Job ID = 9161762 sra ファイルのダウンロード中... Completed: 368386K bytes transferred in 6 seconds (469185K 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 9394978 spots for /home/okishinya/chipatlas/results/sacCer3/SRX1038529/SRR2040152.sra Written 9394978 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: 00:01:38 9394978 reads; of these: 9394978 (100.00%) were unpaired; of these: 1242665 (13.23%) aligned 0 times 7266632 (77.35%) aligned exactly 1 time 885681 (9.43%) aligned >1 times 86.77% overall alignment rate Time searching: 00:01:38 Overall time: 00:01:38 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] 2222418 / 8152313 = 0.2726 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 04:33:17: # Command line: callpeak -t SRX1038529.bam -f BAM -g 12100000 -n SRX1038529.20 -q 1e-20 # ARGUMENTS LIST: # name = SRX1038529.20 # format = BAM # ChIP-seq file = ['SRX1038529.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 04:33:17: #1 read tag files... INFO @ Wed, 28 Jun 2017 04:33:17: #1 read treatment tags... INFO @ Wed, 28 Jun 2017 04:33:17: # Command line: callpeak -t SRX1038529.bam -f BAM -g 12100000 -n SRX1038529.05 -q 1e-05 # ARGUMENTS LIST: # name = SRX1038529.05 # format = BAM # ChIP-seq file = ['SRX1038529.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 04:33:17: #1 read tag files... INFO @ Wed, 28 Jun 2017 04:33:17: #1 read treatment tags... INFO @ Wed, 28 Jun 2017 04:33:17: # Command line: callpeak -t SRX1038529.bam -f BAM -g 12100000 -n SRX1038529.10 -q 1e-10 # ARGUMENTS LIST: # name = SRX1038529.10 # format = BAM # ChIP-seq file = ['SRX1038529.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 04:33:17: #1 read tag files... INFO @ Wed, 28 Jun 2017 04:33:17: #1 read treatment tags... INFO @ Wed, 28 Jun 2017 04:33:25: 1000000 INFO @ Wed, 28 Jun 2017 04:33:25: 1000000 INFO @ Wed, 28 Jun 2017 04:33:26: 1000000 INFO @ Wed, 28 Jun 2017 04:33:34: 2000000 INFO @ Wed, 28 Jun 2017 04:33:34: 2000000 INFO @ Wed, 28 Jun 2017 04:33:35: 2000000 INFO @ Wed, 28 Jun 2017 04:33:43: 3000000 INFO @ Wed, 28 Jun 2017 04:33:43: 3000000 INFO @ Wed, 28 Jun 2017 04:33:44: 3000000 INFO @ Wed, 28 Jun 2017 04:33:52: 4000000 INFO @ Wed, 28 Jun 2017 04:33:52: 4000000 INFO @ Wed, 28 Jun 2017 04:33:53: 4000000 INFO @ Wed, 28 Jun 2017 04:34:01: 5000000 INFO @ Wed, 28 Jun 2017 04:34:01: 5000000 INFO @ Wed, 28 Jun 2017 04:34:02: 5000000 INFO @ Wed, 28 Jun 2017 04:34:09: #1 tag size is determined as 51 bps INFO @ Wed, 28 Jun 2017 04:34:09: #1 tag size is determined as 51 bps INFO @ Wed, 28 Jun 2017 04:34:09: #1 tag size = 51 INFO @ Wed, 28 Jun 2017 04:34:09: #1 tag size = 51 INFO @ Wed, 28 Jun 2017 04:34:09: #1 total tags in treatment: 5929895 INFO @ Wed, 28 Jun 2017 04:34:09: #1 total tags in treatment: 5929895 INFO @ Wed, 28 Jun 2017 04:34:09: #1 user defined the maximum tags... INFO @ Wed, 28 Jun 2017 04:34:09: #1 user defined the maximum tags... INFO @ Wed, 28 Jun 2017 04:34:09: #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 04:34:09: #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 04:34:09: #1 tags after filtering in treatment: 5929895 INFO @ Wed, 28 Jun 2017 04:34:09: #1 tags after filtering in treatment: 5929895 INFO @ Wed, 28 Jun 2017 04:34:09: #1 Redundant rate of treatment: 0.00 INFO @ Wed, 28 Jun 2017 04:34:09: #1 Redundant rate of treatment: 0.00 INFO @ Wed, 28 Jun 2017 04:34:09: #1 finished! INFO @ Wed, 28 Jun 2017 04:34:09: #1 finished! INFO @ Wed, 28 Jun 2017 04:34:09: #2 Build Peak Model... INFO @ Wed, 28 Jun 2017 04:34:09: #2 Build Peak Model... INFO @ Wed, 28 Jun 2017 04:34:09: #2 looking for paired plus/minus strand peaks... INFO @ Wed, 28 Jun 2017 04:34:09: #2 looking for paired plus/minus strand peaks... INFO @ Wed, 28 Jun 2017 04:34:09: #2 number of paired peaks: 0 WARNING @ Wed, 28 Jun 2017 04:34:09: 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 @ Wed, 28 Jun 2017 04:34:09: Process for pairing-model is terminated! INFO @ Wed, 28 Jun 2017 04:34:09: #2 number of paired peaks: 0 WARNING @ Wed, 28 Jun 2017 04:34:09: 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 @ Wed, 28 Jun 2017 04:34:09: Process for pairing-model is terminated! cat: SRX1038529.20_peaks.narrowPeakcat: SRX1038529.05_peaks.narrowPeak: そのようなファイルやディレクトリはありません : 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 pass1 - making usageList (0 chroms): 1 millis needLargeMem: trying to allocate 0 bytes (limit: 17179869184)needLargeMem: trying to allocate 0 bytes (limit: 17179869184) rm: cannot remove `SRX1038529.05_model.r'rm: cannot remove `SRX1038529.20_model.r': そのようなファイルやディレクトリはありません : 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 `SRX1038529.05_*.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 `SRX1038529.20_*.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 `SRX1038529.05_peaks.narrowPeak': そのようなファイルやディレクトリはありません rm: cannot remove `SRX1038529.20_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 CompletedMACS2peakCalling INFO @ Wed, 28 Jun 2017 04:34:11: #1 tag size is determined as 51 bps INFO @ Wed, 28 Jun 2017 04:34:11: #1 tag size = 51 INFO @ Wed, 28 Jun 2017 04:34:11: #1 total tags in treatment: 5929895 INFO @ Wed, 28 Jun 2017 04:34:11: #1 user defined the maximum tags... INFO @ Wed, 28 Jun 2017 04:34:11: #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 04:34:11: #1 tags after filtering in treatment: 5929895 INFO @ Wed, 28 Jun 2017 04:34:11: #1 Redundant rate of treatment: 0.00 INFO @ Wed, 28 Jun 2017 04:34:11: #1 finished! INFO @ Wed, 28 Jun 2017 04:34:11: #2 Build Peak Model... INFO @ Wed, 28 Jun 2017 04:34:11: #2 looking for paired plus/minus strand peaks... INFO @ Wed, 28 Jun 2017 04:34:11: #2 number of paired peaks: 0 WARNING @ Wed, 28 Jun 2017 04:34:11: 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 04:34:11: Process for pairing-model is terminated! cat: SRX1038529.10_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 `SRX1038529.10_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 `SRX1038529.10_*.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 `SRX1038529.10_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。