Job ID = 1294396 sra ファイルのダウンロード中... Read layout: SINGLE fastq に変換中... spots read : 11,258,758 reads read : 11,258,758 reads written : 11,258,758 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: 00:06:01 11258758 reads; of these: 11258758 (100.00%) were unpaired; of these: 550915 (4.89%) aligned 0 times 7134477 (63.37%) aligned exactly 1 time 3573366 (31.74%) aligned >1 times 95.11% overall alignment rate Time searching: 00:06:01 Overall time: 00:06:01 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] 1087280 / 10707843 = 0.1015 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 07:25:02: # Command line: callpeak -t /home/okishinya/chipatlas/results/dm3/SRX287573/SRX287573.bam -f BAM -g dm -n /home/okishinya/chipatlas/results/dm3/SRX287573/SRX287573.05 -q 1e-05 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/dm3/SRX287573/SRX287573.05 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/dm3/SRX287573/SRX287573.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 07:25:02: #1 read tag files... INFO @ Mon, 03 Jun 2019 07:25:02: #1 read treatment tags... INFO @ Mon, 03 Jun 2019 07:25:02: # Command line: callpeak -t /home/okishinya/chipatlas/results/dm3/SRX287573/SRX287573.bam -f BAM -g dm -n /home/okishinya/chipatlas/results/dm3/SRX287573/SRX287573.20 -q 1e-20 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/dm3/SRX287573/SRX287573.20 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/dm3/SRX287573/SRX287573.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 07:25:02: #1 read tag files... INFO @ Mon, 03 Jun 2019 07:25:02: #1 read treatment tags... INFO @ Mon, 03 Jun 2019 07:25:03: # Command line: callpeak -t /home/okishinya/chipatlas/results/dm3/SRX287573/SRX287573.bam -f BAM -g dm -n /home/okishinya/chipatlas/results/dm3/SRX287573/SRX287573.10 -q 1e-10 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/dm3/SRX287573/SRX287573.10 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/dm3/SRX287573/SRX287573.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 07:25:03: #1 read tag files... INFO @ Mon, 03 Jun 2019 07:25:03: #1 read treatment tags... INFO @ Mon, 03 Jun 2019 07:25:11: 1000000 INFO @ Mon, 03 Jun 2019 07:25:11: 1000000 INFO @ Mon, 03 Jun 2019 07:25:11: 1000000 INFO @ Mon, 03 Jun 2019 07:25:18: 2000000 INFO @ Mon, 03 Jun 2019 07:25:18: 2000000 INFO @ Mon, 03 Jun 2019 07:25:19: 2000000 INFO @ Mon, 03 Jun 2019 07:25:26: 3000000 INFO @ Mon, 03 Jun 2019 07:25:26: 3000000 INFO @ Mon, 03 Jun 2019 07:25:27: 3000000 INFO @ Mon, 03 Jun 2019 07:25:34: 4000000 INFO @ Mon, 03 Jun 2019 07:25:34: 4000000 INFO @ Mon, 03 Jun 2019 07:25:35: 4000000 INFO @ Mon, 03 Jun 2019 07:25:42: 5000000 INFO @ Mon, 03 Jun 2019 07:25:42: 5000000 INFO @ Mon, 03 Jun 2019 07:25:43: 5000000 INFO @ Mon, 03 Jun 2019 07:25:50: 6000000 INFO @ Mon, 03 Jun 2019 07:25:50: 6000000 INFO @ Mon, 03 Jun 2019 07:25:51: 6000000 INFO @ Mon, 03 Jun 2019 07:25:57: 7000000 INFO @ Mon, 03 Jun 2019 07:25:58: 7000000 INFO @ Mon, 03 Jun 2019 07:25:58: 7000000 INFO @ Mon, 03 Jun 2019 07:26:04: 8000000 INFO @ Mon, 03 Jun 2019 07:26:05: 8000000 INFO @ Mon, 03 Jun 2019 07:26:06: 8000000 INFO @ Mon, 03 Jun 2019 07:26:12: 9000000 INFO @ Mon, 03 Jun 2019 07:26:12: 9000000 INFO @ Mon, 03 Jun 2019 07:26:14: 9000000 INFO @ Mon, 03 Jun 2019 07:26:16: #1 tag size is determined as 50 bps INFO @ Mon, 03 Jun 2019 07:26:16: #1 tag size = 50 INFO @ Mon, 03 Jun 2019 07:26:16: #1 total tags in treatment: 9620563 INFO @ Mon, 03 Jun 2019 07:26:16: #1 user defined the maximum tags... INFO @ Mon, 03 Jun 2019 07:26:16: #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 