Job ID = 2589816 sra ファイルのダウンロード中... Read layout: SINGLE fastq に変換中... spots read : 6,444,449 reads read : 6,444,449 reads written : 6,444,449 rm: cannot remove ‘[DSE]RR*’: No such file or directory rm: cannot remove ‘/home/okishinya/ncbi/public/sra/SRR947446.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: 00:00:55 6444449 reads; of these: 6444449 (100.00%) were unpaired; of these: 2383123 (36.98%) aligned 0 times 3379559 (52.44%) aligned exactly 1 time 681767 (10.58%) aligned >1 times 63.02% overall alignment rate Time searching: 00:00:55 Overall time: 00:00:55 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] 233722 / 4061326 = 0.0575 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 18:33:00: # Command line: callpeak -t /home/okishinya/chipatlas/results/ce10/SRX331214/SRX331214.bam -f BAM -g ce -n /home/okishinya/chipatlas/results/ce10/SRX331214/SRX331214.05 -q 1e-05 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/ce10/SRX331214/SRX331214.05 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/ce10/SRX331214/SRX331214.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 18:33:00: #1 read tag files... INFO @ Mon, 12 Aug 2019 18:33:00: #1 read treatment tags... INFO @ Mon, 12 Aug 2019 18:33:01: # Command line: callpeak -t /home/okishinya/chipatlas/results/ce10/SRX331214/SRX331214.bam -f BAM -g ce -n /home/okishinya/chipatlas/results/ce10/SRX331214/SRX331214.10 -q 1e-10 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/ce10/SRX331214/SRX331214.10 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/ce10/SRX331214/SRX331214.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 18:33:01: #1 read tag files... INFO @ Mon, 12 Aug 2019 18:33:01: #1 read treatment tags... INFO @ Mon, 12 Aug 2019 18:33:02: # Command line: callpeak -t /home/okishinya/chipatlas/results/ce10/SRX331214/SRX331214.bam -f BAM -g ce -n /home/okishinya/chipatlas/results/ce10/SRX331214/SRX331214.20 -q 1e-20 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/ce10/SRX331214/SRX331214.20 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/ce10/SRX331214/SRX331214.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 18:33:02: #1 read tag files... INFO @ Mon, 12 Aug 2019 18:33:02: #1 read treatment tags... INFO @ Mon, 12 Aug 2019 18:33:06: 1000000 INFO @ Mon, 12 Aug 2019 18:33:09: 1000000 INFO @ Mon, 12 Aug 2019 18:33:09: 1000000 INFO @ Mon, 12 Aug 2019 18:33:13: 2000000 INFO @ Mon, 12 Aug 2019 18:33:16: 2000000 INFO @ Mon, 12 Aug 2019 18:33:16: 2000000 INFO @ Mon, 12 Aug 2019 18:33:19: 3000000 INFO @ Mon, 12 Aug 2019 18:33:23: 3000000 INFO @ Mon, 12 Aug 2019 18:33:24: 3000000 INFO @ Mon, 12 Aug 2019 18:33:25: #1 tag size is determined as 32 bps INFO @ Mon, 12 Aug 2019 18:33:25: #1 tag size = 32 INFO @ Mon, 12 Aug 2019 18:33:25: #1 total tags in treatment: 3827604 INFO @ Mon, 12 Aug 2019 18:33:25: #1 user defined the maximum tags... INFO @ Mon, 12 Aug 2019 18:33:25: #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 18:33:25: #1 tags after filtering in treatment: 3827604 INFO @ Mon, 12 Aug 2019 18:33:25: #1 Redundant rate of treatment: 0.00 INFO @ Mon, 12 Aug 2019 18:33:25: #1 finished! INFO @ Mon, 12 Aug 2019 18:33:25: #2 Build Peak Model... INFO @ Mon, 12 Aug 2019 18:33:25: #2 looking for paired plus/minus strand peaks... INFO @ Mon, 12 Aug 2019 18:33:25: #2 number of paired peaks: 444 WARNING @ Mon, 12 Aug 2019 18:33:25: Fewer