Job ID = 2589715 sra ファイルのダウンロード中... Read layout: SINGLE fastq に変換中... spots read : 4,800,550 reads read : 4,800,550 reads written : 4,800,550 spots read : 5,992,012 reads read : 5,992,012 reads written : 5,992,012 rm: cannot remove ‘/home/okishinya/ncbi/public/sra/SRR947317.sra.cache’: No such file or directory rm: cannot remove ‘/home/okishinya/ncbi/public/sra/SRR947318.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: 00:01:07 10792562 reads; of these: 10792562 (100.00%) were unpaired; of these: 6179469 (57.26%) aligned 0 times 3984205 (36.92%) aligned exactly 1 time 628888 (5.83%) aligned >1 times 42.74% overall alignment rate Time searching: 00:01:07 Overall time: 00:01:07 マッピングが完了しました。 samtools でBAM に変換中... [samopen] SAM header is present: 7 sequences. [bam_rmdupse_core] 1585274 / 4613093 = 0.3436 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, 12 Aug 2019 18:20:55: # Command line: callpeak -t /home/okishinya/chipatlas/results/ce10/SRX331088/SRX331088.bam -f BAM -g ce -n /home/okishinya/chipatlas/results/ce10/SRX331088/SRX331088.05 -q 1e-05 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/ce10/SRX331088/SRX331088.05 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/ce10/SRX331088/SRX331088.bam'] # control file = None # effective genome size = 9.00e+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 @ Mon, 12 Aug 2019 18:20:55: #1 read tag files... INFO @ Mon, 12 Aug 2019 18:20:55: #1 read treatment tags... INFO @ Mon, 12 Aug 2019 18:20:56: # Command line: callpeak -t /home/okishinya/chipatlas/results/ce10/SRX331088/SRX331088.bam -f BAM -g ce -n /home/okishinya/chipatlas/results/ce10/SRX331088/SRX331088.10 -q 1e-10 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/ce10/SRX331088/SRX331088.10 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/ce10/SRX331088/SRX331088.bam'] # control file = None # effective genome size = 9.00e+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 @ Mon, 12 Aug 2019 18:20:56: #1 read tag files... INFO @ Mon, 12 Aug 2019 18:20:56: #1 read treatment tags... INFO @ Mon, 12 Aug 2019 18:20:57: # Command line: callpeak -t /home/okishinya/chipatlas/results/ce10/SRX331088/SRX331088.bam -f BAM -g ce -n /home/okishinya/chipatlas/results/ce10/SRX331088/SRX331088.20 -q 1e-20 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/ce10/SRX331088/SRX331088.20 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/ce10/SRX331088/SRX331088.bam'] # control file = None # effective genome size = 9.00e+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 @ Mon, 12 Aug 2019 18:20:57: #1 read tag files... INFO @ Mon, 12 Aug 2019 18:20:57: #1 read treatment tags... INFO @ Mon, 12 Aug 2019 18:21:04: 1000000 INFO @ Mon, 12 Aug 2019 18:21:04: 1000000 INFO @ Mon, 12 Aug 2019 18:21:04: 1000000 INFO @ Mon, 12 Aug 2019 18:21:11: 2000000 INFO @ Mon, 12 Aug 2019 18:21:12: 2000000 INFO @ Mon, 12 Aug 2019 18:21:13: 2000000 INFO @ Mon, 12 Aug 2019 18:21:19: 3000000 INFO @ Mon, 12 Aug 2019 18:21:19: #1 tag size is determined as 32 bps INFO @ Mon, 12 Aug 2019 