Job ID = 2010857 sra ファイルのダウンロード中... Read layout: SINGLE fastq に変換中... spots read : 7,006,523 reads read : 14,013,046 reads written : 7,006,523 reads 0-length : 7,006,523 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: 00:02:33 7006523 reads; of these: 7006523 (100.00%) were unpaired; of these: 542177 (7.74%) aligned 0 times 5574963 (79.57%) aligned exactly 1 time 889383 (12.69%) aligned >1 times 92.26% overall alignment rate Time searching: 00:02:33 Overall time: 00:02:33 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] 1475545 / 6464346 = 0.2283 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 @ Sat, 06 Jul 2019 01:10:01: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/SRX4140960/SRX4140960.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/SRX4140960/SRX4140960.05 -q 1e-05 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/SRX4140960/SRX4140960.05 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/SRX4140960/SRX4140960.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, 06 Jul 2019 01:10:01: #1 read tag files... INFO @ Sat, 06 Jul 2019 01:10:01: #1 read treatment tags... INFO @ Sat, 06 Jul 2019 01:10:02: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/SRX4140960/SRX4140960.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/SRX4140960/SRX4140960.10 -q 1e-10 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/SRX4140960/SRX4140960.10 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/SRX4140960/SRX4140960.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, 06 Jul 2019 01:10:02: #1 read tag files... INFO @ Sat, 06 Jul 2019 01:10:02: #1 read treatment tags... INFO @ Sat, 06 Jul 2019 01:10:03: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/SRX4140960/SRX4140960.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/SRX4140960/SRX4140960.20 -q 1e-20 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/SRX4140960/SRX4140960.20 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/SRX4140960/SRX4140960.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, 06 Jul 2019 01:10:03: #1 read tag files... INFO @ Sat, 06 Jul 2019 01:10:03: #1 read treatment tags... INFO @ Sat, 06 Jul 2019 01:10:12: 1000000 INFO @ Sat, 06 Jul 2019 01:10:12: 1000000 INFO @ Sat, 06 Jul 2019 01:10:13: 1000000 INFO @ Sat, 06 Jul 2019 01:10:22: 2000000 INFO @ Sat, 06 Jul 2019 01:10:22: 2000000 INFO @ Sat, 06 Jul 2019 01:10:23: 2000000 INFO @ Sat, 06 Jul 2019 01:10:32: 3000000 INFO @ Sat, 06 Jul 2019 01:10:32: 3000000 INFO @ Sat, 06 Jul 2019 01:10:34: 3000000 INFO @ Sat, 06 Jul 2019 01:10:42: 4000000 INFO @ Sat, 06 Jul 2019 01:10:42: 4000000 INFO @ Sat, 06 Jul 2019 01:10:43: 4000000 INFO @ Sat, 06 Jul 2019 01:10:51: #1 tag size is determined as 100 bps INFO @ Sat, 06 Jul 2019 01:10:51: #1 tag size = 100 INFO @ Sat, 06 Jul 2019 01:10:51: #1 total tags in treatment: 4988801 INFO @ Sat, 06 Jul 2019 01:10:51: #1 user defined the maximum tags... INFO @ Sat, 06 Jul 2019 01:10:51: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Sat, 06 Jul 2019 01:10:51: #1 tags after filtering in treatment: 4988801 INFO @ Sat, 06 Jul 2019 01:10:51: #1 Redundant rate of treatment: 0.00 INFO @ Sat, 06 Jul 2019 01:10:51: #1 finished! INFO @ Sat, 06 Jul 2019 01:10:51: #2 Build Peak Model... INFO @ Sat, 06 Jul 2019 01:10:51: #2 looking for paired plus/minus strand peaks... INFO @ Sat, 06 Jul 2019 01:10:52: #2 number of paired peaks: 0 WARNING @ Sat, 06 Jul 2019 01:10:52: 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 @ Sat, 06 Jul 2019 01:10:52: Process for pairing-model is terminated! cut: /home/okishinya/chipatlas/results/sacCer3/SRX4140960/SRX4140960.05_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/SRX4140960/SRX4140960.05_model.r’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX4140960/SRX4140960.05_*.xls’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX4140960/SRX4140960.05_peaks.narrowPeak’: No such file or directory CompletedMACS2peakCalling INFO @ Sat, 06 Jul 2019 01:10:52: #1 tag size is determined as 100 bps INFO @ Sat, 06 Jul 2019 01:10:52: #1 tag size = 100 INFO @ Sat, 06 Jul 2019 01:10:52: #1 total tags in treatment: 4988801 INFO @ Sat, 06 Jul 2019 01:10:52: #1 user defined the maximum tags... INFO @ Sat, 06 Jul 2019 01:10:52: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Sat, 06 Jul 2019 01:10:52: #1 tags after filtering in treatment: 4988801 INFO @ Sat, 06 Jul 2019 01:10:52: #1 Redundant rate of treatment: 0.00 INFO @ Sat, 06 Jul 2019 01:10:52: #1 finished! INFO @ Sat, 06 Jul 2019 01:10:52: #2 Build Peak Model... INFO @ Sat, 06 Jul 2019 01:10:52: #2 looking for paired plus/minus strand peaks... INFO @ Sat, 06 Jul 2019 01:10:53: #2 number of paired peaks: 0 WARNING @ Sat, 06 Jul 2019 01:10:53: 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, 06 Jul 2019 01:10:53: Process for pairing-model is terminated! cut: /home/okishinya/chipatlas/results/sacCer3/SRX4140960/SRX4140960.10_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/SRX4140960/SRX4140960.10_model.r’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX4140960/SRX4140960.10_*.xls’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX4140960/SRX4140960.10_peaks.narrowPeak’: No such file or directory CompletedMACS2peakCalling INFO @ Sat, 06 Jul 2019 01:10:53: #1 tag size is determined as 100 bps INFO @ Sat, 06 Jul 2019 01:10:53: #1 tag size = 100 INFO @ Sat, 06 Jul 2019 01:10:53: #1 total tags in treatment: 4988801 INFO @ Sat, 06 Jul 2019 01:10:53: #1 user defined the maximum tags... INFO @ Sat, 06 Jul 2019 01:10:53: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Sat, 06 Jul 2019 01:10:53: #1 tags after filtering in treatment: 4988801 INFO @ Sat, 06 Jul 2019 01:10:53: #1 Redundant rate of treatment: 0.00 INFO @ Sat, 06 Jul 2019 01:10:53: #1 finished! INFO @ Sat, 06 Jul 2019 01:10:53: #2 Build Peak Model... INFO @ Sat, 06 Jul 2019 01:10:53: #2 looking for paired plus/minus strand peaks... INFO @ Sat, 06 Jul 2019 01:10:54: #2 number of paired peaks: 0 WARNING @ Sat, 06 Jul 2019 01:10:54: 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, 06 Jul 2019 01:10:54: Process for pairing-model is terminated! cut: /home/okishinya/chipatlas/results/sacCer3/SRX4140960/SRX4140960.20_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/SRX4140960/SRX4140960.20_model.r’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX4140960/SRX4140960.20_*.xls’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX4140960/SRX4140960.20_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。