Job ID = 10201988 sra ファイルのダウンロード中... Completed: 361936K bytes transferred in 13 seconds (219907K 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... Written 20456193 spots for /home/okishinya/chipatlas/results/ce10/SRX2576657/SRR5272614.sra Written 20456193 spots total 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: 00:05:01 20456193 reads; of these: 20456193 (100.00%) were unpaired; of these: 1727814 (8.45%) aligned 0 times 15381009 (75.19%) aligned exactly 1 time 3347370 (16.36%) aligned >1 times 91.55% overall alignment rate Time searching: 00:05:01 Overall time: 00:05:01 マッピングが完了しました。 samtools でBAM に変換中... [samopen] SAM header is present: 7 sequences. [bam_sort_core] merging from 8 files... [bam_rmdupse_core] 13196732 / 18728379 = 0.7046 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 @ Mon, 13 Nov 2017 13:17:41: # Command line: callpeak -t SRX2576657.bam -f BAM -g ce -n SRX2576657.05 -q 1e-05 # ARGUMENTS LIST: # name = SRX2576657.05 # format = BAM # ChIP-seq file = ['SRX2576657.bam'] # control file = None # effective genome size = 9.00e+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 @ Mon, 13 Nov 2017 13:17:41: # Command line: callpeak -t SRX2576657.bam -f BAM -g ce -n SRX2576657.20 -q 1e-20 # ARGUMENTS LIST: # name = SRX2576657.20 # format = BAM # ChIP-seq file = ['SRX2576657.bam'] # control file = None # effective genome size = 9.00e+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 @ Mon, 13 Nov 2017 13:17:41: # Command line: callpeak -t SRX2576657.bam -f BAM -g ce -n SRX2576657.10 -q 1e-10 # ARGUMENTS LIST: # name = SRX2576657.10 # format = BAM # ChIP-seq file = ['SRX2576657.bam'] # control file = None # effective genome size = 9.00e+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 @ Mon, 13 Nov 2017 13:17:41: #1 read tag files... INFO @ Mon, 13 Nov 2017 13:17:41: #1 read tag files... INFO @ Mon, 13 Nov 2017 13:17:41: #1 read tag files... INFO @ Mon, 13 Nov 2017 13:17:41: #1 read treatment tags... INFO @ Mon, 13 Nov 2017 13:17:41: #1 read treatment tags... INFO @ Mon, 13 Nov 2017 13:17:41: #1 read treatment tags... INFO @ Mon, 13 Nov 2017 13:17:48: 1000000 INFO @ Mon, 13 Nov 2017 13:17:48: 1000000 INFO @ Mon, 13 Nov 2017 13:17:48: 1000000 INFO @ Mon, 13 Nov 2017 13:17:54: 2000000 INFO @ Mon, 13 Nov 2017 13:17:54: 2000000 INFO @ Mon, 13 Nov 2017 13:17:54: 2000000 INFO @ Mon, 13 Nov 2017 13:18:00: 3000000 INFO @ Mon, 13 Nov 2017 13:18:00: 3000000 INFO @ Mon, 13 Nov 2017 13:18:01: 3000000 INFO @ Mon, 13 Nov 2017 13:18:06: 4000000 INFO @ Mon, 13 Nov 2017 13:18:07: 4000000 INFO @ Mon, 13 Nov 2017 13:18:07: 4000000 INFO @ Mon, 13 Nov 2017 13:18:13: 5000000 INFO @ Mon, 13 Nov 2017 13:18:13: 5000000 INFO @ Mon, 13 Nov 2017 13:18:13: 5000000 INFO @ Mon, 13 Nov 2017 13:18:16: #1 tag size is determined as 51 bps INFO @ Mon, 13 Nov 2017 13:18:16: #1 tag size = 51 INFO @ Mon, 13 Nov 2017 13:18:16: #1 total tags in treatment: 5531647 INFO @ Mon, 13 Nov 2017 13:18:16: #1 user defined the maximum tags... INFO @ Mon, 13 Nov 2017 13:18:16: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Mon, 13 Nov 2017 13:18:16: #1 tag size is determined as 51 bps INFO @ Mon, 13 Nov 2017 13:18:16: #1 tag size = 51 INFO @ Mon, 13 Nov 2017 13:18:16: #1 total tags in treatment: 5531647 INFO @ Mon, 13 Nov 2017 13:18:16: #1 user defined the maximum tags... INFO @ Mon, 13 Nov 2017 