Job ID = 1294082 sra ファイルのダウンロード中... Read layout: SINGLE fastq に変換中... spots read : 30,805,635 reads read : 30,805,635 reads written : 30,805,635 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: 00:04:30 30805635 reads; of these: 30805635 (100.00%) were unpaired; of these: 14296436 (46.41%) aligned 0 times 14941425 (48.50%) aligned exactly 1 time 1567774 (5.09%) aligned >1 times 53.59% overall alignment rate Time searching: 00:04:30 Overall time: 00:04:30 マッピングが完了しました。 samtools でBAM に変換中... [samopen] SAM header is present: 15 sequences. [bam_sort_core] merging from 8 files... [bam_rmdupse_core] 15187097 / 16509199 = 0.9199 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, 03 Jun 2019 04:54:01: # Command line: callpeak -t /home/okishinya/chipatlas/results/dm3/SRX181439/SRX181439.bam -f BAM -g dm -n /home/okishinya/chipatlas/results/dm3/SRX181439/SRX181439.20 -q 1e-20 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/dm3/SRX181439/SRX181439.20 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/dm3/SRX181439/SRX181439.bam'] # control file = None # effective genome size = 1.20e+08 # 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, 03 Jun 2019 04:54:01: #1 read tag files... INFO @ Mon, 03 Jun 2019 04:54:01: #1 read treatment tags... INFO @ Mon, 03 Jun 2019 04:54:01: # Command line: callpeak -t /home/okishinya/chipatlas/results/dm3/SRX181439/SRX181439.bam -f BAM -g dm -n /home/okishinya/chipatlas/results/dm3/SRX181439/SRX181439.05 -q 1e-05 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/dm3/SRX181439/SRX181439.05 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/dm3/SRX181439/SRX181439.bam'] # control file = None # effective genome size = 1.20e+08 # 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, 03 Jun 2019 04:54:01: #1 read tag files... INFO @ Mon, 03 Jun 2019 04:54:01: #1 read treatment tags... INFO @ Mon, 03 Jun 2019 04:54:01: # Command line: callpeak -t /home/okishinya/chipatlas/results/dm3/SRX181439/SRX181439.bam -f BAM -g dm -n /home/okishinya/chipatlas/results/dm3/SRX181439/SRX181439.10 -q 1e-10 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/dm3/SRX181439/SRX181439.10 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/dm3/SRX181439/SRX181439.bam'] # control file = None # effective genome size = 1.20e+08 # 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, 03 Jun 2019 04:54:01: #1 read tag files... INFO @ Mon, 03 Jun 2019 04:54:01: #1 read treatment tags... INFO @ Mon, 03 Jun 2019 04:54:08: 1000000 INFO @ Mon, 03 Jun 2019 04:54:08: 1000000 INFO @ Mon, 03 Jun 2019 04:54:09: 1000000 INFO @ Mon, 03 Jun 2019 04:54:10: #1 tag size is determined as 36 bps INFO @ Mon, 03 Jun 2019 04:54:10: #1 tag size = 36 INFO @ Mon, 03 Jun 2019 04:54:10: #1 total tags in treatment: 1322102 INFO @ Mon, 03 Jun 2019 04:54:10: #1 user defined the maximum tags... INFO @ Mon, 03 Jun 2019 04:54:10: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Mon, 03 Jun 2019 04:54:10: #1 tags after filtering in treatment: 1322102 INFO @ Mon, 03 Jun 2019 04:54:10: #1 Redundant rate of treatment: 0.00 INFO @ Mon, 03 Jun 2019 04:54:10: #1 finished! INFO @ Mon, 03 Jun 2019 04:54:10: #2 Build Peak Model... INFO @ Mon, 03 Jun 2019 04:54:10: #2 looking for paired plus/minus strand peaks... INFO @ Mon, 03 Jun 2019 04:54:10: #2 number of paired peaks: 1639 