Job ID = 14170508 SRX = SRX8689067 Genome = dm3 sra ファイルのダウンロード中... Read layout: SINGLE fastq に変換中... Read 6205748 spots for SRR12174202/SRR12174202.sra Written 6205748 spots for SRR12174202/SRR12174202.sra fastq に変換しました。 bowtie でマッピング中... Your job 14170912 ("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: 00:01:47 6205748 reads; of these: 6205748 (100.00%) were unpaired; of these: 604473 (9.74%) aligned 0 times 4410149 (71.07%) aligned exactly 1 time 1191126 (19.19%) aligned >1 times 90.26% overall alignment rate Time searching: 00:01:47 Overall time: 00:01:47 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] 206834 / 5601275 = 0.0369 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 07:04:27: # Command line: callpeak -t /home/okishinya/chipatlas/results/dm3/SRX8689067/SRX8689067.bam -f BAM -g dm -n /home/okishinya/chipatlas/results/dm3/SRX8689067/SRX8689067.05 -q 1e-05 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/dm3/SRX8689067/SRX8689067.05 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/dm3/SRX8689067/SRX8689067.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 07:04:27: #1 read tag files... INFO @ Sat, 11 Dec 2021 07:04:27: #1 read treatment tags... INFO @ Sat, 11 Dec 2021 07:04:32: 1000000 INFO @ Sat, 11 Dec 2021 07:04:37: 2000000 INFO @ Sat, 11 Dec 2021 07:04:43: 3000000 INFO @ Sat, 11 Dec 2021 07:04:48: 4000000 INFO @ Sat, 11 Dec 2021 07:04:53: 5000000 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 07:04:55: #1 tag size is determined as 50 bps INFO @ Sat, 11 Dec 2021 07:04:55: #1 tag size = 50 INFO @ Sat, 11 Dec 2021 07:04:55: #1 total tags in treatment: 5394441 INFO @ Sat, 11 Dec 2021 07:04:55: #1 user defined the maximum tags... INFO @ Sat, 11 Dec 2021 07:04:55: #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 07:04:55: #1 tags after filtering in treatment: 5394441 INFO @ Sat, 11 Dec 2021 07:04:55: #1 Redundant rate of treatment: 0.00 INFO @ Sat, 11 Dec 2021 07:04:55: #1 finished! INFO @ Sat, 11 Dec 2021 07:04:55: #2 Build Peak Model... INFO @ Sat, 11 Dec 2021 07:04:55: #2 looking for paired plus/minus strand peaks... INFO @ Sat, 11 Dec 2021 07:04:56: #2 number of paired peaks: 158 WARNING @ Sat, 11 Dec 2021 07:04:56: Fewer paired peaks (158) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 158 pairs to build model! INFO @ Sat, 11 Dec 2021 07:04:56: start model_add_line... INFO @ Sat, 11 Dec 2021 07:04:56: start X-correlation... INFO @ Sat, 11 Dec 2021 07:04:56: end of X-cor INFO @ Sat, 11 Dec 2021 07:04:56: #2 finished! INFO @ Sat, 11 Dec 2021 07:04:56: #2 predicted fragment length is 52 bps INFO @ Sat, 11 Dec 2021 07:04:56: #2 alternative fragment length(s) may be 52 bps INFO @ Sat, 11 Dec 2021 07:04:56: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/dm3/SRX8689067/SRX8689067.05_model.r WARNING @ Sat, 11 Dec 2021 07:04:56: #2 Since the d (52) calculated from paired-peaks are smaller than 2*tag length, it may be influenced by unknown sequencing problem! WARNING @ Sat, 11 Dec 2021 07:04:56: #2 You may need to consider one of the other alternative d(s): 52 WARNING @ Sat, 11 Dec 2021 07:04:56: #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 07:04:56: #3 Call peaks... INFO @ Sat, 11 Dec 2021 07:04:56: #3 Pre-compute pvalue-qvalue table... INFO @ Sat, 11 Dec 2021 07:04:57: # Command line: callpeak -t /home/okishinya/chipatlas/results/dm3/SRX8689067/SRX8689067.bam -f BAM -g dm -n /home/okishinya/chipatlas/results/dm3/SRX8689067/SRX8689067.10 -q 1e-10 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/dm3/SRX8689067/SRX8689067.10 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/dm3/SRX8689067/SRX8689067.