Job ID = 2011818 sra ファイルのダウンロード中... Read layout: SINGLE fastq に変換中... spots read : 3,172,287 reads read : 6,344,574 reads written : 3,172,287 reads 0-length : 3,172,287 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: 00:00:47 3172287 reads; of these: 3172287 (100.00%) were unpaired; of these: 243768 (7.68%) aligned 0 times 2601531 (82.01%) aligned exactly 1 time 326988 (10.31%) aligned >1 times 92.32% overall alignment rate Time searching: 00:00:47 Overall time: 00:00:47 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_rmdupse_core] 1139105 / 2928519 = 0.3890 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 02:46:30: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/SRX5028248/SRX5028248.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/SRX5028248/SRX5028248.05 -q 1e-05 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/SRX5028248/SRX5028248.05 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/SRX5028248/SRX5028248.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 02:46:30: #1 read tag files... INFO @ Sat, 06 Jul 2019 02:46:30: #1 read treatment tags... INFO @ Sat, 06 Jul 2019 02:46:31: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/SRX5028248/SRX5028248.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/SRX5028248/SRX5028248.10 -q 1e-10 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/SRX5028248/SRX5028248.10 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/SRX5028248/SRX5028248.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 02:46:31: #1 read tag files... INFO @ Sat, 06 Jul 2019 02:46:31: #1 read treatment tags... INFO @ Sat, 06 Jul 2019 02:46:38: 1000000 INFO @ Sat, 06 Jul 2019 02:46:40: 1000000 INFO @ Sat, 06 Jul 2019 02:46:44: #1 tag size is determined as 51 bps INFO @ Sat, 06 Jul 2019 02:46:44: #1 tag size = 51 INFO @ Sat, 06 Jul 2019 02:46:44: #1 total tags in treatment: 1789414 INFO @ Sat, 06 Jul 2019 02:46:44: #1 user defined the maximum tags... INFO @ Sat, 06 Jul 2019 02:46:44: #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 02:46:44: #1 tags after filtering in treatment: 1789414 INFO @ Sat, 06 Jul 2019 02:46:44: #1 Redundant rate of treatment: 0.00 INFO @ Sat, 06 Jul 2019 02:46:44: #1 finished! INFO @ Sat, 06 Jul 2019 02:46:44: #2 Build Peak Model... INFO @ Sat, 06 Jul 2019 02:46:44: #2 looking for paired plus/minus strand peaks... INFO @ Sat, 06 Jul 2019 02:46:44: #2 number of paired peaks: 32 WARNING @ Sat, 06 Jul 2019 02:46:44: Too few paired peaks (32) 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 02:46:44: Process for pairing-model is terminated! cut: /home/okishinya/chipatlas/results/sacCer3/SRX5028248/SRX5028248.05_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/SRX5028248/SRX5028248.05_model.r’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX5028248/SRX5028248.05_*.xls’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX5028248/SRX5028248.05_peaks.narrowPeak’: No such file or directory CompletedMACS2peakCalling INFO @ Sat, 06 Jul 2019 02:46:47: #1 tag size is determined as 51 bps INFO @ Sat, 06 Jul 2019 02:46:47: #1 tag size = 51 INFO @ Sat, 06 Jul 2019 02:46:47: #1 total tags in treatment: 1789414 INFO @ Sat, 06 Jul 2019 02:46:47: #1 user defined the maximum tags... INFO @ Sat, 06 Jul 2019 02:46:47: #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 02:46:47: #1 tags after filtering in treatment: 1789414 INFO @ Sat, 06 Jul 2019 02:46:47: #1 Redundant rate of treatment: 0.00 INFO @ Sat, 06 Jul 2019 02:46:47: #1 finished! INFO @ Sat, 06 Jul 2019 02:46:47: #2 Build Peak Model... INFO @ Sat, 06 Jul 2019 02:46:47: #2 looking for paired plus/minus strand peaks... INFO @ Sat, 06 Jul 2019 02:46:47: #2 number of paired peaks: 32 WARNING @ Sat, 06 Jul 2019 02:46:47: Too few paired peaks (32) 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 02:46:47: Process for pairing-model is terminated! cut: /home/okishinya/chipatlas/results/sacCer3/SRX5028248/SRX5028248.10_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/SRX5028248/SRX5028248.10_model.r’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX5028248/SRX5028248.10_*.xls’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX5028248/SRX5028248.10_peaks.narrowPeak’: No such file or directory CompletedMACS2peakCalling INFO @ Sat, 06 Jul 2019 02:46:48: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/SRX5028248/SRX5028248.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/SRX5028248/SRX5028248.20 -q 1e-20 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/SRX5028248/SRX5028248.20 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/SRX5028248/SRX5028248.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 02:46:48: #1 read tag files... INFO @ Sat, 06 Jul 2019 02:46:48: #1 read treatment tags... INFO @ Sat, 06 Jul 2019 02:46:56: 1000000 INFO @ Sat, 06 Jul 2019 02:47:02: #1 tag size is determined as 51 bps INFO @ Sat, 06 Jul 2019 02:47:02: #1 tag size = 51 INFO @ Sat, 06 Jul 2019 02:47:02: #1 total tags in treatment: 1789414 INFO @ Sat, 06 Jul 2019 02:47:02: #1 user defined the maximum tags... INFO @ Sat, 06 Jul 2019 02:47:02: #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 02:47:02: #1 tags after filtering in treatment: 1789414 INFO @ Sat, 06 Jul 2019 02:47:02: #1 Redundant rate of treatment: 0.00 INFO @ Sat, 06 Jul 2019 02:47:02: #1 finished! INFO @ Sat, 06 Jul 2019 02:47:02: #2 Build Peak Model... INFO @ Sat, 06 Jul 2019 02:47:02: #2 looking for paired plus/minus strand peaks... INFO @ Sat, 06 Jul 2019 02:47:02: #2 number of paired peaks: 32 WARNING @ Sat, 06 Jul 2019 02:47:02: Too few paired peaks (32) 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 02:47:02: Process for pairing-model is terminated! cut: /home/okishinya/chipatlas/results/sacCer3/SRX5028248/SRX5028248.20_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/SRX5028248/SRX5028248.20_model.r’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX5028248/SRX5028248.20_*.xls’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX5028248/SRX5028248.20_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。