Job ID = 6365937 SRX = SRX043870 Genome = ce11 sra ファイルのダウンロード中... Read layout: SINGLE fastq に変換中... 2020-06-15T22:27:59 prefetch.2.10.7: 1) Downloading 'SRR107332'... 2020-06-15T22:27:59 prefetch.2.10.7: Downloading via HTTPS... 2020-06-15T22:28:26 prefetch.2.10.7: HTTPS download succeed 2020-06-15T22:28:26 prefetch.2.10.7: 'SRR107332' is valid 2020-06-15T22:28:26 prefetch.2.10.7: 1) 'SRR107332' was downloaded successfully Read 2643487 spots for SRR107332/SRR107332.sra Written 2643487 spots for SRR107332/SRR107332.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: 00:00:29 2643487 reads; of these: 2643487 (100.00%) were unpaired; of these: 473174 (17.90%) aligned 0 times 1880542 (71.14%) aligned exactly 1 time 289771 (10.96%) aligned >1 times 82.10% overall alignment rate Time searching: 00:00:29 Overall time: 00:00:29 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] 102425 / 2170313 = 0.0472 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, 16 Jun 2020 07:30:13: # Command line: callpeak -t /home/okishinya/chipatlas/results/ce11/SRX043870/SRX043870.bam -f BAM -g ce -n /home/okishinya/chipatlas/results/ce11/SRX043870/SRX043870.05 -q 1e-05 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/ce11/SRX043870/SRX043870.05 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/ce11/SRX043870/SRX043870.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, 16 Jun 2020 07:30:13: #1 read tag files... INFO @ Tue, 16 Jun 2020 07:30:13: #1 read treatment tags... INFO @ Tue, 16 Jun 2020 07:30:20: 1000000 INFO @ Tue, 16 Jun 2020 07:30:27: 2000000 INFO @ Tue, 16 Jun 2020 07:30:28: #1 tag size is determined as 34 bps INFO @ Tue, 16 Jun 2020 07:30:28: #1 tag size = 34 INFO @ Tue, 16 Jun 2020 07:30:28: #1 total tags in treatment: 2067888 INFO @ Tue, 16 Jun 2020 07:30:28: #1 user defined the maximum tags... INFO @ Tue, 16 Jun 2020 07:30:28: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Tue, 16 Jun 2020 07:30:28: #1 tags after filtering in treatment: 2067888 INFO @ Tue, 16 Jun 2020 07:30:28: #1 Redundant rate of treatment: 0.00 INFO @ Tue, 16 Jun 2020 07:30:28: #1 finished! INFO @ Tue, 16 Jun 2020 07:30:28: #2 Build Peak Model... INFO @ Tue, 16 Jun 2020 07:30:28: #2 looking for paired plus/minus strand peaks... INFO @ Tue, 16 Jun 2020 07:30:28: #2 number of paired peaks: 340 WARNING @ Tue, 16 Jun 2020 07:30:28: Fewer paired peaks (340) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 340 pairs to build model! INFO @ Tue, 16 Jun 2020 07:30:28: start model_add_line... INFO @ Tue, 16 Jun 2020 07:30:28: start X-correlation... INFO @ Tue, 16 Jun 2020 07:30:28: end of X-cor INFO @ Tue, 16 Jun 2020 07:30:28: #2 finished! INFO @ Tue, 16 Jun 2020 07:30:28: #2 predicted fragment length is 45 bps INFO @ Tue, 16 Jun 2020 07:30:28: #2 alternative fragment length(s) may be 45,68,548 bps INFO @ Tue, 16 Jun 2020 07:30:28: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/ce11/SRX043870/SRX043870.05_model.r WARNING @ Tue, 16 Jun 2020 07:30:28: #2 Since the d (45) calculated from paired-peaks are smaller than 2*tag length, it may be influenced by unknown sequencing problem! WARNING @ Tue, 16 Jun 2020 07:30:28: #2 You may need to consider one of the other alternative d(s): 45,68,548 WARNING @ Tue, 16 Jun 2020 07:30:28: #2 You can restart the process with --nomodel --extsize XXX with your choice or an arbitrary number. Nontheless, MACS will continute computing. INFO @ Tue, 16 Jun 2020 07:30:28: #3 Call peaks... INFO @ Tue, 16 Jun 2020 07:30:28: #3 Pre-compute pvalue-qvalue table... INFO @ Tue, 16 Jun 2020 07:30:33: #3 Call