Job ID = 2589538 sra ファイルのダウンロード中... Read layout: SINGLE fastq に変換中... spots read : 9,036,519 reads read : 9,036,519 reads written : 9,036,519 rm: cannot remove ‘[DSE]RR*’: No such file or directory rm: cannot remove ‘/home/okishinya/ncbi/public/sra/SRR701514.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: 00:01:25 9036519 reads; of these: 9036519 (100.00%) were unpaired; of these: 1239958 (13.72%) aligned 0 times 6563509 (72.63%) aligned exactly 1 time 1233052 (13.65%) aligned >1 times 86.28% overall alignment rate Time searching: 00:01:25 Overall time: 00:01:25 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] 748931 / 7796561 = 0.0961 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 17:57:00: # Command line: callpeak -t /home/okishinya/chipatlas/results/ce10/SRX233458/SRX233458.bam -f BAM -g ce -n /home/okishinya/chipatlas/results/ce10/SRX233458/SRX233458.05 -q 1e-05 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/ce10/SRX233458/SRX233458.05 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/ce10/SRX233458/SRX233458.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 17:57:00: #1 read tag files... INFO @ Mon, 12 Aug 2019 17:57:00: #1 read treatment tags... INFO @ Mon, 12 Aug 2019 17:57:01: # Command line: callpeak -t /home/okishinya/chipatlas/results/ce10/SRX233458/SRX233458.bam -f BAM -g ce -n /home/okishinya/chipatlas/results/ce10/SRX233458/SRX233458.10 -q 1e-10 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/ce10/SRX233458/SRX233458.10 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/ce10/SRX233458/SRX233458.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 17:57:01: #1 read tag files... INFO @ Mon, 12 Aug 2019 17:57:01: #1 read treatment tags... INFO @ Mon, 12 Aug 2019 17:57:02: # Command line: callpeak -t /home/okishinya/chipatlas/results/ce10/SRX233458/SRX233458.bam -f BAM -g ce -n /home/okishinya/chipatlas/results/ce10/SRX233458/SRX233458.20 -q 1e-20 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/ce10/SRX233458/SRX233458.20 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/ce10/SRX233458/SRX233458.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 17:57:02: #1 read tag files... INFO @ Mon, 12 Aug 2019 17:57:02: #1 read treatment tags... INFO @ Mon, 12 Aug 2019 17:57:07: 1000000 INFO @ Mon, 12 Aug 2019 17:57:08: 1000000 INFO @ Mon, 12 Aug 2019 17:57:09: 1000000 INFO @ Mon, 12 Aug 2019 17:57:15: 2000000 INFO @ Mon, 12 Aug 2019 17:57:16: 2000000 INFO @ Mon, 12 Aug 2019 17:57:17: 2000000 INFO @ Mon, 12 Aug 2019 17:57:22: 3000000 INFO @ Mon, 12 Aug 2019 17:57:23: 3000000 INFO @ Mon, 12 Aug 2019 17:57:24: 3000000 INFO @ Mon, 12 Aug 2019 17:57:29: 4000000 INFO @ Mon, 12 Aug 2019 17:57:30: 4000000 INFO @ Mon, 12 Aug 2019 17:57:31: 4000000 INFO @ Mon, 12 Aug 2019 17:57:37: 5000000 INFO @ Mon, 12 Aug 2019 17:57:38: 5000000 INFO @ Mon, 12 Aug 2019 17:57:38: 5000000 INFO @ Mon, 12 Aug 2019 17:57:44: 6000000 INFO @ Mon, 12 Aug 2019 17:57:45: 6000000 INFO @ Mon, 12 Aug 2019 17:57:46: 6000000 INFO @ Mon, 12 Aug 2019 17:57:51: 7000000 INFO @ Mon, 12 Aug 2019 17:57:51: #1 tag size is determined as 32 bps INFO @ Mon, 12 Aug 2019 17:57:51: #1 tag size = 32 INFO @ Mon, 12 Aug 2019 17:57:51: #1 total tags in