INFO @ Mon, 03 Jun 2019 04:54:10: start model_add_line... INFO @ Mon, 03 Jun 2019 04:54:10: start X-correlation... INFO @ Mon, 03 Jun 2019 04:54:10: end of X-cor INFO @ Mon, 03 Jun 2019 04:54:10: #2 finished! INFO @ Mon, 03 Jun 2019 04:54:10: #2 predicted fragment length is 69 bps INFO @ Mon, 03 Jun 2019 04:54:10: #2 alternative fragment length(s) may be 69 bps INFO @ Mon, 03 Jun 2019 04:54:10: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/dm3/SRX181439/SRX181439.20_model.r WARNING @ Mon, 03 Jun 2019 04:54:10: #2 Since the d (69) calculated from paired-peaks are smaller than 2*tag length, it may be influenced by unknown sequencing problem! WARNING @ Mon, 03 Jun 2019 04:54:10: #2 You may need to consider one of the other alternative d(s): 69 WARNING @ Mon, 03 Jun 2019 04:54:10: #2 You can restart the process with --nomodel --extsize XXX with your choice or an arbitrary number. Nontheless, MACS will continute computing. INFO @ Mon, 03 Jun 2019 04:54:10: #3 Call peaks... INFO @ Mon, 03 Jun 2019 04:54:10: #3 Pre-compute pvalue-qvalue table... INFO @ Mon, 03 Jun 2019 04:54:10: #1 tag size is determined as 36 bps INFO @ Mon, 03 Jun 2019 04:54:10: #1 tag size = 36 INFO @ Mon, 03 Jun 2019 04:54:10: #1 total tags in treatment: 1322102 INFO @ Mon, 03 Jun 2019 04:54:10: #1 user defined the maximum tags... INFO @ Mon, 03 Jun 2019 04:54:10: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Mon, 03 Jun 2019 04:54:10: #1 tags after filtering in treatment: 1322102 INFO @ Mon, 03 Jun 2019 04:54:10: #1 Redundant rate of treatment: 0.00 INFO @ Mon, 03 Jun 2019 04:54:10: #1 finished! INFO @ Mon, 03 Jun 2019 04:54:10: #2 Build Peak Model... INFO @ Mon, 03 Jun 2019 04:54:10: #2 looking for paired plus/minus strand peaks... INFO @ Mon, 03 Jun 2019 04:54:11: #2 number of paired peaks: 1639 INFO @ Mon, 03 Jun 2019 04:54:11: start model_add_line... INFO @ Mon, 03 Jun 2019 04:54:11: start X-correlation... INFO @ Mon, 03 Jun 2019 04:54:11: end of X-cor INFO @ Mon, 03 Jun 2019 04:54:11: #2 finished! INFO @ Mon, 03 Jun 2019 04:54:11: #2 predicted fragment length is 69 bps INFO @ Mon, 03 Jun 2019 04:54:11: #2 alternative fragment length(s) may be 69 bps INFO @ Mon, 03 Jun 2019 04:54:11: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/dm3/SRX181439/SRX181439.10_model.r WARNING @ Mon, 03 Jun 2019 04:54:11: #2 Since the d (69) calculated from paired-peaks are smaller than 2*tag length, it may be influenced by unknown sequencing problem! WARNING @ Mon, 03 Jun 2019 04:54:11: #2 You may need to consider one of the other alternative d(s): 69 WARNING @ Mon, 03 Jun 2019 04:54:11: #2 You can restart the process with --nomodel --extsize XXX with your choice or an arbitrary number. Nontheless, MACS will continute computing. INFO @ Mon, 03 Jun 2019 04:54:11: #3 Call peaks... INFO @ Mon, 03 Jun 2019 04:54:11: #3 Pre-compute pvalue-qvalue table... INFO @ Mon, 03 Jun 2019 04:54:12: #1 tag size is determined as 36 bps INFO @ Mon, 03 Jun 2019 04:54:12: #1 tag size = 36 INFO @ Mon, 03 Jun 2019 04:54:12: #1 total tags in treatment: 1322102 INFO @ Mon, 03 Jun 2019 04:54:12: #1 user defined the maximum tags... INFO @ Mon, 03 Jun 2019 04:54:12: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Mon, 03 Jun 2019 04:54:12: #1 tags after filtering in treatment: 1322102 INFO @ Mon, 03 Jun 2019 04:54:12: #1 