Job ID = 6627648 SRX = SRX8521385 Genome = dm6 sra ファイルのダウンロード中... Read layout: SINGLE fastq に変換中... 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: 00:06:57 50974137 reads; of these: 50974137 (100.00%) were unpaired; of these: 46830217 (91.87%) aligned 0 times 3038208 (5.96%) aligned exactly 1 time 1105712 (2.17%) aligned >1 times 8.13% overall alignment rate Time searching: 00:06:57 Overall time: 00:06:57 マッピングが完了しました。 samtools でBAM に変換中... [samopen] SAM header is present: 1870 sequences. [bam_rmdupse_core] 578786 / 4143920 = 0.1397 in library ' ' BAM に変換しました。 Bed ファイルを作成中... WARNING: Skipping mount /opt/pkg/singularity/3.5.2/var/singularity/mnt/session/etc/resolv.conf [files]: /etc/resolv.conf doesn't exist in container INFO @ Tue, 14 Jul 2020 12:32:50: # Command line: callpeak -t /home/okishinya/chipatlas/results/dm6/SRX8521385/SRX8521385.bam -f BAM -g dm -n /home/okishinya/chipatlas/results/dm6/SRX8521385/SRX8521385.05 -q 1e-05 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/dm6/SRX8521385/SRX8521385.05 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/dm6/SRX8521385/SRX8521385.bam'] # control file = None # effective genome size = 1.20e+08 # 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 @ Tue, 14 Jul 2020 12:32:50: #1 read tag files... INFO @ Tue, 14 Jul 2020 12:32:50: #1 read treatment tags... INFO @ Tue, 14 Jul 2020 12:32:57: 1000000 INFO @ Tue, 14 Jul 2020 12:33:03: 2000000 INFO @ Tue, 14 Jul 2020 12:33:10: 3000000 INFO @ Tue, 14 Jul 2020 12:33:14: #1 tag size is determined as 66 bps INFO @ Tue, 14 Jul 2020 12:33:14: #1 tag size = 66 INFO @ Tue, 14 Jul 2020 12:33:14: #1 total tags in treatment: 3565134 INFO @ Tue, 14 Jul 2020 12:33:14: #1 user defined the maximum tags... INFO @ Tue, 14 Jul 2020 12:33:14: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Tue, 14 Jul 2020 12:33:14: #1 tags after filtering in treatment: 3564877 INFO @ Tue, 14 Jul 2020 12:33:14: #1 Redundant rate of treatment: 0.00 INFO @ Tue, 14 Jul 2020 12:33:14: #1 finished! INFO @ Tue, 14 Jul 2020 12:33:14: #2 Build Peak Model... INFO @ Tue, 14 Jul 2020 12:33:14: #2 looking for paired plus/minus strand peaks... INFO @ Tue, 14 Jul 2020 12:33:15: #2 number of paired peaks: 854 WARNING @ Tue, 14 Jul 2020 12:33:15: Fewer paired peaks (854) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 854 pairs to build model! INFO @ Tue, 14 Jul 2020 12:33:15: start model_add_line... INFO @ Tue, 14 Jul 2020 12:33:15: start X-correlation... INFO @ Tue, 14 Jul 2020 12:33:15: end of X-cor INFO @ Tue, 14 Jul 2020 12:33:15: #2 finished! INFO @ Tue, 14 Jul 2020 12:33:15: #2 predicted fragment length is 67 bps INFO @ Tue, 14 Jul 2020 12:33:15: #2 alternative fragment length(s) may be 67 bps INFO @ Tue, 14 Jul 2020 12:33:15: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/dm6/SRX8521385/SRX8521385.05_model.r WARNING @ Tue, 14 Jul 2020 12:33:15: #2 Since the d (67) calculated from paired-peaks are smaller than 2*tag length, it may be influenced by unknown sequencing problem! WARNING @ Tue, 14 Jul 2020 12:33:15: #2 You may need to consider one of the other alternative d(s): 67 WARNING @ Tue, 14 Jul 2020 12:33:15: #2 You can restart the process with --nomodel --extsize XXX with your choice or an arbitrary number. Nontheless, MACS will continute computing. INFO @ Tue, 14 Jul 2020 12:33:15: #3 Call peaks... INFO @ Tue, 14 Jul 2020 12:33:15: #3 Pre-compute pvalue-qvalue table... WARNING: Skipping mount /opt/pkg/singularity/3.5.2/var/singularity/mnt/session/etc/resolv.conf [files]: /etc/resolv.conf doesn't exist in container INFO @ Tue, 14 Jul 2020 12:33:20: # Command line: callpeak -t /home/okishinya/chipatlas/results/dm6/SRX8521385/SRX8521385.bam -f BAM -g dm -n /home/okishinya/chipatlas/results/dm6/SRX8521385/SRX8521385.10 -q 1e-10 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/dm6/SRX8521385/SRX8521385.10 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/dm6/SRX8521385/SRX8521385.bam'] # control file = None # effective genome size = 1.20e+08 # 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 @ Tue, 14 Jul 2020 12:33:20: #1 read tag files... INFO @ Tue, 14 Jul 2020 12:33:20: #1 read treatment tags... INFO @ Tue, 14 Jul 2020 12:33:22: #3 Call peaks for each chromosome... INFO @ Tue, 14 Jul 2020 12:33:26: #4 Write output xls file... /home/okishinya/chipatlas/results/dm6/SRX8521385/SRX8521385.05_peaks.xls INFO @ Tue, 14 Jul 2020 12:33:26: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/dm6/SRX8521385/SRX8521385.05_peaks.narrowPeak INFO @ Tue, 14 Jul 2020 12:33:26: #4 Write summits bed file... /home/okishinya/chipatlas/results/dm6/SRX8521385/SRX8521385.05_summits.bed INFO @ Tue, 14 Jul 2020 12:33:26: Done! INFO @ Tue, 14 Jul 2020 12:33:27: 1000000 pass1 - making usageList (176 chroms): 0 millis pass2 - checking and writing primary data (934 records, 4 fields): 7 millis CompletedMACS2peakCalling INFO @ Tue, 14 Jul 2020 12:33:33: 2000000 INFO @ Tue, 14 Jul 2020 12:33:39: 3000000 INFO @ Tue, 14 Jul 2020 12:33:43: #1 tag size is determined as 66 bps INFO @ Tue, 14 Jul 2020 12:33:43: #1 tag size = 66 INFO @ Tue, 14 Jul 2020 12:33:43: #1 total tags in treatment: 3565134 INFO @ Tue, 14 Jul 2020 12:33:43: #1 user defined the maximum tags... INFO @ Tue, 14 Jul 2020 12:33:43: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Tue, 14 Jul 2020 12:33:43: #1 tags after filtering in treatment: 3564877 INFO @ Tue, 14 Jul 2020 12:33:43: #1 Redundant rate of treatment: 0.00 INFO @ Tue, 14 Jul 2020 12:33:43: #1 finished! INFO @ Tue, 14 Jul 2020 12:33:43: #2 Build Peak Model... INFO @ Tue, 14 Jul 2020 12:33:43: #2 looking for paired plus/minus strand peaks... INFO @ Tue, 14 Jul 2020 12:33:43: #2 number of paired peaks: 854 WARNING @ Tue, 14 Jul 2020 12:33:43: Fewer paired peaks (854) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 854 pairs to build model! INFO @ Tue, 14 Jul 2020 12:33:43: start model_add_line... INFO @ Tue, 14 Jul 2020 12:33:43: start X-correlation... INFO @ Tue, 14 Jul 2020 12:33:43: end of X-cor INFO @ Tue, 14 Jul 2020 12:33:43: #2 finished! INFO @ Tue, 14 Jul 2020 12:33:43: #2 predicted fragment length is 67 bps INFO @ Tue, 14 Jul 2020 12:33:43: #2 alternative fragment length(s) may be 67 bps INFO @ Tue, 14 Jul 2020 12:33:43: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/dm6/SRX8521385/SRX8521385.10_model.r WARNING @ Tue, 14 Jul 2020 12:33:43: #2 Since the d (67) calculated from paired-peaks are smaller than 2*tag length, it may be influenced by unknown sequencing problem! WARNING @ Tue, 14 Jul 2020 12:33:43: #2 You may need to consider one of the other alternative d(s): 67 WARNING @ Tue, 14 Jul 2020 12:33:43: #2 You can restart the process with --nomodel --extsize XXX with your choice or an arbitrary number. Nontheless, MACS will continute computing. INFO @ Tue, 14 Jul 2020 12:33:43: #3 Call peaks... INFO @ Tue, 14 Jul 2020 12:33:43: #3 Pre-compute pvalue-qvalue table... BedGraph に変換中... WARNING: Skipping mount /opt/pkg/singularity/3.5.2/var/singularity/mnt/session/etc/resolv.conf [files]: /etc/resolv.conf doesn't exist in container INFO @ Tue, 14 Jul 2020 12:33:50: # Command line: callpeak -t /home/okishinya/chipatlas/results/dm6/SRX8521385/SRX8521385.bam -f BAM -g dm -n /home/okishinya/chipatlas/results/dm6/SRX8521385/SRX8521385.20 -q 1e-20 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/dm6/SRX8521385/SRX8521385.20 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/dm6/SRX8521385/SRX8521385.bam'] # control