Job ID = 2589815 sra ファイルのダウンロード中... Read layout: SINGLE fastq に変換中... spots read : 9,172,619 reads read : 9,172,619 reads written : 9,172,619 rm: cannot remove ‘[DSE]RR*’: No such file or directory rm: cannot remove ‘/home/okishinya/ncbi/public/sra/SRR947445.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: 00:00:01 Time loading mirror index: 00:00:00 Multiseed full-index search: 00:00:51 9172619 reads; of these: 9172619 (100.00%) were unpaired; of these: 6991156 (76.22%) aligned 0 times 1819003 (19.83%) aligned exactly 1 time 362460 (3.95%) aligned >1 times 23.78% overall alignment rate Time searching: 00:00:52 Overall time: 00:00:52 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] 95599 / 2181463 = 0.0438 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 18:32:34: # Command line: callpeak -t /home/okishinya/chipatlas/results/ce10/SRX331213/SRX331213.bam -f BAM -g ce -n /home/okishinya/chipatlas/results/ce10/SRX331213/SRX331213.05 -q 1e-05 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/ce10/SRX331213/SRX331213.05 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/ce10/SRX331213/SRX331213.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 18:32:34: #1 read tag files... INFO @ Mon, 12 Aug 2019 18:32:34: #1 read treatment tags... INFO @ Mon, 12 Aug 2019 18:32:35: # Command line: callpeak -t /home/okishinya/chipatlas/results/ce10/SRX331213/SRX331213.bam -f BAM -g ce -n /home/okishinya/chipatlas/results/ce10/SRX331213/SRX331213.10 -q 1e-10 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/ce10/SRX331213/SRX331213.10 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/ce10/SRX331213/SRX331213.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 18:32:35: #1 read tag files... INFO @ Mon, 12 Aug 2019 18:32:35: #1 read treatment tags... INFO @ Mon, 12 Aug 2019 18:32:36: # Command line: callpeak -t /home/okishinya/chipatlas/results/ce10/SRX331213/SRX331213.bam -f BAM -g ce -n /home/okishinya/chipatlas/results/ce10/SRX331213/SRX331213.20 -q 1e-20 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/ce10/SRX331213/SRX331213.20 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/ce10/SRX331213/SRX331213.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 18:32:36: #1 read tag files... INFO @ Mon, 12 Aug 2019 18:32:36: #1 read treatment tags... INFO @ Mon, 12 Aug 2019 18:32:42: 1000000 INFO @ Mon, 12 Aug 2019 18:32:43: 1000000 INFO @ Mon, 12 Aug 2019 18:32:43: 1000000 INFO @ Mon, 12 Aug 2019 18:32:49: 2000000 INFO @ Mon, 12 Aug 2019 18:32:50: #1 tag size is determined as 32 bps INFO @ Mon, 12 Aug 2019 18:32:50: #1 tag size = 32 INFO @ Mon, 12 Aug 2019 18:32:50: #1 total tags in treatment: 2085864 INFO @ Mon, 12 Aug 2019 18:32:50: #1 user defined the maximum tags... INFO @ Mon, 12 Aug 2019 18:32:50: #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 18:32:50: #1 tags after filtering in treatment: 2085864 INFO @ Mon, 12 Aug 2019 18:32:50: #1 Redundant rate of treatment: 0.00 INFO @ Mon, 12 Aug 2019 18:32:50: #1 finished! INFO @ Mon, 12 Aug 2019 18:32:50: #2 Build Peak Model... INFO @ Mon, 12 Aug 2019 18:32:50: #2 looking for paired plus/minus strand peaks... INFO @ Mon, 12 Aug 2019 18:32:50: #2 number of paired peaks: 422 WARNING @ Mon, 12 Aug 2019 18:32:50: Fewer paired peaks (422) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 422 pairs to build model! INFO @ Mon, 12 Aug 2019 18:32:50: start