Job ID = 1294124 sra ファイルのダウンロード中... Read layout: SINGLE fastq に変換中... spots read : 19,432,784 reads read : 19,432,784 reads written : 19,432,784 rm: cannot remove ‘[DSE]RR*’: No such file or directory rm: cannot remove ‘fastqDump_tmp*’: 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: 00:05:30 19432784 reads; of these: 19432784 (100.00%) were unpaired; of these: 2231756 (11.48%) aligned 0 times 14485773 (74.54%) aligned exactly 1 time 2715255 (13.97%) aligned >1 times 88.52% overall alignment rate Time searching: 00:05:30 Overall time: 00:05:30 マッピングが完了しました。 samtools でBAM に変換中... [samopen] SAM header is present: 15 sequences. [bam_sort_core] merging from 8 files... [bam_rmdupse_core] 12253270 / 17201028 = 0.7124 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, 03 Jun 2019 05:17:07: # Command line: callpeak -t /home/okishinya/chipatlas/results/dm3/SRX191914/SRX191914.bam -f BAM -g dm -n /home/okishinya/chipatlas/results/dm3/SRX191914/SRX191914.20 -q 1e-20 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/dm3/SRX191914/SRX191914.20 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/dm3/SRX191914/SRX191914.bam'] # control file = None # effective genome size = 1.20e+08 # 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, 03 Jun 2019 05:17:07: #1 read tag files... INFO @ Mon, 03 Jun 2019 05:17:07: #1 read treatment tags... INFO @ Mon, 03 Jun 2019 05:17:07: # Command line: callpeak -t /home/okishinya/chipatlas/results/dm3/SRX191914/SRX191914.bam -f BAM -g dm -n /home/okishinya/chipatlas/results/dm3/SRX191914/SRX191914.05 -q 1e-05 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/dm3/SRX191914/SRX191914.05 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/dm3/SRX191914/SRX191914.bam'] # control file = None # effective genome size = 1.20e+08 # 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, 03 Jun 2019 05:17:07: #1 read tag files... INFO @ Mon, 03 Jun 2019 05:17:07: #1 read treatment tags... INFO @ Mon, 03 Jun 2019 05:17:07: # Command line: callpeak -t /home/okishinya/chipatlas/results/dm3/SRX191914/SRX191914.bam -f BAM -g dm -n /home/okishinya/chipatlas/results/dm3/SRX191914/SRX191914.10 -q 1e-10 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/dm3/SRX191914/SRX191914.10 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/dm3/SRX191914/SRX191914.bam'] # control file = None # effective genome size = 1.20e+08 # 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, 03 Jun 2019 05:17:07: #1 read tag files... INFO @ Mon, 03 Jun 2019 05:17:07: #1 read treatment tags... INFO @ Mon, 03 Jun 2019 05:17:15: 1000000 INFO @ Mon, 03 Jun 2019 05:17:15: 1000000 INFO @ Mon, 03 Jun 2019 05:17:15: 1000000 INFO @ Mon, 03 Jun 2019 05:17:22: 2000000 INFO @ Mon, 03 Jun 2019 05:17:22: 2000000 INFO @ Mon, 03 Jun 2019 05:17:22: 2000000 INFO @ Mon, 03 Jun 2019 05:17:28: 3000000 INFO @ Mon, 03 Jun 2019 05:17:29: 3000000 INFO @ Mon, 03 Jun 2019 05:17:30: 3000000 INFO @ Mon, 03 Jun 2019 05:17:34: 4000000 INFO @ Mon, 03 Jun 2019 05:17:37: 4000000 INFO @ Mon, 03 Jun 2019 05:17:37: 4000000 