Job ID = 2008220 sra ファイルのダウンロード中... Read layout: PAIRED fastq に変換中... spots read : 2,341,603 reads read : 4,683,206 reads written : 4,683,206 rm: cannot remove ‘[DSE]RR*’: 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: 00:01:43 2341603 reads; of these: 2341603 (100.00%) were paired; of these: 80477 (3.44%) aligned concordantly 0 times 2054931 (87.76%) aligned concordantly exactly 1 time 206195 (8.81%) aligned concordantly >1 times ---- 80477 pairs aligned concordantly 0 times; of these: 14158 (17.59%) aligned discordantly 1 time ---- 66319 pairs aligned 0 times concordantly or discordantly; of these: 132638 mates make up the pairs; of these: 116757 (88.03%) aligned 0 times 10000 (7.54%) aligned exactly 1 time 5881 (4.43%) aligned >1 times 97.51% overall alignment rate Time searching: 00:01:43 Overall time: 00:01:43 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] 2101710 / 2271067 = 0.9254 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 17:49:35: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/ERX585748/ERX585748.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/ERX585748/ERX585748.05 -q 1e-05 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/ERX585748/ERX585748.05 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/ERX585748/ERX585748.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 17:49:35: #1 read tag files... INFO @ Fri, 05 Jul 2019 17:49:35: #1 read treatment tags... INFO @ Fri, 05 Jul 2019 17:49:36: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/ERX585748/ERX585748.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/ERX585748/ERX585748.10 -q 1e-10 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/ERX585748/ERX585748.10 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/ERX585748/ERX585748.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 17:49:36: #1 read tag files... INFO @ Fri, 05 Jul 2019 17:49:36: #1 read treatment tags... INFO @ Fri, 05 Jul 2019 17:49:37: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/ERX585748/ERX585748.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/ERX585748/ERX585748.20 -q 1e-20 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/ERX585748/ERX585748.20 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/ERX585748/ERX585748.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 17:49:37: #1 read tag files... INFO @ Fri, 05 Jul 2019 17:49:37: #1 read treatment tags... INFO @ Fri, 05 Jul 2019 17:49:38: #1 tag size is determined as 44 bps INFO @ Fri, 05 Jul 2019 17:49:38: #1 tag size = 44 INFO @ Fri, 05 Jul 2019 17:49:38: #1 total tags in treatment: 169715 INFO @ Fri, 05 Jul 2019 17:49:38: #1 user defined the maximum tags... INFO @ Fri, 05 Jul 2019 17:49:38: #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 17:49:38: #1 tags after filtering in treatment: 158375 INFO @ Fri, 05 Jul 2019 17:49:38: #1 Redundant rate of treatment: 0.07 INFO @ Fri, 05 Jul 2019 17:49:38: #1 finished! INFO @ Fri, 05 Jul 2019 17:49:38: #2 Build Peak Model... INFO @ Fri, 05 Jul 2019 17:49:38: #2 looking for paired plus/minus strand peaks... INFO @ Fri, 05 Jul 2019 17:49:38: #2 number of paired peaks: 299 WARNING @ Fri, 05 Jul 2019 17:49:38: Fewer paired peaks (299) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 299 pairs to build model! INFO @ Fri, 05 Jul 2019 17:49:38: start model_add_line... INFO @ Fri, 05 Jul 2019 17:49:38: start X-correlation... INFO @ Fri, 05 Jul 2019 17:49:38: end of X-cor INFO @ Fri, 05 Jul 2019 17:49:38: #2 finished! INFO @ Fri, 05 Jul 2019 17:49:38: #2 predicted fragment length is 148 bps INFO @ Fri, 05 Jul 2019 17:49:38: #2 alternative fragment length(s) may be 4,20,47,103,148,174,196,211,237,284,291,307,444,474,493,529,546,587 bps INFO @ Fri, 05 Jul 2019 17:49:38: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/sacCer3/ERX585748/ERX585748.05_model.r INFO @ Fri, 05 Jul 2019 17:49:38: #3 Call peaks... INFO @ Fri, 05 Jul 2019 17:49:38: #3 Pre-compute pvalue-qvalue table... INFO @ Fri, 05 Jul 2019 17:49:38: #3 Call peaks for each chromosome... INFO @ Fri, 05 Jul 2019 17:49:38: #1 tag size is determined as 44 bps INFO @ Fri, 05 Jul 2019 17:49:38: #1 tag size = 44 INFO @ Fri, 05 Jul 2019 17:49:38: #1 total tags in treatment: 169715 INFO @ Fri, 05 Jul 2019 17:49:38: #1 user defined the maximum tags... INFO @ Fri, 05 Jul 2019 17:49:38: #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 17:49:38: #1 tags after filtering in treatment: 158375 INFO @ Fri, 05 Jul 2019 17:49:38: #1 Redundant rate of treatment: 0.07 INFO @ Fri, 05 Jul 2019 17:49:38: #1 finished! INFO @ Fri, 05 Jul 2019 17:49:38: #2 Build Peak Model... INFO @ Fri, 05 Jul 2019 17:49:38: #2 looking for paired plus/minus strand peaks... INFO @ Fri, 05 Jul 2019 17:49:38: #2 number of paired peaks: 299 WARNING @ Fri, 05 Jul 2019 17:49:38: Fewer paired peaks (299) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 299 pairs to build model! INFO @ Fri, 05 Jul 2019 17:49:38: start model_add_line... INFO @ Fri, 05 Jul 2019 17:49:38: start X-correlation... INFO @ Fri, 05 Jul 2019 17:49:38: end of X-cor INFO @ Fri, 05 Jul 2019 17:49:38: #2 finished! INFO @ Fri, 05 Jul 2019 17:49:38: #2 predicted fragment length is 148 bps INFO @ Fri, 05 Jul 2019 17:49:38: #2 alternative fragment length(s) may be 4,20,47,103,148,174,196,211,237,284,291,307,444,474,493,529,546,587 bps INFO @ Fri, 05 Jul 2019 17:49:38: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/sacCer3/ERX585748/ERX585748.10_model.r INFO @ Fri, 05 Jul 2019 17:49:38: #3 Call peaks... INFO @ Fri, 05 Jul 2019 17:49:38: #3 Pre-compute pvalue-qvalue table... INFO @ Fri, 05 Jul 2019 17:49:39: #4 Write output xls file... /home/okishinya/chipatlas/results/sacCer3/ERX585748/ERX585748.05_peaks.xls INFO @ Fri, 05 Jul 2019 17:49:39: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/sacCer3/ERX585748/ERX585748.05_peaks.narrowPeak INFO @ Fri, 05 Jul 2019 17:49:39: #4 Write summits bed file... /home/okishinya/chipatlas/results/sacCer3/ERX585748/ERX585748.05_summits.bed INFO @ Fri, 05 Jul 2019 17:49:39: Done! pass1 - making usageList (2 chroms): 0 millis pass2 - checking and writing primary data (3 records, 4 fields): 1 millis INFO @ Fri, 05 Jul 2019 17:49:39: #3 Call peaks for each chromosome... INFO @ Fri, 05 Jul 2019 17:49:39: #4 Write output xls file... /home/okishinya/chipatlas/results/sacCer3/ERX585748/ERX585748.10_peaks.xls INFO @ Fri, 05 Jul 2019 17:49:39: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/sacCer3/ERX585748/ERX585748.10_peaks.narrowPeak INFO @ Fri, 05 Jul 2019 17:49:39: #4 Write summits bed file... /home/okishinya/chipatlas/results/sacCer3/ERX585748/ERX585748.10_summits.bed INFO @ Fri, 05 Jul 2019 17:49:39: Done! pass1 - making usageList (0 chroms): 2 millis needLargeMem: trying to allocate 0 bytes (limit: 17179869184) INFO @ Fri, 05 Jul 2019 17:49:40: #1 tag size is determined as 44 bps INFO @ Fri, 05 Jul 2019 17:49:40: #1 tag size = 44 INFO @ Fri, 05 Jul 2019 17:49:40: #1 total tags in treatment: 169715 INFO @ Fri, 05 Jul 2019 17:49:40: #1 user defined the maximum tags... INFO @ Fri, 05 Jul 2019 17:49:40: #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 17:49:40: #1 tags after filtering in treatment: 158375 INFO @ Fri, 05 Jul 2019 17:49:40: #1 Redundant rate of treatment: 0.07 INFO @ Fri, 05 Jul 2019 17:49:40: #1 finished! INFO @ Fri, 05 Jul 2019 17:49:40: #2 Build Peak Model... INFO @ Fri, 05 Jul 2019 17:49:40: #2 looking for paired plus/minus strand peaks... INFO @ Fri, 05 Jul 2019 17:49:40: #2 number of paired peaks: 299 WARNING @ Fri, 05 Jul 2019 17:49:40: Fewer paired peaks (299) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 299 pairs to build model! INFO @ Fri, 05 Jul 2019 17:49:40: start model_add_line... INFO @ Fri, 05 Jul 2019 17:49:40: start X-correlation... INFO @ Fri, 05 Jul 2019 17:49:40: end of X-cor INFO @ Fri, 05 Jul 2019 17:49:40: #2 finished! INFO @ Fri, 05 Jul 2019 17:49:40: #2 predicted fragment length is 148 bps INFO @ Fri, 05 Jul 2019 17:49:40: #2 alternative fragment length(s) may be 4,20,47,103,148,174,196,211,237,284,291,307,444,474,493,529,546,587 bps INFO @ Fri, 05 Jul 2019 17:49:40: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/sacCer3/ERX585748/ERX585748.20_model.r INFO @ Fri, 05 Jul 2019 17:49:40: #3 Call peaks... INFO @ Fri, 05 Jul 2019 17:49:40: #3 Pre-compute pvalue-qvalue table... CompletedMACS2peakCalling INFO @ Fri, 05 Jul 2019 17:49:41: #3 Call peaks for each chromosome... INFO @ Fri, 05 Jul 2019 17:49:41: #4 Write output xls file... /home/okishinya/chipatlas/results/sacCer3/ERX585748/ERX585748.20_peaks.xls INFO @ Fri, 05 Jul 2019 17:49:41: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/sacCer3/ERX585748/ERX585748.20_peaks.narrowPeak INFO @ Fri, 05 Jul 2019 17:49:41: #4 Write summits bed file... /home/okishinya/chipatlas/results/sacCer3/ERX585748/ERX585748.20_summits.bed INFO @ Fri, 05 Jul 2019 17:49:41: Done! pass1 - making usageList (0 chroms): 1 millis needLargeMem: trying to allocate 0 bytes (limit: 17179869184) BedGraph に変換しました。 BigWig に変換中... BigWig に変換しました。 CompletedMACS2peakCalling CompletedMACS2peakCalling