Job ID = 6453994 SRX = SRX1760698 Genome = dm6 sra ファイルのダウンロード中... Read layout: SINGLE fastq に変換中... 2020-06-21T08:51:19 prefetch.2.10.7: 1) Downloading 'SRR3503056'... 2020-06-21T08:51:19 prefetch.2.10.7: Downloading via HTTPS... 2020-06-21T08:53:26 prefetch.2.10.7: HTTPS download succeed 2020-06-21T08:53:27 prefetch.2.10.7: 'SRR3503056' is valid 2020-06-21T08:53:27 prefetch.2.10.7: 1) 'SRR3503056' was downloaded successfully 2020-06-21T08:53:27 prefetch.2.10.7: 'SRR3503056' has 0 unresolved dependencies Read 5513917 spots for SRR3503056/SRR3503056.sra Written 5513917 spots for SRR3503056/SRR3503056.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: 00:00:01 Time loading mirror index: 00:00:00 Multiseed full-index search: 00:04:24 5513917 reads; of these: 5513917 (100.00%) were unpaired; of these: 2058109 (37.33%) aligned 0 times 2516749 (45.64%) aligned exactly 1 time 939059 (17.03%) aligned >1 times 62.67% overall alignment rate Time searching: 00:04:25 Overall time: 00:04:25 マッピングが完了しました。 samtools でBAM に変換中... [samopen] SAM header is present: 1870 sequences. [bam_rmdupse_core] 119706 / 3455808 = 0.0346 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 @ Sun, 21 Jun 2020 18:00:32: # Command line: callpeak -t /home/okishinya/chipatlas/results/dm6/SRX1760698/SRX1760698.bam -f BAM -g dm -n /home/okishinya/chipatlas/results/dm6/SRX1760698/SRX1760698.05 -q 1e-05 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/dm6/SRX1760698/SRX1760698.05 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/dm6/SRX1760698/SRX1760698.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 @ Sun, 21 Jun 2020 18:00:32: #1 read tag files... INFO @ Sun, 21 Jun 2020 18:00:32: #1 read treatment tags... INFO @ Sun, 21 Jun 2020 18:00:40: 1000000 INFO @ Sun, 21 Jun 2020 18:00:47: 2000000 INFO @ Sun, 21 Jun 2020 18:00:55: 3000000 INFO @ Sun, 21 Jun 2020 18:00:58: #1 tag size is determined as 151 bps INFO @ Sun, 21 Jun 2020 18:00:58: #1 tag size = 151 INFO @ Sun, 21 Jun 2020 18:00:58: #1 total tags in treatment: 3336102 INFO @ Sun, 21 Jun 2020 18:00:58: #1 user defined the maximum tags... INFO @ Sun, 21 Jun 2020 18:00:58: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Sun, 21 Jun 2020 18:00:58: #1 tags after filtering in treatment: 3335864 INFO @ Sun, 21 Jun 2020 18:00:58: #1 Redundant rate of treatment: 0.00 INFO @ Sun, 21 Jun 2020 18:00:58: #1 finished! INFO @ Sun, 21 Jun 2020 18:00:58: #2 Build Peak Model... INFO @ Sun, 21 Jun 2020 18:00:58: #2 looking for paired plus/minus strand peaks... INFO @ Sun, 21 Jun 2020 18:00:59: #2 number of paired peaks: 1006 INFO @ Sun, 21 Jun 2020 18:00:59: start model_add_line... INFO @ Sun, 21 Jun 2020 18:00:59: start X-correlation... INFO @ Sun, 21 Jun 2020 18:00:59: end of X-cor INFO @ Sun, 21 Jun 2020 18:00:59: #2 finished! INFO @ Sun, 21 Jun 2020 18:00:59: #2 predicted fragment length is 144 bps INFO @ Sun, 21 Jun 2020 18:00:59: #2 alternative fragment length(s) may be 144 bps INFO @ Sun, 21 Jun 2020 18:00:59: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/dm6/SRX1760698/SRX1760698.05_model.r WARNING @ Sun, 21 Jun 2020 18:00:59: #2 Since the d (144) calculated from paired-peaks are smaller than 2*tag length, it may be influenced by unknown sequencing problem! WARNING @ Sun, 21 Jun 2020 18:00:59: #2 You may need to consider one of the other alternative d(s): 144 WARNING @ Sun, 21 Jun 2020 18:00:59: #2 You can restart the process with --nomodel --extsize XXX with your choice or an arbitrary number. Nontheless, MACS will continute computing. INFO @ Sun, 21 Jun 2020 18:00:59: #3 Call peaks... INFO @ Sun, 21 Jun 2020 18:00:59: #3 Pre-compute pvalue-qvalue table... 