Job ID = 8069724 SRX = SRX7917432 Genome = dm3 sra ファイルのダウンロード中... Read layout: PAIRED fastq に変換中... 2020-08-08T03:47:53 prefetch.2.10.7: 1) Downloading 'SRR11313013'... 2020-08-08T03:47:53 prefetch.2.10.7: Downloading via HTTPS... 2020-08-08T03:48:29 prefetch.2.10.7: HTTPS download succeed 2020-08-08T03:48:29 prefetch.2.10.7: 'SRR11313013' is valid 2020-08-08T03:48:29 prefetch.2.10.7: 1) 'SRR11313013' was downloaded successfully Read 2354587 spots for SRR11313013/SRR11313013.sra Written 2354587 spots for SRR11313013/SRR11313013.sra fastq に変換しました。 bowtie でマッピング中... Your job 8070500 ("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: 00:03:28 2354587 reads; of these: 2354587 (100.00%) were paired; of these: 443092 (18.82%) aligned concordantly 0 times 1611529 (68.44%) aligned concordantly exactly 1 time 299966 (12.74%) aligned concordantly >1 times ---- 443092 pairs aligned concordantly 0 times; of these: 198607 (44.82%) aligned discordantly 1 time ---- 244485 pairs aligned 0 times concordantly or discordantly; of these: 488970 mates make up the pairs; of these: 217732 (44.53%) aligned 0 times 137200 (28.06%) aligned exactly 1 time 134038 (27.41%) aligned >1 times 95.38% overall alignment rate Time searching: 00:03:28 Overall time: 00:03:28 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] 995472 / 2103709 = 0.4732 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 12:53:32: # Command line: callpeak -t /home/okishinya/chipatlas/results/dm3/SRX7917432/SRX7917432.bam -f BAM -g dm -n /home/okishinya/chipatlas/results/dm3/SRX7917432/SRX7917432.05 -q 1e-05 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/dm3/SRX7917432/SRX7917432.05 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/dm3/SRX7917432/SRX7917432.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 12:53:32: #1 read tag files... INFO @ Sat, 08 Aug 2020 12:53:32: #1 read treatment tags... INFO @ Sat, 08 Aug 2020 12:53:37: 1000000 INFO @ Sat, 08 Aug 2020 12:53:41: 2000000 INFO @ Sat, 08 Aug 2020 12:53:43: #1 tag size is determined as 62 bps INFO @ Sat, 08 Aug 2020 12:53:43: #1 tag size = 62 INFO @ Sat, 08 Aug 2020 12:53:43: #1 total tags in treatment: 957505 INFO @ Sat, 08 Aug 2020 12:53:43: #1 user defined the maximum tags... INFO @ Sat, 08 Aug 2020 12:53:43: #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 12:53:44: #1 tags after filtering in treatment: 706292 INFO @ Sat, 08 Aug 2020 12:53:44: #1 Redundant rate of treatment: 0.26 INFO @ Sat, 08 Aug 2020 12:53:44: #1 finished! INFO @ Sat, 08 Aug 2020 12:53:44: #2 Build Peak Model... INFO @ Sat, 08 Aug 2020 12:53:44: #2 looking for paired plus/minus strand peaks... INFO @ Sat, 08 Aug 2020 12:53:44: #2 number of paired peaks: 2724 INFO @ Sat, 08 Aug 2020 12:53:44: start model_add_line... INFO @ Sat, 08 Aug 2020 12:53:44: start X-correlation... INFO @ Sat, 08 Aug 2020 12:53:44: end of X-cor INFO @ Sat, 08 Aug 2020 12:53:44: #2 finished! INFO @ Sat, 08 Aug 2020 12:53:44: #2 predicted fragment length is 191 bps INFO @ Sat, 08 Aug 2020 12:53:44: #2 alternative fragment length(s) may be 