Job ID = 14167244 SRX = SRX8688909 Genome = dm3 sra ファイルのダウンロード中... Read layout: SINGLE fastq に変換中... Read 7722577 spots for SRR12174261/SRR12174261.sra Written 7722577 spots for SRR12174261/SRR12174261.sra fastq に変換しました。 bowtie でマッピング中... Your job 14167812 ("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: 00:02:50 7722577 reads; of these: 7722577 (100.00%) were unpaired; of these: 299317 (3.88%) aligned 0 times 5355902 (69.35%) aligned exactly 1 time 2067358 (26.77%) aligned >1 times 96.12% overall alignment rate Time searching: 00:02:50 Overall time: 00:02:50 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] 348754 / 7423260 = 0.0470 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 @ Fri, 10 Dec 2021 11:20:32: # Command line: callpeak -t /home/okishinya/chipatlas/results/dm3/SRX8688909/SRX8688909.bam -f BAM -g dm -n /home/okishinya/chipatlas/results/dm3/SRX8688909/SRX8688909.05 -q 1e-05 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/dm3/SRX8688909/SRX8688909.05 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/dm3/SRX8688909/SRX8688909.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 @ Fri, 10 Dec 2021 11:20:32: #1 read tag files... INFO @ Fri, 10 Dec 2021 11:20:32: #1 read treatment tags... INFO @ Fri, 10 Dec 2021 11:20:38: 1000000 INFO @ Fri, 10 Dec 2021 11:20:45: 2000000 INFO @ Fri, 10 Dec 2021 11:20:51: 3000000 INFO @ Fri, 10 Dec 2021 11:20:58: 4000000 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 @ Fri, 10 Dec 2021 11:21:02: # Command line: callpeak -t /home/okishinya/chipatlas/results/dm3/SRX8688909/SRX8688909.bam -f BAM -g dm -n /home/okishinya/chipatlas/results/dm3/SRX8688909/SRX8688909.10 -q 1e-10 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/dm3/SRX8688909/SRX8688909.10 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/dm3/SRX8688909/SRX8688909.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 @ Fri, 10 Dec 2021 11:21:02: #1 read tag files... INFO @ Fri, 10 Dec 2021 11:21:02: #1 read treatment tags... INFO @ Fri, 10 Dec 2021 11:21:04: 5000000 INFO @ Fri, 10 Dec 2021 11:21:08: 1000000 INFO @ Fri, 10 Dec 2021 11:21:11: 6000000 INFO @ Fri, 10 Dec 2021 11:21:15: 2000000 INFO @ Fri, 10 Dec 2021 11:21:19: 7000000 INFO @ Fri, 10 Dec 2021 11:21:19: #1 tag size is determined as 50 bps INFO @ Fri, 10 Dec 2021 11:21:19: #1 tag size = 50 INFO @ Fri, 10 Dec 2021 11:21:19: #1 total tags in treatment: 7074506 INFO @ Fri, 10 Dec 2021 11:21:19: #1 user defined the maximum tags... INFO @ Fri, 10 Dec 2021 11:21:19: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Fri, 10 Dec 2021 11:21:19: #1 tags after filtering in treatment: 7074506 INFO @ Fri, 10 Dec 2021 11:21:19: #1 Redundant rate of treatment: 0.00 INFO @ Fri, 10 Dec 2021 11:21:19: #1 finished! INFO @ Fri, 10 Dec 2021 11:21:19: #2 Build Peak Model... INFO @ Fri, 10 Dec 2021 11:21:19: #2 looking for paired plus/minus strand peaks... INFO @ Fri, 10 Dec 2021 11:21:20: #2 number of paired peaks: 272 WARNING @ Fri, 10 Dec 2021 11:21:20: Fewer paired peaks (272) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 272 pairs to build model! INFO @ Fri, 10 Dec 2021 11:21:20: start model_add_line... INFO @ Fri, 10 Dec 2021 11:21:20: start X-correlation... INFO @ Fri, 10 Dec 2021 11:21:20: end of X-cor INFO @ Fri, 10 Dec 2021 11:21:20: #2 finished! INFO @ Fri, 10 Dec 2021 11:21:20: #2 predicted fragment length is 47 bps INFO @ Fri, 10 Dec 2021 11:21:20: #2 alternative fragment length(s) may be 47 bps INFO @ Fri, 10 Dec 2021 11:21:20: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/dm3/SRX8688909/SRX8688909.05_model.r WARNING @ Fri, 10 Dec 2021 11:21:20: #2 Since the d (47) calculated from paired-peaks are smaller than 2*tag length, it may be influenced by unknown