Job ID = 2006280 sra ファイルのダウンロード中... Read layout: SINGLE fastq に変換中... spots read : 1,665,362 reads read : 1,665,362 reads written : 1,665,362 spots read : 1,579,604 reads read : 1,579,604 reads written : 1,579,604 spots read : 1,619,220 reads read : 1,619,220 reads written : 1,619,220 spots read : 1,589,513 reads read : 1,589,513 reads written : 1,589,513 rm: cannot remove ‘/home/okishinya/ncbi/public/sra/ERR2529414.sra.cache’: No such file or directory rm: cannot remove ‘/home/okishinya/ncbi/public/sra/ERR2529416.sra.cache’: No such file or directory rm: cannot remove ‘/home/okishinya/ncbi/public/sra/ERR2529417.sra.cache’: 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: 00:08:10 6453699 reads; of these: 6453699 (100.00%) were unpaired; of these: 181952 (2.82%) aligned 0 times 5386778 (83.47%) aligned exactly 1 time 884969 (13.71%) aligned >1 times 97.18% overall alignment rate Time searching: 00:08:10 Overall time: 00:08:10 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] 5757917 / 6271747 = 0.9181 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 15:27:29: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/ERX2548131/ERX2548131.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/ERX2548131/ERX2548131.05 -q 1e-05 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/ERX2548131/ERX2548131.05 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/ERX2548131/ERX2548131.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 15:27:29: #1 read tag files... INFO @ Fri, 05 Jul 2019 15:27:29: #1 read treatment tags... INFO @ Fri, 05 Jul 2019 15:27:29: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/ERX2548131/ERX2548131.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/ERX2548131/ERX2548131.10 -q 1e-10 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/ERX2548131/ERX2548131.10 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/ERX2548131/ERX2548131.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 15:27:29: #1 read tag files... INFO @ Fri, 05 Jul 2019 15:27:29: #1 read treatment tags... INFO @ Fri, 05 Jul 2019 15:27:30: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/ERX2548131/ERX2548131.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/ERX2548131/ERX2548131.20 -q 1e-20 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/ERX2548131/ERX2548131.20 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/ERX2548131/ERX2548131.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 15:27:30: #1 read tag files... INFO @ Fri, 05 Jul 2019 15:27:30: #1 read treatment tags... INFO @ Fri, 05 Jul 2019 15:27:33: #1 tag size is determined as 75 bps INFO @ Fri, 05 Jul 2019 15:27:33: #1 tag size = 75 INFO @ Fri, 05 Jul 2019 15:27:33: #1 total tags in treatment: 513830 INFO @ Fri, 05 Jul 2019 15:27:33: #1 user defined the maximum tags... INFO @ Fri, 05 Jul 2019 15:27:33: #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 15:27:33: #1 tags after filtering in treatment: 513830 INFO @ Fri, 05 Jul 2019 15:27:33: #1 Redundant rate of treatment: 0.00 INFO @ Fri, 05 Jul 2019 15:27:33: #1 finished! INFO @ Fri, 05 Jul 2019 15:27:33: #2 Build Peak Model... INFO @ Fri, 05 Jul 2019 15:27:33: #2 looking for paired plus/minus strand peaks... INFO @ Fri, 05 Jul 2019 15:27:33: #2 number of paired peaks: 283 WARNING @ Fri, 05 Jul 2019 15:27:33: Fewer paired peaks (283) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 283 pairs to build model! INFO @ Fri, 05 Jul 2019 15:27:33: start model_add_line... INFO @ Fri, 05 Jul 2019 15:27:33: start X-correlation... INFO @ Fri, 05 Jul 2019 15:27:33: end of X-cor INFO @ Fri, 05 Jul 2019 15:27:33: #2 finished! INFO @ Fri, 05 Jul 2019 15:27:33: #2 predicted fragment length is 179 bps INFO @ Fri, 05 Jul 2019 15:27:33: #2 alternative fragment length(s) may be 179 bps INFO @ Fri, 05 Jul 2019 15:27:33: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/sacCer3/ERX2548131/ERX2548131.05_model.r INFO @ Fri, 05 Jul 2019 15:27:33: #3 Call peaks... INFO @ Fri, 05 Jul 2019 15:27:33: #3 Pre-compute pvalue-qvalue table... INFO @ Fri, 05 Jul 2019 15:27:34: #1 tag size is determined as 75 bps INFO @ Fri, 05 Jul 2019 15:27:34: #1 tag size = 75 INFO @ Fri, 05 Jul 2019 15:27:34: #1 total tags in treatment: 513830 INFO @ Fri, 05 Jul 2019 15:27:34: #1 user defined the maximum tags... INFO @ Fri, 05 Jul 2019 15:27:34: #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 15:27:34: #1 tags after filtering in treatment: 513830 INFO @ Fri, 05 Jul 2019 15:27:34: #1 Redundant rate of treatment: 0.00 INFO @ Fri, 05 Jul 2019 15:27:34: #1 finished! INFO @ Fri, 05 Jul 2019 15:27:34: #2 Build Peak Model... INFO @ Fri, 05 Jul 2019 15:27:34: #2 looking for paired plus/minus strand peaks... INFO @ Fri, 05 Jul 2019 15:27:35: #2 number of paired peaks: 283 WARNING @ Fri, 05 Jul 2019 15:27:35: Fewer paired peaks (283) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 283 pairs to build model! INFO @ Fri, 05 Jul 2019 15:27:35: start model_add_line... INFO @ Fri, 05 Jul 2019 15:27:35: start X-correlation... INFO @ Fri, 05 Jul 2019 15:27:35: end of X-cor INFO @ Fri, 05 Jul 2019 15:27:35: #2 finished! INFO @ Fri, 05 Jul 2019 15:27:35: #2 predicted fragment length is 179 bps INFO @ Fri, 05 Jul 2019 15:27:35: #2 alternative fragment length(s) may be 179 bps INFO @ Fri, 05 Jul 2019 15:27:35: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/sacCer3/ERX2548131/ERX2548131.10_model.r INFO @ Fri, 05 Jul 2019 15:27:35: #3 Call peaks... INFO @ Fri, 05 Jul 2019 15:27:35: #3 Pre-compute pvalue-qvalue table... INFO @ Fri, 05 Jul 2019 15:27:35: #3 Call peaks for each chromosome... INFO @ Fri, 05 Jul 2019 15:27:36: #4 Write output xls file... /home/okishinya/chipatlas/results/sacCer3/ERX2548131/ERX2548131.05_peaks.xls INFO @ Fri, 05 Jul 2019 15:27:36: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/sacCer3/ERX2548131/ERX2548131.05_peaks.narrowPeak INFO @ Fri, 05 Jul 2019 15:27:36: #4 Write summits bed file... /home/okishinya/chipatlas/results/sacCer3/ERX2548131/ERX2548131.05_summits.bed INFO @ Fri, 05 Jul 2019 15:27:36: Done! INFO @ Fri, 05 Jul 2019 15:27:36: #1 tag size is determined as 75 bps INFO @ Fri, 05 Jul 2019 15:27:36: #1 tag size = 75 INFO @ Fri, 05 Jul 2019 15:27:36: #1 total tags in treatment: 513830 INFO @ Fri, 05 Jul 2019 15:27:36: #1 user defined the maximum tags... INFO @ Fri, 05 Jul 2019 15:27:36: #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 15:27:36: #1 tags after filtering in treatment: 513830 INFO @ Fri, 05 Jul 2019 15:27:36: #1 Redundant rate of treatment: 0.00 INFO @ Fri, 05 Jul 2019 15:27:36: #1 finished! INFO @ Fri, 05 Jul 2019 15:27:36: #2 Build Peak Model... INFO @ Fri, 05 Jul 2019 15:27:36: #2 looking for paired plus/minus strand peaks... pass1 - making usageList (16 chroms): 1 millis pass2 - checking and writing primary data (459 records, 4 fields): 4 millis INFO @ Fri, 05 Jul 2019 15:27:36: #2 number of paired peaks: 283 WARNING @ Fri, 05 Jul 2019 15:27:36: Fewer paired peaks (283) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 283 pairs to build model! INFO @ Fri, 05 Jul 2019 15:27:36: start model_add_line... INFO @ Fri, 05 Jul 2019 15:27:36: start X-correlation... INFO @ Fri, 05 Jul 2019 15:27:36: end of X-cor INFO @ Fri, 05 Jul 2019 15:27:36: #2 finished! INFO @ Fri, 05 Jul 2019 15:27:36: #2 predicted fragment length is 179 bps INFO @ Fri, 05 Jul 2019 15:27:36: #2 alternative fragment length(s) may be 179 bps INFO @ Fri, 05 Jul 2019 15:27:36: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/sacCer3/ERX2548131/ERX2548131.20_model.r INFO @ Fri, 05 Jul 2019 15:27:36: #3 Call peaks... INFO @ Fri, 05 Jul 2019 15:27:36: #3 Pre-compute pvalue-qvalue table... INFO @ Fri, 05 Jul 2019 15:27:37: #3 Call peaks for each chromosome... INFO @ Fri, 05 Jul 2019 15:27:37: #4 Write output xls file... /home/okishinya/chipatlas/results/sacCer3/ERX2548131/ERX2548131.10_peaks.xls INFO @ Fri, 05 Jul 2019 15:27:37: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/sacCer3/ERX2548131/ERX2548131.10_peaks.narrowPeak INFO @ Fri, 05 Jul 2019 15:27:37: #4 Write summits bed file... /home/okishinya/chipatlas/results/sacCer3/ERX2548131/ERX2548131.10_summits.bed INFO @ Fri, 05 Jul 2019 15:27:37: Done! pass1 - making usageList (16 chroms): 1 millis pass2 - checking and writing primary data (273 records, 4 fields): 3 millis INFO @ Fri, 05 Jul 2019 15:27:38: #3 Call peaks for each chromosome... CompletedMACS2peakCalling INFO @ Fri, 05 Jul 2019 15:27:39: #4 Write output xls file... /home/okishinya/chipatlas/results/sacCer3/ERX2548131/ERX2548131.20_peaks.xls INFO @ Fri, 05 Jul 2019 15:27:39: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/sacCer3/ERX2548131/ERX2548131.20_peaks.narrowPeak INFO @ Fri, 05 Jul 2019 15:27:39: #4 Write summits bed file... /home/okishinya/chipatlas/results/sacCer3/ERX2548131/ERX2548131.20_summits.bed INFO @ Fri, 05 Jul 2019 15:27:39: Done! pass1 - making usageList (15 chroms): 1 millis pass2 - checking and writing primary data (164 records, 4 fields): 3 millis BedGraph に変換しました。 BigWig に変換中... CompletedMACS2peakCalling CompletedMACS2peakCalling BigWig に変換しました。