13:18:16: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Mon, 13 Nov 2017 13:18:16: #1 tags after filtering in treatment: 5531647 INFO @ Mon, 13 Nov 2017 13:18:16: #1 Redundant rate of treatment: 0.00 INFO @ Mon, 13 Nov 2017 13:18:16: #1 finished! INFO @ Mon, 13 Nov 2017 13:18:16: #2 Build Peak Model... INFO @ Mon, 13 Nov 2017 13:18:16: #2 looking for paired plus/minus strand peaks... INFO @ Mon, 13 Nov 2017 13:18:16: #1 tags after filtering in treatment: 5531647 INFO @ Mon, 13 Nov 2017 13:18:16: #1 Redundant rate of treatment: 0.00 INFO @ Mon, 13 Nov 2017 13:18:16: #1 finished! INFO @ Mon, 13 Nov 2017 13:18:16: #2 Build Peak Model... INFO @ Mon, 13 Nov 2017 13:18:16: #2 looking for paired plus/minus strand peaks... INFO @ Mon, 13 Nov 2017 13:18:16: #2 number of paired peaks: 794 WARNING @ Mon, 13 Nov 2017 13:18:16: Fewer paired peaks (794) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 794 pairs to build model! INFO @ Mon, 13 Nov 2017 13:18:16: start model_add_line... INFO @ Mon, 13 Nov 2017 13:18:17: start X-correlation... INFO @ Mon, 13 Nov 2017 13:18:17: end of X-cor INFO @ Mon, 13 Nov 2017 13:18:17: #2 finished! INFO @ Mon, 13 Nov 2017 13:18:17: #2 predicted fragment length is 94 bps INFO @ Mon, 13 Nov 2017 13:18:17: #2 alternative fragment length(s) may be 94 bps INFO @ Mon, 13 Nov 2017 13:18:17: #2.2 Generate R script for model : SRX2576657.10_model.r WARNING @ Mon, 13 Nov 2017 13:18:17: #2 Since the d (94) calculated from paired-peaks are smaller than 2*tag length, it may be influenced by unknown sequencing problem! WARNING @ Mon, 13 Nov 2017 13:18:17: #2 You may need to consider one of the other alternative d(s): 94 WARNING @ Mon, 13 Nov 2017 13:18:17: #2 You can restart the process with --nomodel --extsize XXX with your choice or an arbitrary number. Nontheless, MACS will continute computing. INFO @ Mon, 13 Nov 2017 13:18:17: #3 Call peaks... INFO @ Mon, 13 Nov 2017 13:18:17: #3 Pre-compute pvalue-qvalue table... INFO @ Mon, 13 Nov 2017 13:18:17: #2 number of paired peaks: 794 WARNING @ Mon, 13 Nov 2017 13:18:17: Fewer paired peaks (794) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 794 pairs to build model! INFO @ Mon, 13 Nov 2017 13:18:17: start model_add_line... INFO @ Mon, 13 Nov 2017 13:18:17: start X-correlation... INFO @ Mon, 13 Nov 2017 13:18:17: end of X-cor INFO @ Mon, 13 Nov 2017 13:18:17: #2 finished! INFO @ Mon, 13 Nov 2017 13:18:17: #2 predicted fragment length is 94 bps INFO @ Mon, 13 Nov 2017 13:18:17: #2 alternative fragment length(s) may be 94 bps INFO @ Mon, 13 Nov 2017 13:18:17: #2.2 Generate R script for model : SRX2576657.05_model.r WARNING @ Mon, 13 Nov 2017 13:18:17: #2 Since the d (94) calculated from paired-peaks are smaller than 2*tag length, it may be influenced by unknown sequencing problem! WARNING @ Mon, 13 Nov 2017 13:18:17: #2 You may need to consider one of the other alternative d(s): 94 WARNING @ Mon, 13 Nov 2017 13:18:17: #2 You can restart the process with --nomodel --extsize XXX with your choice or an arbitrary number. Nontheless, MACS will continute computing. INFO @ Mon, 13 Nov 2017 13:18:17: #3 Call peaks... INFO @ Mon, 13 Nov 2017 13:18:17: #3 Pre-compute pvalue-qvalue table... INFO @ Mon, 13 Nov 2017 13:18:17: #1 tag size is determined as 51 bps INFO @ Mon, 13 Nov 2017 13:18:17: #1 tag size = 51 INFO @ Mon, 13 Nov 2017 13:18:17: #1 total tags in