Job ID = 2640786 sra ファイルのダウンロード中... Read layout: SINGLE fastq に変換中... spots read : 2,805,347 reads read : 2,805,347 reads written : 2,805,347 spots read : 2,444,130 reads read : 2,444,130 reads written : 2,444,130 rm: cannot remove ‘/home/okishinya/ncbi/public/sra/SRR3351562.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: 00:00:27 5249477 reads; of these: 5249477 (100.00%) were unpaired; of these: 5183661 (98.75%) aligned 0 times 1618 (0.03%) aligned exactly 1 time 64198 (1.22%) aligned >1 times 1.25% overall alignment rate Time searching: 00:00:27 Overall time: 00:00:27 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] 59450 / 65816 = 0.9033 in library ' ' BAM に変換しました。 Bed ファイルを作成中... INFO @ Sat, 24 Aug 2019 19:13:46: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/SRX1629956/SRX1629956.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/SRX1629956/SRX1629956.05 -q 1e-05 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/SRX1629956/SRX1629956.05 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/SRX1629956/SRX1629956.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, 24 Aug 2019 19:13:46: #1 read tag files... INFO @ Sat, 24 Aug 2019 19:13:46: #1 read treatment tags... INFO @ Sat, 24 Aug 2019 19:13:46: #1 tag size is determined as 51 bps INFO @ Sat, 24 Aug 2019 19:13:46: #1 tag size = 51 INFO @ Sat, 24 Aug 2019 19:13:46: #1 total tags in treatment: 6366 INFO @ Sat, 24 Aug 2019 19:13:46: #1 user defined the maximum tags... INFO @ Sat, 24 Aug 2019 19:13:46: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Sat, 24 Aug 2019 19:13:46: #1 tags after filtering in treatment: 6366 INFO @ Sat, 24 Aug 2019 19:13:46: #1 Redundant rate of treatment: 0.00 INFO @ Sat, 24 Aug 2019 19:13:46: #1 finished! INFO @ Sat, 24 Aug 2019 19:13:46: #2 Build Peak Model... INFO @ Sat, 24 Aug 2019 19:13:46: #2 looking for paired plus/minus strand peaks... INFO @ Sat, 24 Aug 2019 19:13:46: #2 number of paired peaks: 40 WARNING @ Sat, 24 Aug 2019 19:13:46: Too few paired peaks (40) 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, 24 Aug 2019 19:13:46: Process for pairing-model is terminated! cut: /home/okishinya/chipatlas/results/sacCer3/SRX1629956/SRX1629956.05_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/SRX1629956/SRX1629956.05_model.r’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX1629956/SRX1629956.05_*.xls’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX1629956/SRX1629956.05_peaks.narrowPeak’: No such file or directory CompletedMACS2peakCalling INFO @ Sat, 24 Aug 2019 19:14:16: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/SRX1629956/SRX1629956.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/SRX1629956/SRX1629956.10 -q 1e-10 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/SRX1629956/SRX1629956.10 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/SRX1629956/SRX1629956.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, 24 Aug 2019 19:14:16: #1 read tag files... INFO @ Sat, 24 Aug 2019 19:14:16: #1 read treatment tags... INFO @ Sat, 24 Aug 2019 19:14:16: #1 tag size is determined as 51 bps INFO @ Sat, 24 Aug 2019 19:14:16: #1 tag size = 51 INFO @ Sat, 24 Aug 2019 19:14:16: #1 total tags in treatment: 6366 INFO @ Sat, 24 Aug 2019 19:14:16: #1 user defined the maximum tags... INFO @ Sat, 24 Aug 2019 19:14:16: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Sat, 24 Aug 2019 19:14:16: #1 tags after filtering in treatment: 6366 INFO @ Sat, 24 Aug 2019 19:14:16: #1 Redundant rate of treatment: 0.00 INFO @ Sat, 24 Aug 2019 19:14:16: #1 finished! INFO @ Sat, 24 Aug 2019 19:14:16: #2 Build Peak Model... INFO @ Sat, 24 Aug 2019 19:14:16: #2 looking for paired plus/minus strand peaks... INFO @ Sat, 24 Aug 2019 19:14:16: #2 number of paired peaks: 40 WARNING @ Sat, 24 Aug 2019 19:14:16: Too few paired peaks (40) 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, 24 Aug 2019 19:14:16: Process for pairing-model is terminated! cut: /home/okishinya/chipatlas/results/sacCer3/SRX1629956/SRX1629956.10_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/SRX1629956/SRX1629956.10_model.r’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX1629956/SRX1629956.10_*.xls’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX1629956/SRX1629956.10_peaks.narrowPeak’: No such file or directory CompletedMACS2peakCalling BedGraph に変換中... BedGraph に変換しました。 BigWig に変換中... BigWig に変換しました。 INFO @ Sat, 24 Aug 2019 19:14:46: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/SRX1629956/SRX1629956.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/SRX1629956/SRX1629956.20 -q 1e-20 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/SRX1629956/SRX1629956.20 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/SRX1629956/SRX1629956.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, 24 Aug 2019 19:14:46: #1 read tag files... INFO @ Sat, 24 Aug 2019 19:14:46: #1 read treatment tags... INFO @ Sat, 24 Aug 2019 19:14:46: #1 tag size is determined as 51 bps INFO @ Sat, 24 Aug 2019 19:14:46: #1 tag size = 51 INFO @ Sat, 24 Aug 2019 19:14:46: #1 total tags in treatment: 6366 INFO @ Sat, 24 Aug 2019 19:14:46: #1 user defined the maximum tags... INFO @ Sat, 24 Aug 2019 19:14:46: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Sat, 24 Aug 2019 19:14:46: #1 tags after filtering in treatment: 6366 INFO @ Sat, 24 Aug 2019 19:14:46: #1 Redundant rate of treatment: 0.00 INFO @ Sat, 24 Aug 2019 19:14:46: #1 finished! INFO @ Sat, 24 Aug 2019 19:14:46: #2 Build Peak Model... INFO @ Sat, 24 Aug 2019 19:14:46: #2 looking for paired plus/minus strand peaks... INFO @ Sat, 24 Aug 2019 19:14:46: #2 number of paired peaks: 40 WARNING @ Sat, 24 Aug 2019 19:14:46: Too few paired peaks (40) 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, 24 Aug 2019 19:14:46: Process for pairing-model is terminated! cut: /home/okishinya/chipatlas/results/sacCer3/SRX1629956/SRX1629956.20_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/SRX1629956/SRX1629956.20_model.r’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX1629956/SRX1629956.20_*.xls’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX1629956/SRX1629956.20_peaks.narrowPeak’: No such file or directory CompletedMACS2peakCalling