Job ID = 2009885 sra ファイルのダウンロード中... Read layout: SINGLE fastq に変換中... spots read : 14,119,692 reads read : 14,119,692 reads written : 14,119,692 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: 00:02:31 14119692 reads; of these: 14119692 (100.00%) were unpaired; of these: 398291 (2.82%) aligned 0 times 11800709 (83.58%) aligned exactly 1 time 1920692 (13.60%) aligned >1 times 97.18% overall alignment rate Time searching: 00:02:31 Overall time: 00:02:31 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] 4560231 / 13721401 = 0.3323 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 @ Fri, 05 Jul 2019 20:42:42: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/SRX2148736/SRX2148736.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/SRX2148736/SRX2148736.05 -q 1e-05 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/SRX2148736/SRX2148736.05 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/SRX2148736/SRX2148736.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 @ Fri, 05 Jul 2019 20:42:42: #1 read tag files... INFO @ Fri, 05 Jul 2019 20:42:42: #1 read treatment tags... INFO @ Fri, 05 Jul 2019 20:42:43: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/SRX2148736/SRX2148736.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/SRX2148736/SRX2148736.10 -q 1e-10 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/SRX2148736/SRX2148736.10 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/SRX2148736/SRX2148736.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 @ Fri, 05 Jul 2019 20:42:43: #1 read tag files... INFO @ Fri, 05 Jul 2019 20:42:43: #1 read treatment tags... INFO @ Fri, 05 Jul 2019 20:42:44: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/SRX2148736/SRX2148736.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/SRX2148736/SRX2148736.20 -q 1e-20 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/SRX2148736/SRX2148736.20 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/SRX2148736/SRX2148736.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 @ Fri, 05 Jul 2019 20:42:44: #1 read tag files... INFO @ Fri, 05 Jul 2019 20:42:44: #1 read treatment tags... INFO @ Fri, 05 Jul 2019 20:42:49: 1000000 INFO @ Fri, 05 Jul 2019 20:42:51: 1000000 INFO @ Fri, 05 Jul 2019 20:42:51: 1000000 INFO @ Fri, 05 Jul 2019 20:42:56: 2000000 INFO @ Fri, 05 Jul 2019 20:42:59: 2000000 INFO @ Fri, 05 Jul 2019 20:42:59: 2000000 INFO @ Fri, 05 Jul 2019 20:43:03: 3000000 INFO @ Fri, 05 Jul 2019 20:43:06: 3000000 INFO @ Fri, 05 Jul 2019 20:43:07: 3000000 INFO @ Fri, 05 Jul 2019 20:43:10: 4000000 INFO @ Fri, 05 Jul 2019 20:43:13: 4000000 INFO @ Fri, 05 Jul 2019 20:43:15: 4000000 INFO @ Fri, 05 Jul 2019 20:43:17: 5000000 INFO @ Fri, 05 Jul 2019 20:43:20: 5000000 INFO @ Fri, 05 Jul 2019 20:43:22: 5000000 INFO @ Fri, 05 Jul 2019 20:43:23: 6000000 INFO @ Fri, 05 Jul 2019 20:43:26: 6000000 INFO @ Fri, 05 Jul 2019 20:43:29: 6000000 INFO @ Fri, 05 Jul 2019 20:43:30: 7000000 INFO @ Fri, 05 Jul 2019 20:43:33: 7000000 INFO @ Fri, 05 Jul 2019 20:43:37: 8000000 INFO @ Fri, 05 Jul 2019 20:43:37: 7000000 INFO @ Fri, 05 Jul 2019 20:43:40: 8000000 INFO @ Fri, 05 Jul 2019 20:43:43: 9000000 INFO @ Fri, 05 Jul 2019 20:43:44: 8000000 INFO @ Fri, 05 Jul 2019 20:43:45: #1 tag size is determined as 50 bps INFO @ Fri, 05 Jul 2019 20:43:45: #1 tag size = 50 INFO @ Fri, 05 Jul 2019 20:43:45: #1 total tags in treatment: 9161170 INFO @ Fri, 05 Jul 2019 20:43:45: #1 user defined the maximum tags... INFO @ Fri, 05 Jul 2019 20:43:45: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Fri, 05 Jul 2019 20:43:45: #1 tags after filtering in treatment: 9161170 INFO @ Fri, 05 Jul 2019 