Job ID = 11633766 sra ファイルのダウンロード中... Completed: 84603K bytes transferred in 4 seconds (146360K 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 2713866 spots for /home/okishinya/chipatlas/results/sacCer3/ERX1420385/ERR1348861.sra Written 2713866 spots for /home/okishinya/chipatlas/results/sacCer3/ERX1420385/ERR1348861.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: 00:00:26 2713866 reads; of these: 2713866 (100.00%) were unpaired; of these: 450406 (16.60%) aligned 0 times 1906460 (70.25%) aligned exactly 1 time 357000 (13.15%) aligned >1 times 83.40% overall alignment rate Time searching: 00:00:26 Overall time: 00:00:26 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_rmdupse_core] 427072 / 2263460 = 0.1887 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 09:14:46: # Command line: callpeak -t ERX1420385.bam -f BAM -g 12100000 -n ERX1420385.05 -q 1e-05 # ARGUMENTS LIST: # name = ERX1420385.05 # format = BAM # ChIP-seq file = ['ERX1420385.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 09:14:46: #1 read tag files... INFO @ Fri, 15 Feb 2019 09:14:46: #1 read treatment tags... INFO @ Fri, 15 Feb 2019 09:14:46: # Command line: callpeak -t ERX1420385.bam -f BAM -g 12100000 -n ERX1420385.10 -q 1e-10 # ARGUMENTS LIST: # name = ERX1420385.10 # format = BAM # ChIP-seq file = ['ERX1420385.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 09:14:46: #1 read tag files... INFO @ Fri, 15 Feb 2019 09:14:46: #1 read treatment tags... INFO @ Fri, 15 Feb 2019 09:14:46: # Command line: callpeak -t ERX1420385.bam -f BAM -g 12100000 -n ERX1420385.20 -q 1e-20 # ARGUMENTS LIST: # name = ERX1420385.20 # format = BAM # ChIP-seq file = ['ERX1420385.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 09:14:46: #1 read tag files... INFO @ Fri, 15 Feb 2019 09:14:46: #1 read treatment tags... INFO @ Fri, 15 Feb 2019 09:14:53: 1000000 INFO @ Fri, 15 Feb 2019 09:14:53: 1000000 INFO @ Fri, 15 Feb 2019 09:14:54: 1000000 INFO @ Fri, 15 Feb 2019 09:14:59: #1 tag size is determined as 51 bps INFO @ Fri, 15 Feb 2019 09:14:59: #1 tag size = 51 INFO @ Fri, 15 Feb 2019 09:14:59: #1 total tags in treatment: 1836388 INFO @ Fri, 15 Feb 2019 09:14:59: #1 user defined the maximum tags... INFO @ Fri, 15 Feb 2019 09:14:59: #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 09:14:59: #1 tags after filtering in treatment: 1836388 INFO @ Fri, 15 Feb 2019 09:14:59: #1 Redundant rate of treatment: 0.00 INFO @ Fri, 15 Feb 2019 09:14:59: #1 finished! INFO @ Fri, 15 Feb 2019 09:14:59: #2 Build Peak Model... INFO @ Fri, 15 Feb 2019 09:14:59: #2 looking for paired plus/minus strand peaks... INFO @ Fri, 15 Feb 2019 09:14:59: #2 number of paired peaks: 190 WARNING @ Fri, 15 Feb 2019 09:14:59: Fewer paired peaks (190) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 190 pairs to build model! INFO @ Fri, 15 Feb 2019 09:14:59: start model_add_line... INFO @ Fri, 15 Feb 2019 09:14:59: start X-correlation... INFO @ Fri, 15 Feb 2019 09:14:59: end of X-cor INFO @ Fri, 15 Feb 2019 09:14:59: #2 finished! INFO @ Fri, 15 Feb 2019 09:14:59: #2 predicted fragment length is 249 bps INFO @ Fri, 15 Feb 2019 09:14:59: #2 alternative fragment length(s) may be 0,173,218,249,290,581 bps INFO @ Fri, 15 Feb 2019 09:14:59: #2.2 Generate R script for model : ERX1420385.05_model.r INFO @ Fri, 15 Feb 2019 09:14:59: #3 Call peaks... INFO @ Fri, 15 Feb 2019 09:14:59: #3 Pre-compute pvalue-qvalue table... INFO @ Fri, 15 Feb 2019 09:15:00: #1 tag size is determined as 51 bps INFO @ Fri, 15 Feb 2019 09:15:00: #1 tag size = 51 INFO @ Fri, 15 Feb 2019 09:15:00: #1 total tags in treatment: 1836388 INFO @ Fri, 15 Feb 2019 09:15:00: #1 user defined the maximum tags... INFO @ Fri, 15 Feb 2019 09:15:00: #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 09:15:00: #1 tags after filtering in treatment: 1836388 INFO @ Fri, 15 Feb 2019 09:15:00: #1 Redundant rate of treatment: 0.00 INFO @ Fri, 15 Feb 2019 09:15:00: #1 finished! INFO @ Fri, 15 Feb 2019 09:15:00: #2 Build