Job ID = 2010498 sra ファイルのダウンロード中... Read layout: SINGLE fastq に変換中... spots read : 10,696,754 reads read : 10,696,754 reads written : 10,696,754 rm: cannot remove ‘[DSE]RR*’: No such file or directory rm: cannot remove ‘/home/okishinya/ncbi/public/sra/SRR1029333.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: 00:01:32 10696754 reads; of these: 10696754 (100.00%) were unpaired; of these: 4296909 (40.17%) aligned 0 times 5045637 (47.17%) aligned exactly 1 time 1354208 (12.66%) aligned >1 times 59.83% overall alignment rate Time searching: 00:01:32 Overall time: 00:01:32 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] 3130146 / 6399845 = 0.4891 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 22:50:02: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/SRX377176/SRX377176.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/SRX377176/SRX377176.05 -q 1e-05 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/SRX377176/SRX377176.05 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/SRX377176/SRX377176.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 22:50:02: #1 read tag files... INFO @ Fri, 05 Jul 2019 22:50:02: #1 read treatment tags... INFO @ Fri, 05 Jul 2019 22:50:03: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/SRX377176/SRX377176.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/SRX377176/SRX377176.10 -q 1e-10 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/SRX377176/SRX377176.10 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/SRX377176/SRX377176.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 22:50:03: #1 read tag files... INFO @ Fri, 05 Jul 2019 22:50:03: #1 read treatment tags... INFO @ Fri, 05 Jul 2019 22:50:04: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/SRX377176/SRX377176.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/SRX377176/SRX377176.20 -q 1e-20 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/SRX377176/SRX377176.20 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/SRX377176/SRX377176.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 22:50:04: #1 read tag files... INFO @ Fri, 05 Jul 2019 22:50:04: #1 read treatment tags... INFO @ Fri, 05 Jul 2019 22:50:11: 1000000 INFO @ Fri, 05 Jul 2019 22:50:13: 1000000 INFO @ Fri, 05 Jul 2019 22:50:16: 1000000 INFO @ Fri, 05 Jul 2019 22:50:19: 2000000 INFO @ Fri, 05 Jul 2019 22:50:24: 2000000 INFO @ Fri, 05 Jul 2019 22:50:27: 3000000 INFO @ Fri, 05 Jul 2019 22:50:27: 2000000 INFO @ Fri, 05 Jul 2019 22:50:29: #1 tag size is determined as 50 bps INFO @ Fri, 05 Jul 2019 22:50:29: #1 tag size = 50 INFO @ Fri, 05 Jul 2019 22:50:29: #1 total tags in treatment: 3269699 INFO @ Fri, 05 Jul 2019 22:50:29: #1 user defined the maximum tags... INFO @ Fri, 05 Jul 2019 22:50:29: #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 22:50:29: #1 tags after filtering in treatment: 3269699 INFO @ Fri, 05 Jul 2019 22:50:29: #1 Redundant rate of treatment: 0.00 INFO @ Fri, 05 Jul 2019 22:50:29: #1 finished! INFO @ Fri, 05 Jul 2019 22:50:29: #2 Build Peak Model... INFO @ Fri, 05 Jul 2019 22:50:29: #2 looking for paired plus/minus strand peaks... INFO @ Fri, 05 Jul 2019 22:50:29: #2 number of paired peaks: 42 WARNING @ Fri, 05 Jul 2019 22:50:29: Too few paired peaks (42) 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 22:50:29: Process for pairing-model is terminated! cut: /home/okishinya/chipatlas/results/sacCer3/SRX377176/SRX377176.05_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/SRX377176/SRX377176.05_model.r’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX377176/SRX377176.05_*.xls’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX377176/SRX377176.05_peaks.narrowPeak’: No such file or directory CompletedMACS2peakCalling INFO @ Fri, 05 Jul 2019 22:50:34: 3000000 INFO @ Fri, 05 Jul 2019 22:50:36: #1 tag size is determined as 50 bps INFO @ Fri, 05 Jul 2019 22:50:36: #1 tag size = 50 INFO @ Fri, 05 Jul 2019 22:50:36: #1 total tags in treatment: 3269699 INFO @ Fri, 05 Jul 2019 22:50:36: #1 user defined the maximum tags... INFO @ Fri, 05 Jul 2019 22:50:36: #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 22:50:36: #1 tags after filtering in treatment: 3269699 INFO @ Fri, 05 Jul 2019 22:50:36: #1 Redundant rate of treatment: 0.00 INFO @ Fri, 05 Jul 2019 22:50:36: #1 finished! INFO @ Fri, 05 Jul 2019 22:50:36: #2 Build Peak Model... INFO @ Fri, 05 Jul 2019 22:50:36: #2 looking for paired plus/minus strand peaks... INFO @ Fri, 05 Jul 2019 22:50:37: #2 number of paired peaks: 42 WARNING @ Fri, 05 Jul 2019 22:50:37: Too few paired peaks (42) 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 22:50:37: Process for pairing-model is terminated! cut: /home/okishinya/chipatlas/results/sacCer3/SRX377176/SRX377176.10_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/SRX377176/SRX377176.10_model.r’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX377176/SRX377176.10_*.xls’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX377176/SRX377176.10_peaks.narrowPeak’: No such file or directory CompletedMACS2peakCalling INFO @ Fri, 05 Jul 2019 22:50:39: 3000000 INFO @ Fri, 05 Jul 2019 22:50:42: #1 tag size is determined as 50 bps INFO @ Fri, 05 Jul 2019 22:50:42: #1 tag size = 50 INFO @ Fri, 05 Jul 2019 22:50:42: #1 total tags in treatment: 3269699 INFO @ Fri, 05 Jul 2019 22:50:42: #1 user defined the maximum tags... INFO @ Fri, 05 Jul 2019 22:50:42: #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 22:50:42: #1 tags after filtering in treatment: 3269699 INFO @ Fri, 05 Jul 2019 22:50:42: #1 Redundant rate of treatment: 0.00 INFO @ Fri, 05 Jul 2019 22:50:42: #1 finished! INFO @ Fri, 05 Jul 2019 22:50:42: #2 Build Peak Model... INFO @ Fri, 05 Jul 2019 22:50:42: #2 looking for paired plus/minus strand peaks... INFO @ Fri, 05 Jul 2019 22:50:42: #2 number of paired peaks: 42 WARNING @ Fri, 05 Jul 2019 22:50:42: Too few paired peaks (42) 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 22:50:42: Process for pairing-model is terminated! cut: /home/okishinya/chipatlas/results/sacCer3/SRX377176/SRX377176.20_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/SRX377176/SRX377176.20_model.r’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX377176/SRX377176.20_*.xls’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX377176/SRX377176.20_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。