Job ID = 2009023 sra ファイルのダウンロード中... Read layout: SINGLE fastq に変換中... spots read : 5,889,142 reads read : 5,889,142 reads written : 5,889,142 rm: cannot remove ‘[DSE]RR*’: No such file or directory rm: cannot remove ‘/home/okishinya/ncbi/public/sra/ERR637602.sra.cache’: 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: 00:00:58 5889142 reads; of these: 5889142 (100.00%) were unpaired; of these: 673604 (11.44%) aligned 0 times 4354577 (73.94%) aligned exactly 1 time 860961 (14.62%) aligned >1 times 88.56% overall alignment rate Time searching: 00:00:58 Overall time: 00:00:58 マッピングが完了しました。 samtools でBAM に変換中... [samopen] SAM header is present: 17 sequences. [bam_rmdupse_core] 989629 / 5215538 = 0.1897 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 @ Fri, 05 Jul 2019 19:11:38: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/ERX594039/ERX594039.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/ERX594039/ERX594039.05 -q 1e-05 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/ERX594039/ERX594039.05 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/ERX594039/ERX594039.bam'] # control file = None # effective genome size = 1.21e+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 @ Fri, 05 Jul 2019 19:11:38: #1 read tag files... INFO @ Fri, 05 Jul 2019 19:11:38: #1 read treatment tags... INFO @ Fri, 05 Jul 2019 19:11:39: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/ERX594039/ERX594039.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/ERX594039/ERX594039.10 -q 1e-10 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/ERX594039/ERX594039.10 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/ERX594039/ERX594039.bam'] # control file = None # effective genome size = 1.21e+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 @ Fri, 05 Jul 2019 19:11:39: #1 read tag files... INFO @ Fri, 05 Jul 2019 19:11:39: #1 read treatment tags... INFO @ Fri, 05 Jul 2019 19:11:44: 1000000 INFO @ Fri, 05 Jul 2019 19:11:48: 1000000 INFO @ Fri, 05 Jul 2019 19:11:51: 2000000 INFO @ Fri, 05 Jul 2019 19:11:53: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/ERX594039/ERX594039.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/ERX594039/ERX594039.20 -q 1e-20 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/ERX594039/ERX594039.20 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/ERX594039/ERX594039.bam'] # control file = None # effective genome size = 1.21e+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 @ Fri, 05 Jul 2019 19:11:53: #1 read tag files... INFO @ Fri, 05 Jul 2019 19:11:53: #1 read treatment tags... INFO @ Fri, 05 Jul 2019 19:11:58: 2000000 INFO @ Fri, 05 Jul 2019 19:11:58: 3000000 INFO @ Fri, 05 Jul 2019 19:12:02: 1000000 INFO @ Fri, 05 Jul 2019 19:12:05: 4000000 INFO @ Fri, 05 Jul 2019 19:12:06: #1 tag size is determined as 50 bps INFO @ Fri, 05 Jul 2019 19:12:06: #1 tag size = 50 INFO @ Fri, 05 Jul 2019 19:12:06: #1 total tags in treatment: 4225909 INFO @ Fri, 05 Jul 2019 19:12:06: #1 user defined the maximum tags... INFO @ Fri, 05 Jul 2019 19:12:06: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Fri, 05 Jul 2019 19:12:06: #1 tags after filtering in treatment: 4225909 INFO @ Fri, 05 Jul 2019 19:12:06: #1 Redundant rate of treatment: 0.00 INFO @ Fri, 05 Jul 2019 19:12:06: #1 finished! INFO @ Fri, 05 Jul 2019 19:12:06: #2 Build Peak Model... INFO @ Fri, 05 Jul 2019 19:12:06: #2 looking for paired plus/minus strand peaks... INFO @ Fri, 05 Jul 2019 19:12:07: #2 number of paired peaks: 29 WARNING @ Fri, 05 Jul 2019 19:12:07: Too few paired peaks (29) so I can not build the model! Broader your MFOLD range parameter may erase this error. If it still can't build the model, we suggest to use --nomodel and --extsize 147 or other fixed number instead. WARNING @ Fri, 05 Jul 2019 19:12:07: Process for pairing-model is terminated! cut: /home/okishinya/chipatlas/results/sacCer3/ERX594039/ERX594039.05_peaks.narrowPeak: No such