Job ID = 11293688 sra ファイルのダウンロード中... Completed: 69305K bytes transferred in 6 seconds (93185K 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 2009251 spots for /home/okishinya/chipatlas/results/dm3/SRX4375850/SRR7506504.sra Written 2009251 spots for /home/okishinya/chipatlas/results/dm3/SRX4375850/SRR7506504.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: 00:00:35 2009251 reads; of these: 2009251 (100.00%) were unpaired; of these: 845260 (42.07%) aligned 0 times 886174 (44.10%) aligned exactly 1 time 277817 (13.83%) aligned >1 times 57.93% overall alignment rate Time searching: 00:00:35 Overall time: 00:00:35 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_rmdupse_core] 93508 / 1163991 = 0.0803 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, 04 Nov 2018 17:48:16: # Command line: callpeak -t SRX4375850.bam -f BAM -g dm -n SRX4375850.20 -q 1e-20 # ARGUMENTS LIST: # name = SRX4375850.20 # format = BAM # ChIP-seq file = ['SRX4375850.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, 04 Nov 2018 17:48:16: # Command line: callpeak -t SRX4375850.bam -f BAM -g dm -n SRX4375850.05 -q 1e-05 # ARGUMENTS LIST: # name = SRX4375850.05 # format = BAM # ChIP-seq file = ['SRX4375850.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, 04 Nov 2018 17:48:16: # Command line: callpeak -t SRX4375850.bam -f BAM -g dm -n SRX4375850.10 -q 1e-10 # ARGUMENTS LIST: # name = SRX4375850.10 # format = BAM # ChIP-seq file = ['SRX4375850.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, 04 Nov 2018 17:48:16: #1 read tag files... INFO @ Sun, 04 Nov 2018 17:48:16: #1 read tag files... INFO @ Sun, 04 Nov 2018 17:48:16: #1 read tag files... INFO @ Sun, 04 Nov 2018 17:48:16: #1 read treatment tags... INFO @ Sun, 04 Nov 2018 17:48:16: #1 read treatment tags... INFO @ Sun, 04 Nov 2018 17:48:16: #1 read treatment tags... INFO @ Sun, 04 Nov 2018 17:48:23: 1000000 INFO @ Sun, 04 Nov 2018 17:48:23: 1000000 INFO @ Sun, 04 Nov 2018 17:48:23: 1000000 INFO @ Sun, 04 Nov 2018 17:48:23: #1 tag size is determined as 51 bps INFO @ Sun, 04 Nov 2018 17:48:23: #1 tag size = 51 INFO @ Sun, 04 Nov 2018 17:48:23: #1 total tags in treatment: 1070483 INFO @ Sun, 04 Nov 2018 17:48:23: #1 user defined the maximum tags... INFO @ Sun, 04 Nov 2018 17:48:23: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Sun, 04 Nov 2018 17:48:23: #1 tag size is determined as 51 bps INFO @ Sun, 04 Nov 2018 17:48:23: #1 tag size = 51 INFO @ Sun, 04 Nov 2018 17:48:23: #1 total tags in treatment: 1070483 INFO @ Sun, 04 Nov 2018 17:48:23: #1 user defined the maximum tags... INFO @ Sun, 04 Nov 2018 17:48:23: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Sun, 04 Nov 2018 17:48:23: #1 tag size is determined as 51 bps INFO @ Sun, 04 Nov 2018 17:48:23: #1 tag size = 51 INFO @ Sun, 04 Nov 2018 17:48:23: #1 total tags in treatment: 1070483 INFO @ Sun, 04 Nov 2018 17:48:23: #1 user defined the maximum tags... INFO @ Sun, 04 Nov 2018 17:48:23: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Sun, 