Job ID = 5720573 sra ファイルのダウンロード中... Read layout: SINGLE fastq に変換中... spots read : 12,412,264 reads read : 12,412,264 reads written : 12,412,264 rm: cannot remove ‘[DSE]RR*’: No such file or directory rm: cannot remove ‘/home/okishinya/ncbi/public/sra/SRR5289710.sra.cache’: No such file or directory 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: 00:00:01 Time loading mirror index: 00:00:00 Multiseed full-index search: 00:03:04 12412264 reads; of these: 12412264 (100.00%) were unpaired; of these: 1248511 (10.06%) aligned 0 times 9890353 (79.68%) aligned exactly 1 time 1273400 (10.26%) aligned >1 times 89.94% overall alignment rate Time searching: 00:03:05 Overall time: 00:03:05 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_sort_core] merging from 8 files... [bam_rmdupse_core] 4160460 / 11163753 = 0.3727 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 @ Thu, 16 Apr 2020 00:40:05: # Command line: callpeak -t /home/okishinya/chipatlas/results/dm3/SRX2592433/SRX2592433.bam -f BAM -g dm -n /home/okishinya/chipatlas/results/dm3/SRX2592433/SRX2592433.05 -q 1e-05 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/dm3/SRX2592433/SRX2592433.05 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/dm3/SRX2592433/SRX2592433.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 @ Thu, 16 Apr 2020 00:40:05: #1 read tag files... INFO @ Thu, 16 Apr 2020 00:40:05: #1 read treatment tags... INFO @ Thu, 16 Apr 2020 00:40:10: 1000000 INFO @ Thu, 16 Apr 2020 00:40:14: 2000000 INFO @ Thu, 16 Apr 2020 00:40:19: 3000000 INFO @ Thu, 16 Apr 2020 00:40:24: 4000000 INFO @ Thu, 16 Apr 2020 00:40:29: 5000000 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 @ Thu, 16 Apr 2020 00:40:34: 6000000 INFO @ Thu, 16 Apr 2020 00:40:35: # Command line: callpeak -t /home/okishinya/chipatlas/results/dm3/SRX2592433/SRX2592433.bam -f BAM -g dm -n /home/okishinya/chipatlas/results/dm3/SRX2592433/SRX2592433.10 -q 1e-10 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/dm3/SRX2592433/SRX2592433.10 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/dm3/SRX2592433/SRX2592433.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 @ Thu, 16 Apr 2020 00:40:35: #1 read tag files... INFO @ Thu, 16 Apr 2020 00:40:35: #1 read treatment tags... INFO @ Thu, 16 Apr 2020 00:40:39: 7000000 INFO @ Thu, 16 Apr 2020 00:40:39: #1 tag size is determined as 51 bps INFO @ Thu, 16 Apr 2020 00:40:39: #1 tag size = 51 INFO @ Thu, 16 Apr 2020 00:40:39: #1 total tags in treatment: 7003293 INFO @ Thu, 16 Apr 2020 00:40:39: #1 user defined the maximum tags... INFO @ Thu, 16 Apr 2020 00:40:39: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Thu, 16 Apr 2020 00:40:39: #1 tags after filtering in treatment: 7003293 INFO @ Thu, 16 Apr 2020 00:40:39: #1 Redundant rate of treatment: 0.00 INFO @ Thu, 16 Apr 2020 00:40:39: #1 finished! INFO @ Thu, 16 Apr 2020 00:40:39: #2 Build Peak Model... INFO @ Thu, 16 Apr 2020 00:40:39: #2 looking for paired plus/minus strand peaks... INFO @ Thu, 16 Apr 2020 00:40:40: 1000000 INFO @ Thu, 16 Apr 2020 00:40:40: #2 number of paired peaks: 311 WARNING @ Thu, 16 Apr 2020 00:40:40: Fewer paired peaks (311) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 311 pairs to build model! INFO @ Thu, 16 Apr 2020 00:40:40: start model_add_line... INFO @ Thu, 16 Apr 2020 00:40:40: start X-correlation... INFO @ Thu, 16 Apr 2020 00:40:40: end of X-cor INFO @ Thu, 16 Apr 2020 00:40:40: #2 finished! INFO @ Thu, 16 Apr 2020 00:40:40: #2 predicted fragment length is 272 bps INFO @ Thu, 16 Apr 2020 00:40:40: #2 alternative fragment length(s) may be 272 bps INFO @ Thu, 16 Apr 2020 00:40:40: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/dm3/SRX2592433/SRX2592433.05_model.r INFO @ Thu, 16 Apr 2020 00:40:40: #3 Call peaks... INFO @ Thu, 16 Apr 2020 00:40:40: #3 Pre-compute pvalue-qvalue table... INFO @ Thu, 16 Apr 2020 00:40:45: 2000000 INFO @ Thu, 16 Apr 2020 00:40:50: 3000000 INFO @ Thu, 16 Apr 2020 00:40:55: 4000000 INFO @ Thu, 16 Apr 2020 00:41:01: 5000000 INFO @ Thu, 16 Apr 2020 00:41:02: #3 Call peaks for each chromosome... 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 @ Thu, 16 Apr 2020 00:41:05: # Command line: callpeak -t /home/okishinya/chipatlas/results/dm3/SRX2592433/SRX2592433.bam -f BAM -g dm -n /home/okishinya/chipatlas/results/dm3/SRX2592433/SRX2592433.20 -q 1e-20 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/dm3/SRX2592433/SRX2592433.20 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/dm3/SRX2592433/SRX2592433.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 @ Thu, 16 Apr 2020 00:41:05: #1 read tag files... INFO @ Thu, 16 Apr 2020 00:41:05: #1 read treatment tags... INFO @ Thu, 16 Apr 2020 00:41:06: 6000000 INFO @ Thu, 16 Apr 2020 00:41:10: 1000000 INFO @ Thu, 16 Apr 2020 00:41:11: 7000000 INFO @ Thu, 16 Apr 2020 00:41:11: #1 tag size is determined as 51 bps INFO @ Thu, 16 Apr 2020 00:41:11: #1 tag size = 51 INFO @ Thu, 16 Apr 2020 00:41:11: #1 total tags in treatment: 7003293 INFO @ Thu, 16 Apr 2020 00:41:11: #1 user defined the maximum tags... INFO @ Thu, 16 Apr 2020 00:41:11: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Thu, 16 Apr 2020 00:41:11: #1 tags after filtering in treatment: 7003293 INFO @ Thu, 16 Apr 2020 00:41:11: #1 Redundant rate of treatment: 0.00 INFO @ Thu, 16 Apr 2020 00:41:11: #1 finished! INFO @ Thu, 16 Apr 2020 00:41:11: #2 Build Peak Model... INFO @ Thu, 16 Apr 2020 00:41:11: #2 looking for paired plus/minus strand peaks... INFO @ Thu, 16 Apr 2020 00:41:12: #2 number of paired peaks: 311 WARNING @ Thu, 16 Apr 2020 00:41:12: Fewer paired peaks (311) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 311 pairs to build model! INFO @ Thu, 16 Apr 2020 00:41:12: start model_add_line... INFO @ Thu, 16 Apr 2020 00:41:12: start X-correlation... INFO @ Thu, 16 Apr 2020 00:41:12: end of X-cor INFO @ Thu, 16 Apr 2020 00:41:12: #2 finished! INFO @ Thu, 16 Apr 2020 00:41:12: #2 predicted fragment length is 272 bps INFO @ Thu, 16 Apr 2020 00:41:12: #2 alternative fragment length(s) may be 272 bps INFO @ Thu, 16 Apr 2020 00:41:12: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/dm3/SRX2592433/SRX2592433.10_model.r INFO @ Thu, 16 Apr 2020 00:41:12: #3 Call peaks... INFO @ Thu, 16 Apr 2020 00:41:12: #3 Pre-compute pvalue-qvalue table... INFO @ Thu, 16 Apr 2020 00:41:12: #4 Write output xls file... /home/okishinya/chipatlas/results/dm3/SRX2592433/SRX2592433.05_peaks.xls INFO @ Thu, 16 Apr 2020 00:41:12: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/dm3/SRX2592433/SRX2592433.05_peaks.narrowPeak INFO @ Thu, 16 Apr 2020 00:41:12: #4 Write summits bed file... /home/okishinya/chipatlas/results/dm3/SRX2592433/SRX2592433.05_summits.bed