Job ID = 2589841 sra ファイルのダウンロード中... Read layout: SINGLE fastq に変換中... spots read : 7,182,298 reads read : 7,182,298 reads written : 7,182,298 rm: cannot remove ‘[DSE]RR*’: No such file or directory rm: cannot remove ‘/home/okishinya/ncbi/public/sra/SRR947470.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: 00:00:01 Multiseed full-index search: 00:01:22 7182298 reads; of these: 7182298 (100.00%) were unpaired; of these: 336146 (4.68%) aligned 0 times 5650636 (78.67%) aligned exactly 1 time 1195516 (16.65%) aligned >1 times 95.32% overall alignment rate Time searching: 00:01:23 Overall time: 00:01:23 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] 874697 / 6846152 = 0.1278 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 18:37:34: # Command line: callpeak -t /home/okishinya/chipatlas/results/ce10/SRX331238/SRX331238.bam -f BAM -g ce -n /home/okishinya/chipatlas/results/ce10/SRX331238/SRX331238.05 -q 1e-05 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/ce10/SRX331238/SRX331238.05 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/ce10/SRX331238/SRX331238.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 18:37:34: #1 read tag files... INFO @ Mon, 12 Aug 2019 18:37:34: #1 read treatment tags... INFO @ Mon, 12 Aug 2019 18:37:35: # Command line: callpeak -t /home/okishinya/chipatlas/results/ce10/SRX331238/SRX331238.bam -f BAM -g ce -n /home/okishinya/chipatlas/results/ce10/SRX331238/SRX331238.10 -q 1e-10 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/ce10/SRX331238/SRX331238.10 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/ce10/SRX331238/SRX331238.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 18:37:35: #1 read tag files... INFO @ Mon, 12 Aug 2019 18:37:35: #1 read treatment tags... INFO @ Mon, 12 Aug 2019 18:37:36: # Command line: callpeak -t /home/okishinya/chipatlas/results/ce10/SRX331238/SRX331238.bam -f BAM -g ce -n /home/okishinya/chipatlas/results/ce10/SRX331238/SRX331238.20 -q 1e-20 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/ce10/SRX331238/SRX331238.20 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/ce10/SRX331238/SRX331238.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 18:37:36: #1 read tag files... INFO @ Mon, 12 Aug 2019 18:37:36: #1 read treatment tags... INFO @ Mon, 12 Aug 2019 18:37:41: 1000000 INFO @ Mon, 12 Aug 2019 18:37:42: 1000000 INFO @ Mon, 12 Aug 2019 18:37:45: 1000000 INFO @ Mon, 12 Aug 2019 18:37:48: 2000000 INFO @ Mon, 12 Aug 2019 18:37:49: 2000000 INFO @ Mon, 12 Aug 2019 18:37:55: 2000000 INFO @ Mon, 12 Aug 2019 18:37:55: 3000000 INFO @ Mon, 12 Aug 2019 18:37:55: 3000000 INFO @ Mon, 12 Aug 2019 18:38:01: 4000000 INFO @ Mon, 12 Aug 2019 18:38:02: 4000000 INFO @ Mon, 12 Aug 2019 18:38:05: 3000000 INFO @ Mon, 12 Aug 2019 18:38:08: 5000000 INFO @ Mon, 12 Aug 2019 18:38:09: 5000000 INFO @ Mon, 12 Aug 2019 18:38:14: #1 tag size is determined as 32 bps INFO @ Mon, 12 Aug 2019 18:38:14: #1 tag size = 32 INFO @ Mon, 12 Aug 2019 18:38:14: #1 total tags in treatment: 5971455 INFO @ Mon, 12 Aug 2019 18:38:14: #1 user defined the maximum tags... INFO @ Mon, 12 Aug 2019 18:38:14: #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 18:38:14: #1 tags after filtering in treatment: 5971455 INFO @ Mon, 12 Aug 2019 18:38:14: #1 Redundant rate of treatment: 0.00 INFO @ Mon, 12 Aug 2019 18:38:14: #1 finished! INFO @ Mon, 12 Aug 2019 18:38:14: #2 Build Peak Model... INFO @ Mon, 12 Aug 2019 18:38:14: #2 looking for paired plus/minus strand peaks... INFO @ Mon, 12 Aug 2019 18:38:14: 4000000 INFO @ Mon, 12 Aug 2019 18:38:14: #2 number of paired peaks: 515 WARNING @ Mon, 