04 Nov 2018 17:48:23: #1 tags after filtering in treatment: 1070483 INFO @ Sun, 04 Nov 2018 17:48:23: #1 tags after filtering in treatment: 1070483 INFO @ Sun, 04 Nov 2018 17:48:23: #1 Redundant rate of treatment: 0.00 INFO @ Sun, 04 Nov 2018 17:48:23: #1 Redundant rate of treatment: 0.00 INFO @ Sun, 04 Nov 2018 17:48:23: #1 finished! INFO @ Sun, 04 Nov 2018 17:48:23: #1 finished! INFO @ Sun, 04 Nov 2018 17:48:23: #2 Build Peak Model... INFO @ Sun, 04 Nov 2018 17:48:23: #2 Build Peak Model... INFO @ Sun, 04 Nov 2018 17:48:23: #1 tags after filtering in treatment: 1070483 INFO @ Sun, 04 Nov 2018 17:48:23: #1 Redundant rate of treatment: 0.00 INFO @ Sun, 04 Nov 2018 17:48:23: #1 finished! INFO @ Sun, 04 Nov 2018 17:48:23: #2 Build Peak Model... INFO @ Sun, 04 Nov 2018 17:48:23: #2 looking for paired plus/minus strand peaks... INFO @ Sun, 04 Nov 2018 17:48:23: #2 looking for paired plus/minus strand peaks... INFO @ Sun, 04 Nov 2018 17:48:23: #2 looking for paired plus/minus strand peaks... INFO @ Sun, 04 Nov 2018 17:48:24: #2 number of paired peaks: 1534 INFO @ Sun, 04 Nov 2018 17:48:24: start model_add_line... INFO @ Sun, 04 Nov 2018 17:48:24: #2 number of paired peaks: 1534 INFO @ Sun, 04 Nov 2018 17:48:24: start model_add_line... INFO @ Sun, 04 Nov 2018 17:48:24: #2 number of paired peaks: 1534 INFO @ Sun, 04 Nov 2018 17:48:24: start model_add_line... INFO @ Sun, 04 Nov 2018 17:48:24: start X-correlation... INFO @ Sun, 04 Nov 2018 17:48:24: start X-correlation... INFO @ Sun, 04 Nov 2018 17:48:24: start X-correlation... INFO @ Sun, 04 Nov 2018 17:48:24: end of X-cor INFO @ Sun, 04 Nov 2018 17:48:24: end of X-cor INFO @ Sun, 04 Nov 2018 17:48:24: end of X-cor INFO @ Sun, 04 Nov 2018 17:48:24: #2 finished! INFO @ Sun, 04 Nov 2018 17:48:24: #2 finished! INFO @ Sun, 04 Nov 2018 17:48:24: #2 finished! INFO @ Sun, 04 Nov 2018 17:48:24: #2 predicted fragment length is 55 bps INFO @ Sun, 04 Nov 2018 17:48:24: #2 predicted fragment length is 55 bps INFO @ Sun, 04 Nov 2018 17:48:24: #2 predicted fragment length is 55 bps INFO @ Sun, 04 Nov 2018 17:48:24: #2 alternative fragment length(s) may be 55 bps INFO @ Sun, 04 Nov 2018 17:48:24: #2 alternative fragment length(s) may be 55 bps INFO @ Sun, 04 Nov 2018 17:48:24: #2 alternative fragment length(s) may be 55 bps INFO @ Sun, 04 Nov 2018 17:48:24: #2.2 Generate R script for model : SRX4375850.05_model.r INFO @ Sun, 04 Nov 2018 17:48:24: #2.2 Generate R script for model : SRX4375850.20_model.r INFO @ Sun, 04 Nov 2018 17:48:24: #2.2 Generate R script for model : SRX4375850.10_model.r WARNING @ Sun, 04 Nov 2018 17:48:24: #2 Since the d (55) calculated from paired-peaks are smaller than 2*tag length, it may be influenced by unknown sequencing problem! WARNING @ Sun, 04 Nov 2018 17:48:24: #2 You may need to consider one of the other alternative d(s): 55 WARNING @ Sun, 04 Nov 2018 17:48:24: #2 You can restart the process with --nomodel --extsize XXX with your choice or an arbitrary number. Nontheless, MACS