlation... INFO @ Tue, 14 Jul 2020 07:04:58: end of X-cor INFO @ Tue, 14 Jul 2020 07:04:58: #2 finished! INFO @ Tue, 14 Jul 2020 07:04:58: #2 predicted fragment length is 52 bps INFO @ Tue, 14 Jul 2020 07:04:58: #2 alternative fragment length(s) may be 52,240,423,456,474,538 bps INFO @ Tue, 14 Jul 2020 07:04:58: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/ce10/SRX7630545/SRX7630545.10_model.r WARNING @ Tue, 14 Jul 2020 07:04:58: #2 Since the d (52) calculated from paired-peaks are smaller than 2*tag length, it may be influenced by unknown sequencing problem! WARNING @ Tue, 14 Jul 2020 07:04:58: #2 You may need to consider one of the other alternative d(s): 52,240,423,456,474,538 WARNING @ Tue, 14 Jul 2020 07:04:58: #2 You can restart the process with --nomodel --extsize XXX with your choice or an arbitrary number. Nontheless, MACS will continute computing. INFO @ Tue, 14 Jul 2020 07:04:58: #3 Call peaks... INFO @ Tue, 14 Jul 2020 07:04:58: #3 Pre-compute pvalue-qvalue table... INFO @ Tue, 14 Jul 2020 07:05:01: #3 Call peaks for each chromosome... INFO @ Tue, 14 Jul 2020 07:05:02: #4 Write output xls file... /home/okishinya/chipatlas/results/ce10/SRX7630545/SRX7630545.10_peaks.xls INFO @ Tue, 14 Jul 2020 07:05:02: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/ce10/SRX7630545/SRX7630545.10_peaks.narrowPeak INFO @ Tue, 14 Jul 2020 07:05:02: #4 Write summits bed file... /home/okishinya/chipatlas/results/ce10/SRX7630545/SRX7630545.10_summits.bed INFO @ Tue, 14 Jul 2020 07:05:02: Done! pass1 - making usageList (6 chroms): 1 millis pass2 - checking and writing primary data (120 records, 4 fields): 20 millis CompletedMACS2peakCalling BedGraph に変換中... WARNING: Skipping mount /opt/pkg/singularity/3.5.2/var/singularity/mnt/session/etc/resolv.conf [files]: /etc/resolv.conf doesn't exist in container INFO @ Tue, 14 Jul 2020 07:05:22: # Command line: callpeak -t /home/okishinya/chipatlas/results/ce10/SRX7630545/SRX7630545.bam -f BAM -g ce -n /home/okishinya/chipatlas/results/ce10/SRX7630545/SRX7630545.20 -q 1e-20 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/ce10/SRX7630545/SRX7630545.20 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/ce10/SRX7630545/SRX7630545.bam'] # control file = None # effective genome size = 9.00e+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 @ Tue, 14 Jul 2020 07:05:22: #1 read tag files... INFO @ Tue, 14 Jul 2020 07:05:22: #1 read treatment tags... BedGraph に変換しました。 BigWig に変換中... INFO @ Tue, 14 Jul 2020 07:05:27: 1000000 INFO @ Tue, 14 Jul 2020 07:05:27: #1 tag size is determined as 51 bps INFO @ Tue, 14 Jul 2020 07:05:27: #1 tag size = 51 INFO @ Tue, 14 Jul 2020 07:05:27: #1 total tags in treatment: 1119671 INFO @ Tue, 14 Jul 2020 07:05:27: #1 user defined the maximum tags... INFO @ Tue, 14 Jul 2020 07:05:27: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Tue, 14 Jul 2020 07:05:27: #1 tags after filtering in treatment: 1119671 INFO @ Tue, 14 Jul 2020 07:05:27: #1 Redundant rate of treatment: 0.00 INFO @ Tue, 14 Jul 2020 07:05:27: #1 finished! INFO @ Tue, 14 Jul 2020 07:05:27: #2 Build Peak Model... INFO @ Tue, 14 Jul 2020 07:05:27: #2 looking for paired plus/minus strand peaks... INFO @ Tue, 14 Jul 2020 07:05:27: #2 number of paired peaks: 411 WARNING @ Tue, 14 Jul 2020 07:05:27: Fewer paired peaks (411) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 411 pairs to build model! INFO @ Tue, 14 Jul 2020 07:05:27: start model_add_line... INFO @ Tue, 14 Jul 2020 07:05:27: start X-correlation... INFO @ Tue, 14 Jul 2020 07:05:27: end of X-cor INFO @ Tue, 14 Jul 2020 07:05:27: #2 finished! INFO @ Tue, 14 Jul 2020 07:05:27: #2 predicted fragment length is 52 bps INFO @ Tue, 14 Jul 2020 07:05:27: #2 alternative fragment length(s) may be 52,240,423,456,474,538 bps INFO @ Tue, 14 Jul 2020 07:05:27: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/ce10/SRX7630545/SRX7630545.20_model.r WARNING @ Tue, 14 Jul 2020 07:05:27: #2 Since the d (52) calculated from paired-peaks are smaller than 2*tag length, it may be influenced by unknown sequencing problem! WARNING @ Tue, 14 Jul 2020 07:05:27: #2 You may need to consider one of the other alternative d(s): 52,240,423,456,474,538 WARNING @ Tue, 14 Jul 2020 07:05:27: #2 You can restart the process with --nomodel --extsize XXX with your choice or an arbitrary number. Nontheless, MACS will continute computing. INFO @ Tue, 14 Jul 2020 07:05:27: #3 Call peaks... INFO @ Tue, 14 Jul 2020 07:05:27: #3 Pre-compute pvalue-qvalue table... BigWig に変換しました。 INFO @ Tue, 14 Jul 2020 07:05:30: #3 Call peaks for each chromosome... INFO @ Tue, 14 Jul 2020 07:05:31: #4 Write output xls file... /home/okishinya/chipatlas/results/ce10/SRX7630545/SRX7630545.20_peaks.xls INFO @ Tue, 14 Jul 2020 07:05:31: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/ce10/SRX7630545/SRX7630545.20_peaks.narrowPeak INFO @ Tue, 14 Jul 2020 07:05:31: #4 Write summits bed file... /home/okishinya/chipatlas/results/ce10/SRX7630545/SRX7630545.20_summits.bed INFO @ Tue, 14 Jul 2020 07:05:31: Done! pass1 - making usageList (6 chroms): 0 millis pass2 - checking and writing primary data (43 records, 4 fields): 19 millis CompletedMACS2peakCalling