Job ID = 9160077 sra ファイルのダウンロード中... Completed: 98973K bytes transferred in 4 seconds (182799K 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 4758402 spots for /home/okishinya/chipatlas/results/sacCer3/SRX2619021/SRR5319606.sra Written 4758402 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: 00:00:34 4758402 reads; of these: 4758402 (100.00%) were unpaired; of these: 3020059 (63.47%) aligned 0 times 1487224 (31.25%) aligned exactly 1 time 251119 (5.28%) aligned >1 times 36.53% overall alignment rate Time searching: 00:00:34 Overall time: 00:00:34 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] 629233 / 1738343 = 0.3620 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 01:51:04: # Command line: callpeak -t SRX2619021.bam -f BAM -g 12100000 -n SRX2619021.10 -q 1e-10 # ARGUMENTS LIST: # name = SRX2619021.10 # format = BAM # ChIP-seq file = ['SRX2619021.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 01:51:04: #1 read tag files... INFO @ Wed, 28 Jun 2017 01:51:04: #1 read treatment tags... INFO @ Wed, 28 Jun 2017 01:51:04: # Command line: callpeak -t SRX2619021.bam -f BAM -g 12100000 -n SRX2619021.20 -q 1e-20 # ARGUMENTS LIST: # name = SRX2619021.20 # format = BAM # ChIP-seq file = ['SRX2619021.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 01:51:04: #1 read tag files... INFO @ Wed, 28 Jun 2017 01:51:04: #1 read treatment tags... INFO @ Wed, 28 Jun 2017 01:51:04: # Command line: callpeak -t SRX2619021.bam -f BAM -g 12100000 -n SRX2619021.05 -q 1e-05 # ARGUMENTS LIST: # name = SRX2619021.05 # format = BAM # ChIP-seq file = ['SRX2619021.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 01:51:04: #1 read tag files... INFO @ Wed, 28 Jun 2017 01:51:04: #1 read treatment tags... INFO @ Wed, 28 Jun 2017 01:51:11: 1000000 INFO @ Wed, 28 Jun 2017 01:51:11: 1000000 INFO @ Wed, 28 Jun 2017 01:51:11: 1000000 INFO @ Wed, 28 Jun 2017 01:51:12: #1 tag size is determined as 50 bps INFO @ Wed, 28 Jun 2017 01:51:12: #1 tag size = 50 INFO @ Wed, 28 Jun 2017 01:51:12: #1 total tags in treatment: 1109110 INFO @ Wed, 28 Jun 2017 01:51:12: #1 user defined the maximum tags... INFO @ Wed, 28 Jun 2017 01:51:12: #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 01:51:12: #1 tags after filtering in treatment: 1109110 INFO @ Wed, 28 Jun 2017 01:51:12: #1 Redundant rate of treatment: 0.00 INFO @ Wed, 28 Jun 2017 01:51:12: #1 finished! INFO @ Wed, 28 Jun 2017 01:51:12: #2 Build Peak Model... INFO @ Wed, 28 Jun 2017 01:51:12: #2 looking for paired plus/minus strand peaks... INFO @ Wed, 28 Jun 2017 01:51:12: #2 number of paired peaks: 60 WARNING @ Wed, 28 Jun 2017 01:51:12: Too few paired peaks (60) 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 01:51:12: Process for pairing-model is terminated! cat: SRX2619021.10_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 `SRX2619021.10_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 `SRX2619021.10_*.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 `SRX2619021.10_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 01:51:12: #1 tag size is determined as 50 bps INFO @ Wed, 28 Jun 2017 01:51:12: #1 tag size = 50 INFO @ Wed, 28 Jun 2017 01:51:12: #1 total tags in treatment: 1109110 INFO @ Wed, 28 Jun 2017 01:51:12: #1 user defined the maximum tags... INFO @ Wed, 28 Jun 2017 01:51:12: #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 01:51:12: #1 tag size is determined as 50 bps INFO @ Wed, 28 Jun 2017 01:51:12: #1 tag size = 50 INFO @ Wed, 28 Jun 2017 01:51:12: #1 total tags in treatment: 1109110 INFO @ Wed, 28 Jun 2017 01:51:12: #1 user defined the maximum tags... INFO @ Wed, 28 Jun 2017 01:51:12: #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 01:51:12: #1 tags after filtering in treatment: 1109110 INFO @ Wed, 28 Jun 2017 01:51:12: #1 Redundant rate of treatment: 0.00 INFO @ Wed, 28 Jun 2017 01:51:12: #1 finished! INFO @ Wed, 28 Jun 2017 01:51:12: #2 Build Peak Model... INFO @ Wed, 28 Jun 2017 01:51:12: #2 looking for paired plus/minus strand peaks... INFO @ Wed, 28 Jun 2017 01:51:12: #1 tags after filtering in treatment: 1109110 INFO @ Wed, 28 Jun 2017 01:51:12: #1 Redundant rate of treatment: 0.00 INFO @ Wed, 28 Jun 2017 01:51:12: #1 finished! INFO @ Wed, 28 Jun 2017 01:51:12: #2 Build Peak Model... INFO @ Wed, 28 Jun 2017 01:51:12: #2 looking for paired plus/minus strand peaks... INFO @ Wed, 28 Jun 2017 01:51:12: #2 number of paired peaks: 60 WARNING @ Wed, 28 Jun 2017 01:51:12: Too few paired peaks (60) 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 01:51:12: Process for pairing-model is terminated! INFO @ Wed, 28 Jun 2017 01:51:12: #2 number of paired peaks: 60 WARNING @ Wed, 28 Jun 2017 01:51:12: Too few paired peaks (60) 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 01:51:12: Process for pairing-model is terminated! cat: SRX2619021.20_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: SRX2619021.05_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): 1 millis needLargeMem: trying to allocate 0 bytes (limit: 17179869184) rm: cannot remove `SRX2619021.20_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 `SRX2619021.20_*.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 `SRX2619021.20_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 `SRX2619021.05_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 `SRX2619021.05_*.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 `SRX2619021.05_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。