Job ID = 2010475 sra ファイルのダウンロード中... Read layout: SINGLE fastq に変換中... spots read : 11,488,511 reads read : 11,488,511 reads written : 11,488,511 rm: cannot remove ‘[DSE]RR*’: No such file or directory rm: cannot remove ‘/home/okishinya/ncbi/public/sra/SRR1029314.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: 00:01:15 11488511 reads; of these: 11488511 (100.00%) were unpaired; of these: 8807461 (76.66%) aligned 0 times 2208948 (19.23%) aligned exactly 1 time 472102 (4.11%) aligned >1 times 23.34% overall alignment rate Time searching: 00:01:15 Overall time: 00:01:15 マッピングが完了しました。 samtools でBAM に変換中... [samopen] SAM header is present: 17 sequences. [bam_rmdupse_core] 1872786 / 2681050 = 0.6985 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 @ Fri, 05 Jul 2019 22:43:49: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/SRX377157/SRX377157.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/SRX377157/SRX377157.05 -q 1e-05 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/SRX377157/SRX377157.05 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/SRX377157/SRX377157.bam'] # control file = None # effective genome size = 1.21e+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 @ Fri, 05 Jul 2019 22:43:49: #1 read tag files... INFO @ Fri, 05 Jul 2019 22:43:49: #1 read treatment tags... INFO @ Fri, 05 Jul 2019 22:43:50: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/SRX377157/SRX377157.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/SRX377157/SRX377157.10 -q 1e-10 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/SRX377157/SRX377157.10 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/SRX377157/SRX377157.bam'] # control file = None # effective genome size = 1.21e+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 @ Fri, 05 Jul 2019 22:43:50: #1 read tag files... INFO @ Fri, 05 Jul 2019 22:43:50: #1 read treatment tags... INFO @ Fri, 05 Jul 2019 22:43:51: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/SRX377157/SRX377157.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/SRX377157/SRX377157.20 -q 1e-20 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/SRX377157/SRX377157.20 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/SRX377157/SRX377157.bam'] # control file = None # effective genome size = 1.21e+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 @ Fri, 05 Jul 2019 22:43:51: #1 read tag files... INFO @ Fri, 05 Jul 2019 22:43:51: #1 read treatment tags... INFO @ Fri, 05 Jul 2019 22:43:55: #1 tag size is determined as 50 bps INFO @ Fri, 05 Jul 2019 22:43:55: #1 tag size = 50 INFO @ Fri, 05 Jul 2019 22:43:55: #1 total tags in treatment: 808264 INFO @ Fri, 05 Jul 2019 22:43:55: #1 user defined the maximum tags... INFO @ Fri, 05 Jul 2019 22:43:55: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Fri, 05 Jul 2019 22:43:55: #1 tags after filtering in treatment: 808264 INFO @ Fri, 05 Jul 2019 22:43:55: #1 Redundant rate of treatment: 0.00 INFO @ Fri, 05 Jul 2019 22:43:55: #1 finished! INFO @ Fri, 05 Jul 2019 22:43:55: #2 Build Peak Model... INFO @ Fri, 05 Jul 2019 22:43:55: #2 looking for paired plus/minus strand peaks... INFO @ Fri, 05 Jul 2019 22:43:55: #2 number of paired peaks: 193 WARNING @ Fri, 05 Jul 2019 22:43:55: Fewer paired peaks (193) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 193 pairs to build model! INFO @ Fri, 05 Jul 2019 22:43:55: start model_add_line... INFO @ Fri, 05 Jul 2019 22:43:55: start X-correlation... INFO @ Fri, 05 Jul 2019 22:43:55: end of X-cor INFO @ Fri, 05 Jul 2019 22:43:55: #2 finished! INFO @ Fri, 05 Jul 2019 22:43:55: #2 predicted fragment length is 187 bps INFO @ Fri, 05 Jul 2019 22:43:55: #2 alternative fragment length(s) may be 187 bps INFO @ Fri, 05 Jul 2019 22:43:55: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/sacCer3/SRX377157/SRX377157.05_model.r INFO @ Fri, 05 Jul 2019 22:43:55: #3 Call peaks... INFO @ Fri, 05 Jul 2019 22:43:55: #3 Pre-compute pvalue-qvalue table... INFO @ Fri, 05 Jul 2019 22:43:56: #1 tag size is determined as 50 bps INFO @ Fri, 05 Jul 2019 22:43:56: #1 tag size = 50 INFO @ Fri, 05 Jul 2019 22:43:56: #1 total tags in treatment: 808264 INFO @ Fri, 05 Jul 2019 22:43:56: #1 user defined the maximum tags... INFO @ Fri, 05 Jul 2019 22:43:56: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Fri, 05 Jul 2019 22:43:56: #1 tags after filtering in treatment: 808264 INFO @ Fri, 05 Jul 2019 22:43:56: #1 Redundant rate of treatment: 0.00 INFO @ Fri, 05 Jul 2019 22:43:56: #1 finished! INFO @ Fri, 05 