Job ID = 1297462 sra ファイルのダウンロード中... Read layout: PAIRED fastq に変換中... spots read : 10,687,273 reads read : 21,374,546 reads written : 21,374,546 rm: cannot remove ‘[DSE]RR*’: No such file or directory rm: cannot remove ‘fastqDump_tmp*’: 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: 00:02:17 10687273 reads; of these: 10687273 (100.00%) were paired; of these: 10469286 (97.96%) aligned concordantly 0 times 154482 (1.45%) aligned concordantly exactly 1 time 63505 (0.59%) aligned concordantly >1 times ---- 10469286 pairs aligned concordantly 0 times; of these: 728 (0.01%) aligned discordantly 1 time ---- 10468558 pairs aligned 0 times concordantly or discordantly; of these: 20937116 mates make up the pairs; of these: 20771580 (99.21%) aligned 0 times 72915 (0.35%) aligned exactly 1 time 92621 (0.44%) aligned >1 times 2.82% overall alignment rate Time searching: 00:02:17 Overall time: 00:02:17 マッピングが完了しました。 samtools でBAM に変換中... [samopen] SAM header is present: 15 sequences. [bam_rmdup_core] processing reference chr2L... [bam_rmdup_core] processing reference chr2LHet... [bam_rmdup_core] processing reference chr2R... [bam_rmdup_core] processing reference chr2RHet... [bam_rmdup_core] processing reference chr3L... [bam_rmdup_core] processing reference chr3LHet... [bam_rmdup_core] processing reference chr3R... [bam_rmdup_core] processing reference chr3RHet... [bam_rmdup_core] processing reference chr4... [bam_rmdup_core] processing reference chrM... [bam_rmdup_core] processing reference chrU... [bam_rmdup_core] processing reference chrUextra... [bam_rmdup_core] processing reference chrX... [bam_rmdup_core] processing reference chrXHet... [bam_rmdup_core] processing reference chrYHet... [bam_rmdup_core] 4817 / 218072 = 0.0221 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 @ Mon, 03 Jun 2019 16:59:32: # Command line: callpeak -t /home/okishinya/chipatlas/results/dm3/SRX4650853/SRX4650853.bam -f BAM -g dm -n /home/okishinya/chipatlas/results/dm3/SRX4650853/SRX4650853.05 -q 1e-05 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/dm3/SRX4650853/SRX4650853.05 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/dm3/SRX4650853/SRX4650853.bam'] # control file = None # effective genome size = 1.20e+08 # 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 @ Mon, 03 Jun 2019 16:59:32: # Command line: callpeak -t /home/okishinya/chipatlas/results/dm3/SRX4650853/SRX4650853.bam -f BAM -g dm -n /home/okishinya/chipatlas/results/dm3/SRX4650853/SRX4650853.20 -q 1e-20 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/dm3/SRX4650853/SRX4650853.20 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/dm3/SRX4650853/SRX4650853.bam'] # control file = None # effective genome size = 1.20e+08 # 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 @ Mon, 03 Jun 2019 16:59:32: #1 read tag files... INFO @ Mon, 03 Jun 2019 16:59:32: #1 read treatment tags... INFO @ Mon, 03 Jun 2019 16:59:32: #1 read tag files... INFO @ Mon, 03 Jun 2019 16:59:32: #1 read treatment tags... INFO @ Mon, 03 Jun 2019 16:59:32: # Command line: callpeak -t /home/okishinya/chipatlas/results/dm3/SRX4650853/SRX4650853.bam -f BAM -g dm -n /home/okishinya/chipatlas/results/dm3/SRX4650853/SRX4650853.10 -q 1e-10 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/dm3/SRX4650853/SRX4650853.10 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/dm3/SRX4650853/SRX4650853.bam'] # control