Job ID = 11171323 sra ファイルのダウンロード中... Completed: 207826K bytes transferred in 5 seconds (327369K 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 5248049 spots for /home/okishinya/chipatlas/results/dm3/SRX3511952/SRR6418937.sra Written 5248049 spots for /home/okishinya/chipatlas/results/dm3/SRX3511952/SRR6418937.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: 00:03:10 5248049 reads; of these: 5248049 (100.00%) were unpaired; of these: 494499 (9.42%) aligned 0 times 3524290 (67.15%) aligned exactly 1 time 1229260 (23.42%) aligned >1 times 90.58% overall alignment rate Time searching: 00:03:10 Overall time: 00:03:10 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] 443479 / 4753550 = 0.0933 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 @ Sat, 08 Sep 2018 13:47:16: # Command line: callpeak -t SRX3511952.bam -f BAM -g dm -n SRX3511952.20 -q 1e-20 # ARGUMENTS LIST: # name = SRX3511952.20 # format = BAM # ChIP-seq file = ['SRX3511952.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 @ Sat, 08 Sep 2018 13:47:16: #1 read tag files... INFO @ Sat, 08 Sep 2018 13:47:16: #1 read treatment tags... INFO @ Sat, 08 Sep 2018 13:47:16: # Command line: callpeak -t SRX3511952.bam -f BAM -g dm -n SRX3511952.05 -q 1e-05 # ARGUMENTS LIST: # name = SRX3511952.05 # format = BAM # ChIP-seq file = ['SRX3511952.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 @ Sat, 08 Sep 2018 13:47:16: #1 read tag files... INFO @ Sat, 08 Sep 2018 13:47:16: #1 read treatment tags... INFO @ Sat, 08 Sep 2018 13:47:16: # Command line: callpeak -t SRX3511952.bam -f BAM -g dm -n SRX3511952.10 -q 1e-10 # ARGUMENTS LIST: # name = SRX3511952.10 # format = BAM # ChIP-seq file = ['SRX3511952.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 @ Sat, 08 Sep 2018 13:47:16: #1 read tag files... INFO @ Sat, 08 Sep 2018 13:47:16: #1 read treatment tags... INFO @ Sat, 08 Sep 2018 13:47:24: 1000000 INFO @ Sat, 08 Sep 2018 13:47:24: 1000000 INFO @ Sat, 08 Sep 2018 13:47:24: 1000000 INFO @ Sat, 08 Sep 2018 13:47:31: 2000000 INFO @ Sat, 08 Sep 2018 13:47:32: 2000000 INFO @ Sat, 08 Sep 2018 13:47:32: 2000000 INFO @ Sat, 08 Sep 2018 13:47:39: 3000000 INFO @ Sat, 08 Sep 2018 13:47:40: 3000000 INFO @ Sat, 08 Sep 2018 13:47:40: 3000000 INFO @ Sat, 08 Sep 2018 13:47:46: 4000000 INFO @ Sat, 08 Sep 2018 13:47:48: 4000000 INFO @ Sat, 08 Sep 2018 13:47:48: 4000000 INFO @ Sat, 08 Sep 2018 13:47:49: #1 tag size is determined as 98 bps INFO @ Sat, 08 Sep 2018 13:47:49: #1 tag size = 98 INFO @ Sat, 08 Sep 2018 13:47:49: #1 total tags in treatment: 4310071 INFO @ Sat, 08 Sep 2018 13:47:49: #1 user defined the maximum tags... INFO @ Sat, 08 Sep 2018 13:47:49: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Sat, 08 Sep 2018 13:47:49: #1 tags after filtering in treatment: 4310071 INFO @ Sat, 08 Sep 2018 13:47:49: #1 Redundant rate of treatment: 0.00 INFO @ Sat, 08 Sep 2018 13:47:49: #1 finished! INFO @ Sat, 08 Sep 2018 13:47:49: #2 Build Peak Model... INFO @ Sat, 08 Sep 2018 13:47:49: #2 looking for paired plus/minus strand peaks... INFO @ Sat, 08 Sep 2018 13:47:49: #2 number of paired peaks: 611 WARNING @ Sat, 08 Sep 2018 13:47:49: Fewer paired peaks (611) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 611 pairs to build model! INFO @ Sat, 08 Sep 2018 13:47:49: