Job ID = 2589215 sra ファイルのダウンロード中... Read layout: SINGLE fastq に変換中... spots read : 12,769,350 reads read : 12,769,350 reads written : 12,769,350 spots read : 16,223,713 reads read : 16,223,713 reads written : 16,223,713 rm: cannot remove ‘/home/okishinya/ncbi/public/sra/SRR107605.sra.cache’: No such file or directory rm: cannot remove ‘/home/okishinya/ncbi/public/sra/SRR107606.sra.cache’: No such file or directory 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: 00:02:00 28993063 reads; of these: 28993063 (100.00%) were unpaired; of these: 27798444 (95.88%) aligned 0 times 1014211 (3.50%) aligned exactly 1 time 180408 (0.62%) aligned >1 times 4.12% overall alignment rate Time searching: 00:02:00 Overall time: 00:02:00 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_rmdupse_core] 34821 / 1194619 = 0.0291 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, 12 Aug 2019 17:13:28: # Command line: callpeak -t /home/okishinya/chipatlas/results/ce10/SRX044023/SRX044023.bam -f BAM -g ce -n /home/okishinya/chipatlas/results/ce10/SRX044023/SRX044023.05 -q 1e-05 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/ce10/SRX044023/SRX044023.05 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/ce10/SRX044023/SRX044023.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, 12 Aug 2019 17:13:28: #1 read tag files... INFO @ Mon, 12 Aug 2019 17:13:28: #1 read treatment tags... INFO @ Mon, 12 Aug 2019 17:13:29: # Command line: callpeak -t /home/okishinya/chipatlas/results/ce10/SRX044023/SRX044023.bam -f BAM -g ce -n /home/okishinya/chipatlas/results/ce10/SRX044023/SRX044023.10 -q 1e-10 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/ce10/SRX044023/SRX044023.10 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/ce10/SRX044023/SRX044023.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, 12 Aug 2019 17:13:29: #1 read tag files... INFO @ Mon, 12 Aug 2019 17:13:29: #1 read treatment tags... INFO @ Mon, 12 Aug 2019 17:13:30: # Command line: callpeak -t /home/okishinya/chipatlas/results/ce10/SRX044023/SRX044023.bam -f BAM -g ce -n /home/okishinya/chipatlas/results/ce10/SRX044023/SRX044023.20 -q 1e-20 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/ce10/SRX044023/SRX044023.20 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/ce10/SRX044023/SRX044023.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, 12 Aug 2019 17:13:30: #1 read tag files... INFO @ Mon, 12 Aug 2019 17:13:30: #1 read treatment tags... INFO @ Mon, 12 Aug 2019 17:13:37: 1000000 INFO @ Mon, 12 Aug 2019 17:13:38: 1000000 INFO @ Mon, 12 Aug 2019 17:13:38: #1 tag size is determined as 34 bps INFO @ Mon, 12 Aug 2019 17:13:38: #1 tag size = 34 INFO @ Mon, 12 Aug 2019 17:13:38: #1 total tags in treatment: 1159798 INFO @ Mon, 12 Aug 2019 17:13:38: #1 user defined the maximum tags... INFO @ Mon, 12 Aug 2019 17:13:38: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Mon, 12 Aug 2019 17:13:38: #1 tags after filtering in treatment: 1159798 INFO @ Mon, 12 Aug 2019 17:13:38: #1 Redundant rate of treatment: 0.00 INFO @ Mon, 12 Aug 2019 17:13:38: #1 finished! INFO @ Mon, 12 Aug 2019 17:13:38: #2 Build Peak Model... INFO @ Mon, 12 Aug 2019 17:13:38: #2 looking for paired plus/minus strand peaks... INFO @ Mon, 12 Aug 2019 17:13:38: #2 number of paired peaks: 304 WARNING @ Mon, 12 Aug 2019 17:13:38: Fewer paired peaks (304) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 304 pairs to build model! INFO @ Mon, 12 Aug 2019 17:13:38: start model_add_line... INFO @ Mon, 