Job ID = 1290679 sra ファイルのダウンロード中... Read layout: SINGLE fastq に変換中... spots read : 5,031,238 reads read : 5,031,238 reads written : 5,031,238 rm: cannot remove ‘[DSE]RR*’: No such file or directory rm: cannot remove ‘fastqDump_tmp*’: 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: 00:00:31 5031238 reads; of these: 5031238 (100.00%) were unpaired; of these: 4963842 (98.66%) aligned 0 times 44484 (0.88%) aligned exactly 1 time 22912 (0.46%) aligned >1 times 1.34% overall alignment rate Time searching: 00:00:31 Overall time: 00:00:31 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] 14456 / 67396 = 0.2145 in library ' ' BAM に変換しました。 Bed ファイルを作成中... BedGraph に変換中... BedGraph に変換しました。 BigWig に変換中... BigWig に変換しました。 INFO @ Sat, 01 Jun 2019 21:56:14: # Command line: callpeak -t /home/okishinya/chipatlas/results/ce10/SRX278067/SRX278067.bam -f BAM -g ce -n /home/okishinya/chipatlas/results/ce10/SRX278067/SRX278067.20 -q 1e-20 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/ce10/SRX278067/SRX278067.20 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/ce10/SRX278067/SRX278067.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 @ Sat, 01 Jun 2019 21:56:14: #1 read tag files... INFO @ Sat, 01 Jun 2019 21:56:14: #1 read treatment tags... INFO @ Sat, 01 Jun 2019 21:56:14: # Command line: callpeak -t /home/okishinya/chipatlas/results/ce10/SRX278067/SRX278067.bam -f BAM -g ce -n /home/okishinya/chipatlas/results/ce10/SRX278067/SRX278067.05 -q 1e-05 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/ce10/SRX278067/SRX278067.05 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/ce10/SRX278067/SRX278067.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 @ Sat, 01 Jun 2019 21:56:14: #1 read tag files... INFO @ Sat, 01 Jun 2019 21:56:14: #1 read treatment tags... INFO @ Sat, 01 Jun 2019 21:56:14: # Command line: callpeak -t /home/okishinya/chipatlas/results/ce10/SRX278067/SRX278067.bam -f BAM -g ce -n /home/okishinya/chipatlas/results/ce10/SRX278067/SRX278067.10 -q 1e-10 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/ce10/SRX278067/SRX278067.10 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/ce10/SRX278067/SRX278067.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 @ Sat, 01 Jun 2019 21:56:14: #1 read tag files... INFO @ Sat, 01 Jun 2019 21:56:14: #1 read treatment tags... INFO @ Sat, 01 Jun 2019 21:56:14: #1 tag size is determined as 36 bps INFO @ Sat, 01 Jun 2019 21:56:14: #1 tag size = 36 INFO @ Sat, 01 Jun 2019 21:56:14: #1 total tags in treatment: 52940 INFO @ Sat, 01 Jun 2019 21:56:14: #1 user defined the maximum tags... INFO @ Sat, 01 Jun 2019 21:56:14: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Sat, 01 Jun 2019 21:56:14: #1 tags after filtering in treatment: 52940 INFO @ Sat, 01 Jun 2019 21:56:14: #1 Redundant rate of treatment: 0.00 INFO @ Sat, 01 Jun 2019 21:56:14: #1 finished! INFO @ Sat, 01 Jun 2019 21:56:14: #2 Build Peak Model... INFO @ Sat, 01 Jun 2019 21:56:14: #2 looking for paired plus/minus strand peaks... INFO @ Sat, 01 Jun 2019 21:56:14: #1 tag size is determined as 36 bps INFO @ Sat, 01 Jun 2019 21:56:14: #1 tag size = 36 INFO @ Sat, 01 Jun 2019 21:56:14: #1 total tags in treatment: 52940 INFO @ Sat, 01 Jun 2019 21:56:14: #1 user defined the maximum tags... INFO @ Sat, 01 Jun 2019 21:56:14: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Sat, 01 Jun 2019 21:56:14: #1 tags after filtering in treatment: 52940 INFO @ Sat, 01 Jun 2019 21:56:14: #1 Redundant rate of treatment: 0.00 INFO @ Sat, 01 Jun 2019 21:56:14: #1 finished! INFO @ Sat, 01 Jun 2019 21:56:14: #2 Build Peak Model... INFO @ Sat, 01 Jun 2019 21:56:14: #2 looking for paired plus/minus strand peaks... INFO @ Sat, 01 Jun 2019 21:56:14: #1 tag size is determined as 36 bps INFO @ Sat, 01 Jun 2019 21:56:14: #1 tag size = 36 INFO @ Sat, 01 Jun 2019 21:56:14: #1 total tags in treatment: 52940 INFO @ Sat, 01 Jun 2019 21:56:14: #1 user defined the maximum tags... INFO @ Sat, 01 Jun 2019 21:56:14: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Sat, 01 Jun 2019 21:56:14: #1 tags after filtering in treatment: 52940 INFO @ Sat, 01 Jun 2019 21:56:14: #1 Redundant rate of treatment: 0.00 INFO @ Sat, 01 Jun 2019 21:56:14: #1 