Jul 2019 22:43:56: #2 Build Peak Model... INFO @ Fri, 05 Jul 2019 22:43:56: #2 looking for paired plus/minus strand peaks... INFO @ Fri, 05 Jul 2019 22:43:56: #2 number of paired peaks: 193 WARNING @ Fri, 05 Jul 2019 22:43:56: Fewer paired peaks (193) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 193 pairs to build model! INFO @ Fri, 05 Jul 2019 22:43:56: start model_add_line... INFO @ Fri, 05 Jul 2019 22:43:56: start X-correlation... INFO @ Fri, 05 Jul 2019 22:43:56: end of X-cor INFO @ Fri, 05 Jul 2019 22:43:56: #2 finished! INFO @ Fri, 05 Jul 2019 22:43:56: #2 predicted fragment length is 187 bps INFO @ Fri, 05 Jul 2019 22:43:56: #2 alternative fragment length(s) may be 187 bps INFO @ Fri, 05 Jul 2019 22:43:56: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/sacCer3/SRX377157/SRX377157.10_model.r INFO @ Fri, 05 Jul 2019 22:43:56: #3 Call peaks... INFO @ Fri, 05 Jul 2019 22:43:56: #3 Pre-compute pvalue-qvalue table... INFO @ Fri, 05 Jul 2019 22:43:57: #1 tag size is determined as 50 bps INFO @ Fri, 05 Jul 2019 22:43:57: #1 tag size = 50 INFO @ Fri, 05 Jul 2019 22:43:57: #1 total tags in treatment: 808264 INFO @ Fri, 05 Jul 2019 22:43:57: #1 user defined the maximum tags... INFO @ Fri, 05 Jul 2019 22:43:57: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Fri, 05 Jul 2019 22:43:57: #1 tags after filtering in treatment: 808264 INFO @ Fri, 05 Jul 2019 22:43:57: #1 Redundant rate of treatment: 0.00 INFO @ Fri, 05 Jul 2019 22:43:57: #1 finished! INFO @ Fri, 05 Jul 2019 22:43:57: #2 Build Peak Model... INFO @ Fri, 05 Jul 2019 22:43:57: #2 looking for paired plus/minus strand peaks... INFO @ Fri, 05 Jul 2019 22:43:57: #2 number of paired peaks: 193 WARNING @ Fri, 05 Jul 2019 22:43:57: Fewer paired peaks (193) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 193 pairs to build model! INFO @ Fri, 05 Jul 2019 22:43:57: start model_add_line... INFO @ Fri, 05 Jul 2019 22:43:57: start X-correlation... INFO @ Fri, 05 Jul 2019 22:43:57: end of X-cor INFO @ Fri, 05 Jul 2019 22:43:57: #2 finished! INFO @ Fri, 05 Jul 2019 22:43:57: #2 predicted fragment length is 187 bps INFO @ Fri, 05 Jul 2019 22:43:57: #2 alternative fragment length(s) may be 187 bps INFO @ Fri, 05 Jul 2019 22:43:57: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/sacCer3/SRX377157/SRX377157.20_model.r INFO @ Fri, 05 Jul 2019 22:43:57: #3 Call peaks... INFO @ Fri, 05 Jul 2019 22:43:57: #3 Pre-compute pvalue-qvalue table... INFO @ Fri, 05 Jul 2019 22:43:58: #3 Call peaks for each chromosome... INFO @ Fri, 05 Jul 2019 22:43:59: #3 Call peaks for each chromosome... INFO @ Fri, 05 Jul 2019 22:44:00: #4 Write output xls file... /home/okishinya/chipatlas/results/sacCer3/SRX377157/SRX377157.05_peaks.xls INFO @ Fri, 05 Jul 2019 22:44:00: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/sacCer3/SRX377157/SRX377157.05_peaks.narrowPeak INFO @ Fri, 05 Jul 2019 22:44:00: #4 Write summits bed file... /home/okishinya/chipatlas/results/sacCer3/SRX377157/SRX377157.05_summits.bed INFO @ Fri, 05 Jul 2019 22:44:00: Done! pass1 - making usageList (17 chroms): 1 millis pass2 - checking and writing primary data (578 records, 4 fields): 12 millis INFO @ Fri, 05 Jul 2019 22:44:00: #3 Call peaks for each chromosome... INFO @ Fri, 05 Jul 2019 22:44:00: #4 Write output xls file... /home/okishinya/chipatlas/results/sacCer3/SRX377157/SRX377157.10_peaks.xls INFO @ Fri, 05 Jul 2019 22:44:00: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/sacCer3/SRX377157/SRX377157.10_peaks.narrowPeak INFO @ Fri, 05 Jul 2019 22:44:00: #4 Write summits bed file... /home/okishinya/chipatlas/results/sacCer3/SRX377157/SRX377157.10_summits.bed INFO @ Fri, 05 Jul 2019 22:44:00: Done! pass1 - making usageList (17 chroms): 1 millis pass2 - checking and writing primary data (382 records, 4 fields): 3 millis CompletedMACS2peakCalling CompletedMACS2peakCalling INFO @ Fri, 05 Jul 2019 22:44:01: #4 Write output xls file... /home/okishinya/chipatlas/results/sacCer3/SRX377157/SRX377157.20_peaks.xls INFO @ Fri, 05 Jul 2019 22:44:01: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/sacCer3/SRX377157/SRX377157.20_peaks.narrowPeak INFO @ Fri, 05 Jul 2019 22:44:01: #4 Write summits bed file... /home/okishinya/chipatlas/results/sacCer3/SRX377157/SRX377157.20_summits.bed INFO @ Fri, 05 Jul 2019 22:44:01: Done! pass1 - making usageList (17 chroms): 1 millis pass2 - checking and writing primary data (209 records, 4 fields): 23 millis CompletedMACS2peakCalling BedGraph に変換しました。 BigWig に変換中... BigWig に変換しました。