Job ID = 2589680 sra ファイルのダウンロード中... Read layout: SINGLE fastq に変換中... spots read : 5,297,747 reads read : 5,297,747 reads written : 5,297,747 rm: cannot remove ‘[DSE]RR*’: No such file or directory rm: cannot remove ‘/home/okishinya/ncbi/public/sra/SRR947281.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: 00:00:57 5297747 reads; of these: 5297747 (100.00%) were unpaired; of these: 1008493 (19.04%) aligned 0 times 3656789 (69.03%) aligned exactly 1 time 632465 (11.94%) aligned >1 times 80.96% overall alignment rate Time searching: 00:00:57 Overall time: 00:00:57 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] 335656 / 4289254 = 0.0783 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 18:15:08: # Command line: callpeak -t /home/okishinya/chipatlas/results/ce10/SRX331057/SRX331057.bam -f BAM -g ce -n /home/okishinya/chipatlas/results/ce10/SRX331057/SRX331057.05 -q 1e-05 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/ce10/SRX331057/SRX331057.05 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/ce10/SRX331057/SRX331057.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 18:15:08: #1 read tag files... INFO @ Mon, 12 Aug 2019 18:15:08: #1 read treatment tags... INFO @ Mon, 12 Aug 2019 18:15:09: # Command line: callpeak -t /home/okishinya/chipatlas/results/ce10/SRX331057/SRX331057.bam -f BAM -g ce -n /home/okishinya/chipatlas/results/ce10/SRX331057/SRX331057.10 -q 1e-10 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/ce10/SRX331057/SRX331057.10 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/ce10/SRX331057/SRX331057.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 18:15:09: #1 read tag files... INFO @ Mon, 12 Aug 2019 18:15:09: #1 read treatment tags... INFO @ Mon, 12 Aug 2019 18:15:10: # Command line: callpeak -t /home/okishinya/chipatlas/results/ce10/SRX331057/SRX331057.bam -f BAM -g ce -n /home/okishinya/chipatlas/results/ce10/SRX331057/SRX331057.20 -q 1e-20 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/ce10/SRX331057/SRX331057.20 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/ce10/SRX331057/SRX331057.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 18:15:10: #1 read tag files... INFO @ Mon, 12 Aug 2019 18:15:10: #1 read treatment tags... INFO @ Mon, 12 Aug 2019 18:15:15: 1000000 INFO @ Mon, 12 Aug 2019 18:15:16: 1000000 INFO @ Mon, 12 Aug 2019 18:15:18: 1000000 INFO @ Mon, 12 Aug 2019 18:15:23: 2000000 INFO @ Mon, 12 Aug 2019 18:15:23: 2000000 INFO @ Mon, 12 Aug 2019 18:15:27: 2000000 INFO @ Mon, 12 Aug 2019 18:15:29: 3000000 INFO @ Mon, 12 Aug 2019 18:15:30: 3000000 INFO @ Mon, 12 Aug 2019 18:15:35: #1 tag size is determined as 32 bps INFO @ Mon, 12 Aug 2019 18:15:35: #1 tag size = 32 INFO @ Mon, 12 Aug 2019 18:15:35: #1 total tags in treatment: 3953598 INFO @ Mon, 12 Aug 2019 18:15:35: #1 user defined the maximum tags... INFO @ Mon, 12 Aug 2019 18:15:35: #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 18:15:35: 3000000 INFO @ Mon, 12 Aug 2019 18:15:35: #1 tags after filtering in treatment: 3953598 INFO @ Mon, 12 Aug 2019 18:15:35: #1 Redundant rate of treatment: 0.00 INFO @ Mon, 12 Aug 2019 18:15:35: #1 finished! INFO @ Mon, 12 Aug 2019 18:15:35: #2 Build Peak Model... INFO @ Mon, 12 Aug 2019 18:15:35: #2 looking for paired plus/minus