Job ID = 11633941 sra ファイルのダウンロード中... Completed: 183956K bytes transferred in 4 seconds (318238K 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 4948781 spots for /home/okishinya/chipatlas/results/sacCer3/ERX1424528/ERR1353053.sra Written 4948781 spots for /home/okishinya/chipatlas/results/sacCer3/ERX1424528/ERR1353053.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: 00:00:56 4948781 reads; of these: 4948781 (100.00%) were unpaired; of these: 532610 (10.76%) aligned 0 times 3581549 (72.37%) aligned exactly 1 time 834622 (16.87%) aligned >1 times 89.24% overall alignment rate Time searching: 00:00:56 Overall time: 00:00:56 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] 1828297 / 4416171 = 0.4140 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 09:20:53: # Command line: callpeak -t ERX1424528.bam -f BAM -g 12100000 -n ERX1424528.05 -q 1e-05 # ARGUMENTS LIST: # name = ERX1424528.05 # format = BAM # ChIP-seq file = ['ERX1424528.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 09:20:53: #1 read tag files... INFO @ Fri, 15 Feb 2019 09:20:53: #1 read treatment tags... INFO @ Fri, 15 Feb 2019 09:20:53: # Command line: callpeak -t ERX1424528.bam -f BAM -g 12100000 -n ERX1424528.20 -q 1e-20 # ARGUMENTS LIST: # name = ERX1424528.20 # format = BAM # ChIP-seq file = ['ERX1424528.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 09:20:53: #1 read tag files... INFO @ Fri, 15 Feb 2019 09:20:53: #1 read treatment tags... INFO @ Fri, 15 Feb 2019 09:20:53: # Command line: callpeak -t ERX1424528.bam -f BAM -g 12100000 -n ERX1424528.10 -q 1e-10 # ARGUMENTS LIST: # name = ERX1424528.10 # format = BAM # ChIP-seq file = ['ERX1424528.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 09:20:53: #1 read tag files... INFO @ Fri, 15 Feb 2019 09:20:53: #1 read treatment tags... INFO @ Fri, 15 Feb 2019 09:20:59: 1000000 INFO @ Fri, 15 Feb 2019 09:20:59: 1000000 INFO @ Fri, 15 Feb 2019 09:21:00: 1000000 INFO @ Fri, 15 Feb 2019 09:21:05: 2000000 INFO @ Fri, 15 Feb 2019 09:21:06: 2000000 INFO @ Fri, 15 Feb 2019 09:21:07: 2000000 INFO @ Fri, 15 Feb 2019 09:21:09: #1 tag size is determined as 51 bps INFO @ Fri, 15 Feb 2019 09:21:09: #1 tag size = 51 INFO @ Fri, 15 Feb 2019 09:21:09: #1 total tags in treatment: 2587874 INFO @ Fri, 15 Feb 2019 09:21:09: #1 user defined the maximum tags... INFO @ Fri, 15 Feb 2019 09:21:09: #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 09:21:09: #1 tags after filtering in treatment: 2587874 INFO @ Fri, 15 Feb 2019 09:21:09: #1 Redundant rate of treatment: 0.00 INFO @ Fri, 15 Feb 2019 09:21:09: #1 finished! INFO @ Fri, 15 Feb 2019 09:21:09: #2 Build Peak Model... INFO @ Fri, 15 Feb 2019 09:21:09: #2 looking for paired plus/minus strand peaks... INFO @ Fri, 15 Feb 2019 09:21:10: #2 number of paired peaks: 247 WARNING @ Fri, 15 Feb 2019 09:21:10: Fewer paired peaks (247) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 247 pairs to build model! INFO @ Fri, 15 Feb 2019 09:21:10: start model_add_line... INFO @ Fri, 15 Feb 2019 09:21:10: start X-correlation... INFO @ Fri, 15 Feb 2019 09:21:10: end of X-cor INFO @ Fri, 15 Feb 2019 09:21:10: #2 finished! INFO @ Fri, 15 Feb 2019 09:21:10: #2 predicted fragment length is 164 bps INFO @ Fri, 15 Feb 2019 09:21:10: #2 alternative fragment length(s) may be 164 bps INFO @ Fri, 15 Feb 2019 09:21:10: #2.2 Generate R script for model : ERX1424528.20_model.r INFO @ Fri, 15 Feb 2019 09:21:10: #3 Call peaks... INFO @ Fri, 15 Feb 2019 09:21:10: #3 Pre-compute pvalue-qvalue table... INFO @ Fri, 15 Feb 2019 09:21:10: #1 tag size is determined as 51 bps INFO @ Fri, 15 Feb 2019 09:21:10: #1 tag size = 51 INFO @ Fri, 15 Feb 2019 09:21:10: #1 total tags in treatment: 2587874 INFO @ Fri, 15 Feb 2019 09:21:10: #1 user defined the maximum tags... INFO @ Fri, 15 Feb 2019 09:21:10: #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 09:21:10: #1 tags after filtering in treatment: 2587874 INFO @ Fri, 15 Feb 2019 09:21:10: #1 Redundant rate of treatment: 0.00 INFO @ Fri, 15 Feb 2019 09:21:10: #1 finished! INFO @ Fri, 15 Feb 2019 09:21:10: #2 Build Peak Model... INFO @ Fri, 15 Feb 2019 09:21:10: #2 looking for paired plus/minus strand peaks... INFO @ Fri, 15 Feb 2019 09:21:10: #2 number of paired peaks: 247 WARNING @ Fri, 15 Feb 2019 09:21:10: Fewer paired peaks (247) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 247 pairs to build model! INFO @ Fri, 15 Feb 2019 09:21:10: start model_add_line... INFO @ Fri, 15 Feb 2019 09:21:10: start X-correlation... INFO @ Fri, 15 Feb 2019 09:21:10: end of X-cor INFO @ Fri, 15 Feb 2019 09:21:10: #2 finished! INFO @ Fri, 15 Feb 2019 09:21:10: #2 predicted fragment length is 164 bps INFO @ Fri, 15 Feb 2019 09:21:10: #2 alternative fragment length(s) may be 164 bps INFO @ Fri, 15 Feb 2019 09:21:10: #2.2 Generate R script for model : ERX1424528.05_model.r INFO @ Fri, 15 Feb 2019 09:21:10: #3 Call peaks... INFO @ Fri, 15 Feb 2019 09:21:10: #3 Pre-compute pvalue-qvalue table... INFO @ Fri, 15 Feb 2019 09:21:11: #1 tag size is determined as 51 bps INFO @ Fri, 15 Feb 2019 09:21:11: #1 tag size = 51 INFO @ Fri, 15 Feb 2019 09:21:11: #1 total tags in treatment: 2587874 INFO @ Fri, 15 Feb 2019 09:21:11: #1 user defined the maximum tags... INFO @ Fri, 15 Feb 2019 09:21:11: #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 09:21:11: #1 tags after filtering in treatment: 2587874 INFO @ Fri, 15 Feb 2019 09:21:11: #1 Redundant rate of treatment: 0.00 INFO @ Fri, 15 Feb 2019 09:21:11: #1 finished! INFO @ Fri, 15 Feb 2019 09:21:11: #2 Build Peak Model... INFO @ Fri, 15 Feb 2019 09:21:11: #2 looking for paired plus/minus strand peaks... INFO @ Fri, 15 Feb 2019 09:21:11: #2 number of paired peaks: 247 WARNING @ Fri, 15 Feb 2019 09:21:11: Fewer paired peaks (247) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 247 pairs to build model! INFO @ Fri, 15 Feb 2019 09:21:11: start model_add_line... INFO @ Fri, 15 Feb 2019 09:21:11: start X-correlation... INFO @ Fri, 15 Feb 2019 09:21:11: end of X-cor INFO @ Fri, 15 Feb 2019 09:21:11: #2 finished! INFO @ Fri, 15 Feb 2019 09:21:11: #2 predicted fragment length is 164 bps INFO @ Fri, 15 Feb 2019 09:21:11: #2 alternative fragment length(s) may be 164 bps INFO @ Fri, 15 Feb 2019 09:21:11: #2.2 Generate R script for model : ERX1424528.10_model.r INFO @ Fri, 15 Feb 2019 09:21:11: #3 Call peaks... INFO @ Fri, 15 Feb 2019 09:21:11: #3 Pre-compute pvalue-qvalue table... INFO @ Fri, 15 Feb 2019 09:21:20: #3 Call peaks for each chromosome... INFO @ Fri, 15 Feb 2019 09:21:21: #3 Call peaks for each chromosome... INFO @ Fri, 15 Feb 2019 09:21:22: #3 Call peaks for each chromosome... INFO @ Fri, 15 Feb 2019 09:21:23: #4 Write output xls file... ERX1424528.20_peaks.xls INFO @ Fri, 15 Feb 2019 09:21:23: #4 Write peak in narrowPeak format file... ERX1424528.20_peaks.narrowPeak INFO @ Fri, 15 Feb 2019 09:21:23: #4 Write summits bed file... ERX1424528.20_summits.bed INFO @ Fri, 15 Feb 2019 09:21:23: Done! pass1 - making usageList (16 chroms): 2 millis pass2 - checking and writing primary data (1855 records, 4 fields): 4 millis CompletedMACS2peakCalling INFO @ Fri, 15 Feb 2019 09:21:24: #4 Write output xls file... ERX1424528.05_peaks.xls INFO @ Fri, 15 Feb 2019 09:21:24: #4 Write peak in narrowPeak format file... ERX1424528.05_peaks.narrowPeak INFO @ Fri, 15 Feb 2019 09:21:24: #4 Write summits bed file... ERX1424528.05_summits.bed INFO @ Fri, 15 Feb 2019 09:21:24: Done! pass1 - making usageList (16 chroms): 3 millis pass2 - checking and writing primary data (4118 records, 4 fields): 7 millis CompletedMACS2peakCalling INFO @ Fri, 15 Feb 2019 09:21:25: #4 Write output xls file... ERX1424528.10_peaks.xls INFO @ Fri, 15 Feb 2019 09:21:25: #4 Write peak in narrowPeak format file... ERX1424528.10_peaks.narrowPeak INFO @ Fri, 15 Feb 2019 09:21:25: #4 Write summits bed file... ERX1424528.10_summits.bed INFO @ Fri, 15 Feb 2019 09:21:25: Done! pass1 - making usageList (16 chroms): 3 millis pass2 - checking and writing primary data (3118 records, 4 fields): 6 millis CompletedMACS2peakCalling BedGraph に変換しました。 BigWig に変換中... BigWig に変換しました。