sequencing problem! WARNING @ Fri, 10 Dec 2021 11:21:20: #2 You may need to consider one of the other alternative d(s): 47 WARNING @ Fri, 10 Dec 2021 11:21:20: #2 You can restart the process with --nomodel --extsize XXX with your choice or an arbitrary number. Nontheless, MACS will continute computing. INFO @ Fri, 10 Dec 2021 11:21:20: #3 Call peaks... INFO @ Fri, 10 Dec 2021 11:21:20: #3 Pre-compute pvalue-qvalue table... INFO @ Fri, 10 Dec 2021 11:21:21: 3000000 INFO @ Fri, 10 Dec 2021 11:21:27: 4000000 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 @ Fri, 10 Dec 2021 11:21:32: # Command line: callpeak -t /home/okishinya/chipatlas/results/dm3/SRX8688909/SRX8688909.bam -f BAM -g dm -n /home/okishinya/chipatlas/results/dm3/SRX8688909/SRX8688909.20 -q 1e-20 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/dm3/SRX8688909/SRX8688909.20 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/dm3/SRX8688909/SRX8688909.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 @ Fri, 10 Dec 2021 11:21:32: #1 read tag files... INFO @ Fri, 10 Dec 2021 11:21:32: #1 read treatment tags... INFO @ Fri, 10 Dec 2021 11:21:33: 5000000 INFO @ Fri, 10 Dec 2021 11:21:34: #3 Call peaks for each chromosome... INFO @ Fri, 10 Dec 2021 11:21:38: 1000000 INFO @ Fri, 10 Dec 2021 11:21:39: 6000000 INFO @ Fri, 10 Dec 2021 11:21:41: #4 Write output xls file... /home/okishinya/chipatlas/results/dm3/SRX8688909/SRX8688909.05_peaks.xls INFO @ Fri, 10 Dec 2021 11:21:41: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/dm3/SRX8688909/SRX8688909.05_peaks.narrowPeak INFO @ Fri, 10 Dec 2021 11:21:41: #4 Write summits bed file... /home/okishinya/chipatlas/results/dm3/SRX8688909/SRX8688909.05_summits.bed INFO @ Fri, 10 Dec 2021 11:21:41: Done! pass1 - making usageList (9 chroms): 0 millis pass2 - checking and writing primary data (1211 records, 4 fields): 3 millis CompletedMACS2peakCalling INFO @ Fri, 10 Dec 2021 11:21:44: 2000000 INFO @ Fri, 10 Dec 2021 11:21:45: 7000000 INFO @ Fri, 10 Dec 2021 11:21:45: #1 tag size is determined as 50 bps INFO @ Fri, 10 Dec 2021 11:21:45: #1 tag size = 50 INFO @ Fri, 10 Dec 2021 11:21:45: #1 total tags in treatment: 7074506 INFO @ Fri, 10 Dec 2021 11:21:45: #1 user defined the maximum tags... INFO @ Fri, 10 Dec 2021 11:21:45: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Fri, 10 Dec 2021 11:21:45: #1 tags after filtering in treatment: 7074506 INFO @ Fri, 10 Dec 2021 11:21:45: #1 Redundant rate of treatment: 0.00 INFO @ Fri, 10 Dec 2021 11:21:45: #1 finished! INFO @ Fri, 10 Dec 2021 11:21:45: #2 Build Peak Model... INFO @ Fri, 10 Dec 2021 11:21:45: #2 looking for paired plus/minus strand peaks... INFO @ Fri, 10 Dec 2021 11:21:46: #2 number of paired peaks: 272 WARNING @ Fri, 10 Dec 2021 11:21:46: Fewer paired peaks (272) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 272 pairs to build model! INFO @ Fri, 10 Dec 2021 11:21:46: start model_add_line... INFO @ Fri, 10 Dec 2021 11:21:46: start X-correlation... INFO @ Fri, 10 Dec 2021 11:21:46: end of X-cor INFO @ Fri, 10 Dec 2021 11:21:46: #2 finished! INFO @ Fri, 10 Dec 2021 11:21:46: #2 predicted fragment length is 47 bps INFO @ Fri, 10 Dec 2021 11:21:46: #2 alternative fragment length(s) may be 47 bps INFO @ Fri, 10 Dec 2021 11:21:46: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/dm3/SRX8688909/SRX8688909.10_model.r WARNING @ Fri, 10 Dec 2021 11:21:46: #2 Since the d (47) calculated from paired-peaks are smaller than 2*tag length, it may be influenced by unknown sequencing problem! WARNING @ Fri, 10 Dec 2021 11:21:46: #2 You may need to consider one of the other alternative d(s): 47 WARNING @ Fri, 10 Dec 2021 11:21:46: #2 You can restart the process with --nomodel --extsize XXX with your choice or an arbitrary number. Nontheless, MACS will continute computing. INFO @ Fri, 10 Dec 2021 11:21:46: #3 Call peaks... INFO @ Fri, 10 Dec 2021 11:21:46: #3 Pre-compute pvalue-qvalue table... INFO @ Fri, 10 Dec 2021 11:21:50: 3000000 INFO @ Fri, 10 Dec 2021 11:21:56: 4000000 INFO @ Fri, 10 Dec 2021 11:22:00: #3 Call peaks for each chromosome... INFO @ Fri, 10 Dec 2021 11:22:01: 5000000 BedGraph に変換しました。 