Job ID = 10937571 sra ファイルのダウンロード中... Completed: 471416K bytes transferred in 14 seconds (273479K bits/sec), in 1 file. Completed: 105605K bytes transferred in 4 seconds (184067K 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 1134269 spots for /home/okishinya/chipatlas/results/sacCer3/SRX3010347/SRR5833352.sra Written 1134269 spots for /home/okishinya/chipatlas/results/sacCer3/SRX3010347/SRR5833352.sra Read 4804410 spots for /home/okishinya/chipatlas/results/sacCer3/SRX3010347/SRR5833351.sra Written 4804410 spots for /home/okishinya/chipatlas/results/sacCer3/SRX3010347/SRR5833351.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 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: 00:02:16 5938679 reads; of these: 5938679 (100.00%) were paired; of these: 4888444 (82.32%) aligned concordantly 0 times 654451 (11.02%) aligned concordantly exactly 1 time 395784 (6.66%) aligned concordantly >1 times ---- 4888444 pairs aligned concordantly 0 times; of these: 4882 (0.10%) aligned discordantly 1 time ---- 4883562 pairs aligned 0 times concordantly or discordantly; of these: 9767124 mates make up the pairs; of these: 9739523 (99.72%) aligned 0 times 11590 (0.12%) aligned exactly 1 time 16011 (0.16%) aligned >1 times 18.00% overall alignment rate Time searching: 00:02:16 Overall time: 00:02:16 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] 85228 / 1054524 = 0.0808 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, 10 Aug 2018 02:39:34: # Command line: callpeak -t SRX3010347.bam -f BAM -g 12100000 -n SRX3010347.20 -q 1e-20 # ARGUMENTS LIST: # name = SRX3010347.20 # format = BAM # ChIP-seq file = ['SRX3010347.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, 10 Aug 2018 02:39:34: #1 read tag files... INFO @ Fri, 10 Aug 2018 02:39:34: #1 read treatment tags... INFO @ Fri, 10 Aug 2018 02:39:34: # Command line: callpeak -t SRX3010347.bam -f BAM -g 12100000 -n SRX3010347.05 -q 1e-05 # ARGUMENTS LIST: # name = SRX3010347.05 # format = BAM # ChIP-seq file = ['SRX3010347.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, 10 Aug 2018 02:39:34: #1 read tag files... INFO @ Fri, 10 Aug 2018 02:39:34: #1 read treatment tags... INFO @ Fri, 10 Aug 2018 02:39:34: # Command line: callpeak -t SRX3010347.bam -f BAM -g 12100000 -n SRX3010347.10 -q 1e-10 # ARGUMENTS LIST: # name = SRX3010347.10 # format = BAM # ChIP-seq file = ['SRX3010347.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, 10 Aug 2018 02:39:34: #1 read tag files... INFO @ Fri, 10 Aug 2018 02:39:34: #1 read treatment tags... INFO @ Fri, 10 Aug 2018 02:39:42: 1000000 INFO @ Fri, 10 Aug 2018 02:39:42: 1000000 INFO @ Fri, 10 Aug 2018 02:39:42: 1000000 INFO @ Fri, 10 Aug 2018 02:39:49: #1 tag size is determined as 101 bps INFO @ Fri, 10 Aug 2018 02:39:49: #1 tag size = 101 INFO @ Fri, 10 Aug 2018 02:39:49: #1 total tags in treatment: 965114 INFO @ Fri, 10 Aug 2018 02:39:49: #1 user defined the maximum tags... INFO @ Fri, 10 Aug 2018 02:39:49: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Fri, 10 Aug 2018 02:39:49: #1 tags after filtering in treatment: 662945 INFO @ Fri, 10 Aug 2018 02:39:49: #1 Redundant rate of treatment: 0.31 INFO @ Fri, 10 Aug 2018 02:39:49: #1 finished! INFO @ Fri, 10 Aug 2018 02:39:49: #2 Build Peak Model... INFO @ Fri, 10 Aug 2018 02:39:49: #2 looking for paired plus/minus strand peaks... INFO @ Fri, 10 Aug 