Job ID = 2589250 sra ファイルのダウンロード中... Read layout: SINGLE fastq に変換中... spots read : 1,387,623 reads read : 1,387,623 reads written : 1,387,623 rm: cannot remove ‘[DSE]RR*’: No such file or directory rm: cannot remove ‘/home/okishinya/ncbi/public/sra/SRR164281.sra.cache’: No such file or directory 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: 00:00:08 1387623 reads; of these: 1387623 (100.00%) were unpaired; of these: 1191066 (85.83%) aligned 0 times 174341 (12.56%) aligned exactly 1 time 22216 (1.60%) aligned >1 times 14.17% overall alignment rate Time searching: 00:00:08 Overall time: 00:00:08 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] 2244 / 196557 = 0.0114 in library ' ' BAM に変換しました。 Bed ファイルを作成中... BedGraph に変換中... INFO @ Mon, 12 Aug 2019 17:14:06: # Command line: callpeak -t /home/okishinya/chipatlas/results/ce10/SRX054310/SRX054310.bam -f BAM -g ce -n /home/okishinya/chipatlas/results/ce10/SRX054310/SRX054310.05 -q 1e-05 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/ce10/SRX054310/SRX054310.05 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/ce10/SRX054310/SRX054310.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 @ Mon, 12 Aug 2019 17:14:06: #1 read tag files... INFO @ Mon, 12 Aug 2019 17:14:06: #1 read treatment tags... INFO @ Mon, 12 Aug 2019 17:14:07: # Command line: callpeak -t /home/okishinya/chipatlas/results/ce10/SRX054310/SRX054310.bam -f BAM -g ce -n /home/okishinya/chipatlas/results/ce10/SRX054310/SRX054310.10 -q 1e-10 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/ce10/SRX054310/SRX054310.10 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/ce10/SRX054310/SRX054310.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 @ Mon, 12 Aug 2019 17:14:07: #1 read tag files... INFO @ Mon, 12 Aug 2019 17:14:07: #1 read treatment tags... INFO @ Mon, 12 Aug 2019 17:14:08: #1 tag size is determined as 34 bps INFO @ Mon, 12 Aug 2019 17:14:08: #1 tag size = 34 INFO @ Mon, 12 Aug 2019 17:14:08: #1 total tags in treatment: 194313 INFO @ Mon, 12 Aug 2019 17:14:08: #1 user defined the maximum tags... INFO @ Mon, 12 Aug 2019 17:14:08: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Mon, 12 Aug 2019 17:14:08: #1 tags after filtering in treatment: 194313 INFO @ Mon, 12 Aug 2019 17:14:08: #1 Redundant rate of treatment: 0.00 INFO @ Mon, 12 Aug 2019 17:14:08: #1 finished! INFO @ Mon, 12 Aug 2019 17:14:08: #2 Build Peak Model... INFO @ Mon, 12 Aug 2019 17:14:08: #2 looking for paired plus/minus strand peaks... INFO @ Mon, 12 Aug 2019 17:14:08: #2 number of paired peaks: 2334 INFO @ Mon, 12 Aug 2019 17:14:08: start model_add_line... INFO @ Mon, 12 Aug 2019 17:14:08: start X-correlation... INFO @ Mon, 12 Aug 2019 17:14:08: end of X-cor INFO @ Mon, 12 Aug 2019 17:14:08: #2 finished! INFO @ Mon, 12 Aug 2019 17:14:08: #2 predicted fragment length is 175 bps INFO @ Mon, 12 Aug 2019 17:14:08: #2 alternative fragment length(s) may be 175 bps INFO @ Mon, 12 Aug 2019 17:14:08: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/ce10/SRX054310/SRX054310.05_model.r INFO @ Mon, 12 Aug 2019 17:14:08: #3 Call peaks... INFO @ Mon, 12 Aug 2019 17:14:08: #3 Pre-compute pvalue-qvalue table... INFO @ Mon, 12 Aug 2019 17:14:08: # Command line: callpeak -t /home/okishinya/chipatlas/results/ce10/SRX054310/SRX054310.bam -f BAM -g ce -n /home/okishinya/chipatlas/results/ce10/SRX054310/SRX054310.20 -q 1e-20 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/ce10/SRX054310/SRX054310.20 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/ce10/SRX054310/SRX054310.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 @ Mon, 12 Aug 2019 17:14:08: #1 read tag files... INFO @ Mon, 12 Aug 2019 17:14:08: #1 read treatment tags... INFO @ Mon, 12 Aug 2019 17:14:08: #3 Call peaks for each chromosome... INFO @ Mon, 12 Aug 2019 17:14:09: #1 tag size is determined as 34 bps INFO @ Mon, 12 Aug 2019 17:14:09: #1 tag size = 34 INFO @ Mon, 12 Aug 2019 17:14:09: #1 total tags in treatment: 194313 INFO @ Mon, 12 Aug 2019 17:14:09: #1 user defined the maximum tags... INFO @ Mon, 12 Aug 2019 17:14:09: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Mon, 12 Aug 2019 17:14:09: #1 tags after filtering in treatment: 194313 INFO @ Mon, 12 Aug 2019 