Job ID = 9161854 sra ファイルのダウンロード中... Completed: 150607K bytes transferred in 5 seconds (242301K 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 6972254 spots for /home/okishinya/chipatlas/results/sacCer3/SRX1142479/SRR2155474.sra Written 6972254 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: 00:01:15 6972254 reads; of these: 6972254 (100.00%) were unpaired; of these: 180273 (2.59%) aligned 0 times 4505592 (64.62%) aligned exactly 1 time 2286389 (32.79%) aligned >1 times 97.41% overall alignment rate Time searching: 00:01:15 Overall time: 00:01:15 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] 2706255 / 6791981 = 0.3984 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 @ Wed, 28 Jun 2017 04:50:15: # Command line: callpeak -t SRX1142479.bam -f BAM -g 12100000 -n SRX1142479.05 -q 1e-05 # ARGUMENTS LIST: # name = SRX1142479.05 # format = BAM # ChIP-seq file = ['SRX1142479.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 @ Wed, 28 Jun 2017 04:50:15: #1 read tag files... INFO @ Wed, 28 Jun 2017 04:50:15: #1 read treatment tags... INFO @ Wed, 28 Jun 2017 04:50:15: # Command line: callpeak -t SRX1142479.bam -f BAM -g 12100000 -n SRX1142479.20 -q 1e-20 # ARGUMENTS LIST: # name = SRX1142479.20 # format = BAM # ChIP-seq file = ['SRX1142479.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 @ Wed, 28 Jun 2017 04:50:15: #1 read tag files... INFO @ Wed, 28 Jun 2017 04:50:15: #1 read treatment tags... INFO @ Wed, 28 Jun 2017 04:50:15: # Command line: callpeak -t SRX1142479.bam -f BAM -g 12100000 -n SRX1142479.10 -q 1e-10 # ARGUMENTS LIST: # name = SRX1142479.10 # format = BAM # ChIP-seq file = ['SRX1142479.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 @ Wed, 28 Jun 2017 04:50:15: #1 read tag files... INFO @ Wed, 28 Jun 2017 04:50:15: #1 read treatment tags... INFO @ Wed, 28 Jun 2017 04:50:23: 1000000 INFO @ Wed, 28 Jun 2017 04:50:23: 1000000 INFO @ Wed, 28 Jun 2017 04:50:23: 1000000 INFO @ Wed, 28 Jun 2017 04:50:31: 2000000 INFO @ Wed, 28 Jun 2017 04:50:31: 2000000 INFO @ Wed, 28 Jun 2017 04:50:31: 2000000 INFO @ Wed, 28 Jun 2017 04:50:39: 3000000 INFO @ Wed, 28 Jun 2017 04:50:39: 3000000 INFO @ Wed, 28 Jun 2017 04:50:39: 3000000 INFO @ Wed, 28 Jun 2017 04:50:47: 4000000 INFO @ Wed, 28 Jun 2017 04:50:47: 4000000 INFO @ Wed, 28 Jun 2017 04:50:47: 4000000 INFO @ Wed, 28 Jun 2017 04:50:47: #1 tag size is determined as 50 bps INFO @ Wed, 28 Jun 2017 04:50:47: #1 tag size = 50 INFO @ Wed, 28 Jun 2017 04:50:47: #1 total tags in treatment: 4085726 INFO @ Wed, 28 Jun 2017 04:50:47: #1 user defined the maximum tags... INFO @ Wed, 28 Jun 2017 04:50:47: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Wed, 28 Jun 2017 04:50:47: #1 tag size is determined as 50 bps INFO @ Wed, 28 Jun 2017 04:50:47: #1 tag size = 50 INFO @ Wed, 28 Jun 2017 04:50:47: #1 total tags in treatment: 4085726 INFO @ Wed, 28 Jun 2017 04:50:47: #1 user defined the maximum tags... INFO @ Wed, 28 Jun 2017 04:50:47: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Wed, 28 Jun 2017 04:50:47: #1 tag size is determined as 50 bps INFO @ Wed, 28 Jun 2017 04:50:47: #1 tag size = 50 INFO @ Wed, 28 Jun 2017 04:50:47: #1 total tags in treatment: 4085726 INFO @ Wed, 28 Jun 2017 04:50:47: #1 user defined the maximum tags... INFO @ Wed, 28 Jun 2017 04:50:47: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Wed, 28 Jun 2017 04:50:47: #1 tags after filtering in treatment: 4085726 INFO @ Wed, 28 Jun 2017 04:50:47: #1 Redundant rate of treatment: 0.00 INFO @ Wed, 28 Jun 2017 04:50:47: #1 finished! INFO @ Wed, 28 Jun 2017 04:50:47: #2 Build Peak Model... INFO @ Wed, 28 Jun 2017 04:50:47: #2 looking for paired plus/minus strand peaks... INFO @ Wed, 28 Jun 2017 04:50:47: #1 tags after filtering in treatment: 4085726 INFO @ Wed, 28 Jun 2017 04:50:47: #1 Redundant rate of treatment: 0.00 INFO @ Wed, 28 Jun 2017 04:50:47: #1 finished! INFO @ Wed, 28 Jun 2017 04:50:47: #2 Build Peak Model... INFO @ Wed, 28 Jun 2017 04:50:47: #2 looking for paired plus/minus strand peaks... INFO @ Wed, 28 Jun 2017 04:50:47: #1 tags after filtering in treatment: 4085726 INFO @ Wed, 28 Jun 2017 04:50:47: #1 Redundant rate of treatment: 0.00 INFO @ Wed, 28 Jun 2017 04:50:47: #1 finished! INFO @ Wed, 28 Jun 2017 04:50:47: #2 Build Peak Model... INFO @ Wed, 28 Jun 2017 04:50:47: #2 looking for paired plus/minus strand peaks... INFO @ Wed, 28 Jun 2017 04:50:48: #2 number of paired peaks: 84 WARNING @ Wed, 28 Jun 2017 04:50:48: Too few paired peaks (84) 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 @ Wed, 28 Jun 2017 04:50:48: Process for pairing-model is terminated! cat: SRX1142479.20_peaks.narrowPeak: そのようなファイルやディレクトリはありません INFO @ Wed, 28 Jun 2017 04:50:48: #2 number of paired peaks: 84 WARNING @ Wed, 28 Jun 2017 04:50:48: Too few paired peaks (84) 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 @ Wed, 28 Jun 2017 04:50:48: Process for pairing-model is terminated! pass1 - making usageList (0 chroms): 1 millis needLargeMem: trying to allocate 0 bytes (limit: 17179869184) rm: cannot remove `SRX1142479.20_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 `SRX1142479.20_*.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 `SRX1142479.20_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 cat: SRX1142479.05_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 `SRX1142479.05_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 `SRX1142479.05_*.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 `SRX1142479.05_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 INFO @ Wed, 28 Jun 2017 04:50:48: #2 number of paired peaks: 84 WARNING @ Wed, 28 Jun 2017 04:50:48: Too few paired peaks (84) 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 @ Wed, 28 Jun 2017 04:50:48: Process for pairing-model is terminated! cat: SRX1142479.10_peaks.narrowPeak: そのようなファイルやディレクトリはありません pass1 - making usageList (0 chroms): 1 millis needLargeMem: trying to allocate 0 bytes (limit: 17179869184) rm: cannot remove `SRX1142479.10_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 `SRX1142479.10_*.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 `SRX1142479.10_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 BedGraph に変換しました。 BigWig に変換中... BigWig に変換しました。