BigWig に変換中... INFO @ Fri, 10 Dec 2021 11:22:07: 6000000 INFO @ Fri, 10 Dec 2021 11:22:07: #4 Write output xls file... /home/okishinya/chipatlas/results/dm3/SRX8688909/SRX8688909.10_peaks.xls INFO @ Fri, 10 Dec 2021 11:22:07: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/dm3/SRX8688909/SRX8688909.10_peaks.narrowPeak INFO @ Fri, 10 Dec 2021 11:22:07: #4 Write summits bed file... /home/okishinya/chipatlas/results/dm3/SRX8688909/SRX8688909.10_summits.bed INFO @ Fri, 10 Dec 2021 11:22:07: Done! pass1 - making usageList (8 chroms): 1 millis pass2 - checking and writing primary data (986 records, 4 fields): 2 millis CompletedMACS2peakCalling INFO @ Fri, 10 Dec 2021 11:22:12: 7000000 INFO @ Fri, 10 Dec 2021 11:22:13: #1 tag size is determined as 50 bps INFO @ Fri, 10 Dec 2021 11:22:13: #1 tag size = 50 INFO @ Fri, 10 Dec 2021 11:22:13: #1 total tags in treatment: 7074506 INFO @ Fri, 10 Dec 2021 11:22:13: #1 user defined the maximum tags... INFO @ Fri, 10 Dec 2021 11:22:13: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Fri, 10 Dec 2021 11:22:13: #1 tags after filtering in treatment: 7074506 INFO @ Fri, 10 Dec 2021 11:22:13: #1 Redundant rate of treatment: 0.00 INFO @ Fri, 10 Dec 2021 11:22:13: #1 finished! INFO @ Fri, 10 Dec 2021 11:22:13: #2 Build Peak Model... INFO @ Fri, 10 Dec 2021 11:22:13: #2 looking for paired plus/minus strand peaks... INFO @ Fri, 10 Dec 2021 11:22:13: #2 number of paired peaks: 272 WARNING @ Fri, 10 Dec 2021 11:22:13: Fewer paired peaks (272) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 272 pairs to build model! INFO @ Fri, 10 Dec 2021 11:22:13: start model_add_line... INFO @ Fri, 10 Dec 2021 11:22:13: start X-correlation... INFO @ Fri, 10 Dec 2021 11:22:13: end of X-cor INFO @ Fri, 10 Dec 2021 11:22:13: #2 finished! INFO @ Fri, 10 Dec 2021 11:22:13: #2 predicted fragment length is 47 bps INFO @ Fri, 10 Dec 2021 11:22:13: #2 alternative fragment length(s) may be 47 bps INFO @ Fri, 10 Dec 2021 11:22:13: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/dm3/SRX8688909/SRX8688909.20_model.r WARNING @ Fri, 10 Dec 2021 11:22:13: #2 Since the d (47) calculated from paired-peaks are smaller than 2*tag length, it may be influenced by unknown sequencing problem! WARNING @ Fri, 10 Dec 2021 11:22:13: #2 You may need to consider one of the other alternative d(s): 47 WARNING @ Fri, 10 Dec 2021 11:22:13: #2 You can restart the process with --nomodel --extsize XXX with your choice or an arbitrary number. Nontheless, MACS will continute computing. INFO @ Fri, 10 Dec 2021 11:22:13: #3 Call peaks... INFO @ Fri, 10 Dec 2021 11:22:13: #3 Pre-compute pvalue-qvalue table... BigWig に変換しました。 INFO @ Fri, 10 Dec 2021 11:22:28: #3 Call peaks for each chromosome... INFO @ Fri, 10 Dec 2021 11:22:35: #4 Write output xls file... /home/okishinya/chipatlas/results/dm3/SRX8688909/SRX8688909.20_peaks.xls INFO @ Fri, 10 Dec 2021 11:22:35: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/dm3/SRX8688909/SRX8688909.20_peaks.narrowPeak INFO @ Fri, 10 Dec 2021 11:22:35: #4 Write summits bed file... /home/okishinya/chipatlas/results/dm3/SRX8688909/SRX8688909.20_summits.bed INFO @ Fri, 10 Dec 2021 11:22:35: Done! pass1 - making usageList (7 chroms): 2 millis pass2 - checking and writing primary data (703 records, 4 fields): 1 millis CompletedMACS2peakCalling