Job ID = 2010966 sra ファイルのダウンロード中... Read layout: SINGLE fastq に変換中... spots read : 10,874,414 reads read : 21,748,828 reads written : 10,874,414 reads 0-length : 10,874,414 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: 00:02:29 10874414 reads; of these: 10874414 (100.00%) were unpaired; of these: 1940497 (17.84%) aligned 0 times 6799347 (62.53%) aligned exactly 1 time 2134570 (19.63%) aligned >1 times 82.16% overall alignment rate Time searching: 00:02:29 Overall time: 00:02:29 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] 3179150 / 8933917 = 0.3559 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 @ Sat, 06 Jul 2019 01:36:12: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/SRX4342616/SRX4342616.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/SRX4342616/SRX4342616.05 -q 1e-05 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/SRX4342616/SRX4342616.05 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/SRX4342616/SRX4342616.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 @ Sat, 06 Jul 2019 01:36:12: #1 read tag files... INFO @ Sat, 06 Jul 2019 01:36:12: #1 read treatment tags... INFO @ Sat, 06 Jul 2019 01:36:13: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/SRX4342616/SRX4342616.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/SRX4342616/SRX4342616.10 -q 1e-10 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/SRX4342616/SRX4342616.10 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/SRX4342616/SRX4342616.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 @ Sat, 06 Jul 2019 01:36:13: #1 read tag files... INFO @ Sat, 06 Jul 2019 01:36:13: #1 read treatment tags... INFO @ Sat, 06 Jul 2019 01:36:14: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/SRX4342616/SRX4342616.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/SRX4342616/SRX4342616.20 -q 1e-20 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/SRX4342616/SRX4342616.20 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/SRX4342616/SRX4342616.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 @ Sat, 06 Jul 2019 01:36:14: #1 read tag files... INFO @ Sat, 06 Jul 2019 01:36:14: #1 read treatment tags... INFO @ Sat, 06 Jul 2019 01:36:23: 1000000 INFO @ Sat, 06 Jul 2019 01:36:24: 1000000 INFO @ Sat, 06 Jul 2019 01:36:24: 1000000 INFO @ Sat, 06 Jul 2019 01:36:33: 2000000 INFO @ Sat, 06 Jul 2019 01:36:35: 2000000 INFO @ Sat, 06 Jul 2019 01:36:35: 2000000 INFO @ Sat, 06 Jul 2019 01:36:43: 3000000 INFO @ Sat, 06 Jul 2019 01:36:46: 3000000 INFO @ Sat, 06 Jul 2019 01:36:46: 3000000 INFO @ Sat, 06 Jul 2019 01:36:53: 4000000 INFO @ Sat, 06 Jul 2019 01:36:56: 4000000 INFO @ Sat, 06 Jul 2019 01:36:56: 4000000 INFO @ Sat, 06 Jul 2019 01:37:03: 5000000 INFO @ Sat, 06 Jul 2019 01:37:05: 5000000 INFO @ Sat, 06 Jul 2019 01:37:06: 5000000 INFO @ Sat, 06 Jul 2019 01:37:10: #1 tag size is determined as 68 bps INFO @ Sat, 06 Jul 2019 01:37:10: #1 tag size = 68 INFO @ Sat, 06 Jul 2019 01:37:10: #1 total tags in treatment: 5754767 INFO @ Sat, 06 Jul 2019 01:37:10: #1 user defined the maximum tags... INFO @ Sat, 06 Jul 2019 01:37:10: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Sat, 06 Jul 2019 01:37:10: #1 tags after filtering in treatment: 5754767 INFO @ Sat, 06 Jul 2019 01:37:10: #1 Redundant rate of treatment: 0.00 INFO @ Sat, 06 Jul 2019 01:37:10: #1 finished! INFO @ Sat, 06 Jul 2019 01:37:10: #2 Build Peak Model... INFO @ Sat, 06 Jul 2019 01:37:10: #2 looking for paired plus/minus strand peaks... INFO @ Sat, 06 Jul 2019 01:37:10: #2 number of paired peaks: 0 WARNING @ Sat, 06 Jul 2019 01:37:10: 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 @ Sat, 06 Jul 2019 01:37:10: Process for pairing-model is terminated! cut: /home/okishinya/chipatlas/results/sacCer3/SRX4342616/SRX4342616.05_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/SRX4342616/SRX4342616.05_model.r’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX4342616/SRX4342616.05_*.xls’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX4342616/SRX4342616.05_peaks.narrowPeak’: No such file or directory CompletedMACS2peakCalling INFO @ Sat, 06 Jul 2019 01:37:12: #1 tag size is determined as 68 bps INFO @ Sat, 06 Jul 2019 01:37:12: #1 tag size = 68 INFO @ Sat, 06 Jul 2019 01:37:12: #1 total tags in treatment: 5754767 INFO @ Sat, 06 Jul 2019 01:37:12: #1 user defined the maximum tags... INFO @ Sat, 06 Jul 2019 01:37:12: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Sat, 06 Jul 2019 01:37:12: #1 tags after filtering in treatment: 5754767 INFO @ Sat, 06 Jul 2019 01:37:12: #1 Redundant rate of treatment: 0.00 INFO @ Sat, 06 Jul 2019 01:37:12: #1 finished! INFO @ Sat, 06 Jul 2019 01:37:12: #2 Build Peak Model... INFO @ Sat, 06 Jul 2019 01:37:12: #2 looking for paired plus/minus strand peaks... INFO @ Sat, 06 Jul 2019 01:37:13: #2 number of paired peaks: 0 WARNING @ Sat, 06 Jul 2019 01:37:13: 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 @ Sat, 06 Jul 2019 01:37:13: Process for pairing-model is terminated! cut: /home/okishinya/chipatlas/results/sacCer3/SRX4342616/SRX4342616.20_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/SRX4342616/SRX4342616.20_model.r’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX4342616/SRX4342616.20_*.xls’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX4342616/SRX4342616.20_peaks.narrowPeak’: No such file or directory CompletedMACS2peakCalling INFO @ Sat, 06 Jul 2019 01:37:13: #1 tag size is determined as 68 bps INFO @ Sat, 06 Jul 2019 01:37:13: #1 tag size = 68 INFO @ Sat, 06 Jul 2019 01:37:13: #1 total tags in treatment: 5754767 INFO @ Sat, 06 Jul 2019 01:37:13: #1 user defined the maximum tags... INFO @ Sat, 06 Jul 2019 01:37:13: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Sat, 06 Jul 2019 01:37:14: #1 tags after filtering in treatment: 5754767 INFO @ Sat, 06 Jul 2019 01:37:14: #1 Redundant rate of treatment: 0.00 INFO @ Sat, 06 Jul 2019 01:37:14: #1 finished! INFO @ Sat, 06 Jul 2019 01:37:14: #2 Build Peak Model... INFO @ Sat, 06 Jul 2019 01:37:14: #2 looking for paired plus/minus strand peaks... INFO @ Sat, 06 Jul 2019 01:37:14: #2 number of paired peaks: 0 WARNING @ Sat, 06 Jul 2019 01:37:14: 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 @ Sat, 06 Jul 2019 01:37:14: Process for pairing-model is terminated! cut: /home/okishinya/chipatlas/results/sacCer3/SRX4342616/SRX4342616.10_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/SRX4342616/SRX4342616.10_model.r’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX4342616/SRX4342616.10_*.xls’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX4342616/SRX4342616.10_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。