Job ID = 1294096 sra ファイルのダウンロード中... Read layout: SINGLE fastq に変換中... spots read : 9,170,607 reads read : 9,170,607 reads written : 9,170,607 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: 00:03:51 9170607 reads; of these: 9170607 (100.00%) were unpaired; of these: 1802120 (19.65%) aligned 0 times 3625672 (39.54%) aligned exactly 1 time 3742815 (40.81%) aligned >1 times 80.35% overall alignment rate Time searching: 00:03:51 Overall time: 00:03:51 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] 1955632 / 7368487 = 0.2654 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 04:53:42: # Command line: callpeak -t /home/okishinya/chipatlas/results/dm3/SRX183885/SRX183885.bam -f BAM -g dm -n /home/okishinya/chipatlas/results/dm3/SRX183885/SRX183885.20 -q 1e-20 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/dm3/SRX183885/SRX183885.20 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/dm3/SRX183885/SRX183885.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 04:53:42: #1 read tag files... INFO @ Mon, 03 Jun 2019 04:53:42: #1 read treatment tags... INFO @ Mon, 03 Jun 2019 04:53:42: # Command line: callpeak -t /home/okishinya/chipatlas/results/dm3/SRX183885/SRX183885.bam -f BAM -g dm -n /home/okishinya/chipatlas/results/dm3/SRX183885/SRX183885.10 -q 1e-10 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/dm3/SRX183885/SRX183885.10 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/dm3/SRX183885/SRX183885.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 04:53:42: #1 read tag files... INFO @ Mon, 03 Jun 2019 04:53:42: #1 read treatment tags... INFO @ Mon, 03 Jun 2019 04:53:42: # Command line: callpeak -t /home/okishinya/chipatlas/results/dm3/SRX183885/SRX183885.bam -f BAM -g dm -n /home/okishinya/chipatlas/results/dm3/SRX183885/SRX183885.05 -q 1e-05 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/dm3/SRX183885/SRX183885.05 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/dm3/SRX183885/SRX183885.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 04:53:42: #1 read tag files... INFO @ Mon, 03 Jun 2019 04:53:42: #1 read treatment tags... INFO @ Mon, 03 Jun 2019 04:53:51: 1000000 INFO @ Mon, 03 Jun 2019 04:53:51: 1000000 INFO @ Mon, 03 Jun 2019 04:53:51: 1000000 INFO @ Mon, 03 Jun 2019 04:53:58: 2000000 INFO @ Mon, 03 Jun 2019 04:54:00: 2000000 INFO @ Mon, 03 Jun 2019 04:54:00: 2000000 INFO @ Mon, 03 Jun 2019 04:54:05: 3000000 INFO @ Mon, 03 Jun 2019 04:54:08: 3000000 INFO @ Mon, 03 Jun 2019 04:54:08: 3000000 INFO @ Mon, 03 Jun 2019 04:54:12: 4000000 INFO @ Mon, 03 Jun 2019 04:54:16: 4000000 INFO @ Mon, 03 Jun 2019 04:54:16: 4000000 INFO @ Mon, 03 Jun 2019 04:54:19: 5000000 INFO @ Mon, 03 Jun 2019 04:54:22: #1 tag size is determined as 18 bps INFO @ Mon, 03 Jun 2019 04:54:22: #1 tag size = 18 INFO @ Mon, 03 Jun 2019 04:54:22: #1 total tags in treatment: 5412855 INFO @ Mon, 03 Jun 2019 04:54:22: #1 user defined the maximum tags... INFO @ Mon, 03 Jun 2019 04:54:22: #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 04:54:22: #1 tags after filtering in treatment: 5412855 INFO @ Mon, 03 Jun 2019 04:54:22: #1 Redundant rate of treatment: 0.00 INFO @ Mon, 03 Jun 2019 04:54:22: #1 finished! INFO @ Mon, 03 Jun 2019 04:54:22: #2 Build Peak Model... INFO @ Mon, 03 Jun 2019 04:54:22: #2 looking for paired plus/minus strand peaks... INFO @ Mon, 03 Jun 2019 04:54:23: #2 number of paired peaks: 1064 INFO @ Mon, 03 Jun 2019 04:54:23: start model_add_line... INFO @ Mon, 03 Jun 2019 04:54:23: start X-correlation... INFO @ Mon, 03 Jun 2019 04:54:23: end of X-cor INFO @ Mon, 03 Jun 2019 04:54:23: #2 finished! INFO @ Mon, 03 Jun 2019 04:54:23: #2 predicted fragment length is 30 bps INFO @ Mon, 03 Jun 2019 04:54:23: #2 alternative fragment length(s) may be 30 bps INFO @ Mon, 03 Jun 2019 04:54:23: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/dm3/SRX183885/SRX183885.05_model.r WARNING @ Mon, 03 Jun 2019 04:54:23: #2 Since the d (30) calculated from paired-peaks are smaller than 2*tag length, it may be influenced by unknown sequencing problem! WARNING @ Mon, 03 Jun 2019 04:54:23: #2 You may need to consider one of the other alternative d(s): 30 WARNING @ Mon, 03 Jun 2019 04:54:23: #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 04:54:23: #3 Call peaks... INFO @ Mon, 03 Jun 2019 04:54:23: #3 Pre-compute pvalue-qvalue table... INFO @ Mon, 03 Jun 2019 04:54:24: 5000000 INFO @ Mon, 03 Jun 2019 04:54:24: 5000000 INFO @ Mon, 03 Jun 2019 04:54:28: #1 tag size is determined as 18 bps INFO @ Mon, 03 Jun 2019 04:54:28: #1 tag size = 18 INFO @ Mon, 03 Jun 2019 04:54:28: #1 total tags in treatment: 5412855 INFO @ Mon, 03 Jun 2019 04:54:28: #1 user defined the maximum tags... INFO @ Mon, 03 Jun 2019 04:54:28: #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 04:54:28: #1 tag size is determined as 18 bps INFO @ Mon, 03 Jun 2019 04:54:28: #1 tag size = 18 INFO @ Mon, 03 Jun 2019 04:54:28: #1 total tags in treatment: 5412855 INFO @ Mon, 03 Jun 2019 04:54:28: #1 user defined the maximum tags... INFO @ Mon, 03 Jun 2019 04:54:28: #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 04:54:28: #1 tags after filtering in treatment: 5412855 INFO @ Mon, 03 Jun 2019 04:54:28: #1 Redundant rate of treatment: 0.00 INFO @ Mon, 03 Jun 2019 04:54:28: #1 finished! INFO @ Mon, 03 Jun 2019 04:54:28: #2 Build Peak Model... INFO @ Mon, 03 Jun 2019 04:54:28: #2 looking for paired plus/minus strand peaks... INFO @ Mon, 03 Jun 2019 04:54:28: #1 tags after filtering in treatment: 5412855 INFO @ Mon, 03 Jun 2019 04:54:28: #1 Redundant rate of treatment: 0.00 INFO @ Mon, 03 Jun 2019 04:54:28: #1 finished! INFO @ Mon, 03 Jun 2019 04:54:28: #2 Build Peak Model... INFO @ Mon, 03 Jun 2019 04:54:28: #2 looking for paired plus/minus strand peaks... INFO @ Mon, 03 Jun 2019 04:54:29: #2 number of paired peaks: 1064 INFO @ Mon, 03 Jun 2019 04:54:29: start model_add_line... INFO @ Mon, 03 Jun 2019 04:54:29: #2 number of paired peaks: 1064 INFO @ Mon, 03 Jun 2019 04:54:29: start model_add_line... INFO @ Mon, 03 Jun 2019 04:54:29: start X-correlation... INFO @ Mon, 03 Jun 2019 04:54:29: end of X-cor INFO @ Mon, 03 Jun 2019 04:54:29: #2 finished! INFO @ Mon, 03 Jun 2019 04:54:29: #2 predicted fragment length is 30 bps INFO @ Mon, 03 Jun 2019 04:54:29: #2 alternative fragment length(s) may be 30 bps INFO @ Mon, 03 Jun 2019 04:54:29: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/dm3/SRX183885/SRX183885.20_model.r WARNING @ Mon, 03 Jun 2019 04:54:29: #2 Since the d (30) calculated from paired-peaks are smaller than 2*tag length, it