Job ID = 6366426 SRX = SRX146466 Genome = ce11 sra ファイルのダウンロード中... Read layout: SINGLE fastq に変換中... 2020-06-15T22:49:52 prefetch.2.10.7: 1) Downloading 'SRR494627'... 2020-06-15T22:49:52 prefetch.2.10.7: Downloading via HTTPS... 2020-06-15T22:50:12 prefetch.2.10.7: HTTPS download succeed 2020-06-15T22:50:12 prefetch.2.10.7: 'SRR494627' is valid 2020-06-15T22:50:12 prefetch.2.10.7: 1) 'SRR494627' was downloaded successfully Read 2939714 spots for SRR494627/SRR494627.sra Written 2939714 spots for SRR494627/SRR494627.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: 00:00:28 2939714 reads; of these: 2939714 (100.00%) were unpaired; of these: 92909 (3.16%) aligned 0 times 2354309 (80.09%) aligned exactly 1 time 492496 (16.75%) aligned >1 times 96.84% overall alignment rate Time searching: 00:00:28 Overall time: 00:00:28 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] 100697 / 2846805 = 0.0354 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 07:51:52: # Command line: callpeak -t /home/okishinya/chipatlas/results/ce11/SRX146466/SRX146466.bam -f BAM -g ce -n /home/okishinya/chipatlas/results/ce11/SRX146466/SRX146466.05 -q 1e-05 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/ce11/SRX146466/SRX146466.05 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/ce11/SRX146466/SRX146466.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 07:51:52: #1 read tag files... INFO @ Tue, 16 Jun 2020 07:51:52: #1 read treatment tags... INFO @ Tue, 16 Jun 2020 07:51:58: 1000000 INFO @ Tue, 16 Jun 2020 07:52:04: 2000000 INFO @ Tue, 16 Jun 2020 07:52:09: #1 tag size is determined as 32 bps INFO @ Tue, 16 Jun 2020 07:52:09: #1 tag size = 32 INFO @ Tue, 16 Jun 2020 07:52:09: #1 total tags in treatment: 2746108 INFO @ Tue, 16 Jun 2020 07:52:09: #1 user defined the maximum tags... INFO @ Tue, 16 Jun 2020 07:52:09: #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 07:52:09: #1 tags after filtering in treatment: 2746108 INFO @ Tue, 16 Jun 2020 07:52:09: #1 Redundant rate of treatment: 0.00 INFO @ Tue, 16 Jun 2020 07:52:09: #1 finished! INFO @ Tue, 16 Jun 2020 07:52:09: #2 Build Peak Model... INFO @ Tue, 16 Jun 2020 07:52:09: #2 looking for paired plus/minus strand peaks... INFO @ Tue, 16 Jun 2020 07:52:09: #2 number of paired peaks: 453 WARNING @ Tue, 16 Jun 2020 07:52:09: Fewer paired peaks (453) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 453 pairs to build model! INFO @ Tue, 16 Jun 2020 07:52:09: start model_add_line... INFO @ Tue, 16 Jun 2020 07:52:09: start X-correlation... INFO @ Tue, 16 Jun 2020 07:52:09: end of X-cor INFO @ Tue, 16 Jun 2020 07:52:09: #2 finished! INFO @ Tue, 16 Jun 2020 07:52:09: #2 predicted fragment length is 33 bps INFO @ Tue, 16 Jun 2020 07:52:09: #2 alternative fragment length(s) may be 4,33,535 bps INFO @ Tue, 16 Jun 2020 07:52:09: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/ce11/SRX146466/SRX146466.05_model.r WARNING @ Tue, 16 Jun 2020 07:52:09: #2 Since the d (33) calculated from paired-peaks are smaller than 2*tag length, it may be influenced by unknown sequencing problem! WARNING @ Tue, 16 Jun 2020 07:52:09: #2 You may need to consider one of the other alternative d(s): 4,33,535 WARNING @ Tue, 16 Jun 2020 07:52:09: #2 You can restart the process with --nomodel --extsize XXX with your choice or an arbitrary number. Nontheless, MACS will continute computing. INFO @ Tue, 16 Jun 2020 07:52:09: #3 Call peaks... INFO @ Tue, 16 Jun 2020 07:52:09: #3 Pre-compute pvalue-qvalue table... INFO @ Tue, 16 Jun 2020 07:52:15: #3 Call peaks for each chromosome... INFO @ Tue, 16 Jun 2020 07:52:18: #4 Write output xls file... /home/okishinya/chipatlas/results/ce11/SRX146466/SRX146466.05_peaks.xls INFO @ Tue, 16 Jun 2020 07:52:18: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/ce11/SRX146466/SRX146466.05_peaks.narrowPeak INFO @ Tue, 16 Jun 2020 07:52:18: #4 Write summits bed file... /home/okishinya/chipatlas/results/ce11/SRX146466/SRX146466.05_summits.bed INFO @ Tue, 16 Jun 2020 07:52:18: Done! pass1 - making usageList (6 chroms): 1 millis pass2 - checking and writing primary data (339 records, 4 fields): 1 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 07:52:22: # Command line: callpeak -t /home/okishinya/chipatlas/results/ce11/SRX146466/SRX146466.bam -f BAM -g ce -n /home/okishinya/chipatlas/results/ce11/SRX146466/SRX146466.10 -q 1e-10 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/ce11/SRX146466/SRX146466.10 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/ce11/SRX146466/SRX146466.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 07:52:22: #1 read tag files... INFO @ Tue, 16 Jun 2020 07:52:22: #1 read treatment tags... INFO @ Tue, 16 Jun 2020 07:52:29: 1000000 INFO @ Tue, 16 Jun 2020 07:52:35: 2000000 INFO @ Tue, 16 Jun 2020 07:52:40: #1 tag size is determined as 32 bps INFO @ Tue, 16 Jun 2020 07:52:40: #1 tag size = 32 INFO @ Tue, 16 Jun 2020 07:52:40: #1 total tags in treatment: 2746108 INFO @ Tue, 16 Jun 2020 07:52:40: #1 user defined the maximum tags... INFO @ Tue, 16 Jun 2020 07:52:40: #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 07:52:40: #1 tags after filtering in treatment: 2746108 INFO @ Tue, 16 Jun 2020 07:52:40: #1 Redundant rate of treatment: 0.00 INFO @ Tue, 16 Jun 2020 07:52:40: #1 finished! INFO @ Tue, 16 Jun 2020 07:52:40: #2 Build Peak Model... INFO @ Tue, 16 Jun 2020 07:52:40: #2 looking for paired plus/minus strand peaks... INFO @ Tue, 16 Jun 2020 07:52:40: #2 number of paired peaks: 453 WARNING @ Tue, 16 Jun 2020 07:52:40: Fewer paired peaks (453) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 453 pairs to build model! INFO @ Tue, 16 Jun 2020 07:52:40: start model_add_line... INFO @ Tue, 16 Jun 2020 07:52:40: start X-correlation... INFO @ Tue, 16 Jun 2020 07:52:40: end of X-cor INFO @ Tue, 16 Jun 2020 07:52:40: #2 finished! INFO @ Tue, 16 Jun 2020 07:52:40: #2 predicted fragment length is 33 bps INFO @ Tue, 16 Jun 2020 07:52:40: #2 alternative fragment length(s) may be 4,33,535 bps INFO @ Tue, 16 Jun 2020 07:52:40: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/ce11/SRX146466/SRX146466.10_model.r WARNING @ Tue, 16 Jun 2020 07:52:40: #2 Since the d (33) calculated from paired-peaks are smaller than 2*tag length, it may be influenced by unknown sequencing problem! WARNING @ Tue, 16 Jun 2020 07:52:40: #2 You may need to consider one of the other alternative d(s): 4,33,535 WARNING @ Tue, 16 Jun 2020 07:52:40: #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 07:52:40: #3 Call peaks... INFO @ Tue, 16 Jun 2020 07:52:40: #3 Pre-compute pvalue-qvalue table... INFO @ Tue, 16 Jun 2020 07:52:46: #3 Call peaks for each chromosome... INFO @ Tue, 16 Jun 2020 07:52:49: #4 Write output xls file... /home/okishinya/chipatlas/results/ce11/SRX146466/SRX146466.10_peaks.xls INFO @ Tue, 16 Jun 2020 07:52:49: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/ce11/SRX146466/SRX146466.10_peaks.narrowPeak INFO @ Tue, 16 Jun 2020 07:52:49: #4 Write summits bed