Job ID = 10254360 sra ファイルのダウンロード中... Completed: 170318K bytes transferred in 5 seconds (256991K 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... Written 5534660 spots for /home/okishinya/chipatlas/results/sacCer3/SRX2587983/SRR5284411.sra Written 5534660 spots total 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: 00:01:13 5534660 reads; of these: 5534660 (100.00%) were unpaired; of these: 2641925 (47.73%) aligned 0 times 2535925 (45.82%) aligned exactly 1 time 356810 (6.45%) aligned >1 times 52.27% overall alignment rate Time searching: 00:01:13 Overall time: 00:01:13 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] 1271455 / 2892735 = 0.4395 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, 06 Dec 2017 17:38:52: # Command line: callpeak -t SRX2587983.bam -f BAM -g 12100000 -n SRX2587983.10 -q 1e-10 # ARGUMENTS LIST: # name = SRX2587983.10 # format = BAM # ChIP-seq file = ['SRX2587983.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, 06 Dec 2017 17:38:52: #1 read tag files... INFO @ Wed, 06 Dec 2017 17:38:52: #1 read treatment tags... INFO @ Wed, 06 Dec 2017 17:38:52: # Command line: callpeak -t SRX2587983.bam -f BAM -g 12100000 -n SRX2587983.05 -q 1e-05 # ARGUMENTS LIST: # name = SRX2587983.05 # format = BAM # ChIP-seq file = ['SRX2587983.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, 06 Dec 2017 17:38:52: #1 read tag files... INFO @ Wed, 06 Dec 2017 17:38:52: #1 read treatment tags... INFO @ Wed, 06 Dec 2017 17:38:52: # Command line: callpeak -t SRX2587983.bam -f BAM -g 12100000 -n SRX2587983.20 -q 1e-20 # ARGUMENTS LIST: # name = SRX2587983.20 # format = BAM # ChIP-seq file = ['SRX2587983.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, 06 Dec 2017 17:38:52: #1 read tag files... INFO @ Wed, 06 Dec 2017 17:38:52: #1 read treatment tags... INFO @ Wed, 06 Dec 2017 17:38:58: 1000000 INFO @ Wed, 06 Dec 2017 17:38:58: 1000000 INFO @ Wed, 06 Dec 2017 17:38:59: 1000000 INFO @ Wed, 06 Dec 2017 17:39:02: #1 tag size is determined as 50 bps INFO @ Wed, 06 Dec 2017 17:39:02: #1 tag size = 50 INFO @ Wed, 06 Dec 2017 17:39:02: #1 total tags in treatment: 1621280 INFO @ Wed, 06 Dec 2017 17:39:02: #1 user defined the maximum tags... INFO @ Wed, 06 Dec 2017 17:39:02: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Wed, 06 Dec 2017 17:39:02: #1 tags after filtering in treatment: 1621280 INFO @ Wed, 06 Dec 2017 17:39:02: #1 Redundant rate of treatment: 0.00 INFO @ Wed, 06 Dec 2017 17:39:02: #1 finished! INFO @ Wed, 06 Dec 2017 17:39:02: #2 Build Peak Model... INFO @ Wed, 06 Dec 2017 17:39:02: #2 looking for paired plus/minus strand peaks... INFO @ Wed, 06 Dec 2017 17:39:02: #2 number of paired peaks: 0 WARNING @ Wed, 06 Dec 2017 17:39:02: 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, 06 Dec 2017 17:39:02: Process for pairing-model is terminated! cat: SRX2587983.20_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 `SRX2587983.20_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 `SRX2587983.20_*.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 `SRX2587983.20_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, 06 Dec 2017 17:39:02: #1 tag size is determined as 50 bps INFO @ Wed, 06 Dec 2017 17:39:02: #1 tag size = 50 INFO @ Wed, 06 Dec 2017 17:39:02: #1 total tags in treatment: 1621280 INFO @ Wed, 06 Dec 2017 17:39:02: #1 user defined the maximum tags... INFO @ Wed, 06 Dec 2017 17:39:02: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Wed, 06 Dec 2017 17:39:02: #1 tags after filtering in treatment: 1621280 INFO @ Wed, 06 Dec 2017 17:39:02: #1 Redundant rate of treatment: 0.00 INFO @ Wed, 06 Dec 2017 17:39:02: #1 finished! INFO @ Wed, 06 Dec 2017 17:39:02: #2 Build Peak Model... INFO @ Wed, 06 Dec 2017 17:39:02: #2 looking for paired plus/minus strand peaks... INFO @ Wed, 06 Dec 2017 17:39:03: #2 number of paired peaks: 0 WARNING @ Wed, 06 Dec 2017 17:39:03: 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 @ Wed, 06 Dec 2017 17:39:03: Process for pairing-model is terminated! cat: SRX2587983.10_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 `SRX2587983.10_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 `SRX2587983.10_*.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 `SRX2587983.10_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, 06 Dec 2017 17:39:03: #1 tag size is determined as 50 bps INFO @ Wed, 06 Dec 2017 17:39:03: #1 tag size = 50 INFO @ Wed, 06 Dec 2017 17:39:03: #1 total tags in treatment: 1621280 INFO @ Wed, 06 Dec 2017 17:39:03: #1 user defined the maximum tags... INFO @ Wed, 06 Dec 2017 17:39:03: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Wed, 06 Dec 2017 17:39:03: #1 tags after filtering in treatment: 1621280 INFO @ Wed, 06 Dec 2017 17:39:03: #1 Redundant rate of treatment: 0.00 INFO @ Wed, 06 Dec 2017 17:39:03: #1 finished! INFO @ Wed, 06 Dec 2017 17:39:03: #2 Build Peak Model... INFO @ Wed, 06 Dec 2017 17:39:03: #2 looking for paired plus/minus strand peaks... INFO @ Wed, 06 Dec 2017 17:39:03: #2 number of paired peaks: 0 WARNING @ Wed, 06 Dec 2017 17:39:03: 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 @ Wed, 06 Dec 2017 17:39:03: Process for pairing-model is terminated! cat: SRX2587983.05_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 `SRX2587983.05_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 `SRX2587983.05_*.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 `SRX2587983.05_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。