treatment: 7047630 INFO @ Mon, 12 Aug 2019 17:57:51: #1 user defined the maximum tags... INFO @ Mon, 12 Aug 2019 17:57:51: #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 17:57:52: #1 tags after filtering in treatment: 7047630 INFO @ Mon, 12 Aug 2019 17:57:52: #1 Redundant rate of treatment: 0.00 INFO @ Mon, 12 Aug 2019 17:57:52: #1 finished! INFO @ Mon, 12 Aug 2019 17:57:52: #2 Build Peak Model... INFO @ Mon, 12 Aug 2019 17:57:52: #2 looking for paired plus/minus strand peaks... INFO @ Mon, 12 Aug 2019 17:57:52: 7000000 INFO @ Mon, 12 Aug 2019 17:57:52: #2 number of paired peaks: 432 WARNING @ Mon, 12 Aug 2019 17:57:52: Fewer paired peaks (432) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 432 pairs to build model! INFO @ Mon, 12 Aug 2019 17:57:52: start model_add_line... INFO @ Mon, 12 Aug 2019 17:57:52: start X-correlation... INFO @ Mon, 12 Aug 2019 17:57:52: end of X-cor INFO @ Mon, 12 Aug 2019 17:57:52: #2 finished! INFO @ Mon, 12 Aug 2019 17:57:52: #2 predicted fragment length is 92 bps INFO @ Mon, 12 Aug 2019 17:57:52: #2 alternative fragment length(s) may be 4,40,92,564,571,578 bps INFO @ Mon, 12 Aug 2019 17:57:52: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/ce10/SRX233458/SRX233458.05_model.r INFO @ Mon, 12 Aug 2019 17:57:52: #3 Call peaks... INFO @ Mon, 12 Aug 2019 17:57:52: #3 Pre-compute pvalue-qvalue table... INFO @ Mon, 12 Aug 2019 17:57:52: #1 tag size is determined as 32 bps INFO @ Mon, 12 Aug 2019 17:57:52: #1 tag size = 32 INFO @ Mon, 12 Aug 2019 17:57:52: #1 total tags in treatment: 7047630 INFO @ Mon, 12 Aug 2019 17:57:52: #1 user defined the maximum tags... INFO @ Mon, 12 Aug 2019 17:57:52: #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 17:57:53: #1 tags after filtering in treatment: 7047630 INFO @ Mon, 12 Aug 2019 17:57:53: #1 Redundant rate of treatment: 0.00 INFO @ Mon, 12 Aug 2019 17:57:53: #1 finished! INFO @ Mon, 12 Aug 2019 17:57:53: #2 Build Peak Model... INFO @ Mon, 12 Aug 2019 17:57:53: #2 looking for paired plus/minus strand peaks... INFO @ Mon, 12 Aug 2019 17:57:53: 7000000 INFO @ Mon, 12 Aug 2019 17:57:53: #2 number of paired peaks: 432 WARNING @ Mon, 12 Aug 2019 17:57:53: Fewer paired peaks (432) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 432 pairs to build model! INFO @ Mon, 12 Aug 2019 17:57:53: start model_add_line... INFO @ Mon, 12 Aug 2019 17:57:53: #1 tag size is determined as 32 bps INFO @ Mon, 12 Aug 2019 17:57:53: #1 tag size = 32 INFO @ Mon, 12 Aug 2019 17:57:53: #1 total tags in treatment: 7047630 INFO @ Mon, 12 Aug 2019 17:57:53: #1 user defined the maximum tags... INFO @ Mon, 12 Aug 2019 17:57:53: #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 17:57:53: start X-correlation... INFO @ Mon, 12 Aug 2019 17:57:53: end of X-cor INFO @ Mon, 12 Aug 2019 17:57:53: #2 finished! INFO @ Mon, 12 Aug 2019 17:57:53: #2 predicted fragment length is 92 bps INFO @ Mon, 12 Aug 2019 17:57:53: #2 alternative fragment length(s) may be 4,40,92,564,571,578 bps INFO @ Mon, 12 Aug 2019 17:57:53: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/ce10/SRX233458/SRX233458.10_model.r INFO @ Mon, 12 Aug 2019 17:57:53: #3 Call peaks... INFO @ Mon, 12 Aug 2019 17:57:53: #3 Pre-compute pvalue-qvalue