Job ID = 14170469 SRX = SRX8689035 Genome = dm3 sra ファイルのダウンロード中... Read layout: SINGLE fastq に変換中... Read 4301773 spots for SRR12174389/SRR12174389.sra Written 4301773 spots for SRR12174389/SRR12174389.sra fastq に変換しました。 bowtie でマッピング中... Your job 14170866 ("srTdm6") has been submitted Time loading reference: 00:00:00 Time loading forward index: 00:00:00 Time loading mirror index: 00:00:00 Multiseed full-index search: 00:01:41 4301773 reads; of these: 4301773 (100.00%) were unpaired; of these: 212580 (4.94%) aligned 0 times 2417378 (56.19%) aligned exactly 1 time 1671815 (38.86%) aligned >1 times 95.06% overall alignment rate Time searching: 00:01:41 Overall time: 00:01:41 マッピングが完了しました。 samtools でBAM に変換中... [samopen] SAM header is present: 15 sequences. [bam_rmdupse_core] 220116 / 4089193 = 0.0538 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/3.8.3/var/singularity/mnt/session/etc/resolv.conf [files]: /etc/resolv.conf doesn't exist in container INFO @ Sat, 11 Dec 2021 06:54:06: # Command line: callpeak -t /home/okishinya/chipatlas/results/dm3/SRX8689035/SRX8689035.bam -f BAM -g dm -n /home/okishinya/chipatlas/results/dm3/SRX8689035/SRX8689035.05 -q 1e-05 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/dm3/SRX8689035/SRX8689035.05 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/dm3/SRX8689035/SRX8689035.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 @ Sat, 11 Dec 2021 06:54:06: #1 read tag files... INFO @ Sat, 11 Dec 2021 06:54:06: #1 read treatment tags... INFO @ Sat, 11 Dec 2021 06:54:11: 1000000 INFO @ Sat, 11 Dec 2021 06:54:16: 2000000 INFO @ Sat, 11 Dec 2021 06:54:21: 3000000 INFO @ Sat, 11 Dec 2021 06:54:25: #1 tag size is determined as 50 bps INFO @ Sat, 11 Dec 2021 06:54:25: #1 tag size = 50 INFO @ Sat, 11 Dec 2021 06:54:25: #1 total tags in treatment: 3869077 INFO @ Sat, 11 Dec 2021 06:54:25: #1 user defined the maximum tags... INFO @ Sat, 11 Dec 2021 06:54:25: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Sat, 11 Dec 2021 06:54:25: #1 tags after filtering in treatment: 3869077 INFO @ Sat, 11 Dec 2021 06:54:25: #1 Redundant rate of treatment: 0.00 INFO @ Sat, 11 Dec 2021 06:54:25: #1 finished! INFO @ Sat, 11 Dec 2021 06:54:25: #2 Build Peak Model... INFO @ Sat, 11 Dec 2021 06:54:25: #2 looking for paired plus/minus strand peaks... INFO @ Sat, 11 Dec 2021 06:54:25: #2 number of paired peaks: 813 WARNING @ Sat, 11 Dec 2021 06:54:25: Fewer paired peaks (813) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 813 pairs to build model! INFO @ Sat, 11 Dec 2021 06:54:25: start model_add_line... INFO @ Sat, 11 Dec 2021 06:54:25: start X-correlation... INFO @ Sat, 11 Dec 2021 06:54:25: end of X-cor INFO @ Sat, 11 Dec 2021 06:54:25: #2 finished! INFO @ Sat, 11 Dec 2021 06:54:25: #2 predicted fragment length is 50 bps INFO @ Sat, 11 Dec 2021 06:54:25: #2 alternative fragment length(s) may be 50 bps INFO @ Sat, 11 Dec 2021 06:54:25: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/dm3/SRX8689035/SRX8689035.05_model.r WARNING @ Sat, 11 Dec 2021 06:54:25: #2 Since the d (50) calculated from paired-peaks are smaller than 2*tag length, it may be influenced by unknown sequencing problem! WARNING @ Sat, 11 Dec 2021 06:54:25: #2 You may need to consider one of the other alternative d(s): 50 WARNING @ Sat, 11 Dec 2021 06:54:25: #2 You can restart the process with --nomodel --extsize XXX with your choice or an arbitrary number. Nontheless, MACS will continute computing. INFO @ Sat, 11 Dec 2021 06:54:25: #3 Call peaks... INFO @ Sat, 11 Dec 2021 06:54:25: #3 Pre-compute pvalue-qvalue table... INFO @ Sat, 11 Dec 2021 06:54:33: #3 Call peaks for each chromosome... WARNING: Skipping mount /opt/pkg/singularity/3.8.3/var/singularity/mnt/session/etc/resolv.conf [files]: /etc/resolv.conf doesn't exist in container INFO @ Sat, 11 Dec 2021 06:54:36: # Command line: callpeak -t /home/okishinya/chipatlas/results/dm3/SRX8689035/SRX8689035.bam -f BAM -g dm -n /home/okishinya/chipatlas/results/dm3/SRX8689035/SRX8689035.10 -q 1e-10 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/dm3/SRX8689035/SRX8689035.10 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/dm3/SRX8689035/SRX8689035.