Job ID = 11245091 sra ファイルのダウンロード中... Completed: 243054K bytes transferred in 5 seconds (337768K 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 14345126 spots for /home/okishinya/chipatlas/results/sacCer3/SRX4590910/SRR7734551.sra Written 14345126 spots for /home/okishinya/chipatlas/results/sacCer3/SRX4590910/SRR7734551.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: 00:02:24 14345126 reads; of these: 14345126 (100.00%) were unpaired; of these: 753812 (5.25%) aligned 0 times 11861406 (82.69%) aligned exactly 1 time 1729908 (12.06%) aligned >1 times 94.75% overall alignment rate Time searching: 00:02:24 Overall time: 00:02:24 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] 5263422 / 13591314 = 0.3873 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 @ Tue, 09 Oct 2018 23:25:52: # Command line: callpeak -t SRX4590910.bam -f BAM -g 12100000 -n SRX4590910.05 -q 1e-05 # ARGUMENTS LIST: # name = SRX4590910.05 # format = BAM # ChIP-seq file = ['SRX4590910.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 @ Tue, 09 Oct 2018 23:25:52: #1 read tag files... INFO @ Tue, 09 Oct 2018 23:25:52: #1 read treatment tags... INFO @ Tue, 09 Oct 2018 23:25:52: # Command line: callpeak -t SRX4590910.bam -f BAM -g 12100000 -n SRX4590910.10 -q 1e-10 # ARGUMENTS LIST: # name = SRX4590910.10 # format = BAM # ChIP-seq file = ['SRX4590910.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 @ Tue, 09 Oct 2018 23:25:52: #1 read tag files... INFO @ Tue, 09 Oct 2018 23:25:52: #1 read treatment tags... INFO @ Tue, 09 Oct 2018 23:25:52: # Command line: callpeak -t SRX4590910.bam -f BAM -g 12100000 -n SRX4590910.20 -q 1e-20 # ARGUMENTS LIST: # name = SRX4590910.20 # format = BAM # ChIP-seq file = ['SRX4590910.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 @ Tue, 09 Oct 2018 23:25:52: #1 read tag files... INFO @ Tue, 09 Oct 2018 23:25:52: #1 read treatment tags... INFO @ Tue, 09 Oct 2018 23:25:59: 1000000 INFO @ Tue, 09 Oct 2018 23:25:59: 1000000 INFO @ Tue, 09 Oct 2018 23:25:59: 1000000 INFO @ Tue, 09 Oct 2018 23:26:06: 2000000 INFO @ Tue, 09 Oct 2018 23:26:06: 2000000 INFO @ Tue, 09 Oct 2018 23:26:06: 2000000 INFO @ Tue, 09 Oct 2018 23:26:13: 3000000 INFO @ Tue, 09 Oct 2018 23:26:13: 3000000 INFO @ Tue, 09 Oct 2018 23:26:13: 3000000 INFO @ Tue, 09 Oct 2018 23:26:20: 4000000 INFO @ Tue, 09 Oct 2018 23:26:21: 4000000 INFO @ Tue, 09 Oct 2018 23:26:21: 4000000 INFO @ Tue, 09 Oct 2018 23:26:27: 5000000 INFO @ Tue, 09 Oct 2018 23:26:28: 5000000 INFO @ Tue, 09 Oct 2018 23:26:28: 5000000 INFO @ Tue, 09 Oct 2018 23:26:34: 6000000 INFO @ Tue, 09 Oct 2018 23:26:35: 6000000 INFO @ Tue, 09 Oct 2018 23:26:35: 6000000 INFO @ Tue, 09 Oct 2018 23:26:40: 7000000 INFO @ Tue, 09 Oct 2018 23:26:42: 7000000 INFO @ Tue, 09 Oct 2018 23:26:42: 7000000 INFO @ Tue, 09 Oct 2018 23:26:47: 8000000 INFO @ Tue, 09 Oct 2018 23:26:50: #1 tag size is determined as 51 bps INFO @ Tue, 09 Oct 2018 23:26:50: #1 tag size = 51 INFO @ Tue, 09 Oct 2018 23:26:50: #1 total tags in treatment: 8327892 INFO @ Tue, 09 Oct 2018 23:26:50: #1 user defined the maximum tags... INFO @ Tue, 09 Oct 2018 23:26:50: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Tue, 09 Oct 2018 23:26:50: 8000000 INFO @ Tue, 09 Oct 2018 23:26:50: 8000000 INFO @ Tue, 09 Oct 2018 23:26:50: #1 