Job ID = 2010143 sra ファイルのダウンロード中... Read layout: SINGLE fastq に変換中... spots read : 13,190,796 reads read : 13,190,796 reads written : 13,190,796 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: 00:01:31 13190796 reads; of these: 13190796 (100.00%) were unpaired; of these: 8098878 (61.40%) aligned 0 times 4157860 (31.52%) aligned exactly 1 time 934058 (7.08%) aligned >1 times 38.60% overall alignment rate Time searching: 00:01:31 Overall time: 00:01:31 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] 1142149 / 5091918 = 0.2243 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 21:36:28: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/SRX2772218/SRX2772218.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/SRX2772218/SRX2772218.05 -q 1e-05 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/SRX2772218/SRX2772218.05 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/SRX2772218/SRX2772218.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 21:36:28: #1 read tag files... INFO @ Fri, 05 Jul 2019 21:36:28: #1 read treatment tags... INFO @ Fri, 05 Jul 2019 21:36:29: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/SRX2772218/SRX2772218.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/SRX2772218/SRX2772218.10 -q 1e-10 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/SRX2772218/SRX2772218.10 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/SRX2772218/SRX2772218.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 21:36:29: #1 read tag files... INFO @ Fri, 05 Jul 2019 21:36:29: #1 read treatment tags... INFO @ Fri, 05 Jul 2019 21:36:30: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/SRX2772218/SRX2772218.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/SRX2772218/SRX2772218.20 -q 1e-20 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/SRX2772218/SRX2772218.20 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/SRX2772218/SRX2772218.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 21:36:30: #1 read tag files... INFO @ Fri, 05 Jul 2019 21:36:30: #1 read treatment tags... INFO @ Fri, 05 Jul 2019 21:36:39: 1000000 INFO @ Fri, 05 Jul 2019 21:36:40: 1000000 INFO @ Fri, 05 Jul 2019 21:36:42: 1000000 INFO @ Fri, 05 Jul 2019 21:36:50: 2000000 INFO @ Fri, 05 Jul 2019 21:36:50: 2000000 INFO @ Fri, 05 Jul 2019 21:36:53: 2000000 INFO @ Fri, 05 Jul 2019 21:37:00: 3000000 INFO @ Fri, 05 Jul 2019 21:37:00: 3000000 INFO @ Fri, 05 Jul 2019 21:37:02: 3000000 INFO @ Fri, 05 Jul 2019 21:37:10: #1 tag size is determined as 50 bps INFO @ Fri, 05 Jul 2019 21:37:10: #1 tag size = 50 INFO @ Fri, 05 Jul 2019 21:37:10: #1 total tags in treatment: 3949769 INFO @ Fri, 05 Jul 2019 21:37:10: #1 user defined the maximum tags... INFO @ Fri, 05 Jul 2019 21:37:10: #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 21:37:10: #1 tag size is determined as 50 bps INFO @ Fri, 05 Jul 2019 21:37:10: #1 tag size = 50 INFO @ Fri, 05 Jul 2019 21:37:10: #1 total tags in treatment: 3949769 INFO @ Fri, 05 Jul 2019 21:37:10: #1 user defined the maximum tags... INFO @ Fri, 05 Jul 2019 21:37:10: #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 21:37:10: #1 tags after filtering in treatment: 3949769 INFO @ Fri, 05 Jul 2019 21:37:10: #1 Redundant rate of treatment: 0.00 INFO @ Fri, 05 Jul 2019 21:37:10: #1 finished! INFO @ Fri, 05 Jul 2019 21:37:10: #2 Build Peak Model... INFO @ Fri, 05 Jul 2019 21:37:10: #2 looking for paired plus/minus strand peaks... INFO @ Fri, 05 Jul 2019 21:37:10: #1 tags after filtering in treatment: 3949769 INFO @ Fri, 05 Jul 2019 21:37:10: #1 Redundant rate of treatment: 0.00 INFO @ Fri, 05 Jul 2019 21:37:10: #1 finished! INFO @ Fri, 05 Jul 2019 21:37:10: #2 Build Peak Model... INFO @ Fri, 05 Jul 2019 21:37:10: #2 looking for paired plus/minus strand peaks... INFO @ Fri, 05 Jul 2019 21:37:11: #2 number of paired peaks: 29 WARNING @ Fri, 05 Jul 2019 21:37:11: Too few paired peaks (29) 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 21:37:11: Process for pairing-model is terminated! INFO @ Fri, 05 Jul 2019 21:37:11: #2 number of paired peaks: 29 WARNING @ Fri, 05 Jul 2019 21:37:11: Too few paired peaks (29) 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 21:37:11: Process for pairing-model is terminated! cut: /home/okishinya/chipatlas/results/sacCer3/SRX2772218/SRX2772218.10_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/SRX2772218/SRX2772218.10_model.r’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX2772218/SRX2772218.10_*.xls’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX2772218/SRX2772218.10_peaks.narrowPeak’: No such file or directory CompletedMACS2peakCalling cut: /home/okishinya/chipatlas/results/sacCer3/SRX2772218/SRX2772218.05_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/SRX2772218/SRX2772218.05_model.r’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX2772218/SRX2772218.05_*.xls’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX2772218/SRX2772218.05_peaks.narrowPeak’: No such file or directory CompletedMACS2peakCalling INFO @ Fri, 05 Jul 2019 21:37:12: #1 tag size is determined as 50 bps INFO @ Fri, 05 Jul 2019 21:37:12: #1 tag size = 50 INFO @ Fri, 05 Jul 2019 21:37:12: #1 total tags in treatment: 3949769 INFO @ Fri, 05 Jul 2019 21:37:12: #1 user defined the maximum tags... INFO @ Fri, 05 Jul 2019 21:37:12: #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 21:37:12: #1 tags after filtering in treatment: 3949769 INFO @ Fri, 05 Jul 2019 21:37:12: #1 Redundant rate of treatment: 0.00 INFO @ Fri, 05 Jul 2019 21:37:12: #1 finished! INFO @ Fri, 05 Jul 2019 21:37:12: #2 Build Peak Model... INFO @ Fri, 05 Jul 2019 21:37:12: #2 looking for paired plus/minus strand peaks... INFO @ Fri, 05 Jul 2019 21:37:12: #2 number of paired peaks: 29 WARNING @ Fri, 05 Jul 2019 21:37:12: Too few paired peaks (29) 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 21:37:12: Process for pairing-model is terminated! cut: /home/okishinya/chipatlas/results/sacCer3/SRX2772218/SRX2772218.20_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/SRX2772218/SRX2772218.20_model.r’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX2772218/SRX2772218.20_*.xls’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX2772218/SRX2772218.20_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。