Job ID = 1294025 sra ファイルのダウンロード中... Read layout: SINGLE fastq に変換中... spots read : 4,326,356 reads read : 8,652,712 reads written : 4,326,356 reads 0-length : 4,326,356 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: 00:08:53 4326356 reads; of these: 4326356 (100.00%) were unpaired; of these: 1445587 (33.41%) aligned 0 times 971054 (22.45%) aligned exactly 1 time 1909715 (44.14%) aligned >1 times 66.59% overall alignment rate Time searching: 00:08:53 Overall time: 00:08:53 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_rmdupse_core] 311837 / 2880769 = 0.1082 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 04:24:24: # Command line: callpeak -t /home/okishinya/chipatlas/results/dm3/SRX1760701/SRX1760701.bam -f BAM -g dm -n /home/okishinya/chipatlas/results/dm3/SRX1760701/SRX1760701.10 -q 1e-10 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/dm3/SRX1760701/SRX1760701.10 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/dm3/SRX1760701/SRX1760701.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 04:24:24: #1 read tag files... INFO @ Mon, 03 Jun 2019 04:24:24: #1 read treatment tags... INFO @ Mon, 03 Jun 2019 04:24:24: # Command line: callpeak -t /home/okishinya/chipatlas/results/dm3/SRX1760701/SRX1760701.bam -f BAM -g dm -n /home/okishinya/chipatlas/results/dm3/SRX1760701/SRX1760701.05 -q 1e-05 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/dm3/SRX1760701/SRX1760701.05 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/dm3/SRX1760701/SRX1760701.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 04:24:24: #1 read tag files... INFO @ Mon, 03 Jun 2019 04:24:24: #1 read treatment tags... INFO @ Mon, 03 Jun 2019 04:24:24: # Command line: callpeak -t /home/okishinya/chipatlas/results/dm3/SRX1760701/SRX1760701.bam -f BAM -g dm -n /home/okishinya/chipatlas/results/dm3/SRX1760701/SRX1760701.20 -q 1e-20 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/dm3/SRX1760701/SRX1760701.20 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/dm3/SRX1760701/SRX1760701.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 04:24:24: #1 read tag files... INFO @ Mon, 03 Jun 2019 04:24:24: #1 read treatment tags... INFO @ Mon, 03 Jun 2019 04:24:37: 1000000 INFO @ Mon, 03 Jun 2019 04:24:38: 1000000 INFO @ Mon, 03 Jun 2019 04:24:43: 1000000 INFO @ Mon, 03 Jun 2019 04:24:52: 2000000 INFO @ Mon, 03 Jun 2019 04:24:54: 2000000 INFO @ Mon, 03 Jun 2019 04:25:00: #1 tag size is determined as 151 bps INFO @ Mon, 03 Jun 2019 04:25:00: #1 tag size = 151 INFO @ Mon, 03 Jun 2019 04:25:00: #1 total tags in treatment: 2568932 INFO @ Mon, 03 Jun 2019 04:25:00: #1 user defined the maximum tags... INFO @ Mon, 03 Jun 2019 04:25:00: #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 04:25:00: #1 tags after filtering in treatment: 2568932 INFO @ Mon, 03 Jun 2019 04:25:00: #1 Redundant rate of treatment: 0.00 INFO @ Mon, 03 Jun 2019 04:25:00: #1 finished! INFO @ Mon, 03 Jun 2019 04:25:00: #2 Build Peak Model... INFO @ Mon, 03 Jun 2019 04:25:00: #2 looking for paired plus/minus strand peaks... INFO @ Mon, 03 Jun 2019 04:25:00: #2 number of paired peaks: 2924 INFO @ Mon, 03 Jun 2019 04:25:00: start model_add_line... INFO @ Mon, 03 Jun 2019 04:25:00: start X-correlation... INFO @ Mon, 03 Jun 2019 04:25:00: end of X-cor INFO @ Mon, 03 Jun 2019 04:25:00: #2 finished! INFO @ Mon, 03 Jun 2019 04:25:00: #2 predicted fragment length is 134 bps INFO @ Mon, 03 Jun 2019 04:25:00: #2 alternative fragment length(s) may be 134 bps INFO @ Mon, 03 Jun 2019 04:25:00: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/dm3/SRX1760701/SRX1760701.05_model.r WARNING @ Mon, 03 Jun 2019 04:25:01: #2 Since the d (134) calculated from paired-peaks are smaller than 2*tag length, it may be influenced by unknown sequencing problem! WARNING @ Mon, 03 Jun 2019 04:25:01: #2 You may need to consider one of the other alternative d(s): 134 WARNING @ Mon, 03 Jun 2019 04:25:01: #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 04:25:01: #3 Call peaks... INFO @ Mon, 03 Jun 2019 04:25:01: #3 Pre-compute pvalue-qvalue table... INFO @ Mon, 03 Jun 2019 04:25:02: 2000000 INFO @ Mon, 03 Jun 2019 04:25:02: #1 tag size is determined as 151 bps INFO @ Mon, 03 Jun 2019 04:25:02: #1 tag size = 151 INFO @ Mon, 03 Jun 2019 04:25:02: #1 total tags in treatment: 2568932 INFO @ Mon, 03 Jun 2019 04:25:02: #1 user defined the maximum tags... INFO @ Mon, 03 Jun 2019 04:25:02: #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 04:25:02: #1 tags after filtering in treatment: 2568932 INFO @ Mon, 03 Jun 2019 04:25:02: #1 Redundant rate of treatment: 0.00 INFO @ Mon, 03 Jun 2019 04:25:02: #1 finished! INFO @ Mon, 03 Jun 2019 04:25:02: #2 Build Peak Model... INFO @ Mon, 03 Jun 2019 04:25:02: #2 looking for paired plus/minus strand peaks... INFO @ Mon, 03 Jun 2019 04:25:03: #2 number of paired peaks: 2924 INFO @ Mon, 03 Jun 2019 04:25:03: start model_add_line... INFO @ Mon, 03 Jun 2019 04:25:03: start X-correlation... INFO @ Mon, 03 Jun 2019 04:25:03: end of X-cor INFO @ Mon, 03 Jun 2019 04:25:03: #2 finished! INFO @ Mon, 03 Jun 2019 04:25:03: #2 predicted fragment length is 134 bps INFO @ Mon, 03 Jun 2019 04:25:03: #2 alternative fragment length(s) may be 134 bps INFO @ Mon, 03 Jun 2019 04:25:03: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/dm3/SRX1760701/SRX1760701.10_model.r WARNING @ Mon, 03 Jun 2019 04:25:03: #2 Since the d (134) calculated from paired-peaks are smaller than 2*tag length, it may be influenced by unknown sequencing problem! WARNING @ Mon, 03 Jun 2019 04:25:03: #2 You may need to consider one of the other alternative d(s): 134 WARNING @ Mon, 03 Jun 2019 04:25:03: #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 04:25:03: #3 Call peaks... INFO @ Mon, 03 Jun 2019 04:25:03: #3 Pre-compute pvalue-qvalue table... INFO @ Mon, 03 Jun 2019 04:25:09: #3 Call peaks for each chromosome... INFO @ Mon, 03 Jun 2019 04:25:11: #3 Call peaks for each chromosome... INFO @ Mon, 03 Jun 2019 04:25:12: #1 tag size is determined as 151 bps INFO @ Mon, 03 Jun 2019 04:25:12: #1 tag size = 151 INFO @ Mon, 03 Jun 2019 04:25:12: #1 total tags in treatment: 2568932 INFO @ Mon, 03 Jun 2019 04:25:12: #1 user defined the maximum tags... INFO @ Mon, 03 Jun 2019 04:25:12: #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 04:25:12: #1 tags after filtering in treatment: 2568932 INFO @ Mon, 03 Jun 2019 04:25:12: #1 Redundant rate of treatment: 0.00 INFO @ Mon, 03 Jun 2019 04:25:12: #1 finished! INFO @ Mon, 03 Jun 2019 04:25:12: #2 Build Peak Model... INFO @ Mon, 03 Jun 2019 04:25:12: #2 looking for paired plus/minus strand peaks... INFO @ Mon, 03 Jun 2019 04:25:12: #2 number of paired peaks: 2924 INFO @ Mon, 03 Jun 2019 04:25:12: start model_add_line... INFO @ Mon, 03 Jun 2019 04:25:12: start X-correlation... INFO @ Mon, 03 Jun 2019 04:25:12: end of X-cor INFO @ Mon, 03 Jun 2019 04:25:12: #2 finished! INFO @ Mon, 03 Jun 2019 04:25:12: #2 predicted fragment length is 134 bps INFO @ Mon, 03 Jun 2019 04:25:12: #2 alternative fragment length(s) may be 134 bps INFO @ Mon, 03 Jun 2019 04:25:12: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/dm3/SRX1760701/SRX1760701.20_model.r WARNING @ Mon, 03 Jun 2019 04:25:12: #2 Since the d (134) calculated from paired-peaks are smaller than 2*tag length, it may be influenced by unknown sequencing problem! WARNING @ Mon, 03 Jun 2019 04:25:12: #2 You may need to consider one of the other alternative d(s): 134 WARNING @ Mon, 03 Jun 2019 04:25:12: #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 04:25:12: #3 Call peaks... INFO @ Mon, 03 Jun 2019 04:25:12: #3 Pre-compute pvalue-qvalue table... INFO @ Mon, 03 Jun 2019 04:25:14: #4 Write output xls file... /home/okishinya/chipatlas/results/dm3/SRX1760701/SRX1760701.05_peaks.xls INFO @ Mon, 03 Jun 2019 04:25:14: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/dm3/SRX1760701/SRX1760701.05_peaks.narrowPeak INFO @ Mon, 03 Jun 2019 04:25:14: #4 Write summits bed file... /home/okishinya/chipatlas/results/dm3/SRX1760701/SRX1760701.05_summits.bed INFO @ Mon, 03 Jun 2019 04:25:14: Done! pass1 - making usageList (14 chroms): 3 millis pass2 - checking and writing primary data (3157 records, 4 fields): 9 millis CompletedMACS2peakCalling INFO @ Mon, 03 Jun 2019 04:25:15: #4 Write output xls file... /home/okishinya/chipatlas/results/dm3/SRX1760701/SRX1760701.10_peaks.xls INFO @ Mon, 03 Jun 2019 04:25:15: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/dm3/SRX1760701/SRX1760701.10_peaks.narrowPeak INFO @ Mon, 03 Jun 2019 04:25:15: #4 Write summits bed file... /home/okishinya/chipatlas/results/dm3/SRX1760701/SRX1760701.10_summits.bed INFO @ Mon, 03 Jun 2019 04:25:15: Done! pass1 - making usageList (13 chroms): 2 millis pass2 - checking and writing primary data (1425 records, 4 fields): 7 millis CompletedMACS2peakCalling INFO @ Mon, 03 Jun 2019 04:25:21: #3 Call peaks for each chromosome... BedGraph に変換しました。 BigWig に変換中... INFO @ Mon, 03 Jun 2019 04:25:25: #4 Write output xls file... /home/okishinya/chipatlas/results/dm3/SRX1760701/SRX1760701.20_peaks.xls INFO @ Mon, 03 Jun 2019 04:25:25: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/dm3/SRX1760701/SRX1760701.20_peaks.narrowPeak INFO @ Mon, 03 Jun 2019 04:25:25: #4 Write summits bed file... /home/okishinya/chipatlas/results/dm3/SRX1760701/SRX1760701.20_summits.bed INFO @ Mon, 03 Jun 2019 04:25:25: Done! pass1 - making usageList (12 chroms): 1 millis pass2 - checking and writing primary data (564 records, 4 fields): 4 millis CompletedMACS2peakCalling BigWig に変換しました。