07:26:16: #1 tags after filtering in treatment: 9620563 INFO @ Mon, 03 Jun 2019 07:26:16: #1 Redundant rate of treatment: 0.00 INFO @ Mon, 03 Jun 2019 07:26:16: #1 finished! INFO @ Mon, 03 Jun 2019 07:26:16: #2 Build Peak Model... INFO @ Mon, 03 Jun 2019 07:26:16: #2 looking for paired plus/minus strand peaks... INFO @ Mon, 03 Jun 2019 07:26:17: #1 tag size is determined as 50 bps INFO @ Mon, 03 Jun 2019 07:26:17: #1 tag size = 50 INFO @ Mon, 03 Jun 2019 07:26:17: #1 total tags in treatment: 9620563 INFO @ Mon, 03 Jun 2019 07:26:17: #1 user defined the maximum tags... INFO @ Mon, 03 Jun 2019 07:26:17: #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 07:26:17: #2 number of paired peaks: 390 WARNING @ Mon, 03 Jun 2019 07:26:17: Fewer paired peaks (390) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 390 pairs to build model! INFO @ Mon, 03 Jun 2019 07:26:17: start model_add_line... INFO @ Mon, 03 Jun 2019 07:26:17: start X-correlation... INFO @ Mon, 03 Jun 2019 07:26:17: end of X-cor INFO @ Mon, 03 Jun 2019 07:26:17: #2 finished! INFO @ Mon, 03 Jun 2019 07:26:17: #2 predicted fragment length is 49 bps INFO @ Mon, 03 Jun 2019 07:26:17: #2 alternative fragment length(s) may be 49 bps INFO @ Mon, 03 Jun 2019 07:26:17: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/dm3/SRX287573/SRX287573.05_model.r WARNING @ Mon, 03 Jun 2019 07:26:17: #2 Since the d (49) calculated from paired-peaks are smaller than 2*tag length, it may be influenced by unknown sequencing problem! WARNING @ Mon, 03 Jun 2019 07:26:17: #2 You may need to consider one of the other alternative d(s): 49 WARNING @ Mon, 03 Jun 2019 07:26:17: #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 07:26:17: #3 Call peaks... INFO @ Mon, 03 Jun 2019 07:26:17: #3 Pre-compute pvalue-qvalue table... INFO @ Mon, 03 Jun 2019 07:26:17: #1 tags after filtering in treatment: 9620563 INFO @ Mon, 03 Jun 2019 07:26:17: #1 Redundant rate of treatment: 0.00 INFO @ Mon, 03 Jun 2019 07:26:17: #1 finished! INFO @ Mon, 03 Jun 2019 07:26:17: #2 Build Peak Model... INFO @ Mon, 03 Jun 2019 07:26:17: #2 looking for paired plus/minus strand peaks... INFO @ Mon, 03 Jun 2019 07:26:18: #2 number of paired peaks: 390 WARNING @ Mon, 03 Jun 2019 07:26:18: Fewer paired peaks (390) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 390 pairs to build model! INFO @ Mon, 03 Jun 2019 07:26:18: start model_add_line... INFO @ Mon, 03 Jun 2019 07:26:18: start X-correlation... INFO @ Mon, 03 Jun 2019 07:26:18: end of X-cor INFO @ Mon, 03 Jun 2019 07:26:18: #2 finished! INFO @ Mon, 03 Jun 2019 07:26:18: #2 predicted fragment length is 49 bps INFO @ Mon, 03 Jun 2019 07:26:18: #2 alternative fragment length(s) may be 49 bps INFO @ Mon, 03 Jun 2019 07:26:18: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/dm3/SRX287573/SRX287573.20_model.r WARNING @ Mon, 03 Jun 2019 07:26:18: #2 Since the d (49) calculated from paired-peaks are smaller than 2*tag length, it may be influenced by unknown sequencing problem! WARNING @ Mon, 03 Jun 2019 07:26:18: #2 You may need to consider one of the other alternative d(s): 49 WARNING @ Mon, 03 Jun 2019 07:26:18: #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 07:26:18: #3 Call peaks... INFO @ Mon, 03 Jun 2019 07:26:18: #3 Pre-compute pvalue-qvalue table... INFO @ Mon, 03 Jun 2019 07:26:19: #1 tag size is determined as 50 bps INFO @ Mon, 03 Jun 2019 07:26:19: #1 tag size = 50 INFO @ Mon, 03 Jun 2019 07:26:19: #1 total tags in treatment: 9620563 INFO @ Mon, 03 Jun 2019 07:26:19: #1 user defined the maximum tags... INFO @ Mon, 03 Jun 2019 07:26:19: #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 07:26:19: #1 tags after filtering in treatment: 9620563 INFO @ Mon, 03 Jun 2019 07:26:19: #1 Redundant rate of treatment: 0.00 INFO @ Mon, 03 Jun 2019 07:26:19: #1 finished! INFO @ Mon, 03 Jun 2019 07:26:19: #2 Build Peak Model... INFO @ Mon, 03 Jun 2019 07:26:19: #2 looking for paired plus/minus strand peaks... INFO @ Mon, 03 Jun 2019 07:26:20: #2 number of paired peaks: 390 WARNING @ Mon, 03 Jun 2019 07:26:20: Fewer paired peaks (390) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 390 pairs to build model! INFO @ Mon, 03 Jun 2019 07:26:20: start model_add_line... INFO @ Mon, 03 Jun 2019 07:26:20: start X-correlation... INFO @ Mon, 03 Jun 2019 07:26:20: end of X-cor INFO @ Mon, 03 Jun 2019 07:26:20: #2 finished! INFO @ Mon, 03 Jun 2019 07:26:20: #2 predicted fragment length is 49 bps INFO @ Mon, 03 Jun 2019 07:26:20: #2 alternative fragment length(s) may be 49 bps INFO @ Mon, 03 Jun 2019 07:26:20: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/dm3/SRX287573/SRX287573.10_model.r WARNING @ Mon, 03 Jun 2019 07:26:20: #2 Since the d (49) calculated from paired-peaks are smaller than 2*tag length, it may be influenced by unknown sequencing problem! WARNING @ Mon, 03 Jun 2019 07:26:20: #2 You may need to consider one of the other alternative d(s): 49 WARNING @ Mon, 03 Jun 2019 07:26:20: #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 07:26:20: #3 Call peaks... INFO @ Mon, 03 Jun 2019 07:26:20: #3 Pre-compute pvalue-qvalue table... INFO @ Mon, 03 Jun 2019 07:26:44: #3 Call peaks for each chromosome... INFO @ Mon, 03 Jun 2019 07:26:45: #3 Call peaks for each chromosome... INFO @ Mon, 03 Jun 2019 07:26:47: #3 Call peaks for each chromosome... INFO @ Mon, 03 Jun 2019 07:26:58: #4 Write output xls file... /home/okishinya/chipatlas/results/dm3/SRX287573/SRX287573.05_peaks.xls INFO @ Mon, 03 Jun 2019 07:26:58: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/dm3/SRX287573/SRX287573.05_peaks.narrowPeak INFO @ Mon, 03 Jun 2019 07:26:58: #4 Write summits bed file... /home/okishinya/chipatlas/results/dm3/SRX287573/SRX287573.05_summits.bed INFO @ Mon, 03 Jun 2019 07:26:58: Done! pass1 - making usageList (13 chroms): 1 millis pass2 - checking and writing primary data (1954 records, 4 fields): 5 millis CompletedMACS2peakCalling INFO @ Mon, 03 Jun 2019 07:26:58: #4 Write output xls file... /home/okishinya/chipatlas/results/dm3/SRX287573/SRX287573.20_peaks.xls INFO @ Mon, 03 Jun 2019 07:26:58: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/dm3/SRX287573/SRX287573.20_peaks.narrowPeak INFO @ Mon, 03 Jun 2019 07:26:58: #4 Write summits bed file... /home/okishinya/chipatlas/results/dm3/SRX287573/SRX287573.20_summits.bed INFO @ Mon, 03 Jun 2019 07:26:58: Done! pass1 - making usageList (11 chroms): 1 millis pass2 - checking and writing primary data (1166 records, 4 fields): 3 millis CompletedMACS2peakCalling INFO @ Mon, 03 Jun 2019 07:27:00: #4 Write output xls file... /home/okishinya/chipatlas/results/dm3/SRX287573/SRX287573.10_peaks.xls INFO @ Mon, 03 Jun 2019 07:27:00: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/dm3/SRX287573/SRX287573.10_peaks.narrowPeak INFO @ Mon, 03 Jun 2019 07:27:00: #4 Write summits bed file... /home/okishinya/chipatlas/results/dm3/SRX287573/SRX287573.10_summits.bed INFO @ Mon, 03 Jun 2019 07:27:00: Done! pass1 - making usageList (13 chroms): 2 millis pass2 - checking and writing primary data (1646 records, 4 fields): 6 millis CompletedMACS2peakCalling BedGraph に変換しました。 BigWig に変換中... BigWig に変換しました。