Job ID = 8070994 SRX = SRX7917498 Genome = dm3 sra ファイルのダウンロード中... Read layout: PAIRED fastq に変換中... 2020-08-08T04:16:53 prefetch.2.10.7: 1) Downloading 'SRR11313079'... 2020-08-08T04:16:53 prefetch.2.10.7: Downloading via HTTPS... 2020-08-08T04:17:21 prefetch.2.10.7: HTTPS download succeed 2020-08-08T04:17:21 prefetch.2.10.7: 'SRR11313079' is valid 2020-08-08T04:17:21 prefetch.2.10.7: 1) 'SRR11313079' was downloaded successfully Read 2528769 spots for SRR11313079/SRR11313079.sra Written 2528769 spots for SRR11313079/SRR11313079.sra fastq に変換しました。 bowtie でマッピング中... Your job 8071881 ("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: 00:02:59 2528769 reads; of these: 2528769 (100.00%) were paired; of these: 470003 (18.59%) aligned concordantly 0 times 1807065 (71.46%) aligned concordantly exactly 1 time 251701 (9.95%) aligned concordantly >1 times ---- 470003 pairs aligned concordantly 0 times; of these: 234482 (49.89%) aligned discordantly 1 time ---- 235521 pairs aligned 0 times concordantly or discordantly; of these: 471042 mates make up the pairs; of these: 270357 (57.40%) aligned 0 times 107430 (22.81%) aligned exactly 1 time 93255 (19.80%) aligned >1 times 94.65% overall alignment rate Time searching: 00:02:59 Overall time: 00:02:59 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] 1069584 / 2285833 = 0.4679 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 @ Sat, 08 Aug 2020 13:21:56: # Command line: callpeak -t /home/okishinya/chipatlas/results/dm3/SRX7917498/SRX7917498.bam -f BAM -g dm -n /home/okishinya/chipatlas/results/dm3/SRX7917498/SRX7917498.05 -q 1e-05 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/dm3/SRX7917498/SRX7917498.05 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/dm3/SRX7917498/SRX7917498.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, 08 Aug 2020 13:21:56: #1 read tag files... INFO @ Sat, 08 Aug 2020 13:21:56: #1 read treatment tags... INFO @ Sat, 08 Aug 2020 13:22:03: 1000000 INFO @ Sat, 08 Aug 2020 13:22:11: 2000000 INFO @ Sat, 08 Aug 2020 13:22:15: #1 tag size is determined as 62 bps INFO @ Sat, 08 Aug 2020 13:22:15: #1 tag size = 62 INFO @ Sat, 08 Aug 2020 13:22:15: #1 total tags in treatment: 1032150 INFO @ Sat, 08 Aug 2020 13:22:15: #1 user defined the maximum tags... INFO @ Sat, 08 Aug 2020 13:22:15: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Sat, 08 Aug 2020 13:22:15: #1 tags after filtering in treatment: 690205 INFO @ Sat, 08 Aug 2020 13:22:15: #1 Redundant rate of treatment: 0.33 INFO @ Sat, 08 Aug 2020 13:22:15: #1 finished! INFO @ Sat, 08 Aug 2020 13:22:15: #2 Build Peak Model... INFO @ Sat, 08 Aug 2020 13:22:15: #2 looking for paired plus/minus strand peaks... INFO @ Sat, 08 Aug 2020 13:22:15: #2 number of paired peaks: 4721 INFO @ Sat, 08 Aug 2020 13:22:15: start model_add_line... INFO @ Sat, 08 Aug 2020 13:22:15: start X-correlation... INFO @ Sat, 08 Aug 2020 13:22:15: end of X-cor INFO @ Sat, 08 Aug 2020 13:22:15: #2 finished! INFO @ Sat, 08 Aug 2020 13:22:15: #2 predicted fragment length is 169 bps INFO @ Sat, 08 Aug 2020 13:22:15: #2 alternative fragment length(s) may be 2,45,169,206 bps INFO @ Sat, 08 Aug 2020 