Job ID = 9037688 sra ファイルのダウンロード中... Completed: 242336K bytes transferred in 5 seconds (349322K bits/sec), in 1 file, 2 directories. % Total % Received % Xferd Average Speed Time Time Time Current Dload Upload Total Spent Left Speed 0 0 0 0 0 0 0 0 --:--:-- 0:00:06 --:--:-- 0 0 0 0 0 0 0 0 0 --:--:-- 0:00:07 --:--:-- 0 100 13455 0 13455 0 0 1678 0 --:--:-- 0:00:08 --:--:-- 8120 100 40382 0 40382 0 0 4480 0 --:--:-- 0:00:09 --:--:-- 15221 100 46651 0 46651 0 0 4992 0 --:--:-- 0:00:09 --:--:-- 15628 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 11131442 spots for /home/okishinya/chipatlas/results/sacCer3/SRX977479/SRR1951325.sra Written 11131442 spots total 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: 00:01:23 11131442 reads; of these: 11131442 (100.00%) were unpaired; of these: 2293338 (20.60%) aligned 0 times 7805529 (70.12%) aligned exactly 1 time 1032575 (9.28%) aligned >1 times 79.40% overall alignment rate Time searching: 00:01:23 Overall time: 00:01:23 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] 8283353 / 8838104 = 0.9372 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 Jun 2017 05:12:18: # Command line: callpeak -t SRX977479.bam -f BAM -g 12100000 -n SRX977479.05 -q 1e-05 # ARGUMENTS LIST: # name = SRX977479.05 # format = BAM # ChIP-seq file = ['SRX977479.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 INFO @ Sun, 04 Jun 2017 05:12:18: #1 read tag files... INFO @ Sun, 04 Jun 2017 05:12:18: #1 read treatment tags... INFO @ Sun, 04 Jun 2017 05:12:18: # Command line: callpeak -t SRX977479.bam -f BAM -g 12100000 -n SRX977479.20 -q 1e-20 # ARGUMENTS LIST: # name = SRX977479.20 # format = BAM # ChIP-seq file = ['SRX977479.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 INFO @ Sun, 04 Jun 2017 05:12:18: #1 read tag files... INFO @ Sun, 04 Jun 2017 05:12:18: #1 read treatment tags... INFO @ Sun, 04 Jun 2017 05:12:18: # Command line: callpeak -t SRX977479.bam -f BAM -g 12100000 -n SRX977479.10 -q 1e-10 # ARGUMENTS LIST: # name = SRX977479.10 # format = BAM # ChIP-seq file = ['SRX977479.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 INFO @ Sun, 04 Jun 2017 05:12:18: #1 read tag files... INFO @ Sun, 04 Jun 2017 05:12:18: #1 read treatment tags... INFO @ Sun, 04 Jun 2017 05:12:21: #1 tag size is determined as 40 bps INFO @ Sun, 04 Jun 2017 05:12:21: #1 tag size = 40 INFO @ Sun, 04 Jun 2017 05:12:21: #1 total tags in treatment: 554751 INFO @ Sun, 04 Jun 2017 05:12:21: #1 user defined the maximum tags... INFO @ Sun, 04 Jun 2017 05:12:21: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Sun, 04 Jun 2017 05:12:21: #1 tag size is determined as 40 bps INFO @ Sun, 04 Jun 2017 05:12:21: #1 tag size = 40 INFO @ Sun, 04 Jun 2017 05:12:21: #1 total tags in treatment: 554751 INFO @ Sun, 04 Jun 2017 05:12:21: #1 user defined the maximum tags... INFO @ Sun, 04 Jun 2017 05:12:21: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Sun, 04 Jun 2017 05:12:21: #1 tag size is determined as 40 bps INFO @ Sun, 04 Jun 2017 05:12:21: #1 tag size = 40 INFO @ Sun, 04 Jun 2017 05:12:21: #1 total tags in treatment: 554751 INFO @ Sun, 04 Jun 2017 05:12:21: #1 user defined the maximum tags... INFO @ Sun, 04 Jun 2017 05:12:21: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Sun, 04 Jun 2017 05:12:21: #1 tags after filtering in treatment: 553839 INFO @ Sun, 04 Jun 2017 05:12:21: #1 Redundant rate of treatment: 0.00 INFO @ Sun, 04 Jun 2017 05:12:21: #1 finished! INFO @ Sun, 04 Jun 2017 05:12:21: #2 Build Peak Model... INFO @ Sun, 04 Jun 2017 05:12:21: #1 tags after filtering in treatment: 553839 INFO @ Sun, 04 Jun 2017 05:12:21: #1 Redundant rate of treatment: 0.00 INFO @ Sun, 04 Jun 2017 05:12:21: #1 finished! INFO @ Sun, 04 Jun 2017 05:12:21: #2 Build Peak Model... INFO @ Sun, 04 Jun 2017 05:12:21: #1 tags after filtering in treatment: 553839 INFO @ Sun, 04 Jun 2017 05:12:21: #1 Redundant rate of treatment: 0.00 INFO @ Sun, 04 Jun 2017 05:12:21: #1 finished! INFO @ Sun, 04 Jun 2017 05:12:21: #2 Build Peak Model... INFO @ Sun, 04 Jun 2017 05:12:21: #2 number of paired peaks: 441 WARNING @ Sun, 04 Jun 2017 05:12:21: Fewer paired peaks (441) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 441 pairs to build model! INFO @ Sun, 04 Jun 2017 05:12:21: start model_add_line... INFO @ Sun, 04 Jun 2017 05:12:22: #2 number of paired peaks: 441 WARNING @ Sun, 04 Jun 2017 05:12:22: Fewer paired peaks (441) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 441 pairs to build model! INFO @ Sun, 04 Jun 2017 05:12:22: start model_add_line... INFO @ Sun, 04 Jun 2017 05:12:22: #2 number of paired peaks: 441 WARNING @ Sun, 04 Jun 2017 05:12:22: Fewer paired peaks (441) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 441 pairs to build model! INFO @ Sun, 04 Jun 2017 05:12:22: start model_add_line... INFO @ Sun, 04 Jun 2017 05:12:23: start X-correlation... INFO @ Sun, 04 Jun 2017 05:12:23: end of X-cor INFO @ Sun, 04 Jun 2017 05:12:23: #2 finished! INFO @ Sun, 04 Jun 2017 05:12:23: #2 predicted fragment length is 48 bps INFO @ Sun, 04 Jun 2017 05:12:23: #2 alternative fragment length(s) may be 48 bps INFO @ Sun, 04 Jun 2017 05:12:23: #2.2 Generate R script for model : SRX977479.20_model.r WARNING @ Sun, 04 Jun 2017 05:12:23: #2 Since the d (48) calculated from paired-peaks are smaller than 2*tag length, it may be influenced by unknown sequencing problem! WARNING @ Sun, 04 Jun 2017 05:12:23: #2 You may need to consider one of the other alternative d(s): 48 WARNING @ Sun, 04 Jun 2017 05:12:23: #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 Jun 2017 05:12:23: #3 Call peaks... INFO @ Sun, 04 Jun 2017 05:12:23: #3 Pre-compute pvalue-qvalue table... INFO @ Sun, 04 Jun 2017 05:12:24: start X-correlation... INFO @ Sun, 04 Jun 2017 05:12:24: end of X-cor INFO @ Sun, 04 Jun 2017 05:12:24: #2 finished! INFO @ Sun, 04 Jun 2017 05:12:24: #2 predicted fragment length is 48 bps INFO @ Sun, 04 Jun 2017 05:12:24: #2 alternative fragment length(s) may be 48 bps INFO @ Sun, 04 Jun 2017 05:12:24: #2.2 Generate R script for model : SRX977479.10_model.r WARNING @ Sun, 04 Jun 2017 05:12:24: #2 Since the d (48) calculated from paired-peaks are smaller than 2*tag length, it may be influenced by unknown sequencing problem! WARNING @ Sun, 04 Jun 2017 05:12:24: #2 You may need to consider one of the other alternative d(s): 48 WARNING @ Sun, 04 Jun 2017 05:12:24: #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 Jun 2017 05:12:24: #3 Call peaks... INFO @ Sun, 04 Jun 2017 05:12:24: #3 Pre-compute pvalue-qvalue table... INFO @ Sun, 04 Jun 2017 05:12:24: start X-correlation... INFO @ Sun, 04 Jun 2017 05:12:24: end of X-cor INFO @ Sun, 04 Jun 2017 05:12:24: #2 finished! INFO @ Sun, 04 Jun 2017 05:12:24: #2 predicted fragment length is 48 bps INFO @ Sun, 04 Jun 2017 05:12:24: #2 alternative fragment length(s) may be 48 bps INFO @ Sun, 04 Jun 2017 05:12:24: #2.2 Generate R script for model : SRX977479.05_model.r WARNING @ Sun, 04 Jun 2017 05:12:24: #2 Since the d (48) calculated from paired-peaks are smaller than 2*tag length, it may be influenced by unknown sequencing problem! WARNING @ Sun, 04 Jun 2017 05:12:24: #2 You may need to consider one of the other alternative d(s): 48 WARNING @ Sun, 04 Jun 2017 05:12:24: #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 Jun 2017 05:12:24: #3 Call peaks... INFO @ Sun, 04 Jun 2017 05:12:24: #3 Pre-compute pvalue-qvalue table... INFO @ Sun, 04 Jun 2017 05:12:27: #3 Call peaks for each chromosome... INFO @ Sun, 04 Jun 2017 05:12:27: #3 Call peaks for each chromosome... INFO @ Sun, 04 Jun 2017 05:12:27: #3 Call peaks for each chromosome... INFO @ Sun, 04 Jun 2017 05:12:29: #4 Write output xls file... SRX977479.20_peaks.xls INFO @ Sun, 04 Jun 2017 05:12:29: #4 Write peak in narrowPeak format file... SRX977479.20_peaks.narrowPeak INFO @ Sun, 04 Jun 2017 05:12:29: #4 Write summits bed file... SRX977479.20_summits.bed INFO @ Sun, 04 Jun 2017 05:12:29: Done! pass1 - making usageList (16 chroms): 0 millis pass2 - checking and writing primary data (210 records, 4 fields): 2 millis CompletedMACS2peakCalling INFO @ Sun, 04 Jun 2017 05:12:29: #4 Write output xls file... SRX977479.10_peaks.xls INFO @ Sun, 04 Jun 2017 05:12:29: #4 Write peak in narrowPeak format file... SRX977479.10_peaks.narrowPeak INFO @ Sun, 04 Jun 2017 05:12:29: #4 Write summits bed file... SRX977479.10_summits.bed INFO @ Sun, 04 Jun 2017 05:12:29: Done! pass1 - making usageList (16 chroms): 0 millis pass2 - checking and writing primary data (479 records, 4 fields): 3 millis CompletedMACS2peakCalling INFO @ Sun, 04 Jun 2017 05:12:29: #4 Write output xls file... SRX977479.05_peaks.xls INFO @ Sun, 04 Jun 2017 05:12:29: #4 Write peak in narrowPeak format file... SRX977479.05_peaks.narrowPeak INFO @ Sun, 04 Jun 2017 05:12:29: #4 Write summits bed file... SRX977479.05_summits.bed INFO @ Sun, 04 Jun 2017 05:12:29: Done! pass1 - making usageList (16 chroms): 0 millis pass2 - checking and writing primary data (983 records, 4 fields): 3 millis CompletedMACS2peakCalling BedGraph に変換しました。 BigWig に変換中... BigWig に変換しました。