Job ID = 2589146 sra ファイルのダウンロード中... Read layout: SINGLE fastq に変換中... spots read : 2,864,459 reads read : 2,864,459 reads written : 2,864,459 spots read : 3,379,553 reads read : 3,379,553 reads written : 3,379,553 spots read : 1,231,928 reads read : 1,231,928 reads written : 1,231,928 rm: cannot remove ‘/home/okishinya/ncbi/public/sra/SRR107345.sra.cache’: No such file or directory rm: cannot remove ‘/home/okishinya/ncbi/public/sra/SRR107346.sra.cache’: No such file or directory rm: cannot remove ‘/home/okishinya/ncbi/public/sra/SRR107347.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: 00:00:44 7475940 reads; of these: 7475940 (100.00%) were unpaired; of these: 6665344 (89.16%) aligned 0 times 709323 (9.49%) aligned exactly 1 time 101273 (1.35%) aligned >1 times 10.84% overall alignment rate Time searching: 00:00:44 Overall time: 00:00:44 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] 21182 / 810596 = 0.0261 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 17:02:48: # Command line: callpeak -t /home/okishinya/chipatlas/results/ce10/SRX043875/SRX043875.bam -f BAM -g ce -n /home/okishinya/chipatlas/results/ce10/SRX043875/SRX043875.05 -q 1e-05 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/ce10/SRX043875/SRX043875.05 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/ce10/SRX043875/SRX043875.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 17:02:48: #1 read tag files... INFO @ Mon, 12 Aug 2019 17:02:48: #1 read treatment tags... INFO @ Mon, 12 Aug 2019 17:02:49: # Command line: callpeak -t /home/okishinya/chipatlas/results/ce10/SRX043875/SRX043875.bam -f BAM -g ce -n /home/okishinya/chipatlas/results/ce10/SRX043875/SRX043875.10 -q 1e-10 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/ce10/SRX043875/SRX043875.10 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/ce10/SRX043875/SRX043875.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 17:02:49: #1 read tag files... INFO @ Mon, 12 Aug 2019 17:02:49: #1 read treatment tags... INFO @ Mon, 12 Aug 2019 17:02:50: # Command line: callpeak -t /home/okishinya/chipatlas/results/ce10/SRX043875/SRX043875.bam -f BAM -g ce -n /home/okishinya/chipatlas/results/ce10/SRX043875/SRX043875.20 -q 1e-20 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/ce10/SRX043875/SRX043875.20 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/ce10/SRX043875/SRX043875.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 17:02:50: #1 read tag files... INFO @ Mon, 12 Aug 2019 17:02:50: #1 read treatment tags... INFO @ Mon, 12 Aug 2019 17:02:54: #1 tag size is determined as 34 bps INFO @ Mon, 12 Aug 2019 17:02:54: #1 tag size = 34 INFO @ Mon, 12 Aug 2019 17:02:54: #1 total tags in treatment: 789414 INFO @ Mon, 12 Aug 2019 17:02:54: #1 user defined the maximum tags... INFO @ Mon, 12 Aug 2019 17:02:54: #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 17:02:54: #1 tags after filtering in treatment: 789414 INFO @ Mon, 12 Aug 2019 17:02:54: #1 Redundant rate of treatment: 0.00 INFO @ Mon, 12 Aug 2019 17:02:54: #1 finished! INFO @ Mon, 12 Aug 2019 17:02:54: #2 Build Peak Model... INFO @ Mon, 12 Aug 2019 17:02:54: #2 looking for paired plus/minus strand peaks... INFO @ Mon, 12 Aug 2019 17:02:54: #2 number of paired peaks: 275 WARNING @ Mon, 12 Aug 2019 17:02:54: Fewer paired peaks (275) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 275 pairs to build model! INFO @ Mon, 12 Aug 2019 17:02:54: start model_add_line... INFO @ Mon, 12 Aug 2019 17:02:54: start X-correlation... INFO @ Mon, 12 Aug 2019 17:02:54: end of X-cor INFO @ Mon, 12 Aug 2019 17:02:54: #2 finished! INFO @ Mon, 12 Aug 2019 17:02:54: #2 predicted fragment length is 39 bps INFO @ Mon, 12 Aug 2019 17:02:54: #2 alternative fragment length(s) may be 39,86,110,117,419,459,491,565 bps INFO @ Mon, 12 Aug 2019 17:02:54: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/ce10/SRX043875/SRX043875.05_model.r WARNING @ Mon, 12 Aug 2019 17:02:54: #2 Since the d (39) calculated from paired-peaks are smaller than 2*tag length, it may be influenced by unknown sequencing problem! WARNING @ Mon, 12 Aug 2019 17:02:54: #2 You may need to consider one of the other alternative d(s): 39,86,110,117,419,459,491,565 WARNING @ Mon, 12 Aug 2019 17:02:54: #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 17:02:54: #3 Call peaks... INFO @ Mon, 12 Aug 2019 17:02:54: #3 Pre-compute pvalue-qvalue table... INFO @ Mon, 12 Aug 2019 17:02:55: #1 tag size is determined as 34 bps INFO @ Mon, 12 Aug 2019 17:02:55: #1 tag size = 34 INFO @ Mon, 12 Aug 2019 17:02:55: #1 total tags in treatment: 789414 INFO @ Mon, 12 Aug 2019 17:02:55: #1 user defined the maximum tags... INFO @ Mon, 12 Aug 2019 17:02:55: #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 17:02:55: #1 tags after filtering in treatment: 789414 INFO @ Mon, 12 Aug 2019 17:02:55: #1 Redundant rate of treatment: 0.00 INFO @ Mon, 12 Aug 2019 17:02:55: #1 finished! INFO @ Mon, 12 Aug 2019 17:02:55: #2 Build Peak Model... INFO @ Mon, 12 Aug 2019 17:02:55: #2 looking for paired plus/minus strand peaks... INFO @ Mon, 12 Aug 2019 17:02:55: #2 number of paired peaks: 275 WARNING @ Mon, 12 Aug 2019 17:02:55: Fewer paired peaks (275) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 275 pairs to build model! INFO @ Mon, 12 Aug 2019 17:02:55: start model_add_line... INFO @ Mon, 12 Aug 2019 17:02:55: start X-correlation... INFO @ Mon, 12 Aug 2019 17:02:55: end of X-cor INFO @ Mon, 12 Aug 2019 17:02:55: #2 finished! INFO @ Mon, 12 Aug 2019 17:02:55: #2 predicted fragment length is 39 bps INFO @ Mon, 12 Aug 2019 17:02:55: #2 alternative fragment length(s) may be 39,86,110,117,419,459,491,565 bps INFO @ Mon, 12 Aug 2019 17:02:55: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/ce10/SRX043875/SRX043875.10_model.r WARNING @ Mon, 12 Aug 2019 17:02:55: #2 Since the d (39) calculated from paired-peaks are smaller than 2*tag length, it may be influenced by unknown sequencing problem! WARNING @ Mon, 12 Aug 2019 17:02:55: #2 You may need to consider one of the other alternative d(s): 39,86,110,117,419,459,491,565 WARNING @ Mon, 12 Aug 2019 17:02:55: #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 17:02:55: #3 Call peaks... INFO @ Mon, 12 Aug 2019 17:02:55: #3 Pre-compute pvalue-qvalue table... INFO @ Mon, 12 Aug 2019 17:02:57: #3 Call peaks for each chromosome... INFO @ Mon, 12 Aug 2019 17:02:57: #1 tag size is determined as 34 bps INFO @ Mon, 12 Aug 2019 17:02:57: #1 tag size = 34 INFO @ Mon, 12 Aug 2019 17:02:57: #1 total tags in treatment: 789414 INFO @ Mon, 12 Aug 2019 17:02:57: #1 user defined the maximum tags... INFO @ Mon, 12 Aug 2019 17:02:57: #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 17:02:57: #1 tags after filtering in treatment: 789414 INFO @ Mon, 12 Aug 2019 17:02:57: #1 