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 07:04:57: #1 read tag files... INFO @ Sat, 11 Dec 2021 07:04:57: #1 read treatment tags... INFO @ Sat, 11 Dec 2021 07:05:02: 1000000 INFO @ Sat, 11 Dec 2021 07:05:07: #3 Call peaks for each chromosome... INFO @ Sat, 11 Dec 2021 07:05:08: 2000000 INFO @ Sat, 11 Dec 2021 07:05:13: 3000000 INFO @ Sat, 11 Dec 2021 07:05:13: #4 Write output xls file... /home/okishinya/chipatlas/results/dm3/SRX8689067/SRX8689067.05_peaks.xls INFO @ Sat, 11 Dec 2021 07:05:13: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/dm3/SRX8689067/SRX8689067.05_peaks.narrowPeak INFO @ Sat, 11 Dec 2021 07:05:13: #4 Write summits bed file... /home/okishinya/chipatlas/results/dm3/SRX8689067/SRX8689067.05_summits.bed INFO @ Sat, 11 Dec 2021 07:05:13: Done! pass1 - making usageList (10 chroms): 1 millis pass2 - checking and writing primary data (1165 records, 4 fields): 2 millis CompletedMACS2peakCalling INFO @ Sat, 11 Dec 2021 07:05:18: 4000000 INFO @ Sat, 11 Dec 2021 07:05:24: 5000000 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 07:05:26: #1 tag size is determined as 50 bps INFO @ Sat, 11 Dec 2021 07:05:26: #1 tag size = 50 INFO @ Sat, 11 Dec 2021 07:05:26: #1 total tags in treatment: 5394441 INFO @ Sat, 11 Dec 2021 07:05:26: #1 user defined the maximum tags... INFO @ Sat, 11 Dec 2021 07:05:26: #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 07:05:26: #1 tags after filtering in treatment: 5394441 INFO @ Sat, 11 Dec 2021 07:05:26: #1 Redundant rate of treatment: 0.00 INFO @ Sat, 11 Dec 2021 07:05:26: #1 finished! INFO @ Sat, 11 Dec 2021 07:05:26: #2 Build Peak Model... INFO @ Sat, 11 Dec 2021 07:05:26: #2 looking for paired plus/minus strand peaks... INFO @ Sat, 11 Dec 2021 07:05:26: #2 number of paired peaks: 158 WARNING @ Sat, 11 Dec 2021 07:05:26: Fewer paired peaks (158) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 158 pairs to build model! INFO @ Sat, 11 Dec 2021 07:05:26: start model_add_line... INFO @ Sat, 11 Dec 2021 07:05:26: start X-correlation... INFO @ Sat, 11 Dec 2021 07:05:26: end of X-cor INFO @ Sat, 11 Dec 2021 07:05:26: #2 finished! INFO @ Sat, 11 Dec 2021 07:05:26: #2 predicted fragment length is 52 bps INFO @ Sat, 11 Dec 2021 07:05:26: #2 alternative fragment length(s) may be 52 bps INFO @ Sat, 11 Dec 2021 07:05:26: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/dm3/SRX8689067/SRX8689067.10_model.r WARNING @ Sat, 11 Dec 2021 07:05:26: #2 Since the d (52) calculated from paired-peaks are smaller than 2*tag length, it may be influenced by unknown sequencing problem! WARNING @ Sat, 11 Dec 2021 07:05:26: #2 You may need to consider one of the other alternative d(s): 52 WARNING @ Sat, 11 Dec 2021 07:05:26: #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 07:05:26: #3 Call peaks... INFO @ Sat, 11 Dec 2021 07:05:26: #3 Pre-compute pvalue-qvalue table... INFO @ Sat, 11 Dec 2021 07:05:27: # Command line: callpeak -t /home/okishinya/chipatlas/results/dm3/SRX8689067/SRX8689067.bam -f BAM -g dm -n /home/okishinya/chipatlas/results/dm3/SRX8689067/SRX8689067.20 -q 1e-20 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/dm3/SRX8689067/SRX8689067.20 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/dm3/SRX8689067/SRX8689067.