Job ID = 6626411 SRX = SRX7262226 Genome = ce11 sra ファイルのダウンロード中... Read layout: SINGLE fastq に変換中... 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: 00:00:19 1462729 reads; of these: 1462729 (100.00%) were unpaired; of these: 284853 (19.47%) aligned 0 times 925327 (63.26%) aligned exactly 1 time 252549 (17.27%) aligned >1 times 80.53% overall alignment rate Time searching: 00:00:19 Overall time: 00:00:19 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] 111409 / 1177876 = 0.0946 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 07:00:03: # Command line: callpeak -t /home/okishinya/chipatlas/results/ce11/SRX7262226/SRX7262226.bam -f BAM -g ce -n /home/okishinya/chipatlas/results/ce11/SRX7262226/SRX7262226.05 -q 1e-05 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/ce11/SRX7262226/SRX7262226.05 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/ce11/SRX7262226/SRX7262226.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 07:00:03: #1 read tag files... INFO @ Tue, 14 Jul 2020 07:00:03: #1 read treatment tags... INFO @ Tue, 14 Jul 2020 07:00:09: 1000000 INFO @ Tue, 14 Jul 2020 07:00:09: #1 tag size is determined as 50 bps INFO @ Tue, 14 Jul 2020 07:00:09: #1 tag size = 50 INFO @ Tue, 14 Jul 2020 07:00:09: #1 total tags in treatment: 1066467 INFO @ Tue, 14 Jul 2020 07:00:09: #1 user defined the maximum tags... INFO @ Tue, 14 Jul 2020 07:00:09: #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 07:00:09: #1 tags after filtering in treatment: 1066467 INFO @ Tue, 14 Jul 2020 07:00:09: #1 Redundant rate of treatment: 0.00 INFO @ Tue, 14 Jul 2020 07:00:09: #1 finished! INFO @ Tue, 14 Jul 2020 07:00:09: #2 Build Peak Model... INFO @ Tue, 14 Jul 2020 07:00:09: #2 looking for paired plus/minus strand peaks... INFO @ Tue, 14 Jul 2020 07:00:09: #2 number of paired peaks: 462 WARNING @ Tue, 14 Jul 2020 07:00:09: Fewer paired peaks (462) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 462 pairs to build model! INFO @ Tue, 14 Jul 2020 07:00:09: start model_add_line... INFO @ Tue, 14 Jul 2020 07:00:09: start X-correlation... INFO @ Tue, 14 Jul 2020 07:00:09: end of X-cor INFO @ Tue, 14 Jul 2020 07:00:09: #2 finished! INFO @ Tue, 14 Jul 2020 07:00:09: #2 predicted fragment length is 49 bps INFO @ Tue, 14 Jul 2020 07:00:09: #2 alternative fragment length(s) may be 49,209,249,419 bps INFO @ Tue, 14 Jul 2020 07:00:09: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/ce11/SRX7262226/SRX7262226.05_model.r WARNING @ Tue, 14 Jul 2020 07:00:09: #2 Since the d (49) calculated from paired-peaks are smaller than 2*tag length, it may be influenced by unknown sequencing problem! WARNING @ Tue, 14 Jul 2020 07:00:09: #2 You may need to consider one of the other alternative d(s): 49,209,249,419 WARNING @ Tue, 14 Jul 2020 07:00:09: #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 07:00:09: #3 Call peaks... INFO @ Tue, 14 Jul 2020 07:00:09: #3 Pre-compute pvalue-qvalue table... INFO @ Tue, 14 Jul 2020 07:00:12: #3 Call peaks for each chromosome... INFO @ Tue, 14 Jul 2020 07:00:13: #4 Write output xls file... /home/okishinya/chipatlas/results/ce11/SRX7262226/SRX7262226.05_peaks.xls INFO @ Tue, 14 Jul 2020 07:00:13: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/ce11/SRX7262226/SRX7262226.05_peaks.narrowPeak