Job ID = 11634669 sra ファイルのダウンロード中... Completed: 134672K bytes transferred in 4 seconds (231541K 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 6881074 spots for /home/okishinya/chipatlas/results/sacCer3/SRX4092949/SRR7175377.sra Written 6881074 spots for /home/okishinya/chipatlas/results/sacCer3/SRX4092949/SRR7175377.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: 00:01:02 6881074 reads; of these: 6881074 (100.00%) were unpaired; of these: 1366559 (19.86%) aligned 0 times 3464191 (50.34%) aligned exactly 1 time 2050324 (29.80%) aligned >1 times 80.14% overall alignment rate Time searching: 00:01:02 Overall time: 00:01:02 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] 2921509 / 5514515 = 0.5298 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 10:36:32: # Command line: callpeak -t SRX4092949.bam -f BAM -g 12100000 -n SRX4092949.20 -q 1e-20 # ARGUMENTS LIST: # name = SRX4092949.20 # format = BAM # ChIP-seq file = ['SRX4092949.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 10:36:32: #1 read tag files... INFO @ Fri, 15 Feb 2019 10:36:32: #1 read treatment tags... INFO @ Fri, 15 Feb 2019 10:36:32: # Command line: callpeak -t SRX4092949.bam -f BAM -g 12100000 -n SRX4092949.10 -q 1e-10 # ARGUMENTS LIST: # name = SRX4092949.10 # format = BAM # ChIP-seq file = ['SRX4092949.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 10:36:32: #1 read tag files... INFO @ Fri, 15 Feb 2019 10:36:32: #1 read treatment tags... INFO @ Fri, 15 Feb 2019 10:36:32: # Command line: callpeak -t SRX4092949.bam -f BAM -g 12100000 -n SRX4092949.05 -q 1e-05 # ARGUMENTS LIST: # name = SRX4092949.05 # format = BAM # ChIP-seq file = ['SRX4092949.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 10:36:32: #1 read tag files... INFO @ Fri, 15 Feb 2019 10:36:32: #1 read treatment tags... INFO @ Fri, 15 Feb 2019 10:36:39: 1000000 INFO @ Fri, 15 Feb 2019 10:36:39: 1000000 INFO @ Fri, 15 Feb 2019 10:36:39: 1000000 INFO @ Fri, 15 Feb 2019 10:36:45: 2000000 INFO @ Fri, 15 Feb 2019 10:36:45: 2000000 INFO @ Fri, 15 Feb 2019 10:36:45: 2000000 INFO @ Fri, 15 Feb 2019 10:36:49: #1 tag size is determined as 50 bps INFO @ Fri, 15 Feb 2019 10:36:49: #1 tag size = 50 INFO @ Fri, 15 Feb 2019 10:36:49: #1 total tags in treatment: 2593006 INFO @ Fri, 15 Feb 2019 10:36:49: #1 user defined the maximum tags... INFO @ Fri, 15 Feb 2019 10:36:49: #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 10:36:49: #1 tags after filtering in treatment: 2593006 INFO @ Fri, 15 Feb 2019 10:36:49: #1 Redundant rate of treatment: 0.00 INFO @ Fri, 15 Feb 2019 10:36:49: #1 finished! INFO @ Fri, 15 Feb 2019 10:36:49: #2 Build Peak Model... INFO @ Fri, 15 Feb 2019 10:36:49: #2 looking for paired plus/minus strand peaks... INFO @ Fri, 15 Feb 2019 10:36:49: #1 tag size is determined as 50 bps INFO @ Fri, 15 Feb 2019 10:36:49: #1 tag size = 50 INFO @ Fri, 15 Feb 2019 10:36:49: #1 total tags in treatment: 2593006 INFO @ Fri, 15 Feb 2019 10:36:49: #1 user defined the maximum tags... INFO @ Fri, 15 Feb 2019 10:36:49: #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 10:36:49: #1 tag size is determined as 50 bps INFO @ Fri, 15 Feb 2019 10:36:49: #1 tag size = 50 INFO @ Fri, 15 Feb 2019 10:36:49: #1 total tags in treatment: 2593006 INFO @ Fri, 15 Feb 2019 10:36:49: #1 user defined the maximum tags... INFO @ Fri, 15 Feb 2019 10:36:49: #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 10:36:49: #1 tags after filtering in treatment: 2593006 INFO @ Fri, 15 Feb 2019 10:36:49: #1 Redundant rate of treatment: 0.00 INFO @ Fri, 15 Feb 2019 10:36:49: #1 finished! INFO @ Fri, 15 Feb 2019 10:36:49: #2 Build Peak Model... INFO @ Fri, 15 Feb 2019 10:36:49: #2 looking for paired plus/minus strand peaks... INFO @ Fri, 15 Feb 2019 10:36:49: #1 tags after filtering in treatment: 2593006 INFO @ Fri, 15 Feb 2019 10:36:49: #1 Redundant rate of treatment: 0.00 INFO @ Fri, 15 Feb 2019 10:36:49: #1 finished! INFO @ Fri, 15 Feb 2019 10:36:49: #2 Build Peak Model... INFO @ Fri, 15 Feb 2019 10:36:49: #2 looking for paired plus/minus strand peaks... INFO @ Fri, 15 Feb 2019 10:36:49: #2 number of paired peaks: 36 WARNING @ Fri, 15 Feb 2019 10:36:49: Too few paired peaks (36) 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 10:36:49: Process for pairing-model is terminated! cat: SRX4092949.20_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): 3 millis needLargeMem: trying to allocate 0 bytes (limit: 17179869184) rm: cannot remove `SRX4092949.20_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 `SRX4092949.20_*.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 `SRX4092949.20_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 @ Fri, 15 Feb 2019 10:36:49: #2 number of paired peaks: 36 WARNING @ Fri, 15 Feb 2019 10:36:49: Too few paired peaks (36) 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 10:36:49: Process for pairing-model is terminated! cat: SRX4092949.05_peaks.narrowPeak: そのようなファイルやディレクトリはありません INFO @ Fri, 15 Feb 2019 10:36:49: #2 number of paired peaks: 36 WARNING @ Fri, 15 Feb 2019 10:36:49: Too few paired peaks (36) 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 10:36:49: Process for pairing-model is terminated! pass1 - making usageList (0 chroms): 5 millis cat: needLargeMem: trying to allocate 0 bytes (limit: 17179869184)SRX4092949.10_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 `SRX4092949.05_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 `SRX4092949.05_*.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 `SRX4092949.05_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 pass1 - making usageList (0 chroms): 2 millis needLargeMem: trying to allocate 0 bytes (limit: 17179869184) rm: cannot remove `SRX4092949.10_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 `SRX4092949.10_*.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 `SRX4092949.10_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。