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 @ Sat, 11 Dec 2021 06:54:36: #1 read tag files... INFO @ Sat, 11 Dec 2021 06:54:36: #1 read treatment tags... INFO @ Sat, 11 Dec 2021 06:54:38: #4 Write output xls file... /home/okishinya/chipatlas/results/dm3/SRX8689035/SRX8689035.05_peaks.xls INFO @ Sat, 11 Dec 2021 06:54:38: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/dm3/SRX8689035/SRX8689035.05_peaks.narrowPeak INFO @ Sat, 11 Dec 2021 06:54:38: #4 Write summits bed file... /home/okishinya/chipatlas/results/dm3/SRX8689035/SRX8689035.05_summits.bed INFO @ Sat, 11 Dec 2021 06:54:38: Done! pass1 - making usageList (11 chroms): 0 millis pass2 - checking and writing primary data (1395 records, 4 fields): 4 millis CompletedMACS2peakCalling INFO @ Sat, 11 Dec 2021 06:54:41: 1000000 INFO @ Sat, 11 Dec 2021 06:54:45: 2000000 INFO @ Sat, 11 Dec 2021 06:54:50: 3000000 INFO @ Sat, 11 Dec 2021 06:54:54: #1 tag size is determined as 50 bps INFO @ Sat, 11 Dec 2021 06:54:54: #1 tag size = 50 INFO @ Sat, 11 Dec 2021 06:54:54: #1 total tags in treatment: 3869077 INFO @ Sat, 11 Dec 2021 06:54:54: #1 user defined the maximum tags... INFO @ Sat, 11 Dec 2021 06:54:54: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Sat, 11 Dec 2021 06:54:54: #1 tags after filtering in treatment: 3869077 INFO @ Sat, 11 Dec 2021 06:54:54: #1 Redundant rate of treatment: 0.00 INFO @ Sat, 11 Dec 2021 06:54:54: #1 finished! INFO @ Sat, 11 Dec 2021 06:54:54: #2 Build Peak Model... INFO @ Sat, 11 Dec 2021 06:54:54: #2 looking for paired plus/minus strand peaks... INFO @ Sat, 11 Dec 2021 06:54:55: #2 number of paired peaks: 813 WARNING @ Sat, 11 Dec 2021 06:54:55: Fewer paired peaks (813) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 813 pairs to build model! INFO @ Sat, 11 Dec 2021 06:54:55: start model_add_line... INFO @ Sat, 11 Dec 2021 06:54:55: start X-correlation... INFO @ Sat, 11 Dec 2021 06:54:55: end of X-cor INFO @ Sat, 11 Dec 2021 06:54:55: #2 finished! INFO @ Sat, 11 Dec 2021 06:54:55: #2 predicted fragment length is 50 bps INFO @ Sat, 11 Dec 2021 06:54:55: #2 alternative fragment length(s) may be 50 bps INFO @ Sat, 11 Dec 2021 06:54:55: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/dm3/SRX8689035/SRX8689035.10_model.r WARNING @ Sat, 11 Dec 2021 06:54:55: #2 Since the d (50) calculated from paired-peaks are smaller than 2*tag length, it may be influenced by unknown sequencing problem! WARNING @ Sat, 11 Dec 2021 06:54:55: #2 You may need to consider one of the other alternative d(s): 50 WARNING @ Sat, 11 Dec 2021 06:54:55: #2 You can restart the process with --nomodel --extsize XXX with your choice or an arbitrary number. Nontheless, MACS will continute computing. INFO @ Sat, 11 Dec 2021 06:54:55: #3 Call peaks... INFO @ Sat, 11 Dec 2021 06:54:55: #3 Pre-compute pvalue-qvalue table... INFO @ Sat, 11 Dec 2021 06:55:03: #3 Call peaks for each chromosome... BedGraph に変換中... WARNING: Skipping mount /opt/pkg/singularity/3.8.3/var/singularity/mnt/session/etc/resolv.conf [files]: /etc/resolv.conf doesn't exist in container INFO @ Sat, 11 Dec 2021 06:55:06: # Command line: callpeak -t /home/okishinya/chipatlas/results/dm3/SRX8689035/SRX8689035.bam -f BAM -g dm -n /home/okishinya/chipatlas/results/dm3/SRX8689035/SRX8689035.20 -q 1e-20 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/dm3/SRX8689035/SRX8689035.20 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/dm3/SRX8689035/SRX8689035.