13:22:15: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/dm3/SRX7917498/SRX7917498.05_model.r INFO @ Sat, 08 Aug 2020 13:22:15: #3 Call peaks... INFO @ Sat, 08 Aug 2020 13:22:15: #3 Pre-compute pvalue-qvalue table... INFO @ Sat, 08 Aug 2020 13:22:17: #3 Call peaks for each chromosome... INFO @ Sat, 08 Aug 2020 13:22:17: #4 Write output xls file... /home/okishinya/chipatlas/results/dm3/SRX7917498/SRX7917498.05_peaks.xls INFO @ Sat, 08 Aug 2020 13:22:17: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/dm3/SRX7917498/SRX7917498.05_peaks.narrowPeak INFO @ Sat, 08 Aug 2020 13:22:17: #4 Write summits bed file... /home/okishinya/chipatlas/results/dm3/SRX7917498/SRX7917498.05_summits.bed INFO @ Sat, 08 Aug 2020 13:22:17: Done! pass1 - making usageList (3 chroms): 0 millis pass2 - checking and writing primary data (18 records, 4 fields): 1 millis CompletedMACS2peakCalling 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 @ Sat, 08 Aug 2020 13:22:26: # Command line: callpeak -t /home/okishinya/chipatlas/results/dm3/SRX7917498/SRX7917498.bam -f BAM -g dm -n /home/okishinya/chipatlas/results/dm3/SRX7917498/SRX7917498.10 -q 1e-10 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/dm3/SRX7917498/SRX7917498.10 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/dm3/SRX7917498/SRX7917498.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, 08 Aug 2020 13:22:26: #1 read tag files... INFO @ Sat, 08 Aug 2020 13:22:26: #1 read treatment tags... INFO @ Sat, 08 Aug 2020 13:22:33: 1000000 INFO @ Sat, 08 Aug 2020 13:22:40: 2000000 INFO @ Sat, 08 Aug 2020 13:22:44: #1 tag size is determined as 62 bps INFO @ Sat, 08 Aug 2020 13:22:44: #1 tag size = 62 INFO @ Sat, 08 Aug 2020 13:22:44: #1 total tags in treatment: 1032150 INFO @ Sat, 08 Aug 2020 13:22:44: #1 user defined the maximum tags... INFO @ Sat, 08 Aug 2020 13:22:44: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Sat, 08 Aug 2020 13:22:44: #1 tags after filtering in treatment: 690205 INFO @ Sat, 08 Aug 2020 13:22:44: #1 Redundant rate of treatment: 0.33 INFO @ Sat, 08 Aug 2020 13:22:44: #1 finished! INFO @ Sat, 08 Aug 2020 13:22:44: #2 Build Peak Model... INFO @ Sat, 08 Aug 2020 13:22:44: #2 looking for paired plus/minus strand peaks... INFO @ Sat, 08 Aug 2020 13:22:45: #2 number of paired peaks: 4721 INFO @ Sat, 08 Aug 2020 13:22:45: start model_add_line... INFO @ Sat, 08 Aug 2020 13:22:45: start X-correlation... INFO @ Sat, 08 Aug 2020 13:22:45: end of X-cor INFO @ Sat, 08 Aug 2020 13:22:45: #2 finished! INFO @ Sat, 08 Aug 2020 13:22:45: #2 predicted fragment length is 169 bps INFO @ Sat, 08 Aug 2020 13:22:45: #2 alternative fragment length(s) may be 2,45,169,206 bps INFO @ Sat, 08 Aug 2020 13:22:45: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/dm3/SRX7917498/SRX7917498.10_model.r INFO @ Sat, 08 Aug 2020 13:22:45: #3 Call peaks... INFO @ Sat, 08 Aug 2020 13:22:45: #3 Pre-compute pvalue-qvalue table... INFO @ Sat, 08 Aug 2020 13:22:46: #3 Call peaks for each chromosome... INFO @ Sat, 08 Aug 2020 13:22:47: #4 Write output xls file... /home/okishinya/chipatlas/results/dm3/SRX7917498/SRX7917498.10_peaks.xls INFO @ Sat, 08 Aug 2020 