Job ID = 9161638 sra ファイルのダウンロード中... Completed: 17550K bytes transferred in 3 seconds (46874K 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 1422677 spots for /home/okishinya/chipatlas/results/sacCer3/SRX043822/SRR107277.sra Written 1422677 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: 00:00:07 1422677 reads; of these: 1422677 (100.00%) were unpaired; of these: 1261368 (88.66%) aligned 0 times 62460 (4.39%) aligned exactly 1 time 98849 (6.95%) aligned >1 times 11.34% overall alignment rate Time searching: 00:00:07 Overall time: 00:00:07 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] 160941 / 161309 = 0.9977 in library ' ' BAM に変換しました。 Bed ファイルを作成中... BedGraph に変換中... BedGraph に変換しました。 BigWig に変換中... BigWig に変換しました。 INFO @ Wed, 28 Jun 2017 04:14:12: # Command line: callpeak -t SRX043822.bam -f BAM -g 12100000 -n SRX043822.20 -q 1e-20 # ARGUMENTS LIST: # name = SRX043822.20 # format = BAM # ChIP-seq file = ['SRX043822.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 04:14:12: #1 read tag files... INFO @ Wed, 28 Jun 2017 04:14:12: #1 read treatment tags... INFO @ Wed, 28 Jun 2017 04:14:12: # Command line: callpeak -t SRX043822.bam -f BAM -g 12100000 -n SRX043822.05 -q 1e-05 # ARGUMENTS LIST: # name = SRX043822.05 # format = BAM # ChIP-seq file = ['SRX043822.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 04:14:12: #1 read tag files... INFO @ Wed, 28 Jun 2017 04:14:12: #1 read treatment tags... INFO @ Wed, 28 Jun 2017 04:14:12: # Command line: callpeak -t SRX043822.bam -f BAM -g 12100000 -n SRX043822.10 -q 1e-10 # ARGUMENTS LIST: # name = SRX043822.10 # format = BAM # ChIP-seq file = ['SRX043822.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 04:14:12: #1 read tag files... INFO @ Wed, 28 Jun 2017 04:14:12: #1 read treatment tags... INFO @ Wed, 28 Jun 2017 04:14:12: #1 tag size is determined as 36 bps INFO @ Wed, 28 Jun 2017 04:14:12: #1 tag size = 36 INFO @ Wed, 28 Jun 2017 04:14:12: #1 total tags in treatment: 368 INFO @ Wed, 28 Jun 2017 04:14:12: #1 user defined the maximum tags... INFO @ Wed, 28 Jun 2017 04:14:12: #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 04:14:12: #1 tag size is determined as 36 bps INFO @ Wed, 28 Jun 2017 04:14:12: #1 tag size = 36 INFO @ Wed, 28 Jun 2017 04:14:12: #1 total tags in treatment: 368 INFO @ Wed, 28 Jun 2017 04:14:12: #1 user defined the maximum tags... INFO @ Wed, 28 Jun 2017 04:14:12: #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 04:14:12: #1 tag size is determined as 36 bps INFO @ Wed, 28 Jun 2017 04:14:12: #1 tag size = 36 INFO @ Wed, 28 Jun 2017 04:14:12: #1 total tags in treatment: 368 INFO @ Wed, 28 Jun 2017 04:14:12: #1 user defined the maximum tags... INFO @ Wed, 28 Jun 2017 04:14:12: #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 04:14:12: #1 tags after filtering in treatment: 365 INFO @ Wed, 28 Jun 2017 04:14:12: #1 Redundant rate of treatment: 0.01 INFO @ Wed, 28 Jun 2017 04:14:12: #1 finished! INFO @ Wed, 28 Jun 2017 04:14:12: #2 Build Peak Model... INFO @ Wed, 28 Jun 2017 04:14:12: #2 looking for paired plus/minus strand peaks... INFO @ Wed, 28 Jun 2017 04:14:12: #2 number of paired peaks: 0 INFO @ Wed, 28 Jun 2017 04:14:12: #1 tags after filtering in treatment: 365 WARNING @ Wed, 28 Jun 2017 04:14:12: 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 @ Wed, 28 Jun 2017 04:14:12: #1 Redundant rate of treatment: 0.01 WARNING @ Wed, 28 Jun 2017 04:14:12: Process for pairing-model is terminated! INFO @ Wed, 28 Jun 2017 04:14:12: #1 finished! INFO @ Wed, 28 Jun 2017 04:14:12: #2 Build Peak Model... INFO @ Wed, 28 Jun 2017 04:14:12: #2 looking for paired plus/minus strand peaks... INFO @ Wed, 28 Jun 2017 04:14:12: #2 number of paired peaks: 0 WARNING @ Wed, 28 Jun 2017 04:14:12: 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 04:14:12: Process for pairing-model is terminated! INFO @ Wed, 28 Jun 2017 04:14:12: #1 tags after filtering in treatment: 365 INFO @ Wed, 28 Jun 2017 04:14:12: #1 Redundant rate of treatment: 0.01 INFO @ Wed, 28 Jun 2017 04:14:12: #1 finished! INFO @ Wed, 28 Jun 2017 04:14:12: #2 Build Peak Model... INFO @ Wed, 28 Jun 2017 04:14:12: #2 looking for paired plus/minus strand peaks... INFO @ Wed, 28 Jun 2017 04:14:12: #2 number of paired peaks: 0 WARNING @ Wed, 28 Jun 2017 04:14:12: 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 04:14:12: Process for pairing-model is terminated! cat: SRX043822.20_peaks.narrowPeakcat: SRX043822.05_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 cat: SRX043822.10_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 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 `SRX043822.20_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 `SRX043822.20_*.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 `SRX043822.05_model.r'rm: cannot remove `SRX043822.20_peaks.narrowPeak': そのようなファイルやディレクトリはありません : 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 rm: cannot remove `SRX043822.05_*.xls': 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 `SRX043822.05_peaks.narrowPeak': そのようなファイルやディレクトリはありません needLargeMem: trying to allocate 0 bytes (limit: 17179869184) CompletedMACS2peakCalling rm: cannot remove `SRX043822.10_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 `SRX043822.10_*.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 `SRX043822.10_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