Job ID = 2009777 sra ファイルのダウンロード中... Read layout: SINGLE fastq に変換中... spots read : 22,246,077 reads read : 22,246,077 reads written : 22,246,077 rm: cannot remove ‘[DSE]RR*’: No such file or directory rm: cannot remove ‘/home/okishinya/ncbi/public/sra/SRR502961.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: 00:03:52 22246077 reads; of these: 22246077 (100.00%) were unpaired; of these: 9535736 (42.86%) aligned 0 times 9975577 (44.84%) aligned exactly 1 time 2734764 (12.29%) aligned >1 times 57.14% overall alignment rate Time searching: 00:03:52 Overall time: 00:03:52 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] 6251188 / 12710341 = 0.4918 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 19:59:09: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/SRX150897/SRX150897.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/SRX150897/SRX150897.05 -q 1e-05 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/SRX150897/SRX150897.05 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/SRX150897/SRX150897.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 19:59:09: #1 read tag files... INFO @ Fri, 05 Jul 2019 19:59:09: #1 read treatment tags... INFO @ Fri, 05 Jul 2019 19:59:10: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/SRX150897/SRX150897.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/SRX150897/SRX150897.10 -q 1e-10 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/SRX150897/SRX150897.10 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/SRX150897/SRX150897.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 19:59:10: #1 read tag files... INFO @ Fri, 05 Jul 2019 19:59:10: #1 read treatment tags... INFO @ Fri, 05 Jul 2019 19:59:11: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/SRX150897/SRX150897.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/SRX150897/SRX150897.20 -q 1e-20 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/SRX150897/SRX150897.20 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/SRX150897/SRX150897.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 19:59:11: #1 read tag files... INFO @ Fri, 05 Jul 2019 19:59:11: #1 read treatment tags... INFO @ Fri, 05 Jul 2019 19:59:17: 1000000 INFO @ Fri, 05 Jul 2019 19:59:18: 1000000 INFO @ Fri, 05 Jul 2019 19:59:19: 1000000 INFO @ Fri, 05 Jul 2019 19:59:25: 2000000 INFO @ Fri, 05 Jul 2019 19:59:26: 2000000 INFO @ Fri, 05 Jul 2019 19:59:27: 2000000 INFO @ Fri, 05 Jul 2019 19:59:33: 3000000 INFO @ Fri, 05 Jul 2019 19:59:33: 3000000 INFO @ Fri, 05 Jul 2019 19:59:35: 3000000 INFO @ Fri, 05 Jul 2019 19:59:41: 4000000 INFO @ Fri, 05 Jul 2019 19:59:42: 4000000 INFO @ Fri, 05 Jul 2019 19:59:43: 4000000 INFO @ Fri, 05 Jul 2019 19:59:48: 5000000 INFO @ Fri, 05 Jul 2019 19:59:50: 5000000 INFO @ Fri, 05 Jul 2019 19:59:51: 5000000 INFO @ Fri, 05 Jul 2019 19:59:56: 6000000 INFO @ Fri, 05 Jul 2019 19:59:58: 6000000 INFO @ Fri, 05 Jul 2019 19:59:59: #1 tag size is determined as 36 bps INFO @ Fri, 05 Jul 2019 19:59:59: #1 tag size = 36 INFO @ Fri, 05 Jul 2019 19:59:59: #1 total tags in treatment: 6459153 INFO @ Fri, 05 Jul 2019 19:59:59: #1 user defined the maximum tags... INFO @ Fri, 05 Jul 2019 19:59:59: #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 19:59:59: #1 tags after filtering in treatment: 6459153 INFO @ Fri, 05 Jul 2019 19:59:59: #1 Redundant rate of treatment: 0.00 INFO @ Fri, 05 Jul 2019 19:59:59: #1 finished! INFO @ Fri, 05 Jul 2019 19:59:59: #2 Build Peak Model... INFO @ Fri, 05 Jul 2019 19:59:59: #2 looking for paired plus/minus strand peaks... INFO @ Fri, 05 Jul 2019 20:00:00: #2 number of paired peaks: 0 WARNING @ Fri, 05 Jul 2019 20:00:00: 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 20:00:00: Process for pairing-model is terminated! cut: /home/okishinya/chipatlas/results/sacCer3/SRX150897/SRX150897.20_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/SRX150897/SRX150897.20_model.r’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX150897/SRX150897.20_*.xls’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX150897/SRX150897.20_peaks.narrowPeak’: No such file or directory CompletedMACS2peakCalling INFO @ Fri, 05 Jul 2019 20:00:02: 6000000 INFO @ Fri, 05 Jul 2019 20:00:02: #1 tag size is determined as 36 bps INFO @ Fri, 05 Jul 2019 20:00:02: #1 tag size = 36 INFO @ Fri, 05 Jul 2019 20:00:02: #1 total tags in treatment: 6459153 INFO @ Fri, 05 Jul 2019 20:00:02: #1 user defined the maximum tags... INFO @ Fri, 05 Jul 2019 20:00:02: #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 20:00:02: #1 tags after filtering in treatment: 6459153 INFO @ Fri, 05 Jul 2019 20:00:02: #1 Redundant rate of treatment: 0.00 INFO @ Fri, 05 Jul 2019 20:00:02: #1 finished! INFO @ Fri, 05 Jul 2019 20:00:02: #2 Build Peak Model... INFO @ Fri, 05 Jul 2019 20:00:02: #2 looking for paired plus/minus strand peaks... INFO @ Fri, 05 Jul 2019 20:00:02: #2 number of paired peaks: 0 WARNING @ Fri, 05 Jul 2019 20:00:02: 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 @ Fri, 05 Jul 2019 20:00:02: Process for pairing-model is terminated! cut: /home/okishinya/chipatlas/results/sacCer3/SRX150897/SRX150897.05_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/SRX150897/SRX150897.05_model.r’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX150897/SRX150897.05_*.xls’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX150897/SRX150897.05_peaks.narrowPeak’: No such file or directory CompletedMACS2peakCalling INFO @ Fri, 05 Jul 2019 20:00:06: #1 tag size is determined as 36 bps INFO @ Fri, 05 Jul 2019 20:00:06: #1 tag size = 36 INFO @ Fri, 05 Jul 2019 20:00:06: #1 total tags in treatment: 6459153 INFO @ Fri, 05 Jul 2019 20:00:06: #1 user defined the maximum tags... INFO @ Fri, 05 Jul 2019 20:00:06: #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 20:00:06: #1 tags after filtering in treatment: 6459153 INFO @ Fri, 05 Jul 2019 20:00:06: #1 Redundant rate of treatment: 0.00 INFO @ Fri, 05 Jul 2019 20:00:06: #1 finished! INFO @ Fri, 05 Jul 2019 20:00:06: #2 Build Peak Model... INFO @ Fri, 05 Jul 2019 20:00:06: #2 looking for paired plus/minus strand peaks... INFO @ Fri, 05 Jul 2019 20:00:06: #2 number of paired peaks: 0 WARNING @ Fri, 05 Jul 2019 20:00:06: 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 20:00:06: Process for pairing-model is terminated! cut: /home/okishinya/chipatlas/results/sacCer3/SRX150897/SRX150897.10_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/SRX150897/SRX150897.10_model.r’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX150897/SRX150897.10_*.xls’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX150897/SRX150897.10_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。