INFO @ Thu, 16 Apr 2020 00:41:12: Done! pass1 - making usageList (13 chroms): 2 millis pass2 - checking and writing primary data (12203 records, 4 fields): 13 millis CompletedMACS2peakCalling INFO @ Thu, 16 Apr 2020 00:41:16: 2000000 INFO @ Thu, 16 Apr 2020 00:41:21: 3000000 INFO @ Thu, 16 Apr 2020 00:41:27: 4000000 INFO @ Thu, 16 Apr 2020 00:41:32: #3 Call peaks for each chromosome... INFO @ Thu, 16 Apr 2020 00:41:32: 5000000 INFO @ Thu, 16 Apr 2020 00:41:38: 6000000 INFO @ Thu, 16 Apr 2020 00:41:42: #4 Write output xls file... /home/okishinya/chipatlas/results/dm3/SRX2592433/SRX2592433.10_peaks.xls INFO @ Thu, 16 Apr 2020 00:41:42: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/dm3/SRX2592433/SRX2592433.10_peaks.narrowPeak INFO @ Thu, 16 Apr 2020 00:41:42: #4 Write summits bed file... /home/okishinya/chipatlas/results/dm3/SRX2592433/SRX2592433.10_summits.bed INFO @ Thu, 16 Apr 2020 00:41:42: Done! pass1 - making usageList (13 chroms): 2 millis pass2 - checking and writing primary data (9527 records, 4 fields): 11 millis CompletedMACS2peakCalling INFO @ Thu, 16 Apr 2020 00:41:43: 7000000 INFO @ Thu, 16 Apr 2020 00:41:43: #1 tag size is determined as 51 bps INFO @ Thu, 16 Apr 2020 00:41:43: #1 tag size = 51 INFO @ Thu, 16 Apr 2020 00:41:43: #1 total tags in treatment: 7003293 INFO @ Thu, 16 Apr 2020 00:41:43: #1 user defined the maximum tags... INFO @ Thu, 16 Apr 2020 00:41:43: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Thu, 16 Apr 2020 00:41:43: #1 tags after filtering in treatment: 7003293 INFO @ Thu, 16 Apr 2020 00:41:43: #1 Redundant rate of treatment: 0.00 INFO @ Thu, 16 Apr 2020 00:41:43: #1 finished! INFO @ Thu, 16 Apr 2020 00:41:43: #2 Build Peak Model... INFO @ Thu, 16 Apr 2020 00:41:43: #2 looking for paired plus/minus strand peaks... INFO @ Thu, 16 Apr 2020 00:41:44: #2 number of paired peaks: 311 WARNING @ Thu, 16 Apr 2020 00:41:44: Fewer paired peaks (311) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 311 pairs to build model! INFO @ Thu, 16 Apr 2020 00:41:44: start model_add_line... INFO @ Thu, 16 Apr 2020 00:41:44: start X-correlation... INFO @ Thu, 16 Apr 2020 00:41:44: end of X-cor INFO @ Thu, 16 Apr 2020 00:41:44: #2 finished! INFO @ Thu, 16 Apr 2020 00:41:44: #2 predicted fragment length is 272 bps INFO @ Thu, 16 Apr 2020 00:41:44: #2 alternative fragment length(s) may be 272 bps INFO @ Thu, 16 Apr 2020 00:41:44: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/dm3/SRX2592433/SRX2592433.20_model.r INFO @ Thu, 16 Apr 2020 00:41:44: #3 Call peaks... INFO @ Thu, 16 Apr 2020 00:41:44: #3 Pre-compute pvalue-qvalue table... INFO @ Thu, 16 Apr 2020 00:42:05: #3 Call peaks for each chromosome... INFO @ Thu, 16 Apr 2020 00:42:14: #4 Write output xls file... /home/okishinya/chipatlas/results/dm3/SRX2592433/SRX2592433.20_peaks.xls INFO @ Thu, 16 Apr 2020 00:42:14: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/dm3/SRX2592433/SRX2592433.20_peaks.narrowPeak INFO @ Thu, 16 Apr 2020 00:42:14: #4 Write summits bed file... /home/okishinya/chipatlas/results/dm3/SRX2592433/SRX2592433.20_summits.bed INFO @ Thu, 16 Apr 2020 00:42:14: Done! pass1 - making usageList (13 chroms): 1 millis pass2 - checking and writing primary data (6874 records, 4 fields): 8 millis CompletedMACS2peakCalling BedGraph に変換しました。 BigWig に変換中... BigWig に変換しました。