Job ID = 11244838 sra ファイルのダウンロード中... Completed: 99897K bytes transferred in 4 seconds (191331K bits/sec), in 1 file. Completed: 218455K bytes transferred in 11 seconds (153551K 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 3638569 spots for /home/okishinya/chipatlas/results/sacCer3/SRX3732399/SRR6759902.sra Written 3638569 spots for /home/okishinya/chipatlas/results/sacCer3/SRX3732399/SRR6759902.sra Read 7722455 spots for /home/okishinya/chipatlas/results/sacCer3/SRX3732399/SRR6759903.sra Written 7722455 spots for /home/okishinya/chipatlas/results/sacCer3/SRX3732399/SRR6759903.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 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: 00:01:57 11361024 reads; of these: 11361024 (100.00%) were unpaired; of these: 2130554 (18.75%) aligned 0 times 7098856 (62.48%) aligned exactly 1 time 2131614 (18.76%) aligned >1 times 81.25% overall alignment rate Time searching: 00:01:57 Overall time: 00:01:57 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] 4913429 / 9230470 = 0.5323 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, 09 Oct 2018 22:04:03: # Command line: callpeak -t SRX3732399.bam -f BAM -g 12100000 -n SRX3732399.10 -q 1e-10 # ARGUMENTS LIST: # name = SRX3732399.10 # format = BAM # ChIP-seq file = ['SRX3732399.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 @ Tue, 09 Oct 2018 22:04:03: # Command line: callpeak -t SRX3732399.bam -f BAM -g 12100000 -n SRX3732399.05 -q 1e-05 # ARGUMENTS LIST: # name = SRX3732399.05 # format = BAM # ChIP-seq file = ['SRX3732399.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 @ Tue, 09 Oct 2018 22:04:03: # Command line: callpeak -t SRX3732399.bam -f BAM -g 12100000 -n SRX3732399.20 -q 1e-20 # ARGUMENTS LIST: # name = SRX3732399.20 # format = BAM # ChIP-seq file = ['SRX3732399.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 @ Tue, 09 Oct 2018 22:04:03: #1 read tag files... INFO @ Tue, 09 Oct 2018 22:04:03: #1 read tag files... INFO @ Tue, 09 Oct 2018 22:04:03: #1 read tag files... INFO @ Tue, 09 Oct 2018 22:04:03: #1 read treatment tags... INFO @ Tue, 09 Oct 2018 22:04:03: #1 read treatment tags... INFO @ Tue, 09 Oct 2018 22:04:03: #1 read treatment tags... INFO @ Tue, 09 Oct 2018 22:04:10: 1000000 INFO @ Tue, 09 Oct 2018 22:04:10: 1000000 INFO @ Tue, 09 Oct 2018 22:04:10: 1000000 INFO @ Tue, 09 Oct 2018 22:04:17: 2000000 INFO @ Tue, 09 Oct 2018 22:04:17: 2000000 INFO @ Tue, 09 Oct 2018 22:04:17: 2000000 INFO @ Tue, 09 Oct 2018 22:04:23: 3000000 INFO @ Tue, 09 Oct 2018 22:04:24: 3000000 INFO @ Tue, 09 Oct 2018 22:04:24: 3000000 INFO @ Tue, 09 Oct 2018 22:04:30: 4000000 INFO @ Tue, 09 Oct 2018 22:04:31: 4000000 INFO @ Tue, 09 Oct 2018 22:04:31: 4000000 INFO @ Tue, 09 Oct 2018 22:04:32: #1 tag size is determined as 50 bps INFO @ Tue, 09 Oct 2018 22:04:32: #1 tag size = 50 INFO @ Tue, 09 Oct 2018 22:04:32: #1 total tags in treatment: 4317041 INFO @ Tue, 09 Oct 2018 22:04:32: #1 user defined the maximum tags... INFO @ Tue, 09 Oct 2018 22:04:32: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Tue, 09 Oct 2018 22:04:32: #1 tags after filtering in treatment: 4317041 INFO @ Tue, 09 Oct 2018 22:04:32: #1 Redundant rate of treatment: 0.00 INFO @ Tue, 09 Oct 2018 22:04:32: #1 finished! INFO @ Tue, 09 Oct 2018 22:04:32: #2 Build Peak Model... INFO @ Tue, 09 Oct 2018 22:04:32: #2 looking for paired plus/minus strand peaks... INFO @ Tue, 09 Oct 2018 22:04:32: #2 number of paired peaks: 30 WARNING @ Tue, 09 Oct 2018 22:04:32: Too few paired peaks (30) 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, 09 Oct 2018 22:04:32: Process for pairing-model is terminated! cat: SRX3732399.10_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 `SRX3732399.10_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 `SRX3732399.10_*.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 `SRX3732399.10_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 @ Tue, 09 Oct 2018 22:04:33: #1 tag size is determined as 50 bps INFO @ Tue, 09 Oct 2018 22:04:33: #1 tag size = 50 INFO @ Tue, 09 Oct 2018 22:04:33: #1 total tags in treatment: 4317041 INFO @ Tue, 09 Oct 2018 22:04:33: #1 user defined the maximum tags... INFO @ Tue, 09 Oct 2018 22:04:33: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Tue, 09 Oct 2018 22:04:33: #1 tag size is determined as 50 bps INFO @ Tue, 09 Oct 2018 22:04:33: #1 tag size = 50 INFO @ Tue, 09 Oct 2018 22:04:33: #1 total tags in treatment: 4317041 INFO @ Tue, 09 Oct 2018 22:04:33: #1 user defined the maximum tags... INFO @ Tue, 09 Oct 2018 22:04:33: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Tue, 09 Oct 2018 22:04:34: #1 tags after filtering in treatment: 4317041 INFO @ Tue, 09 Oct 2018 22:04:34: #1 Redundant rate of treatment: 0.00 INFO @ Tue, 09 Oct 2018 22:04:34: #1 finished! INFO @ Tue, 09 Oct 2018 22:04:34: #2 Build Peak Model... INFO @ Tue, 09 Oct 2018 22:04:34: #2 looking for paired plus/minus strand peaks... INFO @ Tue, 09 Oct 2018 22:04:34: #1 tags after filtering in treatment: 4317041 INFO @ Tue, 09 Oct 2018 22:04:34: #1 Redundant rate of treatment: 0.00 INFO @ Tue, 09 Oct 2018 22:04:34: #1 finished! INFO @ Tue, 09 Oct 2018 22:04:34: #2 Build Peak Model... INFO @ Tue, 09 Oct 2018 22:04:34: #2 looking for paired plus/minus strand peaks... INFO @ Tue, 09 Oct 2018 22:04:34: #2 number of paired peaks: 30 WARNING @ Tue, 09 Oct 2018 22:04:34: Too few paired peaks (30) 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, 09 Oct 2018 22:04:34: Process for pairing-model is terminated! INFO @ Tue, 09 Oct 2018 22:04:34: #2 number of paired peaks: 30 WARNING @ Tue, 09 Oct 2018 22:04:34: Too few paired peaks (30) 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, 09 Oct 2018 22:04:34: Process for pairing-model is terminated! cat: SRX3732399.20_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: SRX3732399.05_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) pass1 - making usageList (0 chroms): 0 millis rm: cannot remove `SRX3732399.20_model.r'needLargeMem: trying to allocate 0 bytes (limit: 17179869184) : 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 `SRX3732399.20_*.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 `SRX3732399.20_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 rm: cannot remove `SRX3732399.05_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 `SRX3732399.05_*.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 `SRX3732399.05_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。