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 07:05:27: #1 read tag files... INFO @ Sat, 11 Dec 2021 07:05:27: #1 read treatment tags... INFO @ Sat, 11 Dec 2021 07:05:33: 1000000 INFO @ Sat, 11 Dec 2021 07:05:37: #3 Call peaks for each chromosome... INFO @ Sat, 11 Dec 2021 07:05:38: 2000000 INFO @ Sat, 11 Dec 2021 07:05:43: #4 Write output xls file... /home/okishinya/chipatlas/results/dm3/SRX8689067/SRX8689067.10_peaks.xls INFO @ Sat, 11 Dec 2021 07:05:43: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/dm3/SRX8689067/SRX8689067.10_peaks.narrowPeak INFO @ Sat, 11 Dec 2021 07:05:43: #4 Write summits bed file... /home/okishinya/chipatlas/results/dm3/SRX8689067/SRX8689067.10_summits.bed INFO @ Sat, 11 Dec 2021 07:05:43: Done! pass1 - making usageList (8 chroms): 1 millis pass2 - checking and writing primary data (935 records, 4 fields): 2 millis CompletedMACS2peakCalling INFO @ Sat, 11 Dec 2021 07:05:43: 3000000 INFO @ Sat, 11 Dec 2021 07:05:49: 4000000 BedGraph に変換しました。 BigWig に変換中... INFO @ Sat, 11 Dec 2021 07:05:54: 5000000 INFO @ Sat, 11 Dec 2021 07:05:56: #1 tag size is determined as 50 bps INFO @ Sat, 11 Dec 2021 07:05:56: #1 tag size = 50 INFO @ Sat, 11 Dec 2021 07:05:56: #1 total tags in treatment: 5394441 INFO @ Sat, 11 Dec 2021 07:05:56: #1 user defined the maximum tags... INFO @ Sat, 11 Dec 2021 07:05:56: #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 07:05:56: #1 tags after filtering in treatment: 5394441 INFO @ Sat, 11 Dec 2021 07:05:56: #1 Redundant rate of treatment: 0.00 INFO @ Sat, 11 Dec 2021 07:05:56: #1 finished! INFO @ Sat, 11 Dec 2021 07:05:56: #2 Build Peak Model... INFO @ Sat, 11 Dec 2021 07:05:56: #2 looking for paired plus/minus strand peaks... INFO @ Sat, 11 Dec 2021 07:05:57: #2 number of paired peaks: 158 WARNING @ Sat, 11 Dec 2021 07:05:57: Fewer paired peaks (158) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 158 pairs to build model! INFO @ Sat, 11 Dec 2021 07:05:57: start model_add_line... INFO @ Sat, 11 Dec 2021 07:05:57: start X-correlation... INFO @ Sat, 11 Dec 2021 07:05:57: end of X-cor INFO @ Sat, 11 Dec 2021 07:05:57: #2 finished! INFO @ Sat, 11 Dec 2021 07:05:57: #2 predicted fragment length is 52 bps INFO @ Sat, 11 Dec 2021 07:05:57: #2 alternative fragment length(s) may be 52 bps INFO @ Sat, 11 Dec 2021 07:05:57: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/dm3/SRX8689067/SRX8689067.20_model.r WARNING @ Sat, 11 Dec 2021 07:05:57: #2 Since the d (52) calculated from paired-peaks are smaller than 2*tag length, it may be influenced by unknown sequencing problem! WARNING @ Sat, 11 Dec 2021 07:05:57: #2 You may need to consider one of the other alternative d(s): 52 WARNING @ Sat, 11 Dec 2021 07:05:57: #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 07:05:57: #3 Call peaks... INFO @ Sat, 11 Dec 2021 07:05:57: #3 Pre-compute pvalue-qvalue table... BigWig に変換しました。 INFO @ Sat, 11 Dec 2021 07:06:07: #3 Call peaks for each chromosome... INFO @ Sat, 11 Dec 2021 07:06:13: #4 Write output xls file... /home/okishinya/chipatlas/results/dm3/SRX8689067/SRX8689067.20_peaks.xls INFO @ Sat, 11 Dec 2021 07:06:13: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/dm3/SRX8689067/SRX8689067.20_peaks.narrowPeak INFO @ Sat, 11 Dec 2021 07:06:13: #4 Write summits bed file... /home/okishinya/chipatlas/results/dm3/SRX8689067/SRX8689067.20_summits.bed INFO @ Sat, 11 Dec 2021 07:06:13: Done! pass1 - making usageList (7 chroms): 0 millis pass2 - checking and writing primary data (580 records, 4 fields): 2 millis CompletedMACS2peakCalling