Job ID = 10714584 sra ファイルのダウンロード中... Completed: 283133K bytes transferred in 25 seconds (90404K 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: SINGLE fastq に変換中... Read 18474302 spots for /home/okishinya/chipatlas/results/dm3/SRX4053338/SRR7132375.sra Written 18474302 spots for /home/okishinya/chipatlas/results/dm3/SRX4053338/SRR7132375.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: 00:06:55 18474302 reads; of these: 18474302 (100.00%) were unpaired; of these: 3659468 (19.81%) aligned 0 times 10303930 (55.77%) aligned exactly 1 time 4510904 (24.42%) aligned >1 times 80.19% overall alignment rate Time searching: 00:06:55 Overall time: 00:06:55 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_sort_core] merging from 8 files... [bam_rmdupse_core] 2552273 / 14814834 = 0.1723 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 @ Sun, 03 Jun 2018 13:47:25: # Command line: callpeak -t SRX4053338.bam -f BAM -g dm -n SRX4053338.20 -q 1e-20 # ARGUMENTS LIST: # name = SRX4053338.20 # format = BAM # ChIP-seq file = ['SRX4053338.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 @ Sun, 03 Jun 2018 13:47:25: #1 read tag files... INFO @ Sun, 03 Jun 2018 13:47:25: #1 read treatment tags... INFO @ Sun, 03 Jun 2018 13:47:25: # Command line: callpeak -t SRX4053338.bam -f BAM -g dm -n SRX4053338.05 -q 1e-05 # ARGUMENTS LIST: # name = SRX4053338.05 # format = BAM # ChIP-seq file = ['SRX4053338.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 @ Sun, 03 Jun 2018 13:47:25: #1 read tag files... INFO @ Sun, 03 Jun 2018 13:47:25: #1 read treatment tags... INFO @ Sun, 03 Jun 2018 13:47:25: # Command line: callpeak -t SRX4053338.bam -f BAM -g dm -n SRX4053338.10 -q 1e-10 # ARGUMENTS LIST: # name = SRX4053338.10 # format = BAM # ChIP-seq file = ['SRX4053338.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 @ Sun, 03 Jun 2018 13:47:25: #1 read tag files... INFO @ Sun, 03 Jun 2018 13:47:25: #1 read treatment tags... INFO @ Sun, 03 Jun 2018 13:47:32: 1000000 INFO @ Sun, 03 Jun 2018 13:47:32: 1000000 INFO @ Sun, 03 Jun 2018 13:47:32: 1000000 INFO @ Sun, 03 Jun 2018 13:47:38: 2000000 INFO @ Sun, 03 Jun 2018 13:47:38: 2000000 INFO @ Sun, 03 Jun 2018 13:47:38: 2000000 INFO @ Sun, 03 Jun 2018 13:47:44: 3000000 INFO @ Sun, 03 Jun 2018 13:47:44: 3000000 INFO @ Sun, 03 Jun 2018 13:47:44: 3000000 INFO @ Sun, 03 Jun 2018 13:47:50: 4000000 INFO @ Sun, 03 Jun 2018 13:47:50: 4000000 INFO @ Sun, 03 Jun 2018 13:47:50: 4000000 INFO @ Sun, 03 Jun 2018 13:47:56: 5000000 INFO @ Sun, 03 Jun 2018 13:47:56: 5000000 INFO @ Sun, 03 Jun 2018 13:47:56: 5000000 INFO @ Sun, 03 Jun 2018 13:48:03: 6000000 INFO @ Sun, 03 Jun 2018 13:48:03: 6000000 INFO @ Sun, 03 Jun 2018 13:48:03: 6000000 INFO @ Sun, 03 Jun 2018 13:48:09: 7000000 INFO @ Sun, 03 Jun 2018 13:48:09: 7000000 INFO @ Sun, 03 Jun 2018 13:48:09: 7000000 INFO @ Sun, 03 Jun 2018 13:48:15: 8000000 INFO @ Sun, 03 Jun 2018 13:48:15: 8000000 INFO @ Sun, 03 Jun 2018 13:48:15: 8000000 INFO @ Sun, 03 Jun 2018 13:48:21: 9000000 INFO @ Sun, 03 Jun 2018 13:48:21: 9000000 INFO @ Sun, 03 Jun 2018 13:48:21: 9000000 INFO @ Sun, 03 Jun 2018 13:48:28: 10000000 INFO @ Sun, 03 Jun 2018 13:48:28: 10000000 INFO @ Sun, 03 Jun 2018 13:48:28: 10000000 INFO @ Sun, 03 Jun 2018 13:48:34: 11000000 INFO @ Sun, 03 Jun 2018 13:48:34: 11000000 INFO @ Sun, 03 Jun 2018 13:48:34: 11000000 INFO @ Sun, 03 Jun 2018 13:48:40: 12000000 INFO @ Sun, 03 Jun 2018 13:48:40: 12000000 INFO @ Sun, 03 Jun 2018 13:48:40: 12000000 INFO @ Sun, 03 Jun 2018 13:48:42: #1 tag size is determined as 50 bps INFO @ Sun, 03 Jun 2018 13:48:42: #1 tag size = 50 INFO @ Sun, 03 Jun 2018 