Job ID = 2011028 sra ファイルのダウンロード中... Read layout: SINGLE fastq に変換中... spots read : 8,311,917 reads read : 16,623,834 reads written : 8,311,917 reads 0-length : 8,311,917 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: 00:01:30 8311917 reads; of these: 8311917 (100.00%) were unpaired; of these: 866268 (10.42%) aligned 0 times 6569973 (79.04%) aligned exactly 1 time 875676 (10.54%) aligned >1 times 89.58% overall alignment rate Time searching: 00:01:30 Overall time: 00:01:30 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] 1744318 / 7445649 = 0.2343 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 @ Sat, 06 Jul 2019 01:49:49: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/SRX4550108/SRX4550108.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/SRX4550108/SRX4550108.05 -q 1e-05 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/SRX4550108/SRX4550108.05 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/SRX4550108/SRX4550108.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 @ Sat, 06 Jul 2019 01:49:49: #1 read tag files... INFO @ Sat, 06 Jul 2019 01:49:49: #1 read treatment tags... INFO @ Sat, 06 Jul 2019 01:49:50: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/SRX4550108/SRX4550108.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/SRX4550108/SRX4550108.10 -q 1e-10 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/SRX4550108/SRX4550108.10 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/SRX4550108/SRX4550108.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 @ Sat, 06 Jul 2019 01:49:50: #1 read tag files... INFO @ Sat, 06 Jul 2019 01:49:50: #1 read treatment tags... INFO @ Sat, 06 Jul 2019 01:49:51: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/SRX4550108/SRX4550108.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/SRX4550108/SRX4550108.20 -q 1e-20 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/SRX4550108/SRX4550108.20 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/SRX4550108/SRX4550108.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 @ Sat, 06 Jul 2019 01:49:51: #1 read tag files... INFO @ Sat, 06 Jul 2019 01:49:51: #1 read treatment tags... INFO @ Sat, 06 Jul 2019 01:49:57: 1000000 INFO @ Sat, 06 Jul 2019 01:49:58: 1000000 INFO @ Sat, 06 Jul 2019 01:50:01: 1000000 INFO @ Sat, 06 Jul 2019 01:50:04: 2000000 INFO @ Sat, 06 Jul 2019 01:50:05: 2000000 INFO @ Sat, 06 Jul 2019 01:50:11: 2000000 INFO @ Sat, 06 Jul 2019 01:50:12: 3000000 INFO @ Sat, 06 Jul 2019 01:50:13: 3000000 INFO @ Sat, 06 Jul 2019 01:50:19: 4000000 INFO @ Sat, 06 Jul 2019 01:50:20: 4000000 INFO @ Sat, 06 Jul 2019 01:50:20: 3000000 INFO @ Sat, 06 Jul 2019 01:50:27: 5000000 INFO @ Sat, 06 Jul 2019 01:50:28: 5000000 INFO @ Sat, 06 Jul 2019 01:50:31: 4000000 INFO @ Sat, 06 Jul 2019 01:50:32: #1 tag size is determined as 50 bps INFO @ Sat, 06 Jul 2019 01:50:32: #1 tag size = 50 INFO @ Sat, 06 Jul 2019 01:50:32: #1 total tags in treatment: 5701331 INFO @ Sat, 06 Jul 2019 01:50:32: #1 user defined the maximum tags... INFO @ Sat, 06 Jul 2019 01:50:32: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Sat, 06 Jul 2019 01:50:32: #1 tags after filtering in treatment: 5701331 INFO @ Sat, 06 Jul 2019 01:50:32: #1 Redundant rate of treatment: 0.00 INFO @ Sat, 06 Jul 2019 01:50:32: #1 finished! INFO @ Sat, 06 Jul 2019 01:50:32: #2 Build Peak Model... INFO @ Sat, 06 Jul 2019 01:50:32: #2 looking for paired plus/minus strand peaks... INFO @ Sat, 06 Jul 2019 01:50:33: #2 number of paired peaks: 0 WARNING @ Sat, 06 Jul 2019 01:50:33: 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 @ Sat, 06 Jul 2019 01:50:33: Process for pairing-model is terminated! cut: /home/okishinya/chipatlas/results/sacCer3/SRX4550108/SRX4550108.05_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/SRX4550108/SRX4550108.05_model.r’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX4550108/SRX4550108.05_*.xls’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX4550108/SRX4550108.05_peaks.narrowPeak’: No such file or directory CompletedMACS2peakCalling INFO @ Sat, 06 Jul 2019 01:50:33: #1 tag size is determined as 50 bps INFO @ Sat, 06 Jul 2019 01:50:33: #1 tag size = 50 INFO @ Sat, 06 Jul 2019 01:50:33: #1 total tags in treatment: 5701331 INFO @ Sat, 06 Jul 2019 01:50:33: #1 user defined the maximum tags... INFO @ Sat, 06 Jul 2019 01:50:33: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Sat, 06 Jul 2019 01:50:33: #1 tags after filtering in treatment: 5701331 INFO @ Sat, 06 Jul 2019 01:50:33: #1 Redundant rate of treatment: 0.00 INFO @ Sat, 06 Jul 2019 01:50:33: #1 finished! INFO @ Sat, 06 Jul 2019 01:50:33: #2 Build Peak Model... INFO @ Sat, 06 Jul 2019 01:50:33: #2 looking for paired plus/minus strand peaks... INFO @ Sat, 06 Jul 2019 01:50:34: #2 number of paired peaks: 0 WARNING @ Sat, 06 Jul 2019 01:50:34: 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 @ Sat, 06 Jul 2019 01:50:34: Process for pairing-model is terminated! cut: /home/okishinya/chipatlas/results/sacCer3/SRX4550108/SRX4550108.10_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/SRX4550108/SRX4550108.10_model.r’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX4550108/SRX4550108.10_*.xls’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX4550108/SRX4550108.10_peaks.narrowPeak’: No such file or directory CompletedMACS2peakCalling INFO @ Sat, 06 Jul 2019 01:50:40: 5000000 INFO @ Sat, 06 Jul 2019 01:50:47: #1 tag size is determined as 50 bps INFO @ Sat, 06 Jul 2019 01:50:47: #1 tag size = 50 INFO @ Sat, 06 Jul 2019 01:50:47: #1 total tags in treatment: 5701331 INFO @ Sat, 06 Jul 2019 01:50:47: #1 user defined the maximum tags... INFO @ Sat, 06 Jul 2019 01:50:47: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Sat, 06 Jul 2019 01:50:47: #1 tags after filtering in treatment: 5701331 INFO @ Sat, 06 Jul 2019 01:50:47: #1 Redundant rate of treatment: 0.00 INFO @ Sat, 06 Jul 2019 01:50:47: #1 finished! INFO @ Sat, 06 Jul 2019 01:50:47: #2 Build Peak Model... INFO @ Sat, 06 Jul 2019 01:50:47: #2 looking for paired plus/minus strand peaks... INFO @ Sat, 06 Jul 2019 01:50:47: #2 number of paired peaks: 0 WARNING @ Sat, 06 Jul 2019 01:50:47: 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 @ Sat, 06 Jul 2019 01:50:47: Process for pairing-model is terminated! cut: /home/okishinya/chipatlas/results/sacCer3/SRX4550108/SRX4550108.20_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/SRX4550108/SRX4550108.20_model.r’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX4550108/SRX4550108.20_*.xls’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX4550108/SRX4550108.20_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。