Job ID = 9160068 sra ファイルのダウンロード中... Completed: 84151K bytes transferred in 5 seconds (134806K 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 3705965 spots for /home/okishinya/chipatlas/results/sacCer3/SRX2619013/SRR5319598.sra Written 3705965 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: 00:00:49 3705965 reads; of these: 3705965 (100.00%) were unpaired; of these: 194234 (5.24%) aligned 0 times 2583790 (69.72%) aligned exactly 1 time 927941 (25.04%) aligned >1 times 94.76% overall alignment rate Time searching: 00:00:49 Overall time: 00:00:49 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] 1032132 / 3511731 = 0.2939 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 01:50:36: # Command line: callpeak -t SRX2619013.bam -f BAM -g 12100000 -n SRX2619013.10 -q 1e-10 # ARGUMENTS LIST: # name = SRX2619013.10 # format = BAM # ChIP-seq file = ['SRX2619013.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 01:50:36: #1 read tag files... INFO @ Wed, 28 Jun 2017 01:50:36: #1 read treatment tags... INFO @ Wed, 28 Jun 2017 01:50:36: # Command line: callpeak -t SRX2619013.bam -f BAM -g 12100000 -n SRX2619013.05 -q 1e-05 # ARGUMENTS LIST: # name = SRX2619013.05 # format = BAM # ChIP-seq file = ['SRX2619013.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 01:50:36: #1 read tag files... INFO @ Wed, 28 Jun 2017 01:50:36: #1 read treatment tags... INFO @ Wed, 28 Jun 2017 01:50:36: # Command line: callpeak -t SRX2619013.bam -f BAM -g 12100000 -n SRX2619013.20 -q 1e-20 # ARGUMENTS LIST: # name = SRX2619013.20 # format = BAM # ChIP-seq file = ['SRX2619013.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 01:50:36: #1 read tag files... INFO @ Wed, 28 Jun 2017 01:50:36: #1 read treatment tags... INFO @ Wed, 28 Jun 2017 01:50:42: 1000000 INFO @ Wed, 28 Jun 2017 01:50:42: 1000000 INFO @ Wed, 28 Jun 2017 01:50:42: 1000000 INFO @ Wed, 28 Jun 2017 01:50:48: 2000000 INFO @ Wed, 28 Jun 2017 01:50:48: 2000000 INFO @ Wed, 28 Jun 2017 01:50:49: 2000000 INFO @ Wed, 28 Jun 2017 01:50:52: #1 tag size is determined as 50 bps INFO @ Wed, 28 Jun 2017 01:50:52: #1 tag size = 50 INFO @ Wed, 28 Jun 2017 01:50:52: #1 total tags in treatment: 2479599 INFO @ Wed, 28 Jun 2017 01:50:52: #1 user defined the maximum tags... INFO @ Wed, 28 Jun 2017 01:50:52: #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 01:50:52: #1 tag size is determined as 50 bps INFO @ Wed, 28 Jun 2017 01:50:52: #1 tag size = 50 INFO @ Wed, 28 Jun 2017 01:50:52: #1 total tags in treatment: 2479599 INFO @ Wed, 28 Jun 2017 01:50:52: #1 user defined the maximum tags... INFO @ Wed, 28 Jun 2017 01:50:52: #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 01:50:52: #1 tags after filtering in treatment: 2479599 INFO @ Wed, 28 Jun 2017 01:50:52: #1 Redundant rate of treatment: 0.00 INFO @ Wed, 28 Jun 2017 01:50:52: #1 finished! INFO @ Wed, 28 Jun 2017 01:50:52: #2 Build Peak Model... INFO @ Wed, 28 Jun 2017 01:50:52: #2 looking for paired plus/minus strand peaks... INFO @ Wed, 28 Jun 2017 01:50:52: #1 tags after filtering in treatment: 2479599 INFO @ Wed, 28 Jun 2017 01:50:52: #1 Redundant rate of treatment: 0.00 INFO @ Wed, 28 Jun 2017 01:50:52: #1 finished! INFO @ Wed, 28 Jun 2017 01:50:52: #2 Build Peak Model... INFO @ Wed, 28 Jun 2017 01:50:52: #2 looking for paired plus/minus strand peaks... INFO @ Wed, 28 Jun 2017 01:50:52: #1 tag size is determined as 50 bps INFO @ Wed, 28 Jun 2017 01:50:52: #1 tag size = 50 INFO @ Wed, 28 Jun 2017 01:50:52: #1 total tags in treatment: 2479599 INFO @ Wed, 28 Jun 2017 01:50:52: #1 user defined the maximum tags... INFO @ Wed, 28 Jun 2017 01:50:52: #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 01:50:52: #1 tags after filtering in treatment: 2479599 INFO @ Wed, 28 Jun 2017 01:50:52: #1 Redundant rate of treatment: 0.00 INFO @ Wed, 28 Jun 2017 01:50:52: #1 finished! INFO @ Wed, 28 Jun 2017 01:50:52: #2 Build Peak Model... INFO @ Wed, 28 Jun 2017 01:50:52: #2 looking for paired plus/minus strand peaks... INFO @ Wed, 28 Jun 2017 01:50:52: #2 number of paired peaks: 38 WARNING @ Wed, 28 Jun 2017 01:50:52: Too few paired peaks (38) 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 01:50:52: Process for pairing-model is terminated! cat: SRX2619013.05_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 `SRX2619013.05_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 `SRX2619013.05_*.xls': そのようなファイルやディレクトリはありません INFO @ Wed, 28 Jun 2017 01:50:52: #2 number of paired peaks: 38 WARNING @ Wed, 28 Jun 2017 01:50:52: Too few paired peaks (38) 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 01:50:52: Process for pairing-model is terminated! rm: cannot remove `SRX2619013.05_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 cat: SRX2619013.20_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 `SRX2619013.20_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 `SRX2619013.20_*.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 `SRX2619013.20_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 01:50:52: #2 number of paired peaks: 38 WARNING @ Wed, 28 Jun 2017 01:50:52: Too few paired peaks (38) 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 01:50:52: Process for pairing-model is terminated! cat: SRX2619013.10_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 `SRX2619013.10_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 `SRX2619013.10_*.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 `SRX2619013.10_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 BedGraph に変換しました。 BigWig に変換中... BigWig に変換しました。