12 Aug 2019 18:38:14: Fewer paired peaks (515) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 515 pairs to build model! INFO @ Mon, 12 Aug 2019 18:38:14: start model_add_line... INFO @ Mon, 12 Aug 2019 18:38:15: start X-correlation... INFO @ Mon, 12 Aug 2019 18:38:15: end of X-cor INFO @ Mon, 12 Aug 2019 18:38:15: #2 finished! INFO @ Mon, 12 Aug 2019 18:38:15: #2 predicted fragment length is 32 bps INFO @ Mon, 12 Aug 2019 18:38:15: #2 alternative fragment length(s) may be 2,32,551,560,593 bps INFO @ Mon, 12 Aug 2019 18:38:15: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/ce10/SRX331238/SRX331238.20_model.r WARNING @ Mon, 12 Aug 2019 18:38:15: #2 Since the d (32) calculated from paired-peaks are smaller than 2*tag length, it may be influenced by unknown sequencing problem! WARNING @ Mon, 12 Aug 2019 18:38:15: #2 You may need to consider one of the other alternative d(s): 2,32,551,560,593 WARNING @ Mon, 12 Aug 2019 18:38:15: #2 You can restart the process with --nomodel --extsize XXX with your choice or an arbitrary number. Nontheless, MACS will continute computing. INFO @ Mon, 12 Aug 2019 18:38:15: #3 Call peaks... INFO @ Mon, 12 Aug 2019 18:38:15: #3 Pre-compute pvalue-qvalue table... INFO @ Mon, 12 Aug 2019 18:38:16: #1 tag size is determined as 32 bps INFO @ Mon, 12 Aug 2019 18:38:16: #1 tag size = 32 INFO @ Mon, 12 Aug 2019 18:38:16: #1 total tags in treatment: 5971455 INFO @ Mon, 12 Aug 2019 18:38:16: #1 user defined the maximum tags... INFO @ Mon, 12 Aug 2019 18:38:16: #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 18:38:16: #1 tags after filtering in treatment: 5971455 INFO @ Mon, 12 Aug 2019 18:38:16: #1 Redundant rate of treatment: 0.00 INFO @ Mon, 12 Aug 2019 18:38:16: #1 finished! INFO @ Mon, 12 Aug 2019 18:38:16: #2 Build Peak Model... INFO @ Mon, 12 Aug 2019 18:38:16: #2 looking for paired plus/minus strand peaks... INFO @ Mon, 12 Aug 2019 18:38:17: #2 number of paired peaks: 515 WARNING @ Mon, 12 Aug 2019 18:38:17: Fewer paired peaks (515) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 515 pairs to build model! INFO @ Mon, 12 Aug 2019 18:38:17: start model_add_line... INFO @ Mon, 12 Aug 2019 18:38:17: start X-correlation... INFO @ Mon, 12 Aug 2019 18:38:17: end of X-cor INFO @ Mon, 12 Aug 2019 18:38:17: #2 finished! INFO @ Mon, 12 Aug 2019 18:38:17: #2 predicted fragment length is 32 bps INFO @ Mon, 12 Aug 2019 18:38:17: #2 alternative fragment length(s) may be 2,32,551,560,593 bps INFO @ Mon, 12 Aug 2019 18:38:17: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/ce10/SRX331238/SRX331238.05_model.r WARNING @ Mon, 12 Aug 2019 18:38:17: #2 Since the d (32) calculated from paired-peaks are smaller than 2*tag length, it may be influenced by unknown sequencing problem! WARNING @ Mon, 12 Aug 2019 18:38:17: #2 You may need to consider one of the other alternative d(s): 2,32,551,560,593 WARNING @ Mon, 12 Aug 2019 18:38:17: #2 You can restart the process with --nomodel --extsize XXX with your choice or an arbitrary number. Nontheless, MACS will continute computing. INFO @ Mon, 12 Aug 2019 18:38:17: #3 Call peaks... INFO @ Mon, 12 Aug 2019 18:38:17: #3 Pre-compute pvalue-qvalue table... INFO @ Mon, 12 Aug 2019 18:38:24: 5000000 INFO @ Mon, 12 Aug 2019 18:38:31: #3 Call peaks for each chromosome... INFO @ Mon, 12 Aug 2019 18:38:33: #1 tag size is determined as 32 bps INFO @ Mon, 12 Aug 2019 18:38:33: #1 tag size = 32 INFO @ Mon, 12 Aug 2019 18:38:33: #1 total tags in treatment: 5971455 INFO @ Mon, 12 Aug 2019 18:38:33: #1 user defined the maximum tags... INFO @ Mon, 12 Aug 2019 18:38:33: #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 18:38:33: #1 tags after filtering in treatment: 5971455 INFO @ Mon, 12 Aug 2019 18:38:33: #1 Redundant rate of treatment: 0.00 INFO @ Mon, 12 Aug 2019 18:38:33: #1 finished! INFO @ Mon, 12 Aug 2019 18:38:33: #2 Build Peak Model... INFO @ Mon, 12 Aug 2019 18:38:33: #2 looking for paired plus/minus strand peaks... INFO @ Mon, 12 Aug 2019 18:38:33: #2 number of paired peaks: 515 WARNING @ Mon, 12 Aug 2019 18:38:33: Fewer paired peaks (515) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 515 pairs to build model! INFO @ Mon, 12 Aug 2019 18:38:33: start model_add_line... INFO @ Mon, 12 Aug 2019 18:38:33: start X-correlation... INFO @ Mon, 12 Aug 2019 18:38:33: end of X-cor INFO @ Mon, 12 Aug 2019 18:38:33: #2 finished! INFO @ Mon, 12 Aug 2019 18:38:33: #2 predicted fragment length is 32 bps INFO @ Mon, 12 Aug 2019 18:38:33: #2 alternative fragment length(s) may be 2,32,551,560,593 bps INFO @ Mon, 12 Aug 2019 18:38:33: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/ce10/SRX331238/SRX331238.10_model.r WARNING @ Mon, 12 Aug 2019 18:38:33: #2 Since the d (32) calculated from paired-peaks are smaller than 2*tag length, it may be influenced by unknown sequencing problem! WARNING @ Mon, 12 Aug 2019 18:38:33: #2 You may need to consider one of the other alternative d(s): 2,32,551,560,593 WARNING @ Mon, 12 Aug 2019 18:38:33: #2 You can restart the process with --nomodel --extsize XXX with your choice or an arbitrary number. Nontheless, MACS will continute computing. INFO @ Mon, 12 Aug 2019 18:38:33: #3 Call peaks... INFO @ Mon, 12 Aug 2019 18:38:33: #3 Pre-compute pvalue-qvalue table... INFO @ Mon, 12 Aug 2019 18:38:34: #3 Call peaks for each chromosome... INFO @ Mon, 12 Aug 2019 18:38:40: #4 Write output xls file... /home/okishinya/chipatlas/results/ce10/SRX331238/SRX331238.20_peaks.xls INFO @ Mon, 12 Aug 2019 18:38:40: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/ce10/SRX331238/SRX331238.20_peaks.narrowPeak INFO @ Mon, 12 Aug 2019 18:38:40: #4 Write summits bed file... /home/okishinya/chipatlas/results/ce10/SRX331238/SRX331238.20_summits.bed INFO @ Mon, 12 Aug 2019 18:38:40: Done! pass1 - making usageList (6 chroms): 1 millis pass2 - checking and writing primary data (71 records, 4 fields): 1 millis CompletedMACS2peakCalling INFO @ Mon, 12 Aug 2019 18:38:42: #4 Write output xls file... /home/okishinya/chipatlas/results/ce10/SRX331238/SRX331238.05_peaks.xls INFO @ Mon, 12 Aug 2019 18:38:42: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/ce10/SRX331238/SRX331238.05_peaks.narrowPeak INFO @ Mon, 12 Aug 2019 18:38:42: #4 Write summits bed file... /home/okishinya/chipatlas/results/ce10/SRX331238/SRX331238.05_summits.bed INFO @ Mon, 12 Aug 2019 18:38:42: Done! pass1 - making usageList (6 chroms): 2 millis pass2 - checking and writing primary data (607 records, 4 fields): 3 millis CompletedMACS2peakCalling INFO @ Mon, 12 Aug 2019 18:38:50: #3 Call peaks for each chromosome... INFO @ Mon, 12 Aug 2019 18:38:59: #4 Write output xls file... /home/okishinya/chipatlas/results/ce10/SRX331238/SRX331238.10_peaks.xls INFO @ Mon, 12 Aug 2019 18:38:59: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/ce10/SRX331238/SRX331238.10_peaks.narrowPeak INFO @ Mon, 12 Aug 2019 18:38:59: #4 Write summits bed file... /home/okishinya/chipatlas/results/ce10/SRX331238/SRX331238.10_summits.bed INFO @ Mon, 12 Aug 2019 18:38:59: Done! pass1 - making usageList (6 chroms): 1 millis pass2 - checking and writing primary data (319 records, 4 fields): 2 millis CompletedMACS2peakCalling BedGraph に変換しました。 BigWig に変換中... BigWig に変換しました。