18:21:19: #1 tag size = 32 INFO @ Mon, 12 Aug 2019 18:21:19: #1 total tags in treatment: 3027819 INFO @ Mon, 12 Aug 2019 18:21:19: #1 user defined the maximum tags... INFO @ Mon, 12 Aug 2019 18:21:19: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Mon, 12 Aug 2019 18:21:19: #1 tags after filtering in treatment: 3027819 INFO @ Mon, 12 Aug 2019 18:21:19: #1 Redundant rate of treatment: 0.00 INFO @ Mon, 12 Aug 2019 18:21:19: #1 finished! INFO @ Mon, 12 Aug 2019 18:21:19: #2 Build Peak Model... INFO @ Mon, 12 Aug 2019 18:21:19: #2 looking for paired plus/minus strand peaks... INFO @ Mon, 12 Aug 2019 18:21:19: #2 number of paired peaks: 2178 INFO @ Mon, 12 Aug 2019 18:21:19: start model_add_line... INFO @ Mon, 12 Aug 2019 18:21:19: start X-correlation... INFO @ Mon, 12 Aug 2019 18:21:19: end of X-cor INFO @ Mon, 12 Aug 2019 18:21:19: #2 finished! INFO @ Mon, 12 Aug 2019 18:21:19: #2 predicted fragment length is 141 bps INFO @ Mon, 12 Aug 2019 18:21:19: #2 alternative fragment length(s) may be 141 bps INFO @ Mon, 12 Aug 2019 18:21:19: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/ce10/SRX331088/SRX331088.10_model.r INFO @ Mon, 12 Aug 2019 18:21:19: #3 Call peaks... INFO @ Mon, 12 Aug 2019 18:21:19: #3 Pre-compute pvalue-qvalue table... INFO @ Mon, 12 Aug 2019 18:21:19: 3000000 INFO @ Mon, 12 Aug 2019 18:21:20: #1 tag size is determined as 32 bps INFO @ Mon, 12 Aug 2019 18:21:20: #1 tag size = 32 INFO @ Mon, 12 Aug 2019 18:21:20: #1 total tags in treatment: 3027819 INFO @ Mon, 12 Aug 2019 18:21:20: #1 user defined the maximum tags... INFO @ Mon, 12 Aug 2019 18:21:20: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Mon, 12 Aug 2019 18:21:20: #1 tags after filtering in treatment: 3027819 INFO @ Mon, 12 Aug 2019 18:21:20: #1 Redundant rate of treatment: 0.00 INFO @ Mon, 12 Aug 2019 18:21:20: #1 finished! INFO @ Mon, 12 Aug 2019 18:21:20: #2 Build Peak Model... INFO @ Mon, 12 Aug 2019 18:21:20: #2 looking for paired plus/minus strand peaks... INFO @ Mon, 12 Aug 2019 18:21:20: #2 number of paired peaks: 2178 INFO @ Mon, 12 Aug 2019 18:21:20: start model_add_line... INFO @ Mon, 12 Aug 2019 18:21:20: start X-correlation... INFO @ Mon, 12 Aug 2019 18:21:20: end of X-cor INFO @ Mon, 12 Aug 2019 18:21:20: #2 finished! INFO @ Mon, 12 Aug 2019 18:21:20: #2 predicted fragment length is 141 bps INFO @ Mon, 12 Aug 2019 18:21:20: #2 alternative fragment length(s) may be 141 bps INFO @ Mon, 12 Aug 2019 18:21:20: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/ce10/SRX331088/SRX331088.20_model.r INFO @ Mon, 12 Aug 2019 18:21:20: #3 Call peaks... INFO @ Mon, 12 Aug 2019 18:21:20: #3 Pre-compute pvalue-qvalue table... INFO @ Mon, 12 Aug 2019 18:21:21: 3000000 INFO @ Mon, 12 Aug 2019 18:21:21: #1 tag size is determined as 32 bps INFO @ Mon, 12 Aug 2019 18:21:21: #1 tag size = 32 INFO @ Mon, 12 Aug 2019 18:21:21: #1 total tags in treatment: 3027819 INFO @ Mon, 12 Aug 2019 18:21:21: #1 user defined the maximum tags... INFO @ Mon, 12 Aug 2019 18:21:21: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Mon, 