finished! INFO @ Sat, 01 Jun 2019 21:56:14: #2 Build Peak Model... INFO @ Sat, 01 Jun 2019 21:56:14: #2 looking for paired plus/minus strand peaks... INFO @ Sat, 01 Jun 2019 21:56:14: #2 number of paired peaks: 2344 INFO @ Sat, 01 Jun 2019 21:56:14: start model_add_line... INFO @ Sat, 01 Jun 2019 21:56:14: start X-correlation... INFO @ Sat, 01 Jun 2019 21:56:14: end of X-cor INFO @ Sat, 01 Jun 2019 21:56:14: #2 finished! INFO @ Sat, 01 Jun 2019 21:56:14: #2 predicted fragment length is 300 bps INFO @ Sat, 01 Jun 2019 21:56:14: #2 alternative fragment length(s) may be 39,117,167,203,262,300 bps INFO @ Sat, 01 Jun 2019 21:56:14: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/ce10/SRX278067/SRX278067.20_model.r INFO @ Sat, 01 Jun 2019 21:56:14: #3 Call peaks... INFO @ Sat, 01 Jun 2019 21:56:14: #3 Pre-compute pvalue-qvalue table... INFO @ Sat, 01 Jun 2019 21:56:14: #2 number of paired peaks: 2344 INFO @ Sat, 01 Jun 2019 21:56:14: start model_add_line... INFO @ Sat, 01 Jun 2019 21:56:14: start X-correlation... INFO @ Sat, 01 Jun 2019 21:56:14: end of X-cor INFO @ Sat, 01 Jun 2019 21:56:14: #2 finished! INFO @ Sat, 01 Jun 2019 21:56:14: #2 predicted fragment length is 300 bps INFO @ Sat, 01 Jun 2019 21:56:14: #2 alternative fragment length(s) may be 39,117,167,203,262,300 bps INFO @ Sat, 01 Jun 2019 21:56:14: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/ce10/SRX278067/SRX278067.10_model.r INFO @ Sat, 01 Jun 2019 21:56:14: #3 Call peaks... INFO @ Sat, 01 Jun 2019 21:56:14: #3 Pre-compute pvalue-qvalue table... INFO @ Sat, 01 Jun 2019 21:56:14: #2 number of paired peaks: 2344 INFO @ Sat, 01 Jun 2019 21:56:14: start model_add_line... INFO @ Sat, 01 Jun 2019 21:56:14: start X-correlation... INFO @ Sat, 01 Jun 2019 21:56:14: end of X-cor INFO @ Sat, 01 Jun 2019 21:56:14: #2 finished! INFO @ Sat, 01 Jun 2019 21:56:14: #2 predicted fragment length is 300 bps INFO @ Sat, 01 Jun 2019 21:56:14: #2 alternative fragment length(s) may be 39,117,167,203,262,300 bps INFO @ Sat, 01 Jun 2019 21:56:14: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/ce10/SRX278067/SRX278067.05_model.r INFO @ Sat, 01 Jun 2019 21:56:14: #3 Call peaks... INFO @ Sat, 01 Jun 2019 21:56:14: #3 Pre-compute pvalue-qvalue table... INFO @ Sat, 01 Jun 2019 21:56:14: #3 Call peaks for each chromosome... INFO @ Sat, 01 Jun 2019 21:56:14: #3 Call peaks for each chromosome... INFO @ Sat, 01 Jun 2019 21:56:14: #4 Write output xls file... /home/okishinya/chipatlas/results/ce10/SRX278067/SRX278067.20_peaks.xls INFO @ Sat, 01 Jun 2019 21:56:14: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/ce10/SRX278067/SRX278067.20_peaks.narrowPeak INFO @ Sat, 01 Jun 2019 21:56:14: #4 Write summits bed file... /home/okishinya/chipatlas/results/ce10/SRX278067/SRX278067.20_summits.bed INFO @ Sat, 01 Jun 2019 21:56:14: Done! INFO @ Sat, 01 Jun 2019 21:56:14: #4 Write output xls file... /home/okishinya/chipatlas/results/ce10/SRX278067/SRX278067.10_peaks.xls INFO @ Sat, 01 Jun 2019 21:56:14: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/ce10/SRX278067/SRX278067.10_peaks.narrowPeak INFO @ Sat, 01 Jun 2019 21:56:14: #4 Write summits bed file... /home/okishinya/chipatlas/results/ce10/SRX278067/SRX278067.10_summits.bed INFO @ Sat, 01 Jun 2019 21:56:14: Done! INFO @ Sat, 01 Jun 2019 21:56:14: #3 Call peaks for each chromosome... pass1 - making usageList (1 chroms): 1 millis pass2 - checking and writing primary data (1 records, 4 fields): 3 millis CompletedMACS2peakCalling INFO @ Sat, 01 Jun 2019 21:56:15: #4 Write output xls file... /home/okishinya/chipatlas/results/ce10/SRX278067/SRX278067.05_peaks.xls pass1 - making usageList (4 chroms): 1 millis pass2 - checking and writing primary data (7 records, 4 fields): 2 millis INFO @ Sat, 01 Jun 2019 21:56:15: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/ce10/SRX278067/SRX278067.05_peaks.narrowPeak INFO @ Sat, 01 Jun 2019 21:56:15: #4 Write summits bed file... /home/okishinya/chipatlas/results/ce10/SRX278067/SRX278067.05_summits.bed INFO @ Sat, 01 Jun 2019 21:56:15: Done! CompletedMACS2peakCalling pass1 - making usageList (6 chroms): 1 millis pass2 - checking and writing primary data (28 records, 4 fields): 2 millis CompletedMACS2peakCalling