Job ID = 9384036 sra ファイルのダウンロード中... Completed: 98628K bytes transferred in 4 seconds (178004K bits/sec), in 1 file, 2 directories. sra ファイルのダウンロードが完了しました。 Read layout: SINGLE fastq に変換中... Written 3434342 spots for /home/okishinya/chipatlas/results/sacCer3/SRX2481693/SRR5164667.sra Written 3434342 spots total rm: cannot remove `[DSE]RR*.fastq': そのようなファイルやディレクトリはありません 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: 00:00:47 3434342 reads; of these: 3434342 (100.00%) were unpaired; of these: 1522511 (44.33%) aligned 0 times 1704526 (49.63%) aligned exactly 1 time 207305 (6.04%) aligned >1 times 55.67% overall alignment rate Time searching: 00:00:47 Overall time: 00:00:47 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] 639281 / 1911831 = 0.3344 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 @ Sun, 06 Aug 2017 00:14:00: # Command line: callpeak -t SRX2481693.bam -f BAM -g 12100000 -n SRX2481693.10 -q 1e-10 # ARGUMENTS LIST: # name = SRX2481693.10 # format = BAM # ChIP-seq file = ['SRX2481693.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 @ Sun, 06 Aug 2017 00:14:00: #1 read tag files... INFO @ Sun, 06 Aug 2017 00:14:00: #1 read treatment tags... INFO @ Sun, 06 Aug 2017 00:14:00: # Command line: callpeak -t SRX2481693.bam -f BAM -g 12100000 -n SRX2481693.20 -q 1e-20 # ARGUMENTS LIST: # name = SRX2481693.20 # format = BAM # ChIP-seq file = ['SRX2481693.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 @ Sun, 06 Aug 2017 00:14:00: #1 read tag files... INFO @ Sun, 06 Aug 2017 00:14:00: #1 read treatment tags... INFO @ Sun, 06 Aug 2017 00:14:00: # Command line: callpeak -t SRX2481693.bam -f BAM -g 12100000 -n SRX2481693.05 -q 1e-05 # ARGUMENTS LIST: # name = SRX2481693.05 # format = BAM # ChIP-seq file = ['SRX2481693.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 @ Sun, 06 Aug 2017 00:14:00: #1 read tag files... INFO @ Sun, 06 Aug 2017 00:14:00: #1 read treatment tags... INFO @ Sun, 06 Aug 2017 00:14:07: 1000000 INFO @ Sun, 06 Aug 2017 00:14:07: 1000000 INFO @ Sun, 06 Aug 2017 00:14:08: 1000000 INFO @ Sun, 06 Aug 2017 00:14:09: #1 tag size is determined as 50 bps INFO @ Sun, 06 Aug 2017 00:14:09: #1 tag size = 50 INFO @ Sun, 06 Aug 2017 00:14:09: #1 total tags in treatment: 1272550 INFO @ Sun, 06 Aug 2017 00:14:09: #1 user defined the maximum tags... INFO @ Sun, 06 Aug 2017 00:14:09: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Sun, 06 Aug 2017 00:14:09: #1 tag size is determined as 50 bps INFO @ Sun, 06 Aug 2017 00:14:09: #1 tag size = 50 INFO @ Sun, 06 Aug 2017 00:14:09: #1 total tags in treatment: 1272550 INFO @ Sun, 06 Aug 2017 00:14:09: #1 user defined the maximum tags... INFO @ Sun, 06 Aug 2017 00:14:09: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Sun, 06 Aug 2017 00:14:09: #1 tags after filtering in treatment: 1272550 INFO @ Sun, 06 Aug 2017 00:14:09: #1 Redundant rate of treatment: 0.00 INFO @ Sun, 06 Aug 2017 00:14:09: #1 finished! INFO @ Sun, 06 Aug 2017 00:14:09: #2 Build Peak Model... INFO @ Sun, 