Job ID = 11633580 sra ファイルのダウンロード中... Completed: 127199K bytes transferred in 4 seconds (223909K bits/sec), in 1 file. sra ファイルのダウンロードが完了しました。 Read layout: PAIRED fastq に変換中... Read 2340802 spots for /home/okishinya/chipatlas/results/sacCer3/ERX1303542/ERR1231603.sra Written 2340802 spots for /home/okishinya/chipatlas/results/sacCer3/ERX1303542/ERR1231603.sra rm: cannot remove `[DSE]RX*': そのようなファイルやディレクトリはありません rm: cannot remove `[DSE]RR*.fastq': そのようなファイルやディレクトリはありません 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: 00:02:18 2340802 reads; of these: 2340802 (100.00%) were paired; of these: 1724185 (73.66%) aligned concordantly 0 times 483528 (20.66%) aligned concordantly exactly 1 time 133089 (5.69%) aligned concordantly >1 times ---- 1724185 pairs aligned concordantly 0 times; of these: 699294 (40.56%) aligned discordantly 1 time ---- 1024891 pairs aligned 0 times concordantly or discordantly; of these: 2049782 mates make up the pairs; of these: 1308559 (63.84%) aligned 0 times 493930 (24.10%) aligned exactly 1 time 247293 (12.06%) aligned >1 times 72.05% overall alignment rate Time searching: 00:02:18 Overall time: 00:02:18 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_rmdup_core] processing reference chrI... [bam_rmdup_core] processing reference chrII... [bam_rmdup_core] processing reference chrIII... [bam_rmdup_core] processing reference chrIV... [bam_rmdup_core] processing reference chrIX... [bam_rmdup_core] processing reference chrM... [bam_rmdup_core] processing reference chrV... [bam_rmdup_core] processing reference chrVI... [bam_rmdup_core] processing reference chrVII... [bam_rmdup_core] processing reference chrVIII... [bam_rmdup_core] processing reference chrX... [bam_rmdup_core] processing reference chrXI... [bam_rmdup_core] processing reference chrXII... [bam_rmdup_core] processing reference chrXIII... [bam_rmdup_core] processing reference chrXIV... [bam_rmdup_core] processing reference chrXV... [bam_rmdup_core] processing reference chrXVI... [bam_rmdup_core] 67836 / 782126 = 0.0867 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, 15 Feb 2019 09:09:21: # Command line: callpeak -t ERX1303542.bam -f BAM -g 12100000 -n ERX1303542.10 -q 1e-10 # ARGUMENTS LIST: # name = ERX1303542.10 # format = BAM # ChIP-seq file = ['ERX1303542.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, 15 Feb 2019 09:09:21: #1 read tag files... INFO @ Fri, 15 Feb 2019 09:09:21: #1 read treatment tags... INFO @ Fri, 15 Feb 2019 09:09:21: # Command line: callpeak -t ERX1303542.bam -f BAM -g 12100000 -n ERX1303542.05 -q 1e-05 # ARGUMENTS LIST: # name = ERX1303542.05 # format = BAM # ChIP-seq file = ['ERX1303542.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, 15 Feb 2019 09:09:21: #1 read tag files... INFO @ Fri, 15 Feb 2019 09:09:21: #1 read treatment tags... INFO @ Fri, 15 Feb 2019 09:09:21: # Command line: callpeak -t ERX1303542.bam -f BAM -g 12100000 -n ERX1303542.20 -q 1e-20 # ARGUMENTS LIST: # name = ERX1303542.20 # format = BAM # ChIP-seq file = ['ERX1303542.