Job ID = 9161833 sra ファイルのダウンロード中... Completed: 763256K bytes transferred in 9 seconds (678362K 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 23128786 spots for /home/okishinya/chipatlas/results/sacCer3/SRX1100131/SRR2125092.sra Written 23128786 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: 00:04:08 23128786 reads; of these: 23128786 (100.00%) were unpaired; of these: 1202640 (5.20%) aligned 0 times 15734976 (68.03%) aligned exactly 1 time 6191170 (26.77%) aligned >1 times 94.80% overall alignment rate Time searching: 00:04:08 Overall time: 00:04:08 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_sort_core] merging from 12 files... [bam_rmdupse_core] 10704729 / 21926146 = 0.4882 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 04:52:45: # Command line: callpeak -t SRX1100131.bam -f BAM -g 12100000 -n SRX1100131.10 -q 1e-10 # ARGUMENTS LIST: # name = SRX1100131.10 # format = BAM # ChIP-seq file = ['SRX1100131.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 04:52:45: #1 read tag files... INFO @ Wed, 28 Jun 2017 04:52:45: #1 read treatment tags... INFO @ Wed, 28 Jun 2017 04:52:45: # Command line: callpeak -t SRX1100131.bam -f BAM -g 12100000 -n SRX1100131.05 -q 1e-05 # ARGUMENTS LIST: # name = SRX1100131.05 # format = BAM # ChIP-seq file = ['SRX1100131.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 04:52:45: #1 read tag files... INFO @ Wed, 28 Jun 2017 04:52:45: #1 read treatment tags... INFO @ Wed, 28 Jun 2017 04:52:45: # Command line: callpeak -t SRX1100131.bam -f BAM -g 12100000 -n SRX1100131.20 -q 1e-20 # ARGUMENTS LIST: # name = SRX1100131.20 # format = BAM # ChIP-seq file = ['SRX1100131.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 04:52:45: #1 read tag files... INFO @ Wed, 28 Jun 2017 04:52:45: #1 read treatment tags... INFO @ Wed, 28 Jun 2017 04:52:51: 1000000 INFO @ Wed, 28 Jun 2017 04:52:51: 1000000 INFO @ Wed, 28 Jun 2017 04:52:51: 1000000 INFO @ Wed, 28 Jun 2017 04:52:57: 2000000 INFO @ Wed, 28 Jun 2017 04:52:57: 2000000 INFO @ Wed, 28 Jun 2017 04:52:57: 2000000 INFO @ Wed, 28 Jun 2017 04:53:02: 3000000 INFO @ Wed, 28 Jun 2017 04:53:03: 3000000 INFO @ Wed, 28 Jun 2017 04:53:03: 3000000 INFO @ Wed, 28 Jun 2017 04:53:08: 4000000 INFO @ Wed, 28 Jun 2017 04:53:09: 4000000 INFO @ Wed, 28 Jun 2017 04:53:09: 4000000 INFO @ Wed, 28 Jun 2017 04:53:14: 5000000 INFO @ Wed, 28 Jun 2017 04:53:15: 5000000 INFO @ Wed, 28 Jun 2017 04:53:15: 5000000 INFO @ Wed, 28 Jun 2017 04:53:20: 6000000 INFO @ Wed, 28 Jun 2017 04:53:21: 6000000 INFO @ Wed, 28 Jun 2017 04:53:21: 6000000 INFO @ Wed, 28 Jun 2017 04:53:25: 7000000 INFO @ Wed, 28 Jun 2017 04:53:27: 7000000 INFO @ Wed, 28 Jun 2017 04:53:27: 7000000 INFO @ Wed, 28 Jun 2017 04:53:31: 8000000 INFO @ Wed, 28 Jun 2017 04:53:33: 8000000 INFO @ Wed, 28 Jun 2017 04:53:33: 8000000 INFO @ Wed, 28 Jun 2017 04:53:37: 9000000 INFO @ Wed, 28 Jun 2017 04:53:38: 9000000 INFO @ Wed, 28 Jun 2017 04:53:38: 9000000 INFO @ Wed, 28 Jun 2017 04:53:42: 10000000 INFO @ Wed, 28 Jun 2017 04:53:45: 10000000 INFO @ Wed, 28 Jun 2017 04:53:45: 10000000 INFO @ Wed, 28 Jun 2017 04:53:49: 11000000 INFO @ Wed, 28 Jun 2017 04:53:50: #1 tag size is determined as 51 bps INFO @ Wed, 28 Jun 2017 04:53:50: #1 tag size = 51 INFO @ Wed, 28 Jun 2017 04:53:50: #1 total tags in treatment: 11221417 INFO @ Wed, 28 Jun 2017 04:53:50: #1 user defined the maximum tags... INFO @ Wed, 28 Jun 2017 04:53:50: #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 04:53:50: #1 tags after filtering in treatment: 11221417 INFO @ Wed, 28 Jun 2017 04:53:50: #1 Redundant rate of treatment: 0.00 INFO @ Wed, 28 Jun 2017 04:53:50: #1 finished! INFO @ Wed, 28 Jun 2017 04:53:50: #2 Build Peak Model... INFO @ Wed, 28 Jun 2017 04:53:50: #2 looking for paired plus/minus strand peaks... INFO @ Wed, 28 Jun 2017 04:53:51: #2 number of paired peaks: 0 WARNING @ Wed, 28 Jun 2017 04:53:51: 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 04:53:51: Process for pairing-model is terminated! cat: SRX1100131.10_peaks.narrowPeak: そのようなファイルやディレクトリはありません INFO @ Wed, 28 Jun 2017 04:53:51: 11000000 pass1 - making usageList (0 chroms): 1 millis needLargeMem: trying to allocate 0 bytes (limit: 17179869184) rm: cannot remove `SRX1100131.10_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 `SRX1100131.10_*.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 `SRX1100131.10_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 @ Wed, 28 Jun 2017 04:53:51: 11000000 INFO @ Wed, 28 Jun 2017 04:53:52: #1 tag size is determined as 51 bps INFO @ Wed, 28 Jun 2017 04:53:52: #1 tag size = 51 INFO @ Wed, 28 Jun 2017 04:53:52: #1 total tags in treatment: 11221417 INFO @ Wed, 28 Jun 2017 04:53:52: #1 user defined the maximum tags... INFO @ Wed, 28 Jun 2017 04:53:52: #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 04:53:52: #1 tag size is determined as 51 bps INFO @ Wed, 28 Jun 2017 04:53:52: #1 tag size = 51 INFO @ Wed, 28 Jun 2017 04:53:52: #1 total tags in treatment: 11221417 INFO @ Wed, 28 Jun 2017 04:53:52: #1 user defined the maximum tags... INFO @ Wed, 28 Jun 2017 04:53:52: #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 04:53:53: #1 tags after filtering in treatment: 11221417 INFO @ Wed, 28 Jun 2017 04:53:53: #1 Redundant rate of treatment: 0.00 INFO @ Wed, 28 Jun 2017 04:53:53: #1 finished! INFO @ Wed, 28 Jun 2017 04:53:53: #2 Build Peak Model... INFO @ Wed, 28 Jun 2017 04:53:53: #2 looking for paired plus/minus strand peaks... INFO @ Wed, 28 Jun 2017 04:53:53: #1 tags after filtering in treatment: 11221417 INFO @ Wed, 28 Jun 2017 04:53:53: #1 Redundant rate of treatment: 0.00 INFO @ Wed, 28 Jun 2017 04:53:53: #1 finished! INFO @ Wed, 28 Jun 2017 04:53:53: #2 Build Peak Model... INFO @ Wed, 28 Jun 2017 04:53:53: #2 looking for paired plus/minus strand peaks... INFO @ Wed, 28 Jun 2017 04:53:53: #2 number of paired peaks: 0 WARNING @ Wed, 28 Jun 2017 04:53:53: 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 04:53:53: Process for pairing-model is terminated! cat: SRX1100131.05_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 `SRX1100131.05_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 `SRX1100131.05_*.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 `SRX1100131.05_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 INFO @ Wed, 28 Jun 2017 04:53:53: #2 number of paired peaks: 0 WARNING @ Wed, 28 Jun 2017 04:53:53: 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 04:53:53: Process for pairing-model is terminated! cat: SRX1100131.20_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 `SRX1100131.20_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 `SRX1100131.20_*.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 `SRX1100131.20_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 BedGraph に変換しました。 BigWig に変換中... BigWig に変換しました。