06 Aug 2017 00:14:09: #2 looking for paired plus/minus strand peaks... INFO @ Sun, 06 Aug 2017 00:14:09: #1 tags after filtering in treatment: 1272550 INFO @ Sun, 06 Aug 2017 00:14:09: #1 Redundant rate of treatment: 0.00 INFO @ Sun, 06 Aug 2017 00:14:09: #1 finished! INFO @ Sun, 06 Aug 2017 00:14:09: #2 Build Peak Model... INFO @ Sun, 06 Aug 2017 00:14:09: #2 looking for paired plus/minus strand peaks... INFO @ Sun, 06 Aug 2017 00:14:09: #2 number of paired peaks: 0 WARNING @ Sun, 06 Aug 2017 00:14:09: 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 @ Sun, 06 Aug 2017 00:14:09: Process for pairing-model is terminated! INFO @ Sun, 06 Aug 2017 00:14:09: #2 number of paired peaks: 0 WARNING @ Sun, 06 Aug 2017 00:14:09: 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 @ Sun, 06 Aug 2017 00:14:09: Process for pairing-model is terminated! cat: SRX2481693.10_peaks.narrowPeak: そのようなファイルやディレクトリはありません cat: SRX2481693.20_peaks.narrowPeak: そのようなファイルやディレクトリはありません pass1 - making usageList (0 chroms): 1 millis needLargeMem: trying to allocate 0 bytes (limit: 17179869184) rm: cannot remove `SRX2481693.10_model.r': そのようなファイルやディレクトリはありません rm: cannot remove `SRX2481693.10_*.xls': そのようなファイルやディレクトリはありません rm: cannot remove `SRX2481693.10_peaks.narrowPeak': そのようなファイルやディレクトリはありません CompletedMACS2peakCalling pass1 - making usageList (0 chroms): 1 millis needLargeMem: trying to allocate 0 bytes (limit: 17179869184) rm: cannot remove `SRX2481693.20_model.r': そのようなファイルやディレクトリはありません rm: cannot remove `SRX2481693.20_*.xls': そのようなファイルやディレクトリはありません rm: cannot remove `SRX2481693.20_peaks.narrowPeak': そのようなファイルやディレクトリはありません CompletedMACS2peakCalling INFO @ Sun, 06 Aug 2017 00:14:10: #1 tag size is determined as 50 bps INFO @ Sun, 06 Aug 2017 00:14:10: #1 tag size = 50 INFO @ Sun, 06 Aug 2017 00:14:10: #1 total tags in treatment: 1272550 INFO @ Sun, 06 Aug 2017 00:14:10: #1 user defined the maximum tags... INFO @ Sun, 06 Aug 2017 00:14:10: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Sun, 06 Aug 2017 00:14:10: #1 tags after filtering in treatment: 1272550 INFO @ Sun, 06 Aug 2017 00:14:10: #1 Redundant rate of treatment: 0.00 INFO @ Sun, 06 Aug 2017 00:14:10: #1 finished! INFO @ Sun, 06 Aug 2017 00:14:10: #2 Build Peak Model... INFO @ Sun, 06 Aug 2017 00:14:10: #2 looking for paired plus/minus strand peaks... INFO @ Sun, 06 Aug 2017 00:14:10: #2 number of paired peaks: 0 WARNING @ Sun, 06 Aug 2017 00:14:10: 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 @ Sun, 06 Aug 2017 00:14:10: Process for pairing-model is terminated! cat: SRX2481693.05_peaks.narrowPeak: そのようなファイルやディレクトリはありません pass1 - making usageList (0 chroms): 1 millis needLargeMem: trying to allocate 0 bytes (limit: 17179869184) rm: cannot remove `SRX2481693.05_model.r': そのようなファイルやディレクトリはありません rm: cannot remove `SRX2481693.05_*.xls': そのようなファイルやディレクトリはありません rm: cannot remove `SRX2481693.05_peaks.narrowPeak': そのようなファイルやディレクトリはありません CompletedMACS2peakCalling BedGraph に変換しました。 BigWig に変換中... BigWig に変換しました。