Job ID = 9160130 sra ファイルのダウンロード中... Completed: 339738K bytes transferred in 7 seconds (361059K 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 15041383 spots for /home/okishinya/chipatlas/results/sacCer3/SRX2619074/SRR5319659.sra Written 15041383 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: 00:02:42 15041383 reads; of these: 15041383 (100.00%) were unpaired; of these: 473530 (3.15%) aligned 0 times 13229326 (87.95%) aligned exactly 1 time 1338527 (8.90%) aligned >1 times 96.85% overall alignment rate Time searching: 00:02:42 Overall time: 00:02:42 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_sort_core] merging from 8 files... [bam_rmdupse_core] 7779615 / 14567853 = 0.5340 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 02:01:00: # Command line: callpeak -t SRX2619074.bam -f BAM -g 12100000 -n SRX2619074.10 -q 1e-10 # ARGUMENTS LIST: # name = SRX2619074.10 # format = BAM # ChIP-seq file = ['SRX2619074.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 02:01:00: #1 read tag files... INFO @ Wed, 28 Jun 2017 02:01:00: #1 read treatment tags... INFO @ Wed, 28 Jun 2017 02:01:00: # Command line: callpeak -t SRX2619074.bam -f BAM -g 12100000 -n SRX2619074.20 -q 1e-20 # ARGUMENTS LIST: # name = SRX2619074.20 # format = BAM # ChIP-seq file = ['SRX2619074.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 02:01:00: #1 read tag files... INFO @ Wed, 28 Jun 2017 02:01:00: #1 read treatment tags... INFO @ Wed, 28 Jun 2017 02:01:00: # Command line: callpeak -t SRX2619074.bam -f BAM -g 12100000 -n SRX2619074.05 -q 1e-05 # ARGUMENTS LIST: # name = SRX2619074.05 # format = BAM # ChIP-seq file = ['SRX2619074.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 02:01:00: #1 read tag files... INFO @ Wed, 28 Jun 2017 02:01:00: #1 read treatment tags... INFO @ Wed, 28 Jun 2017 02:01:06: 1000000 INFO @ Wed, 28 Jun 2017 02:01:06: 1000000 INFO @ Wed, 28 Jun 2017 02:01:07: 1000000 INFO @ Wed, 28 Jun 2017 02:01:13: 2000000 INFO @ Wed, 28 Jun 2017 02:01:13: 2000000 INFO @ Wed, 28 Jun 2017 02:01:13: 2000000 INFO @ Wed, 28 Jun 2017 02:01:19: 3000000 INFO @ Wed, 28 Jun 2017 02:01:19: 3000000 INFO @ Wed, 28 Jun 2017 02:01:20: 3000000 INFO @ Wed, 28 Jun 2017 02:01:25: 4000000 INFO @ Wed, 28 Jun 2017 02:01:26: 4000000 INFO @ Wed, 28 Jun 2017 02:01:27: 4000000 INFO @ Wed, 28 Jun 2017 02:01:31: 5000000 INFO @ Wed, 28 Jun 2017 02:01:33: 5000000 INFO @ Wed, 28 Jun 2017 02:01:34: 5000000 INFO @ Wed, 28 Jun 2017 02:01:38: 6000000 INFO @ Wed, 28 Jun 2017 02:01:39: 6000000 INFO @ Wed, 28 Jun 2017 02:01:41: 6000000 INFO @ Wed, 28 Jun 2017 02:01:43: #1 tag size is determined as 50 bps INFO @ Wed, 28 Jun 2017 02:01:43: #1 tag size = 50 INFO @ Wed, 28 Jun 2017 02:01:43: #1 total tags in treatment: 6788238 INFO @ Wed, 28 Jun 2017 02:01:43: #1 user defined the maximum tags... INFO @ Wed, 28 Jun 2017 02:01:43: #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 02:01:43: #1 tags after filtering in treatment: 6788238 INFO @ Wed, 28 Jun 2017 02:01:43: #1 Redundant rate of treatment: 0.00 INFO @ Wed, 28 Jun 2017 02:01:43: #1 finished! INFO @ Wed, 28 Jun 2017 02:01:43: #2 Build Peak Model... INFO @ Wed, 28 Jun 2017 02:01:43: #2 looking for paired plus/minus strand peaks... INFO @ Wed, 28 Jun 2017 02:01:43: #2 number of paired peaks: 0 WARNING @ Wed, 28 Jun 2017 02:01:43: 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 02:01:43: Process for pairing-model is terminated! cat: SRX2619074.20_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 `SRX2619074.20_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 `SRX2619074.20_*.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 `SRX2619074.20_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 @ Wed, 28 Jun 2017 02:01:45: #1 tag size is determined as 50 bps INFO @ Wed, 28 Jun 2017 02:01:45: #1 tag size = 50 INFO @ Wed, 28 Jun 2017 02:01:45: #1 total tags in treatment: 6788238 INFO @ Wed, 28 Jun 2017 02:01:45: #1 user defined the maximum tags... INFO @ Wed, 28 Jun 2017 02:01:45: #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 02:01:45: #1 tags after filtering in treatment: 6788238 INFO @ Wed, 28 Jun 2017 02:01:45: #1 Redundant rate of treatment: 0.00 INFO @ Wed, 28 Jun 2017 02:01:45: #1 finished! INFO @ Wed, 28 Jun 2017 02:01:45: #2 Build Peak Model... INFO @ Wed, 28 Jun 2017 02:01:45: #2 looking for paired plus/minus strand peaks... INFO @ Wed, 28 Jun 2017 02:01:45: #2 number of paired peaks: 0 WARNING @ Wed, 28 Jun 2017 02:01:45: 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 02:01:45: Process for pairing-model is terminated! cat: SRX2619074.10_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): 0 millis needLargeMem: trying to allocate 0 bytes (limit: 17179869184) rm: cannot remove `SRX2619074.10_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 `SRX2619074.10_*.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 `SRX2619074.10_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 02:01:46: #1 tag size is determined as 50 bps INFO @ Wed, 28 Jun 2017 02:01:46: #1 tag size = 50 INFO @ Wed, 28 Jun 2017 02:01:46: #1 total tags in treatment: 6788238 INFO @ Wed, 28 Jun 2017 02:01:46: #1 user defined the maximum tags... INFO @ Wed, 28 Jun 2017 02:01:46: #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 02:01:46: #1 tags after filtering in treatment: 6788238 INFO @ Wed, 28 Jun 2017 02:01:46: #1 Redundant rate of treatment: 0.00 INFO @ Wed, 28 Jun 2017 02:01:46: #1 finished! INFO @ Wed, 28 Jun 2017 02:01:46: #2 Build Peak Model... INFO @ Wed, 28 Jun 2017 02:01:46: #2 looking for paired plus/minus strand peaks... INFO @ Wed, 28 Jun 2017 02:01:47: #2 number of paired peaks: 0 WARNING @ Wed, 28 Jun 2017 02:01:47: 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 02:01:47: Process for pairing-model is terminated! cat: SRX2619074.05_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 `SRX2619074.05_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 `SRX2619074.05_*.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 `SRX2619074.05_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。