Job ID = 10937609 sra ファイルのダウンロード中... Completed: 87690K bytes transferred in 6 seconds (118978K 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 2619012 spots for /home/okishinya/chipatlas/results/sacCer3/SRX3463279/SRR6367818.sra Written 2619012 spots for /home/okishinya/chipatlas/results/sacCer3/SRX3463279/SRR6367818.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: 00:00:24 2619012 reads; of these: 2619012 (100.00%) were unpaired; of these: 249189 (9.51%) aligned 0 times 2167085 (82.74%) aligned exactly 1 time 202738 (7.74%) aligned >1 times 90.49% overall alignment rate Time searching: 00:00:24 Overall time: 00:00:24 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] 533276 / 2369823 = 0.2250 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, 10 Aug 2018 02:41:33: # Command line: callpeak -t SRX3463279.bam -f BAM -g 12100000 -n SRX3463279.05 -q 1e-05 # ARGUMENTS LIST: # name = SRX3463279.05 # format = BAM # ChIP-seq file = ['SRX3463279.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, 10 Aug 2018 02:41:33: #1 read tag files... INFO @ Fri, 10 Aug 2018 02:41:33: #1 read treatment tags... INFO @ Fri, 10 Aug 2018 02:41:33: # Command line: callpeak -t SRX3463279.bam -f BAM -g 12100000 -n SRX3463279.20 -q 1e-20 # ARGUMENTS LIST: # name = SRX3463279.20 # format = BAM # ChIP-seq file = ['SRX3463279.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, 10 Aug 2018 02:41:33: #1 read tag files... INFO @ Fri, 10 Aug 2018 02:41:33: #1 read treatment tags... INFO @ Fri, 10 Aug 2018 02:41:33: # Command line: callpeak -t SRX3463279.bam -f BAM -g 12100000 -n SRX3463279.10 -q 1e-10 # ARGUMENTS LIST: # name = SRX3463279.10 # format = BAM # ChIP-seq file = ['SRX3463279.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, 10 Aug 2018 02:41:33: #1 read tag files... INFO @ Fri, 10 Aug 2018 02:41:33: #1 read treatment tags... INFO @ Fri, 10 Aug 2018 02:41:39: 1000000 INFO @ Fri, 10 Aug 2018 02:41:39: 1000000 INFO @ Fri, 10 Aug 2018 02:41:39: 1000000 INFO @ Fri, 10 Aug 2018 02:41:44: #1 tag size is determined as 45 bps INFO @ Fri, 10 Aug 2018 02:41:44: #1 tag size = 45 INFO @ Fri, 10 Aug 2018 02:41:44: #1 total tags in treatment: 1836547 INFO @ Fri, 10 Aug 2018 02:41:44: #1 user defined the maximum tags... INFO @ Fri, 10 Aug 2018 02:41:44: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Fri, 10 Aug 2018 02:41:44: #1 tags after filtering in treatment: 1836547 INFO @ Fri, 10 Aug 2018 02:41:44: #1 Redundant rate of treatment: 0.00 INFO @ Fri, 10 Aug 2018 02:41:44: #1 finished! INFO @ Fri, 10 Aug 2018 02:41:44: #2 Build Peak Model... INFO @ Fri, 10 Aug 2018 02:41:44: #2 looking for paired plus/minus strand peaks... INFO @ Fri, 10 Aug 2018 02:41:44: #2 number of paired peaks: 213 WARNING @ Fri, 10 Aug 2018 02:41:44: Fewer paired peaks (213) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 213 pairs to build model! INFO @ Fri, 10 Aug 2018 02:41:44: start model_add_line... INFO @ Fri, 10 Aug 2018 02:41:44: start X-correlation... INFO @ Fri, 10 Aug 2018 02:41:44: end of X-cor INFO @ Fri, 10 Aug 2018 02:41:44: #2 finished! INFO @ Fri, 10 Aug 2018 02:41:44: #2 predicted fragment length is 128 bps INFO @ Fri, 10 Aug 2018 02:41:44: #2 alternative fragment length(s) may be 128 bps INFO @ Fri, 10 Aug 2018 02:41:44: #2.2 Generate R script for model : SRX3463279.10_model.r INFO @ Fri, 10 Aug 2018 02:41:44: #3 Call peaks... INFO @ Fri, 10 Aug 2018 02:41:44: #3 Pre-compute pvalue-qvalue table... INFO @ Fri, 10 Aug 2018 02:41:44: #1 tag size is determined as 45 bps INFO @ Fri, 10 Aug 2018 02:41:44: #1 tag size = 45 INFO @ Fri, 10 Aug 2018 02:41:44: #1 total tags in treatment: 1836547 INFO @ Fri, 10 Aug 2018 02:41:44: #1 user defined the maximum tags... INFO @ Fri, 10 Aug 2018 02:41:44: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Fri, 10 Aug 2018 02:41:44: #1 tags after filtering in treatment: 1836547 INFO @ Fri, 10 Aug 2018 02:41:44: #1 Redundant rate of treatment: 0.00 INFO @ Fri, 10 Aug 2018 02:41:44: #1 finished! INFO @ Fri, 10 Aug 2018 02:41:44: #2 