INFO @ Mon, 03 Jun 2019 05:17:40: #1 tag size is determined as 36 bps INFO @ Mon, 03 Jun 2019 05:17:40: #1 tag size = 36 INFO @ Mon, 03 Jun 2019 05:17:40: #1 total tags in treatment: 4947758 INFO @ Mon, 03 Jun 2019 05:17:40: #1 user defined the maximum tags... INFO @ Mon, 03 Jun 2019 05:17:40: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Mon, 03 Jun 2019 05:17:41: #1 tags after filtering in treatment: 4947758 INFO @ Mon, 03 Jun 2019 05:17:41: #1 Redundant rate of treatment: 0.00 INFO @ Mon, 03 Jun 2019 05:17:41: #1 finished! INFO @ Mon, 03 Jun 2019 05:17:41: #2 Build Peak Model... INFO @ Mon, 03 Jun 2019 05:17:41: #2 looking for paired plus/minus strand peaks... INFO @ Mon, 03 Jun 2019 05:17:41: #2 number of paired peaks: 2164 INFO @ Mon, 03 Jun 2019 05:17:41: start model_add_line... INFO @ Mon, 03 Jun 2019 05:17:41: start X-correlation... INFO @ Mon, 03 Jun 2019 05:17:41: end of X-cor INFO @ Mon, 03 Jun 2019 05:17:41: #2 finished! INFO @ Mon, 03 Jun 2019 05:17:41: #2 predicted fragment length is 113 bps INFO @ Mon, 03 Jun 2019 05:17:41: #2 alternative fragment length(s) may be 113 bps INFO @ Mon, 03 Jun 2019 05:17:41: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/dm3/SRX191914/SRX191914.10_model.r INFO @ Mon, 03 Jun 2019 05:17:41: #3 Call peaks... INFO @ Mon, 03 Jun 2019 05:17:41: #3 Pre-compute pvalue-qvalue table... INFO @ Mon, 03 Jun 2019 05:17:43: #1 tag size is determined as 36 bps INFO @ Mon, 03 Jun 2019 05:17:43: #1 tag size = 36 INFO @ Mon, 03 Jun 2019 05:17:43: #1 total tags in treatment: 4947758 INFO @ Mon, 03 Jun 2019 05:17:43: #1 user defined the maximum tags... INFO @ Mon, 03 Jun 2019 05:17:43: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Mon, 03 Jun 2019 05:17:43: #1 tags after filtering in treatment: 4947758 INFO @ Mon, 03 Jun 2019 05:17:43: #1 Redundant rate of treatment: 0.00 INFO @ Mon, 03 Jun 2019 05:17:43: #1 finished! INFO @ Mon, 03 Jun 2019 05:17:43: #2 Build Peak Model... INFO @ Mon, 03 Jun 2019 05:17:43: #2 looking for paired plus/minus strand peaks... INFO @ Mon, 03 Jun 2019 05:17:44: #2 number of paired peaks: 2164 INFO @ Mon, 03 Jun 2019 05:17:44: start model_add_line... INFO @ Mon, 03 Jun 2019 05:17:44: start X-correlation... INFO @ Mon, 03 Jun 2019 05:17:44: end of X-cor INFO @ Mon, 03 Jun 2019 05:17:44: #2 finished! INFO @ Mon, 03 Jun 2019 05:17:44: #2 predicted fragment length is 113 bps INFO @ Mon, 03 Jun 2019 05:17:44: #2 alternative fragment length(s) may be 113 bps INFO @ Mon, 03 Jun 2019 05:17:44: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/dm3/SRX191914/SRX191914.05_model.r INFO @ Mon, 03 Jun 2019 05:17:44: #3 Call peaks... INFO @ Mon, 03 Jun 2019 05:17:44: #3 Pre-compute pvalue-qvalue table... INFO @ Mon, 03 Jun 2019 05:17:44: #1 tag size is determined as 36 bps INFO @ Mon, 03 Jun 2019 05:17:44: #1 tag size = 36 INFO @ Mon, 03 Jun 2019 05:17:44: #1 total tags in treatment: 4947758 INFO @ Mon, 03 Jun 2019 05:17:44: #1 user defined the maximum tags... INFO @ Mon, 03 Jun 2019 05:17:44: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Mon, 