Job ID = 11193165 sra ファイルのダウンロード中... Completed: 74694K bytes transferred in 4 seconds (122393K 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 3266890 spots for /home/okishinya/chipatlas/results/sacCer3/SRX4337757/SRR7467846.sra Written 3266890 spots for /home/okishinya/chipatlas/results/sacCer3/SRX4337757/SRR7467846.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: 00:00:29 3266890 reads; of these: 3266890 (100.00%) were unpaired; of these: 1268518 (38.83%) aligned 0 times 1743599 (53.37%) aligned exactly 1 time 254773 (7.80%) aligned >1 times 61.17% overall alignment rate Time searching: 00:00:29 Overall time: 00:00:29 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] 521921 / 1998372 = 0.2612 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 11:04:23: # Command line: callpeak -t SRX4337757.bam -f BAM -g 12100000 -n SRX4337757.10 -q 1e-10 # ARGUMENTS LIST: # name = SRX4337757.10 # format = BAM # ChIP-seq file = ['SRX4337757.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 11:04:23: #1 read tag files... INFO @ Sat, 15 Sep 2018 11:04:23: #1 read treatment tags... INFO @ Sat, 15 Sep 2018 11:04:23: # Command line: callpeak -t SRX4337757.bam -f BAM -g 12100000 -n SRX4337757.05 -q 1e-05 # ARGUMENTS LIST: # name = SRX4337757.05 # format = BAM # ChIP-seq file = ['SRX4337757.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 11:04:23: #1 read tag files... INFO @ Sat, 15 Sep 2018 11:04:23: #1 read treatment tags... INFO @ Sat, 15 Sep 2018 11:04:23: # Command line: callpeak -t SRX4337757.bam -f BAM -g 12100000 -n SRX4337757.20 -q 1e-20 # ARGUMENTS LIST: # name = SRX4337757.20 # format = BAM # ChIP-seq file = ['SRX4337757.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 11:04:23: #1 read tag files... INFO @ Sat, 15 Sep 2018 11:04:23: #1 read treatment tags... INFO @ Sat, 15 Sep 2018 11:04:30: 1000000 INFO @ Sat, 15 Sep 2018 11:04:30: 1000000 INFO @ Sat, 15 Sep 2018 11:04:30: 1000000 INFO @ Sat, 15 Sep 2018 11:04:33: #1 tag size is determined as 51 bps INFO @ Sat, 15 Sep 2018 11:04:33: #1 tag size = 51 INFO @ Sat, 15 Sep 2018 11:04:33: #1 total tags in treatment: 1476451 INFO @ Sat, 15 Sep 2018 11:04:33: #1 user defined the maximum tags... INFO @ Sat, 15 Sep 2018 11:04:33: #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 11:04:33: #1 tags after filtering in treatment: 1476451 INFO @ Sat, 15 Sep 2018 11:04:33: #1 Redundant rate of treatment: 0.00 INFO @ Sat, 15 Sep 2018 11:04:33: #1 finished! INFO @ Sat, 15 Sep 2018 11:04:33: #2 Build Peak Model... INFO @ Sat, 15 Sep 2018 11:04:33: #2 looking for paired plus/minus strand peaks... INFO @ Sat, 15 Sep 2018 11:04:33: #1 tag size is determined as 51 bps INFO @ Sat, 15 Sep 2018 11:04:33: #1 tag size = 51 INFO @ Sat, 15 Sep 2018 11:04:33: #1 total tags in treatment: 1476451 INFO @ Sat, 15 Sep 2018 11:04:33: #1 user defined the maximum tags... INFO @ Sat, 15 Sep 2018 11:04:33: #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 11:04:33: #1 tags after filtering in treatment: 1476451 INFO @ Sat, 15 Sep 2018 11:04:33: #1 Redundant rate of treatment: 0.00 INFO @ Sat, 15 Sep 2018 11:04:33: #1 finished! INFO @ Sat, 15 Sep 2018 11:04:33: #2 Build Peak Model... INFO @ Sat, 15 Sep 2018 11:04:33: #2 looking for paired plus/minus strand peaks... INFO @ Sat, 15 Sep 2018 11:04:33: #2 number of paired peaks: 67 WARNING @ Sat, 15 Sep 2018 11:04:33: Too few paired peaks (67) 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 11:04:33: Process for pairing-model is terminated! cat: SRX4337757.05_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 `SRX4337757.05_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 `SRX4337757.05_*.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 `SRX4337757.05_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 @ Sat, 15 Sep 2018 11:04:33: #1 tag size is determined as 51 bps INFO @ Sat, 15 Sep 2018 11:04:33: #1 tag size = 51 INFO @ Sat, 15 Sep 2018 11:04:33: #1 total tags in treatment: 1476451 INFO @ Sat, 15 Sep 2018 11:04:33: #1 user defined the maximum tags... INFO @ Sat, 15 Sep 2018 11:04:33: #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 11:04:33: #2 number of paired peaks: 67 WARNING @ Sat, 15 Sep 2018 11:04:33: Too few paired peaks (67) 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 11:04:33: Process for pairing-model is terminated! INFO @ Sat, 15 Sep 2018 11:04:33: #1 tags after filtering in treatment: 1476451 INFO @ Sat, 15 Sep 2018 11:04:33: #1 Redundant rate of treatment: 0.00 INFO @ Sat, 15 Sep 2018 11:04:33: #1 finished! INFO @ Sat, 15 Sep 2018 11:04:33: #2 Build Peak Model... INFO @ Sat, 15 Sep 2018 11:04:33: #2 looking for paired plus/minus strand peaks... cat: SRX4337757.20_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): 0 millis needLargeMem: trying to allocate 0 bytes (limit: 17179869184) rm: cannot remove `SRX4337757.20_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 `SRX4337757.20_*.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 `SRX4337757.20_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 @ Sat, 15 Sep 2018 11:04:33: #2 number of paired peaks: 67 WARNING @ Sat, 15 Sep 2018 11:04:33: Too few paired peaks (67) 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 11:04:33: Process for pairing-model is terminated! cat: SRX4337757.10_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 `SRX4337757.10_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 `SRX4337757.10_*.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 `SRX4337757.10_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。