Build Peak Model... INFO @ Fri, 10 Aug 2018 02:41:44: #2 looking for paired plus/minus strand peaks... INFO @ Fri, 10 Aug 2018 02:41:45: #2 number of paired peaks: 213 WARNING @ Fri, 10 Aug 2018 02:41:45: Fewer paired peaks (213) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 213 pairs to build model! INFO @ Fri, 10 Aug 2018 02:41:45: start model_add_line... INFO @ Fri, 10 Aug 2018 02:41:45: start X-correlation... INFO @ Fri, 10 Aug 2018 02:41:45: end of X-cor INFO @ Fri, 10 Aug 2018 02:41:45: #2 finished! INFO @ Fri, 10 Aug 2018 02:41:45: #2 predicted fragment length is 128 bps INFO @ Fri, 10 Aug 2018 02:41:45: #2 alternative fragment length(s) may be 128 bps INFO @ Fri, 10 Aug 2018 02:41:45: #2.2 Generate R script for model : SRX3463279.20_model.r INFO @ Fri, 10 Aug 2018 02:41:45: #3 Call peaks... INFO @ Fri, 10 Aug 2018 02:41:45: #3 Pre-compute pvalue-qvalue table... INFO @ Fri, 10 Aug 2018 02:41:45: #1 tag size is determined as 45 bps INFO @ Fri, 10 Aug 2018 02:41:45: #1 tag size = 45 INFO @ Fri, 10 Aug 2018 02:41:45: #1 total tags in treatment: 1836547 INFO @ Fri, 10 Aug 2018 02:41:45: #1 user defined the maximum tags... INFO @ Fri, 10 Aug 2018 02:41:45: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Fri, 10 Aug 2018 02:41:45: #1 tags after filtering in treatment: 1836547 INFO @ Fri, 10 Aug 2018 02:41:45: #1 Redundant rate of treatment: 0.00 INFO @ Fri, 10 Aug 2018 02:41:45: #1 finished! INFO @ Fri, 10 Aug 2018 02:41:45: #2 Build Peak Model... INFO @ Fri, 10 Aug 2018 02:41:45: #2 looking for paired plus/minus strand peaks... INFO @ Fri, 10 Aug 2018 02:41:45: #2 number of paired peaks: 213 WARNING @ Fri, 10 Aug 2018 02:41:45: Fewer paired peaks (213) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 213 pairs to build model! INFO @ Fri, 10 Aug 2018 02:41:45: start model_add_line... INFO @ Fri, 10 Aug 2018 02:41:45: start X-correlation... INFO @ Fri, 10 Aug 2018 02:41:45: end of X-cor INFO @ Fri, 10 Aug 2018 02:41:45: #2 finished! INFO @ Fri, 10 Aug 2018 02:41:45: #2 predicted fragment length is 128 bps INFO @ Fri, 10 Aug 2018 02:41:45: #2 alternative fragment length(s) may be 128 bps INFO @ Fri, 10 Aug 2018 02:41:45: #2.2 Generate R script for model : SRX3463279.05_model.r INFO @ Fri, 10 Aug 2018 02:41:45: #3 Call peaks... INFO @ Fri, 10 Aug 2018 02:41:45: #3 Pre-compute pvalue-qvalue table... INFO @ Fri, 10 Aug 2018 02:41:49: #3 Call peaks for each chromosome... INFO @ Fri, 10 Aug 2018 02:41:50: #3 Call peaks for each chromosome... INFO @ Fri, 10 Aug 2018 02:41:50: #3 Call peaks for each chromosome... INFO @ Fri, 10 Aug 2018 02:41:51: #4 Write output xls file... SRX3463279.10_peaks.xls INFO @ Fri, 10 Aug 2018 02:41:51: #4 Write peak in narrowPeak format file... SRX3463279.10_peaks.narrowPeak INFO @ Fri, 10 Aug 2018 02:41:51: #4 Write summits bed file... SRX3463279.10_summits.bed INFO @ Fri, 10 Aug 2018 02:41:51: Done! pass1 - making usageList (16 chroms): 0 millis pass2 - checking and writing primary data (1241 records, 4 fields): 4 millis CompletedMACS2peakCalling INFO @ Fri, 10 Aug 2018 02:41:52: #4 Write output xls file... SRX3463279.20_peaks.xls INFO @ Fri, 10 Aug 2018 02:41:52: #4 Write peak in narrowPeak format file... SRX3463279.20_peaks.narrowPeak INFO @ Fri, 10 Aug 2018 02:41:52: #4 Write summits bed file... SRX3463279.20_summits.bed INFO @ Fri, 10 Aug 2018 02:41:52: Done! pass1 - making usageList (16 chroms): 1 millis pass2 - checking and writing primary data (617 records, 4 fields): 3 millis CompletedMACS2peakCalling INFO @ Fri, 10 Aug 2018 02:41:52: #4 Write output xls file... SRX3463279.05_peaks.xls INFO @ Fri, 10 Aug 2018 02:41:53: #4 Write peak in narrowPeak format file... SRX3463279.05_peaks.narrowPeak INFO @ Fri, 10 Aug 2018 02:41:53: #4 Write summits bed file... SRX3463279.05_summits.bed INFO @ Fri, 10 Aug 2018 02:41:53: Done! pass1 - making usageList (16 chroms): 1 millis pass2 - checking and writing primary data (2120 records, 4 fields): 5 millis CompletedMACS2peakCalling BedGraph に変換しました。 BigWig に変換中... BigWig に変換しました。