model_add_line... INFO @ Mon, 12 Aug 2019 18:32:50: start X-correlation... INFO @ Mon, 12 Aug 2019 18:32:50: end of X-cor INFO @ Mon, 12 Aug 2019 18:32:50: #2 finished! INFO @ Mon, 12 Aug 2019 18:32:50: #2 predicted fragment length is 33 bps INFO @ Mon, 12 Aug 2019 18:32:50: #2 alternative fragment length(s) may be 33,155,212,238,420,425,432,525,588 bps INFO @ Mon, 12 Aug 2019 18:32:50: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/ce10/SRX331213/SRX331213.20_model.r WARNING @ Mon, 12 Aug 2019 18:32:50: #2 Since the d (33) calculated from paired-peaks are smaller than 2*tag length, it may be influenced by unknown sequencing problem! WARNING @ Mon, 12 Aug 2019 18:32:50: #2 You may need to consider one of the other alternative d(s): 33,155,212,238,420,425,432,525,588 WARNING @ Mon, 12 Aug 2019 18:32:50: #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 18:32:50: #3 Call peaks... INFO @ Mon, 12 Aug 2019 18:32:50: #3 Pre-compute pvalue-qvalue table... INFO @ Mon, 12 Aug 2019 18:32:51: 2000000 INFO @ Mon, 12 Aug 2019 18:32:52: #1 tag size is determined as 32 bps INFO @ Mon, 12 Aug 2019 18:32:52: #1 tag size = 32 INFO @ Mon, 12 Aug 2019 18:32:52: #1 total tags in treatment: 2085864 INFO @ Mon, 12 Aug 2019 18:32:52: #1 user defined the maximum tags... INFO @ Mon, 12 Aug 2019 18:32:52: #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 18:32:52: #1 tags after filtering in treatment: 2085864 INFO @ Mon, 12 Aug 2019 18:32:52: #1 Redundant rate of treatment: 0.00 INFO @ Mon, 12 Aug 2019 18:32:52: #1 finished! INFO @ Mon, 12 Aug 2019 18:32:52: #2 Build Peak Model... INFO @ Mon, 12 Aug 2019 18:32:52: #2 looking for paired plus/minus strand peaks... INFO @ Mon, 12 Aug 2019 18:32:52: 2000000 INFO @ Mon, 12 Aug 2019 18:32:52: #2 number of paired peaks: 422 WARNING @ Mon, 12 Aug 2019 18:32:52: Fewer paired peaks (422) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 422 pairs to build model! INFO @ Mon, 12 Aug 2019 18:32:52: start model_add_line... INFO @ Mon, 12 Aug 2019 18:32:52: start X-correlation... INFO @ Mon, 12 Aug 2019 18:32:52: end of X-cor INFO @ Mon, 12 Aug 2019 18:32:52: #2 finished! INFO @ Mon, 12 Aug 2019 18:32:52: #2 predicted fragment length is 33 bps INFO @ Mon, 12 Aug 2019 18:32:52: #2 alternative fragment length(s) may be 33,155,212,238,420,425,432,525,588 bps INFO @ Mon, 12 Aug 2019 18:32:52: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/ce10/SRX331213/SRX331213.05_model.r WARNING @ Mon, 12 Aug 2019 18:32:52: #2 Since the d (33) calculated from paired-peaks are smaller than 2*tag length, it may be influenced by unknown sequencing problem! WARNING @ Mon, 12 Aug 2019 18:32:52: #2 You may need to consider one of the other alternative d(s): 33,155,212,238,420,425,432,525,588 WARNING @ Mon, 12 Aug 2019 18:32:52: #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 18:32:52: #3 Call peaks... INFO @ Mon, 12 Aug 2019 18:32:52: #3 Pre-compute pvalue-qvalue table... INFO @ Mon, 12 Aug 2019 18:32:52: #1 tag size is determined as 32 bps INFO @ Mon, 12 Aug 2019 18:32:52: #1 tag size = 32 INFO @ Mon, 12 Aug 2019 18:32:52: #1 total tags in treatment: 2085864 INFO @ Mon, 12 Aug 2019 18:32:52: #1 user defined the maximum tags... INFO @ Mon, 12 Aug 2019 18:32:52: #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 18:32:52: #1 tags after filtering in treatment: 2085864 INFO @ Mon, 12 Aug 2019 18:32:52: #1 Redundant rate of treatment: 