Job ID = 2011937 sra ファイルのダウンロード中... Read layout: SINGLE fastq に変換中... spots read : 4,667,649 reads read : 4,667,649 reads written : 4,667,649 rm: cannot remove ‘[DSE]RR*’: No such file or directory rm: cannot remove ‘/home/okishinya/ncbi/public/sra/SRR1284650.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: 00:00:55 4667649 reads; of these: 4667649 (100.00%) were unpaired; of these: 89640 (1.92%) aligned 0 times 3622595 (77.61%) aligned exactly 1 time 955414 (20.47%) aligned >1 times 98.08% overall alignment rate Time searching: 00:00:55 Overall time: 00:00:55 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] 1032770 / 4578009 = 0.2256 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 03:27:08: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/SRX541163/SRX541163.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/SRX541163/SRX541163.05 -q 1e-05 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/SRX541163/SRX541163.05 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/SRX541163/SRX541163.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 03:27:08: #1 read tag files... INFO @ Sat, 06 Jul 2019 03:27:08: #1 read treatment tags... INFO @ Sat, 06 Jul 2019 03:27:08: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/SRX541163/SRX541163.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/SRX541163/SRX541163.10 -q 1e-10 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/SRX541163/SRX541163.10 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/SRX541163/SRX541163.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 03:27:08: #1 read tag files... INFO @ Sat, 06 Jul 2019 03:27:08: #1 read treatment tags... INFO @ Sat, 06 Jul 2019 03:27:09: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/SRX541163/SRX541163.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/SRX541163/SRX541163.20 -q 1e-20 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/SRX541163/SRX541163.20 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/SRX541163/SRX541163.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 03:27:09: #1 read tag files... INFO @ Sat, 06 Jul 2019 03:27:09: #1 read treatment tags... INFO @ Sat, 06 Jul 2019 03:27:18: 1000000 INFO @ Sat, 06 Jul 2019 03:27:18: 1000000 INFO @ Sat, 06 Jul 2019 03:27:18: 1000000 INFO @ Sat, 06 Jul 2019 03:27:27: 2000000 INFO @ Sat, 06 Jul 2019 03:27:28: 2000000 INFO @ Sat, 06 Jul 2019 03:27:28: 2000000 INFO @ Sat, 06 Jul 2019 03:27:36: 3000000 INFO @ Sat, 06 Jul 2019 03:27:37: 3000000 INFO @ Sat, 06 Jul 2019 03:27:39: 3000000 INFO @ Sat, 06 Jul 2019 03:27:40: #1 tag size is determined as 50 bps INFO @ Sat, 06 Jul 2019 03:27:40: #1 tag size = 50 INFO @ Sat, 06 Jul 2019 03:27:40: #1 total tags in treatment: 3545239 INFO @ Sat, 06 Jul 2019 03:27:40: #1 user defined the maximum tags... INFO @ Sat, 06 Jul 2019 03:27:40: #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 03:27:40: #1 tags after filtering in treatment: 3545239 INFO @ Sat, 06 Jul 2019 03:27:40: #1 Redundant rate of treatment: 0.00 INFO @ Sat, 06 Jul 2019 03:27:40: #1 finished! INFO @ Sat, 06 Jul 2019 03:27:40: #2 Build Peak Model... INFO @ Sat, 06 Jul 2019 03:27:40: #2 looking for paired plus/minus strand peaks... INFO @ Sat, 06 Jul 2019 03:27:41: #2 number of paired peaks: 48 WARNING @ Sat, 06 Jul 2019 03:27:41: Too few paired peaks (48) 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 03:27:41: Process for pairing-model is terminated! cut: /home/okishinya/chipatlas/results/sacCer3/SRX541163/SRX541163.10_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/SRX541163/SRX541163.10_model.r’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX541163/SRX541163.10_*.xls’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX541163/SRX541163.10_peaks.narrowPeak’: No such file or directory CompletedMACS2peakCalling INFO @ Sat, 06 Jul 2019 03:27:42: #1 tag size is determined as 50 bps INFO @ Sat, 06 Jul 2019 03:27:42: #1 tag size = 50 INFO @ Sat, 06 Jul 2019 03:27:42: #1 total tags in treatment: 3545239 INFO @ Sat, 06 Jul 2019 03:27:42: #1 user defined the maximum tags... INFO @ Sat, 06 Jul 2019 03:27:42: #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 03:27:42: #1 tags after filtering in treatment: 3545239 INFO @ Sat, 06 Jul 2019 03:27:42: #1 Redundant rate of treatment: 0.00 INFO @ Sat, 06 Jul 2019 03:27:42: #1 finished! INFO @ Sat, 06 Jul 2019 03:27:42: #2 Build Peak Model... INFO @ Sat, 06 Jul 2019 03:27:42: #2 looking for paired plus/minus strand peaks... INFO @ Sat, 06 Jul 2019 03:27:42: #2 number of paired peaks: 48 WARNING @ Sat, 06 Jul 2019 03:27:42: Too few paired peaks (48) 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 03:27:42: Process for pairing-model is terminated! cut: /home/okishinya/chipatlas/results/sacCer3/SRX541163/SRX541163.20_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/SRX541163/SRX541163.20_model.r’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX541163/SRX541163.20_*.xls’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX541163/SRX541163.20_peaks.narrowPeak’: No such file or directory CompletedMACS2peakCalling INFO @ Sat, 06 Jul 2019 03:27:44: #1 tag size is determined as 50 bps INFO @ Sat, 06 Jul 2019 03:27:44: #1 tag size = 50 INFO @ Sat, 06 Jul 2019 03:27:44: #1 total tags in treatment: 3545239 INFO @ Sat, 06 Jul 2019 03:27:44: #1 user defined the maximum tags... INFO @ Sat, 06 Jul 2019 03:27:44: #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 03:27:45: #1 tags after filtering in treatment: 3545239 INFO @ Sat, 06 Jul 2019 03:27:45: #1 Redundant rate of treatment: 0.00 INFO @ Sat, 06 Jul 2019 03:27:45: #1 finished! INFO @ Sat, 06 Jul 2019 03:27:45: #2 Build Peak Model... INFO @ Sat, 06 Jul 2019 03:27:45: #2 looking for paired plus/minus strand peaks... INFO @ Sat, 06 Jul 2019 03:27:45: #2 number of paired peaks: 48 WARNING @ Sat, 06 Jul 2019 03:27:45: Too few paired peaks (48) 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 03:27:45: Process for pairing-model is terminated! cut: /home/okishinya/chipatlas/results/sacCer3/SRX541163/SRX541163.05_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/SRX541163/SRX541163.05_model.r’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX541163/SRX541163.05_*.xls’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX541163/SRX541163.05_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。