paired peaks (444) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 444 pairs to build model! INFO @ Mon, 12 Aug 2019 18:33:25: start model_add_line... INFO @ Mon, 12 Aug 2019 18:33:25: start X-correlation... INFO @ Mon, 12 Aug 2019 18:33:25: end of X-cor INFO @ Mon, 12 Aug 2019 18:33:25: #2 finished! INFO @ Mon, 12 Aug 2019 18:33:25: #2 predicted fragment length is 35 bps INFO @ Mon, 12 Aug 2019 18:33:25: #2 alternative fragment length(s) may be 4,35,564,598 bps INFO @ Mon, 12 Aug 2019 18:33:25: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/ce10/SRX331214/SRX331214.05_model.r WARNING @ Mon, 12 Aug 2019 18:33:25: #2 Since the d (35) calculated from paired-peaks are smaller than 2*tag length, it may be influenced by unknown sequencing problem! WARNING @ Mon, 12 Aug 2019 18:33:25: #2 You may need to consider one of the other alternative d(s): 4,35,564,598 WARNING @ Mon, 12 Aug 2019 18:33:25: #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 18:33:25: #3 Call peaks... INFO @ Mon, 12 Aug 2019 18:33:25: #3 Pre-compute pvalue-qvalue table... INFO @ Mon, 12 Aug 2019 18:33:28: #1 tag size is determined as 32 bps INFO @ Mon, 12 Aug 2019 18:33:28: #1 tag size = 32 INFO @ Mon, 12 Aug 2019 18:33:28: #1 total tags in treatment: 3827604 INFO @ Mon, 12 Aug 2019 18:33:28: #1 user defined the maximum tags... INFO @ Mon, 12 Aug 2019 18:33:28: #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 18:33:28: #1 tags after filtering in treatment: 3827604 INFO @ Mon, 12 Aug 2019 18:33:28: #1 Redundant rate of treatment: 0.00 INFO @ Mon, 12 Aug 2019 18:33:28: #1 finished! INFO @ Mon, 12 Aug 2019 18:33:28: #2 Build Peak Model... INFO @ Mon, 12 Aug 2019 18:33:28: #2 looking for paired plus/minus strand peaks... INFO @ Mon, 12 Aug 2019 18:33:28: #2 number of paired peaks: 444 WARNING @ Mon, 12 Aug 2019 18:33:28: Fewer paired peaks (444) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 444 pairs to build model! INFO @ Mon, 12 Aug 2019 18:33:28: start model_add_line... INFO @ Mon, 12 Aug 2019 18:33:28: start X-correlation... INFO @ Mon, 12 Aug 2019 18:33:28: end of X-cor INFO @ Mon, 12 Aug 2019 18:33:28: #2 finished! INFO @ Mon, 12 Aug 2019 18:33:28: #2 predicted fragment length is 35 bps INFO @ Mon, 12 Aug 2019 18:33:28: #2 alternative fragment length(s) may be 4,35,564,598 bps INFO @ Mon, 12 Aug 2019 18:33:28: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/ce10/SRX331214/SRX331214.20_model.r WARNING @ Mon, 12 Aug 2019 18:33:28: #2 Since the d (35) calculated from paired-peaks are smaller than 2*tag length, it may be influenced by unknown sequencing problem! WARNING @ Mon, 12 Aug 2019 18:33:28: #2 You may need to consider one of the other alternative d(s): 4,35,564,598 WARNING @ Mon, 12 Aug 2019 18:33:28: #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 18:33:28: #3 Call peaks... INFO @ Mon, 12 Aug 2019 18:33:28: #3 Pre-compute pvalue-qvalue table... INFO @ Mon, 12 Aug 2019 18:33:30: #1 tag size is determined as 32 bps INFO @ Mon, 12 Aug 2019 18:33:30: #1 tag size = 32 INFO @ Mon, 12 Aug 2019 18:33:30: #1 total tags in treatment: 3827604 INFO @ Mon, 12 Aug 2019 18:33:30: #1 user defined the maximum tags... INFO @ Mon, 12 Aug 2019 18:33:30: #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 18:33:30: #1 tags after filtering in treatment: 3827604 INFO @ Mon, 12 Aug 2019 18:33:30: #1 Redundant rate of treatment: 0.00 INFO @ Mon, 12 Aug 2019 18:33:30: #1 finished! INFO @ Mon, 12 Aug 2019 18:33:30: #2 Build Peak Model... INFO @ Mon, 12 Aug 2019 18:33:30: #2 looking for paired plus/minus strand peaks... INFO @ Mon, 12 Aug 2019 18:33:31: #2 number of paired peaks: 444 WARNING @ Mon, 12 Aug 2019 18:33:31: Fewer paired peaks (444) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 444 pairs to build model! INFO @ Mon, 12 Aug 2019 18:33:31: start model_add_line... INFO @ Mon, 12 Aug 2019 18:33:31: start X-correlation... INFO @ Mon, 12 Aug 2019 18:33:31: end of X-cor INFO @ Mon, 12 Aug 2019 18:33:31: #2 finished! INFO @ Mon, 12 Aug 2019 18:33:31: #2 predicted fragment length is 35 bps INFO @ Mon, 12 Aug 2019 18:33:31: #2 alternative fragment length(s) may be 4,35,564,598 bps INFO @ Mon, 12 Aug 2019 18:33:31: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/ce10/SRX331214/SRX331214.10_model.r WARNING @ Mon, 12 Aug 2019 18:33:31: #2 Since the d (35) calculated from paired-peaks are smaller than 2*tag length, it may be influenced by unknown sequencing problem! WARNING @ Mon, 12 Aug 2019 18:33:31: #2 You may need to consider one of the other alternative d(s): 4,35,564,598 WARNING @ Mon, 12 Aug 2019 18:33:31: #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 18:33:31: #3 Call peaks... INFO @ Mon, 12 Aug 2019 18:33:31: #3 Pre-compute pvalue-qvalue table... INFO @ Mon, 12 Aug 2019 18:33:36: #3 Call peaks for each chromosome... INFO @ Mon, 12 Aug 2019 18:33:40: #3 Call peaks for each chromosome... INFO @ Mon, 12 Aug 2019 18:33:42: #4 Write output xls file... /home/okishinya/chipatlas/results/ce10/SRX331214/SRX331214.05_peaks.xls INFO @ Mon, 12 Aug 2019 18:33:42: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/ce10/SRX331214/SRX331214.05_peaks.narrowPeak INFO @ Mon, 12 Aug 2019 18:33:42: #4 Write summits bed file... /home/okishinya/chipatlas/results/ce10/SRX331214/SRX331214.05_summits.bed INFO @ Mon, 12 Aug 2019 18:33:42: #3 Call peaks for each chromosome... INFO @ Mon, 12 Aug 2019 18:33:42: Done! pass1 - making usageList (7 chroms): 1 millis pass2 - checking and writing primary data (448 records, 4 fields): 3 millis CompletedMACS2peakCalling INFO @ Mon, 12 Aug 2019 18:33:46: #4 Write output xls file... /home/okishinya/chipatlas/results/ce10/SRX331214/SRX331214.20_peaks.xls INFO @ Mon, 12 Aug 2019 18:33:46: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/ce10/SRX331214/SRX331214.20_peaks.narrowPeak INFO @ Mon, 12 Aug 2019 18:33:46: #4 Write summits bed file... /home/okishinya/chipatlas/results/ce10/SRX331214/SRX331214.20_summits.bed INFO @ Mon, 12 Aug 2019 18:33:46: Done! pass1 - making usageList (6 chroms): 1 millis pass2 - checking and writing primary data (59 records, 4 fields): 1 millis CompletedMACS2peakCalling INFO @ Mon, 12 Aug 2019 18:33:48: #4 Write output xls file... /home/okishinya/chipatlas/results/ce10/SRX331214/SRX331214.10_peaks.xls INFO @ Mon, 12 Aug 2019 18:33:48: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/ce10/SRX331214/SRX331214.10_peaks.narrowPeak INFO @ Mon, 12 Aug 2019 18:33:48: #4 Write summits bed file... /home/okishinya/chipatlas/results/ce10/SRX331214/SRX331214.10_summits.bed INFO @ Mon, 12 Aug 2019 18:33:48: Done! pass1 - making usageList (6 chroms): 1 millis pass2 - checking and writing primary data (194 records, 4 fields): 1 millis CompletedMACS2peakCalling BedGraph に変換しました。 BigWig に変換中... BigWig に変換しました。