Job ID = 2640965 sra ファイルのダウンロード中... Read layout: SINGLE fastq に変換中... spots read : 4,890,521 reads read : 4,890,521 reads written : 4,890,521 rm: cannot remove ‘[DSE]RR*’: 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: 00:01:22 4890521 reads; of these: 4890521 (100.00%) were unpaired; of these: 752073 (15.38%) aligned 0 times 3346590 (68.43%) aligned exactly 1 time 791858 (16.19%) aligned >1 times 84.62% overall alignment rate Time searching: 00:01:22 Overall time: 00:01:22 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] 1765334 / 4138448 = 0.4266 in library ' ' BAM に変換しました。 Bed ファイルを作成中... INFO @ Sat, 24 Aug 2019 20:11:30: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/SRX472148/SRX472148.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/SRX472148/SRX472148.05 -q 1e-05 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/SRX472148/SRX472148.05 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/SRX472148/SRX472148.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 @ Sat, 24 Aug 2019 20:11:30: #1 read tag files... INFO @ Sat, 24 Aug 2019 20:11:30: #1 read treatment tags... INFO @ Sat, 24 Aug 2019 20:11:41: 1000000 INFO @ Sat, 24 Aug 2019 20:11:52: 2000000 INFO @ Sat, 24 Aug 2019 20:11:56: #1 tag size is determined as 51 bps INFO @ Sat, 24 Aug 2019 20:11:56: #1 tag size = 51 INFO @ Sat, 24 Aug 2019 20:11:56: #1 total tags in treatment: 2373114 INFO @ Sat, 24 Aug 2019 20:11:56: #1 user defined the maximum tags... INFO @ Sat, 24 Aug 2019 20:11:56: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Sat, 24 Aug 2019 20:11:56: #1 tags after filtering in treatment: 2373114 INFO @ Sat, 24 Aug 2019 20:11:56: #1 Redundant rate of treatment: 0.00 INFO @ Sat, 24 Aug 2019 20:11:56: #1 finished! INFO @ Sat, 24 Aug 2019 20:11:56: #2 Build Peak Model... INFO @ Sat, 24 Aug 2019 20:11:56: #2 looking for paired plus/minus strand peaks... INFO @ Sat, 24 Aug 2019 20:11:56: #2 number of paired peaks: 0 WARNING @ Sat, 24 Aug 2019 20:11:56: 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 @ Sat, 24 Aug 2019 20:11:56: Process for pairing-model is terminated! cut: /home/okishinya/chipatlas/results/sacCer3/SRX472148/SRX472148.05_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/sacCer3/SRX472148/SRX472148.05_model.r’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX472148/SRX472148.05_*.xls’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX472148/SRX472148.05_peaks.narrowPeak’: No such file or directory CompletedMACS2peakCalling INFO @ Sat, 24 Aug 2019 20:12:00: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/SRX472148/SRX472148.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/SRX472148/SRX472148.10 -q 1e-10 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/SRX472148/SRX472148.10 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/SRX472148/SRX472148.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 @ Sat, 24 Aug 2019 20:12:00: #1 read tag files... INFO @ Sat, 24 Aug 2019 20:12:00: #1 read treatment tags... INFO @ Sat, 24 Aug 2019 20:12:11: 1000000 INFO @ Sat, 24 Aug 2019 20:12:21: 2000000 INFO @ Sat, 24 Aug 2019 20:12:25: #1 tag size is determined as 51 bps INFO @ Sat, 24 Aug 2019 20:12:25: #1 tag size = 51 INFO @ Sat, 24 Aug 2019 20:12:25: #1 total tags in treatment: 2373114 INFO @ Sat, 24 Aug 2019 20:12:25: #1 user defined the maximum tags... INFO @ Sat, 24 Aug 2019 20:12:25: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Sat, 24 Aug 2019 20:12:25: #1 tags after filtering in treatment: 2373114 INFO @ Sat, 24 Aug 2019 20:12:25: #1 Redundant rate of treatment: 0.00 INFO @ Sat, 24 Aug 2019 20:12:25: #1 finished! INFO @ Sat, 24 Aug 2019 20:12:25: #2 Build Peak Model... INFO @ Sat, 24 Aug 2019 20:12:25: #2 looking for paired plus/minus strand peaks... INFO @ Sat, 24 Aug 2019 20:12:26: #2 number of paired peaks: 0 WARNING @ Sat, 24 Aug 2019 20:12:26: 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 @ Sat, 24 Aug 2019 20:12:26: Process for pairing-model is terminated! cut: /home/okishinya/chipatlas/results/sacCer3/SRX472148/SRX472148.10_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/sacCer3/SRX472148/SRX472148.10_model.r’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX472148/SRX472148.10_*.xls’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX472148/SRX472148.10_peaks.narrowPeak’: No such file or directory CompletedMACS2peakCalling BedGraph に変換中... INFO @ Sat, 24 Aug 2019 20:12:30: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/SRX472148/SRX472148.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/SRX472148/SRX472148.20 -q 1e-20 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/SRX472148/SRX472148.20 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/SRX472148/SRX472148.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 @ Sat, 24 Aug 2019 20:12:30: #1 read tag files... INFO @ Sat, 24 Aug 2019 20:12:30: #1 read treatment tags... INFO @ Sat, 24 Aug 2019 20:12:41: 1000000 INFO @ Sat, 24 Aug 2019 20:12:51: 2000000 INFO @ Sat, 24 Aug 2019 20:12:54: #1 tag size is determined as 51 bps INFO @ Sat, 24 Aug 2019 20:12:54: #1 tag size = 51 INFO @ Sat, 24 Aug 2019 20:12:54: #1 total tags in treatment: 2373114 INFO @ Sat, 24 Aug 2019 20:12:54: #1 user defined the maximum tags... INFO @ Sat, 24 Aug 2019 20:12:54: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Sat, 24 Aug 2019 20:12:54: #1 tags after filtering in treatment: 2373114 INFO @ Sat, 24 Aug 2019 20:12:54: #1 Redundant rate of treatment: 0.00 INFO @ Sat, 24 Aug 2019 20:12:54: #1 finished! INFO @ Sat, 24 Aug 2019 20:12:54: #2 Build Peak Model... INFO @ Sat, 24 Aug 2019 20:12:54: #2 looking for paired plus/minus strand peaks... INFO @ Sat, 24 Aug 2019 20:12:55: #2 number of paired peaks: 0 WARNING @ Sat, 24 Aug 2019 20:12:55: 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 @ Sat, 24 Aug 2019 20:12:55: Process for pairing-model is terminated! cut: /home/okishinya/chipatlas/results/sacCer3/SRX472148/SRX472148.20_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/sacCer3/SRX472148/SRX472148.20_model.r’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX472148/SRX472148.20_*.xls’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX472148/SRX472148.20_peaks.narrowPeak’: No such file or directory CompletedMACS2peakCalling BedGraph に変換しました。 BigWig に変換中... BigWig に変換しました。