Job ID = 11193113 sra ファイルのダウンロード中... Completed: 203826K bytes transferred in 5 seconds (301843K 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 10153651 spots for /home/okishinya/chipatlas/results/sacCer3/SRX4234102/SRR7360999.sra Written 10153651 spots for /home/okishinya/chipatlas/results/sacCer3/SRX4234102/SRR7360999.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 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: 00:02:11 10153651 reads; of these: 10153651 (100.00%) were unpaired; of these: 912458 (8.99%) aligned 0 times 8600094 (84.70%) aligned exactly 1 time 641099 (6.31%) aligned >1 times 91.01% overall alignment rate Time searching: 00:02:11 Overall time: 00:02:11 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] 2243883 / 9241193 = 0.2428 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 @ Sat, 15 Sep 2018 11:02:06: # Command line: callpeak -t SRX4234102.bam -f BAM -g 12100000 -n SRX4234102.20 -q 1e-20 # ARGUMENTS LIST: # name = SRX4234102.20 # format = BAM # ChIP-seq file = ['SRX4234102.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 @ Sat, 15 Sep 2018 11:02:06: #1 read tag files... INFO @ Sat, 15 Sep 2018 11:02:06: # Command line: callpeak -t SRX4234102.bam -f BAM -g 12100000 -n SRX4234102.10 -q 1e-10 # ARGUMENTS LIST: # name = SRX4234102.10 # format = BAM # ChIP-seq file = ['SRX4234102.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 @ Sat, 15 Sep 2018 11:02:06: #1 read treatment tags... INFO @ Sat, 15 Sep 2018 11:02:06: #1 read tag files... INFO @ Sat, 15 Sep 2018 11:02:06: #1 read treatment tags... INFO @ Sat, 15 Sep 2018 11:02:06: # Command line: callpeak -t SRX4234102.bam -f BAM -g 12100000 -n SRX4234102.05 -q 1e-05 # ARGUMENTS LIST: # name = SRX4234102.05 # format = BAM # ChIP-seq file = ['SRX4234102.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 @ Sat, 15 Sep 2018 11:02:06: #1 read tag files... INFO @ Sat, 15 Sep 2018 11:02:06: #1 read treatment tags... INFO @ Sat, 15 Sep 2018 11:02:14: 1000000 INFO @ Sat, 15 Sep 2018 11:02:14: 1000000 INFO @ Sat, 15 Sep 2018 11:02:14: 1000000 INFO @ Sat, 15 Sep 2018 11:02:21: 2000000 INFO @ Sat, 15 Sep 2018 11:02:22: 2000000 INFO @ Sat, 15 Sep 2018 11:02:22: 2000000 INFO @ Sat, 15 Sep 2018 11:02:28: 3000000 INFO @ Sat, 15 Sep 2018 11:02:29: 3000000 INFO @ Sat, 15 Sep 2018 11:02:29: 3000000 INFO @ Sat, 15 Sep 2018 11:02:36: 4000000 INFO @ Sat, 15 Sep 2018 11:02:38: 4000000 INFO @ Sat, 15 Sep 2018 11:02:38: 4000000 INFO @ Sat, 15 Sep 2018 11:02:43: 5000000 INFO @ Sat, 15 Sep 2018 11:02:46: 5000000 INFO @ Sat, 15 Sep 2018 11:02:46: 5000000 INFO @ Sat, 15 Sep 2018 11:02:50: 6000000 INFO @ Sat, 15 Sep 2018 11:02:54: 6000000 INFO @ Sat, 15 Sep 2018 11:02:54: 6000000 INFO @ Sat, 15 Sep 2018 11:02:58: #1 tag size is determined as 49 bps INFO @ Sat, 15 Sep 2018 11:02:58: #1 tag size = 49 INFO @ Sat, 15 Sep 2018 11:02:58: #1 total tags in treatment: 6997310 INFO @ Sat, 15 Sep 2018 11:02:58: #1 user defined the maximum tags... INFO @ Sat, 15 Sep 2018 11:02:58: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Sat, 15 Sep 2018 11:02:58: #1 tags after filtering in treatment: 6997310 INFO @ Sat, 15 Sep 2018 11:02:58: #1 Redundant rate of