Job ID = 2641221 sra ファイルのダウンロード中... Read layout: SINGLE fastq に変換中... spots read : 21,973,770 reads read : 21,973,770 reads written : 21,973,770 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: 00:03:37 21973770 reads; of these: 21973770 (100.00%) were unpaired; of these: 2679883 (12.20%) aligned 0 times 17586127 (80.03%) aligned exactly 1 time 1707760 (7.77%) aligned >1 times 87.80% overall alignment rate Time searching: 00:03:37 Overall time: 00:03:37 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] 15540885 / 19293887 = 0.8055 in library ' ' BAM に変換しました。 Bed ファイルを作成中... INFO @ Sat, 24 Aug 2019 22:06:05: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/SRX5820055/SRX5820055.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/SRX5820055/SRX5820055.05 -q 1e-05 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/SRX5820055/SRX5820055.05 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/SRX5820055/SRX5820055.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, 24 Aug 2019 22:06:05: #1 read tag files... INFO @ Sat, 24 Aug 2019 22:06:05: #1 read treatment tags... INFO @ Sat, 24 Aug 2019 22:06:13: 1000000 INFO @ Sat, 24 Aug 2019 22:06:21: 2000000 INFO @ Sat, 24 Aug 2019 22:06:29: 3000000 INFO @ Sat, 24 Aug 2019 22:06:34: #1 tag size is determined as 51 bps INFO @ Sat, 24 Aug 2019 22:06:34: #1 tag size = 51 INFO @ Sat, 24 Aug 2019 22:06:34: #1 total tags in treatment: 3753002 INFO @ Sat, 24 Aug 2019 22:06:34: #1 user defined the maximum tags... INFO @ Sat, 24 Aug 2019 22:06:34: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Sat, 24 Aug 2019 22:06:34: #1 tags after filtering in treatment: 3753002 INFO @ Sat, 24 Aug 2019 22:06:34: #1 Redundant rate of treatment: 0.00 INFO @ Sat, 24 Aug 2019 22:06:34: #1 finished! INFO @ Sat, 24 Aug 2019 22:06:34: #2 Build Peak Model... INFO @ Sat, 24 Aug 2019 22:06:34: #2 looking for paired plus/minus strand peaks... INFO @ Sat, 24 Aug 2019 22:06:35: #2 number of paired peaks: 45 WARNING @ Sat, 24 Aug 2019 22:06:35: Too few paired peaks (45) 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, 24 Aug 2019 22:06:35: Process for pairing-model is terminated! cut: /home/okishinya/chipatlas/results/sacCer3/SRX5820055/SRX5820055.05_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/SRX5820055/SRX5820055.05_model.r’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX5820055/SRX5820055.05_*.xls’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX5820055/SRX5820055.05_peaks.narrowPeak’: No such file or directory CompletedMACS2peakCalling INFO @ Sat, 24 Aug 2019 22:06:36: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/SRX5820055/SRX5820055.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/SRX5820055/SRX5820055.10 -q 1e-10 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/SRX5820055/SRX5820055.10 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/SRX5820055/SRX5820055.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, 24 Aug 2019 22:06:36: #1 read tag files... INFO @ Sat, 24 Aug 2019 22:06:36: #1 read treatment tags... INFO @ Sat, 24 Aug 2019 22:06:43: 1000000 INFO @ Sat, 24 Aug 2019 22:06:50: 2000000 INFO @ Sat, 24 Aug 2019 22:06:56: 3000000 INFO @ Sat, 24 Aug 2019 22:07:02: #1 tag size is determined as 51 bps INFO @ Sat, 24 Aug 2019 22:07:02: #1 tag size = 51 INFO @ Sat, 24 Aug 2019 22:07:02: #1 total tags in treatment: 3753002 INFO @ Sat, 24 Aug 2019 22:07:02: #1 user defined the maximum tags... INFO @ Sat, 24 Aug 2019 22:07:02: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Sat, 24 Aug 2019 22:07:02: #1 tags after filtering in treatment: 3753002 INFO @ Sat, 24 Aug 2019 22:07:02: #1 Redundant rate of treatment: 0.00 INFO @ Sat, 24 Aug 2019 22:07:02: #1 finished! INFO @ Sat, 24 Aug 2019 22:07:02: #2 Build Peak Model... INFO @ Sat, 24 Aug 2019 22:07:02: #2 looking for paired plus/minus strand peaks... INFO @ Sat, 24 Aug 2019 22:07:02: #2 number of paired peaks: 45 WARNING @ Sat, 24 Aug 2019 22:07:02: Too few paired peaks (45) 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, 24 Aug 2019 22:07:02: Process for pairing-model is terminated! cut: /home/okishinya/chipatlas/results/sacCer3/SRX5820055/SRX5820055.10_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/SRX5820055/SRX5820055.10_model.r’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX5820055/SRX5820055.10_*.xls’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX5820055/SRX5820055.10_peaks.narrowPeak’: No such file or directory CompletedMACS2peakCalling BedGraph に変換中... INFO @ Sat, 24 Aug 2019 22:07:05: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/SRX5820055/SRX5820055.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/SRX5820055/SRX5820055.20 -q 1e-20 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/SRX5820055/SRX5820055.20 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/SRX5820055/SRX5820055.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, 24 Aug 2019 22:07:05: #1 read tag files... INFO @ Sat, 24 Aug 2019 22:07:05: #1 read treatment tags... INFO @ Sat, 24 Aug 2019 22:07:14: 1000000 INFO @ Sat, 24 Aug 2019 22:07:23: 2000000 INFO @ Sat, 24 Aug 2019 22:07:32: 3000000 INFO @ Sat, 24 Aug 2019 22:07:38: #1 tag size is determined as 51 bps INFO @ Sat, 24 Aug 2019 22:07:38: #1 tag size = 51 INFO @ Sat, 24 Aug 2019 22:07:38: #1 total tags in treatment: 3753002 INFO @ Sat, 24 Aug 2019 22:07:38: #1 user defined the maximum tags... INFO @ Sat, 24 Aug 2019 22:07:38: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Sat, 24 Aug 2019 22:07:38: #1 tags after filtering in treatment: 3753002 INFO @ Sat, 24 Aug 2019 22:07:38: #1 Redundant rate of treatment: 0.00 INFO @ Sat, 24 Aug 2019 22:07:38: #1 finished! INFO @ Sat, 24 Aug 2019 22:07:38: #2 Build Peak Model... INFO @ Sat, 24 Aug 2019 22:07:38: #2 looking for paired plus/minus strand peaks... INFO @ Sat, 24 Aug 2019 22:07:39: #2 number of paired peaks: 45 WARNING @ Sat, 24 Aug 2019 22:07:39: Too few paired peaks (45) 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, 24 Aug 2019 22:07:39: Process for pairing-model is terminated! cut: /home/okishinya/chipatlas/results/sacCer3/SRX5820055/SRX5820055.20_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/SRX5820055/SRX5820055.20_model.r’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX5820055/SRX5820055.20_*.xls’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX5820055/SRX5820055.20_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。