strand peaks... INFO @ Mon, 12 Aug 2019 18:15:36: #2 number of paired peaks: 397 WARNING @ Mon, 12 Aug 2019 18:15:36: Fewer paired peaks (397) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 397 pairs to build model! INFO @ Mon, 12 Aug 2019 18:15:36: start model_add_line... INFO @ Mon, 12 Aug 2019 18:15:36: start X-correlation... INFO @ Mon, 12 Aug 2019 18:15:36: end of X-cor INFO @ Mon, 12 Aug 2019 18:15:36: #2 finished! INFO @ Mon, 12 Aug 2019 18:15:36: #2 predicted fragment length is 32 bps INFO @ Mon, 12 Aug 2019 18:15:36: #2 alternative fragment length(s) may be 3,32,157,586 bps INFO @ Mon, 12 Aug 2019 18:15:36: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/ce10/SRX331057/SRX331057.10_model.r WARNING @ Mon, 12 Aug 2019 18:15:36: #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 18:15:36: #2 You may need to consider one of the other alternative d(s): 3,32,157,586 WARNING @ Mon, 12 Aug 2019 18:15:36: #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 18:15:36: #3 Call peaks... INFO @ Mon, 12 Aug 2019 18:15:36: #3 Pre-compute pvalue-qvalue table... INFO @ Mon, 12 Aug 2019 18:15:37: #1 tag size is determined as 32 bps INFO @ Mon, 12 Aug 2019 18:15:37: #1 tag size = 32 INFO @ Mon, 12 Aug 2019 18:15:37: #1 total tags in treatment: 3953598 INFO @ Mon, 12 Aug 2019 18:15:37: #1 user defined the maximum tags... INFO @ Mon, 12 Aug 2019 18:15:37: #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 18:15:37: #1 tags after filtering in treatment: 3953598 INFO @ Mon, 12 Aug 2019 18:15:37: #1 Redundant rate of treatment: 0.00 INFO @ Mon, 12 Aug 2019 18:15:37: #1 finished! INFO @ Mon, 12 Aug 2019 18:15:37: #2 Build Peak Model... INFO @ Mon, 12 Aug 2019 18:15:37: #2 looking for paired plus/minus strand peaks... INFO @ Mon, 12 Aug 2019 18:15:37: #2 number of paired peaks: 397 WARNING @ Mon, 12 Aug 2019 18:15:37: Fewer paired peaks (397) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 397 pairs to build model! INFO @ Mon, 12 Aug 2019 18:15:37: start model_add_line... INFO @ Mon, 12 Aug 2019 18:15:38: start X-correlation... INFO @ Mon, 12 Aug 2019 18:15:38: end of X-cor INFO @ Mon, 12 Aug 2019 18:15:38: #2 finished! INFO @ Mon, 12 Aug 2019 18:15:38: #2 predicted fragment length is 32 bps INFO @ Mon, 12 Aug 2019 18:15:38: #2 alternative fragment length(s) may be 3,32,157,586 bps INFO @ Mon, 12 Aug 2019 18:15:38: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/ce10/SRX331057/SRX331057.05_model.r WARNING @ Mon, 12 Aug 2019 18:15:38: #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 18:15:38: #2 You may need to consider one of the other alternative d(s): 3,32,157,586 WARNING @ Mon, 12 Aug 2019 18:15:38: #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 18:15:38: #3 Call peaks... INFO @ Mon, 12 Aug 2019 18:15:38: #3 Pre-compute pvalue-qvalue table... INFO @ Mon, 12 Aug 2019 18:15:43: #1 tag size is determined as 32 bps INFO @ Mon, 12 Aug 2019 18:15:43: #1 tag size = 32 INFO @ Mon, 12 Aug 2019 18:15:43: #1 total tags in treatment: 3953598 INFO @ Mon, 12 Aug 2019 18:15:43: #1 user defined the maximum tags... INFO @ Mon, 12 Aug 2019 18:15:43: #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 18:15:43: #1 tags after filtering in treatment: 3953598 INFO @ Mon, 12 Aug 2019 18:15:43: #1 Redundant