Job ID = 2010112 sra ファイルのダウンロード中... Read layout: SINGLE fastq に変換中... spots read : 25,852,737 reads read : 25,852,737 reads written : 25,852,737 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: 00:05:09 25852737 reads; of these: 25852737 (100.00%) were unpaired; of these: 16290364 (63.01%) aligned 0 times 8037300 (31.09%) aligned exactly 1 time 1525073 (5.90%) aligned >1 times 36.99% overall alignment rate Time searching: 00:05:09 Overall time: 00:05:09 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] 2612264 / 9562373 = 0.2732 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 21:34:26: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/SRX2772191/SRX2772191.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/SRX2772191/SRX2772191.05 -q 1e-05 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/SRX2772191/SRX2772191.05 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/SRX2772191/SRX2772191.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 21:34:26: #1 read tag files... INFO @ Fri, 05 Jul 2019 21:34:26: #1 read treatment tags... INFO @ Fri, 05 Jul 2019 21:34:27: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/SRX2772191/SRX2772191.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/SRX2772191/SRX2772191.10 -q 1e-10 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/SRX2772191/SRX2772191.10 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/SRX2772191/SRX2772191.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 21:34:27: #1 read tag files... INFO @ Fri, 05 Jul 2019 21:34:27: #1 read treatment tags... INFO @ Fri, 05 Jul 2019 21:34:28: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/SRX2772191/SRX2772191.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/SRX2772191/SRX2772191.20 -q 1e-20 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/SRX2772191/SRX2772191.20 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/SRX2772191/SRX2772191.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 21:34:28: #1 read tag files... INFO @ Fri, 05 Jul 2019 21:34:28: #1 read treatment tags... INFO @ Fri, 05 Jul 2019 21:34:34: 1000000 INFO @ Fri, 05 Jul 2019 21:34:36: 1000000 INFO @ Fri, 05 Jul 2019 21:34:38: 1000000 INFO @ Fri, 05 Jul 2019 21:34:43: 2000000 INFO @ Fri, 05 Jul 2019 21:34:47: 2000000 INFO @ Fri, 05 Jul 2019 21:34:48: 2000000 INFO @ Fri, 05 Jul 2019 21:34:52: 3000000 INFO @ Fri, 05 Jul 2019 21:34:56: 3000000 INFO @ Fri, 05 Jul 2019 21:34:57: 3000000 INFO @ Fri, 05 Jul 2019 21:35:01: 4000000 INFO @ Fri, 05 Jul 2019 21:35:07: 4000000 INFO @ Fri, 05 Jul 2019 21:35:08: 4000000 INFO @ Fri, 05 Jul 2019 21:35:10: 5000000 INFO @ Fri, 05 Jul 2019 21:35:17: 5000000 INFO @ Fri, 05 Jul 2019 21:35:18: 5000000 INFO @ Fri, 05 Jul 2019 21:35:19: 6000000 INFO @ Fri, 05 Jul 2019 21:35:27: #1 tag size is determined as 50 bps INFO @ Fri, 05 Jul 2019 21:35:27: #1 tag size = 50 INFO @ Fri, 05 Jul 2019 21:35:27: #1 total tags in treatment: 6950109 INFO @ Fri, 05 Jul 2019 21:35:27: #1 user defined the maximum tags... INFO @ Fri, 05 Jul 2019 21:35:27: #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 21:35:27: #1 tags after filtering in treatment: 6950109 INFO @ Fri, 05 Jul 2019 21:35:27: #1 Redundant rate of treatment: 0.00 INFO @ Fri, 05 Jul 2019 21:35:27: #1 finished! INFO @ Fri, 05 Jul 2019 21:35:27: #2 Build Peak Model... INFO @ Fri, 05 Jul 2019 21:35:27: #2 looking for paired plus/minus strand peaks... INFO @ Fri, 05 Jul 2019 21:35:27: #2 number of paired peaks: 0 WARNING @ Fri, 05 Jul 2019 21:35:27: 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 21:35:27: Process for pairing-model is terminated! cut: /home/okishinya/chipatlas/results/sacCer3/SRX2772191/SRX2772191.05_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/SRX2772191/SRX2772191.05_model.r’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX2772191/SRX2772191.05_*.xls’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX2772191/SRX2772191.05_peaks.narrowPeak’: No such file or directory CompletedMACS2peakCalling INFO @ Fri, 05 Jul 2019 21:35:28: 6000000 INFO @ Fri, 05 Jul 2019 21:35:29: 6000000 INFO @ Fri, 05 Jul 2019 21:35:37: #1 tag size is determined as 50 bps INFO @ Fri, 05 Jul 2019 21:35:37: #1 tag size = 50 INFO @ Fri, 05 Jul 2019 21:35:37: #1 total tags in treatment: 6950109 INFO @ Fri, 05 Jul 2019 21:35:37: #1 user defined the maximum tags... INFO @ Fri, 05 Jul 2019 21:35:37: #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 21:35:37: #1 tags after filtering in treatment: 6950109 INFO @ Fri, 05 Jul 2019 21:35:37: #1 Redundant rate of treatment: 0.00 INFO @ Fri, 05 Jul 2019 21:35:37: #1 finished! INFO @ Fri, 05 Jul 2019 21:35:37: #2 Build Peak Model... INFO @ Fri, 05 Jul 2019 21:35:37: #2 looking for paired plus/minus strand peaks... INFO @ Fri, 05 Jul 2019 21:35:38: #2 number of paired peaks: 0 WARNING @ Fri, 05 Jul 2019 21:35:38: 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 21:35:38: Process for pairing-model is terminated! cut: /home/okishinya/chipatlas/results/sacCer3/SRX2772191/SRX2772191.10_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/SRX2772191/SRX2772191.10_model.r’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX2772191/SRX2772191.10_*.xls’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX2772191/SRX2772191.10_peaks.narrowPeak’: No such file or directory CompletedMACS2peakCalling INFO @ Fri, 05 Jul 2019 21:35:38: #1 tag size is determined as 50 bps INFO @ Fri, 05 Jul 2019 21:35:38: #1 tag size = 50 INFO @ Fri, 05 Jul 2019 21:35:38: #1 total tags in treatment: 6950109 INFO @ Fri, 05 Jul 2019 21:35:38: #1 user defined the maximum tags... INFO @ Fri, 05 Jul 2019 21:35:38: #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 21:35:38: #1 tags after filtering in treatment: 6950109 INFO @ Fri, 05 Jul 2019 21:35:38: #1 Redundant rate of treatment: 0.00 INFO @ Fri, 05 Jul 2019 21:35:38: #1 finished! INFO @ Fri, 05 Jul 2019 21:35:38: #2 Build Peak Model... INFO @ Fri, 05 Jul 2019 21:35:38: #2 looking for paired plus/minus strand peaks... INFO @ Fri, 05 Jul 2019 21:35:39: #2 number of paired peaks: 0 WARNING @ Fri, 05 Jul 2019 21:35:39: 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 21:35:39: Process for pairing-model is terminated! cut: /home/okishinya/chipatlas/results/sacCer3/SRX2772191/SRX2772191.20_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/SRX2772191/SRX2772191.20_model.r’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX2772191/SRX2772191.20_*.xls’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX2772191/SRX2772191.20_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。