13:48:42: #1 total tags in treatment: 12262561 INFO @ Sun, 03 Jun 2018 13:48:42: #1 user defined the maximum tags... INFO @ Sun, 03 Jun 2018 13:48:42: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Sun, 03 Jun 2018 13:48:42: #1 tags after filtering in treatment: 12262561 INFO @ Sun, 03 Jun 2018 13:48:42: #1 Redundant rate of treatment: 0.00 INFO @ Sun, 03 Jun 2018 13:48:42: #1 finished! INFO @ Sun, 03 Jun 2018 13:48:42: #2 Build Peak Model... INFO @ Sun, 03 Jun 2018 13:48:42: #2 looking for paired plus/minus strand peaks... INFO @ Sun, 03 Jun 2018 13:48:42: #1 tag size is determined as 50 bps INFO @ Sun, 03 Jun 2018 13:48:42: #1 tag size is determined as 50 bps INFO @ Sun, 03 Jun 2018 13:48:42: #1 tag size = 50 INFO @ Sun, 03 Jun 2018 13:48:42: #1 tag size = 50 INFO @ Sun, 03 Jun 2018 13:48:42: #1 total tags in treatment: 12262561 INFO @ Sun, 03 Jun 2018 13:48:42: #1 total tags in treatment: 12262561 INFO @ Sun, 03 Jun 2018 13:48:42: #1 user defined the maximum tags... INFO @ Sun, 03 Jun 2018 13:48:42: #1 user defined the maximum tags... INFO @ Sun, 03 Jun 2018 13:48:42: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Sun, 03 Jun 2018 13:48:42: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Sun, 03 Jun 2018 13:48:42: #1 tags after filtering in treatment: 12262561 INFO @ Sun, 03 Jun 2018 13:48:42: #1 tags after filtering in treatment: 12262561 INFO @ Sun, 03 Jun 2018 13:48:42: #1 Redundant rate of treatment: 0.00 INFO @ Sun, 03 Jun 2018 13:48:42: #1 Redundant rate of treatment: 0.00 INFO @ Sun, 03 Jun 2018 13:48:42: #1 finished! INFO @ Sun, 03 Jun 2018 13:48:42: #1 finished! INFO @ Sun, 03 Jun 2018 13:48:42: #2 Build Peak Model... INFO @ Sun, 03 Jun 2018 13:48:42: #2 Build Peak Model... INFO @ Sun, 03 Jun 2018 13:48:42: #2 looking for paired plus/minus strand peaks... INFO @ Sun, 03 Jun 2018 13:48:42: #2 looking for paired plus/minus strand peaks... INFO @ Sun, 03 Jun 2018 13:48:43: #2 number of paired peaks: 158 WARNING @ Sun, 03 Jun 2018 13:48:43: Fewer paired peaks (158) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 158 pairs to build model! INFO @ Sun, 03 Jun 2018 13:48:43: start model_add_line... INFO @ Sun, 03 Jun 2018 13:48:43: start X-correlation... INFO @ Sun, 03 Jun 2018 13:48:43: end of X-cor INFO @ Sun, 03 Jun 2018 13:48:43: #2 finished! INFO @ Sun, 03 Jun 2018 13:48:43: #2 predicted fragment length is 49 bps INFO @ Sun, 03 Jun 2018 13:48:43: #2 alternative fragment length(s) may be 49 bps INFO @ Sun, 03 Jun 2018 13:48:43: #2.2 Generate R script for model : SRX4053338.20_model.r WARNING @ Sun, 03 Jun 2018 13:48:43: #2 Since the d (49) calculated from paired-peaks are smaller than 2*tag length, it may be influenced by unknown sequencing problem! WARNING @ Sun, 03 Jun 2018 13:48:43: #2 You may need to consider one of the other alternative d(s): 49 WARNING @ Sun, 03 Jun 2018 13:48:43: #2 You can restart the process with --nomodel --extsize XXX with your choice or an arbitrary number. Nontheless, MACS will continute computing. INFO @ Sun, 03 Jun 2018 13:48:43: #3 Call peaks... INFO @ Sun, 03 Jun 2018 13:48:43: #3 Pre-compute pvalue-qvalue table... INFO @ Sun, 03 Jun 2018 13:48:43: #2 number of paired peaks: 158 WARNING @ Sun, 03 Jun 2018 13:48:43: Fewer paired peaks (158) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 158 pairs to build model! INFO @ Sun, 03 Jun 2018 13:48:43: start model_add_line... INFO @ Sun, 03 Jun 2018 13:48:43: #2 number of paired peaks: 158 WARNING @ Sun, 03 Jun 2018 13:48:43: Fewer paired peaks (158) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 158 pairs to build model! INFO @ Sun, 03 