12 Aug 2019 17:13:38: start X-correlation... INFO @ Mon, 12 Aug 2019 17:13:38: end of X-cor INFO @ Mon, 12 Aug 2019 17:13:38: #2 finished! INFO @ Mon, 12 Aug 2019 17:13:38: #2 predicted fragment length is 35 bps INFO @ Mon, 12 Aug 2019 17:13:38: #2 alternative fragment length(s) may be 35,96,533,537,547 bps INFO @ Mon, 12 Aug 2019 17:13:38: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/ce10/SRX044023/SRX044023.05_model.r WARNING @ Mon, 12 Aug 2019 17:13:38: #2 Since the d (35) calculated from paired-peaks are smaller than 2*tag length, it may be influenced by unknown sequencing problem! WARNING @ Mon, 12 Aug 2019 17:13:38: #2 You may need to consider one of the other alternative d(s): 35,96,533,537,547 WARNING @ Mon, 12 Aug 2019 17:13:38: #2 You can restart the process with --nomodel --extsize XXX with your choice or an arbitrary number. Nontheless, MACS will continute computing. INFO @ Mon, 12 Aug 2019 17:13:38: #3 Call peaks... INFO @ Mon, 12 Aug 2019 17:13:38: #3 Pre-compute pvalue-qvalue table... INFO @ Mon, 12 Aug 2019 17:13:39: 1000000 INFO @ Mon, 12 Aug 2019 17:13:39: #1 tag size is determined as 34 bps INFO @ Mon, 12 Aug 2019 17:13:39: #1 tag size = 34 INFO @ Mon, 12 Aug 2019 17:13:39: #1 total tags in treatment: 1159798 INFO @ Mon, 12 Aug 2019 17:13:39: #1 user defined the maximum tags... INFO @ Mon, 12 Aug 2019 17:13:39: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Mon, 12 Aug 2019 17:13:39: #1 tags after filtering in treatment: 1159798 INFO @ Mon, 12 Aug 2019 17:13:39: #1 Redundant rate of treatment: 0.00 INFO @ Mon, 12 Aug 2019 17:13:39: #1 finished! INFO @ Mon, 12 Aug 2019 17:13:39: #2 Build Peak Model... INFO @ Mon, 12 Aug 2019 17:13:39: #2 looking for paired plus/minus strand peaks... INFO @ Mon, 12 Aug 2019 17:13:39: #2 number of paired peaks: 304 WARNING @ Mon, 12 Aug 2019 17:13:39: Fewer paired peaks (304) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 304 pairs to build model! INFO @ Mon, 12 Aug 2019 17:13:39: start model_add_line... INFO @ Mon, 12 Aug 2019 17:13:39: start X-correlation... INFO @ Mon, 12 Aug 2019 17:13:39: end of X-cor INFO @ Mon, 12 Aug 2019 17:13:39: #2 finished! INFO @ Mon, 12 Aug 2019 17:13:39: #2 predicted fragment length is 35 bps INFO @ Mon, 12 Aug 2019 17:13:39: #2 alternative fragment length(s) may be 35,96,533,537,547 bps INFO @ Mon, 12 Aug 2019 17:13:39: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/ce10/SRX044023/SRX044023.10_model.r WARNING @ Mon, 12 Aug 2019 17:13:39: #2 Since the d (35) calculated from paired-peaks are smaller than 2*tag length, it may be influenced by unknown sequencing problem! WARNING @ Mon, 12 Aug 2019 17:13:39: #2 You may need to consider one of the other alternative d(s): 35,96,533,537,547 WARNING @ Mon, 12 Aug 2019 17:13:39: #2 You can restart the process with --nomodel --extsize XXX with your choice or an arbitrary number. Nontheless, MACS will continute computing. INFO @ Mon, 12 Aug 2019 17:13:39: #3 Call peaks... INFO @ Mon, 12 Aug 2019 17:13:39: #3 Pre-compute pvalue-qvalue table... INFO @ Mon, 12 Aug 2019 17:13:40: #1 tag size is determined as 34 bps INFO @ Mon, 12 Aug 2019 17:13:40: #1 tag size = 34 INFO @ Mon, 12 Aug 2019 17:13:40: #1 total tags in treatment: 1159798 INFO @ Mon, 12 Aug 2019 17:13:40: #1 user defined the maximum tags... INFO @ Mon, 12 Aug 2019 17:13:40: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Mon, 12 Aug 2019 17:13:40: #1 tags after filtering in treatment: 1159798 INFO @ Mon, 12 Aug 2019 17:13:40: #1 