file = None # effective genome size = 1.20e+08 # 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 @ Tue, 14 Jul 2020 12:33:50: #1 read tag files... INFO @ Tue, 14 Jul 2020 12:33:50: #1 read treatment tags... INFO @ Tue, 14 Jul 2020 12:33:51: #3 Call peaks for each chromosome... INFO @ Tue, 14 Jul 2020 12:33:55: #4 Write output xls file... /home/okishinya/chipatlas/results/dm6/SRX8521385/SRX8521385.10_peaks.xls INFO @ Tue, 14 Jul 2020 12:33:55: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/dm6/SRX8521385/SRX8521385.10_peaks.narrowPeak INFO @ Tue, 14 Jul 2020 12:33:55: #4 Write summits bed file... /home/okishinya/chipatlas/results/dm6/SRX8521385/SRX8521385.10_summits.bed INFO @ Tue, 14 Jul 2020 12:33:55: Done! pass1 - making usageList (118 chroms): 1 millis pass2 - checking and writing primary data (367 records, 4 fields): 5 millis CompletedMACS2peakCalling INFO @ Tue, 14 Jul 2020 12:33:57: 1000000 INFO @ Tue, 14 Jul 2020 12:34:02: 2000000 BedGraph に変換しました。 BigWig に変換中... INFO @ Tue, 14 Jul 2020 12:34:08: 3000000 INFO @ Tue, 14 Jul 2020 12:34:12: #1 tag size is determined as 66 bps INFO @ Tue, 14 Jul 2020 12:34:12: #1 tag size = 66 INFO @ Tue, 14 Jul 2020 12:34:12: #1 total tags in treatment: 3565134 INFO @ Tue, 14 Jul 2020 12:34:12: #1 user defined the maximum tags... INFO @ Tue, 14 Jul 2020 12:34:12: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Tue, 14 Jul 2020 12:34:12: #1 tags after filtering in treatment: 3564877 INFO @ Tue, 14 Jul 2020 12:34:12: #1 Redundant rate of treatment: 0.00 INFO @ Tue, 14 Jul 2020 12:34:12: #1 finished! INFO @ Tue, 14 Jul 2020 12:34:12: #2 Build Peak Model... INFO @ Tue, 14 Jul 2020 12:34:12: #2 looking for paired plus/minus strand peaks... INFO @ Tue, 14 Jul 2020 12:34:13: #2 number of paired peaks: 854 WARNING @ Tue, 14 Jul 2020 12:34:13: Fewer paired peaks (854) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 854 pairs to build model! INFO @ Tue, 14 Jul 2020 12:34:13: start model_add_line... INFO @ Tue, 14 Jul 2020 12:34:13: start X-correlation... INFO @ Tue, 14 Jul 2020 12:34:13: end of X-cor INFO @ Tue, 14 Jul 2020 12:34:13: #2 finished! INFO @ Tue, 14 Jul 2020 12:34:13: #2 predicted fragment length is 67 bps INFO @ Tue, 14 Jul 2020 12:34:13: #2 alternative fragment length(s) may be 67 bps INFO @ Tue, 14 Jul 2020 12:34:13: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/dm6/SRX8521385/SRX8521385.20_model.r WARNING @ Tue, 14 Jul 2020 12:34:13: #2 Since the d (67) calculated from paired-peaks are smaller than 2*tag length, it may be influenced by unknown sequencing problem! WARNING @ Tue, 14 Jul 2020 12:34:13: #2 You may need to consider one of the other alternative d(s): 67 WARNING @ Tue, 14 Jul 2020 12:34:13: #2 You can restart the process with --nomodel --extsize XXX with your choice or an arbitrary number. Nontheless, MACS will continute computing. INFO @ Tue, 14 Jul 2020 12:34:13: #3 Call peaks... INFO @ Tue, 14 Jul 2020 12:34:13: #3 Pre-compute pvalue-qvalue table... BigWig に変換しました。 INFO @ Tue, 14 Jul 2020 12:34:21: #3 Call peaks for each chromosome... INFO @ Tue, 14 Jul 2020 12:34:25: #4 Write output xls file... /home/okishinya/chipatlas/results/dm6/SRX8521385/SRX8521385.20_peaks.xls INFO @ Tue, 14 Jul 2020 12:34:25: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/dm6/SRX8521385/SRX8521385.20_peaks.narrowPeak INFO @ Tue, 14 Jul 2020 12:34:25: #4 Write summits bed file... /home/okishinya/chipatlas/results/dm6/SRX8521385/SRX8521385.20_summits.bed INFO @ Tue, 14 Jul 2020 12:34:25: Done! pass1 - making usageList (77 chroms): 0 millis pass2 - checking and writing primary data (136 records, 4 fields): 5 millis CompletedMACS2peakCalling