Redundant rate of treatment: 0.00 INFO @ Mon, 03 Jun 2019 04:54:12: #1 finished! INFO @ Mon, 03 Jun 2019 04:54:12: #2 Build Peak Model... INFO @ Mon, 03 Jun 2019 04:54:12: #2 looking for paired plus/minus strand peaks... INFO @ Mon, 03 Jun 2019 04:54:12: #2 number of paired peaks: 1639 INFO @ Mon, 03 Jun 2019 04:54:12: start model_add_line... INFO @ Mon, 03 Jun 2019 04:54:12: start X-correlation... INFO @ Mon, 03 Jun 2019 04:54:12: end of X-cor INFO @ Mon, 03 Jun 2019 04:54:12: #2 finished! INFO @ Mon, 03 Jun 2019 04:54:12: #2 predicted fragment length is 69 bps INFO @ Mon, 03 Jun 2019 04:54:12: #2 alternative fragment length(s) may be 69 bps INFO @ Mon, 03 Jun 2019 04:54:12: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/dm3/SRX181439/SRX181439.05_model.r WARNING @ Mon, 03 Jun 2019 04:54:12: #2 Since the d (69) calculated from paired-peaks are smaller than 2*tag length, it may be influenced by unknown sequencing problem! WARNING @ Mon, 03 Jun 2019 04:54:12: #2 You may need to consider one of the other alternative d(s): 69 WARNING @ Mon, 03 Jun 2019 04:54:12: #2 You can restart the process with --nomodel --extsize XXX with your choice or an arbitrary number. Nontheless, MACS will continute computing. INFO @ Mon, 03 Jun 2019 04:54:12: #3 Call peaks... INFO @ Mon, 03 Jun 2019 04:54:12: #3 Pre-compute pvalue-qvalue table... INFO @ Mon, 03 Jun 2019 04:54:14: #3 Call peaks for each chromosome... INFO @ Mon, 03 Jun 2019 04:54:15: #3 Call peaks for each chromosome... INFO @ Mon, 03 Jun 2019 04:54:16: #4 Write output xls file... /home/okishinya/chipatlas/results/dm3/SRX181439/SRX181439.20_peaks.xls INFO @ Mon, 03 Jun 2019 04:54:16: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/dm3/SRX181439/SRX181439.20_peaks.narrowPeak INFO @ Mon, 03 Jun 2019 04:54:16: #4 Write summits bed file... /home/okishinya/chipatlas/results/dm3/SRX181439/SRX181439.20_summits.bed INFO @ Mon, 03 Jun 2019 04:54:16: Done! pass1 - making usageList (3 chroms): 1 millis pass2 - checking and writing primary data (35 records, 4 fields): 2 millis CompletedMACS2peakCalling INFO @ Mon, 03 Jun 2019 04:54:16: #3 Call peaks for each chromosome... INFO @ Mon, 03 Jun 2019 04:54:17: #4 Write output xls file... /home/okishinya/chipatlas/results/dm3/SRX181439/SRX181439.10_peaks.xls INFO @ Mon, 03 Jun 2019 04:54:17: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/dm3/SRX181439/SRX181439.10_peaks.narrowPeak INFO @ Mon, 03 Jun 2019 04:54:17: #4 Write summits bed file... /home/okishinya/chipatlas/results/dm3/SRX181439/SRX181439.10_summits.bed INFO @ Mon, 03 Jun 2019 04:54:17: Done! pass1 - making usageList (11 chroms): 1 millis pass2 - checking and writing primary data (151 records, 4 fields): 3 millis CompletedMACS2peakCalling INFO @ Mon, 03 Jun 2019 04:54:18: #4 Write output xls file... /home/okishinya/chipatlas/results/dm3/SRX181439/SRX181439.05_peaks.xls INFO @ Mon, 03 Jun 2019 04:54:18: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/dm3/SRX181439/SRX181439.05_peaks.narrowPeak INFO @ Mon, 03 Jun 2019 04:54:18: #4 Write summits bed file... /home/okishinya/chipatlas/results/dm3/SRX181439/SRX181439.05_summits.bed INFO @ Mon, 03 Jun 2019 04:54:18: Done! pass1 - making usageList (13 chroms): 1 millis pass2 - checking and writing primary data (503 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。