Job ID = 14170075 SRX = SRX8556366 Genome = dm3 sra ファイルのダウンロード中... Read layout: PAIRED fastq に変換中... Read 28285078 spots for SRR12024922/SRR12024922.sra Written 28285078 spots for SRR12024922/SRR12024922.sra fastq に変換しました。 bowtie でマッピング中... Your job 14170664 ("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: 00:11:32 28285078 reads; of these: 28285078 (100.00%) were paired; of these: 27166579 (96.05%) aligned concordantly 0 times 839589 (2.97%) aligned concordantly exactly 1 time 278910 (0.99%) aligned concordantly >1 times ---- 27166579 pairs aligned concordantly 0 times; of these: 136035 (0.50%) aligned discordantly 1 time ---- 27030544 pairs aligned 0 times concordantly or discordantly; of these: 54061088 mates make up the pairs; of these: 53677948 (99.29%) aligned 0 times 178234 (0.33%) aligned exactly 1 time 204906 (0.38%) aligned >1 times 5.11% overall alignment rate Time searching: 00:11:32 Overall time: 00:11:32 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_rmdup_core] processing reference chr2L... [bam_rmdup_core] processing reference chr2LHet... [bam_rmdup_core] processing reference chr2R... [bam_rmdup_core] processing reference chr2RHet... [bam_rmdup_core] processing reference chr3L... [bam_rmdup_core] processing reference chr3LHet... [bam_rmdup_core] processing reference chr3R... [bam_rmdup_core] processing reference chr3RHet... [bam_rmdup_core] processing reference chr4... [bam_rmdup_core] processing reference chrM... [bam_rmdup_core] processing reference chrU... [bam_rmdup_core] processing reference chrUextra... [bam_rmdup_core] processing reference chrX... [bam_rmdup_core] processing reference chrXHet... [bam_rmdup_core] processing reference chrYHet... [bam_rmdup_core] 888671 / 1240078 = 0.7166 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 05:16:07: # Command line: callpeak -t /home/okishinya/chipatlas/results/dm3/SRX8556366/SRX8556366.bam -f BAM -g dm -n /home/okishinya/chipatlas/results/dm3/SRX8556366/SRX8556366.05 -q 1e-05 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/dm3/SRX8556366/SRX8556366.05 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/dm3/SRX8556366/SRX8556366.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 05:16:07: #1 read tag files... INFO @ Sat, 11 Dec 2021 05:16:07: #1 read treatment tags... INFO @ Sat, 11 Dec 2021 05:16:15: 1000000 INFO @ Sat, 11 Dec 2021 05:16:15: #1 tag size is determined as 150 bps INFO @ Sat, 11 Dec 2021 05:16:15: #1 tag size = 150 INFO @ Sat, 11 Dec 2021 05:16:15: #1 total tags in treatment: 302719 INFO @ Sat, 11 Dec 2021 05:16:15: #1 user defined the maximum tags... INFO @ Sat, 11 Dec 2021 05:16:15: #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 05:16:15: #1 tags after filtering in treatment: 264698 INFO @ Sat, 11 Dec 2021 05:16:15: #1 Redundant rate of treatment: 0.13 INFO @ Sat, 11 Dec 2021 05:16:15: #1 finished! INFO @ Sat, 11 Dec 2021 05:16:15: #2 Build Peak Model... INFO @ Sat, 11 Dec 2021 05:16:15: #2 looking for paired plus/minus strand peaks... INFO @ Sat, 11 Dec 2021 05:16:16: #2 number of paired peaks: 3046 INFO @ Sat, 11 Dec 2021 05:16:16: start model_add_line... INFO @ Sat, 11 Dec 2021 05:16:16: start X-correlation... INFO @ Sat, 11 Dec 2021 05:16:16: end of X-cor INFO @ Sat, 11 Dec 2021 05:16:16: #2 finished! INFO @ Sat, 11 Dec 2021 05:16:16: #2 predicted fragment length is 174 bps INFO @ Sat, 11 Dec 2021 05:16:16: #2 alternative fragment length(s) may be 174 bps INFO @ Sat, 11 Dec 2021 05:16:16: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/dm3/SRX8556366/SRX8556366.05_model.r