Job ID = 2640824 sra ファイルのダウンロード中... Read layout: SINGLE fastq に変換中... spots read : 8,351,298 reads read : 8,351,298 reads written : 8,351,298 rm: cannot remove ‘[DSE]RR*’: No such file or directory rm: cannot remove ‘/home/okishinya/ncbi/public/sra/SRR6322054.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: 00:01:38 8351298 reads; of these: 8351298 (100.00%) were unpaired; of these: 297999 (3.57%) aligned 0 times 7430537 (88.97%) aligned exactly 1 time 622762 (7.46%) aligned >1 times 96.43% overall alignment rate Time searching: 00:01:38 Overall time: 00:01:38 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] 1699322 / 8053299 = 0.2110 in library ' ' BAM に変換しました。 Bed ファイルを作成中... INFO @ Sat, 24 Aug 2019 19:24:13: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/SRX3421877/SRX3421877.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/SRX3421877/SRX3421877.05 -q 1e-05 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/SRX3421877/SRX3421877.05 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/SRX3421877/SRX3421877.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 19:24:13: #1 read tag files... INFO @ Sat, 24 Aug 2019 19:24:13: #1 read treatment tags... INFO @ Sat, 24 Aug 2019 19:24:21: 1000000 INFO @ Sat, 24 Aug 2019 19:24:28: 2000000 INFO @ Sat, 24 Aug 2019 19:24:35: 3000000 INFO @ Sat, 24 Aug 2019 19:24:42: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/SRX3421877/SRX3421877.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/SRX3421877/SRX3421877.10 -q 1e-10 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/SRX3421877/SRX3421877.10 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/SRX3421877/SRX3421877.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 19:24:42: #1 read tag files... INFO @ Sat, 24 Aug 2019 19:24:42: #1 read treatment tags... INFO @ Sat, 24 Aug 2019 19:24:42: 4000000 INFO @ Sat, 24 Aug 2019 19:24:50: 5000000 INFO @ Sat, 24 Aug 2019 19:24:51: 1000000 INFO @ Sat, 24 Aug 2019 19:24:59: 6000000 INFO @ Sat, 24 Aug 2019 19:24:59: 2000000 INFO @ Sat, 24 Aug 2019 19:25:01: #1 tag size is determined as 51 bps INFO @ Sat, 24 Aug 2019 19:25:01: #1 tag size = 51 INFO @ Sat, 24 Aug 2019 19:25:01: #1 total tags in treatment: 6353977 INFO @ Sat, 24 Aug 2019 19:25:01: #1 user defined the maximum tags... INFO @ Sat, 24 Aug 2019 19:25:01: #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 19:25:01: #1 tags after filtering in treatment: 6353977 INFO @ Sat, 24 Aug 2019 19:25:01: #1 Redundant rate of treatment: 0.00 INFO @ Sat, 24 Aug 2019 19:25:01: #1 finished! INFO @ Sat, 24 Aug 2019 19:25:01: #2 Build Peak Model... INFO @ Sat, 24 Aug 2019 19:25:01: #2 looking for paired plus/minus strand peaks... INFO @ Sat, 24 Aug 2019 19:25:02: #2 number of paired peaks: 0 WARNING @ Sat, 24 Aug 2019 19:25:02: 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 19:25:02: Process for pairing-model is terminated! cut: /home/okishinya/chipatlas/results/sacCer3/SRX3421877/SRX3421877.05_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/sacCer3/SRX3421877/SRX3421877.05_model.r’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX3421877/SRX3421877.05_*.xls’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX3421877/SRX3421877.05_peaks.narrowPeak’: No such file or directory CompletedMACS2peakCalling INFO @ Sat, 24 Aug 2019 19:25:07: 3000000 BedGraph に変換中... INFO @ Sat, 24 Aug 2019 19:25:12: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/SRX3421877/SRX3421877.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/SRX3421877/SRX3421877.20 -q 1e-20 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/SRX3421877/SRX3421877.20 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/SRX3421877/SRX3421877.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 19:25:12: #1 read tag files... INFO @ Sat, 24 Aug 2019 19:25:12: #1 read treatment tags... INFO @ Sat, 24 Aug 2019 19:25:14: 4000000 INFO @ Sat, 24 Aug 2019 19:25:21: 1000000 INFO @ Sat, 24 Aug 2019 19:25:21: 5000000 INFO @ Sat, 24 Aug 2019 19:25:28: 6000000 INFO @ Sat, 24 Aug 2019 19:25:29: 2000000 INFO @ Sat, 24 Aug 2019 19:25:31: #1 tag size is determined as 51 bps INFO @ Sat, 24 Aug 2019 19:25:31: #1 tag size = 51 INFO @ Sat, 24 Aug 2019 19:25:31: #1 total tags in treatment: 6353977 INFO @ Sat, 24 Aug 2019 19:25:31: #1 user defined the maximum tags... INFO @ Sat, 24 Aug 2019 19:25:31: #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 19:25:31: #1 tags after filtering in treatment: 6353977 INFO @ Sat, 24 Aug 2019 19:25:31: #1 Redundant rate of treatment: 0.00 INFO @ Sat, 24 Aug 2019 19:25:31: #1 finished! INFO @ Sat, 24 Aug 2019 19:25:31: #2 Build Peak Model... INFO @ Sat, 24 Aug 2019 19:25:31: #2 looking for paired plus/minus strand peaks... INFO @ Sat, 24 Aug 2019 19:25:31: #2 number of paired peaks: 0 WARNING @ Sat, 24 Aug 2019 19:25:31: 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 19:25:31: Process for pairing-model is terminated! cut: /home/okishinya/chipatlas/results/sacCer3/SRX3421877/SRX3421877.10_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/SRX3421877/SRX3421877.10_model.r’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX3421877/SRX3421877.10_*.xls’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX3421877/SRX3421877.10_peaks.narrowPeak’: No such file or directory CompletedMACS2peakCalling INFO @ Sat, 24 Aug 2019 19:25:37: 3000000 INFO @ Sat, 24 Aug 2019 19:25:44: 4000000 INFO @ Sat, 24 Aug 2019 19:25:52: 5000000 INFO @ Sat, 24 Aug 2019 19:26:00: 6000000 INFO @ Sat, 24 Aug 2019 19:26:03: #1 tag size is determined as 51 bps INFO @ Sat, 24 Aug 2019 19:26:03: #1 tag size = 51 INFO @ Sat, 24 Aug 2019 19:26:03: #1 total tags in treatment: 6353977 INFO @ Sat, 24 Aug 2019 19:26:03: #1 user defined the maximum tags... INFO @ Sat, 24 Aug 2019 19:26:03: #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 19:26:03: #1 tags after filtering in treatment: 6353977 INFO @ Sat, 24 Aug 2019 19:26:03: #1 Redundant rate of treatment: 0.00 INFO @ Sat, 24 Aug 2019 19:26:03: #1 finished! INFO @ Sat, 24 Aug 2019 19:26:03: #2 Build Peak Model... INFO @ Sat, 24 Aug 2019 19:26:03: #2 looking for paired plus/minus strand peaks... INFO @ Sat, 24 Aug 2019 19:26:03: #2 number of paired peaks: 0 WARNING @ Sat, 24 Aug 2019 19:26:03: 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 19:26:03: Process for pairing-model is terminated! cut: /home/okishinya/chipatlas/results/sacCer3/SRX3421877/SRX3421877.20_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/SRX3421877/SRX3421877.20_model.r’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX3421877/SRX3421877.20_*.xls’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX3421877/SRX3421877.20_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。