tags after filtering in treatment: 8327892 INFO @ Tue, 09 Oct 2018 23:26:50: #1 Redundant rate of treatment: 0.00 INFO @ Tue, 09 Oct 2018 23:26:50: #1 finished! INFO @ Tue, 09 Oct 2018 23:26:50: #2 Build Peak Model... INFO @ Tue, 09 Oct 2018 23:26:50: #2 looking for paired plus/minus strand peaks... INFO @ Tue, 09 Oct 2018 23:26:50: #2 number of paired peaks: 0 WARNING @ Tue, 09 Oct 2018 23:26:50: 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 @ Tue, 09 Oct 2018 23:26:50: Process for pairing-model is terminated! cat: SRX4590910.05_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 `SRX4590910.05_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 `SRX4590910.05_*.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 `SRX4590910.05_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 @ Tue, 09 Oct 2018 23:26:52: #1 tag size is determined as 51 bps INFO @ Tue, 09 Oct 2018 23:26:52: #1 tag size = 51 INFO @ Tue, 09 Oct 2018 23:26:52: #1 total tags in treatment: 8327892 INFO @ Tue, 09 Oct 2018 23:26:52: #1 user defined the maximum tags... INFO @ Tue, 09 Oct 2018 23:26:52: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Tue, 09 Oct 2018 23:26:52: #1 tag size is determined as 51 bps INFO @ Tue, 09 Oct 2018 23:26:52: #1 tag size = 51 INFO @ Tue, 09 Oct 2018 23:26:52: #1 total tags in treatment: 8327892 INFO @ Tue, 09 Oct 2018 23:26:52: #1 user defined the maximum tags... INFO @ Tue, 09 Oct 2018 23:26:52: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Tue, 09 Oct 2018 23:26:52: #1 tags after filtering in treatment: 8327892 INFO @ Tue, 09 Oct 2018 23:26:52: #1 Redundant rate of treatment: 0.00 INFO @ Tue, 09 Oct 2018 23:26:52: #1 finished! INFO @ Tue, 09 Oct 2018 23:26:52: #2 Build Peak Model... INFO @ Tue, 09 Oct 2018 23:26:52: #2 looking for paired plus/minus strand peaks... INFO @ Tue, 09 Oct 2018 23:26:52: #1 tags after filtering in treatment: 8327892 INFO @ Tue, 09 Oct 2018 23:26:52: #1 Redundant rate of treatment: 0.00 INFO @ Tue, 09 Oct 2018 23:26:52: #1 finished! INFO @ Tue, 09 Oct 2018 23:26:52: #2 Build Peak Model... INFO @ Tue, 09 Oct 2018 23:26:52: #2 looking for paired plus/minus strand peaks... INFO @ Tue, 09 Oct 2018 23:26:52: #2 number of paired peaks: 0 WARNING @ Tue, 09 Oct 2018 23:26:52: 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 @ Tue, 09 Oct 2018 23:26:52: Process for pairing-model is terminated! cat: SRX4590910.20_peaks.narrowPeak: そのようなファイルやディレクトリはありません INFO @ Tue, 09 Oct 2018 23:26:52: #2 number of paired peaks: 0 WARNING @ Tue, 09 Oct 2018 23:26:52: 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 @ Tue, 09 Oct 2018 23:26:52: Process for pairing-model is terminated! pass1 - making usageList (0 chroms): 1 millis needLargeMem: trying to allocate 0 bytes (limit: 17179869184) rm: cannot remove `SRX4590910.20_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 `SRX4590910.20_*.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 `SRX4590910.20_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 cat: SRX4590910.10_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 `SRX4590910.10_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 `SRX4590910.10_*.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 `SRX4590910.10_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。