file or directory pass1 - making usageList (0 chroms): 1 millis needLargeMem: trying to allocate 0 bytes (limit: 17179869184) rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/ERX594039/ERX594039.05_model.r’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/ERX594039/ERX594039.05_*.xls’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/ERX594039/ERX594039.05_peaks.narrowPeak’: No such file or directory CompletedMACS2peakCalling INFO @ Fri, 05 Jul 2019 19:12:07: 3000000 INFO @ Fri, 05 Jul 2019 19:12:11: 2000000 INFO @ Fri, 05 Jul 2019 19:12:17: 4000000 INFO @ Fri, 05 Jul 2019 19:12:19: #1 tag size is determined as 50 bps INFO @ Fri, 05 Jul 2019 19:12:19: #1 tag size = 50 INFO @ Fri, 05 Jul 2019 19:12:19: #1 total tags in treatment: 4225909 INFO @ Fri, 05 Jul 2019 19:12:19: #1 user defined the maximum tags... INFO @ Fri, 05 Jul 2019 19:12:19: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Fri, 05 Jul 2019 19:12:19: #1 tags after filtering in treatment: 4225909 INFO @ Fri, 05 Jul 2019 19:12:19: #1 Redundant rate of treatment: 0.00 INFO @ Fri, 05 Jul 2019 19:12:19: #1 finished! INFO @ Fri, 05 Jul 2019 19:12:19: #2 Build Peak Model... INFO @ Fri, 05 Jul 2019 19:12:19: #2 looking for paired plus/minus strand peaks... INFO @ Fri, 05 Jul 2019 19:12:19: #2 number of paired peaks: 29 WARNING @ Fri, 05 Jul 2019 19:12:19: Too few paired peaks (29) so I can not build the model! Broader your MFOLD range parameter may erase this error. If it still can't build the model, we suggest to use --nomodel and --extsize 147 or other fixed number instead. WARNING @ Fri, 05 Jul 2019 19:12:19: Process for pairing-model is terminated! cut: /home/okishinya/chipatlas/results/sacCer3/ERX594039/ERX594039.10_peaks.narrowPeak: No such file or directory pass1 - making usageList (0 chroms): 2 millis needLargeMem: trying to allocate 0 bytes (limit: 17179869184) rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/ERX594039/ERX594039.10_model.r’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/ERX594039/ERX594039.10_*.xls’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/ERX594039/ERX594039.10_peaks.narrowPeak’: No such file or directory CompletedMACS2peakCalling INFO @ Fri, 05 Jul 2019 19:12:20: 3000000 INFO @ Fri, 05 Jul 2019 19:12:28: 4000000 INFO @ Fri, 05 Jul 2019 19:12:30: #1 tag size is determined as 50 bps INFO @ Fri, 05 Jul 2019 19:12:30: #1 tag size = 50 INFO @ Fri, 05 Jul 2019 19:12:30: #1 total tags in treatment: 4225909 INFO @ Fri, 05 Jul 2019 19:12:30: #1 user defined the maximum tags... INFO @ Fri, 05 Jul 2019 19:12:30: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Fri, 05 Jul 2019 19:12:30: #1 tags after filtering in treatment: 4225909 INFO @ Fri, 05 Jul 2019 19:12:30: #1 Redundant rate of treatment: 0.00 INFO @ Fri, 05 Jul 2019 19:12:30: #1 finished! INFO @ Fri, 05 Jul 2019 19:12:30: #2 Build Peak Model... INFO @ Fri, 05 Jul 2019 19:12:30: #2 looking for paired plus/minus strand peaks... INFO @ Fri, 05 Jul 2019 19:12:30: #2 number of paired peaks: 29 WARNING @ Fri, 05 Jul 2019 19:12:30: Too few paired peaks (29) so I can not build the model! Broader your MFOLD range parameter may erase this error. If it still can't build the model, we suggest to use --nomodel and --extsize 147 or other fixed number instead. WARNING @ Fri, 05 Jul 2019 19:12:30: Process for pairing-model is terminated! cut: /home/okishinya/chipatlas/results/sacCer3/ERX594039/ERX594039.20_peaks.narrowPeak: No such file or directory pass1 - making usageList (0 chroms): 2 millis needLargeMem: trying to allocate 0 bytes (limit: 17179869184) rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/ERX594039/ERX594039.20_model.r’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/ERX594039/ERX594039.20_*.xls’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/ERX594039/ERX594039.20_peaks.narrowPeak’: No such file or directory CompletedMACS2peakCalling BedGraph に変換しました。 BigWig に変換中... BigWig に変換しました。