start model_add_line... INFO @ Sat, 08 Sep 2018 13:47:49: start X-correlation... INFO @ Sat, 08 Sep 2018 13:47:49: end of X-cor INFO @ Sat, 08 Sep 2018 13:47:49: #2 finished! INFO @ Sat, 08 Sep 2018 13:47:49: #2 predicted fragment length is 144 bps INFO @ Sat, 08 Sep 2018 13:47:49: #2 alternative fragment length(s) may be 1,144,226,590 bps INFO @ Sat, 08 Sep 2018 13:47:49: #2.2 Generate R script for model : SRX3511952.10_model.r WARNING @ Sat, 08 Sep 2018 13:47:49: #2 Since the d (144) calculated from paired-peaks are smaller than 2*tag length, it may be influenced by unknown sequencing problem! WARNING @ Sat, 08 Sep 2018 13:47:49: #2 You may need to consider one of the other alternative d(s): 1,144,226,590 WARNING @ Sat, 08 Sep 2018 13:47:49: #2 You can restart the process with --nomodel --extsize XXX with your choice or an arbitrary number. Nontheless, MACS will continute computing. INFO @ Sat, 08 Sep 2018 13:47:49: #3 Call peaks... INFO @ Sat, 08 Sep 2018 13:47:49: #3 Pre-compute pvalue-qvalue table... INFO @ Sat, 08 Sep 2018 13:47:50: #1 tag size is determined as 98 bps INFO @ Sat, 08 Sep 2018 13:47:50: #1 tag size = 98 INFO @ Sat, 08 Sep 2018 13:47:50: #1 total tags in treatment: 4310071 INFO @ Sat, 08 Sep 2018 13:47:50: #1 user defined the maximum tags... INFO @ Sat, 08 Sep 2018 13:47:50: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Sat, 08 Sep 2018 13:47:50: #1 tag size is determined as 98 bps INFO @ Sat, 08 Sep 2018 13:47:50: #1 tag size = 98 INFO @ Sat, 08 Sep 2018 13:47:50: #1 total tags in treatment: 4310071 INFO @ Sat, 08 Sep 2018 13:47:50: #1 user defined the maximum tags... INFO @ Sat, 08 Sep 2018 13:47:50: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Sat, 08 Sep 2018 13:47:50: #1 tags after filtering in treatment: 4310071 INFO @ Sat, 08 Sep 2018 13:47:50: #1 Redundant rate of treatment: 0.00 INFO @ Sat, 08 Sep 2018 13:47:50: #1 tags after filtering in treatment: 4310071 INFO @ Sat, 08 Sep 2018 13:47:50: #1 finished! INFO @ Sat, 08 Sep 2018 13:47:50: #2 Build Peak Model... INFO @ Sat, 08 Sep 2018 13:47:50: #1 Redundant rate of treatment: 0.00 INFO @ Sat, 08 Sep 2018 13:47:50: #1 finished! INFO @ Sat, 08 Sep 2018 13:47:50: #2 looking for paired plus/minus strand peaks... INFO @ Sat, 08 Sep 2018 13:47:50: #2 Build Peak Model... INFO @ Sat, 08 Sep 2018 13:47:50: #2 looking for paired plus/minus strand peaks... INFO @ Sat, 08 Sep 2018 13:47:50: #2 number of paired peaks: 611 WARNING @ Sat, 08 Sep 2018 13:47:50: Fewer paired peaks (611) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 611 pairs to build model! INFO @ Sat, 08 Sep 2018 13:47:50: start model_add_line... INFO @ Sat, 08 Sep 2018 13:47:50: #2 number of paired peaks: 611 WARNING @ Sat, 08 Sep 2018 13:47:50: Fewer paired peaks (611) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 611 pairs to build model! INFO @ Sat, 08 Sep 2018 13:47:50: start model_add_line... INFO @ Sat, 08 Sep 2018 13:47:51: start X-correlation... INFO @ Sat, 08 Sep 2018 13:47:51: end of X-cor INFO @ Sat, 08 Sep 2018 13:47:51: #2 finished! INFO @ Sat, 08 Sep 2018 13:47:51: #2 predicted fragment length is 144 bps INFO @ Sat, 08 Sep 2018 13:47:51: #2 alternative fragment length(s) may be 1,144,226,590 bps INFO @ Sat, 08 Sep 2018 13:47:51: #2.2 Generate R script for