Job ID = 6528430 SRX = SRX6441116 Genome = dm3 sra ファイルのダウンロード中... Read layout: PAIRED fastq に変換中... 2020-06-29T14:56:14 prefetch.2.10.7: 1) Downloading 'SRR9680914'... 2020-06-29T14:56:14 prefetch.2.10.7: Downloading via HTTPS... 2020-06-29T14:56:53 prefetch.2.10.7: HTTPS download succeed 2020-06-29T14:56:53 prefetch.2.10.7: 'SRR9680914' is valid 2020-06-29T14:56:53 prefetch.2.10.7: 1) 'SRR9680914' was downloaded successfully 2020-06-29T14:56:53 prefetch.2.10.7: 'SRR9680914' has 0 unresolved dependencies Read 1601766 spots for SRR9680914/SRR9680914.sra Written 1601766 spots for SRR9680914/SRR9680914.sra fastq に変換しました。 bowtie でマッピング中... Time loading reference: 00:00:00 Time loading forward index: 00:00:00 Time loading mirror index: 00:00:00 Multiseed full-index search: 00:02:47 1601766 reads; of these: 1601766 (100.00%) were paired; of these: 519762 (32.45%) aligned concordantly 0 times 814994 (50.88%) aligned concordantly exactly 1 time 267010 (16.67%) aligned concordantly >1 times ---- 519762 pairs aligned concordantly 0 times; of these: 142023 (27.32%) aligned discordantly 1 time ---- 377739 pairs aligned 0 times concordantly or discordantly; of these: 755478 mates make up the pairs; of these: 396753 (52.52%) aligned 0 times 204727 (27.10%) aligned exactly 1 time 153998 (20.38%) aligned >1 times 87.62% overall alignment rate Time searching: 00:02:47 Overall time: 00:02:47 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_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] 791271 / 1221411 = 0.6478 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 @ Tue, 30 Jun 2020 00:02:09: # Command line: callpeak -t /home/okishinya/chipatlas/results/dm3/SRX6441116/SRX6441116.bam -f BAM -g dm -n /home/okishinya/chipatlas/results/dm3/SRX6441116/SRX6441116.05 -q 1e-05 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/dm3/SRX6441116/SRX6441116.05 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/dm3/SRX6441116/SRX6441116.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 @ Tue, 30 Jun 2020 00:02:09: #1 read tag files... INFO @ Tue, 30 Jun 2020 00:02:09: #1 read treatment tags... INFO @ Tue, 30 Jun 2020 00:02:15: 1000000 INFO @ Tue, 30 Jun 2020 00:02:16: #1 tag size is determined as 82 bps INFO @ Tue, 30 Jun 2020 00:02:16: #1 tag size = 82 INFO @ Tue, 30 Jun 2020 00:02:16: #1 total tags in treatment: 371429 INFO @ Tue, 30 Jun 2020 00:02:16: #1 user defined the maximum tags... INFO @ Tue, 30 Jun 2020 00:02:16: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Tue, 30 Jun 2020 00:02:16: #1 tags after filtering in treatment: 300519 INFO @ Tue, 30 Jun 2020 00:02:16: #1 Redundant rate of treatment: 0.19 INFO @ Tue, 30 Jun 2020 00:02:16: #1 finished! INFO @ Tue, 30 Jun 2020 00:02:16: #2 Build Peak Model... INFO @ Tue, 30 Jun 2020 00:02:16: #2 looking for paired plus/minus strand peaks... INFO @ Tue, 30 Jun 2020 00:02:16: #2 number of paired peaks: 4228 INFO @ Tue, 30 Jun 2020 00:02:16: start model_add_line... INFO @ Tue, 30 Jun 2020 00:02:16: start X-correlation... INFO @ Tue, 30 Jun 2020 00:02:16: end of X-cor INFO @ Tue, 30 Jun 2020 00:02:16: #2 finished! INFO @ Tue, 30 Jun 2020 00:02:16: #2 predicted fragment length is 356 bps INFO @ Tue, 30 Jun 2020 00:02:16: #2 alternative fragment length(s) may be 9,245,356 bps INFO @ Tue, 30 Jun 2020 00:02:16: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/dm3/SRX6441116/SRX6441116.05_model.r INFO @ Tue, 30 Jun 2020 00:02:16: #3 Call peaks... INFO @ Tue, 30 Jun 2020 00:02:16: #3 Pre-compute pvalue-qvalue table... INFO @ Tue, 30 Jun 2020 00:02:17: #3 Call peaks for each chromosome... INFO @ Tue, 30 Jun 2020 00:02:17: #4 Write output xls file... /home/okishinya/chipatlas/results/dm3/SRX6441116/SRX6441116.05_peaks.xls INFO @ Tue, 30 Jun 2020 00:02:17: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/dm3/SRX6441116/SRX6441116.05_peaks.narrowPeak INFO @ Tue, 30 Jun 2020 00:02:17: #4 Write summits bed file... /home/okishinya/chipatlas/results/dm3/SRX6441116/SRX6441116.05_summits.bed INFO @ Tue, 30 Jun 2020 00:02:17: Done! pass1 - making usageList (6 chroms): 0 millis pass2 - checking and writing primary data (38 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 @ Tue, 30 Jun 2020 00:02:39: # Command line: callpeak -t /home/okishinya/chipatlas/results/dm3/SRX6441116/SRX6441116.bam -f BAM -g dm -n /home/okishinya/chipatlas/results/dm3/SRX6441116/SRX6441116.10 -q 1e-10 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/dm3/SRX6441116/SRX6441116.10 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/dm3/SRX6441116/SRX6441116.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 @ Tue, 30 Jun 2020 00:02:39: #1 read tag files... INFO @ Tue, 30 Jun 2020 00:02:39: #1 read treatment tags... INFO @ Tue, 30 Jun 2020 00:02:45: 1000000 INFO @ Tue, 30 Jun 2020 00:02:46: #1 tag size is determined as 82 bps INFO @ Tue, 30 Jun 2020 00:02:46: #1 tag size = 82 INFO @ Tue, 30 Jun 2020 00:02:46: #1 total tags in treatment: 371429 INFO @ Tue, 30 Jun 2020 00:02:46: #1 user defined the maximum tags... INFO @ Tue, 30 Jun 2020 00:02:46: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Tue, 30 Jun 2020 00:02:46: #1 tags after filtering in treatment: 300519 INFO @ Tue, 30 Jun 2020 00:02:46: #1 Redundant rate of treatment: 0.19 INFO @ Tue, 30 Jun 2020 00:02:46: #1 finished! INFO @ Tue, 30 Jun 2020 00:02:46: #2 Build Peak Model... INFO @ Tue, 30 Jun 2020 00:02:46: #2 looking for paired plus/minus strand peaks... INFO @ Tue, 30 Jun 2020 00:02:46: #2 number of paired peaks: 4228 INFO @ Tue, 30 Jun 2020 00:02:46: start model_add_line... INFO @ Tue, 30 Jun 2020 00:02:46: start X-correlation... INFO @ Tue, 30 Jun 2020 00:02:46: end of X-cor INFO @ Tue, 30 Jun 2020 00:02:46: #2 finished! INFO @ Tue, 30 Jun 2020 00:02:46: #2 predicted fragment length is 356 bps INFO @ Tue, 30 Jun 2020 00:02:46: #2 alternative fragment length(s) may be 9,245,356 bps INFO @ Tue, 30 Jun 2020 00:02:46: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/dm3/SRX6441116/SRX6441116.10_model.r INFO @ Tue, 30 Jun 2020 00:02:46: #3 Call peaks... INFO @ Tue, 30 Jun 2020 00:02:46: #3 Pre-compute pvalue-qvalue table... INFO @ Tue, 30 Jun 2020 00:02:47: #3 Call peaks for each chromosome... INFO @ Tue, 30 Jun 2020 00:02:47: #4 Write output xls file... /home/okishinya/chipatlas/results/dm3/SRX6441116/SRX6441116.10_peaks.xls INFO @ Tue, 30 Jun 2020 00:02:47: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/dm3/SRX6441116/SRX6441116.10_peaks.narrowPeak INFO @ Tue, 30 Jun 2020 00:02:47: #4 Write summits bed file... /home/okishinya/chipatlas/results/dm3/SRX6441116/SRX6441116.10_summits.bed INFO @ Tue, 30 Jun 2020 00:02:47: Done! pass1 - making usageList (2 chroms): 1 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 @ Tue, 30 Jun 2020 00:03:09: # Command line: callpeak -t /home/okishinya/chipatlas/results/dm3/SRX6441116/SRX6441116.bam -f BAM -g dm -n /home/okishinya/chipatlas/results/dm3/SRX6441116/SRX6441116.20 -q 1e-20 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/dm3/SRX6441116/SRX6441116.20 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/dm3/SRX6441116/SRX6441116.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 @ Tue, 30 Jun 2020 00:03:09: #1 read tag files... INFO @ Tue, 30 Jun 2020 00:03:09: #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 @ Tue, 30 Jun 2020 00:03:16: 1000000 INFO @ Tue, 30 Jun 2020 00:03:18: #1 tag size is determined as 82 bps INFO @ Tue, 30 Jun 2020 00:03:18: #1 tag size = 82 INFO @ Tue, 30 Jun 2020 00:03:18: #1 total tags in treatment: 371429 INFO @ Tue, 30 Jun 2020 00:03:18: #1 user defined the maximum tags... INFO @ Tue, 30 Jun 2020 00:03:18: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Tue, 30 Jun 2020 00:03:18: #1 tags after filtering in treatment: 300519 INFO @ Tue, 30 Jun 2020 00:03:18: #1 Redundant rate of treatment: 0.19 INFO @ Tue, 30 Jun 2020 00:03:18: #1 finished! INFO @ Tue, 30 Jun 2020 00:03:18: #2 Build Peak Model... INFO @ Tue, 30 Jun 2020 00:03:18: #2 looking for paired plus/minus strand peaks... INFO @ Tue, 30 Jun 2020 00:03:18: #2 number of paired peaks: 4228 INFO @ Tue, 30 Jun 2020 00:03:18: start model_add_line... INFO @ Tue, 30 Jun 2020 00:03:18: start X-correlation... INFO @ Tue, 30 Jun 2020 00:03:18: end of X-cor INFO @ Tue, 30 Jun 2020 00:03:18: #2 finished! INFO @ Tue, 30 Jun 2020 00:03:18: #2 predicted fragment length is 356 bps INFO @ Tue, 30 Jun 2020 00:03:18: #2 alternative fragment length(s) may be 9,245,356 bps INFO @ Tue, 30 Jun 2020 00:03:18: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/dm3/SRX6441116/SRX6441116.20_model.r INFO @ Tue, 30 Jun 2020 00:03:18: #3 Call peaks... INFO @ Tue, 30 Jun 2020 00:03:18: #3 Pre-compute pvalue-qvalue table... INFO @ Tue, 30 Jun 2020 00:03:19: #3 Call peaks for each chromosome... INFO @ Tue, 30 Jun 2020 00:03:19: #4 Write output xls file... /home/okishinya/chipatlas/results/dm3/SRX6441116/SRX6441116.20_peaks.xls INFO @ Tue, 30 Jun 2020 00:03:19: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/dm3/SRX6441116/SRX6441116.20_peaks.narrowPeak INFO @ Tue, 30 Jun 2020 00:03:19: #4 Write summits bed file... /home/okishinya/chipatlas/results/dm3/SRX6441116/SRX6441116.20_summits.bed INFO @ Tue, 30 Jun 2020 00:03:19: Done! pass1 - making usageList (0 chroms): 1 millis needLargeMem: trying to allocate 0 bytes (limit: 17179869184) CompletedMACS2peakCalling