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 @ Sun, 21 Jun 2020 18:01:02: # Command line: callpeak -t /home/okishinya/chipatlas/results/dm6/SRX1760698/SRX1760698.bam -f BAM -g dm -n /home/okishinya/chipatlas/results/dm6/SRX1760698/SRX1760698.10 -q 1e-10 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/dm6/SRX1760698/SRX1760698.10 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/dm6/SRX1760698/SRX1760698.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 @ Sun, 21 Jun 2020 18:01:02: #1 read tag files... INFO @ Sun, 21 Jun 2020 18:01:02: #1 read treatment tags... INFO @ Sun, 21 Jun 2020 18:01:07: #3 Call peaks for each chromosome... INFO @ Sun, 21 Jun 2020 18:01:10: 1000000 INFO @ Sun, 21 Jun 2020 18:01:11: #4 Write output xls file... /home/okishinya/chipatlas/results/dm6/SRX1760698/SRX1760698.05_peaks.xls INFO @ Sun, 21 Jun 2020 18:01:11: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/dm6/SRX1760698/SRX1760698.05_peaks.narrowPeak INFO @ Sun, 21 Jun 2020 18:01:11: #4 Write summits bed file... /home/okishinya/chipatlas/results/dm6/SRX1760698/SRX1760698.05_summits.bed INFO @ Sun, 21 Jun 2020 18:01:11: Done! pass1 - making usageList (543 chroms): 1 millis pass2 - checking and writing primary data (1249 records, 4 fields): 17 millis CompletedMACS2peakCalling INFO @ Sun, 21 Jun 2020 18:01:18: 2000000 INFO @ Sun, 21 Jun 2020 18:01:26: 3000000 INFO @ Sun, 21 Jun 2020 18:01:28: #1 tag size is determined as 151 bps INFO @ Sun, 21 Jun 2020 18:01:28: #1 tag size = 151 INFO @ Sun, 21 Jun 2020 18:01:28: #1 total tags in treatment: 3336102 INFO @ Sun, 21 Jun 2020 18:01:28: #1 user defined the maximum tags... INFO @ Sun, 21 Jun 2020 18:01:28: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Sun, 21 Jun 2020 18:01:29: #1 tags after filtering in treatment: 3335864 INFO @ Sun, 21 Jun 2020 18:01:29: #1 Redundant rate of treatment: 0.00 INFO @ Sun, 21 Jun 2020 18:01:29: #1 finished! INFO @ Sun, 21 Jun 2020 18:01:29: #2 Build Peak Model... INFO @ Sun, 21 Jun 2020 18:01:29: #2 looking for paired plus/minus strand peaks... INFO @ Sun, 21 Jun 2020 18:01:29: #2 number of paired peaks: 1006 INFO @ Sun, 21 Jun 2020 18:01:29: start model_add_line... INFO @ Sun, 21 Jun 2020 18:01:29: start X-correlation... INFO @ Sun, 21 Jun 2020 18:01:29: end of X-cor INFO @ Sun, 21 Jun 2020 18:01:29: #2 finished! INFO @ Sun, 21 Jun 2020 18:01:29: #2 predicted fragment length is 144 bps INFO @ Sun, 21 Jun 2020 18:01:29: #2 alternative fragment length(s) may be 144 bps INFO @ Sun, 21 Jun 2020 18:01:29: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/dm6/SRX1760698/SRX1760698.10_model.r WARNING @ Sun, 21 Jun 2020 18:01:29: #2 Since the d (144) calculated from paired-peaks are smaller than 2*tag length, it may be influenced by unknown sequencing problem! WARNING @ Sun, 21 Jun 2020 18:01:29: #2 You may need to consider one of the other alternative d(s): 144 WARNING @ Sun, 21 Jun 2020 18:01:29: #2 You can restart the process with --nomodel --extsize XXX with your choice or an arbitrary number. Nontheless, MACS will continute computing. INFO @ Sun, 21 Jun 2020 18:01:29: #3 Call peaks... INFO @ Sun, 21 Jun 2020 18:01:29: #3 Pre-compute pvalue-qvalue table... 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 @ Sun, 21 Jun 2020 18:01:32: # Command line: callpeak -t /home/okishinya/chipatlas/results/dm6/SRX1760698/SRX1760698.bam -f BAM -g dm -n /home/okishinya/chipatlas/results/dm6/SRX1760698/SRX1760698.20 -q 1e-20 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/dm6/SRX1760698/SRX1760698.20 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/dm6/SRX1760698/SRX1760698.