Job ID = 10721721 sra ファイルのダウンロード中... Completed: 662939K bytes transferred in 15 seconds (355383K 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 19746636 spots for /home/okishinya/chipatlas/results/sacCer3/SRX2766308/SRR5482936.sra Written 19746636 spots for /home/okishinya/chipatlas/results/sacCer3/SRX2766308/SRR5482936.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: 00:03:10 19746636 reads; of these: 19746636 (100.00%) were unpaired; of these: 7200734 (36.47%) aligned 0 times 9248146 (46.83%) aligned exactly 1 time 3297756 (16.70%) aligned >1 times 63.53% overall alignment rate Time searching: 00:03:10 Overall time: 00:03:10 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_sort_core] merging from 8 files... [bam_rmdupse_core] 8144552 / 12545902 = 0.6492 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 @ Mon, 04 Jun 2018 03:48:55: # Command line: callpeak -t SRX2766308.bam -f BAM -g 12100000 -n SRX2766308.20 -q 1e-20 # ARGUMENTS LIST: # name = SRX2766308.20 # format = BAM # ChIP-seq file = ['SRX2766308.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 @ Mon, 04 Jun 2018 03:48:55: # Command line: callpeak -t SRX2766308.bam -f BAM -g 12100000 -n SRX2766308.05 -q 1e-05 # ARGUMENTS LIST: # name = SRX2766308.05 # format = BAM # ChIP-seq file = ['SRX2766308.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 @ Mon, 04 Jun 2018 03:48:55: #1 read tag files... INFO @ Mon, 04 Jun 2018 03:48:55: #1 read tag files... INFO @ Mon, 04 Jun 2018 03:48:55: #1 read treatment tags... INFO @ Mon, 04 Jun 2018 03:48:55: #1 read treatment tags... INFO @ Mon, 04 Jun 2018 03:48:55: # Command line: callpeak -t SRX2766308.bam -f BAM -g 12100000 -n SRX2766308.10 -q 1e-10 # ARGUMENTS LIST: # name = SRX2766308.10 # format = BAM # ChIP-seq file = ['SRX2766308.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 @ Mon, 04 Jun 2018 03:48:55: #1 read tag files... INFO @ Mon, 04 Jun 2018 03:48:55: #1 read treatment tags... INFO @ Mon, 04 Jun 2018 03:49:01: 1000000 INFO @ Mon, 04 Jun 2018 03:49:01: 1000000 INFO @ Mon, 04 Jun 2018 03:49:01: 1000000 INFO @ Mon, 04 Jun 2018 03:49:07: 2000000 INFO @ Mon, 04 Jun 2018 03:49:07: 2000000 INFO @ Mon, 04 Jun 2018 03:49:07: 2000000 INFO @ Mon, 04 Jun 2018 03:49:13: 3000000 INFO @ Mon, 04 Jun 2018 03:49:13: 3000000 INFO @ Mon, 04 Jun 2018 03:49:13: 3000000 INFO @ Mon, 04 Jun 2018 03:49:19: 4000000 INFO @ Mon, 04 Jun 2018 03:49:19: 4000000 INFO @ Mon, 04 Jun 2018 03:49:19: 4000000 INFO @ Mon, 04 Jun 2018 03:49:21: #1 tag size is determined as 50 bps INFO @ Mon, 04 Jun 2018 03:49:21: #1 tag size = 50 INFO @ Mon, 04 Jun 2018 03:49:21: #1 total tags in treatment: 4401350 INFO @ Mon, 04 Jun 2018 03:49:21: #1 user defined the maximum tags... INFO @ Mon, 04 Jun 2018 03:49:21: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Mon, 04 Jun 2018 03:49:22: #1 tags after filtering in treatment: 4401350 INFO @ Mon, 04 Jun 2018 03:49:22: #1 Redundant rate of treatment: 0.00 INFO @ Mon, 04 Jun 2018 03:49:22: #1 finished! INFO @ Mon, 04 Jun 2018 03:49:22: #2 Build Peak Model... INFO @ Mon, 04 Jun 2018 03:49:22: #2 looking for paired plus/minus strand peaks... INFO @ Mon, 04 Jun 2018 03:49:22: #1 tag size is determined as 50 bps INFO @ Mon, 04 Jun 2018 03:49:22: #1 tag size = 50 INFO @ Mon, 04 Jun 2018 03:49:22: #1 total tags in treatment: 4401350 INFO @ Mon, 04 Jun 2018 03:49:22: #1 user defined the maximum tags... INFO @ Mon, 04 Jun 2018 03:49:22: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Mon, 04 Jun 2018 03:49:22: #1 tag size is determined as 50 bps INFO @ Mon, 04 Jun 2018 03:49:22: #1 tag size = 50 INFO @ Mon, 04 Jun 2018 03:49:22: #1 total tags in treatment: 4401350 INFO @ Mon, 04 Jun 2018 03:49:22: #1 user defined the maximum tags... INFO @ Mon, 04 Jun 2018 03:49:22: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Mon, 04 Jun 2018 03:49:22: #1 tags after filtering in treatment: 4401350 INFO @ Mon, 04 Jun 2018 03:49:22: #1 Redundant rate of treatment: 0.00 INFO @ Mon, 04 Jun 2018 03:49:22: #1 finished! INFO @ Mon, 04 Jun 2018 03:49:22: #2 Build Peak Model... INFO @ Mon, 04 Jun 2018 03:49:22: #2 looking for paired plus/minus strand peaks... INFO @ Mon, 04 Jun 2018 03:49:22: #1 tags after filtering in treatment: 4401350 INFO @ Mon, 04 Jun 2018 03:49:22: #1 Redundant rate of treatment: 0.00 INFO @ Mon, 04 Jun 2018 03:49:22: #1 finished! INFO @ Mon, 04 Jun 2018 03:49:22: #2 Build Peak Model... INFO @ Mon, 04 Jun 2018 03:49:22: #2 looking for paired plus/minus strand peaks... INFO @ Mon, 04 Jun 2018 03:49:22: #2 number of paired peaks: 31 WARNING @ Mon, 04 Jun 2018 03:49:22: 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 @ Mon, 04 Jun 2018 03:49:22: Process for pairing-model is terminated! cat: SRX2766308.05_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 `SRX2766308.05_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 `SRX2766308.05_*.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 `SRX2766308.05_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 @ Mon, 04 Jun 2018 03:49:22: #2 number of paired peaks: 31 WARNING @ Mon, 04 Jun 2018 03:49:22: 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 @ Mon, 04 Jun 2018 03:49:22: Process for pairing-model is terminated! cat: SRX2766308.20_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 @ Mon, 04 Jun 2018 03:49:22: #2 number of paired peaks: 31 WARNING @ Mon, 04 Jun 2018 03:49:22: 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 @ Mon, 04 Jun 2018 03:49:22: Process for pairing-model is terminated! pass1 - making usageList (0 chroms): 1 millis needLargeMem: trying to allocate 0 bytes (limit: 17179869184) cat: SRX2766308.10_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 `SRX2766308.20_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 `SRX2766308.20_*.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 `SRX2766308.20_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 pass1 - making usageList (0 chroms): 1 millis needLargeMem: trying to allocate 0 bytes (limit: 17179869184) rm: cannot remove `SRX2766308.10_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 `SRX2766308.10_*.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 `SRX2766308.10_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。