treatment: 5531647 INFO @ Mon, 13 Nov 2017 13:18:17: #1 user defined the maximum tags... INFO @ Mon, 13 Nov 2017 13:18:17: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Mon, 13 Nov 2017 13:18:17: #1 tags after filtering in treatment: 5531647 INFO @ Mon, 13 Nov 2017 13:18:17: #1 Redundant rate of treatment: 0.00 INFO @ Mon, 13 Nov 2017 13:18:17: #1 finished! INFO @ Mon, 13 Nov 2017 13:18:17: #2 Build Peak Model... INFO @ Mon, 13 Nov 2017 13:18:17: #2 looking for paired plus/minus strand peaks... INFO @ Mon, 13 Nov 2017 13:18:17: #2 number of paired peaks: 794 WARNING @ Mon, 13 Nov 2017 13:18:17: Fewer paired peaks (794) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 794 pairs to build model! INFO @ Mon, 13 Nov 2017 13:18:17: start model_add_line... INFO @ Mon, 13 Nov 2017 13:18:17: start X-correlation... INFO @ Mon, 13 Nov 2017 13:18:17: end of X-cor INFO @ Mon, 13 Nov 2017 13:18:17: #2 finished! INFO @ Mon, 13 Nov 2017 13:18:17: #2 predicted fragment length is 94 bps INFO @ Mon, 13 Nov 2017 13:18:17: #2 alternative fragment length(s) may be 94 bps INFO @ Mon, 13 Nov 2017 13:18:17: #2.2 Generate R script for model : SRX2576657.20_model.r WARNING @ Mon, 13 Nov 2017 13:18:17: #2 Since the d (94) calculated from paired-peaks are smaller than 2*tag length, it may be influenced by unknown sequencing problem! WARNING @ Mon, 13 Nov 2017 13:18:17: #2 You may need to consider one of the other alternative d(s): 94 WARNING @ Mon, 13 Nov 2017 13:18:17: #2 You can restart the process with --nomodel --extsize XXX with your choice or an arbitrary number. Nontheless, MACS will continute computing. INFO @ Mon, 13 Nov 2017 13:18:17: #3 Call peaks... INFO @ Mon, 13 Nov 2017 13:18:17: #3 Pre-compute pvalue-qvalue table... INFO @ Mon, 13 Nov 2017 13:18:30: #3 Call peaks for each chromosome... INFO @ Mon, 13 Nov 2017 13:18:31: #3 Call peaks for each chromosome... INFO @ Mon, 13 Nov 2017 13:18:31: #3 Call peaks for each chromosome... INFO @ Mon, 13 Nov 2017 13:18:37: #4 Write output xls file... SRX2576657.05_peaks.xls INFO @ Mon, 13 Nov 2017 13:18:37: #4 Write peak in narrowPeak format file... SRX2576657.05_peaks.narrowPeak INFO @ Mon, 13 Nov 2017 13:18:37: #4 Write summits bed file... SRX2576657.05_summits.bed INFO @ Mon, 13 Nov 2017 13:18:37: Done! pass1 - making usageList (6 chroms): 1 millis pass2 - checking and writing primary data (1438 records, 4 fields): 4 millis CompletedMACS2peakCalling INFO @ Mon, 13 Nov 2017 13:18:37: #4 Write output xls file... SRX2576657.10_peaks.xls INFO @ Mon, 13 Nov 2017 13:18:37: #4 Write peak in narrowPeak format file... SRX2576657.10_peaks.narrowPeak INFO @ Mon, 13 Nov 2017 13:18:37: #4 Write summits bed file... SRX2576657.10_summits.bed INFO @ Mon, 13 Nov 2017 13:18:37: Done! pass1 - making usageList (6 chroms): 1 millis pass2 - checking and writing primary data (982 records, 4 fields): 2 millis CompletedMACS2peakCalling INFO @ Mon, 13 Nov 2017 13:18:37: #4 Write output xls file... SRX2576657.20_peaks.xls INFO @ Mon, 13 Nov 2017 13:18:37: #4 Write peak in narrowPeak format file... SRX2576657.20_peaks.narrowPeak INFO @ Mon, 13 Nov 2017 13:18:37: #4 Write summits bed file... SRX2576657.20_summits.bed INFO @ Mon, 13 Nov 2017 13:18:37: Done! pass1 - making usageList (6 chroms): 1 millis pass2 - checking and writing primary data (567 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。