Job ID = 2010131 sra ファイルのダウンロード中... Read layout: SINGLE fastq に変換中... spots read : 14,274,264 reads read : 14,274,264 reads written : 14,274,264 rm: cannot remove ‘[DSE]RR*’: 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: 00:01:55 14274264 reads; of these: 14274264 (100.00%) were unpaired; of these: 6414175 (44.94%) aligned 0 times 6844662 (47.95%) aligned exactly 1 time 1015427 (7.11%) aligned >1 times 55.06% overall alignment rate Time searching: 00:01:55 Overall time: 00:01:55 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] 2111617 / 7860089 = 0.2687 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 21:32:00: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/SRX2772206/SRX2772206.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/SRX2772206/SRX2772206.05 -q 1e-05 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/SRX2772206/SRX2772206.05 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/SRX2772206/SRX2772206.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 21:32:00: #1 read tag files... INFO @ Fri, 05 Jul 2019 21:32:00: #1 read treatment tags... INFO @ Fri, 05 Jul 2019 21:32:00: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/SRX2772206/SRX2772206.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/SRX2772206/SRX2772206.10 -q 1e-10 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/SRX2772206/SRX2772206.10 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/SRX2772206/SRX2772206.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 21:32:00: #1 read tag files... INFO @ Fri, 05 Jul 2019 21:32:00: #1 read treatment tags... INFO @ Fri, 05 Jul 2019 21:32:01: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/SRX2772206/SRX2772206.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/SRX2772206/SRX2772206.20 -q 1e-20 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/SRX2772206/SRX2772206.20 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/SRX2772206/SRX2772206.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 21:32:01: #1 read tag files... INFO @ Fri, 05 Jul 2019 21:32:01: #1 read treatment tags... INFO @ Fri, 05 Jul 2019 21:32:08: 1000000 INFO @ Fri, 05 Jul 2019 21:32:08: 1000000 INFO @ Fri, 05 Jul 2019 21:32:09: 1000000 INFO @ Fri, 05 Jul 2019 21:32:15: 2000000 INFO @ Fri, 05 Jul 2019 21:32:17: 2000000 INFO @ Fri, 05 Jul 2019 21:32:17: 2000000 INFO @ Fri, 05 Jul 2019 21:32:22: 3000000 INFO @ Fri, 05 Jul 2019 21:32:24: 3000000 INFO @ Fri, 05 Jul 2019 21:32:25: 3000000 INFO @ Fri, 05 Jul 2019 21:32:29: 4000000 INFO @ Fri, 05 Jul 2019 21:32:31: 4000000 INFO @ Fri, 05 Jul 2019 21:32:32: 4000000 INFO @ Fri, 05 Jul 2019 21:32:36: 5000000 INFO @ Fri, 05 Jul 2019 21:32:38: 5000000 INFO @ Fri, 05 Jul 2019 21:32:40: 5000000 INFO @ Fri, 05 Jul 2019 21:32:42: #1 tag size is determined as 50 bps INFO @ Fri, 05 Jul 2019 21:32:42: #1 tag size = 50 INFO @ Fri, 05 Jul 2019 21:32:42: #1 total tags in treatment: 5748472 INFO @ Fri, 05 Jul 2019 21:32:42: #1 user defined the maximum tags... INFO @ Fri, 05 Jul 2019 21:32:42: #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 21:32:42: #1 tags after filtering in treatment: 5748472 INFO @ Fri, 05 Jul 2019 21:32:42: #1 Redundant rate of treatment: 0.00 INFO @ Fri, 05 Jul 2019 21:32:42: #1 finished! INFO @ Fri, 05 Jul 2019 21:32:42: #2 Build Peak Model... INFO @ Fri, 05 Jul 2019 21:32:42: #2 looking for paired plus/minus strand peaks... INFO @ Fri, 05 Jul 2019 21:32:42: #2 number of paired peaks: 0 WARNING @ Fri, 05 Jul 2019 21:32:42: Too few paired peaks (0) 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 21:32:42: Process for pairing-model is terminated! cut: /home/okishinya/chipatlas/results/sacCer3/SRX2772206/SRX2772206.10_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/SRX2772206/SRX2772206.10_model.r’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX2772206/SRX2772206.10_*.xls’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX2772206/SRX2772206.10_peaks.narrowPeak’: No such file or directory CompletedMACS2peakCalling INFO @ Fri, 05 Jul 2019 21:32:44: #1 tag size is determined as 50 bps INFO @ Fri, 05 Jul 2019 21:32:44: #1 tag size = 50 INFO @ Fri, 05 Jul 2019 21:32:44: #1 total tags in treatment: 5748472 INFO @ Fri, 05 Jul 2019 21:32:44: #1 user defined the maximum tags... INFO @ Fri, 05 Jul 2019 21:32:44: #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 21:32:44: #1 tags after filtering in treatment: 5748472 INFO @ Fri, 05 Jul 2019 21:32:44: #1 Redundant rate of treatment: 0.00 INFO @ Fri, 05 Jul 2019 21:32:44: #1 finished! INFO @ Fri, 05 Jul 2019 21:32:44: #2 Build Peak Model... INFO @ Fri, 05 Jul 2019 21:32:44: #2 looking for paired plus/minus strand peaks... INFO @ Fri, 05 Jul 2019 21:32:44: #2 number of paired peaks: 0 WARNING @ Fri, 05 Jul 2019 21:32:44: Too few paired peaks (0) 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 21:32:44: Process for pairing-model is terminated! cut: /home/okishinya/chipatlas/results/sacCer3/SRX2772206/SRX2772206.20_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/SRX2772206/SRX2772206.20_model.r’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX2772206/SRX2772206.20_*.xls’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX2772206/SRX2772206.20_peaks.narrowPeak’: No such file or directory CompletedMACS2peakCalling INFO @ Fri, 05 Jul 2019 21:32:45: #1 tag size is determined as 50 bps INFO @ Fri, 05 Jul 2019 21:32:45: #1 tag size = 50 INFO @ Fri, 05 Jul 2019 21:32:45: #1 total tags in treatment: 5748472 INFO @ Fri, 05 Jul 2019 21:32:45: #1 user defined the maximum tags... INFO @ Fri, 05 Jul 2019 21:32:45: #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 21:32:46: #1 tags after filtering in treatment: 5748472 INFO @ Fri, 05 Jul 2019 21:32:46: #1 Redundant rate of treatment: 0.00 INFO @ Fri, 05 Jul 2019 21:32:46: #1 finished! INFO @ Fri, 05 Jul 2019 21:32:46: #2 Build Peak Model... INFO @ Fri, 05 Jul 2019 21:32:46: #2 looking for paired plus/minus strand peaks... INFO @ Fri, 05 Jul 2019 21:32:46: #2 number of paired peaks: 0 WARNING @ Fri, 05 Jul 2019 21:32:46: Too few paired peaks (0) 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 21:32:46: Process for pairing-model is terminated! cut: /home/okishinya/chipatlas/results/sacCer3/SRX2772206/SRX2772206.05_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/SRX2772206/SRX2772206.05_model.r’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX2772206/SRX2772206.05_*.xls’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX2772206/SRX2772206.05_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。