Job ID = 2010078 sra ファイルのダウンロード中... Read layout: SINGLE fastq に変換中... spots read : 19,680,721 reads read : 19,680,721 reads written : 19,680,721 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: 00:03:46 19680721 reads; of these: 19680721 (100.00%) were unpaired; of these: 8404802 (42.71%) aligned 0 times 9884368 (50.22%) aligned exactly 1 time 1391551 (7.07%) aligned >1 times 57.29% overall alignment rate Time searching: 00:03:47 Overall time: 00:03:47 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] 4257714 / 11275919 = 0.3776 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 21:23:07: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/SRX2772168/SRX2772168.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/SRX2772168/SRX2772168.10 -q 1e-10 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/SRX2772168/SRX2772168.10 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/SRX2772168/SRX2772168.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 21:23:07: #1 read tag files... INFO @ Fri, 05 Jul 2019 21:23:07: #1 read treatment tags... INFO @ Fri, 05 Jul 2019 21:23:07: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/SRX2772168/SRX2772168.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/SRX2772168/SRX2772168.05 -q 1e-05 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/SRX2772168/SRX2772168.05 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/SRX2772168/SRX2772168.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 21:23:07: #1 read tag files... INFO @ Fri, 05 Jul 2019 21:23:07: #1 read treatment tags... INFO @ Fri, 05 Jul 2019 21:23:08: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/SRX2772168/SRX2772168.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/SRX2772168/SRX2772168.20 -q 1e-20 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/SRX2772168/SRX2772168.20 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/SRX2772168/SRX2772168.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 21:23:08: #1 read tag files... INFO @ Fri, 05 Jul 2019 21:23:08: #1 read treatment tags... INFO @ Fri, 05 Jul 2019 21:23:15: 1000000 INFO @ Fri, 05 Jul 2019 21:23:16: 1000000 INFO @ Fri, 05 Jul 2019 21:23:17: 1000000 INFO @ Fri, 05 Jul 2019 21:23:23: 2000000 INFO @ Fri, 05 Jul 2019 21:23:24: 2000000 INFO @ Fri, 05 Jul 2019 21:23:27: 2000000 INFO @ Fri, 05 Jul 2019 21:23:30: 3000000 INFO @ Fri, 05 Jul 2019 21:23:32: 3000000 INFO @ Fri, 05 Jul 2019 21:23:36: 3000000 INFO @ Fri, 05 Jul 2019 21:23:38: 4000000 INFO @ Fri, 05 Jul 2019 21:23:40: 4000000 INFO @ Fri, 05 Jul 2019 21:23:44: 4000000 INFO @ Fri, 05 Jul 2019 21:23:45: 5000000 INFO @ Fri, 05 Jul 2019 21:23:48: 5000000 INFO @ Fri, 05 Jul 2019 21:23:53: 5000000 INFO @ Fri, 05 Jul 2019 21:23:53: 6000000 INFO @ Fri, 05 Jul 2019 21:23:55: 6000000 INFO @ Fri, 05 Jul 2019 21:24:00: 7000000 INFO @ Fri, 05 Jul 2019 21:24:00: #1 tag size is determined as 50 bps INFO @ Fri, 05 Jul 2019 21:24:00: #1 tag size = 50 INFO @ Fri, 05 Jul 2019 21:24:00: #1 total tags in treatment: 7018205 INFO @ Fri, 05 Jul 2019 21:24:00: #1 user defined the maximum tags... INFO @ Fri, 05 Jul 2019 21:24:00: #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 21:24:01: #1 tags after filtering in treatment: 7018205 INFO @ Fri, 05 Jul 2019 21:24:01: #1 Redundant rate of treatment: 0.00 INFO @ Fri, 05 Jul 2019 21:24:01: #1 finished! INFO @ Fri, 05 Jul 2019 21:24:01: #2 Build Peak Model... INFO @ Fri, 05 Jul 2019 21:24:01: #2 looking for paired plus/minus strand peaks... INFO @ Fri, 05 Jul 2019 21:24:01: #2 number of paired peaks: 0 WARNING @ Fri, 05 Jul 2019 21:24:01: 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 21:24:01: Process for pairing-model is terminated! cut: /home/okishinya/chipatlas/results/sacCer3/SRX2772168/SRX2772168.10_peaks.narrowPeak: No such file or directory INFO @ Fri, 05 Jul 2019 21:24:01: 6000000 pass1 - making usageList (0 chroms): 2 millis needLargeMem: trying to allocate 0 bytes (limit: 17179869184) rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX2772168/SRX2772168.10_model.r’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX2772168/SRX2772168.10_*.xls’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX2772168/SRX2772168.10_peaks.narrowPeak’: No such file or directory CompletedMACS2peakCalling INFO @ Fri, 05 Jul 2019 21:24:03: 7000000 INFO @ Fri, 05 Jul 2019 21:24:03: #1 tag size is determined as 50 bps INFO @ Fri, 05 Jul 2019 21:24:03: #1 tag size = 50 INFO @ Fri, 05 Jul 2019 21:24:03: #1 total tags in treatment: 7018205 INFO @ Fri, 05 Jul 2019 21:24:03: #1 user defined the maximum tags... INFO @ Fri, 05 Jul 2019 21:24:03: #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 21:24:04: #1 tags after filtering in treatment: 7018205 INFO @ Fri, 05 Jul 2019 21:24:04: #1 Redundant rate of treatment: 0.00 INFO @ Fri, 05 Jul 2019 21:24:04: #1 finished! INFO @ Fri, 05 Jul 2019 21:24:04: #2 Build Peak Model... INFO @ Fri, 05 Jul 2019 21:24:04: #2 looking for paired plus/minus strand peaks... INFO @ Fri, 05 Jul 2019 21:24:04: #2 number of paired peaks: 0 WARNING @ Fri, 05 Jul 2019 21:24:04: 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 21:24:04: Process for pairing-model is terminated! cut: /home/okishinya/chipatlas/results/sacCer3/SRX2772168/SRX2772168.05_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/SRX2772168/SRX2772168.05_model.r’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX2772168/SRX2772168.05_*.xls’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX2772168/SRX2772168.05_peaks.narrowPeak’: No such file or directory CompletedMACS2peakCalling INFO @ Fri, 05 Jul 2019 21:24:10: 7000000 INFO @ Fri, 05 Jul 2019 21:24:10: #1 tag size is determined as 50 bps INFO @ Fri, 05 Jul 2019 21:24:10: #1 tag size = 50 INFO @ Fri, 05 Jul 2019 21:24:10: #1 total tags in treatment: 7018205 INFO @ Fri, 05 Jul 2019 21:24:10: #1 user defined the maximum tags... INFO @ Fri, 05 Jul 2019 21:24:10: #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 21:24:10: #1 tags after filtering in treatment: 7018205 INFO @ Fri, 05 Jul 2019 21:24:10: #1 Redundant rate of treatment: 0.00 INFO @ Fri, 05 Jul 2019 21:24:10: #1 finished! INFO @ Fri, 05 Jul 2019 21:24:10: #2 Build Peak Model... INFO @ Fri, 05 Jul 2019 21:24:10: #2 looking for paired plus/minus strand peaks... INFO @ Fri, 05 Jul 2019 21:24:11: #2 number of paired peaks: 0 WARNING @ Fri, 05 Jul 2019 21:24:11: 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 21:24:11: Process for pairing-model is terminated! cut: /home/okishinya/chipatlas/results/sacCer3/SRX2772168/SRX2772168.20_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/SRX2772168/SRX2772168.20_model.r’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX2772168/SRX2772168.20_*.xls’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX2772168/SRX2772168.20_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。