Job ID = 2011016 sra ファイルのダウンロード中... Read layout: SINGLE fastq に変換中... spots read : 5,953,428 reads read : 11,906,856 reads written : 5,953,428 reads 0-length : 5,953,428 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: 00:01:06 5953428 reads; of these: 5953428 (100.00%) were unpaired; of these: 435930 (7.32%) aligned 0 times 4786510 (80.40%) aligned exactly 1 time 730988 (12.28%) aligned >1 times 92.68% overall alignment rate Time searching: 00:01:06 Overall time: 00:01:06 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] 1129418 / 5517498 = 0.2047 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 01:42:41: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/SRX4550096/SRX4550096.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/SRX4550096/SRX4550096.05 -q 1e-05 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/SRX4550096/SRX4550096.05 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/SRX4550096/SRX4550096.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 01:42:41: #1 read tag files... INFO @ Sat, 06 Jul 2019 01:42:41: #1 read treatment tags... INFO @ Sat, 06 Jul 2019 01:42:42: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/SRX4550096/SRX4550096.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/SRX4550096/SRX4550096.10 -q 1e-10 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/SRX4550096/SRX4550096.10 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/SRX4550096/SRX4550096.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 01:42:42: #1 read tag files... INFO @ Sat, 06 Jul 2019 01:42:42: #1 read treatment tags... INFO @ Sat, 06 Jul 2019 01:42:43: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/SRX4550096/SRX4550096.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/SRX4550096/SRX4550096.20 -q 1e-20 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/SRX4550096/SRX4550096.20 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/SRX4550096/SRX4550096.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 01:42:43: #1 read tag files... INFO @ Sat, 06 Jul 2019 01:42:43: #1 read treatment tags... INFO @ Sat, 06 Jul 2019 01:42:50: 1000000 INFO @ Sat, 06 Jul 2019 01:42:52: 1000000 INFO @ Sat, 06 Jul 2019 01:42:52: 1000000 INFO @ Sat, 06 Jul 2019 01:42:59: 2000000 INFO @ Sat, 06 Jul 2019 01:43:01: 2000000 INFO @ Sat, 06 Jul 2019 01:43:03: 2000000 INFO @ Sat, 06 Jul 2019 01:43:10: 3000000 INFO @ Sat, 06 Jul 2019 01:43:11: 3000000 INFO @ Sat, 06 Jul 2019 01:43:13: 3000000 INFO @ Sat, 06 Jul 2019 01:43:19: 4000000 INFO @ Sat, 06 Jul 2019 01:43:21: 4000000 INFO @ Sat, 06 Jul 2019 01:43:22: #1 tag size is determined as 50 bps INFO @ Sat, 06 Jul 2019 01:43:22: #1 tag size = 50 INFO @ Sat, 06 Jul 2019 01:43:22: #1 total tags in treatment: 4388080 INFO @ Sat, 06 Jul 2019 01:43:22: #1 user defined the maximum tags... INFO @ Sat, 06 Jul 2019 01:43:22: #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 01:43:23: #1 tags after filtering in treatment: 4388080 INFO @ Sat, 06 Jul 2019 01:43:23: #1 Redundant rate of treatment: 0.00 INFO @ Sat, 06 Jul 2019 01:43:23: #1 finished! INFO @ Sat, 06 Jul 2019 01:43:23: #2 Build Peak Model... INFO @ Sat, 06 Jul 2019 01:43:23: #2 looking for paired plus/minus strand peaks... INFO @ Sat, 06 Jul 2019 01:43:23: 4000000 INFO @ Sat, 06 Jul 2019 01:43:23: #2 number of paired peaks: 30 WARNING @ Sat, 06 Jul 2019 01:43:23: Too few paired peaks (30) 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 01:43:23: Process for pairing-model is terminated! cut: /home/okishinya/chipatlas/results/sacCer3/SRX4550096/SRX4550096.05_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/SRX4550096/SRX4550096.05_model.r’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX4550096/SRX4550096.05_*.xls’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX4550096/SRX4550096.05_peaks.narrowPeak’: No such file or directory CompletedMACS2peakCalling INFO @ Sat, 06 Jul 2019 01:43:24: #1 tag size is determined as 50 bps INFO @ Sat, 06 Jul 2019 01:43:24: #1 tag size = 50 INFO @ Sat, 06 Jul 2019 01:43:24: #1 total tags in treatment: 4388080 INFO @ Sat, 06 Jul 2019 01:43:24: #1 user defined the maximum tags... INFO @ Sat, 06 Jul 2019 01:43:24: #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 01:43:24: #1 tags after filtering in treatment: 4388080 INFO @ Sat, 06 Jul 2019 01:43:24: #1 Redundant rate of treatment: 0.00 INFO @ Sat, 06 Jul 2019 01:43:24: #1 finished! INFO @ Sat, 06 Jul 2019 01:43:24: #2 Build Peak Model... INFO @ Sat, 06 Jul 2019 01:43:24: #2 looking for paired plus/minus strand peaks... INFO @ Sat, 06 Jul 2019 01:43:24: #2 number of paired peaks: 30 WARNING @ Sat, 06 Jul 2019 01:43:24: Too few paired peaks (30) 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 01:43:24: Process for pairing-model is terminated! cut: /home/okishinya/chipatlas/results/sacCer3/SRX4550096/SRX4550096.20_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/SRX4550096/SRX4550096.20_model.r’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX4550096/SRX4550096.20_*.xls’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX4550096/SRX4550096.20_peaks.narrowPeak’: No such file or directory CompletedMACS2peakCalling INFO @ Sat, 06 Jul 2019 01:43:26: #1 tag size is determined as 50 bps INFO @ Sat, 06 Jul 2019 01:43:26: #1 tag size = 50 INFO @ Sat, 06 Jul 2019 01:43:26: #1 total tags in treatment: 4388080 INFO @ Sat, 06 Jul 2019 01:43:26: #1 user defined the maximum tags... INFO @ Sat, 06 Jul 2019 01:43:26: #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 01:43:26: #1 tags after filtering in treatment: 4388080 INFO @ Sat, 06 Jul 2019 01:43:26: #1 Redundant rate of treatment: 0.00 INFO @ Sat, 06 Jul 2019 01:43:26: #1 finished! INFO @ Sat, 06 Jul 2019 01:43:26: #2 Build Peak Model... INFO @ Sat, 06 Jul 2019 01:43:26: #2 looking for paired plus/minus strand peaks... INFO @ Sat, 06 Jul 2019 01:43:27: #2 number of paired peaks: 30 WARNING @ Sat, 06 Jul 2019 01:43:27: Too few paired peaks (30) 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 01:43:27: Process for pairing-model is terminated! cut: /home/okishinya/chipatlas/results/sacCer3/SRX4550096/SRX4550096.10_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/SRX4550096/SRX4550096.10_model.r’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX4550096/SRX4550096.10_*.xls’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX4550096/SRX4550096.10_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。