table... INFO @ Mon, 12 Aug 2019 17:57:53: #1 tags after filtering in treatment: 7047630 INFO @ Mon, 12 Aug 2019 17:57:53: #1 Redundant rate of treatment: 0.00 INFO @ Mon, 12 Aug 2019 17:57:53: #1 finished! INFO @ Mon, 12 Aug 2019 17:57:53: #2 Build Peak Model... INFO @ Mon, 12 Aug 2019 17:57:53: #2 looking for paired plus/minus strand peaks... INFO @ Mon, 12 Aug 2019 17:57:54: #2 number of paired peaks: 432 WARNING @ Mon, 12 Aug 2019 17:57:54: Fewer paired peaks (432) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 432 pairs to build model! INFO @ Mon, 12 Aug 2019 17:57:54: start model_add_line... INFO @ Mon, 12 Aug 2019 17:57:54: start X-correlation... INFO @ Mon, 12 Aug 2019 17:57:54: end of X-cor INFO @ Mon, 12 Aug 2019 17:57:54: #2 finished! INFO @ Mon, 12 Aug 2019 17:57:54: #2 predicted fragment length is 92 bps INFO @ Mon, 12 Aug 2019 17:57:54: #2 alternative fragment length(s) may be 4,40,92,564,571,578 bps INFO @ Mon, 12 Aug 2019 17:57:54: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/ce10/SRX233458/SRX233458.20_model.r INFO @ Mon, 12 Aug 2019 17:57:54: #3 Call peaks... INFO @ Mon, 12 Aug 2019 17:57:54: #3 Pre-compute pvalue-qvalue table... INFO @ Mon, 12 Aug 2019 17:58:12: #3 Call peaks for each chromosome... INFO @ Mon, 12 Aug 2019 17:58:13: #3 Call peaks for each chromosome... INFO @ Mon, 12 Aug 2019 17:58:14: #3 Call peaks for each chromosome... INFO @ Mon, 12 Aug 2019 17:58:22: #4 Write output xls file... /home/okishinya/chipatlas/results/ce10/SRX233458/SRX233458.05_peaks.xls INFO @ Mon, 12 Aug 2019 17:58:22: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/ce10/SRX233458/SRX233458.05_peaks.narrowPeak INFO @ Mon, 12 Aug 2019 17:58:22: #4 Write summits bed file... /home/okishinya/chipatlas/results/ce10/SRX233458/SRX233458.05_summits.bed INFO @ Mon, 12 Aug 2019 17:58:22: Done! pass1 - making usageList (7 chroms): 1 millis pass2 - checking and writing primary data (1623 records, 4 fields): 7 millis CompletedMACS2peakCalling INFO @ Mon, 12 Aug 2019 17:58:23: #4 Write output xls file... /home/okishinya/chipatlas/results/ce10/SRX233458/SRX233458.10_peaks.xls INFO @ Mon, 12 Aug 2019 17:58:23: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/ce10/SRX233458/SRX233458.10_peaks.narrowPeak INFO @ Mon, 12 Aug 2019 17:58:23: #4 Write summits bed file... /home/okishinya/chipatlas/results/ce10/SRX233458/SRX233458.10_summits.bed INFO @ Mon, 12 Aug 2019 17:58:23: Done! pass1 - making usageList (7 chroms): 2 millis pass2 - checking and writing primary data (826 records, 4 fields): 4 millis CompletedMACS2peakCalling INFO @ Mon, 12 Aug 2019 17:58:24: #4 Write output xls file... /home/okishinya/chipatlas/results/ce10/SRX233458/SRX233458.20_peaks.xls INFO @ Mon, 12 Aug 2019 17:58:24: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/ce10/SRX233458/SRX233458.20_peaks.narrowPeak INFO @ Mon, 12 Aug 2019 17:58:24: #4 Write summits bed file... /home/okishinya/chipatlas/results/ce10/SRX233458/SRX233458.20_summits.bed INFO @ Mon, 12 Aug 2019 17:58:24: Done! pass1 - making usageList (6 chroms): 1 millis pass2 - checking and writing primary data (277 records, 4 fields): 3 millis CompletedMACS2peakCalling BedGraph に変換しました。 BigWig に変換中... BigWig に変換しました。