2,41,191,223,269 bps INFO @ Sat, 08 Aug 2020 12:53:44: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/dm3/SRX7917432/SRX7917432.05_model.r INFO @ Sat, 08 Aug 2020 12:53:44: #3 Call peaks... INFO @ Sat, 08 Aug 2020 12:53:44: #3 Pre-compute pvalue-qvalue table... INFO @ Sat, 08 Aug 2020 12:53:45: #3 Call peaks for each chromosome... INFO @ Sat, 08 Aug 2020 12:53:46: #4 Write output xls file... /home/okishinya/chipatlas/results/dm3/SRX7917432/SRX7917432.05_peaks.xls INFO @ Sat, 08 Aug 2020 12:53:46: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/dm3/SRX7917432/SRX7917432.05_peaks.narrowPeak INFO @ Sat, 08 Aug 2020 12:53:46: #4 Write summits bed file... /home/okishinya/chipatlas/results/dm3/SRX7917432/SRX7917432.05_summits.bed INFO @ Sat, 08 Aug 2020 12:53:46: Done! pass1 - making usageList (5 chroms): 1 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 12:54:02: # Command line: callpeak -t /home/okishinya/chipatlas/results/dm3/SRX7917432/SRX7917432.bam -f BAM -g dm -n /home/okishinya/chipatlas/results/dm3/SRX7917432/SRX7917432.10 -q 1e-10 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/dm3/SRX7917432/SRX7917432.10 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/dm3/SRX7917432/SRX7917432.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 12:54:02: #1 read tag files... INFO @ Sat, 08 Aug 2020 12:54:02: #1 read treatment tags... INFO @ Sat, 08 Aug 2020 12:54:07: 1000000 INFO @ Sat, 08 Aug 2020 12:54:12: 2000000 INFO @ Sat, 08 Aug 2020 12:54:14: #1 tag size is determined as 62 bps INFO @ Sat, 08 Aug 2020 12:54:14: #1 tag size = 62 INFO @ Sat, 08 Aug 2020 12:54:14: #1 total tags in treatment: 957505 INFO @ Sat, 08 Aug 2020 12:54:14: #1 user defined the maximum tags... INFO @ Sat, 08 Aug 2020 12:54:14: #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 12:54:14: #1 tags after filtering in treatment: 706292 INFO @ Sat, 08 Aug 2020 12:54:14: #1 Redundant rate of treatment: 0.26 INFO @ Sat, 08 Aug 2020 12:54:14: #1 finished! INFO @ Sat, 08 Aug 2020 12:54:14: #2 Build Peak Model... INFO @ Sat, 08 Aug 2020 12:54:14: #2 looking for paired plus/minus strand peaks... INFO @ Sat, 08 Aug 2020 12:54:14: #2 number of paired peaks: 2724 INFO @ Sat, 08 Aug 2020 12:54:14: start model_add_line... INFO @ Sat, 08 Aug 2020 12:54:14: start X-correlation... INFO @ Sat, 08 Aug 2020 12:54:14: end of X-cor INFO @ Sat, 08 Aug 2020 12:54:14: #2 finished! INFO @ Sat, 08 Aug 2020 12:54:14: #2 predicted fragment length is 191 bps INFO @ Sat, 08 Aug 2020 12:54:14: #2 alternative fragment length(s) may be 2,41,191,223,269 bps INFO @ Sat, 08 Aug 2020 12:54:14: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/dm3/SRX7917432/SRX7917432.10_model.r INFO @ Sat, 08 Aug 2020 12:54:14: #3 Call peaks... INFO @ Sat, 08 Aug 2020 12:54:14: #3 Pre-compute pvalue-qvalue table... INFO @ Sat, 08 Aug 2020 12:54:15: #3 Call peaks for each chromosome... INFO @ Sat, 08 Aug 2020 12:54:16: #4 Write output xls file... /home/okishinya/chipatlas/results/dm3/SRX7917432/SRX7917432.10_peaks.xls INFO @ Sat, 08 Aug 2020 