Job ID = 9161846 sra ファイルのダウンロード中... Completed: 192310K bytes transferred in 4 seconds (326320K 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 8627619 spots for /home/okishinya/chipatlas/results/sacCer3/SRX1142469/SRR2155464.sra Written 8627619 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: 00:01:51 8627619 reads; of these: 8627619 (100.00%) were unpaired; of these: 624744 (7.24%) aligned 0 times 5959790 (69.08%) aligned exactly 1 time 2043085 (23.68%) aligned >1 times 92.76% overall alignment rate Time searching: 00:01:51 Overall time: 00:01:51 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] 3015911 / 8002875 = 0.3769 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 04:49:45: # Command line: callpeak -t SRX1142469.bam -f BAM -g 12100000 -n SRX1142469.05 -q 1e-05 # ARGUMENTS LIST: # name = SRX1142469.05 # format = BAM # ChIP-seq file = ['SRX1142469.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 04:49:45: #1 read tag files... INFO @ Wed, 28 Jun 2017 04:49:45: #1 read treatment tags... INFO @ Wed, 28 Jun 2017 04:49:45: # Command line: callpeak -t SRX1142469.bam -f BAM -g 12100000 -n SRX1142469.20 -q 1e-20 # ARGUMENTS LIST: # name = SRX1142469.20 # format = BAM # ChIP-seq file = ['SRX1142469.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 04:49:45: #1 read tag files... INFO @ Wed, 28 Jun 2017 04:49:45: #1 read treatment tags... INFO @ Wed, 28 Jun 2017 04:49:45: # Command line: callpeak -t SRX1142469.bam -f BAM -g 12100000 -n SRX1142469.10 -q 1e-10 # ARGUMENTS LIST: # name = SRX1142469.10 # format = BAM # ChIP-seq file = ['SRX1142469.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 04:49:45: #1 read tag files... INFO @ Wed, 28 Jun 2017 04:49:45: #1 read treatment tags... INFO @ Wed, 28 Jun 2017 04:49:51: 1000000 INFO @ Wed, 28 Jun 2017 04:49:51: 1000000 INFO @ Wed, 28 Jun 2017 04:49:52: 1000000 INFO @ Wed, 28 Jun 2017 04:49:57: 2000000 INFO @ Wed, 28 Jun 2017 04:49:58: 2000000 INFO @ Wed, 28 Jun 2017 04:49:58: 2000000 INFO @ Wed, 28 Jun 2017 04:50:04: 3000000 INFO @ Wed, 28 Jun 2017 04:50:05: 3000000 INFO @ Wed, 28 Jun 2017 04:50:05: 3000000 INFO @ Wed, 28 Jun 2017 04:50:10: 4000000 INFO @ Wed, 28 Jun 2017 04:50:11: 4000000 INFO @ Wed, 28 Jun 2017 04:50:12: 4000000 INFO @ Wed, 28 Jun 2017 04:50:16: #1 tag size is determined as 50 bps INFO @ Wed, 28 Jun 2017 04:50:16: #1 tag size = 50 INFO @ Wed, 28 Jun 2017 04:50:16: #1 total tags in treatment: 4986964 INFO @ Wed, 28 Jun 2017 04:50:16: #1 user defined the maximum tags... INFO @ Wed, 28 Jun 2017 04:50:16: #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 04:50:16: #1 tags after filtering in treatment: 4986964 INFO @ Wed, 28 Jun 2017 04:50:16: #1 Redundant rate of treatment: 0.00 INFO @ Wed, 28 Jun 2017 04:50:16: #1 finished! INFO @ Wed, 28 Jun 2017 04:50:16: #2 Build Peak Model... INFO @ Wed, 28 Jun 2017 04:50:16: #2 looking for paired plus/minus strand peaks... INFO @ Wed, 28 Jun 2017 04:50:17: #2 number of paired peaks: 0 WARNING @ Wed, 28 Jun 2017 04:50:17: 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 @ Wed, 28 Jun 2017 04:50:17: Process for pairing-model is terminated! cat: SRX1142469.05_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): 0 millis needLargeMem: trying to allocate 0 bytes (limit: 17179869184) rm: cannot remove `SRX1142469.05_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 `SRX1142469.05_*.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 `SRX1142469.05_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 04:50:18: #1 tag size is determined as 50 bps INFO @ Wed, 28 Jun 2017 04:50:18: #1 tag size = 50 INFO @ Wed, 28 Jun 2017 04:50:18: #1 total tags in treatment: 4986964 INFO @ Wed, 28 Jun 2017 04:50:18: #1 user defined the maximum tags... INFO @ Wed, 28 Jun 2017 04:50:18: #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 04:50:18: #1 tags after filtering in treatment: 4986964 INFO @ Wed, 28 Jun 2017 04:50:18: #1 Redundant rate of treatment: 0.00 INFO @ Wed, 28 Jun 2017 04:50:18: #1 finished! INFO @ Wed, 28 Jun 2017 04:50:18: #2 Build Peak Model... INFO @ Wed, 28 Jun 2017 04:50:18: #2 looking for paired plus/minus strand peaks... INFO @ Wed, 28 Jun 2017 04:50:18: #2 number of paired peaks: 0 WARNING @ Wed, 28 Jun 2017 04:50:18: 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 @ Wed, 28 Jun 2017 04:50:18: Process for pairing-model is terminated! cat: SRX1142469.10_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 `SRX1142469.10_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 `SRX1142469.10_*.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 `SRX1142469.10_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 INFO @ Wed, 28 Jun 2017 04:50:19: #1 tag size is determined as 50 bps INFO @ Wed, 28 Jun 2017 04:50:19: #1 tag size = 50 INFO @ Wed, 28 Jun 2017 04:50:19: #1 total tags in treatment: 4986964 INFO @ Wed, 28 Jun 2017 04:50:19: #1 user defined the maximum tags... INFO @ Wed, 28 Jun 2017 04:50:19: #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 04:50:19: #1 tags after filtering in treatment: 4986964 INFO @ Wed, 28 Jun 2017 04:50:19: #1 Redundant rate of treatment: 0.00 INFO @ Wed, 28 Jun 2017 04:50:19: #1 finished! INFO @ Wed, 28 Jun 2017 04:50:19: #2 Build Peak Model... INFO @ Wed, 28 Jun 2017 04:50:19: #2 looking for paired plus/minus strand peaks... INFO @ Wed, 28 Jun 2017 04:50:19: #2 number of paired peaks: 0 WARNING @ Wed, 28 Jun 2017 04:50:19: 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 @ Wed, 28 Jun 2017 04:50:19: Process for pairing-model is terminated! cat: SRX1142469.20_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 `SRX1142469.20_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 `SRX1142469.20_*.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 `SRX1142469.20_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 BedGraph に変換しました。 BigWig に変換中... BigWig に変換しました。