Redundant rate of treatment: 0.00 INFO @ Mon, 12 Aug 2019 17:02:57: #1 finished! INFO @ Mon, 12 Aug 2019 17:02:57: #2 Build Peak Model... INFO @ Mon, 12 Aug 2019 17:02:57: #2 looking for paired plus/minus strand peaks... INFO @ Mon, 12 Aug 2019 17:02:57: #2 number of paired peaks: 275 WARNING @ Mon, 12 Aug 2019 17:02:57: Fewer paired peaks (275) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 275 pairs to build model! INFO @ Mon, 12 Aug 2019 17:02:57: start model_add_line... INFO @ Mon, 12 Aug 2019 17:02:57: start X-correlation... INFO @ Mon, 12 Aug 2019 17:02:57: end of X-cor INFO @ Mon, 12 Aug 2019 17:02:57: #2 finished! INFO @ Mon, 12 Aug 2019 17:02:57: #2 predicted fragment length is 39 bps INFO @ Mon, 12 Aug 2019 17:02:57: #2 alternative fragment length(s) may be 39,86,110,117,419,459,491,565 bps INFO @ Mon, 12 Aug 2019 17:02:57: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/ce10/SRX043875/SRX043875.20_model.r WARNING @ Mon, 12 Aug 2019 17:02:57: #2 Since the d (39) calculated from paired-peaks are smaller than 2*tag length, it may be influenced by unknown sequencing problem! WARNING @ Mon, 12 Aug 2019 17:02:57: #2 You may need to consider one of the other alternative d(s): 39,86,110,117,419,459,491,565 WARNING @ Mon, 12 Aug 2019 17:02:57: #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 17:02:57: #3 Call peaks... INFO @ Mon, 12 Aug 2019 17:02:57: #3 Pre-compute pvalue-qvalue table... INFO @ Mon, 12 Aug 2019 17:02:58: #3 Call peaks for each chromosome... INFO @ Mon, 12 Aug 2019 17:02:58: #4 Write output xls file... /home/okishinya/chipatlas/results/ce10/SRX043875/SRX043875.05_peaks.xls INFO @ Mon, 12 Aug 2019 17:02:58: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/ce10/SRX043875/SRX043875.05_peaks.narrowPeak INFO @ Mon, 12 Aug 2019 17:02:58: #4 Write summits bed file... /home/okishinya/chipatlas/results/ce10/SRX043875/SRX043875.05_summits.bed INFO @ Mon, 12 Aug 2019 17:02:58: Done! pass1 - making usageList (6 chroms): 1 millis pass2 - checking and writing primary data (49 records, 4 fields): 2 millis CompletedMACS2peakCalling INFO @ Mon, 12 Aug 2019 17:02:59: #4 Write output xls file... /home/okishinya/chipatlas/results/ce10/SRX043875/SRX043875.10_peaks.xls INFO @ Mon, 12 Aug 2019 17:02:59: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/ce10/SRX043875/SRX043875.10_peaks.narrowPeak INFO @ Mon, 12 Aug 2019 17:02:59: #4 Write summits bed file... /home/okishinya/chipatlas/results/ce10/SRX043875/SRX043875.10_summits.bed INFO @ Mon, 12 Aug 2019 17:02:59: Done! pass1 - making usageList (6 chroms): 1 millis pass2 - checking and writing primary data (17 records, 4 fields): 2 millis CompletedMACS2peakCalling INFO @ Mon, 12 Aug 2019 17:03:00: #3 Call peaks for each chromosome... BedGraph に変換しました。 BigWig に変換中... INFO @ Mon, 12 Aug 2019 17:03:01: #4 Write output xls file... /home/okishinya/chipatlas/results/ce10/SRX043875/SRX043875.20_peaks.xls INFO @ Mon, 12 Aug 2019 17:03:01: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/ce10/SRX043875/SRX043875.20_peaks.narrowPeak INFO @ Mon, 12 Aug 2019 17:03:01: #4 Write summits bed file... /home/okishinya/chipatlas/results/ce10/SRX043875/SRX043875.20_summits.bed INFO @ Mon, 12 Aug 2019 17:03:01: Done! pass1 - making usageList (4 chroms): 1 millis pass2 - checking and writing primary data (5 records, 4 fields): 1 millis CompletedMACS2peakCalling BigWig に変換しました。