Job ID = 2590890 sra ファイルのダウンロード中... Read layout: SINGLE fastq に変換中... spots read : 1,600 reads read : 1,600 reads written : 1,600 rm: cannot remove ‘[DSE]RR*’: No such file or directory rm: cannot remove ‘/home/okishinya/ncbi/public/sra/SRR8559079.sra.cache’: No such file or directory 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: 00:00:00 1600 reads; of these: 1600 (100.00%) were unpaired; of these: 535 (33.44%) aligned 0 times 1006 (62.88%) aligned exactly 1 time 59 (3.69%) aligned >1 times 66.56% overall alignment rate Time searching: 00:00:00 Overall time: 00:00:00 マッピングが完了しました。 samtools でBAM に変換中... [samopen] SAM header is present: 15 sequences. [bam_rmdupse_core] 29 / 1065 = 0.0272 in library ' ' BAM に変換しました。 Bed ファイルを作成中... BedGraph に変換中... BedGraph に変換しました。 BigWig に変換中... BigWig に変換しました。 INFO @ Mon, 12 Aug 2019 23:50:37: # Command line: callpeak -t /home/okishinya/chipatlas/results/dm3/SRX5360573/SRX5360573.bam -f BAM -g dm -n /home/okishinya/chipatlas/results/dm3/SRX5360573/SRX5360573.05 -q 1e-05 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/dm3/SRX5360573/SRX5360573.05 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/dm3/SRX5360573/SRX5360573.bam'] # control file = None # effective genome size = 1.20e+08 # 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, 12 Aug 2019 23:50:37: #1 read tag files... INFO @ Mon, 12 Aug 2019 23:50:37: #1 read treatment tags... INFO @ Mon, 12 Aug 2019 23:50:37: #1 tag size is determined as 50 bps INFO @ Mon, 12 Aug 2019 23:50:37: #1 tag size = 50 INFO @ Mon, 12 Aug 2019 23:50:37: #1 total tags in treatment: 1036 INFO @ Mon, 12 Aug 2019 23:50:37: #1 user defined the maximum tags... INFO @ Mon, 12 Aug 2019 23:50:37: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Mon, 12 Aug 2019 23:50:37: #1 tags after filtering in treatment: 1033 INFO @ Mon, 12 Aug 2019 23:50:37: #1 Redundant rate of treatment: 0.00 INFO @ Mon, 12 Aug 2019 23:50:37: #1 finished! INFO @ Mon, 12 Aug 2019 23:50:37: #2 Build Peak Model... INFO @ Mon, 12 Aug 2019 23:50:37: #2 looking for paired plus/minus strand peaks... INFO @ Mon, 12 Aug 2019 23:50:37: #2 number of paired peaks: 0 WARNING @ Mon, 12 Aug 2019 23:50:37: 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 @ Mon, 12 Aug 2019 23:50:37: Process for pairing-model is terminated! cut: /home/okishinya/chipatlas/results/dm3/SRX5360573/SRX5360573.05_peaks.narrowPeak: No such file or directory pass1 - making usageList (0 chroms): 1 millis needLargeMem: trying to allocate 0 bytes (limit: 17179869184) rm: cannot remove ‘/home/okishinya/chipatlas/results/dm3/SRX5360573/SRX5360573.05_model.r’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/dm3/SRX5360573/SRX5360573.05_*.xls’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/dm3/SRX5360573/SRX5360573.05_peaks.narrowPeak’: No such file or directory CompletedMACS2peakCalling INFO @ Mon, 12 Aug 2019 23:50:38: # Command line: callpeak -t /home/okishinya/chipatlas/results/dm3/SRX5360573/SRX5360573.bam -f BAM -g dm -n /home/okishinya/chipatlas/results/dm3/SRX5360573/SRX5360573.10 -q 1e-10 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/dm3/SRX5360573/SRX5360573.10 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/dm3/SRX5360573/SRX5360573.bam'] # control file = None # effective genome size = 1.20e+08 # 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, 12 Aug 2019 23:50:38: #1 read tag files... INFO @ Mon, 12 Aug 2019 23:50:38: #1 read treatment tags... INFO @ Mon, 12 