Jun 2018 13:48:43: start model_add_line... INFO @ Sun, 03 Jun 2018 13:48:43: start X-correlation... INFO @ Sun, 03 Jun 2018 13:48:43: end of X-cor INFO @ Sun, 03 Jun 2018 13:48:43: #2 finished! INFO @ Sun, 03 Jun 2018 13:48:43: #2 predicted fragment length is 49 bps INFO @ Sun, 03 Jun 2018 13:48:43: #2 alternative fragment length(s) may be 49 bps INFO @ Sun, 03 Jun 2018 13:48:43: #2.2 Generate R script for model : SRX4053338.10_model.r INFO @ Sun, 03 Jun 2018 13:48:43: start X-correlation... WARNING @ Sun, 03 Jun 2018 13:48:43: #2 Since the d (49) calculated from paired-peaks are smaller than 2*tag length, it may be influenced by unknown sequencing problem! WARNING @ Sun, 03 Jun 2018 13:48:43: #2 You may need to consider one of the other alternative d(s): 49 WARNING @ Sun, 03 Jun 2018 13:48:43: #2 You can restart the process with --nomodel --extsize XXX with your choice or an arbitrary number. Nontheless, MACS will continute computing. INFO @ Sun, 03 Jun 2018 13:48:43: #3 Call peaks... INFO @ Sun, 03 Jun 2018 13:48:43: #3 Pre-compute pvalue-qvalue table... INFO @ Sun, 03 Jun 2018 13:48:43: end of X-cor INFO @ Sun, 03 Jun 2018 13:48:43: #2 finished! INFO @ Sun, 03 Jun 2018 13:48:43: #2 predicted fragment length is 49 bps INFO @ Sun, 03 Jun 2018 13:48:43: #2 alternative fragment length(s) may be 49 bps INFO @ Sun, 03 Jun 2018 13:48:43: #2.2 Generate R script for model : SRX4053338.05_model.r WARNING @ Sun, 03 Jun 2018 13:48:43: #2 Since the d (49) calculated from paired-peaks are smaller than 2*tag length, it may be influenced by unknown sequencing problem! WARNING @ Sun, 03 Jun 2018 13:48:43: #2 You may need to consider one of the other alternative d(s): 49 WARNING @ Sun, 03 Jun 2018 13:48:43: #2 You can restart the process with --nomodel --extsize XXX with your choice or an arbitrary number. Nontheless, MACS will continute computing. INFO @ Sun, 03 Jun 2018 13:48:43: #3 Call peaks... INFO @ Sun, 03 Jun 2018 13:48:43: #3 Pre-compute pvalue-qvalue table... INFO @ Sun, 03 Jun 2018 13:49:08: #3 Call peaks for each chromosome... INFO @ Sun, 03 Jun 2018 13:49:09: #3 Call peaks for each chromosome... INFO @ Sun, 03 Jun 2018 13:49:09: #3 Call peaks for each chromosome... INFO @ Sun, 03 Jun 2018 13:49:24: #4 Write output xls file... SRX4053338.10_peaks.xls INFO @ Sun, 03 Jun 2018 13:49:24: #4 Write peak in narrowPeak format file... SRX4053338.10_peaks.narrowPeak INFO @ Sun, 03 Jun 2018 13:49:24: #4 Write summits bed file... SRX4053338.10_summits.bed INFO @ Sun, 03 Jun 2018 13:49:24: Done! pass1 - making usageList (13 chroms): 0 millis pass2 - checking and writing primary data (1306 records, 4 fields): 4 millis CompletedMACS2peakCalling INFO @ Sun, 03 Jun 2018 13:49:25: #4 Write output xls file... SRX4053338.05_peaks.xls INFO @ Sun, 03 Jun 2018 13:49:25: #4 Write output xls file... SRX4053338.20_peaks.xls INFO @ Sun, 03 Jun 2018 13:49:25: #4 Write peak in narrowPeak format file... SRX4053338.05_peaks.narrowPeak INFO @ Sun, 03 Jun 2018 13:49:25: #4 Write peak in narrowPeak format file... SRX4053338.20_peaks.narrowPeak INFO @ Sun, 03 Jun 2018 13:49:25: #4 Write summits bed file... SRX4053338.20_summits.bed INFO @ Sun, 03 Jun 2018 13:49:25: #4 Write summits bed file... SRX4053338.05_summits.bed INFO @ Sun, 03 Jun 2018 13:49:25: Done! INFO @ Sun, 03 Jun 2018 13:49:25: Done! pass1 - making usageList (10 chroms): 1 millis pass2 - checking and writing primary data (706 records, 4 fields): 3 millis CompletedMACS2peakCalling pass1 - making usageList (14 chroms): 1 millis pass2 - checking and writing primary data (1818 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。