will continute computing. INFO @ Sun, 04 Nov 2018 17:48:24: #3 Call peaks... WARNING @ Sun, 04 Nov 2018 17:48:24: #2 Since the d (55) calculated from paired-peaks are smaller than 2*tag length, it may be influenced by unknown sequencing problem! WARNING @ Sun, 04 Nov 2018 17:48:24: #2 You may need to consider one of the other alternative d(s): 55 WARNING @ Sun, 04 Nov 2018 17:48:24: #2 You can restart the process with --nomodel --extsize XXX with your choice or an arbitrary number. Nontheless, MACS will continute computing. INFO @ Sun, 04 Nov 2018 17:48:24: #3 Call peaks... WARNING @ Sun, 04 Nov 2018 17:48:24: #2 Since the d (55) calculated from paired-peaks are smaller than 2*tag length, it may be influenced by unknown sequencing problem! WARNING @ Sun, 04 Nov 2018 17:48:24: #2 You may need to consider one of the other alternative d(s): 55 WARNING @ Sun, 04 Nov 2018 17:48:24: #2 You can restart the process with --nomodel --extsize XXX with your choice or an arbitrary number. Nontheless, MACS will continute computing. INFO @ Sun, 04 Nov 2018 17:48:24: #3 Call peaks... INFO @ Sun, 04 Nov 2018 17:48:24: #3 Pre-compute pvalue-qvalue table... INFO @ Sun, 04 Nov 2018 17:48:24: #3 Pre-compute pvalue-qvalue table... INFO @ Sun, 04 Nov 2018 17:48:24: #3 Pre-compute pvalue-qvalue table... INFO @ Sun, 04 Nov 2018 17:48:27: #3 Call peaks for each chromosome... INFO @ Sun, 04 Nov 2018 17:48:27: #3 Call peaks for each chromosome... INFO @ Sun, 04 Nov 2018 17:48:27: #3 Call peaks for each chromosome... INFO @ Sun, 04 Nov 2018 17:48:28: #4 Write output xls file... SRX4375850.10_peaks.xls INFO @ Sun, 04 Nov 2018 17:48:28: #4 Write peak in narrowPeak format file... SRX4375850.10_peaks.narrowPeak INFO @ Sun, 04 Nov 2018 17:48:28: #4 Write summits bed file... SRX4375850.10_summits.bed INFO @ Sun, 04 Nov 2018 17:48:28: Done! INFO @ Sun, 04 Nov 2018 17:48:28: #4 Write output xls file... SRX4375850.20_peaks.xls INFO @ Sun, 04 Nov 2018 17:48:28: #4 Write peak in narrowPeak format file... SRX4375850.20_peaks.narrowPeak INFO @ Sun, 04 Nov 2018 17:48:28: #4 Write summits bed file... SRX4375850.20_summits.bed INFO @ Sun, 04 Nov 2018 17:48:28: #4 Write output xls file... SRX4375850.05_peaks.xls INFO @ Sun, 04 Nov 2018 17:48:28: Done! INFO @ Sun, 04 Nov 2018 17:48:28: #4 Write peak in narrowPeak format file... SRX4375850.05_peaks.narrowPeak INFO @ Sun, 04 Nov 2018 17:48:28: #4 Write summits bed file... SRX4375850.05_summits.bed INFO @ Sun, 04 Nov 2018 17:48:28: Done! pass1 - making usageList (12 chroms)pass1 - making usageList (9 chroms)pass1 - making usageList (6 chroms): 20 millis : 20 millis : 20 millis pass2 - checking and writing primary data (381 records, 4 fields): 86 millis pass2 - checking and writing primary data (636 records, 4 fields): 86 millis pass2 - checking and writing primary data (831 records, 4 fields): 87 millis CompletedMACS2peakCalling CompletedMACS2peakCalling CompletedMACS2peakCalling BedGraph に変換しました。 BigWig に変換中... BigWig に変換しました。