Job ID = 6365880 SRX = SRX005637 Genome = ce11 sra ファイルのダウンロード中... Read layout: SINGLE fastq に変換中... 2020-06-15T22:24:30 prefetch.2.10.7: 1) Downloading 'SRR017606'... 2020-06-15T22:24:30 prefetch.2.10.7: Downloading via HTTPS... 2020-06-15T22:24:53 prefetch.2.10.7: HTTPS download succeed 2020-06-15T22:24:54 prefetch.2.10.7: 'SRR017606' is valid 2020-06-15T22:24:54 prefetch.2.10.7: 1) 'SRR017606' was downloaded successfully Read 2245066 spots for SRR017606/SRR017606.sra Written 2245066 spots for SRR017606/SRR017606.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: 00:00:18 2245066 reads; of these: 2245066 (100.00%) were unpaired; of these: 775765 (34.55%) aligned 0 times 1242484 (55.34%) aligned exactly 1 time 226817 (10.10%) aligned >1 times 65.45% overall alignment rate Time searching: 00:00:18 Overall time: 00:00:18 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] 655427 / 1469301 = 0.4461 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 07:26:06: # Command line: callpeak -t /home/okishinya/chipatlas/results/ce11/SRX005637/SRX005637.bam -f BAM -g ce -n /home/okishinya/chipatlas/results/ce11/SRX005637/SRX005637.05 -q 1e-05 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/ce11/SRX005637/SRX005637.05 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/ce11/SRX005637/SRX005637.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 07:26:06: #1 read tag files... INFO @ Tue, 16 Jun 2020 07:26:06: #1 read treatment tags... INFO @ Tue, 16 Jun 2020 07:26:11: #1 tag size is determined as 27 bps INFO @ Tue, 16 Jun 2020 07:26:11: #1 tag size = 27 INFO @ Tue, 16 Jun 2020 07:26:11: #1 total tags in treatment: 813874 INFO @ Tue, 16 Jun 2020 07:26:11: #1 user defined the maximum tags... INFO @ Tue, 16 Jun 2020 07:26:11: #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 07:26:11: #1 tags after filtering in treatment: 813874 INFO @ Tue, 16 Jun 2020 07:26:11: #1 Redundant rate of treatment: 0.00 INFO @ Tue, 16 Jun 2020 07:26:11: #1 finished! INFO @ Tue, 16 Jun 2020 07:26:11: #2 Build Peak Model... INFO @ Tue, 16 Jun 2020 07:26:11: #2 looking for paired plus/minus strand peaks... INFO @ Tue, 16 Jun 2020 07:26:11: #2 number of paired peaks: 1149 INFO @ Tue, 16 Jun 2020 07:26:11: start model_add_line... INFO @ Tue, 16 Jun 2020 07:26:11: start X-correlation... INFO @ Tue, 16 Jun 2020 07:26:11: end of X-cor INFO @ Tue, 16 Jun 2020 07:26:11: #2 finished! INFO @ Tue, 16 Jun 2020 07:26:11: #2 predicted fragment length is 175 bps INFO @ Tue, 16 Jun 2020 07:26:11: #2 alternative fragment length(s) may be 175 bps INFO @ Tue, 16 Jun 2020 07:26:11: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/ce11/SRX005637/SRX005637.05_model.r INFO @ Tue, 16 Jun 2020 07:26:11: #3 Call peaks... INFO @ Tue, 16 Jun 2020 07:26:11: #3 Pre-compute pvalue-qvalue table... INFO @ Tue, 16 Jun 2020 07:26:13: #3 Call peaks for each chromosome... INFO @ Tue, 16 Jun 2020 07:26:14: #4 Write output xls file... /home/okishinya/chipatlas/results/ce11/SRX005637/SRX005637.05_peaks.xls INFO @ Tue, 16 Jun 2020 07:26:14: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/ce11/SRX005637/SRX005637.05_peaks.narrowPeak INFO @ Tue, 16 Jun 2020 07:26:14: #4 Write summits bed file... /home/okishinya/chipatlas/results/ce11/SRX005637/SRX005637.05_summits.bed INFO @ Tue, 16 Jun 2020 07:26:14: Done! pass1 - making usageList (7 chroms): 1 millis pass2 - checking and writing primary data (1185 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 07:26:36: # Command line: callpeak -t /home/okishinya/chipatlas/results/ce11/SRX005637/SRX005637.bam -f BAM -g ce -n /home/okishinya/chipatlas/results/ce11/SRX005637/SRX005637.10 -q 1e-10 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/ce11/SRX005637/SRX005637.10 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/ce11/SRX005637/SRX005637.