Redundant rate of treatment: 0.00 INFO @ Mon, 12 Aug 2019 17:13:40: #1 finished! INFO @ Mon, 12 Aug 2019 17:13:40: #2 Build Peak Model... INFO @ Mon, 12 Aug 2019 17:13:40: #2 looking for paired plus/minus strand peaks... INFO @ Mon, 12 Aug 2019 17:13:40: #2 number of paired peaks: 304 WARNING @ Mon, 12 Aug 2019 17:13:40: Fewer paired peaks (304) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 304 pairs to build model! INFO @ Mon, 12 Aug 2019 17:13:40: start model_add_line... INFO @ Mon, 12 Aug 2019 17:13:40: start X-correlation... INFO @ Mon, 12 Aug 2019 17:13:40: end of X-cor INFO @ Mon, 12 Aug 2019 17:13:40: #2 finished! INFO @ Mon, 12 Aug 2019 17:13:40: #2 predicted fragment length is 35 bps INFO @ Mon, 12 Aug 2019 17:13:40: #2 alternative fragment length(s) may be 35,96,533,537,547 bps INFO @ Mon, 12 Aug 2019 17:13:40: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/ce10/SRX044023/SRX044023.20_model.r WARNING @ Mon, 12 Aug 2019 17:13:40: #2 Since the d (35) calculated from paired-peaks are smaller than 2*tag length, it may be influenced by unknown sequencing problem! WARNING @ Mon, 12 Aug 2019 17:13:40: #2 You may need to consider one of the other alternative d(s): 35,96,533,537,547 WARNING @ Mon, 12 Aug 2019 17:13:40: #2 You can restart the process with --nomodel --extsize XXX with your choice or an arbitrary number. Nontheless, MACS will continute computing. INFO @ Mon, 12 Aug 2019 17:13:40: #3 Call peaks... INFO @ Mon, 12 Aug 2019 17:13:40: #3 Pre-compute pvalue-qvalue table... INFO @ Mon, 12 Aug 2019 17:13:42: #3 Call peaks for each chromosome... INFO @ Mon, 12 Aug 2019 17:13:43: #3 Call peaks for each chromosome... INFO @ Mon, 12 Aug 2019 17:13:44: #4 Write output xls file... /home/okishinya/chipatlas/results/ce10/SRX044023/SRX044023.05_peaks.xls INFO @ Mon, 12 Aug 2019 17:13:44: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/ce10/SRX044023/SRX044023.05_peaks.narrowPeak INFO @ Mon, 12 Aug 2019 17:13:44: #4 Write summits bed file... /home/okishinya/chipatlas/results/ce10/SRX044023/SRX044023.05_summits.bed INFO @ Mon, 12 Aug 2019 17:13:44: Done! pass1 - making usageList (7 chroms): 1 millis pass2 - checking and writing primary data (100 records, 4 fields): 2 millis CompletedMACS2peakCalling INFO @ Mon, 12 Aug 2019 17:13:44: #3 Call peaks for each chromosome... INFO @ Mon, 12 Aug 2019 17:13:45: #4 Write output xls file... /home/okishinya/chipatlas/results/ce10/SRX044023/SRX044023.10_peaks.xls INFO @ Mon, 12 Aug 2019 17:13:45: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/ce10/SRX044023/SRX044023.10_peaks.narrowPeak INFO @ Mon, 12 Aug 2019 17:13:45: #4 Write summits bed file... /home/okishinya/chipatlas/results/ce10/SRX044023/SRX044023.10_summits.bed INFO @ Mon, 12 Aug 2019 17:13:45: Done! pass1 - making usageList (6 chroms): 1 millis pass2 - checking and writing primary data (36 records, 4 fields): 2 millis CompletedMACS2peakCalling INFO @ Mon, 12 Aug 2019 17:13:46: #4 Write output xls file... /home/okishinya/chipatlas/results/ce10/SRX044023/SRX044023.20_peaks.xls INFO @ Mon, 12 Aug 2019 17:13:46: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/ce10/SRX044023/SRX044023.20_peaks.narrowPeak INFO @ Mon, 12 Aug 2019 17:13:46: #4 Write summits bed file... /home/okishinya/chipatlas/results/ce10/SRX044023/SRX044023.20_summits.bed INFO @ Mon, 12 Aug 2019 17:13:46: Done! pass1 - making usageList (5 chroms): 1 millis pass2 - checking and writing primary data (6 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。