treatment: 0.00 INFO @ Sat, 15 Sep 2018 11:02:58: #1 finished! INFO @ Sat, 15 Sep 2018 11:02:58: #2 Build Peak Model... INFO @ Sat, 15 Sep 2018 11:02:58: #2 looking for paired plus/minus strand peaks... INFO @ Sat, 15 Sep 2018 11:02:58: #2 number of paired peaks: 0 WARNING @ Sat, 15 Sep 2018 11:02:58: 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 @ Sat, 15 Sep 2018 11:02:58: Process for pairing-model is terminated! cat: SRX4234102.10_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 `SRX4234102.10_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 `SRX4234102.10_*.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 `SRX4234102.10_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 @ Sat, 15 Sep 2018 11:03:02: #1 tag size is determined as 49 bps INFO @ Sat, 15 Sep 2018 11:03:02: #1 tag size = 49 INFO @ Sat, 15 Sep 2018 11:03:02: #1 total tags in treatment: 6997310 INFO @ Sat, 15 Sep 2018 11:03:02: #1 user defined the maximum tags... INFO @ Sat, 15 Sep 2018 11:03:02: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Sat, 15 Sep 2018 11:03:02: #1 tag size is determined as 49 bps INFO @ Sat, 15 Sep 2018 11:03:02: #1 tag size = 49 INFO @ Sat, 15 Sep 2018 11:03:02: #1 total tags in treatment: 6997310 INFO @ Sat, 15 Sep 2018 11:03:02: #1 user defined the maximum tags... INFO @ Sat, 15 Sep 2018 11:03:02: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Sat, 15 Sep 2018 11:03:02: #1 tags after filtering in treatment: 6997310 INFO @ Sat, 15 Sep 2018 11:03:02: #1 Redundant rate of treatment: 0.00 INFO @ Sat, 15 Sep 2018 11:03:02: #1 finished! INFO @ Sat, 15 Sep 2018 11:03:02: #2 Build Peak Model... INFO @ Sat, 15 Sep 2018 11:03:02: #2 looking for paired plus/minus strand peaks... INFO @ Sat, 15 Sep 2018 11:03:02: #1 tags after filtering in treatment: 6997310 INFO @ Sat, 15 Sep 2018 11:03:02: #1 Redundant rate of treatment: 0.00 INFO @ Sat, 15 Sep 2018 11:03:02: #1 finished! INFO @ Sat, 15 Sep 2018 11:03:02: #2 Build Peak Model... INFO @ Sat, 15 Sep 2018 11:03:02: #2 looking for paired plus/minus strand peaks... INFO @ Sat, 15 Sep 2018 11:03:03: #2 number of paired peaks: 0 WARNING @ Sat, 15 Sep 2018 11:03:03: 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 @ Sat, 15 Sep 2018 11:03:03: Process for pairing-model is terminated! cat: SRX4234102.20_peaks.narrowPeak: そのようなファイルやディレクトリはありません INFO @ Sat, 15 Sep 2018 11:03:03: #2 number of paired peaks: 0 WARNING @ Sat, 15 Sep 2018 11:03:03: 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 @ Sat, 15 Sep 2018 11:03:03: Process for pairing-model is terminated! pass1 - making usageList (0 chroms): 1 millis needLargeMem: trying to allocate 0 bytes (limit: 17179869184) rm: cannot remove `SRX4234102.20_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 `SRX4234102.20_*.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 `SRX4234102.20_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 cat: SRX4234102.05_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 `SRX4234102.05_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 `SRX4234102.05_*.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 `SRX4234102.05_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。