20:43:45: #1 Redundant rate of treatment: 0.00 INFO @ Fri, 05 Jul 2019 20:43:45: #1 finished! INFO @ Fri, 05 Jul 2019 20:43:45: #2 Build Peak Model... INFO @ Fri, 05 Jul 2019 20:43:45: #2 looking for paired plus/minus strand peaks... INFO @ Fri, 05 Jul 2019 20:43:45: #2 number of paired peaks: 0 WARNING @ Fri, 05 Jul 2019 20:43:45: 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 @ Fri, 05 Jul 2019 20:43:45: Process for pairing-model is terminated! cut: /home/okishinya/chipatlas/results/sacCer3/SRX2148736/SRX2148736.05_peaks.narrowPeak: No such file or directory pass1 - making usageList (0 chroms): 3 millis needLargeMem: trying to allocate 0 bytes (limit: 17179869184) rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX2148736/SRX2148736.05_model.r’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX2148736/SRX2148736.05_*.xls’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX2148736/SRX2148736.05_peaks.narrowPeak’: No such file or directory CompletedMACS2peakCalling INFO @ Fri, 05 Jul 2019 20:43:46: 9000000 INFO @ Fri, 05 Jul 2019 20:43:47: #1 tag size is determined as 50 bps INFO @ Fri, 05 Jul 2019 20:43:47: #1 tag size = 50 INFO @ Fri, 05 Jul 2019 20:43:47: #1 total tags in treatment: 9161170 INFO @ Fri, 05 Jul 2019 20:43:47: #1 user defined the maximum tags... INFO @ Fri, 05 Jul 2019 20:43:47: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Fri, 05 Jul 2019 20:43:48: #1 tags after filtering in treatment: 9161170 INFO @ Fri, 05 Jul 2019 20:43:48: #1 Redundant rate of treatment: 0.00 INFO @ Fri, 05 Jul 2019 20:43:48: #1 finished! INFO @ Fri, 05 Jul 2019 20:43:48: #2 Build Peak Model... INFO @ Fri, 05 Jul 2019 20:43:48: #2 looking for paired plus/minus strand peaks... INFO @ Fri, 05 Jul 2019 20:43:48: #2 number of paired peaks: 0 WARNING @ Fri, 05 Jul 2019 20:43:48: 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 @ Fri, 05 Jul 2019 20:43:48: Process for pairing-model is terminated! cut: /home/okishinya/chipatlas/results/sacCer3/SRX2148736/SRX2148736.20_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/SRX2148736/SRX2148736.20_model.r’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX2148736/SRX2148736.20_*.xls’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX2148736/SRX2148736.20_peaks.narrowPeak’: No such file or directory CompletedMACS2peakCalling INFO @ Fri, 05 Jul 2019 20:43:52: 9000000 INFO @ Fri, 05 Jul 2019 20:43:53: #1 tag size is determined as 50 bps INFO @ Fri, 05 Jul 2019 20:43:53: #1 tag size = 50 INFO @ Fri, 05 Jul 2019 20:43:53: #1 total tags in treatment: 9161170 INFO @ Fri, 05 Jul 2019 20:43:53: #1 user defined the maximum tags... INFO @ Fri, 05 Jul 2019 20:43:53: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Fri, 05 Jul 2019 20:43:53: #1 tags after filtering in treatment: 9161170 INFO @ Fri, 05 Jul 2019 20:43:53: #1 Redundant rate of treatment: 0.00 INFO @ Fri, 05 Jul 2019 20:43:53: #1 finished! INFO @ Fri, 05 Jul 2019 20:43:53: #2 Build Peak Model... INFO @ Fri, 05 Jul 2019 20:43:53: #2 looking for paired plus/minus strand peaks... INFO @ Fri, 05 Jul 2019 20:43:54: #2 number of paired peaks: 0 WARNING @ Fri, 05 Jul 2019 20:43:54: 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 @ Fri, 05 Jul 2019 20:43:54: Process for pairing-model is terminated! cut: /home/okishinya/chipatlas/results/sacCer3/SRX2148736/SRX2148736.10_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/SRX2148736/SRX2148736.10_model.r’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX2148736/SRX2148736.10_*.xls’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX2148736/SRX2148736.10_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。