Job ID = 9157332 sra ファイルのダウンロード中... Completed: 786K bytes transferred in 2 seconds (3129K 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 40216 spots for /home/okishinya/chipatlas/results/ce10/SRX015101/SRR032447.sra Written 40216 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: 00:00:01 40216 reads; of these: 40216 (100.00%) were unpaired; of these: 40183 (99.92%) aligned 0 times 17 (0.04%) aligned exactly 1 time 16 (0.04%) aligned >1 times 0.08% overall alignment rate Time searching: 00:00:01 Overall time: 00:00:01 マッピングが完了しました。 samtools でBAM に変換中... [samopen] SAM header is present: 7 sequences. [bam_rmdupse_core] 3 / 33 = 0.0909 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 @ Tue, 27 Jun 2017 11:23:42: # Command line: callpeak -t SRX015101.bam -f BAM -g ce -n SRX015101.20 -q 1e-20 # ARGUMENTS LIST: # name = SRX015101.20 # format = BAM # ChIP-seq file = ['SRX015101.bam'] # control file = None # effective genome size = 9.00e+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 @ Tue, 27 Jun 2017 11:23:42: #1 read tag files... INFO @ Tue, 27 Jun 2017 11:23:42: #1 read treatment tags... INFO @ Tue, 27 Jun 2017 11:23:42: # Command line: callpeak -t SRX015101.bam -f BAM -g ce -n SRX015101.05 -q 1e-05 # ARGUMENTS LIST: # name = SRX015101.05 # format = BAM # ChIP-seq file = ['SRX015101.bam'] # control file = None # effective genome size = 9.00e+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 @ Tue, 27 Jun 2017 11:23:42: #1 read tag files... INFO @ Tue, 27 Jun 2017 11:23:42: #1 read treatment tags... INFO @ Tue, 27 Jun 2017 11:23:42: #1 tag size is determined as 27 bps INFO @ Tue, 27 Jun 2017 11:23:42: #1 tag size = 27 INFO @ Tue, 27 Jun 2017 11:23:42: #1 total tags in treatment: 30 INFO @ Tue, 27 Jun 2017 11:23:42: #1 user defined the maximum tags... INFO @ Tue, 27 Jun 2017 11:23:42: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Tue, 27 Jun 2017 11:23:42: # Command line: callpeak -t SRX015101.bam -f BAM -g ce -n SRX015101.10 -q 1e-10 # ARGUMENTS LIST: # name = SRX015101.10 # format = BAM # ChIP-seq file = ['SRX015101.bam'] # control file = None # effective genome size = 9.00e+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 @ Tue, 27 Jun 2017 11:23:42: #1 read tag files... INFO @ Tue, 27 Jun 2017 11:23:42: #1 read treatment tags... INFO @ Tue, 27 Jun 2017 11:23:42: #1 tags after filtering in treatment: 29 INFO @ Tue, 27 Jun 2017 11:23:42: #1 tag size is determined as 27 bps INFO @ Tue, 27 Jun 2017 11:23:42: #1 Redundant rate of treatment: 0.03 INFO @ Tue, 27 Jun 2017 11:23:42: #1 tag size = 27 INFO @ Tue, 27 Jun 2017 11:23:42: #1 finished! INFO @ Tue, 27 Jun 2017 11:23:42: #1 total tags in treatment: 30 INFO @ Tue, 27 Jun 2017 11:23:42: #2 Build Peak Model... INFO @ Tue, 27 Jun 2017 11:23:42: #1 user defined the maximum tags... INFO @ Tue, 27 Jun 2017 11:23:42: #2 looking for paired plus/minus strand peaks... INFO @ Tue, 27 Jun 2017 11:23:42: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Tue, 27 Jun 2017 11:23:42: #2 number of paired peaks: 0 WARNING @ Tue, 27 Jun 2017 11:23:42: 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 @ Tue, 27 Jun 2017 11:23:42: Process for pairing-model is terminated! INFO @ Tue, 27 Jun 2017 11:23:42: #1 tags after filtering in treatment: 29 INFO @ Tue, 27 Jun 2017 11:23:42: #1 Redundant rate of treatment: 0.03 INFO @ Tue, 27 Jun 2017 11:23:42: #1 finished! INFO @ Tue, 27 Jun 2017 11:23:42: #2 Build Peak Model... INFO @ Tue, 27 Jun 2017 11:23:42: #2 looking for paired plus/minus strand peaks... INFO @ Tue, 27 Jun 2017 11:23:42: #1 tag size is determined as 27 bps INFO @ Tue, 27 Jun 2017 11:23:42: #1 tag size = 27 INFO @ Tue, 27 Jun 2017 11:23:42: #2 number of paired peaks: 0 INFO @ Tue, 27 Jun 2017 11:23:42: #1 total tags in treatment: 30 WARNING @ Tue, 27 Jun 2017 11:23:42: 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. INFO @ Tue, 27 Jun 2017 11:23:42: #1 user defined the maximum tags... WARNING @ Tue, 27 Jun 2017 11:23:42: Process for pairing-model is terminated! INFO @ Tue, 27 Jun 2017 11:23:42: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Tue, 27 Jun 2017 11:23:42: #1 tags after filtering in treatment: 29 INFO @ Tue, 27 Jun 2017 11:23:42: #1 Redundant rate of treatment: 0.03 INFO @ Tue, 27 Jun 2017 11:23:42: #1 finished! INFO @ Tue, 27 Jun 2017 11:23:42: #2 Build Peak Model... INFO @ Tue, 27 Jun 2017 11:23:42: #2 looking for paired plus/minus strand peaks... INFO @ Tue, 27 Jun 2017 11:23:42: #2 number of paired peaks: 0 WARNING @ Tue, 27 Jun 2017 11:23:42: 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 @ Tue, 27 Jun 2017 11:23:42: Process for pairing-model is terminated! cat: SRX015101.20_peaks.narrowPeak: そのようなファイルやディレクトリはありません cat: SRX015101.05_peaks.narrowPeak: そのようなファイルやディレクトリはありません cat: SRX015101.10_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): 2 millis needLargeMem: trying to allocate 0 bytes (limit: 17179869184) rm: cannot remove `SRX015101.20_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 `SRX015101.20_*.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 `SRX015101.20_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 pass1 - making usageList (0 chroms): 1 millis needLargeMem: trying to allocate 0 bytes (limit: 17179869184) pass1 - making usageList (0 chroms): 1 millis needLargeMem: trying to allocate 0 bytes (limit: 17179869184) rm: cannot remove `SRX015101.10_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 `SRX015101.10_*.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 `SRX015101.10_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 rm: cannot remove `SRX015101.05_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 `SRX015101.05_*.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 `SRX015101.05_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。