peaks for each chromosome... INFO @ Tue, 16 Jun 2020 07:30:35: #4 Write output xls file... /home/okishinya/chipatlas/results/ce11/SRX043870/SRX043870.05_peaks.xls INFO @ Tue, 16 Jun 2020 07:30:35: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/ce11/SRX043870/SRX043870.05_peaks.narrowPeak INFO @ Tue, 16 Jun 2020 07:30:35: #4 Write summits bed file... /home/okishinya/chipatlas/results/ce11/SRX043870/SRX043870.05_summits.bed INFO @ Tue, 16 Jun 2020 07:30:35: Done! pass1 - making usageList (7 chroms): 0 millis pass2 - checking and writing primary data (173 records, 4 fields): 2 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, 16 Jun 2020 07:30:43: # Command line: callpeak -t /home/okishinya/chipatlas/results/ce11/SRX043870/SRX043870.bam -f BAM -g ce -n /home/okishinya/chipatlas/results/ce11/SRX043870/SRX043870.10 -q 1e-10 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/ce11/SRX043870/SRX043870.10 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/ce11/SRX043870/SRX043870.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, 16 Jun 2020 07:30:43: #1 read tag files... INFO @ Tue, 16 Jun 2020 07:30:43: #1 read treatment tags... INFO @ Tue, 16 Jun 2020 07:30:50: 1000000 INFO @ Tue, 16 Jun 2020 07:30:57: 2000000 INFO @ Tue, 16 Jun 2020 07:30:58: #1 tag size is determined as 34 bps INFO @ Tue, 16 Jun 2020 07:30:58: #1 tag size = 34 INFO @ Tue, 16 Jun 2020 07:30:58: #1 total tags in treatment: 2067888 INFO @ Tue, 16 Jun 2020 07:30:58: #1 user defined the maximum tags... INFO @ Tue, 16 Jun 2020 07:30:58: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Tue, 16 Jun 2020 07:30:58: #1 tags after filtering in treatment: 2067888 INFO @ Tue, 16 Jun 2020 07:30:58: #1 Redundant rate of treatment: 0.00 INFO @ Tue, 16 Jun 2020 07:30:58: #1 finished! INFO @ Tue, 16 Jun 2020 07:30:58: #2 Build Peak Model... INFO @ Tue, 16 Jun 2020 07:30:58: #2 looking for paired plus/minus strand peaks... INFO @ Tue, 16 Jun 2020 07:30:58: #2 number of paired peaks: 340 WARNING @ Tue, 16 Jun 2020 07:30:58: Fewer paired peaks (340) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 340 pairs to build model! INFO @ Tue, 16 Jun 2020 07:30:58: start model_add_line... INFO @ Tue, 16 Jun 2020 07:30:58: start X-correlation... INFO @ Tue, 16 Jun 2020 07:30:58: end of X-cor INFO @ Tue, 16 Jun 2020 07:30:58: #2 finished! INFO @ Tue, 16 Jun 2020 07:30:58: #2 predicted fragment length is 45 bps INFO @ Tue, 16 Jun 2020 07:30:58: #2 alternative fragment length(s) may be 45,68,548 bps INFO @ Tue, 16 Jun 2020 07:30:58: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/ce11/SRX043870/SRX043870.10_model.r WARNING @ Tue, 16 Jun 2020 07:30:58: #2 Since the d (45) calculated from paired-peaks are smaller than 2*tag length, it may be influenced by unknown sequencing problem! WARNING @ Tue, 16 Jun 2020 07:30:58: #2 You may need to consider one of the other alternative d(s): 45,68,548 WARNING @ Tue, 16 Jun 2020 07:30:58: #2 You can restart the process with --nomodel --extsize XXX with your choice or an arbitrary number. Nontheless, MACS will continute computing. INFO @ Tue, 16 Jun 2020 07:30:58: #3 Call peaks... INFO @ Tue, 16 Jun 2020 07:30:58: #3 Pre-compute pvalue-qvalue table... INFO @ Tue, 16 Jun 2020 07:31:03: #3 Call peaks for each chromosome... INFO @ Tue, 16 Jun 2020 07:31:05: #4 Write output xls file... /home/okishinya/chipatlas/results/ce11/SRX043870/SRX043870.10_peaks.xls INFO @ Tue, 16 Jun 2020 07:31:05: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/ce11/SRX043870/SRX043870.10_peaks.narrowPeak INFO @ Tue, 16 Jun 2020 07:31:05: #4 