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 @ Sat, 11 Dec 2021 06:55:06: #1 read tag files... INFO @ Sat, 11 Dec 2021 06:55:06: #1 read treatment tags... INFO @ Sat, 11 Dec 2021 06:55:07: #4 Write output xls file... /home/okishinya/chipatlas/results/dm3/SRX8689035/SRX8689035.10_peaks.xls INFO @ Sat, 11 Dec 2021 06:55:07: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/dm3/SRX8689035/SRX8689035.10_peaks.narrowPeak INFO @ Sat, 11 Dec 2021 06:55:07: #4 Write summits bed file... /home/okishinya/chipatlas/results/dm3/SRX8689035/SRX8689035.10_summits.bed INFO @ Sat, 11 Dec 2021 06:55:07: Done! pass1 - making usageList (8 chroms): 0 millis pass2 - checking and writing primary data (1084 records, 4 fields): 3 millis CompletedMACS2peakCalling INFO @ Sat, 11 Dec 2021 06:55:11: 1000000 INFO @ Sat, 11 Dec 2021 06:55:16: 2000000 INFO @ Sat, 11 Dec 2021 06:55:20: 3000000 BedGraph に変換しました。 BigWig に変換中... INFO @ Sat, 11 Dec 2021 06:55:25: #1 tag size is determined as 50 bps INFO @ Sat, 11 Dec 2021 06:55:25: #1 tag size = 50 INFO @ Sat, 11 Dec 2021 06:55:25: #1 total tags in treatment: 3869077 INFO @ Sat, 11 Dec 2021 06:55:25: #1 user defined the maximum tags... INFO @ Sat, 11 Dec 2021 06:55:25: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Sat, 11 Dec 2021 06:55:25: #1 tags after filtering in treatment: 3869077 INFO @ Sat, 11 Dec 2021 06:55:25: #1 Redundant rate of treatment: 0.00 INFO @ Sat, 11 Dec 2021 06:55:25: #1 finished! INFO @ Sat, 11 Dec 2021 06:55:25: #2 Build Peak Model... INFO @ Sat, 11 Dec 2021 06:55:25: #2 looking for paired plus/minus strand peaks... INFO @ Sat, 11 Dec 2021 06:55:25: #2 number of paired peaks: 813 WARNING @ Sat, 11 Dec 2021 06:55:25: Fewer paired peaks (813) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 813 pairs to build model! INFO @ Sat, 11 Dec 2021 06:55:25: start model_add_line... INFO @ Sat, 11 Dec 2021 06:55:25: start X-correlation... INFO @ Sat, 11 Dec 2021 06:55:25: end of X-cor INFO @ Sat, 11 Dec 2021 06:55:25: #2 finished! INFO @ Sat, 11 Dec 2021 06:55:25: #2 predicted fragment length is 50 bps INFO @ Sat, 11 Dec 2021 06:55:25: #2 alternative fragment length(s) may be 50 bps INFO @ Sat, 11 Dec 2021 06:55:25: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/dm3/SRX8689035/SRX8689035.20_model.r WARNING @ Sat, 11 Dec 2021 06:55:25: #2 Since the d (50) calculated from paired-peaks are smaller than 2*tag length, it may be influenced by unknown sequencing problem! WARNING @ Sat, 11 Dec 2021 06:55:25: #2 You may need to consider one of the other alternative d(s): 50 WARNING @ Sat, 11 Dec 2021 06:55:25: #2 You can restart the process with --nomodel --extsize XXX with your choice or an arbitrary number. Nontheless, MACS will continute computing. INFO @ Sat, 11 Dec 2021 06:55:25: #3 Call peaks... INFO @ Sat, 11 Dec 2021 06:55:25: #3 Pre-compute pvalue-qvalue table... BigWig に変換しました。 INFO @ Sat, 11 Dec 2021 06:55:33: #3 Call peaks for each chromosome... INFO @ Sat, 11 Dec 2021 06:55:38: #4 Write output xls file... /home/okishinya/chipatlas/results/dm3/SRX8689035/SRX8689035.20_peaks.xls INFO @ Sat, 11 Dec 2021 06:55:38: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/dm3/SRX8689035/SRX8689035.20_peaks.narrowPeak INFO @ Sat, 11 Dec 2021 06:55:38: #4 Write summits bed file... /home/okishinya/chipatlas/results/dm3/SRX8689035/SRX8689035.20_summits.bed INFO @ Sat, 11 Dec 2021 06:55:38: Done! pass1 - making usageList (7 chroms): 1 millis pass2 - checking and writing primary data (774 records, 4 fields): 34 millis CompletedMACS2peakCalling