file = None # effective genome size = 1.20e+08 # 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 @ Mon, 03 Jun 2019 16:59:32: #1 read tag files... INFO @ Mon, 03 Jun 2019 16:59:32: #1 read treatment tags... INFO @ Mon, 03 Jun 2019 16:59:37: #1 tag size is determined as 39 bps INFO @ Mon, 03 Jun 2019 16:59:37: #1 tag size = 39 INFO @ Mon, 03 Jun 2019 16:59:37: #1 total tags in treatment: 213177 INFO @ Mon, 03 Jun 2019 16:59:37: #1 user defined the maximum tags... INFO @ Mon, 03 Jun 2019 16:59:37: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Mon, 03 Jun 2019 16:59:37: #1 tags after filtering in treatment: 210473 INFO @ Mon, 03 Jun 2019 16:59:37: #1 Redundant rate of treatment: 0.01 INFO @ Mon, 03 Jun 2019 16:59:37: #1 finished! INFO @ Mon, 03 Jun 2019 16:59:37: #2 Build Peak Model... INFO @ Mon, 03 Jun 2019 16:59:37: #2 looking for paired plus/minus strand peaks... INFO @ Mon, 03 Jun 2019 16:59:37: #2 number of paired peaks: 726 WARNING @ Mon, 03 Jun 2019 16:59:37: Fewer paired peaks (726) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 726 pairs to build model! INFO @ Mon, 03 Jun 2019 16:59:37: start model_add_line... INFO @ Mon, 03 Jun 2019 16:59:37: start X-correlation... INFO @ Mon, 03 Jun 2019 16:59:37: end of X-cor INFO @ Mon, 03 Jun 2019 16:59:37: #2 finished! INFO @ Mon, 03 Jun 2019 16:59:37: #2 predicted fragment length is 100 bps INFO @ Mon, 03 Jun 2019 16:59:37: #2 alternative fragment length(s) may be 100,160,272,463 bps INFO @ Mon, 03 Jun 2019 16:59:37: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/dm3/SRX4650853/SRX4650853.20_model.r INFO @ Mon, 03 Jun 2019 16:59:37: #3 Call peaks... INFO @ Mon, 03 Jun 2019 16:59:37: #3 Pre-compute pvalue-qvalue table... INFO @ Mon, 03 Jun 2019 16:59:37: #1 tag size is determined as 39 bps INFO @ Mon, 03 Jun 2019 16:59:37: #1 tag size = 39 INFO @ Mon, 03 Jun 2019 16:59:37: #1 total tags in treatment: 213177 INFO @ Mon, 03 Jun 2019 16:59:37: #1 user defined the maximum tags... INFO @ Mon, 03 Jun 2019 16:59:37: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Mon, 03 Jun 2019 16:59:37: #1 tags after filtering in treatment: 210473 INFO @ Mon, 03 Jun 2019 16:59:37: #1 Redundant rate of treatment: 0.01 INFO @ Mon, 03 Jun 2019 16:59:37: #1 finished! INFO @ Mon, 03 Jun 2019 16:59:37: #2 Build Peak Model... INFO @ Mon, 03 Jun 2019 16:59:37: #2 looking for paired plus/minus strand peaks... INFO @ Mon, 03 Jun 2019 16:59:37: #2 number of paired peaks: 726 WARNING @ Mon, 03 Jun 2019 16:59:37: Fewer paired peaks (726) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 726 pairs to build model! INFO @ Mon, 03 Jun 2019 16:59:37: start model_add_line... INFO @ Mon, 03 Jun 2019 16:59:37: start X-correlation... INFO @ Mon, 03 Jun 2019 16:59:37: end of X-cor INFO @ Mon, 03 Jun 2019 16:59:37: #2 finished! INFO @ Mon, 03 Jun 2019 16:59:37: #2 predicted fragment length is 100 bps INFO @ Mon, 03 Jun 2019 16:59:37: #2 alternative fragment length(s) may be 100,160,272,463 bps INFO @ Mon, 03 Jun 2019 16:59:37: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/dm3/SRX4650853/SRX4650853.10_model.r INFO @ Mon, 03 Jun 2019 16:59:37: #3 Call peaks... INFO @ Mon, 03 Jun 2019 16:59:37: #3 Pre-compute pvalue-qvalue table... INFO @ Mon, 03 Jun 2019 16:59:37: #1 tag size is determined as 39 bps INFO @ Mon, 03 Jun 2019 16:59:37: #1 tag size = 39 INFO @ Mon, 03 Jun 2019 16:59:37: #1 total tags in treatment: 213177 INFO @ Mon, 03 Jun 2019 16:59:37: #1 user defined the maximum tags... INFO @ Mon, 03 Jun 2019 16:59:37: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Mon, 03 Jun 2019 16:59:38: #1 tags after filtering in treatment: 210473 INFO @ Mon, 03 Jun 2019 16:59:38: #1 Redundant rate of treatment: 0.01 INFO @ Mon, 03 Jun 2019 16:59:38: #1 finished! INFO @ Mon, 03 Jun 2019 16:59:38: #2 Build Peak Model... INFO @ Mon, 03 Jun 2019 16:59:38: #2 looking for paired plus/minus strand peaks... INFO @ Mon, 03 Jun 2019 16:59:38: #3 Call peaks for each chromosome... INFO @ Mon, 03 Jun 2019 16:59:38: #2 number of paired peaks: 726 WARNING @ Mon, 03 Jun 2019 16:59:38: Fewer paired peaks (726) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 726 pairs to build model! INFO @ Mon, 03 Jun 2019 16:59:38: start model_add_line... INFO @ Mon, 03 Jun 2019 16:59:38: start X-correlation... INFO @ Mon, 03 Jun 2019 16:59:38: end of X-cor INFO @ Mon, 03 Jun 2019 16:59:38: #2 finished! INFO @ Mon, 03 Jun 2019 16:59:38: #2 predicted fragment length is 100 bps INFO @ Mon, 03 Jun 2019 16:59:38: #2 alternative fragment length(s) may be 100,160,272,463 bps INFO @ Mon, 03 Jun 2019 16:59:38: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/dm3/SRX4650853/SRX4650853.05_model.r INFO @ Mon, 03 Jun 2019 16:59:38: #3 Call peaks... INFO @ Mon, 03 Jun 2019 16:59:38: #3 Pre-compute pvalue-qvalue table... INFO @ Mon, 03 Jun 2019 16:59:38: #3 Call peaks for each chromosome... INFO @ Mon, 03 Jun 2019 16:59:38: #4 Write output xls file... /home/okishinya/chipatlas/results/dm3/SRX4650853/SRX4650853.20_peaks.xls INFO @ Mon, 03 Jun 2019 16:59:38: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/dm3/SRX4650853/SRX4650853.20_peaks.narrowPeak INFO @ Mon, 03 Jun 2019 16:59:38: #4 Write summits bed file... /home/okishinya/chipatlas/results/dm3/SRX4650853/SRX4650853.20_summits.bed INFO @ Mon, 03 Jun 2019 16:59:38: Done! pass1 - making usageList (3 chroms): 1 millis pass2 - checking and writing primary data (28 records, 4 fields): 1 millis CompletedMACS2peakCalling BedGraph に変換しました。 BigWig に変換中... INFO @ Mon, 03 Jun 2019 16:59:38: #4 Write output xls file... /home/okishinya/chipatlas/results/dm3/SRX4650853/SRX4650853.10_peaks.xls INFO @ Mon, 03 Jun 2019 16:59:38: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/dm3/SRX4650853/SRX4650853.10_peaks.narrowPeak INFO @ Mon, 03 Jun 2019 16:59:38: #4 Write summits bed file... /home/okishinya/chipatlas/results/dm3/SRX4650853/SRX4650853.10_summits.bed INFO @ Mon, 03 Jun 2019 16:59:38: Done! pass1 - making usageList (6 chroms): 1 millis pass2 - checking and writing primary data (46 records, 4 fields): 2 millis CompletedMACS2peakCalling INFO @ Mon, 03 Jun 2019 16:59:38: #3 Call peaks for each chromosome... INFO @ Mon, 03 Jun 2019 16:59:39: #4 Write output xls file... /home/okishinya/chipatlas/results/dm3/SRX4650853/SRX4650853.05_peaks.xls INFO @ Mon, 03 Jun 2019 16:59:39: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/dm3/SRX4650853/SRX4650853.05_peaks.narrowPeak INFO @ Mon, 03 Jun 2019 16:59:39: #4 Write summits bed file... /home/okishinya/chipatlas/results/dm3/SRX4650853/SRX4650853.05_summits.bed INFO @ Mon, 03 Jun 2019 16:59:39: Done! pass1 - making usageList (6 chroms): 0 millis pass2 - checking and writing primary data (69 records, 4 fields): 3 millis CompletedMACS2peakCalling BigWig に変換しました。