17:14:09: #1 Redundant rate of treatment: 0.00 INFO @ Mon, 12 Aug 2019 17:14:09: #1 finished! INFO @ Mon, 12 Aug 2019 17:14:09: #2 Build Peak Model... INFO @ Mon, 12 Aug 2019 17:14:09: #2 looking for paired plus/minus strand peaks... INFO @ Mon, 12 Aug 2019 17:14:09: #4 Write output xls file... /home/okishinya/chipatlas/results/ce10/SRX054310/SRX054310.05_peaks.xls INFO @ Mon, 12 Aug 2019 17:14:09: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/ce10/SRX054310/SRX054310.05_peaks.narrowPeak INFO @ Mon, 12 Aug 2019 17:14:09: #4 Write summits bed file... /home/okishinya/chipatlas/results/ce10/SRX054310/SRX054310.05_summits.bed INFO @ Mon, 12 Aug 2019 17:14:09: Done! INFO @ Mon, 12 Aug 2019 17:14:09: #2 number of paired peaks: 2334 INFO @ Mon, 12 Aug 2019 17:14:09: start model_add_line... INFO @ Mon, 12 Aug 2019 17:14:09: start X-correlation... INFO @ Mon, 12 Aug 2019 17:14:09: end of X-cor INFO @ Mon, 12 Aug 2019 17:14:09: #2 finished! INFO @ Mon, 12 Aug 2019 17:14:09: #2 predicted fragment length is 175 bps INFO @ Mon, 12 Aug 2019 17:14:09: #2 alternative fragment length(s) may be 175 bps INFO @ Mon, 12 Aug 2019 17:14:09: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/ce10/SRX054310/SRX054310.10_model.r INFO @ Mon, 12 Aug 2019 17:14:09: #3 Call peaks... INFO @ Mon, 12 Aug 2019 17:14:09: #3 Pre-compute pvalue-qvalue table... pass1 - making usageList (5 chroms): 1 millis pass2 - checking and writing primary data (22 records, 4 fields): 1 millis CompletedMACS2peakCalling BedGraph に変換しました。 BigWig に変換中... INFO @ Mon, 12 Aug 2019 17:14:09: #3 Call peaks for each chromosome... BigWig に変換しました。 INFO @ Mon, 12 Aug 2019 17:14:10: #1 tag size is determined as 34 bps INFO @ Mon, 12 Aug 2019 17:14:10: #1 tag size = 34 INFO @ Mon, 12 Aug 2019 17:14:10: #1 total tags in treatment: 194313 INFO @ Mon, 12 Aug 2019 17:14:10: #1 user defined the maximum tags... INFO @ Mon, 12 Aug 2019 17:14:10: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Mon, 12 Aug 2019 17:14:10: #1 tags after filtering in treatment: 194313 INFO @ Mon, 12 Aug 2019 17:14:10: #1 Redundant rate of treatment: 0.00 INFO @ Mon, 12 Aug 2019 17:14:10: #1 finished! INFO @ Mon, 12 Aug 2019 17:14:10: #2 Build Peak Model... INFO @ Mon, 12 Aug 2019 17:14:10: #2 looking for paired plus/minus strand peaks... INFO @ Mon, 12 Aug 2019 17:14:10: #4 Write output xls file... /home/okishinya/chipatlas/results/ce10/SRX054310/SRX054310.10_peaks.xls INFO @ Mon, 12 Aug 2019 17:14:10: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/ce10/SRX054310/SRX054310.10_peaks.narrowPeak INFO @ Mon, 12 Aug 2019 17:14:10: #4 Write summits bed file... /home/okishinya/chipatlas/results/ce10/SRX054310/SRX054310.10_summits.bed INFO @ Mon, 12 Aug 2019 17:14:10: Done! INFO @ Mon, 12 Aug 2019 17:14:10: #2 number of paired peaks: 2334 INFO @ Mon, 12 Aug 2019 17:14:10: start model_add_line... INFO @ Mon, 12 Aug 2019 17:14:10: start X-correlation... INFO @ Mon, 12 Aug 2019 17:14:10: end of X-cor INFO @ Mon, 12 Aug 2019 17:14:10: #2 finished! INFO @ Mon, 12 Aug 2019 17:14:10: #2 predicted fragment length is 175 bps INFO @ Mon, 12 Aug 2019 17:14:10: #2 alternative fragment length(s) may be 175 bps INFO @ Mon, 12 Aug 2019 17:14:10: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/ce10/SRX054310/SRX054310.20_model.r INFO @ Mon, 12 Aug 2019 17:14:10: #3 Call peaks... INFO @ Mon, 12 Aug 2019 17:14:10: #3 Pre-compute pvalue-qvalue table... pass1 - making usageList (2 chroms): 1 millis pass2 - checking and writing primary data (5 records, 4 fields): 1 millis CompletedMACS2peakCalling INFO @ Mon, 12 Aug 2019 17:14:10: #3 Call peaks for each chromosome... INFO @ Mon, 12 Aug 2019 17:14:11: #4 Write output xls file... /home/okishinya/chipatlas/results/ce10/SRX054310/SRX054310.20_peaks.xls INFO @ Mon, 12 Aug 2019 17:14:11: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/ce10/SRX054310/SRX054310.20_peaks.narrowPeak INFO @ Mon, 12 Aug 2019 17:14:11: #4 Write summits bed file... /home/okishinya/chipatlas/results/ce10/SRX054310/SRX054310.20_summits.bed INFO @ Mon, 12 Aug 2019 17:14:11: Done! pass1 - making usageList (1 chroms): 1 millis pass2 - checking and writing primary data (1 records, 4 fields): 1 millis CompletedMACS2peakCalling