Job ID = 1295870 sra ファイルのダウンロード中... Read layout: PAIRED fastq に変換中... spots read : 36,074,539 reads read : 72,149,078 reads written : 72,149,078 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: 00:06:41 36074539 reads; of these: 36074539 (100.00%) were paired; of these: 34882481 (96.70%) aligned concordantly 0 times 959888 (2.66%) aligned concordantly exactly 1 time 232170 (0.64%) aligned concordantly >1 times ---- 34882481 pairs aligned concordantly 0 times; of these: 1478 (0.00%) aligned discordantly 1 time ---- 34881003 pairs aligned 0 times concordantly or discordantly; of these: 69762006 mates make up the pairs; of these: 69552962 (99.70%) aligned 0 times 70826 (0.10%) aligned exactly 1 time 138218 (0.20%) aligned >1 times 3.60% overall alignment rate Time searching: 00:06:41 Overall time: 00:06:41 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] 32490 / 1192685 = 0.0272 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 16:16:26: # Command line: callpeak -t /home/okishinya/chipatlas/results/dm3/SRX4650733/SRX4650733.bam -f BAM -g dm -n /home/okishinya/chipatlas/results/dm3/SRX4650733/SRX4650733.20 -q 1e-20 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/dm3/SRX4650733/SRX4650733.20 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/dm3/SRX4650733/SRX4650733.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 16:16:26: #1 read tag files... INFO @ Mon, 03 Jun 2019 16:16:26: #1 read treatment tags... INFO @ Mon, 03 Jun 2019 16:16:26: # Command line: callpeak -t /home/okishinya/chipatlas/results/dm3/SRX4650733/SRX4650733.bam -f BAM -g dm -n /home/okishinya/chipatlas/results/dm3/SRX4650733/SRX4650733.05 -q 1e-05 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/dm3/SRX4650733/SRX4650733.05 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/dm3/SRX4650733/SRX4650733.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 16:16:26: #1 read tag files... INFO @ Mon, 03 Jun 2019 16:16:26: #1 read treatment tags... INFO @ Mon, 03 Jun 2019 16:16:26: # Command line: callpeak -t /home/okishinya/chipatlas/results/dm3/SRX4650733/SRX4650733.bam -f BAM -g dm -n /home/okishinya/chipatlas/results/dm3/SRX4650733/SRX4650733.10 -q 1e-10 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/dm3/SRX4650733/SRX4650733.10 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/dm3/SRX4650733/SRX4650733.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 16:16:26: #1 read tag files... INFO @ Mon, 03 Jun 2019 16:16:26: #1 read treatment tags... INFO @ Mon, 03 Jun 2019 16:16:33: 1000000 INFO @ Mon, 03 Jun 2019 16:16:35: 1000000 INFO @ Mon, 03 Jun 2019 16:16:35: 1000000 INFO @ Mon, 03 Jun 2019 16:16:40: 2000000 INFO @ Mon, 03 Jun 2019 16:16:42: 2000000 INFO @ Mon, 03 Jun 2019 16:16:44: #1 tag size is determined as 39 bps INFO @ Mon, 03 Jun 2019 16:16:44: #1 tag size = 39 INFO @ Mon, 03 Jun 2019 16:16:44: #1 total tags in treatment: 1159611 INFO @ Mon, 03 Jun 2019 16:16:44: #1 user defined the maximum tags... INFO @ Mon, 03 Jun 2019 16:16:44: #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 16:16:44: #1 tags after filtering in treatment: 1125066 INFO @ Mon, 03 Jun 2019 16:16:44: #1 Redundant rate of treatment: 0.03 INFO @ Mon, 03 Jun 2019 16:16:44: #1 finished! INFO @ Mon, 03 Jun 2019 16:16:44: #2 Build Peak Model... INFO @ Mon, 03 Jun 2019 16:16:44: #2 looking for paired plus/minus strand peaks... INFO @ Mon, 03 Jun 2019 16:16:44: #2 number of paired peaks: 1572 INFO @ Mon, 03 Jun 2019 16:16:44: start model_add_line... INFO @ Mon, 03 Jun 2019 16:16:44: start X-correlation... INFO @ Mon, 03 Jun 2019 16:16:44: 2000000 INFO @ Mon, 03 Jun 2019 16:16:44: end of X-cor INFO @ Mon, 03 Jun 2019 16:16:44: #2 finished! INFO @ Mon, 03 Jun 2019 16:16:44: #2 predicted fragment length is 132 bps INFO @ Mon, 03 Jun 2019 16:16:44: #2 alternative fragment length(s) may be 132 bps INFO @ Mon, 03 Jun 2019 16:16:44: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/dm3/SRX4650733/SRX4650733.20_model.r INFO @ Mon, 03 Jun 2019 16:16:44: #3 Call peaks... INFO @ Mon, 03 Jun 2019 16:16:44: #3 Pre-compute pvalue-qvalue table... INFO @ Mon, 03 Jun 2019 16:16:46: #1 tag size is determined as 39 bps INFO @ Mon, 03 Jun 2019 16:16:46: #1 tag size = 39 INFO @ Mon, 03 Jun 2019 16:16:46: #1 total tags in treatment: 1159611 INFO @ Mon, 03 Jun 2019 16:16:46: #1 user defined the maximum tags... INFO @ Mon, 03 Jun 2019 16:16:46: #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 16:16:46: #1 tags after filtering in treatment: 1125066 INFO @ Mon, 03 Jun 2019 16:16:46: #1 Redundant rate of treatment: 0.03 INFO @ Mon, 03 Jun 2019 16:16:46: #1 finished! INFO @ Mon, 03 Jun 2019 16:16:46: #2 Build Peak Model... INFO @ Mon, 03 Jun 2019 16:16:46: #2 looking for paired plus/minus strand peaks... INFO @ Mon, 03 Jun 2019 16:16:46: #2 number of paired peaks: 1572 INFO @ Mon, 03 Jun 2019 16:16:46: start model_add_line... INFO @ Mon, 03 Jun 2019 16:16:46: start X-correlation... INFO @ Mon, 03 Jun 2019 16:16:46: end of X-cor INFO @ Mon, 03 Jun 2019 16:16:46: #2 finished! INFO @ Mon, 03 Jun 2019 16:16:46: #2 predicted fragment length is 132 bps INFO @ Mon, 03 Jun 2019 16:16:46: #2 alternative fragment length(s) may be 132 bps INFO @ Mon, 03 Jun 2019 16:16:46: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/dm3/SRX4650733/SRX4650733.10_model.r INFO @ Mon, 03 Jun 2019 16:16:46: #3 Call peaks... INFO @ Mon, 03 Jun 2019 16:16:46: #3 Pre-compute pvalue-qvalue table... INFO @ Mon, 03 Jun 2019 16:16:48: #3 Call peaks for each chromosome... INFO @ Mon, 03 Jun 2019 16:16:48: #1 tag size is determined as 39 bps INFO @ Mon, 03 Jun 2019 16:16:48: #1 tag size = 39 INFO @ Mon, 03 Jun 2019 16:16:48: #1 total tags in treatment: 1159611 INFO @ Mon, 03 Jun 2019 16:16:48: #1 user defined the maximum tags... INFO @ Mon, 03 Jun 2019 16:16:48: #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 16:16:48: #1 tags after filtering in treatment: 1125066 INFO @ Mon, 03 Jun 2019 16:16:48: #1 Redundant rate of treatment: 0.03 INFO @ Mon, 03 Jun 2019 16:16:48: #1 finished! INFO @ Mon, 03 Jun 2019 16:16:48: #2 Build Peak Model... INFO @ Mon, 03 Jun 2019 16:16:48: #2 looking for paired plus/minus strand peaks... INFO @ Mon, 03 Jun 2019 16:16:49: #2 number of paired peaks: 1572 INFO @ Mon, 03 Jun 2019 16:16:49: start model_add_line... INFO @ Mon, 03 Jun 2019 16:16:49: start X-correlation... INFO @ Mon, 03 Jun 2019 16:16:49: end of X-cor INFO @ Mon, 03 Jun 2019 16:16:49: #2 finished! INFO @ Mon, 03 Jun 2019 16:16:49: #2 predicted fragment length is 132 bps INFO @ Mon, 03 Jun 2019 16:16:49: #2 alternative fragment length(s) may be 132 bps INFO @ Mon, 03 Jun 2019 16:16:49: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/dm3/SRX4650733/SRX4650733.05_model.r INFO @ Mon, 03 Jun 2019 16:16:49: #3 Call peaks... INFO @ Mon, 03 Jun 2019 16:16:49: #3 Pre-compute pvalue-qvalue table... INFO @ Mon, 03 Jun 2019 16:16:49: #4 Write output xls file... /home/okishinya/chipatlas/results/dm3/SRX4650733/SRX4650733.20_peaks.xls INFO @ Mon, 03 Jun 2019 16:16:49: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/dm3/SRX4650733/SRX4650733.20_peaks.narrowPeak INFO @ Mon, 03 Jun 2019 16:16:49: #4 Write summits bed file... /home/okishinya/chipatlas/results/dm3/SRX4650733/SRX4650733.20_summits.bed INFO @ Mon, 03 Jun 2019 16:16:49: Done! pass1 - making usageList (5 chroms): 1 millis pass2 - checking and writing primary data (61 records, 4 fields): 2 millis CompletedMACS2peakCalling INFO @ Mon, 03 Jun 2019 16:16:50: #3 Call peaks for each chromosome... INFO @ Mon, 03 Jun 2019 16:16:52: #4 Write output xls file... /home/okishinya/chipatlas/results/dm3/SRX4650733/SRX4650733.10_peaks.xls INFO @ Mon, 03 Jun 2019 16:16:52: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/dm3/SRX4650733/SRX4650733.10_peaks.narrowPeak INFO @ Mon, 03 Jun 2019 16:16:52: #4 Write summits bed file... /home/okishinya/chipatlas/results/dm3/SRX4650733/SRX4650733.10_summits.bed INFO @ Mon, 03 Jun 2019 16:16:52: Done! pass1 - making usageList (10 chroms): 1 millis pass2 - checking and writing primary data (182 records, 4 fields): 3 millis CompletedMACS2peakCalling INFO @ Mon, 03 Jun 2019 16:16:52: #3 Call peaks for each chromosome... INFO @ Mon, 03 Jun 2019 16:16:54: #4 Write output xls file... /home/okishinya/chipatlas/results/dm3/SRX4650733/SRX4650733.05_peaks.xls INFO @ Mon, 03 Jun 2019 16:16:54: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/dm3/SRX4650733/SRX4650733.05_peaks.narrowPeak INFO @ Mon, 03 Jun 2019 16:16:54: #4 Write summits bed file... /home/okishinya/chipatlas/results/dm3/SRX4650733/SRX4650733.05_summits.bed INFO @ Mon, 03 Jun 2019 16:16:54: Done! pass1 - making usageList (12 chroms): 1 millis pass2 - checking and writing primary data (347 records, 4 fields): 2 millis CompletedMACS2peakCalling BedGraph に変換しました。 BigWig に変換中... BigWig に変換しました。