model : SRX3511952.05_model.r INFO @ Sat, 08 Sep 2018 13:47:51: start X-correlation... INFO @ Sat, 08 Sep 2018 13:47:51: end of X-cor INFO @ Sat, 08 Sep 2018 13:47:51: #2 finished! INFO @ Sat, 08 Sep 2018 13:47:51: #2 predicted fragment length is 144 bps INFO @ Sat, 08 Sep 2018 13:47:51: #2 alternative fragment length(s) may be 1,144,226,590 bps INFO @ Sat, 08 Sep 2018 13:47:51: #2.2 Generate R script for model : SRX3511952.20_model.r WARNING @ Sat, 08 Sep 2018 13:47:51: #2 Since the d (144) calculated from paired-peaks are smaller than 2*tag length, it may be influenced by unknown sequencing problem! WARNING @ Sat, 08 Sep 2018 13:47:51: #2 You may need to consider one of the other alternative d(s): 1,144,226,590 WARNING @ Sat, 08 Sep 2018 13:47:51: #2 You can restart the process with --nomodel --extsize XXX with your choice or an arbitrary number. Nontheless, MACS will continute computing. INFO @ Sat, 08 Sep 2018 13:47:51: #3 Call peaks... INFO @ Sat, 08 Sep 2018 13:47:51: #3 Pre-compute pvalue-qvalue table... WARNING @ Sat, 08 Sep 2018 13:47:51: #2 Since the d (144) calculated from paired-peaks are smaller than 2*tag length, it may be influenced by unknown sequencing problem! WARNING @ Sat, 08 Sep 2018 13:47:51: #2 You may need to consider one of the other alternative d(s): 1,144,226,590 WARNING @ Sat, 08 Sep 2018 13:47:51: #2 You can restart the process with --nomodel --extsize XXX with your choice or an arbitrary number. Nontheless, MACS will continute computing. INFO @ Sat, 08 Sep 2018 13:47:51: #3 Call peaks... INFO @ Sat, 08 Sep 2018 13:47:51: #3 Pre-compute pvalue-qvalue table... INFO @ Sat, 08 Sep 2018 13:48:01: #3 Call peaks for each chromosome... INFO @ Sat, 08 Sep 2018 13:48:01: #3 Call peaks for each chromosome... INFO @ Sat, 08 Sep 2018 13:48:01: #3 Call peaks for each chromosome... INFO @ Sat, 08 Sep 2018 13:48:07: #4 Write output xls file... SRX3511952.10_peaks.xls INFO @ Sat, 08 Sep 2018 13:48:07: #4 Write peak in narrowPeak format file... SRX3511952.10_peaks.narrowPeak INFO @ Sat, 08 Sep 2018 13:48:07: #4 Write summits bed file... SRX3511952.10_summits.bed INFO @ Sat, 08 Sep 2018 13:48:07: Done! INFO @ Sat, 08 Sep 2018 13:48:07: #4 Write output xls file... SRX3511952.05_peaks.xls INFO @ Sat, 08 Sep 2018 13:48:07: #4 Write output xls file... SRX3511952.20_peaks.xls INFO @ Sat, 08 Sep 2018 13:48:07: #4 Write peak in narrowPeak format file... SRX3511952.05_peaks.narrowPeak INFO @ Sat, 08 Sep 2018 13:48:07: #4 Write peak in narrowPeak format file... SRX3511952.20_peaks.narrowPeak INFO @ Sat, 08 Sep 2018 13:48:07: #4 Write summits bed file... SRX3511952.05_summits.bed INFO @ Sat, 08 Sep 2018 13:48:07: #4 Write summits bed file... SRX3511952.20_summits.bed INFO @ Sat, 08 Sep 2018 13:48:08: Done! INFO @ Sat, 08 Sep 2018 13:48:08: Done! pass1 - making usageList (3 chroms): 0 millis pass2 - checking and writing primary data (62 records, 4 fields): 2 millis CompletedMACS2peakCalling pass1 - making usageList (3 chroms): 0 millis pass1 - making usageList (12 chroms): 0 millis pass2 - checking and writing primary data (23 records, 4 fields): 2 millis pass2 - checking and writing primary data (196 records, 4 fields): 2 millis CompletedMACS2peakCalling CompletedMACS2peakCalling BedGraph に変換しました。 BigWig に変換中... BigWig に変換しました。