Job ID = 2007597 sra ファイルのダウンロード中... Read layout: SINGLE fastq に変換中... spots read : 13,037,075 reads read : 13,037,075 reads written : 13,037,075 rm: cannot remove ‘[DSE]RR*’: No such file or directory rm: cannot remove ‘/home/okishinya/ncbi/public/sra/ERR2529727.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: 00:03:22 13037075 reads; of these: 13037075 (100.00%) were unpaired; of these: 385972 (2.96%) aligned 0 times 10178819 (78.08%) aligned exactly 1 time 2472284 (18.96%) aligned >1 times 97.04% overall alignment rate Time searching: 00:03:22 Overall time: 00:03:22 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] 12481271 / 12651103 = 0.9866 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 16:01:02: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/ERX2548222/ERX2548222.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/ERX2548222/ERX2548222.05 -q 1e-05 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/ERX2548222/ERX2548222.05 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/ERX2548222/ERX2548222.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 16:01:02: #1 read tag files... INFO @ Fri, 05 Jul 2019 16:01:02: #1 read treatment tags... INFO @ Fri, 05 Jul 2019 16:01:02: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/ERX2548222/ERX2548222.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/ERX2548222/ERX2548222.10 -q 1e-10 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/ERX2548222/ERX2548222.10 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/ERX2548222/ERX2548222.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 16:01:02: #1 read tag files... INFO @ Fri, 05 Jul 2019 16:01:02: #1 read treatment tags... INFO @ Fri, 05 Jul 2019 16:01:04: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/ERX2548222/ERX2548222.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/ERX2548222/ERX2548222.20 -q 1e-20 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/ERX2548222/ERX2548222.20 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/ERX2548222/ERX2548222.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 16:01:04: #1 read tag files... INFO @ Fri, 05 Jul 2019 16:01:04: #1 read treatment tags... INFO @ Fri, 05 Jul 2019 16:01:04: #1 tag size is determined as 53 bps INFO @ Fri, 05 Jul 2019 16:01:04: #1 tag size = 53 INFO @ Fri, 05 Jul 2019 16:01:04: #1 total tags in treatment: 169832 INFO @ Fri, 05 Jul 2019 16:01:04: #1 user defined the maximum tags... INFO @ Fri, 05 Jul 2019 16:01:04: #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 16:01:04: #1 tags after filtering in treatment: 169832 INFO @ Fri, 05 Jul 2019 16:01:04: #1 Redundant rate of treatment: 0.00 INFO @ Fri, 05 Jul 2019 16:01:04: #1 finished! INFO @ Fri, 05 Jul 2019 16:01:04: #2 Build Peak Model... INFO @ Fri, 05 Jul 2019 16:01:04: #2 looking for paired plus/minus strand peaks... INFO @ Fri, 05 Jul 2019 16:01:04: #2 number of paired peaks: 491 WARNING @ Fri, 05 Jul 2019 16:01:04: Fewer paired peaks (491) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 491 pairs to build model! INFO @ Fri, 05 Jul 2019 16:01:04: start model_add_line... INFO @ Fri, 05 Jul 2019 16:01:04: start X-correlation... INFO @ Fri, 05 Jul 2019 16:01:04: end of X-cor INFO @ Fri, 05 Jul 2019 16:01:04: #2 finished! INFO @ Fri, 05 Jul 2019 16:01:04: #2 predicted fragment length is 112 bps INFO @ Fri, 05 Jul 2019 16:01:04: #2 alternative fragment length(s) may be 79,112,137,503,538,592,594 bps INFO @ Fri, 05 Jul 2019 16:01:04: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/sacCer3/ERX2548222/ERX2548222.05_model.r INFO @ Fri, 05 Jul 2019 16:01:04: #3 Call peaks... INFO @ Fri, 05 Jul 2019 16:01:04: #3 Pre-compute pvalue-qvalue table... INFO @ Fri, 05 Jul 2019 16:01:04: #1 tag size is determined as 53 bps INFO @ Fri, 05 Jul 2019 16:01:04: #1 tag size = 53 INFO @ Fri, 05 Jul 2019 16:01:04: #1 total tags in treatment: 169832 INFO @ Fri, 05 Jul 2019 16:01:04: #1 user defined the maximum tags... INFO @ Fri, 05 Jul 2019 16:01:04: #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 16:01:04: #1 tags after filtering in treatment: 169832 INFO @ Fri, 05 Jul 2019 16:01:04: #1 Redundant rate of treatment: 0.00 INFO @ Fri, 05 Jul 2019 16:01:04: #1 finished! INFO @ Fri, 05 Jul 2019 16:01:04: #2 Build Peak Model... INFO @ Fri, 05 Jul 2019 16:01:04: #2 looking for paired plus/minus strand peaks... INFO @ Fri, 05 Jul 2019 16:01:04: #2 