0.00 INFO @ Mon, 12 Aug 2019 18:32:52: #1 finished! INFO @ Mon, 12 Aug 2019 18:32:52: #2 Build Peak Model... INFO @ Mon, 12 Aug 2019 18:32:52: #2 looking for paired plus/minus strand peaks... INFO @ Mon, 12 Aug 2019 18:32:53: #2 number of paired peaks: 422 WARNING @ Mon, 12 Aug 2019 18:32:53: Fewer paired peaks (422) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 422 pairs to build model! INFO @ Mon, 12 Aug 2019 18:32:53: start model_add_line... INFO @ Mon, 12 Aug 2019 18:32:53: start X-correlation... INFO @ Mon, 12 Aug 2019 18:32:53: end of X-cor INFO @ Mon, 12 Aug 2019 18:32:53: #2 finished! INFO @ Mon, 12 Aug 2019 18:32:53: #2 predicted fragment length is 33 bps INFO @ Mon, 12 Aug 2019 18:32:53: #2 alternative fragment length(s) may be 33,155,212,238,420,425,432,525,588 bps INFO @ Mon, 12 Aug 2019 18:32:53: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/ce10/SRX331213/SRX331213.10_model.r WARNING @ Mon, 12 Aug 2019 18:32:53: #2 Since the d (33) calculated from paired-peaks are smaller than 2*tag length, it may be influenced by unknown sequencing problem! WARNING @ Mon, 12 Aug 2019 18:32:53: #2 You may need to consider one of the other alternative d(s): 33,155,212,238,420,425,432,525,588 WARNING @ Mon, 12 Aug 2019 18:32:53: #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 18:32:53: #3 Call peaks... INFO @ Mon, 12 Aug 2019 18:32:53: #3 Pre-compute pvalue-qvalue table... INFO @ Mon, 12 Aug 2019 18:32:57: #3 Call peaks for each chromosome... INFO @ Mon, 12 Aug 2019 18:32:58: #3 Call peaks for each chromosome... INFO @ Mon, 12 Aug 2019 18:32:59: #3 Call peaks for each chromosome... INFO @ Mon, 12 Aug 2019 18:33:00: #4 Write output xls file... /home/okishinya/chipatlas/results/ce10/SRX331213/SRX331213.20_peaks.xls INFO @ Mon, 12 Aug 2019 18:33:00: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/ce10/SRX331213/SRX331213.20_peaks.narrowPeak INFO @ Mon, 12 Aug 2019 18:33:00: #4 Write summits bed file... /home/okishinya/chipatlas/results/ce10/SRX331213/SRX331213.20_summits.bed INFO @ Mon, 12 Aug 2019 18:33:00: Done! pass1 - making usageList (6 chroms): 1 millis pass2 - checking and writing primary data (34 records, 4 fields): 2 millis CompletedMACS2peakCalling INFO @ Mon, 12 Aug 2019 18:33:01: #4 Write output xls file... /home/okishinya/chipatlas/results/ce10/SRX331213/SRX331213.05_peaks.xls INFO @ Mon, 12 Aug 2019 18:33:01: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/ce10/SRX331213/SRX331213.05_peaks.narrowPeak INFO @ Mon, 12 Aug 2019 18:33:01: #4 Write summits bed file... /home/okishinya/chipatlas/results/ce10/SRX331213/SRX331213.05_summits.bed INFO @ Mon, 12 Aug 2019 18:33:01: Done! pass1 - making usageList (6 chroms): 2 millis pass2 - checking and writing primary data (274 records, 4 fields): 2 millis CompletedMACS2peakCalling INFO @ Mon, 12 Aug 2019 18:33:02: #4 Write output xls file... /home/okishinya/chipatlas/results/ce10/SRX331213/SRX331213.10_peaks.xls INFO @ Mon, 12 Aug 2019 18:33:02: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/ce10/SRX331213/SRX331213.10_peaks.narrowPeak INFO @ Mon, 12 Aug 2019 18:33:02: #4 Write summits bed file... /home/okishinya/chipatlas/results/ce10/SRX331213/SRX331213.10_summits.bed INFO @ Mon, 12 Aug 2019 18:33:02: Done! pass1 - making usageList (6 chroms): 0 millis pass2 - checking and writing primary data (121 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。