Job ID = 2010474 sra ファイルのダウンロード中... Read layout: SINGLE fastq に変換中... spots read : 11,212,795 reads read : 11,212,795 reads written : 11,212,795 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: 00:01:34 11212795 reads; of these: 11212795 (100.00%) were unpaired; of these: 5192327 (46.31%) aligned 0 times 4986003 (44.47%) aligned exactly 1 time 1034465 (9.23%) aligned >1 times 53.69% overall alignment rate Time searching: 00:01:34 Overall time: 00:01:34 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] 3782209 / 6020468 = 0.6282 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 22:49:04: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/SRX377156/SRX377156.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/SRX377156/SRX377156.05 -q 1e-05 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/SRX377156/SRX377156.05 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/SRX377156/SRX377156.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 22:49:04: #1 read tag files... INFO @ Fri, 05 Jul 2019 22:49:04: #1 read treatment tags... INFO @ Fri, 05 Jul 2019 22:49:05: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/SRX377156/SRX377156.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/SRX377156/SRX377156.10 -q 1e-10 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/SRX377156/SRX377156.10 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/SRX377156/SRX377156.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 22:49:05: #1 read tag files... INFO @ Fri, 05 Jul 2019 22:49:05: #1 read treatment tags... INFO @ Fri, 05 Jul 2019 22:49:13: 1000000 INFO @ Fri, 05 Jul 2019 22:49:14: 1000000 INFO @ Fri, 05 Jul 2019 22:49:21: 2000000 INFO @ Fri, 05 Jul 2019 22:49:23: 2000000 INFO @ Fri, 05 Jul 2019 22:49:23: #1 tag size is determined as 50 bps INFO @ Fri, 05 Jul 2019 22:49:23: #1 tag size = 50 INFO @ Fri, 05 Jul 2019 22:49:23: #1 total tags in treatment: 2238259 INFO @ Fri, 05 Jul 2019 22:49:23: #1 user defined the maximum tags... INFO @ Fri, 05 Jul 2019 22:49:23: #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 22:49:23: #1 tags after filtering in treatment: 2238259 INFO @ Fri, 05 Jul 2019 22:49:23: #1 Redundant rate of treatment: 0.00 INFO @ Fri, 05 Jul 2019 22:49:23: #1 finished! INFO @ Fri, 05 Jul 2019 22:49:23: #2 Build Peak Model... INFO @ Fri, 05 Jul 2019 22:49:23: #2 looking for paired plus/minus strand peaks... INFO @ Fri, 05 Jul 2019 22:49:23: #2 number of paired peaks: 82 WARNING @ Fri, 05 Jul 2019 22:49:23: Too few paired peaks (82) 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 22:49:23: Process for pairing-model is terminated! INFO @ Fri, 05 Jul 2019 22:49:24: #1 tag size is determined as 50 bps INFO @ Fri, 05 Jul 2019 22:49:24: #1 tag size = 50 INFO @ Fri, 05 Jul 2019 22:49:24: #1 total tags in treatment: 2238259 INFO @ Fri, 05 Jul 2019 22:49:24: #1 user defined the maximum tags... INFO @ Fri, 05 Jul 2019 22:49:24: #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 22:49:24: #1 tags after filtering in treatment: 2238259 INFO @ Fri, 05 Jul 2019 22:49:24: #1 Redundant rate of treatment: 0.00 INFO @ Fri, 05 Jul 2019 22:49:24: #1 finished! INFO @ Fri, 05 Jul 2019 22:49:24: #2 Build Peak Model... INFO @ Fri, 05 Jul 2019 22:49:24: #2 looking for paired plus/minus strand peaks... INFO @ Fri, 05 Jul 2019 22:49:25: #2 number of paired peaks: 82 WARNING @ Fri, 05 Jul 2019 22:49:25: Too few paired peaks (82) 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 22:49:25: Process for pairing-model is terminated! cut: /home/okishinya/chipatlas/results/sacCer3/SRX377156/SRX377156.05_peaks.narrowPeak: No such file or directory cut: /home/okishinya/chipatlas/results/sacCer3/SRX377156/SRX377156.10_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/SRX377156/SRX377156.10_model.r’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX377156/SRX377156.10_*.xls’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX377156/SRX377156.10_peaks.narrowPeak’: No such file or directory CompletedMACS2peakCalling pass1 - making usageList (0 chroms): 2 millis needLargeMem: trying to allocate 0 bytes (limit: 17179869184) rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX377156/SRX377156.05_model.r’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX377156/SRX377156.05_*.xls’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX377156/SRX377156.05_peaks.narrowPeak’: No such file or directory CompletedMACS2peakCalling INFO @ Fri, 05 Jul 2019 22:49:33: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/SRX377156/SRX377156.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/SRX377156/SRX377156.20 -q 1e-20 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/SRX377156/SRX377156.20 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/SRX377156/SRX377156.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 22:49:33: #1 read tag files... INFO @ Fri, 05 Jul 2019 22:49:33: #1 read treatment tags... INFO @ Fri, 05 Jul 2019 22:49:44: 1000000 INFO @ Fri, 05 Jul 2019 22:49:55: 2000000 INFO @ Fri, 05 Jul 2019 22:49:57: #1 tag size is determined as 50 bps INFO @ Fri, 05 Jul 2019 22:49:57: #1 tag size = 50 INFO @ Fri, 05 Jul 2019 22:49:57: #1 total tags in treatment: 2238259 INFO @ Fri, 05 Jul 2019 22:49:57: #1 user defined the maximum tags... INFO @ Fri, 05 Jul 2019 22:49:57: #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 22:49:57: #1 tags after filtering in treatment: 2238259 INFO @ Fri, 05 Jul 2019 22:49:57: #1 Redundant rate of treatment: 0.00 INFO @ Fri, 05 Jul 2019 22:49:57: #1 finished! INFO @ Fri, 05 Jul 2019 22:49:57: #2 Build Peak Model... INFO @ Fri, 05 Jul 2019 22:49:57: #2 looking for paired plus/minus strand peaks... INFO @ Fri, 05 Jul 2019 22:49:57: #2 number of paired peaks: 82 WARNING @ Fri, 05 Jul 2019 22:49:57: Too few paired peaks (82) 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 22:49:57: Process for pairing-model is terminated! cut: /home/okishinya/chipatlas/results/sacCer3/SRX377156/SRX377156.20_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/SRX377156/SRX377156.20_model.r’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX377156/SRX377156.20_*.xls’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX377156/SRX377156.20_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。