12 Aug 2019 18:21:21: #1 tags after filtering in treatment: 3027819 INFO @ Mon, 12 Aug 2019 18:21:21: #1 Redundant rate of treatment: 0.00 INFO @ Mon, 12 Aug 2019 18:21:21: #1 finished! INFO @ Mon, 12 Aug 2019 18:21:21: #2 Build Peak Model... INFO @ Mon, 12 Aug 2019 18:21:21: #2 looking for paired plus/minus strand peaks... INFO @ Mon, 12 Aug 2019 18:21:22: #2 number of paired peaks: 2178 INFO @ Mon, 12 Aug 2019 18:21:22: start model_add_line... INFO @ Mon, 12 Aug 2019 18:21:22: start X-correlation... INFO @ Mon, 12 Aug 2019 18:21:22: end of X-cor INFO @ Mon, 12 Aug 2019 18:21:22: #2 finished! INFO @ Mon, 12 Aug 2019 18:21:22: #2 predicted fragment length is 141 bps INFO @ Mon, 12 Aug 2019 18:21:22: #2 alternative fragment length(s) may be 141 bps INFO @ Mon, 12 Aug 2019 18:21:22: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/ce10/SRX331088/SRX331088.05_model.r INFO @ Mon, 12 Aug 2019 18:21:22: #3 Call peaks... INFO @ Mon, 12 Aug 2019 18:21:22: #3 Pre-compute pvalue-qvalue table... INFO @ Mon, 12 Aug 2019 18:21:29: #3 Call peaks for each chromosome... INFO @ Mon, 12 Aug 2019 18:21:30: #3 Call peaks for each chromosome... INFO @ Mon, 12 Aug 2019 18:21:32: #3 Call peaks for each chromosome... INFO @ Mon, 12 Aug 2019 18:21:33: #4 Write output xls file... /home/okishinya/chipatlas/results/ce10/SRX331088/SRX331088.10_peaks.xls INFO @ Mon, 12 Aug 2019 18:21:33: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/ce10/SRX331088/SRX331088.10_peaks.narrowPeak INFO @ Mon, 12 Aug 2019 18:21:33: #4 Write summits bed file... /home/okishinya/chipatlas/results/ce10/SRX331088/SRX331088.10_summits.bed INFO @ Mon, 12 Aug 2019 18:21:34: Done! pass1 - making usageList (7 chroms): 2 millis pass2 - checking and writing primary data (3207 records, 4 fields): 8 millis CompletedMACS2peakCalling INFO @ Mon, 12 Aug 2019 18:21:34: #4 Write output xls file... /home/okishinya/chipatlas/results/ce10/SRX331088/SRX331088.20_peaks.xls INFO @ Mon, 12 Aug 2019 18:21:34: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/ce10/SRX331088/SRX331088.20_peaks.narrowPeak INFO @ Mon, 12 Aug 2019 18:21:34: #4 Write summits bed file... /home/okishinya/chipatlas/results/ce10/SRX331088/SRX331088.20_summits.bed INFO @ Mon, 12 Aug 2019 18:21:34: Done! pass1 - making usageList (6 chroms): 2 millis pass2 - checking and writing primary data (1920 records, 4 fields): 6 millis CompletedMACS2peakCalling INFO @ Mon, 12 Aug 2019 18:21:36: #4 Write output xls file... /home/okishinya/chipatlas/results/ce10/SRX331088/SRX331088.05_peaks.xls INFO @ Mon, 12 Aug 2019 18:21:36: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/ce10/SRX331088/SRX331088.05_peaks.narrowPeak INFO @ Mon, 12 Aug 2019 18:21:36: #4 Write summits bed file... /home/okishinya/chipatlas/results/ce10/SRX331088/SRX331088.05_summits.bed INFO @ Mon, 12 Aug 2019 18:21:36: Done! pass1 - making usageList (7 chroms): 2 millis pass2 - checking and writing primary data (4546 records, 4 fields): 7 millis CompletedMACS2peakCalling BedGraph に変換しました。 BigWig に変換中... BigWig に変換しました。