Job ID = 11634638 sra ファイルのダウンロード中... Completed: 662879K bytes transferred in 9 seconds (596578K 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 16684226 spots for /home/okishinya/chipatlas/results/sacCer3/SRX3933750/SRR7000952.sra Written 16684226 spots for /home/okishinya/chipatlas/results/sacCer3/SRX3933750/SRR7000952.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: 00:04:28 16684226 reads; of these: 16684226 (100.00%) were unpaired; of these: 3397197 (20.36%) aligned 0 times 12070999 (72.35%) aligned exactly 1 time 1216030 (7.29%) aligned >1 times 79.64% overall alignment rate Time searching: 00:04:28 Overall time: 00:04:28 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_sort_core] merging from 8 files... [bam_rmdupse_core] 7502490 / 13287029 = 0.5646 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 10:28:31: # Command line: callpeak -t SRX3933750.bam -f BAM -g 12100000 -n SRX3933750.10 -q 1e-10 # ARGUMENTS LIST: # name = SRX3933750.10 # format = BAM # ChIP-seq file = ['SRX3933750.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 10:28:31: #1 read tag files... INFO @ Fri, 15 Feb 2019 10:28:31: #1 read treatment tags... INFO @ Fri, 15 Feb 2019 10:28:31: # Command line: callpeak -t SRX3933750.bam -f BAM -g 12100000 -n SRX3933750.05 -q 1e-05 # ARGUMENTS LIST: # name = SRX3933750.05 # format = BAM # ChIP-seq file = ['SRX3933750.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 10:28:31: #1 read tag files... INFO @ Fri, 15 Feb 2019 10:28:31: #1 read treatment tags... INFO @ Fri, 15 Feb 2019 10:28:31: # Command line: callpeak -t SRX3933750.bam -f BAM -g 12100000 -n SRX3933750.20 -q 1e-20 # ARGUMENTS LIST: # name = SRX3933750.20 # format = BAM # ChIP-seq file = ['SRX3933750.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 10:28:31: #1 read tag files... INFO @ Fri, 15 Feb 2019 10:28:31: #1 read treatment tags... INFO @ Fri, 15 Feb 2019 10:28:39: 1000000 INFO @ Fri, 15 Feb 2019 10:28:39: 1000000 INFO @ Fri, 15 Feb 2019 10:28:39: 1000000 INFO @ Fri, 15 Feb 2019 10:28:47: 2000000 INFO @ Fri, 15 Feb 2019 10:28:48: 2000000 INFO @ Fri, 15 Feb 2019 10:28:48: 2000000 INFO @ Fri, 15 Feb 2019 10:28:55: 3000000 INFO @ Fri, 15 Feb 2019 10:28:56: 3000000 INFO @ Fri, 15 Feb 2019 10:28:56: 3000000 INFO @ Fri, 15 Feb 2019 10:29:03: 4000000 INFO @ Fri, 15 Feb 2019 10:29:04: 4000000 INFO @ Fri, 15 Feb 2019 10:29:04: 4000000 INFO @ Fri, 15 Feb 2019 10:29:11: 5000000 INFO @ Fri, 15 Feb 2019 10:29:12: 5000000 INFO @ Fri, 15 Feb 2019 10:29:12: 5000000 INFO @ Fri, 15 Feb 2019 10:29:17: #1 tag size is determined as 82 bps INFO @ Fri, 15 Feb 2019 10:29:17: #1 tag size = 82 INFO @ Fri, 15 Feb 2019 10:29:17: #1 total tags in treatment: 5784539 INFO @ Fri, 15 Feb 2019 10:29:17: #1 user defined the maximum tags... INFO @ Fri, 15 Feb 2019 10:29:17: #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 10:29:17: #1 tags after filtering in treatment: 5784539 INFO @ Fri, 15 Feb 2019 10:29:17: #1 Redundant rate of treatment: 0.00 INFO @ Fri, 15 Feb 2019 10:29:17: #1 finished! INFO @ Fri, 15 Feb 2019 10:29:17: #2 Build Peak Model... INFO @ Fri, 15 Feb 2019 10:29:17: #2 looking for paired plus/minus strand peaks... INFO @ Fri, 15 Feb 2019 10:29:17: #2 number of paired peaks: 0 WARNING @ Fri, 15 Feb 2019 10:29:17: 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 @ Fri, 15 Feb 2019 10:29:17: Process for pairing-model is terminated! cat: SRX3933750.10_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): 5 millis needLargeMem: trying to allocate 0 bytes (limit: 17179869184) rm: cannot remove `SRX3933750.10_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 `SRX3933750.10_*.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 `SRX3933750.10_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 @ Fri, 15 Feb 2019 10:29:18: #1 tag size is determined as 82 bps INFO @ Fri, 15 Feb 2019 10:29:18: #1 tag size = 82 INFO @ Fri, 15 Feb 2019 10:29:18: #1 total tags in treatment: 5784539 INFO @ Fri, 15 Feb 2019 10:29:18: #1 user defined the maximum tags... INFO @ Fri, 15 Feb 2019 10:29:18: #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 10:29:18: #1 tags after filtering in treatment: 5784539 INFO @ Fri, 15 Feb 2019 10:29:18: #1 Redundant rate of treatment: 0.00 INFO @ Fri, 15 Feb 2019 10:29:18: #1 finished! INFO @ Fri, 15 Feb 2019 10:29:18: #2 Build Peak Model... INFO @ Fri, 15 Feb 2019 10:29:18: #2 looking for paired plus/minus strand peaks... INFO @ Fri, 15 Feb 2019 10:29:19: #1 tag size is determined as 82 bps INFO @ Fri, 15 Feb 2019 10:29:19: #1 tag size = 82 INFO @ Fri, 15 Feb 2019 10:29:19: #1 total tags in treatment: 5784539 INFO @ Fri, 15 Feb 2019 10:29:19: #1 user defined the maximum tags... INFO @ Fri, 15 Feb 2019 10:29:19: #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 10:29:19: #1 tags after filtering in treatment: 5784539 INFO @ Fri, 15 Feb 2019 10:29:19: #1 Redundant rate of treatment: 0.00 INFO @ Fri, 15 Feb 2019 10:29:19: #1 finished! INFO @ Fri, 15 Feb 2019 10:29:19: #2 Build Peak Model... INFO @ Fri, 15 Feb 2019 10:29:19: #2 looking for paired plus/minus strand peaks... INFO @ Fri, 15 Feb 2019 10:29:19: #2 number of paired peaks: 0 WARNING @ Fri, 15 Feb 2019 10:29:19: 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 @ Fri, 15 Feb 2019 10:29:19: Process for pairing-model is terminated! cat: SRX3933750.05_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): 7 millis needLargeMem: trying to allocate 0 bytes (limit: 17179869184) rm: cannot remove `SRX3933750.05_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 `SRX3933750.05_*.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 `SRX3933750.05_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 10:29:19: #2 number of paired peaks: 0 WARNING @ Fri, 15 Feb 2019 10:29:19: 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 @ Fri, 15 Feb 2019 10:29:19: Process for pairing-model is terminated! cat: SRX3933750.20_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): 7 millis needLargeMem: trying to allocate 0 bytes (limit: 17179869184) rm: cannot remove `SRX3933750.20_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 `SRX3933750.20_*.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 `SRX3933750.20_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。