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 @ Sun, 21 Jun 2020 18:01:32: #1 read tag files... INFO @ Sun, 21 Jun 2020 18:01:32: #1 read treatment tags... INFO @ Sun, 21 Jun 2020 18:01:38: #3 Call peaks for each chromosome... INFO @ Sun, 21 Jun 2020 18:01:40: 1000000 INFO @ Sun, 21 Jun 2020 18:01:42: #4 Write output xls file... /home/okishinya/chipatlas/results/dm6/SRX1760698/SRX1760698.10_peaks.xls INFO @ Sun, 21 Jun 2020 18:01:42: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/dm6/SRX1760698/SRX1760698.10_peaks.narrowPeak INFO @ Sun, 21 Jun 2020 18:01:42: #4 Write summits bed file... /home/okishinya/chipatlas/results/dm6/SRX1760698/SRX1760698.10_summits.bed INFO @ Sun, 21 Jun 2020 18:01:42: Done! pass1 - making usageList (449 chroms): 1 millis pass2 - checking and writing primary data (836 records, 4 fields): 14 millis CompletedMACS2peakCalling INFO @ Sun, 21 Jun 2020 18:01:47: 2000000 BedGraph に変換しました。 BigWig に変換中... INFO @ Sun, 21 Jun 2020 18:01:55: 3000000 INFO @ Sun, 21 Jun 2020 18:01:58: #1 tag size is determined as 151 bps INFO @ Sun, 21 Jun 2020 18:01:58: #1 tag size = 151 INFO @ Sun, 21 Jun 2020 18:01:58: #1 total tags in treatment: 3336102 INFO @ Sun, 21 Jun 2020 18:01:58: #1 user defined the maximum tags... INFO @ Sun, 21 Jun 2020 18:01:58: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Sun, 21 Jun 2020 18:01:58: #1 tags after filtering in treatment: 3335864 INFO @ Sun, 21 Jun 2020 18:01:58: #1 Redundant rate of treatment: 0.00 INFO @ Sun, 21 Jun 2020 18:01:58: #1 finished! INFO @ Sun, 21 Jun 2020 18:01:58: #2 Build Peak Model... INFO @ Sun, 21 Jun 2020 18:01:58: #2 looking for paired plus/minus strand peaks... INFO @ Sun, 21 Jun 2020 18:01:59: #2 number of paired peaks: 1006 INFO @ Sun, 21 Jun 2020 18:01:59: start model_add_line... INFO @ Sun, 21 Jun 2020 18:01:59: start X-correlation... INFO @ Sun, 21 Jun 2020 18:01:59: end of X-cor INFO @ Sun, 21 Jun 2020 18:01:59: #2 finished! INFO @ Sun, 21 Jun 2020 18:01:59: #2 predicted fragment length is 144 bps INFO @ Sun, 21 Jun 2020 18:01:59: #2 alternative fragment length(s) may be 144 bps INFO @ Sun, 21 Jun 2020 18:01:59: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/dm6/SRX1760698/SRX1760698.20_model.r WARNING @ Sun, 21 Jun 2020 18:01:59: #2 Since the d (144) calculated from paired-peaks are smaller than 2*tag length, it may be influenced by unknown sequencing problem! WARNING @ Sun, 21 Jun 2020 18:01:59: #2 You may need to consider one of the other alternative d(s): 144 WARNING @ Sun, 21 Jun 2020 18:01:59: #2 You can restart the process with --nomodel --extsize XXX with your choice or an arbitrary number. Nontheless, MACS will continute computing. INFO @ Sun, 21 Jun 2020 18:01:59: #3 Call peaks... INFO @ Sun, 21 Jun 2020 18:01:59: #3 Pre-compute pvalue-qvalue table... BigWig に変換しました。 INFO @ Sun, 21 Jun 2020 18:02:07: #3 Call peaks for each chromosome... INFO @ Sun, 21 Jun 2020 18:02:11: #4 Write output xls file... /home/okishinya/chipatlas/results/dm6/SRX1760698/SRX1760698.20_peaks.xls INFO @ Sun, 21 Jun 2020 18:02:11: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/dm6/SRX1760698/SRX1760698.20_peaks.narrowPeak INFO @ Sun, 21 Jun 2020 18:02:11: #4 Write summits bed file... /home/okishinya/chipatlas/results/dm6/SRX1760698/SRX1760698.20_summits.bed INFO @ Sun, 21 Jun 2020 18:02:11: Done! pass1 - making usageList (317 chroms): 1 millis pass2 - checking and writing primary data (458 records, 4 fields): 10 millis CompletedMACS2peakCalling