Job ID = 2009779 sra ファイルのダウンロード中... Read layout: SINGLE fastq に変換中... spots read : 25,571,397 reads read : 25,571,397 reads written : 25,571,397 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: 00:03:42 25571397 reads; of these: 25571397 (100.00%) were unpaired; of these: 4361289 (17.06%) aligned 0 times 19399125 (75.86%) aligned exactly 1 time 1810983 (7.08%) aligned >1 times 82.94% overall alignment rate Time searching: 00:03:42 Overall time: 00:03:42 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] 12879477 / 21210108 = 0.6072 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 20:07:36: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/SRX150899/SRX150899.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/SRX150899/SRX150899.05 -q 1e-05 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/SRX150899/SRX150899.05 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/SRX150899/SRX150899.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 20:07:36: #1 read tag files... INFO @ Fri, 05 Jul 2019 20:07:36: #1 read treatment tags... INFO @ Fri, 05 Jul 2019 20:07:37: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/SRX150899/SRX150899.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/SRX150899/SRX150899.10 -q 1e-10 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/SRX150899/SRX150899.10 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/SRX150899/SRX150899.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 20:07:37: #1 read tag files... INFO @ Fri, 05 Jul 2019 20:07:37: #1 read treatment tags... INFO @ Fri, 05 Jul 2019 20:07:38: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/SRX150899/SRX150899.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/SRX150899/SRX150899.20 -q 1e-20 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/SRX150899/SRX150899.20 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/SRX150899/SRX150899.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 20:07:38: #1 read tag files... INFO @ Fri, 05 Jul 2019 20:07:38: #1 read treatment tags... INFO @ Fri, 05 Jul 2019 20:07:43: 1000000 INFO @ Fri, 05 Jul 2019 20:07:44: 1000000 INFO @ Fri, 05 Jul 2019 20:07:46: 1000000 INFO @ Fri, 05 Jul 2019 20:07:51: 2000000 INFO @ Fri, 05 Jul 2019 20:07:52: 2000000 INFO @ Fri, 05 Jul 2019 20:07:54: 2000000 INFO @ Fri, 05 Jul 2019 20:07:58: 3000000 INFO @ Fri, 05 Jul 2019 20:07:59: 3000000 INFO @ Fri, 05 Jul 2019 20:08:02: 3000000 INFO @ Fri, 05 Jul 2019 20:08:04: 4000000 INFO @ Fri, 05 Jul 2019 20:08:06: 4000000 INFO @ Fri, 05 Jul 2019 20:08:09: 4000000 INFO @ Fri, 05 Jul 2019 20:08:11: 5000000 INFO @ Fri, 05 Jul 2019 20:08:13: 5000000 INFO @ Fri, 05 Jul 2019 20:08:17: 5000000 INFO @ Fri, 05 Jul 2019 20:08:18: 6000000 INFO @ Fri, 05 Jul 2019 20:08:21: 6000000 INFO @ Fri, 05 Jul 2019 20:08:24: 6000000 INFO @ Fri, 05 Jul 2019 20:08:25: 7000000 INFO @ Fri, 05 Jul 2019 20:08:28: 7000000 INFO @ Fri, 05 Jul 2019 20:08:33: 7000000 INFO @ Fri, 05 Jul 2019 20:08:33: 8000000 INFO @ Fri, 05 Jul 2019 20:08:35: #1 tag size is determined as 36 bps INFO @ Fri, 05 Jul 2019 20:08:35: #1 tag size = 36 INFO @ Fri, 05 Jul 2019 20:08:35: #1 total tags in treatment: 8330631 INFO @ Fri, 05 Jul 2019 20:08:35: #1 user defined the maximum tags... INFO @ Fri, 05 Jul 2019 20:08:35: #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 20:08:35: #1 tags after filtering in treatment: 8330631 INFO @ Fri, 05 Jul 2019 20:08:35: #1 Redundant rate of treatment: 0.00 INFO @ Fri, 05 Jul 2019 20:08:35: #1 finished! INFO @ Fri, 05 Jul 2019 20:08:35: #2 Build Peak Model... INFO @ Fri, 05 Jul 2019 20:08:35: #2 looking for paired plus/minus strand peaks... INFO @ Fri, 05 Jul 2019 20:08:36: #2 number of paired peaks: 0 WARNING @ Fri, 05 Jul 2019 20:08:36: 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 20:08:36: Process for pairing-model is terminated! cut: /home/okishinya/chipatlas/results/sacCer3/SRX150899/SRX150899.05_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/SRX150899/SRX150899.05_model.r’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX150899/SRX150899.05_*.xls’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX150899/SRX150899.05_peaks.narrowPeak’: No such file or directory CompletedMACS2peakCalling INFO @ Fri, 05 Jul 2019 20:08:36: 8000000 INFO @ Fri, 05 Jul 2019 20:08:38: #1 tag size is determined as 36 bps INFO @ Fri, 05 Jul 2019 20:08:38: #1 tag size = 36 INFO @ Fri, 05 Jul 2019 20:08:38: #1 total tags in treatment: 8330631 INFO @ Fri, 05 Jul 2019 20:08:38: #1 user defined the maximum tags... INFO @ Fri, 05 Jul 2019 20:08:38: #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 20:08:39: #1 tags after filtering in treatment: 8330631 INFO @ Fri, 05 Jul 2019 20:08:39: #1 Redundant rate of treatment: 0.00 INFO @ Fri, 05 Jul 2019 20:08:39: #1 finished! INFO @ Fri, 05 Jul 2019 20:08:39: #2 Build Peak Model... INFO @ Fri, 05 Jul 2019 20:08:39: #2 looking for paired plus/minus strand peaks... INFO @ Fri, 05 Jul 2019 20:08:39: #2 number of paired peaks: 0 WARNING @ Fri, 05 Jul 2019 20:08:39: 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 20:08:39: Process for pairing-model is terminated! cut: /home/okishinya/chipatlas/results/sacCer3/SRX150899/SRX150899.10_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/SRX150899/SRX150899.10_model.r’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX150899/SRX150899.10_*.xls’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX150899/SRX150899.10_peaks.narrowPeak’: No such file or directory CompletedMACS2peakCalling INFO @ Fri, 05 Jul 2019 20:08:41: 8000000 INFO @ Fri, 05 Jul 2019 20:08:43: #1 tag size is determined as 36 bps INFO @ Fri, 05 Jul 2019 20:08:43: #1 tag size = 36 INFO @ Fri, 05 Jul 2019 20:08:43: #1 total tags in treatment: 8330631 INFO @ Fri, 05 Jul 2019 20:08:43: #1 user defined the maximum tags... INFO @ Fri, 05 Jul 2019 20:08:43: #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 20:08:43: #1 tags after filtering in treatment: 8330631 INFO @ Fri, 05 Jul 2019 20:08:43: #1 Redundant rate of treatment: 0.00 INFO @ Fri, 05 Jul 2019 20:08:43: #1 finished! INFO @ Fri, 05 Jul 2019 20:08:43: #2 Build Peak Model... INFO @ Fri, 05 Jul 2019 20:08:43: #2 looking for paired plus/minus strand peaks... INFO @ Fri, 05 Jul 2019 20:08:44: #2 number of paired peaks: 0 WARNING @ Fri, 05 Jul 2019 20:08:44: 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 20:08:44: Process for pairing-model is terminated! cut: /home/okishinya/chipatlas/results/sacCer3/SRX150899/SRX150899.20_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/SRX150899/SRX150899.20_model.r’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX150899/SRX150899.20_*.xls’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX150899/SRX150899.20_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。