WARNING @ Sat, 11 Dec 2021 05:16:16: #2 Since the d (174) calculated from paired-peaks are smaller than 2*tag length, it may be influenced by unknown sequencing problem! WARNING @ Sat, 11 Dec 2021 05:16:16: #2 You may need to consider one of the other alternative d(s): 174 WARNING @ Sat, 11 Dec 2021 05:16:16: #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 05:16:16: #3 Call peaks... INFO @ Sat, 11 Dec 2021 05:16:16: #3 Pre-compute pvalue-qvalue table... INFO @ Sat, 11 Dec 2021 05:16:16: #3 Call peaks for each chromosome... INFO @ Sat, 11 Dec 2021 05:16:17: #4 Write output xls file... /home/okishinya/chipatlas/results/dm3/SRX8556366/SRX8556366.05_peaks.xls INFO @ Sat, 11 Dec 2021 05:16:17: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/dm3/SRX8556366/SRX8556366.05_peaks.narrowPeak INFO @ Sat, 11 Dec 2021 05:16:17: #4 Write summits bed file... /home/okishinya/chipatlas/results/dm3/SRX8556366/SRX8556366.05_summits.bed INFO @ Sat, 11 Dec 2021 05:16:17: Done! pass1 - making usageList (14 chroms): 1 millis pass2 - checking and writing primary data (1069 records, 4 fields): 3 millis CompletedMACS2peakCalling 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 05:16:37: # Command line: callpeak -t /home/okishinya/chipatlas/results/dm3/SRX8556366/SRX8556366.bam -f BAM -g dm -n /home/okishinya/chipatlas/results/dm3/SRX8556366/SRX8556366.10 -q 1e-10 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/dm3/SRX8556366/SRX8556366.10 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/dm3/SRX8556366/SRX8556366.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 05:16:37: #1 read tag files... INFO @ Sat, 11 Dec 2021 05:16:37: #1 read treatment tags... INFO @ Sat, 11 Dec 2021 05:16:45: 1000000 INFO @ Sat, 11 Dec 2021 05:16:46: #1 tag size is determined as 150 bps INFO @ Sat, 11 Dec 2021 05:16:46: #1 tag size = 150 INFO @ Sat, 11 Dec 2021 05:16:46: #1 total tags in treatment: 302719 INFO @ Sat, 11 Dec 2021 05:16:46: #1 user defined the maximum tags... INFO @ Sat, 11 Dec 2021 05:16:46: #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 05:16:46: #1 tags after filtering in treatment: 264698 INFO @ Sat, 11 Dec 2021 05:16:46: #1 Redundant rate of treatment: 0.13 INFO @ Sat, 11 Dec 2021 05:16:46: #1 finished! INFO @ Sat, 11 Dec 2021 05:16:46: #2 Build Peak Model... INFO @ Sat, 11 Dec 2021 05:16:46: #2 looking for paired plus/minus strand peaks... INFO @ Sat, 11 Dec 2021 05:16:46: #2 number of paired peaks: 3046 INFO @ Sat, 11 Dec 2021 05:16:46: start model_add_line... INFO @ Sat, 11 Dec 2021 05:16:46: start X-correlation... INFO @ Sat, 11 Dec 2021 05:16:46: end of X-cor INFO @ Sat, 11 Dec 2021 05:16:46: #2 finished! INFO @ Sat, 11 Dec 2021 05:16:46: #2 predicted fragment length is 174 bps INFO @ Sat, 11 Dec 2021 05:16:46: #2 alternative fragment length(s) may be 174 bps INFO @ Sat, 11 Dec 2021 05:16:46: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/dm3/SRX8556366/SRX8556366.10_model.r WARNING @ Sat, 11 Dec 2021 05:16:46: #2 Since the d (174) calculated from paired-peaks are smaller than 2*tag length, it may be influenced by unknown sequencing problem! WARNING @ Sat, 11 Dec 2021 05:16:46: #2 You may need to consider one of the other alternative d(s): 174 WARNING @ Sat, 11 Dec 2021 05:16:46: #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 05:16:46: #3 Call peaks... INFO @ Sat, 11 Dec 2021 05:16:46: #3 Pre-compute pvalue-qvalue table... INFO @ Sat, 11 Dec 2021 05:16:46: #3 Call peaks for each chromosome... INFO @ Sat, 11 Dec 2021 05:16:47: #4 Write