INFO @ Tue, 14 Jul 2020 07:00:13: #4 Write summits bed file... /home/okishinya/chipatlas/results/ce11/SRX7262226/SRX7262226.05_summits.bed INFO @ Tue, 14 Jul 2020 07:00:13: Done! pass1 - making usageList (6 chroms): 1 millis pass2 - checking and writing primary data (227 records, 4 fields): 73 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 07:00:33: # Command line: callpeak -t /home/okishinya/chipatlas/results/ce11/SRX7262226/SRX7262226.bam -f BAM -g ce -n /home/okishinya/chipatlas/results/ce11/SRX7262226/SRX7262226.10 -q 1e-10 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/ce11/SRX7262226/SRX7262226.10 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/ce11/SRX7262226/SRX7262226.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 07:00:33: #1 read tag files... INFO @ Tue, 14 Jul 2020 07:00:33: #1 read treatment tags... INFO @ Tue, 14 Jul 2020 07:00:40: 1000000 INFO @ Tue, 14 Jul 2020 07:00:41: #1 tag size is determined as 50 bps INFO @ Tue, 14 Jul 2020 07:00:41: #1 tag size = 50 INFO @ Tue, 14 Jul 2020 07:00:41: #1 total tags in treatment: 1066467 INFO @ Tue, 14 Jul 2020 07:00:41: #1 user defined the maximum tags... INFO @ Tue, 14 Jul 2020 07:00:41: #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 07:00:41: #1 tags after filtering in treatment: 1066467 INFO @ Tue, 14 Jul 2020 07:00:41: #1 Redundant rate of treatment: 0.00 INFO @ Tue, 14 Jul 2020 07:00:41: #1 finished! INFO @ Tue, 14 Jul 2020 07:00:41: #2 Build Peak Model... INFO @ Tue, 14 Jul 2020 07:00:41: #2 looking for paired plus/minus strand peaks... INFO @ Tue, 14 Jul 2020 07:00:41: #2 number of paired peaks: 462 WARNING @ Tue, 14 Jul 2020 07:00:41: Fewer paired peaks (462) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 462 pairs to build model! INFO @ Tue, 14 Jul 2020 07:00:41: start model_add_line... INFO @ Tue, 14 Jul 2020 07:00:41: start X-correlation... INFO @ Tue, 14 Jul 2020 07:00:41: end of X-cor INFO @ Tue, 14 Jul 2020 07:00:41: #2 finished! INFO @ Tue, 14 Jul 2020 07:00:41: #2 predicted fragment length is 49 bps INFO @ Tue, 14 Jul 2020 07:00:41: #2 alternative fragment length(s) may be 49,209,249,419 bps INFO @ Tue, 14 Jul 2020 07:00:41: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/ce11/SRX7262226/SRX7262226.10_model.r WARNING @ Tue, 14 Jul 2020 07:00:41: #2 Since the d (49) calculated from paired-peaks are smaller than 2*tag length, it may be influenced by unknown sequencing problem! WARNING @ Tue, 14 Jul 2020 07:00:41: #2 You may need to consider one of the other alternative d(s): 49,209,249,419 WARNING @ Tue, 14 Jul 2020 07:00:41: #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 07:00:41: #3 Call peaks... INFO @ Tue, 14 Jul 2020 07:00:41: #3 Pre-compute pvalue-qvalue table... INFO @ Tue, 14 Jul 2020 07:00:44: #3 Call peaks for each chromosome... INFO @ Tue, 14 Jul 2020 07:00:45: #4 Write output xls file... /home/okishinya/chipatlas/results/ce11/SRX7262226/SRX7262226.10_peaks.xls INFO @ Tue, 14 Jul 2020 07:00:45: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/ce11/SRX7262226/SRX7262226.10_peaks.narrowPeak INFO @ Tue, 14 Jul 2020 07:00:45: #4 Write summits bed file... /home/okishinya/chipatlas/results/ce11/SRX7262226/SRX7262226.10_summits.bed INFO @ Tue, 14 Jul 2020 07:00:45: Done! pass1 - making usageList (6 chroms): 1 millis pass2 - checking and writing primary data (115 records, 4 fields): 15 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 07:01:03: # Command line: callpeak -t /home/okishinya/chipatlas/results/ce11/SRX7262226/SRX7262226.bam -f BAM -g ce -n /home/okishinya/chipatlas/results/ce11/SRX7262226/SRX7262226.20 -q 1e-20 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/ce11/SRX7262226/SRX7262226.20 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/ce11/SRX7262226/SRX7262226.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 07:01:03: #1 read tag files... INFO @ Tue, 14 Jul 2020 07:01:03: #1 read treatment tags... BedGraph に変換しました。 BigWig に変換中... BigWig に変換しました。 INFO @ Tue, 14 Jul 2020 07:01:11: 1000000 INFO @ Tue, 14 Jul 2020 07:01:11: #1 tag size is determined as 50 bps INFO @ Tue, 14 Jul 2020 07:01:11: #1 tag size = 50 INFO @ Tue, 14 Jul 2020 07:01:11: #1 total tags in treatment: 1066467 INFO @ Tue, 14 Jul 2020 07:01:11: #1 user defined the maximum tags... INFO @ Tue, 14 Jul 2020 07:01:11: #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 07:01:11: #1 tags after filtering in treatment: 1066467 INFO @ Tue, 14 Jul 2020 07:01:11: #1 Redundant rate of treatment: 0.00 INFO @ Tue, 14 Jul 2020 07:01:11: #1 finished! INFO @ Tue, 14 Jul 2020 07:01:11: #2 Build Peak Model... INFO @ Tue, 14 Jul 2020 07:01:11: #2 looking for paired plus/minus strand peaks... INFO @ Tue, 14 Jul 2020 07:01:11: #2 number of paired peaks: 462 WARNING @ Tue, 14 Jul 2020 07:01:11: Fewer paired peaks (462) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 462 pairs to build model! INFO @ Tue, 14 Jul 2020 07:01:11: start model_add_line... INFO @ Tue, 14 Jul 2020 07:01:11: start X-correlation... INFO @ Tue, 14 Jul 2020 07:01:11: end of X-cor INFO @ Tue, 14 Jul 2020 07:01:11: #2 finished! INFO @ Tue, 14 Jul 2020 07:01:11: #2 predicted fragment length is 49 bps INFO @ Tue, 14 Jul 2020 07:01:11: #2 alternative fragment length(s) may be 49,209,249,419 bps INFO @ Tue, 14 Jul 2020 07:01:11: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/ce11/SRX7262226/SRX7262226.20_model.r WARNING @ Tue, 14 Jul 2020 07:01:11: #2 Since the d (49) calculated from paired-peaks are smaller than 2*tag length, it may be influenced by unknown sequencing problem! WARNING @ Tue, 14 Jul 2020 07:01:11: #2 You may need to consider one of the other alternative d(s): 49,209,249,419 WARNING @ Tue, 14 Jul 2020 07:01:11: #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 07:01:11: #3 Call peaks... INFO @ Tue, 14 Jul 2020 07:01:11: #3 Pre-compute pvalue-qvalue table... INFO @ Tue, 14 Jul 2020 07:01:14: #3 Call peaks for each chromosome... INFO @ Tue, 14 Jul 2020 07:01:15: #4 Write output xls file... /home/okishinya/chipatlas/results/ce11/SRX7262226/SRX7262226.20_peaks.xls INFO @ Tue, 14 Jul 2020 07:01:15: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/ce11/SRX7262226/SRX7262226.20_peaks.narrowPeak INFO @ Tue, 14 Jul 2020 07:01:15: #4 Write summits bed file... /home/okishinya/chipatlas/results/ce11/SRX7262226/SRX7262226.20_summits.bed INFO @ Tue, 14 Jul 2020 07:01:15: Done! pass1 - making usageList (6 chroms): 0 millis pass2 - checking and writing primary data (46 records, 4 fields): 8 millis CompletedMACS2peakCalling