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, 15 Feb 2019 09:09:21: #1 read tag files... INFO @ Fri, 15 Feb 2019 09:09:21: #1 read treatment tags... INFO @ Fri, 15 Feb 2019 09:09:27: 1000000 INFO @ Fri, 15 Feb 2019 09:09:27: 1000000 INFO @ Fri, 15 Feb 2019 09:09:27: 1000000 INFO @ Fri, 15 Feb 2019 09:09:32: 2000000 INFO @ Fri, 15 Feb 2019 09:09:33: 2000000 INFO @ Fri, 15 Feb 2019 09:09:33: 2000000 INFO @ Fri, 15 Feb 2019 09:09:38: 3000000 INFO @ Fri, 15 Feb 2019 09:09:39: 3000000 INFO @ Fri, 15 Feb 2019 09:09:39: 3000000 INFO @ Fri, 15 Feb 2019 09:09:39: #1 tag size is determined as 51 bps INFO @ Fri, 15 Feb 2019 09:09:39: #1 tag size = 51 INFO @ Fri, 15 Feb 2019 09:09:39: #1 total tags in treatment: 562628 INFO @ Fri, 15 Feb 2019 09:09:39: #1 user defined the maximum tags... INFO @ Fri, 15 Feb 2019 09:09:39: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Fri, 15 Feb 2019 09:09:39: #1 tags after filtering in treatment: 513539 INFO @ Fri, 15 Feb 2019 09:09:39: #1 Redundant rate of treatment: 0.09 INFO @ Fri, 15 Feb 2019 09:09:39: #1 finished! INFO @ Fri, 15 Feb 2019 09:09:39: #2 Build Peak Model... INFO @ Fri, 15 Feb 2019 09:09:39: #2 looking for paired plus/minus strand peaks... INFO @ Fri, 15 Feb 2019 09:09:39: #2 number of paired peaks: 229 WARNING @ Fri, 15 Feb 2019 09:09:39: Fewer paired peaks (229) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 229 pairs to build model! INFO @ Fri, 15 Feb 2019 09:09:39: start model_add_line... INFO @ Fri, 15 Feb 2019 09:09:39: start X-correlation... INFO @ Fri, 15 Feb 2019 09:09:39: end of X-cor INFO @ Fri, 15 Feb 2019 09:09:39: #2 finished! INFO @ Fri, 15 Feb 2019 09:09:39: #2 predicted fragment length is 319 bps INFO @ Fri, 15 Feb 2019 09:09:39: #2 alternative fragment length(s) may be 319 bps INFO @ Fri, 15 Feb 2019 09:09:39: #2.2 Generate R script for model : ERX1303542.20_model.r INFO @ Fri, 15 Feb 2019 09:09:40: #3 Call peaks... INFO @ Fri, 15 Feb 2019 09:09:40: #3 Pre-compute pvalue-qvalue table... INFO @ Fri, 15 Feb 2019 09:09:40: #1 tag size is determined as 51 bps INFO @ Fri, 15 Feb 2019 09:09:40: #1 tag size = 51 INFO @ Fri, 15 Feb 2019 09:09:40: #1 tag size is determined as 51 bps INFO @ Fri, 15 Feb 2019 09:09:40: #1 total tags in treatment: 562628 INFO @ Fri, 15 Feb 2019 09:09:40: #1 tag size = 51 INFO @ Fri, 15 Feb 2019 09:09:40: #1 user defined the maximum tags... INFO @ Fri, 15 Feb 2019 09:09:40: #1 total tags in treatment: 562628 INFO @ Fri, 15 Feb 2019 09:09:40: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Fri, 15 Feb 2019 09:09:40: #1 user defined the maximum tags... INFO @ Fri, 15 Feb 2019 09:09:40: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Fri, 15 Feb 2019 09:09:40: #1 tags after filtering in treatment: 513539 INFO @ Fri, 15 Feb 2019 09:09:40: #1 Redundant rate of treatment: 0.09 INFO @ Fri, 15 Feb 2019 09:09:40: #1 tags after filtering in treatment: 513539 INFO @ Fri, 15 Feb 2019 09:09:40: #1 finished! INFO @ Fri, 15 Feb 2019 09:09:40: #1 Redundant rate of treatment: 0.09 INFO @ Fri, 15 Feb 2019 09:09:40: #2 Build Peak Model... INFO @ Fri, 15 Feb 2019 09:09:40: #1 finished! INFO @ Fri, 15 Feb 2019 09:09:40: #2 looking for paired plus/minus strand peaks... INFO @ Fri, 15 Feb 2019 09:09:40: #2 Build Peak Model... INFO @ Fri, 15 Feb 2019 09:09:40: #2 looking for paired plus/minus strand peaks... INFO @ Fri, 15 Feb 2019 09:09:40: #2 number of paired peaks: 229 WARNING @ Fri, 15 Feb 2019 09:09:40: Fewer paired peaks (229) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 229 pairs to build model! INFO @ Fri, 15 Feb 2019 09:09:40: start model_add_line... INFO @ Fri, 15 Feb 2019 09:09:40: #2 number of paired peaks: 229 WARNING @ Fri, 15 Feb 2019 09:09:40: Fewer paired peaks (229) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 229 pairs to build model! INFO @ Fri, 15 Feb 2019 09:09:40: start model_add_line... INFO @ Fri, 15 Feb 2019 09:09:40: start X-correlation... INFO @ Fri, 15 Feb 2019 09:09:40: start X-correlation... INFO @ Fri, 15 Feb 2019 09:09:40: end of X-cor INFO @ Fri, 15 Feb 2019 09:09:40: #2 finished! INFO @ Fri, 15 Feb 2019 09:09:40: #2 predicted fragment length is 319 bps INFO @ Fri, 15 Feb 2019 09:09:40: #2 alternative fragment length(s) may be 319 bps INFO @ Fri, 15 Feb 2019 09:09:40: #2.2 Generate R script for model : ERX1303542.05_model.r INFO @ Fri, 15 Feb 2019 09:09:40: end of X-cor INFO @ Fri, 15 Feb 2019 09:09:40: #2 finished! INFO @ Fri, 15 Feb 2019 09:09:40: #2 predicted fragment length is 319 bps INFO @ Fri, 15 Feb 2019 09:09:40: #2 alternative fragment length(s) may be 319 bps INFO @ Fri, 15 Feb 2019 09:09:40: #2.2 Generate R script for model : ERX1303542.10_model.r INFO @ Fri, 15 Feb 2019 09:09:40: #3 Call peaks... INFO @ Fri, 15 Feb 2019 09:09:40: #3 Pre-compute pvalue-qvalue table... INFO @ Fri, 15 Feb 2019 09:09:40: #3 Call peaks... INFO @ Fri, 15 Feb 2019 09:09:40: #3 Pre-compute pvalue-qvalue table... INFO @ Fri, 15 Feb 2019 09:09:42: #3 Call peaks for each chromosome... INFO @ Fri, 15 Feb 2019 09:09:42: #4 Write output xls file... ERX1303542.20_peaks.xls INFO @ Fri, 15 Feb 2019 09:09:42: #4 Write peak in narrowPeak format file... ERX1303542.20_peaks.narrowPeak INFO @ Fri, 15 Feb 2019 09:09:42: #4 Write summits bed file... ERX1303542.20_summits.bed INFO @ Fri, 15 Feb 2019 09:09:42: Done! pass1 - making usageList (15 chroms): 2 millis pass2 - checking and writing primary data (70 records, 4 fields): 3 millis CompletedMACS2peakCalling INFO @ Fri, 15 Feb 2019 09:09:43: #3 Call peaks for each chromosome... INFO @ Fri, 15 Feb 2019 09:09:43: #3 Call peaks for each chromosome... INFO @ Fri, 15 Feb 2019 09:09:43: #4 Write output xls file... ERX1303542.05_peaks.xls INFO @ Fri, 15 Feb 2019 09:09:43: #4 Write peak in narrowPeak format file... ERX1303542.05_peaks.narrowPeak INFO @ Fri, 15 Feb 2019 09:09:43: #4 Write summits bed file... ERX1303542.05_summits.bed INFO @ Fri, 15 Feb 2019 09:09:43: Done! pass1 - making usageList (16 chroms): 1 millis pass2 - checking and writing primary data (256 records, 4 fields): 3 millis CompletedMACS2peakCalling INFO @ Fri, 15 Feb 2019 09:09:43: #4 Write output xls file... ERX1303542.10_peaks.xls INFO @ Fri, 15 Feb 2019 09:09:43: #4 Write peak in narrowPeak format file... ERX1303542.10_peaks.narrowPeak INFO @ Fri, 15 Feb 2019 09:09:43: #4 Write summits bed file... ERX1303542.10_summits.bed INFO @ Fri, 15 Feb 2019 09:09:43: Done! pass1 - making usageList (16 chroms): 2 millis pass2 - checking and writing primary data (152 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。