Peak Model... INFO @ Fri, 15 Feb 2019 09:15:00: #2 looking for paired plus/minus strand peaks... INFO @ Fri, 15 Feb 2019 09:15:00: #2 number of paired peaks: 190 WARNING @ Fri, 15 Feb 2019 09:15:00: Fewer paired peaks (190) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 190 pairs to build model! INFO @ Fri, 15 Feb 2019 09:15:00: start model_add_line... INFO @ Fri, 15 Feb 2019 09:15:00: start X-correlation... INFO @ Fri, 15 Feb 2019 09:15:00: end of X-cor INFO @ Fri, 15 Feb 2019 09:15:00: #2 finished! INFO @ Fri, 15 Feb 2019 09:15:00: #2 predicted fragment length is 249 bps INFO @ Fri, 15 Feb 2019 09:15:00: #2 alternative fragment length(s) may be 0,173,218,249,290,581 bps INFO @ Fri, 15 Feb 2019 09:15:00: #2.2 Generate R script for model : ERX1420385.20_model.r INFO @ Fri, 15 Feb 2019 09:15:00: #3 Call peaks... INFO @ Fri, 15 Feb 2019 09:15:00: #3 Pre-compute pvalue-qvalue table... INFO @ Fri, 15 Feb 2019 09:15:01: #1 tag size is determined as 51 bps INFO @ Fri, 15 Feb 2019 09:15:01: #1 tag size = 51 INFO @ Fri, 15 Feb 2019 09:15:01: #1 total tags in treatment: 1836388 INFO @ Fri, 15 Feb 2019 09:15:01: #1 user defined the maximum tags... INFO @ Fri, 15 Feb 2019 09:15:01: #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 09:15:01: #1 tags after filtering in treatment: 1836388 INFO @ Fri, 15 Feb 2019 09:15:01: #1 Redundant rate of treatment: 0.00 INFO @ Fri, 15 Feb 2019 09:15:01: #1 finished! INFO @ Fri, 15 Feb 2019 09:15:01: #2 Build Peak Model... INFO @ Fri, 15 Feb 2019 09:15:01: #2 looking for paired plus/minus strand peaks... INFO @ Fri, 15 Feb 2019 09:15:01: #2 number of paired peaks: 190 WARNING @ Fri, 15 Feb 2019 09:15:01: Fewer paired peaks (190) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 190 pairs to build model! INFO @ Fri, 15 Feb 2019 09:15:01: start model_add_line... INFO @ Fri, 15 Feb 2019 09:15:01: start X-correlation... INFO @ Fri, 15 Feb 2019 09:15:01: end of X-cor INFO @ Fri, 15 Feb 2019 09:15:01: #2 finished! INFO @ Fri, 15 Feb 2019 09:15:01: #2 predicted fragment length is 249 bps INFO @ Fri, 15 Feb 2019 09:15:01: #2 alternative fragment length(s) may be 0,173,218,249,290,581 bps INFO @ Fri, 15 Feb 2019 09:15:01: #2.2 Generate R script for model : ERX1420385.10_model.r INFO @ Fri, 15 Feb 2019 09:15:01: #3 Call peaks... INFO @ Fri, 15 Feb 2019 09:15:01: #3 Pre-compute pvalue-qvalue table... INFO @ Fri, 15 Feb 2019 09:15:04: #3 Call peaks for each chromosome... INFO @ Fri, 15 Feb 2019 09:15:05: #3 Call peaks for each chromosome... INFO @ Fri, 15 Feb 2019 09:15:06: #4 Write output xls file... ERX1420385.05_peaks.xls INFO @ Fri, 15 Feb 2019 09:15:06: #4 Write peak in narrowPeak format file... ERX1420385.05_peaks.narrowPeak INFO @ Fri, 15 Feb 2019 09:15:06: #4 Write summits bed file... ERX1420385.05_summits.bed INFO @ Fri, 15 Feb 2019 09:15:06: Done! pass1 - making usageList (6 chroms): 1 millis pass2 - checking and writing primary data (18 records, 4 fields): 3 millis CompletedMACS2peakCalling INFO @ Fri, 15 Feb 2019 09:15:06: #3 Call peaks for each chromosome... INFO @ Fri, 15 Feb 2019 09:15:07: #4 Write output xls file... ERX1420385.20_peaks.xls INFO @ Fri, 15 Feb 2019 09:15:07: #4 Write peak in narrowPeak format file... ERX1420385.20_peaks.narrowPeak INFO @ Fri, 15 Feb 2019 09:15:07: #4 Write summits bed file... ERX1420385.20_summits.bed INFO @ Fri, 15 Feb 2019 09:15:07: Done! pass1 - making usageList (4 chroms): 1 millis pass2 - checking and writing primary data (6 records, 4 fields): 2 millis CompletedMACS2peakCalling INFO @ Fri, 15 Feb 2019 09:15:08: #4 Write output xls file... ERX1420385.10_peaks.xls INFO @ Fri, 15 Feb 2019 09:15:08: #4 Write peak in narrowPeak format file... ERX1420385.10_peaks.narrowPeak INFO @ Fri, 15 Feb 2019 09:15:08: #4 Write summits bed file... ERX1420385.10_summits.bed INFO @ Fri, 15 Feb 2019 09:15:08: Done! pass1 - making usageList (5 chroms): 1 millis pass2 - checking and writing primary data (14 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。