Job ID = 2589416 sra ファイルのダウンロード中... Read layout: SINGLE fastq に変換中... spots read : 6,303,653 reads read : 6,303,653 reads written : 6,303,653 rm: cannot remove ‘[DSE]RR*’: No such file or directory rm: cannot remove ‘/home/okishinya/ncbi/public/sra/SRR494626.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: 00:00:48 6303653 reads; of these: 6303653 (100.00%) were unpaired; of these: 3765011 (59.73%) aligned 0 times 2182984 (34.63%) aligned exactly 1 time 355658 (5.64%) aligned >1 times 40.27% overall alignment rate Time searching: 00:00:48 Overall time: 00:00:48 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] 586804 / 2538642 = 0.2311 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 17:38:19: # Command line: callpeak -t /home/okishinya/chipatlas/results/ce10/SRX146465/SRX146465.bam -f BAM -g ce -n /home/okishinya/chipatlas/results/ce10/SRX146465/SRX146465.05 -q 1e-05 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/ce10/SRX146465/SRX146465.05 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/ce10/SRX146465/SRX146465.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 17:38:19: #1 read tag files... INFO @ Mon, 12 Aug 2019 17:38:19: #1 read treatment tags... INFO @ Mon, 12 Aug 2019 17:38:20: # Command line: callpeak -t /home/okishinya/chipatlas/results/ce10/SRX146465/SRX146465.bam -f BAM -g ce -n /home/okishinya/chipatlas/results/ce10/SRX146465/SRX146465.10 -q 1e-10 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/ce10/SRX146465/SRX146465.10 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/ce10/SRX146465/SRX146465.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 17:38:20: #1 read tag files... INFO @ Mon, 12 Aug 2019 17:38:20: #1 read treatment tags... INFO @ Mon, 12 Aug 2019 17:38:21: # Command line: callpeak -t /home/okishinya/chipatlas/results/ce10/SRX146465/SRX146465.bam -f BAM -g ce -n /home/okishinya/chipatlas/results/ce10/SRX146465/SRX146465.20 -q 1e-20 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/ce10/SRX146465/SRX146465.20 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/ce10/SRX146465/SRX146465.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 17:38:21: #1 read tag files... INFO @ Mon, 12 Aug 2019 17:38:21: #1 read treatment tags... INFO @ Mon, 12 Aug 2019 17:38:27: 1000000 INFO @ Mon, 12 Aug 2019 17:38:27: 1000000 INFO @ Mon, 12 Aug 2019 17:38:29: 1000000 INFO @ Mon, 12 Aug 2019 17:38:33: #1 tag size is determined as 32 bps INFO @ Mon, 12 Aug 2019 17:38:33: #1 tag size = 32 INFO @ Mon, 12 Aug 2019 17:38:33: #1 total tags in treatment: 1951838 INFO @ Mon, 12 Aug 2019 17:38:33: #1 user defined the maximum tags... INFO @ Mon, 12 Aug 2019 17:38:33: #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 17:38:33: #1 tags after filtering in treatment: 1951838 INFO @ Mon, 12 Aug 2019 17:38:33: #1 Redundant rate of treatment: 0.00 INFO @ Mon, 12 Aug 2019 17:38:33: #1 finished! INFO @ Mon, 12 Aug 2019 17:38:33: #2 Build Peak Model... INFO @ Mon, 12 Aug 2019 17:38:33: #2 looking for paired plus/minus strand peaks... INFO @ Mon, 12 Aug 2019 17:38:33: #2 number of paired peaks: 2382 INFO @ Mon, 12 Aug 2019 17:38:33: start model_add_line... INFO @ Mon, 12 Aug 2019 17:38:33: start X-correlation... INFO @ Mon, 12 Aug 2019 17:38:33: end of X-cor INFO @ Mon, 12 Aug 2019 17:38:33: #2 finished! INFO @ Mon, 12 Aug 2019 17:38:33: #2 predicted fragment length is 139 bps INFO @ Mon, 12 Aug 2019 17:38:33: #2 alternative fragment length(s) may be 139 bps INFO @ Mon, 12 Aug 2019 17:38:33: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/ce10/SRX146465/SRX146465.10_model.r INFO @ Mon, 12 Aug 2019 17:38:33: #3 Call peaks... INFO @ Mon, 12 Aug 2019 17:38:33: #3 Pre-compute pvalue-qvalue table... INFO @ Mon, 12 Aug 2019 17:38:34: #1 tag size is determined as 32 bps INFO @ Mon, 12 Aug 2019 17:38:34: #1 tag size = 32 INFO @ Mon, 12 Aug 2019 17:38:34: #1 total tags in treatment: 1951838 INFO @ Mon, 12 Aug 2019 17:38:34: #1 user defined the maximum tags... INFO @ Mon, 12 Aug 2019 17:38:34: #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 17:38:34: #1 tags after filtering in treatment: 1951838 INFO @ Mon, 12 Aug 2019 17:38:34: #1 Redundant rate of treatment: 0.00 INFO @ Mon, 12 Aug 2019 17:38:34: #1 finished! INFO @ Mon, 12 Aug 2019 17:38:34: #2 Build Peak Model... INFO @ Mon, 12 Aug 2019 17:38:34: #2 looking for paired plus/minus strand peaks... INFO @ Mon, 12 Aug 2019 17:38:34: #2 number of paired peaks: 2382 INFO @ Mon, 12 Aug 2019 17:38:34: start model_add_line... INFO @ Mon, 12 Aug 2019 17:38:34: start X-correlation... INFO @ Mon, 12 Aug 2019 17:38:34: end of X-cor INFO @ Mon, 12 Aug 2019 17:38:34: #2 finished! INFO @ Mon, 12 Aug 2019 17:38:34: #2 predicted fragment length is 139 bps INFO @ Mon, 12 Aug 2019 17:38:34: #2 alternative fragment length(s) may be 139 bps INFO @ Mon, 12 Aug 2019 17:38:34: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/ce10/SRX146465/SRX146465.05_model.r INFO @ Mon, 12 Aug 2019 17:38:34: #3 Call peaks... INFO @ Mon, 12 Aug 2019 17:38:34: #3 Pre-compute pvalue-qvalue table... INFO @ Mon, 12 Aug 2019 17:38:37: #1 tag size is determined as 32 bps INFO @ Mon, 12 Aug 2019 17:38:37: #1 tag size = 32 INFO @ Mon, 12 Aug 2019 17:38:37: #1 total tags in treatment: 1951838 INFO @ Mon, 12 Aug 2019 17:38:37: #1 user defined the maximum tags... INFO @ Mon, 12 Aug 2019 17:38:37: #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 17:38:37: #1 tags after filtering in treatment: 1951838 INFO @ Mon, 12 Aug 2019 17:38:37: #1 Redundant rate of treatment: 0.00 INFO @ Mon, 12 Aug 2019 17:38:37: #1 finished! INFO @ Mon, 12 Aug 2019 17:38:37: #2 Build Peak Model... INFO @ Mon, 12 Aug 2019 17:38:37: #2 looking for paired plus/minus strand peaks... INFO @ Mon, 12 Aug 2019 17:38:37: #2 number of paired peaks: 2382 INFO @ Mon, 12 Aug 2019 17:38:37: start model_add_line... INFO @ Mon, 12 Aug 2019 17:38:37: start X-correlation... INFO @ Mon, 12 Aug 2019 17:38:37: end of X-cor INFO @ Mon, 12 Aug 2019 17:38:37: #2 finished! INFO @ Mon, 12 Aug 2019 17:38:37: #2 predicted fragment length is 139 bps INFO @ Mon, 12 Aug 2019 17:38:37: #2 alternative fragment length(s) may be 139 bps INFO @ Mon, 12 Aug 2019 17:38:37: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/ce10/SRX146465/SRX146465.20_model.r INFO @ Mon, 12 Aug 2019 17:38:37: #3 Call peaks... INFO @ Mon, 12 Aug 2019 17:38:37: #3 Pre-compute pvalue-qvalue table... INFO @ Mon, 12 Aug 2019 17:38:40: #3 Call peaks for each chromosome... INFO @ Mon, 12 Aug 2019 17:38:41: #3 Call peaks for each chromosome... INFO @ Mon, 12 Aug 2019 17:38:43: #4 Write output xls file... /home/okishinya/chipatlas/results/ce10/SRX146465/SRX146465.10_peaks.xls INFO @ Mon, 12 Aug 2019 17:38:43: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/ce10/SRX146465/SRX146465.10_peaks.narrowPeak INFO @ Mon, 12 Aug 2019 17:38:43: #4 Write summits bed file... /home/okishinya/chipatlas/results/ce10/SRX146465/SRX146465.10_summits.bed INFO @ Mon, 12 Aug 2019 17:38:43: Done! pass1 - making usageList (7 chroms): 1 millis pass2 - checking and writing primary data (2682 records, 4 fields): 5 millis CompletedMACS2peakCalling INFO @ Mon, 12 Aug 2019 17:38:44: #3 Call peaks for each chromosome... INFO @ Mon, 12 Aug 2019 17:38:44: #4 Write output xls file... /home/okishinya/chipatlas/results/ce10/SRX146465/SRX146465.05_peaks.xls INFO @ Mon, 12 Aug 2019 17:38:44: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/ce10/SRX146465/SRX146465.05_peaks.narrowPeak INFO @ Mon, 12 Aug 2019 17:38:44: #4 Write summits bed file... /home/okishinya/chipatlas/results/ce10/SRX146465/SRX146465.05_summits.bed INFO @ Mon, 12 Aug 2019 17:38:45: Done! pass1 - making usageList (7 chroms): 2 millis pass2 - checking and writing primary data (3694 records, 4 fields): 6 millis CompletedMACS2peakCalling INFO @ Mon, 12 Aug 2019 17:38:47: #4 Write output xls file... /home/okishinya/chipatlas/results/ce10/SRX146465/SRX146465.20_peaks.xls INFO @ Mon, 12 Aug 2019 17:38:47: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/ce10/SRX146465/SRX146465.20_peaks.narrowPeak INFO @ Mon, 12 Aug 2019 17:38:47: #4 Write summits bed file... /home/okishinya/chipatlas/results/ce10/SRX146465/SRX146465.20_summits.bed INFO @ Mon, 12 Aug 2019 17:38:47: Done! pass1 - making usageList (7 chroms): 2 millis pass2 - checking and writing primary data (1692 records, 4 fields): 7 millis CompletedMACS2peakCalling BedGraph に変換しました。 BigWig に変換中... BigWig に変換しました。