Aug 2019 23:50:38: #1 tag size is determined as 50 bps INFO @ Mon, 12 Aug 2019 23:50:38: #1 tag size = 50 INFO @ Mon, 12 Aug 2019 23:50:38: #1 total tags in treatment: 1036 INFO @ Mon, 12 Aug 2019 23:50:38: #1 user defined the maximum tags... INFO @ Mon, 12 Aug 2019 23:50:38: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Mon, 12 Aug 2019 23:50:38: #1 tags after filtering in treatment: 1033 INFO @ Mon, 12 Aug 2019 23:50:38: #1 Redundant rate of treatment: 0.00 INFO @ Mon, 12 Aug 2019 23:50:38: #1 finished! INFO @ Mon, 12 Aug 2019 23:50:38: #2 Build Peak Model... INFO @ Mon, 12 Aug 2019 23:50:38: #2 looking for paired plus/minus strand peaks... INFO @ Mon, 12 Aug 2019 23:50:38: #2 number of paired peaks: 0 WARNING @ Mon, 12 Aug 2019 23:50:38: 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 @ Mon, 12 Aug 2019 23:50:38: Process for pairing-model is terminated! cut: /home/okishinya/chipatlas/results/dm3/SRX5360573/SRX5360573.10_peaks.narrowPeak: No such file or directory pass1 - making usageList (0 chroms): 2 millis needLargeMem: trying to allocate 0 bytes (limit: 17179869184) rm: cannot remove ‘/home/okishinya/chipatlas/results/dm3/SRX5360573/SRX5360573.10_model.r’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/dm3/SRX5360573/SRX5360573.10_*.xls’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/dm3/SRX5360573/SRX5360573.10_peaks.narrowPeak’: No such file or directory CompletedMACS2peakCalling INFO @ Mon, 12 Aug 2019 23:50:39: # Command line: callpeak -t /home/okishinya/chipatlas/results/dm3/SRX5360573/SRX5360573.bam -f BAM -g dm -n /home/okishinya/chipatlas/results/dm3/SRX5360573/SRX5360573.20 -q 1e-20 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/dm3/SRX5360573/SRX5360573.20 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/dm3/SRX5360573/SRX5360573.bam'] # control file = None # effective genome size = 1.20e+08 # 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, 12 Aug 2019 23:50:39: #1 read tag files... INFO @ Mon, 12 Aug 2019 23:50:39: #1 read treatment tags... INFO @ Mon, 12 Aug 2019 23:50:39: #1 tag size is determined as 50 bps INFO @ Mon, 12 Aug 2019 23:50:39: #1 tag size = 50 INFO @ Mon, 12 Aug 2019 23:50:39: #1 total tags in treatment: 1036 INFO @ Mon, 12 Aug 2019 23:50:39: #1 user defined the maximum tags... INFO @ Mon, 12 Aug 2019 23:50:39: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Mon, 12 Aug 2019 23:50:39: #1 tags after filtering in treatment: 1033 INFO @ Mon, 12 Aug 2019 23:50:39: #1 Redundant rate of treatment: 0.00 INFO @ Mon, 12 Aug 2019 23:50:39: #1 finished! INFO @ Mon, 12 Aug 2019 23:50:39: #2 Build Peak Model... INFO @ Mon, 12 Aug 2019 23:50:39: #2 looking for paired plus/minus strand peaks... INFO @ Mon, 12 Aug 2019 23:50:39: #2 number of paired peaks: 0 WARNING @ Mon, 12 Aug 2019 23:50:39: 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 @ Mon, 12 Aug 2019 23:50:39: Process for pairing-model is terminated! cut: /home/okishinya/chipatlas/results/dm3/SRX5360573/SRX5360573.20_peaks.narrowPeak: No such file or directory pass1 - making usageList (0 chroms): 1 millis needLargeMem: trying to allocate 0 bytes (limit: 17179869184) rm: cannot remove ‘/home/okishinya/chipatlas/results/dm3/SRX5360573/SRX5360573.20_model.r’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/dm3/SRX5360573/SRX5360573.20_*.xls’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/dm3/SRX5360573/SRX5360573.20_peaks.narrowPeak’: No such file or directory CompletedMACS2peakCalling