output xls file... /home/okishinya/chipatlas/results/dm3/SRX8556366/SRX8556366.10_peaks.xls INFO @ Sat, 11 Dec 2021 05:16:47: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/dm3/SRX8556366/SRX8556366.10_peaks.narrowPeak INFO @ Sat, 11 Dec 2021 05:16:47: #4 Write summits bed file... /home/okishinya/chipatlas/results/dm3/SRX8556366/SRX8556366.10_summits.bed INFO @ Sat, 11 Dec 2021 05:16:47: Done! pass1 - making usageList (11 chroms): 1 millis pass2 - checking and writing primary data (621 records, 4 fields): 1 millis CompletedMACS2peakCalling 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 05:17:07: # Command line: callpeak -t /home/okishinya/chipatlas/results/dm3/SRX8556366/SRX8556366.bam -f BAM -g dm -n /home/okishinya/chipatlas/results/dm3/SRX8556366/SRX8556366.20 -q 1e-20 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/dm3/SRX8556366/SRX8556366.20 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/dm3/SRX8556366/SRX8556366.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 05:17:07: #1 read tag files... INFO @ Sat, 11 Dec 2021 05:17:07: #1 read treatment tags... BedGraph に変換しました。 BigWig に変換中... BigWig に変換しました。 INFO @ Sat, 11 Dec 2021 05:17:17: 1000000 INFO @ Sat, 11 Dec 2021 05:17:18: #1 tag size is determined as 150 bps INFO @ Sat, 11 Dec 2021 05:17:18: #1 tag size = 150 INFO @ Sat, 11 Dec 2021 05:17:18: #1 total tags in treatment: 302719 INFO @ Sat, 11 Dec 2021 05:17:18: #1 user defined the maximum tags... INFO @ Sat, 11 Dec 2021 05:17:18: #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 05:17:18: #1 tags after filtering in treatment: 264698 INFO @ Sat, 11 Dec 2021 05:17:18: #1 Redundant rate of treatment: 0.13 INFO @ Sat, 11 Dec 2021 05:17:18: #1 finished! INFO @ Sat, 11 Dec 2021 05:17:18: #2 Build Peak Model... INFO @ Sat, 11 Dec 2021 05:17:18: #2 looking for paired plus/minus strand peaks... INFO @ Sat, 11 Dec 2021 05:17:18: #2 number of paired peaks: 3046 INFO @ Sat, 11 Dec 2021 05:17:18: start model_add_line... INFO @ Sat, 11 Dec 2021 05:17:18: start X-correlation... INFO @ Sat, 11 Dec 2021 05:17:18: end of X-cor INFO @ Sat, 11 Dec 2021 05:17:18: #2 finished! INFO @ Sat, 11 Dec 2021 05:17:18: #2 predicted fragment length is 174 bps INFO @ Sat, 11 Dec 2021 05:17:18: #2 alternative fragment length(s) may be 174 bps INFO @ Sat, 11 Dec 2021 05:17:18: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/dm3/SRX8556366/SRX8556366.20_model.r WARNING @ Sat, 11 Dec 2021 05:17:18: #2 Since the d (174) calculated from paired-peaks are smaller than 2*tag length, it may be influenced by unknown sequencing problem! WARNING @ Sat, 11 Dec 2021 05:17:18: #2 You may need to consider one of the other alternative d(s): 174 WARNING @ Sat, 11 Dec 2021 05:17:18: #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 05:17:18: #3 Call peaks... INFO @ Sat, 11 Dec 2021 05:17:18: #3 Pre-compute pvalue-qvalue table... INFO @ Sat, 11 Dec 2021 05:17:19: #3 Call peaks for each chromosome... INFO @ Sat, 11 Dec 2021 05:17:19: #4 Write output xls file... /home/okishinya/chipatlas/results/dm3/SRX8556366/SRX8556366.20_peaks.xls INFO @ Sat, 11 Dec 2021 05:17:19: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/dm3/SRX8556366/SRX8556366.20_peaks.narrowPeak INFO @ Sat, 11 Dec 2021 05:17:19: #4 Write summits bed file... /home/okishinya/chipatlas/results/dm3/SRX8556366/SRX8556366.20_summits.bed INFO @ Sat, 11 Dec 2021 05:17:19: Done! pass1 - making usageList (10 chroms): 0 millis pass2 - checking and writing primary data (274 records, 4 fields): 2 millis CompletedMACS2peakCalling