Job ID = 2009886 sra ファイルのダウンロード中... Read layout: SINGLE fastq に変換中... spots read : 17,981,719 reads read : 17,981,719 reads written : 17,981,719 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: 00:03:03 17981719 reads; of these: 17981719 (100.00%) were unpaired; of these: 710489 (3.95%) aligned 0 times 13126707 (73.00%) aligned exactly 1 time 4144523 (23.05%) aligned >1 times 96.05% overall alignment rate Time searching: 00:03:03 Overall time: 00:03:03 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] 8995635 / 17271230 = 0.5208 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 20:48:41: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/SRX2148737/SRX2148737.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/SRX2148737/SRX2148737.05 -q 1e-05 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/SRX2148737/SRX2148737.05 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/SRX2148737/SRX2148737.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 20:48:41: #1 read tag files... INFO @ Fri, 05 Jul 2019 20:48:41: #1 read treatment tags... INFO @ Fri, 05 Jul 2019 20:48:42: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/SRX2148737/SRX2148737.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/SRX2148737/SRX2148737.10 -q 1e-10 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/SRX2148737/SRX2148737.10 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/SRX2148737/SRX2148737.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 20:48:42: #1 read tag files... INFO @ Fri, 05 Jul 2019 20:48:42: #1 read treatment tags... INFO @ Fri, 05 Jul 2019 20:48:43: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/SRX2148737/SRX2148737.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/SRX2148737/SRX2148737.20 -q 1e-20 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/SRX2148737/SRX2148737.20 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/SRX2148737/SRX2148737.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 20:48:43: #1 read tag files... INFO @ Fri, 05 Jul 2019 20:48:43: #1 read treatment tags... INFO @ Fri, 05 Jul 2019 20:48:48: 1000000 INFO @ Fri, 05 Jul 2019 20:48:50: 1000000 INFO @ Fri, 05 Jul 2019 20:48:50: 1000000 INFO @ Fri, 05 Jul 2019 20:48:55: 2000000 INFO @ Fri, 05 Jul 2019 20:48:58: 2000000 INFO @ Fri, 05 Jul 2019 20:48:59: 2000000 INFO @ Fri, 05 Jul 2019 20:49:03: 3000000 INFO @ Fri, 05 Jul 2019 20:49:05: 3000000 INFO @ Fri, 05 Jul 2019 20:49:07: 3000000 INFO @ Fri, 05 Jul 2019 20:49:10: 4000000 INFO @ Fri, 05 Jul 2019 20:49:12: 4000000 INFO @ Fri, 05 Jul 2019 20:49:15: 4000000 INFO @ Fri, 05 Jul 2019 20:49:17: 5000000 INFO @ Fri, 05 Jul 2019 20:49:19: 5000000 INFO @ Fri, 05 Jul 2019 20:49:24: 5000000 INFO @ Fri, 05 Jul 2019 20:49:24: 6000000 INFO @ Fri, 05 Jul 2019 20:49:26: 6000000 INFO @ Fri, 05 Jul 2019 20:49:32: 7000000 INFO @ Fri, 05 Jul 2019 20:49:32: 6000000 INFO @ Fri, 05 Jul 2019 20:49:33: 7000000 INFO @ Fri, 05 Jul 2019 20:49:39: 8000000 INFO @ Fri, 05 Jul 2019 20:49:40: 7000000 INFO @ Fri, 05 Jul 2019 20:49:40: 8000000 INFO @ Fri, 05 Jul 2019 20:49:41: #1 tag size is determined as 50 bps INFO @ Fri, 05 Jul 2019 20:49:41: #1 tag size = 50 INFO @ Fri, 05 Jul 2019 20:49:41: #1 total tags in treatment: 8275595 INFO @ Fri, 05 Jul 2019 20:49:41: #1 user defined the maximum tags... INFO @ Fri, 05 Jul 2019 20:49:41: #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 20:49:41: #1 tags after filtering