13:22:47: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/dm3/SRX7917498/SRX7917498.10_peaks.narrowPeak INFO @ Sat, 08 Aug 2020 13:22:47: #4 Write summits bed file... /home/okishinya/chipatlas/results/dm3/SRX7917498/SRX7917498.10_summits.bed INFO @ Sat, 08 Aug 2020 13:22:47: Done! pass1 - making usageList (1 chroms): 1 millis pass2 - checking and writing primary data (3 records, 4 fields): 0 millis CompletedMACS2peakCalling 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 @ Sat, 08 Aug 2020 13:22:56: # Command line: callpeak -t /home/okishinya/chipatlas/results/dm3/SRX7917498/SRX7917498.bam -f BAM -g dm -n /home/okishinya/chipatlas/results/dm3/SRX7917498/SRX7917498.20 -q 1e-20 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/dm3/SRX7917498/SRX7917498.20 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/dm3/SRX7917498/SRX7917498.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, 08 Aug 2020 13:22:56: #1 read tag files... INFO @ Sat, 08 Aug 2020 13:22:56: #1 read treatment tags... INFO @ Sat, 08 Aug 2020 13:23:02: 1000000 BedGraph に変換しました。 BigWig に変換中... INFO @ Sat, 08 Aug 2020 13:23:07: 2000000 BigWig に変換しました。 INFO @ Sat, 08 Aug 2020 13:23:11: #1 tag size is determined as 62 bps INFO @ Sat, 08 Aug 2020 13:23:11: #1 tag size = 62 INFO @ Sat, 08 Aug 2020 13:23:11: #1 total tags in treatment: 1032150 INFO @ Sat, 08 Aug 2020 13:23:11: #1 user defined the maximum tags... INFO @ Sat, 08 Aug 2020 13:23:11: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Sat, 08 Aug 2020 13:23:11: #1 tags after filtering in treatment: 690205 INFO @ Sat, 08 Aug 2020 13:23:11: #1 Redundant rate of treatment: 0.33 INFO @ Sat, 08 Aug 2020 13:23:11: #1 finished! INFO @ Sat, 08 Aug 2020 13:23:11: #2 Build Peak Model... INFO @ Sat, 08 Aug 2020 13:23:11: #2 looking for paired plus/minus strand peaks... INFO @ Sat, 08 Aug 2020 13:23:11: #2 number of paired peaks: 4721 INFO @ Sat, 08 Aug 2020 13:23:11: start model_add_line... INFO @ Sat, 08 Aug 2020 13:23:11: start X-correlation... INFO @ Sat, 08 Aug 2020 13:23:11: end of X-cor INFO @ Sat, 08 Aug 2020 13:23:11: #2 finished! INFO @ Sat, 08 Aug 2020 13:23:11: #2 predicted fragment length is 169 bps INFO @ Sat, 08 Aug 2020 13:23:11: #2 alternative fragment length(s) may be 2,45,169,206 bps INFO @ Sat, 08 Aug 2020 13:23:11: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/dm3/SRX7917498/SRX7917498.20_model.r INFO @ Sat, 08 Aug 2020 13:23:11: #3 Call peaks... INFO @ Sat, 08 Aug 2020 13:23:11: #3 Pre-compute pvalue-qvalue table... INFO @ Sat, 08 Aug 2020 13:23:12: #3 Call peaks for each chromosome... INFO @ Sat, 08 Aug 2020 13:23:13: #4 Write output xls file... /home/okishinya/chipatlas/results/dm3/SRX7917498/SRX7917498.20_peaks.xls INFO @ Sat, 08 Aug 2020 13:23:13: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/dm3/SRX7917498/SRX7917498.20_peaks.narrowPeak INFO @ Sat, 08 Aug 2020 13:23:13: #4 Write summits bed file... /home/okishinya/chipatlas/results/dm3/SRX7917498/SRX7917498.20_summits.bed INFO @ Sat, 08 Aug 2020 13:23:13: Done! pass1 - making usageList (0 chroms): 1 millis needLargeMem: trying to allocate 0 bytes (limit: 17179869184) CompletedMACS2peakCalling