rate of treatment: 0.00 INFO @ Mon, 12 Aug 2019 18:15:43: #1 finished! INFO @ Mon, 12 Aug 2019 18:15:43: #2 Build Peak Model... INFO @ Mon, 12 Aug 2019 18:15:43: #2 looking for paired plus/minus strand peaks... INFO @ Mon, 12 Aug 2019 18:15:43: #2 number of paired peaks: 397 WARNING @ Mon, 12 Aug 2019 18:15:43: Fewer paired peaks (397) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 397 pairs to build model! INFO @ Mon, 12 Aug 2019 18:15:43: start model_add_line... INFO @ Mon, 12 Aug 2019 18:15:43: start X-correlation... INFO @ Mon, 12 Aug 2019 18:15:43: end of X-cor INFO @ Mon, 12 Aug 2019 18:15:43: #2 finished! INFO @ Mon, 12 Aug 2019 18:15:43: #2 predicted fragment length is 32 bps INFO @ Mon, 12 Aug 2019 18:15:44: #2 alternative fragment length(s) may be 3,32,157,586 bps INFO @ Mon, 12 Aug 2019 18:15:44: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/ce10/SRX331057/SRX331057.20_model.r WARNING @ Mon, 12 Aug 2019 18:15:44: #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 18:15:44: #2 You may need to consider one of the other alternative d(s): 3,32,157,586 WARNING @ Mon, 12 Aug 2019 18:15:44: #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 18:15:44: #3 Call peaks... INFO @ Mon, 12 Aug 2019 18:15:44: #3 Pre-compute pvalue-qvalue table... INFO @ Mon, 12 Aug 2019 18:15:47: #3 Call peaks for each chromosome... INFO @ Mon, 12 Aug 2019 18:15:49: #3 Call peaks for each chromosome... INFO @ Mon, 12 Aug 2019 18:15:53: #4 Write output xls file... /home/okishinya/chipatlas/results/ce10/SRX331057/SRX331057.10_peaks.xls INFO @ Mon, 12 Aug 2019 18:15:53: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/ce10/SRX331057/SRX331057.10_peaks.narrowPeak INFO @ Mon, 12 Aug 2019 18:15:53: #4 Write summits bed file... /home/okishinya/chipatlas/results/ce10/SRX331057/SRX331057.10_summits.bed INFO @ Mon, 12 Aug 2019 18:15:53: Done! pass1 - making usageList (6 chroms): 1 millis pass2 - checking and writing primary data (143 records, 4 fields): 2 millis CompletedMACS2peakCalling INFO @ Mon, 12 Aug 2019 18:15:55: #4 Write output xls file... /home/okishinya/chipatlas/results/ce10/SRX331057/SRX331057.05_peaks.xls INFO @ Mon, 12 Aug 2019 18:15:55: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/ce10/SRX331057/SRX331057.05_peaks.narrowPeak INFO @ Mon, 12 Aug 2019 18:15:55: #4 Write summits bed file... /home/okishinya/chipatlas/results/ce10/SRX331057/SRX331057.05_summits.bed INFO @ Mon, 12 Aug 2019 18:15:55: Done! pass1 - making usageList (6 chroms): 1 millis pass2 - checking and writing primary data (346 records, 4 fields): 3 millis CompletedMACS2peakCalling INFO @ Mon, 12 Aug 2019 18:15:55: #3 Call peaks for each chromosome... INFO @ Mon, 12 Aug 2019 18:16:01: #4 Write output xls file... /home/okishinya/chipatlas/results/ce10/SRX331057/SRX331057.20_peaks.xls INFO @ Mon, 12 Aug 2019 18:16:01: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/ce10/SRX331057/SRX331057.20_peaks.narrowPeak INFO @ Mon, 12 Aug 2019 18:16:01: #4 Write summits bed file... /home/okishinya/chipatlas/results/ce10/SRX331057/SRX331057.20_summits.bed INFO @ Mon, 12 Aug 2019 18:16:01: Done! pass1 - making usageList (6 chroms): 1 millis pass2 - checking and writing primary data (29 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。