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 07:26:36: #1 read tag files... INFO @ Tue, 16 Jun 2020 07:26:36: #1 read treatment tags... INFO @ Tue, 16 Jun 2020 07:26:41: #1 tag size is determined as 27 bps INFO @ Tue, 16 Jun 2020 07:26:41: #1 tag size = 27 INFO @ Tue, 16 Jun 2020 07:26:41: #1 total tags in treatment: 813874 INFO @ Tue, 16 Jun 2020 07:26:41: #1 user defined the maximum tags... INFO @ Tue, 16 Jun 2020 07:26:41: #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 07:26:41: #1 tags after filtering in treatment: 813874 INFO @ Tue, 16 Jun 2020 07:26:41: #1 Redundant rate of treatment: 0.00 INFO @ Tue, 16 Jun 2020 07:26:41: #1 finished! INFO @ Tue, 16 Jun 2020 07:26:41: #2 Build Peak Model... INFO @ Tue, 16 Jun 2020 07:26:41: #2 looking for paired plus/minus strand peaks... INFO @ Tue, 16 Jun 2020 07:26:41: #2 number of paired peaks: 1149 INFO @ Tue, 16 Jun 2020 07:26:41: start model_add_line... INFO @ Tue, 16 Jun 2020 07:26:41: start X-correlation... INFO @ Tue, 16 Jun 2020 07:26:41: end of X-cor INFO @ Tue, 16 Jun 2020 07:26:41: #2 finished! INFO @ Tue, 16 Jun 2020 07:26:41: #2 predicted fragment length is 175 bps INFO @ Tue, 16 Jun 2020 07:26:41: #2 alternative fragment length(s) may be 175 bps INFO @ Tue, 16 Jun 2020 07:26:41: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/ce11/SRX005637/SRX005637.10_model.r INFO @ Tue, 16 Jun 2020 07:26:41: #3 Call peaks... INFO @ Tue, 16 Jun 2020 07:26:41: #3 Pre-compute pvalue-qvalue table... INFO @ Tue, 16 Jun 2020 07:26:43: #3 Call peaks for each chromosome... INFO @ Tue, 16 Jun 2020 07:26:44: #4 Write output xls file... /home/okishinya/chipatlas/results/ce11/SRX005637/SRX005637.10_peaks.xls INFO @ Tue, 16 Jun 2020 07:26:44: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/ce11/SRX005637/SRX005637.10_peaks.narrowPeak INFO @ Tue, 16 Jun 2020 07:26:44: #4 Write summits bed file... /home/okishinya/chipatlas/results/ce11/SRX005637/SRX005637.10_summits.bed INFO @ Tue, 16 Jun 2020 07:26:44: Done! pass1 - making usageList (6 chroms): 1 millis pass2 - checking and writing primary data (392 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 07:27:06: # Command line: callpeak -t /home/okishinya/chipatlas/results/ce11/SRX005637/SRX005637.bam -f BAM -g ce -n /home/okishinya/chipatlas/results/ce11/SRX005637/SRX005637.20 -q 1e-20 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/ce11/SRX005637/SRX005637.20 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/ce11/SRX005637/SRX005637.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 07:27:06: #1 read tag files... INFO @ Tue, 16 Jun 2020 07:27:06: #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, 16 Jun 2020 07:27:10: #1 tag size is determined as 27 bps INFO @ Tue, 16 Jun 2020 07:27:10: #1 tag size = 27 INFO @ Tue, 16 Jun 2020 07:27:10: #1 total tags in treatment: 813874 INFO @ Tue, 16 Jun 2020 07:27:10: #1 user defined the maximum tags... INFO @ Tue, 16 Jun 2020 07:27:10: #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 07:27:10: #1 tags after filtering in treatment: 813874 INFO @ Tue, 16 Jun 2020 07:27:10: #1 Redundant rate of treatment: 0.00 INFO @ Tue, 16 Jun 2020 07:27:10: #1 finished! INFO @ Tue, 16 Jun 2020 07:27:10: #2 Build Peak Model... INFO @ Tue, 16 Jun 2020 07:27:10: #2 looking for paired plus/minus strand peaks... INFO @ Tue, 16 Jun 2020 07:27:10: #2 number of paired peaks: 1149 INFO @ Tue, 16 Jun 2020 07:27:10: start model_add_line... INFO @ Tue, 16 Jun 2020 07:27:10: start X-correlation... INFO @ Tue, 16 Jun 2020 07:27:10: end of X-cor INFO @ Tue, 16 Jun 2020 07:27:10: #2 finished! INFO @ Tue, 16 Jun 2020 07:27:10: #2 predicted fragment length is 175 bps INFO @ Tue, 16 Jun 2020 07:27:10: #2 alternative fragment length(s) may be 175 bps INFO @ Tue, 16 Jun 2020 07:27:10: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/ce11/SRX005637/SRX005637.20_model.r INFO @ Tue, 16 Jun 2020 07:27:10: #3 Call peaks... INFO @ Tue, 16 Jun 2020 07:27:10: #3 Pre-compute pvalue-qvalue table... INFO @ Tue, 16 Jun 2020 07:27:13: #3 Call peaks for each chromosome... INFO @ Tue, 16 Jun 2020 07:27:14: #4 Write output xls file... /home/okishinya/chipatlas/results/ce11/SRX005637/SRX005637.20_peaks.xls INFO @ Tue, 16 Jun 2020 07:27:14: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/ce11/SRX005637/SRX005637.20_peaks.narrowPeak INFO @ Tue, 16 Jun 2020 07:27:14: #4 Write summits bed file... /home/okishinya/chipatlas/results/ce11/SRX005637/SRX005637.20_summits.bed INFO @ Tue, 16 Jun 2020 07:27:14: Done! pass1 - making usageList (6 chroms): 0 millis pass2 - checking and writing primary data (71 records, 4 fields): 1 millis CompletedMACS2peakCalling