12:54:16: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/dm3/SRX7917432/SRX7917432.10_peaks.narrowPeak INFO @ Sat, 08 Aug 2020 12:54:16: #4 Write summits bed file... /home/okishinya/chipatlas/results/dm3/SRX7917432/SRX7917432.10_summits.bed INFO @ Sat, 08 Aug 2020 12:54:16: Done! pass1 - making usageList (1 chroms): 0 millis pass2 - checking and writing primary data (4 records, 4 fields): 1 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 12:54:32: # Command line: callpeak -t /home/okishinya/chipatlas/results/dm3/SRX7917432/SRX7917432.bam -f BAM -g dm -n /home/okishinya/chipatlas/results/dm3/SRX7917432/SRX7917432.20 -q 1e-20 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/dm3/SRX7917432/SRX7917432.20 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/dm3/SRX7917432/SRX7917432.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 12:54:32: #1 read tag files... INFO @ Sat, 08 Aug 2020 12:54:32: #1 read treatment tags... INFO @ Sat, 08 Aug 2020 12:54:37: 1000000 BedGraph に変換しました。 BigWig に変換中... INFO @ Sat, 08 Aug 2020 12:54:41: 2000000 BigWig に変換しました。 INFO @ Sat, 08 Aug 2020 12:54:44: #1 tag size is determined as 62 bps INFO @ Sat, 08 Aug 2020 12:54:44: #1 tag size = 62 INFO @ Sat, 08 Aug 2020 12:54:44: #1 total tags in treatment: 957505 INFO @ Sat, 08 Aug 2020 12:54:44: #1 user defined the maximum tags... INFO @ Sat, 08 Aug 2020 12:54:44: #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 12:54:44: #1 tags after filtering in treatment: 706292 INFO @ Sat, 08 Aug 2020 12:54:44: #1 Redundant rate of treatment: 0.26 INFO @ Sat, 08 Aug 2020 12:54:44: #1 finished! INFO @ Sat, 08 Aug 2020 12:54:44: #2 Build Peak Model... INFO @ Sat, 08 Aug 2020 12:54:44: #2 looking for paired plus/minus strand peaks... INFO @ Sat, 08 Aug 2020 12:54:44: #2 number of paired peaks: 2724 INFO @ Sat, 08 Aug 2020 12:54:44: start model_add_line... INFO @ Sat, 08 Aug 2020 12:54:44: start X-correlation... INFO @ Sat, 08 Aug 2020 12:54:44: end of X-cor INFO @ Sat, 08 Aug 2020 12:54:44: #2 finished! INFO @ Sat, 08 Aug 2020 12:54:44: #2 predicted fragment length is 191 bps INFO @ Sat, 08 Aug 2020 12:54:44: #2 alternative fragment length(s) may be 2,41,191,223,269 bps INFO @ Sat, 08 Aug 2020 12:54:44: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/dm3/SRX7917432/SRX7917432.20_model.r INFO @ Sat, 08 Aug 2020 12:54:44: #3 Call peaks... INFO @ Sat, 08 Aug 2020 12:54:44: #3 Pre-compute pvalue-qvalue table... INFO @ Sat, 08 Aug 2020 12:54:45: #3 Call peaks for each chromosome... INFO @ Sat, 08 Aug 2020 12:54:46: #4 Write output xls file... /home/okishinya/chipatlas/results/dm3/SRX7917432/SRX7917432.20_peaks.xls INFO @ Sat, 08 Aug 2020 12:54:46: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/dm3/SRX7917432/SRX7917432.20_peaks.narrowPeak INFO @ Sat, 08 Aug 2020 12:54:46: #4 Write summits bed file... /home/okishinya/chipatlas/results/dm3/SRX7917432/SRX7917432.20_summits.bed INFO @ Sat, 08 Aug 2020 12:54:46: Done! pass1 - making usageList (0 chroms): 1 millis needLargeMem: trying to allocate 0 bytes (limit: 17179869184) CompletedMACS2peakCalling