in treatment: 8275595 INFO @ Fri, 05 Jul 2019 20:49:41: #1 Redundant rate of treatment: 0.00 INFO @ Fri, 05 Jul 2019 20:49:41: #1 finished! INFO @ Fri, 05 Jul 2019 20:49:41: #2 Build Peak Model... INFO @ Fri, 05 Jul 2019 20:49:41: #2 looking for paired plus/minus strand peaks... INFO @ Fri, 05 Jul 2019 20:49:41: #2 number of paired peaks: 0 WARNING @ Fri, 05 Jul 2019 20:49:41: 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 20:49:41: Process for pairing-model is terminated! cut: /home/okishinya/chipatlas/results/sacCer3/SRX2148737/SRX2148737.05_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/SRX2148737/SRX2148737.05_model.r’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX2148737/SRX2148737.05_*.xls’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX2148737/SRX2148737.05_peaks.narrowPeak’: No such file or directory CompletedMACS2peakCalling INFO @ Fri, 05 Jul 2019 20:49:42: #1 tag size is determined as 50 bps INFO @ Fri, 05 Jul 2019 20:49:42: #1 tag size = 50 INFO @ Fri, 05 Jul 2019 20:49:42: #1 total tags in treatment: 8275595 INFO @ Fri, 05 Jul 2019 20:49:42: #1 user defined the maximum tags... INFO @ Fri, 05 Jul 2019 20:49:42: #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 20:49:42: #1 tags after filtering in treatment: 8275595 INFO @ Fri, 05 Jul 2019 20:49:42: #1 Redundant rate of treatment: 0.00 INFO @ Fri, 05 Jul 2019 20:49:42: #1 finished! INFO @ Fri, 05 Jul 2019 20:49:42: #2 Build Peak Model... INFO @ Fri, 05 Jul 2019 20:49:42: #2 looking for paired plus/minus strand peaks... INFO @ Fri, 05 Jul 2019 20:49:43: #2 number of paired peaks: 0 WARNING @ Fri, 05 Jul 2019 20:49:43: 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 20:49:43: Process for pairing-model is terminated! cut: /home/okishinya/chipatlas/results/sacCer3/SRX2148737/SRX2148737.20_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/SRX2148737/SRX2148737.20_model.r’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX2148737/SRX2148737.20_*.xls’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX2148737/SRX2148737.20_peaks.narrowPeak’: No such file or directory CompletedMACS2peakCalling INFO @ Fri, 05 Jul 2019 20:49:47: 8000000 INFO @ Fri, 05 Jul 2019 20:49:50: #1 tag size is determined as 50 bps INFO @ Fri, 05 Jul 2019 20:49:50: #1 tag size = 50 INFO @ Fri, 05 Jul 2019 20:49:50: #1 total tags in treatment: 8275595 INFO @ Fri, 05 Jul 2019 20:49:50: #1 user defined the maximum tags... INFO @ Fri, 05 Jul 2019 20:49:50: #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 20:49:50: #1 tags after filtering in treatment: 8275595 INFO @ Fri, 05 Jul 2019 20:49:50: #1 Redundant rate of treatment: 0.00 INFO @ Fri, 05 Jul 2019 20:49:50: #1 finished! INFO @ Fri, 05 Jul 2019 20:49:50: #2 Build Peak Model... INFO @ Fri, 05 Jul 2019 20:49:50: #2 looking for paired plus/minus strand peaks... INFO @ Fri, 05 Jul 2019 20:49:50: #2 number of paired peaks: 0 WARNING @ Fri, 05 Jul 2019 20:49:50: 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 20:49:50: Process for pairing-model is terminated! cut: /home/okishinya/chipatlas/results/sacCer3/SRX2148737/SRX2148737.10_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/SRX2148737/SRX2148737.10_model.r’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX2148737/SRX2148737.10_*.xls’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX2148737/SRX2148737.10_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。