Job ID = 2010040 sra ファイルのダウンロード中... Read layout: SINGLE fastq に変換中... spots read : 14,631,757 reads read : 14,631,757 reads written : 14,631,757 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: 00:02:32 14631757 reads; of these: 14631757 (100.00%) were unpaired; of these: 814822 (5.57%) aligned 0 times 11097192 (75.84%) aligned exactly 1 time 2719743 (18.59%) aligned >1 times 94.43% overall alignment rate Time searching: 00:02:32 Overall time: 00:02:32 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] 6279043 / 13816935 = 0.4544 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 21:15:30: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/SRX2609705/SRX2609705.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/SRX2609705/SRX2609705.05 -q 1e-05 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/SRX2609705/SRX2609705.05 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/SRX2609705/SRX2609705.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 21:15:30: #1 read tag files... INFO @ Fri, 05 Jul 2019 21:15:30: #1 read treatment tags... INFO @ Fri, 05 Jul 2019 21:15:31: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/SRX2609705/SRX2609705.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/SRX2609705/SRX2609705.10 -q 1e-10 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/SRX2609705/SRX2609705.10 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/SRX2609705/SRX2609705.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 21:15:31: #1 read tag files... INFO @ Fri, 05 Jul 2019 21:15:31: #1 read treatment tags... INFO @ Fri, 05 Jul 2019 21:15:33: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/SRX2609705/SRX2609705.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/SRX2609705/SRX2609705.20 -q 1e-20 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/SRX2609705/SRX2609705.20 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/SRX2609705/SRX2609705.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 21:15:33: #1 read tag files... INFO @ Fri, 05 Jul 2019 21:15:33: #1 read treatment tags... INFO @ Fri, 05 Jul 2019 21:15:38: 1000000 INFO @ Fri, 05 Jul 2019 21:15:39: 1000000 INFO @ Fri, 05 Jul 2019 21:15:42: 1000000 INFO @ Fri, 05 Jul 2019 21:15:46: 2000000 INFO @ Fri, 05 Jul 2019 21:15:46: 2000000 INFO @ Fri, 05 Jul 2019 21:15:51: 2000000 INFO @ Fri, 05 Jul 2019 21:15:54: 3000000 INFO @ Fri, 05 Jul 2019 21:15:54: 3000000 INFO @ Fri, 05 Jul 2019 21:16:00: 3000000 INFO @ Fri, 05 Jul 2019 21:16:02: 4000000 INFO @ Fri, 05 Jul 2019 21:16:02: 4000000 INFO @ Fri, 05 Jul 2019 21:16:08: 4000000 INFO @ Fri, 05 Jul 2019 21:16:09: 5000000 INFO @ Fri, 05 Jul 2019 21:16:10: 5000000 INFO @ Fri, 05 Jul 2019 21:16:17: 6000000 INFO @ Fri, 05 Jul 2019 21:16:17: 5000000 INFO @ Fri, 05 Jul 2019 21:16:17: 6000000 INFO @ Fri, 05 Jul 2019 21:16:24: 7000000 INFO @ Fri, 05 Jul 2019 21:16:25: 7000000 INFO @ Fri, 05 Jul 2019 21:16:25: 6000000 INFO @ Fri, 05 Jul 2019 21:16:28: #1 tag size is determined as 51 bps INFO @ Fri, 05 Jul 2019 21:16:28: #1 tag size = 51 INFO @ Fri, 05 Jul 2019 21:16:28: #1 total tags in treatment: 7537892 INFO @ Fri, 05 Jul 2019 21:16:28: #1 user defined the maximum tags... INFO @ Fri, 05 Jul 2019 21:16:28: #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 21:16:28: #1 tags after filtering in treatment: 7537892 INFO @ Fri, 05 Jul 2019 21:16:28: #1 Redundant rate of treatment: 0.00 INFO @ Fri, 05 Jul 2019 21:16:28: #1 finished! INFO @ Fri, 05 Jul 2019 21:16:28: #2 Build Peak Model... INFO @ Fri, 05 Jul 2019 21:16:28: #2 looking for paired plus/minus strand peaks... INFO @ Fri, 05 Jul 2019 21:16:29: #1 tag size is determined as 51 bps INFO @ Fri, 05 Jul 2019 21:16:29: #1 tag size = 51 INFO @ Fri, 05 Jul 2019 21:16:29: #1 total tags in treatment: 7537892 INFO @ Fri, 05 Jul 2019 21:16:29: #1 user defined the maximum tags... INFO @ Fri, 05 Jul 2019 21:16:29: #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 21:16:29: #1 tags after filtering in treatment: 7537892 INFO @ Fri, 05 Jul 2019 21:16:29: #1 Redundant rate of treatment: 0.00 INFO @ Fri, 05 Jul 2019 21:16:29: #1 finished! INFO @ Fri, 05 Jul 2019 21:16:29: #2 Build Peak Model... INFO @ Fri, 05 Jul 2019 21:16:29: #2 looking for paired plus/minus strand peaks... INFO @ Fri, 05 Jul 2019 21:16:29: #2 number of paired peaks: 0 WARNING @ Fri, 05 Jul 2019 21:16:29: 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 21:16:29: Process for pairing-model is terminated! cut: /home/okishinya/chipatlas/results/sacCer3/SRX2609705/SRX2609705.05_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/SRX2609705/SRX2609705.05_model.r’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX2609705/SRX2609705.05_*.xls’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX2609705/SRX2609705.05_peaks.narrowPeak’: No such file or directory CompletedMACS2peakCalling INFO @ Fri, 05 Jul 2019 21:16:29: #2 number of paired peaks: 0 WARNING @ Fri, 05 Jul 2019 21:16:29: 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 21:16:29: Process for pairing-model is terminated! cut: /home/okishinya/chipatlas/results/sacCer3/SRX2609705/SRX2609705.10_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/SRX2609705/SRX2609705.10_model.r’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX2609705/SRX2609705.10_*.xls’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX2609705/SRX2609705.10_peaks.narrowPeak’: No such file or directory CompletedMACS2peakCalling INFO @ Fri, 05 Jul 2019 21:16:34: 7000000 INFO @ Fri, 05 Jul 2019 21:16:38: #1 tag size is determined as 51 bps INFO @ Fri, 05 Jul 2019 21:16:38: #1 tag size = 51 INFO @ Fri, 05 Jul 2019 21:16:38: #1 total tags in treatment: 7537892 INFO @ Fri, 05 Jul 2019 21:16:38: #1 user defined the maximum tags... INFO @ Fri, 05 Jul 2019 21:16:38: #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 21:16:38: #1 tags after filtering in treatment: 7537892 INFO @ Fri, 05 Jul 2019 21:16:38: #1 Redundant rate of treatment: 0.00 INFO @ Fri, 05 Jul 2019 21:16:38: #1 finished! INFO @ Fri, 05 Jul 2019 21:16:38: #2 Build Peak Model... INFO @ Fri, 05 Jul 2019 21:16:38: #2 looking for paired plus/minus strand peaks... INFO @ Fri, 05 Jul 2019 21:16:39: #2 number of paired peaks: 0 WARNING @ Fri, 05 Jul 2019 21:16:39: 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 21:16:39: Process for pairing-model is terminated! cut: /home/okishinya/chipatlas/results/sacCer3/SRX2609705/SRX2609705.20_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/SRX2609705/SRX2609705.20_model.r’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX2609705/SRX2609705.20_*.xls’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX2609705/SRX2609705.20_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。