file... /home/okishinya/chipatlas/results/ce11/SRX146466/SRX146466.10_summits.bed INFO @ Tue, 16 Jun 2020 07:52:49: Done! pass1 - making usageList (6 chroms): 0 millis pass2 - checking and writing primary data (148 records, 4 fields): 2 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 07:52:52: # Command line: callpeak -t /home/okishinya/chipatlas/results/ce11/SRX146466/SRX146466.bam -f BAM -g ce -n /home/okishinya/chipatlas/results/ce11/SRX146466/SRX146466.20 -q 1e-20 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/ce11/SRX146466/SRX146466.20 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/ce11/SRX146466/SRX146466.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 07:52:52: #1 read tag files... INFO @ Tue, 16 Jun 2020 07:52:52: #1 read treatment tags... INFO @ Tue, 16 Jun 2020 07:52:58: 1000000 BedGraph に変換しました。 BigWig に変換中... INFO @ Tue, 16 Jun 2020 07:53:04: 2000000 INFO @ Tue, 16 Jun 2020 07:53:09: #1 tag size is determined as 32 bps INFO @ Tue, 16 Jun 2020 07:53:09: #1 tag size = 32 INFO @ Tue, 16 Jun 2020 07:53:09: #1 total tags in treatment: 2746108 INFO @ Tue, 16 Jun 2020 07:53:09: #1 user defined the maximum tags... INFO @ Tue, 16 Jun 2020 07:53:09: #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 07:53:09: #1 tags after filtering in treatment: 2746108 INFO @ Tue, 16 Jun 2020 07:53:09: #1 Redundant rate of treatment: 0.00 INFO @ Tue, 16 Jun 2020 07:53:09: #1 finished! INFO @ Tue, 16 Jun 2020 07:53:09: #2 Build Peak Model... INFO @ Tue, 16 Jun 2020 07:53:09: #2 looking for paired plus/minus strand peaks... BigWig に変換しました。 INFO @ Tue, 16 Jun 2020 07:53:09: #2 number of paired peaks: 453 WARNING @ Tue, 16 Jun 2020 07:53:09: Fewer paired peaks (453) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 453 pairs to build model! INFO @ Tue, 16 Jun 2020 07:53:09: start model_add_line... INFO @ Tue, 16 Jun 2020 07:53:09: start X-correlation... INFO @ Tue, 16 Jun 2020 07:53:09: end of X-cor INFO @ Tue, 16 Jun 2020 07:53:09: #2 finished! INFO @ Tue, 16 Jun 2020 07:53:09: #2 predicted fragment length is 33 bps INFO @ Tue, 16 Jun 2020 07:53:09: #2 alternative fragment length(s) may be 4,33,535 bps INFO @ Tue, 16 Jun 2020 07:53:09: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/ce11/SRX146466/SRX146466.20_model.r WARNING @ Tue, 16 Jun 2020 07:53:09: #2 Since the d (33) calculated from paired-peaks are smaller than 2*tag length, it may be influenced by unknown sequencing problem! WARNING @ Tue, 16 Jun 2020 07:53:09: #2 You may need to consider one of the other alternative d(s): 4,33,535 WARNING @ Tue, 16 Jun 2020 07:53:09: #2 You can restart the process with --nomodel --extsize XXX with your choice or an arbitrary number. Nontheless, MACS will continute computing. INFO @ Tue, 16 Jun 2020 07:53:09: #3 Call peaks... INFO @ Tue, 16 Jun 2020 07:53:09: #3 Pre-compute pvalue-qvalue table... INFO @ Tue, 16 Jun 2020 07:53:15: #3 Call peaks for each chromosome... INFO @ Tue, 16 Jun 2020 07:53:18: #4 Write output xls file... /home/okishinya/chipatlas/results/ce11/SRX146466/SRX146466.20_peaks.xls INFO @ Tue, 16 Jun 2020 07:53:18: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/ce11/SRX146466/SRX146466.20_peaks.narrowPeak INFO @ Tue, 16 Jun 2020 07:53:18: #4 Write summits bed file... /home/okishinya/chipatlas/results/ce11/SRX146466/SRX146466.20_summits.bed INFO @ Tue, 16 Jun 2020 07:53:18: Done! pass1 - making usageList (6 chroms): 0 millis pass2 - checking and writing primary data (26 records, 4 fields): 1 millis CompletedMACS2peakCalling