Job ID = 11633722 sra ファイルのダウンロード中... Completed: 40428K bytes transferred in 3 seconds (87058K 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 1264337 spots for /home/okishinya/chipatlas/results/sacCer3/ERX1420341/ERR1348817.sra Written 1264337 spots for /home/okishinya/chipatlas/results/sacCer3/ERX1420341/ERR1348817.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: 00:00:10 1264337 reads; of these: 1264337 (100.00%) were unpaired; of these: 708513 (56.04%) aligned 0 times 486469 (38.48%) aligned exactly 1 time 69355 (5.49%) aligned >1 times 43.96% overall alignment rate Time searching: 00:00:10 Overall time: 00:00:10 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] 24053 / 555824 = 0.0433 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 @ Fri, 15 Feb 2019 09:10:30: # Command line: callpeak -t ERX1420341.bam -f BAM -g 12100000 -n ERX1420341.05 -q 1e-05 # ARGUMENTS LIST: # name = ERX1420341.05 # format = BAM # ChIP-seq file = ['ERX1420341.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 @ Fri, 15 Feb 2019 09:10:30: #1 read tag files... INFO @ Fri, 15 Feb 2019 09:10:30: #1 read treatment tags... INFO @ Fri, 15 Feb 2019 09:10:30: # Command line: callpeak -t ERX1420341.bam -f BAM -g 12100000 -n ERX1420341.20 -q 1e-20 # ARGUMENTS LIST: # name = ERX1420341.20 # format = BAM # ChIP-seq file = ['ERX1420341.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 @ Fri, 15 Feb 2019 09:10:30: #1 read tag files... INFO @ Fri, 15 Feb 2019 09:10:30: #1 read treatment tags... INFO @ Fri, 15 Feb 2019 09:10:30: # Command line: callpeak -t ERX1420341.bam -f BAM -g 12100000 -n ERX1420341.10 -q 1e-10 # ARGUMENTS LIST: # name = ERX1420341.10 # format = BAM # ChIP-seq file = ['ERX1420341.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 @ Fri, 15 Feb 2019 09:10:30: #1 read tag files... INFO @ Fri, 15 Feb 2019 09:10:30: #1 read treatment tags... INFO @ Fri, 15 Feb 2019 09:10:34: #1 tag size is determined as 51 bps INFO @ Fri, 15 Feb 2019 09:10:34: #1 tag size = 51 INFO @ Fri, 15 Feb 2019 09:10:34: #1 total tags in treatment: 531771 INFO @ Fri, 15 Feb 2019 09:10:34: #1 user defined the maximum tags... INFO @ Fri, 15 Feb 2019 09:10:34: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Fri, 15 Feb 2019 09:10:34: #1 tag size is determined as 51 bps INFO @ Fri, 15 Feb 2019 09:10:34: #1 tag size = 51 INFO @ Fri, 15 Feb 2019 09:10:34: #1 total tags in treatment: 531771 INFO @ Fri, 15 Feb 2019 09:10:34: #1 user defined the maximum tags... INFO @ Fri, 15 Feb 2019 09:10:34: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Fri, 15 Feb 2019 09:10:34: #1 tags after filtering in treatment: 531771 INFO @ Fri, 15 Feb 2019 09:10:34: #1 Redundant rate of treatment: 0.00 INFO @ Fri, 15 Feb 2019 09:10:34: #1 finished! INFO @ Fri, 15 Feb 2019 09:10:34: #2 Build Peak Model... INFO @ Fri, 15 Feb 2019 09:10:34: #2 looking for paired plus/minus strand peaks... INFO @ Fri, 15 Feb 2019 09:10:34: #1 tags after filtering in treatment: 531771 INFO @ Fri, 15 Feb 2019 09:10:34: #1 Redundant rate of treatment: 0.00 INFO @ Fri, 15 Feb 2019 09:10:34: #1 finished! INFO @ Fri, 15 Feb 2019 09:10:34: #2 Build Peak Model... INFO @ Fri, 15 Feb 2019 09:10:34: #2 looking for paired plus/minus strand peaks... INFO @ Fri, 15 Feb 2019 09:10:34: #2 number of paired peaks: 31 WARNING @ Fri, 15 Feb 2019 09:10:34: Too few paired peaks (31) 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 @ Fri, 15 Feb 2019 09:10:34: Process for pairing-model is terminated! INFO @ Fri, 15 Feb 2019 09:10:34: #2 number of paired peaks: 31 WARNING @ Fri, 15 Feb 2019 09:10:34: Too few paired peaks (31) 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 @ Fri, 15 Feb 2019 09:10:34: Process for pairing-model is terminated! cat: ERX1420341.10_peaks.narrowPeak: そのようなファイルやディレクトリはありません cat: ERX1420341.05_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): 4 millis needLargeMem: trying to allocate 0 bytes (limit: 17179869184) pass1 - making usageList (0 chroms): 3 millis needLargeMem: trying to allocate 0 bytes (limit: 17179869184) rm: cannot remove `ERX1420341.10_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 `ERX1420341.10_*.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 `ERX1420341.10_peaks.narrowPeak': そのようなファイルやディレクトリはありません rm: cannot remove `ERX1420341.05_model.r': そのようなファイルやディレクトリはありません CompletedMACS2peakCalling rm: cannot remove `ERX1420341.05_*.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 `ERX1420341.05_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 @ Fri, 15 Feb 2019 09:10:34: #1 tag size is determined as 51 bps INFO @ Fri, 15 Feb 2019 09:10:34: #1 tag size = 51 INFO @ Fri, 15 Feb 2019 09:10:34: #1 total tags in treatment: 531771 INFO @ Fri, 15 Feb 2019 09:10:34: #1 user defined the maximum tags... INFO @ Fri, 15 Feb 2019 09:10:34: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Fri, 15 Feb 2019 09:10:34: #1 tags after filtering in treatment: 531771 INFO @ Fri, 15 Feb 2019 09:10:34: #1 Redundant rate of treatment: 0.00 INFO @ Fri, 15 Feb 2019 09:10:34: #1 finished! INFO @ Fri, 15 Feb 2019 09:10:34: #2 Build Peak Model... INFO @ Fri, 15 Feb 2019 09:10:34: #2 looking for paired plus/minus strand peaks... INFO @ Fri, 15 Feb 2019 09:10:34: #2 number of paired peaks: 31 WARNING @ Fri, 15 Feb 2019 09:10:34: Too few paired peaks (31) 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 @ Fri, 15 Feb 2019 09:10:34: Process for pairing-model is terminated! cat: ERX1420341.20_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): 2 millis needLargeMem: trying to allocate 0 bytes (limit: 17179869184) rm: cannot remove `ERX1420341.20_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 `ERX1420341.20_*.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 `ERX1420341.20_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。