may be influenced by unknown sequencing problem! WARNING @ Mon, 03 Jun 2019 04:54:29: #2 You may need to consider one of the other alternative d(s): 30 WARNING @ Mon, 03 Jun 2019 04:54:29: #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 04:54:29: #3 Call peaks... INFO @ Mon, 03 Jun 2019 04:54:29: #3 Pre-compute pvalue-qvalue table... INFO @ Mon, 03 Jun 2019 04:54:29: start X-correlation... INFO @ Mon, 03 Jun 2019 04:54:29: end of X-cor INFO @ Mon, 03 Jun 2019 04:54:29: #2 finished! INFO @ Mon, 03 Jun 2019 04:54:29: #2 predicted fragment length is 30 bps INFO @ Mon, 03 Jun 2019 04:54:29: #2 alternative fragment length(s) may be 30 bps INFO @ Mon, 03 Jun 2019 04:54:29: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/dm3/SRX183885/SRX183885.10_model.r WARNING @ Mon, 03 Jun 2019 04:54:29: #2 Since the d (30) calculated from paired-peaks are smaller than 2*tag length, it may be influenced by unknown sequencing problem! WARNING @ Mon, 03 Jun 2019 04:54:29: #2 You may need to consider one of the other alternative d(s): 30 WARNING @ Mon, 03 Jun 2019 04:54:29: #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 04:54:29: #3 Call peaks... INFO @ Mon, 03 Jun 2019 04:54:29: #3 Pre-compute pvalue-qvalue table... INFO @ Mon, 03 Jun 2019 04:54:39: #3 Call peaks for each chromosome... INFO @ Mon, 03 Jun 2019 04:54:45: #3 Call peaks for each chromosome... INFO @ Mon, 03 Jun 2019 04:54:45: #3 Call peaks for each chromosome... INFO @ Mon, 03 Jun 2019 04:54:47: #4 Write output xls file... /home/okishinya/chipatlas/results/dm3/SRX183885/SRX183885.05_peaks.xls INFO @ Mon, 03 Jun 2019 04:54:47: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/dm3/SRX183885/SRX183885.05_peaks.narrowPeak INFO @ Mon, 03 Jun 2019 04:54:47: #4 Write summits bed file... /home/okishinya/chipatlas/results/dm3/SRX183885/SRX183885.05_summits.bed INFO @ Mon, 03 Jun 2019 04:54:47: Done! pass1 - making usageList (14 chroms): 2 millis pass2 - checking and writing primary data (4110 records, 4 fields): 10 millis CompletedMACS2peakCalling INFO @ Mon, 03 Jun 2019 04:54:52: #4 Write output xls file... /home/okishinya/chipatlas/results/dm3/SRX183885/SRX183885.20_peaks.xls INFO @ Mon, 03 Jun 2019 04:54:52: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/dm3/SRX183885/SRX183885.20_peaks.narrowPeak INFO @ Mon, 03 Jun 2019 04:54:52: #4 Write summits bed file... /home/okishinya/chipatlas/results/dm3/SRX183885/SRX183885.20_summits.bed INFO @ Mon, 03 Jun 2019 04:54:52: Done! pass1 - making usageList (10 chroms): 1 millis pass2 - checking and writing primary data (1065 records, 4 fields): 5 millis CompletedMACS2peakCalling INFO @ Mon, 03 Jun 2019 04:54:53: #4 Write output xls file... /home/okishinya/chipatlas/results/dm3/SRX183885/SRX183885.10_peaks.xls INFO @ Mon, 03 Jun 2019 04:54:53: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/dm3/SRX183885/SRX183885.10_peaks.narrowPeak INFO @ Mon, 03 Jun 2019 04:54:53: #4 Write summits bed file... /home/okishinya/chipatlas/results/dm3/SRX183885/SRX183885.10_summits.bed INFO @ Mon, 03 Jun 2019 04:54:53: Done! pass1 - making usageList (11 chroms): 2 millis pass2 - checking and writing primary data (2262 records, 4 fields): 7 millis CompletedMACS2peakCalling BedGraph に変換しました。 BigWig に変換中... BigWig に変換しました。