number of paired peaks: 491 WARNING @ Fri, 05 Jul 2019 16:01:04: Fewer paired peaks (491) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 491 pairs to build model! INFO @ Fri, 05 Jul 2019 16:01:04: start model_add_line... INFO @ Fri, 05 Jul 2019 16:01:04: start X-correlation... INFO @ Fri, 05 Jul 2019 16:01:04: end of X-cor INFO @ Fri, 05 Jul 2019 16:01:04: #2 finished! INFO @ Fri, 05 Jul 2019 16:01:04: #2 predicted fragment length is 112 bps INFO @ Fri, 05 Jul 2019 16:01:04: #2 alternative fragment length(s) may be 79,112,137,503,538,592,594 bps INFO @ Fri, 05 Jul 2019 16:01:04: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/sacCer3/ERX2548222/ERX2548222.10_model.r INFO @ Fri, 05 Jul 2019 16:01:04: #3 Call peaks... INFO @ Fri, 05 Jul 2019 16:01:04: #3 Pre-compute pvalue-qvalue table... INFO @ Fri, 05 Jul 2019 16:01:05: #3 Call peaks for each chromosome... INFO @ Fri, 05 Jul 2019 16:01:05: #3 Call peaks for each chromosome... INFO @ Fri, 05 Jul 2019 16:01:05: #4 Write output xls file... /home/okishinya/chipatlas/results/sacCer3/ERX2548222/ERX2548222.05_peaks.xls INFO @ Fri, 05 Jul 2019 16:01:05: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/sacCer3/ERX2548222/ERX2548222.05_peaks.narrowPeak INFO @ Fri, 05 Jul 2019 16:01:05: #4 Write summits bed file... /home/okishinya/chipatlas/results/sacCer3/ERX2548222/ERX2548222.05_summits.bed INFO @ Fri, 05 Jul 2019 16:01:05: Done! pass1 - making usageList (16 chroms): 1 millis pass2 - checking and writing primary data (245 records, 4 fields): 2 millis INFO @ Fri, 05 Jul 2019 16:01:05: #4 Write output xls file... /home/okishinya/chipatlas/results/sacCer3/ERX2548222/ERX2548222.10_peaks.xls INFO @ Fri, 05 Jul 2019 16:01:05: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/sacCer3/ERX2548222/ERX2548222.10_peaks.narrowPeak INFO @ Fri, 05 Jul 2019 16:01:05: #4 Write summits bed file... /home/okishinya/chipatlas/results/sacCer3/ERX2548222/ERX2548222.10_summits.bed INFO @ Fri, 05 Jul 2019 16:01:05: Done! pass1 - making usageList (15 chroms): 0 millis pass2 - checking and writing primary data (107 records, 4 fields): 3 millis INFO @ Fri, 05 Jul 2019 16:01:05: #1 tag size is determined as 53 bps INFO @ Fri, 05 Jul 2019 16:01:05: #1 tag size = 53 INFO @ Fri, 05 Jul 2019 16:01:05: #1 total tags in treatment: 169832 INFO @ Fri, 05 Jul 2019 16:01:05: #1 user defined the maximum tags... INFO @ Fri, 05 Jul 2019 16:01:05: #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 16:01:05: #1 tags after filtering in treatment: 169832 INFO @ Fri, 05 Jul 2019 16:01:05: #1 Redundant rate of treatment: 0.00 INFO @ Fri, 05 Jul 2019 16:01:05: #1 finished! INFO @ Fri, 05 Jul 2019 16:01:05: #2 Build Peak Model... INFO @ Fri, 05 Jul 2019 16:01:05: #2 looking for paired plus/minus strand peaks... INFO @ Fri, 05 Jul 2019 16:01:05: #2 number of paired peaks: 491 WARNING @ Fri, 05 Jul 2019 16:01:05: Fewer paired peaks (491) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 491 pairs to build model! INFO @ Fri, 05 Jul 2019 16:01:05: start model_add_line... INFO @ Fri, 05 Jul 2019 16:01:05: start X-correlation... INFO @ Fri, 05 Jul 2019 16:01:05: end of X-cor INFO @ Fri, 05 Jul 2019 16:01:05: #2 finished! INFO @ Fri, 05 Jul 2019 16:01:05: #2 predicted fragment length is 112 bps INFO @ Fri, 05 Jul 2019 16:01:05: #2 alternative fragment length(s) may be 79,112,137,503,538,592,594 bps INFO @ Fri, 05 Jul 2019 16:01:05: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/sacCer3/ERX2548222/ERX2548222.20_model.r INFO @ Fri, 05 Jul 2019 16:01:05: #3 Call peaks... INFO @ Fri, 05 Jul 2019 16:01:05: #3 Pre-compute pvalue-qvalue table... INFO @ Fri, 05 Jul 2019 16:01:06: #3 Call peaks for each chromosome... INFO @ Fri, 05 Jul 2019 16:01:06: #4 Write output xls file... /home/okishinya/chipatlas/results/sacCer3/ERX2548222/ERX2548222.20_peaks.xls INFO @ Fri, 05 Jul 2019 16:01:06: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/sacCer3/ERX2548222/ERX2548222.20_peaks.narrowPeak INFO @ Fri, 05 Jul 2019 16:01:06: #4 Write summits bed file... /home/okishinya/chipatlas/results/sacCer3/ERX2548222/ERX2548222.20_summits.bed INFO @ Fri, 05 Jul 2019 16:01:06: Done! pass1 - making usageList (14 chroms): 1 millis pass2 - checking and writing primary data (54 records, 4 fields): 2 millis CompletedMACS2peakCalling BedGraph に変換しました。 BigWig に変換中... CompletedMACS2peakCalling BigWig に変換しました。 CompletedMACS2peakCalling