Write summits bed file... /home/okishinya/chipatlas/results/ce11/SRX043870/SRX043870.10_summits.bed INFO @ Tue, 16 Jun 2020 07:31:05: Done! pass1 - making usageList (6 chroms): 1 millis pass2 - checking and writing primary data (44 records, 4 fields): 1 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, 16 Jun 2020 07:31:13: # Command line: callpeak -t /home/okishinya/chipatlas/results/ce11/SRX043870/SRX043870.bam -f BAM -g ce -n /home/okishinya/chipatlas/results/ce11/SRX043870/SRX043870.20 -q 1e-20 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/ce11/SRX043870/SRX043870.20 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/ce11/SRX043870/SRX043870.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, 16 Jun 2020 07:31:13: #1 read tag files... INFO @ Tue, 16 Jun 2020 07:31:13: #1 read treatment tags... INFO @ Tue, 16 Jun 2020 07:31:21: 1000000 BedGraph に変換しました。 BigWig に変換中... INFO @ Tue, 16 Jun 2020 07:31:29: 2000000 INFO @ Tue, 16 Jun 2020 07:31:29: #1 tag size is determined as 34 bps INFO @ Tue, 16 Jun 2020 07:31:29: #1 tag size = 34 INFO @ Tue, 16 Jun 2020 07:31:29: #1 total tags in treatment: 2067888 INFO @ Tue, 16 Jun 2020 07:31:29: #1 user defined the maximum tags... INFO @ Tue, 16 Jun 2020 07:31:29: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Tue, 16 Jun 2020 07:31:29: #1 tags after filtering in treatment: 2067888 INFO @ Tue, 16 Jun 2020 07:31:29: #1 Redundant rate of treatment: 0.00 INFO @ Tue, 16 Jun 2020 07:31:29: #1 finished! INFO @ Tue, 16 Jun 2020 07:31:29: #2 Build Peak Model... INFO @ Tue, 16 Jun 2020 07:31:29: #2 looking for paired plus/minus strand peaks... BigWig に変換しました。 INFO @ Tue, 16 Jun 2020 07:31:29: #2 number of paired peaks: 340 WARNING @ Tue, 16 Jun 2020 07:31:29: Fewer paired peaks (340) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 340 pairs to build model! INFO @ Tue, 16 Jun 2020 07:31:29: start model_add_line... INFO @ Tue, 16 Jun 2020 07:31:29: start X-correlation... INFO @ Tue, 16 Jun 2020 07:31:29: end of X-cor INFO @ Tue, 16 Jun 2020 07:31:29: #2 finished! INFO @ Tue, 16 Jun 2020 07:31:29: #2 predicted fragment length is 45 bps INFO @ Tue, 16 Jun 2020 07:31:29: #2 alternative fragment length(s) may be 45,68,548 bps INFO @ Tue, 16 Jun 2020 07:31:29: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/ce11/SRX043870/SRX043870.20_model.r WARNING @ Tue, 16 Jun 2020 07:31:29: #2 Since the d (45) calculated from paired-peaks are smaller than 2*tag length, it may be influenced by unknown sequencing problem! WARNING @ Tue, 16 Jun 2020 07:31:29: #2 You may need to consider one of the other alternative d(s): 45,68,548 WARNING @ Tue, 16 Jun 2020 07:31:29: #2 You can restart the process with --nomodel --extsize XXX with your choice or an arbitrary number. Nontheless, MACS will continute computing. INFO @ Tue, 16 Jun 2020 07:31:29: #3 Call peaks... INFO @ Tue, 16 Jun 2020 07:31:29: #3 Pre-compute pvalue-qvalue table... INFO @ Tue, 16 Jun 2020 07:31:34: #3 Call peaks for each chromosome... INFO @ Tue, 16 Jun 2020 07:31:36: #4 Write output xls file... /home/okishinya/chipatlas/results/ce11/SRX043870/SRX043870.20_peaks.xls INFO @ Tue, 16 Jun 2020 07:31:36: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/ce11/SRX043870/SRX043870.20_peaks.narrowPeak INFO @ Tue, 16 Jun 2020 07:31:36: #4 Write summits bed file... /home/okishinya/chipatlas/results/ce11/SRX043870/SRX043870.20_summits.bed INFO @ Tue, 16 Jun 2020 07:31:36: Done! pass1 - making usageList (5 chroms): 0 millis pass2 - checking and writing primary data (6 records, 4 fields): 1 millis CompletedMACS2peakCalling