2018 02:39:49: #2 number of paired peaks: 531 WARNING @ Fri, 10 Aug 2018 02:39:49: Fewer paired peaks (531) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 531 pairs to build model! INFO @ Fri, 10 Aug 2018 02:39:49: start model_add_line... INFO @ Fri, 10 Aug 2018 02:39:49: start X-correlation... INFO @ Fri, 10 Aug 2018 02:39:49: end of X-cor INFO @ Fri, 10 Aug 2018 02:39:49: #2 finished! INFO @ Fri, 10 Aug 2018 02:39:49: #2 predicted fragment length is 201 bps INFO @ Fri, 10 Aug 2018 02:39:49: #2 alternative fragment length(s) may be 201 bps INFO @ Fri, 10 Aug 2018 02:39:49: #2.2 Generate R script for model : SRX3010347.10_model.r WARNING @ Fri, 10 Aug 2018 02:39:49: #2 Since the d (201) calculated from paired-peaks are smaller than 2*tag length, it may be influenced by unknown sequencing problem! WARNING @ Fri, 10 Aug 2018 02:39:49: #2 You may need to consider one of the other alternative d(s): 201 WARNING @ Fri, 10 Aug 2018 02:39:49: #2 You can restart the process with --nomodel --extsize XXX with your choice or an arbitrary number. Nontheless, MACS will continute computing. INFO @ Fri, 10 Aug 2018 02:39:49: #3 Call peaks... INFO @ Fri, 10 Aug 2018 02:39:49: #3 Pre-compute pvalue-qvalue table... INFO @ Fri, 10 Aug 2018 02:39:50: #1 tag size is determined as 101 bps INFO @ Fri, 10 Aug 2018 02:39:50: #1 tag size = 101 INFO @ Fri, 10 Aug 2018 02:39:50: #1 total tags in treatment: 965114 INFO @ Fri, 10 Aug 2018 02:39:50: #1 user defined the maximum tags... INFO @ Fri, 10 Aug 2018 02:39:50: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Fri, 10 Aug 2018 02:39:50: #1 tag size is determined as 101 bps INFO @ Fri, 10 Aug 2018 02:39:50: #1 tag size = 101 INFO @ Fri, 10 Aug 2018 02:39:50: #1 total tags in treatment: 965114 INFO @ Fri, 10 Aug 2018 02:39:50: #1 user defined the maximum tags... INFO @ Fri, 10 Aug 2018 02:39:50: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Fri, 10 Aug 2018 02:39:50: #1 tags after filtering in treatment: 662945 INFO @ Fri, 10 Aug 2018 02:39:50: #1 Redundant rate of treatment: 0.31 INFO @ Fri, 10 Aug 2018 02:39:50: #1 finished! INFO @ Fri, 10 Aug 2018 02:39:50: #2 Build Peak Model... INFO @ Fri, 10 Aug 2018 02:39:50: #2 looking for paired plus/minus strand peaks... INFO @ Fri, 10 Aug 2018 02:39:50: #1 tags after filtering in treatment: 662945 INFO @ Fri, 10 Aug 2018 02:39:50: #1 Redundant rate of treatment: 0.31 INFO @ Fri, 10 Aug 2018 02:39:50: #1 finished! INFO @ Fri, 10 Aug 2018 02:39:50: #2 Build Peak Model... INFO @ Fri, 10 Aug 2018 02:39:50: #2 looking for paired plus/minus strand peaks... INFO @ Fri, 10 Aug 2018 02:39:50: #2 number of paired peaks: 531 WARNING @ Fri, 10 Aug 2018 02:39:50: Fewer paired peaks (531) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 531 pairs to build model! INFO @ Fri, 10 Aug 2018 02:39:50: start model_add_line... INFO @ Fri, 10 Aug 2018 02:39:50: #2 number of paired peaks: 531 WARNING @ Fri, 10 Aug 2018 02:39:50: Fewer paired peaks (531) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 531 pairs to build model! INFO @ Fri, 10 Aug 2018 02:39:50: start model_add_line... INFO @ Fri, 10 Aug 2018 02:39:50: start X-correlation... INFO @ Fri, 10 Aug 2018 02:39:50: start X-correlation... INFO @ Fri, 10 Aug 2018 02:39:50: end of X-cor INFO @ Fri, 10 Aug 2018 02:39:50: end of X-cor INFO @ Fri, 10 Aug 2018 02:39:50: #2 finished! INFO @ Fri, 10 Aug 2018 02:39:50: #2 finished! INFO @ Fri, 10 Aug 2018 02:39:50: #2 predicted fragment length is 201 bps INFO @ Fri, 10 Aug 2018 02:39:50: #2 predicted fragment length is 201 bps INFO @ Fri, 10 Aug 2018 02:39:50: #2 alternative fragment length(s) may be 201 bps INFO @ Fri, 10 Aug 2018 02:39:50: #2 alternative fragment length(s) may be 201 bps INFO @ Fri, 10 Aug 2018 02:39:50: #2.2 Generate R script for model : SRX3010347.05_model.r INFO @ Fri, 10 Aug 2018 02:39:50: #2.2 Generate R script for model : SRX3010347.20_model.r WARNING @ Fri, 10 Aug 2018 02:39:50: #2 Since the d (201) calculated from paired-peaks are smaller than 2*tag length, it may be influenced by unknown sequencing problem! WARNING @ Fri, 10 Aug 2018 02:39:50: #2 You may need to consider one of the other alternative d(s): 201 WARNING @ Fri, 10 Aug 2018 02:39:50: #2 Since the d (201) calculated from paired-peaks are smaller than 2*tag length, it may be influenced by unknown sequencing problem! WARNING @ Fri, 10 Aug 2018 02:39:50: #2 You can restart the process with --nomodel --extsize XXX with your choice or an arbitrary number. Nontheless, MACS will continute computing. WARNING @ Fri, 10 Aug 2018 02:39:50: #2 You may need to consider one of the other alternative d(s): 201 INFO @ Fri, 10 Aug 2018 02:39:50: #3 Call peaks... WARNING @ Fri, 10 Aug 2018 02:39:50: #2 You can restart the process with --nomodel --extsize XXX with your choice or an arbitrary number. Nontheless, MACS will continute computing. INFO @ Fri, 10 Aug 2018 02:39:50: #3 Call peaks... INFO @ Fri, 10 Aug 2018 02:39:50: #3 Pre-compute pvalue-qvalue table... INFO @ Fri, 10 Aug 2018 02:39:50: #3 Pre-compute pvalue-qvalue table... INFO @ Fri, 10 Aug 2018 02:39:52: #3 Call peaks for each chromosome... INFO @ Fri, 10 Aug 2018 02:39:52: #3 Call peaks for each chromosome... INFO @ Fri, 10 Aug 2018 02:39:52: #3 Call peaks for each chromosome... INFO @ Fri, 10 Aug 2018 02:39:53: #4 Write output xls file... SRX3010347.10_peaks.xls INFO @ Fri, 10 Aug 2018 02:39:53: #4 Write peak in narrowPeak format file... SRX3010347.10_peaks.narrowPeak INFO @ Fri, 10 Aug 2018 02:39:53: #4 Write summits bed file... SRX3010347.10_summits.bed INFO @ Fri, 10 Aug 2018 02:39:53: Done! pass1 - making usageList (16 chroms): 1 millis pass2 - checking and writing primary data (471 records, 4 fields): 4 millis CompletedMACS2peakCalling INFO @ Fri, 10 Aug 2018 02:39:53: #4 Write output xls file... SRX3010347.20_peaks.xls INFO @ Fri, 10 Aug 2018 02:39:53: #4 Write peak in narrowPeak format file... SRX3010347.20_peaks.narrowPeak INFO @ Fri, 10 Aug 2018 02:39:53: #4 Write summits bed file... SRX3010347.20_summits.bed INFO @ Fri, 10 Aug 2018 02:39:53: Done! pass1 - making usageList (16 chroms): 1 millis pass2 - checking and writing primary data (426 records, 4 fields): 3 millis CompletedMACS2peakCalling INFO @ Fri, 10 Aug 2018 02:39:53: #4 Write output xls file... SRX3010347.05_peaks.xls INFO @ Fri, 10 Aug 2018 02:39:53: #4 Write peak in narrowPeak format file... SRX3010347.05_peaks.narrowPeak INFO @ Fri, 10 Aug 2018 02:39:53: #4 Write summits bed file... SRX3010347.05_summits.bed INFO @ Fri, 10 Aug 2018 02:39:53: Done! pass1 - making usageList (17 chroms): 0 millis pass2 - checking and writing primary data (531 records, 4 fields): 4 millis CompletedMACS2peakCalling BedGraph に変換しました。 BigWig に変換中... BigWig に変換しました。