03 Jun 2019 05:17:44: #1 tags after filtering in treatment: 4947758 INFO @ Mon, 03 Jun 2019 05:17:44: #1 Redundant rate of treatment: 0.00 INFO @ Mon, 03 Jun 2019 05:17:44: #1 finished! INFO @ Mon, 03 Jun 2019 05:17:44: #2 Build Peak Model... INFO @ Mon, 03 Jun 2019 05:17:44: #2 looking for paired plus/minus strand peaks... INFO @ Mon, 03 Jun 2019 05:17:45: #2 number of paired peaks: 2164 INFO @ Mon, 03 Jun 2019 05:17:45: start model_add_line... INFO @ Mon, 03 Jun 2019 05:17:45: start X-correlation... INFO @ Mon, 03 Jun 2019 05:17:45: end of X-cor INFO @ Mon, 03 Jun 2019 05:17:45: #2 finished! INFO @ Mon, 03 Jun 2019 05:17:45: #2 predicted fragment length is 113 bps INFO @ Mon, 03 Jun 2019 05:17:45: #2 alternative fragment length(s) may be 113 bps INFO @ Mon, 03 Jun 2019 05:17:45: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/dm3/SRX191914/SRX191914.20_model.r INFO @ Mon, 03 Jun 2019 05:17:45: #3 Call peaks... INFO @ Mon, 03 Jun 2019 05:17:45: #3 Pre-compute pvalue-qvalue table... INFO @ Mon, 03 Jun 2019 05:17:57: #3 Call peaks for each chromosome... INFO @ Mon, 03 Jun 2019 05:18:00: #3 Call peaks for each chromosome... INFO @ Mon, 03 Jun 2019 05:18:00: #3 Call peaks for each chromosome... INFO @ Mon, 03 Jun 2019 05:18:05: #4 Write output xls file... /home/okishinya/chipatlas/results/dm3/SRX191914/SRX191914.10_peaks.xls INFO @ Mon, 03 Jun 2019 05:18:05: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/dm3/SRX191914/SRX191914.10_peaks.narrowPeak INFO @ Mon, 03 Jun 2019 05:18:05: #4 Write summits bed file... /home/okishinya/chipatlas/results/dm3/SRX191914/SRX191914.10_summits.bed INFO @ Mon, 03 Jun 2019 05:18:05: Done! pass1 - making usageList (14 chroms): 2 millis pass2 - checking and writing primary data (3881 records, 4 fields): 10 millis CompletedMACS2peakCalling INFO @ Mon, 03 Jun 2019 05:18:07: #4 Write output xls file... /home/okishinya/chipatlas/results/dm3/SRX191914/SRX191914.05_peaks.xls INFO @ Mon, 03 Jun 2019 05:18:07: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/dm3/SRX191914/SRX191914.05_peaks.narrowPeak INFO @ Mon, 03 Jun 2019 05:18:08: #4 Write summits bed file... /home/okishinya/chipatlas/results/dm3/SRX191914/SRX191914.05_summits.bed INFO @ Mon, 03 Jun 2019 05:18:08: Done! pass1 - making usageList (15 chroms): 1 millis pass2 - checking and writing primary data (5850 records, 4 fields): 10 millis CompletedMACS2peakCalling INFO @ Mon, 03 Jun 2019 05:18:08: #4 Write output xls file... /home/okishinya/chipatlas/results/dm3/SRX191914/SRX191914.20_peaks.xls INFO @ Mon, 03 Jun 2019 05:18:08: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/dm3/SRX191914/SRX191914.20_peaks.narrowPeak INFO @ Mon, 03 Jun 2019 05:18:08: #4 Write summits bed file... /home/okishinya/chipatlas/results/dm3/SRX191914/SRX191914.20_summits.bed INFO @ Mon, 03 Jun 2019 05:18:08: Done! pass1 - making usageList (14 chroms): 1 millis pass2 - checking and writing primary data (2650 records, 4 fields): 11 millis CompletedMACS2peakCalling BedGraph に変換しました。 BigWig に変換中... BigWig に変換しました。