Job ID = 11192624 sra ファイルのダウンロード中... Completed: 350371K bytes transferred in 6 seconds (418246K bits/sec), in 1 file. 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... Read 9882274 spots for /home/okishinya/chipatlas/results/sacCer3/SRX1143278/SRR2156290.sra Written 9882274 spots for /home/okishinya/chipatlas/results/sacCer3/SRX1143278/SRR2156290.sra rm: cannot remove `[DSE]RX*': 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 `[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: 00:02:25 9882274 reads; of these: 9882274 (100.00%) were unpaired; of these: 831378 (8.41%) aligned 0 times 7642170 (77.33%) aligned exactly 1 time 1408726 (14.26%) aligned >1 times 91.59% overall alignment rate Time searching: 00:02:25 Overall time: 00:02:25 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] 2514208 / 9050896 = 0.2778 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, 15 Sep 2018 09:40:08: # Command line: callpeak -t SRX1143278.bam -f BAM -g 12100000 -n SRX1143278.10 -q 1e-10 # ARGUMENTS LIST: # name = SRX1143278.10 # format = BAM # ChIP-seq file = ['SRX1143278.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, 15 Sep 2018 09:40:08: # Command line: callpeak -t SRX1143278.bam -f BAM -g 12100000 -n SRX1143278.05 -q 1e-05 # ARGUMENTS LIST: # name = SRX1143278.05 # format = BAM # ChIP-seq file = ['SRX1143278.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, 15 Sep 2018 09:40:08: # Command line: callpeak -t SRX1143278.bam -f BAM -g 12100000 -n SRX1143278.20 -q 1e-20 # ARGUMENTS LIST: # name = SRX1143278.20 # format = BAM # ChIP-seq file = ['SRX1143278.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, 15 Sep 2018 09:40:08: #1 read tag files... INFO @ Sat, 15 Sep 2018 09:40:08: #1 read tag files... INFO @ Sat, 15 Sep 2018 09:40:08: #1 read tag files... INFO @ Sat, 15 Sep 2018 09:40:08: #1 read treatment tags... INFO @ Sat, 15 Sep 2018 09:40:08: #1 read treatment tags... INFO @ Sat, 15 Sep 2018 09:40:08: #1 read treatment tags... INFO @ Sat, 15 Sep 2018 09:40:16: 1000000 INFO @ Sat, 15 Sep 2018 09:40:16: 1000000 INFO @ Sat, 15 Sep 2018 09:40:16: 1000000 INFO @ Sat, 15 Sep 2018 09:40:23: 2000000 INFO @ Sat, 15 Sep 2018 09:40:23: 2000000 INFO @ Sat, 15 Sep 2018 09:40:23: 2000000 INFO @ Sat, 15 Sep 2018 09:40:30: 3000000 INFO @ Sat, 15 Sep 2018 09:40:31: 3000000 INFO @ Sat, 15 Sep 2018 09:40:31: 3000000 INFO @ Sat, 15 Sep 2018 09:40:38: 4000000 INFO @ Sat, 15 Sep 2018 09:40:38: 4000000 INFO @ Sat, 15 Sep 2018 09:40:38: 4000000 INFO @ Sat, 15 Sep 2018 09:40:45: 5000000 INFO @ Sat, 15 Sep 2018 09:40:45: 5000000 INFO @ Sat, 15 Sep 2018 09:40:45: 5000000 INFO @ Sat, 15 Sep 2018 09:40:52: 6000000 INFO @ Sat, 15 Sep 2018 09:40:53: 6000000 INFO @ Sat, 15 Sep 2018 09:40:53: 6000000 INFO @ Sat, 15 Sep 2018 09:40:56: #1 tag size is determined as 75 bps INFO @ Sat, 15 Sep 2018 09:40:56: #1 tag size = 75 INFO @ Sat, 15 Sep 2018 09:40:56: #1 total tags in treatment: 6536688 INFO @ Sat, 15 Sep 2018 09:40:56: #1 user defined the maximum tags... INFO @ Sat, 15 Sep 2018 09:40:56: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Sat, 15 Sep 2018 09:40:56: #1 tags after filtering in treatment: 6536688 INFO @ Sat, 15 Sep 2018 09:40:56: #1 Redundant rate of treatment: 0.00 INFO @ Sat, 15 Sep 2018 09:40:56: #1 finished! INFO @ Sat, 15 Sep 2018 09:40:56: #2 Build Peak Model... INFO @ Sat, 15 Sep 2018 09:40:56: #2 looking for paired plus/minus strand peaks... INFO @ Sat, 15 Sep 2018 09:40:57: #1 tag size is determined as 75 bps INFO @ Sat, 15 Sep 2018 09:40:57: #1 tag size = 75 INFO @ Sat, 15 Sep 2018 09:40:57: #1 total tags in treatment: 6536688 INFO @ Sat, 15 Sep 2018 09:40:57: #1 user defined the maximum tags... INFO @ Sat, 15 Sep 2018 09:40:57: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Sat, 15 Sep 2018 09:40:57: #2 number of paired peaks: 0 WARNING @ Sat, 15 Sep 2018 09:40:57: 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 @ Sat, 15 Sep 2018 09:40:57: Process for pairing-model is terminated! cat: SRX1143278.10_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 `SRX1143278.10_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 `SRX1143278.10_*.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 `SRX1143278.10_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 @ Sat, 15 Sep 2018 09:40:57: #1 tags after filtering in treatment: 6536688 INFO @ Sat, 15 Sep 2018 09:40:57: #1 Redundant rate of treatment: 0.00 INFO @ Sat, 15 Sep 2018 09:40:57: #1 finished! INFO @ Sat, 15 Sep 2018 09:40:57: #2 Build Peak Model... INFO @ Sat, 15 Sep 2018 09:40:57: #2 looking for paired plus/minus strand peaks... INFO @ Sat, 15 Sep 2018 09:40:57: #1 tag size is determined as 75 bps INFO @ Sat, 15 Sep 2018 09:40:57: #1 tag size = 75 INFO @ Sat, 15 Sep 2018 09:40:57: #1 total tags in treatment: 6536688 INFO @ Sat, 15 Sep 2018 09:40:57: #1 user defined the maximum tags... INFO @ Sat, 15 Sep 2018 09:40:57: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Sat, 15 Sep 2018 09:40:57: #1 tags after filtering in treatment: 6536688 INFO @ Sat, 15 Sep 2018 09:40:57: #1 Redundant rate of treatment: 0.00 INFO @ Sat, 15 Sep 2018 09:40:57: #1 finished! INFO @ Sat, 15 Sep 2018 09:40:57: #2 Build Peak Model... INFO @ Sat, 15 Sep 2018 09:40:57: #2 looking for paired plus/minus strand peaks... INFO @ Sat, 15 Sep 2018 09:40:57: #2 number of paired peaks: 0 WARNING @ Sat, 15 Sep 2018 09:40:57: 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 @ Sat, 15 Sep 2018 09:40:57: Process for pairing-model is terminated! cat: SRX1143278.20_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 `SRX1143278.20_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 `SRX1143278.20_*.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 `SRX1143278.20_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 @ Sat, 15 Sep 2018 09:40:58: #2 number of paired peaks: 0 WARNING @ Sat, 15 Sep 2018 09:40:58: 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 @ Sat, 15 Sep 2018 09:40:58: Process for pairing-model is terminated! cat: SRX1143278.05_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 `SRX1143278.05_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 `SRX1143278.05_*.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 `SRX1143278.05_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。