Job ID = 6367276 SRX = SRX330986 Genome = ce11 sra ファイルのダウンロード中... Read layout: SINGLE fastq に変換中... 2020-06-15T23:18:01 prefetch.2.10.7: 1) Downloading 'SRR947191'... 2020-06-15T23:18:01 prefetch.2.10.7: Downloading via HTTPS... 2020-06-15T23:19:46 prefetch.2.10.7: HTTPS download succeed 2020-06-15T23:19:46 prefetch.2.10.7: 1) 'SRR947191' was downloaded successfully Read 13785217 spots for SRR947191/SRR947191.sra Written 13785217 spots for SRR947191/SRR947191.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: 00:04:30 13785217 reads; of these: 13785217 (100.00%) were unpaired; of these: 992026 (7.20%) aligned 0 times 10333517 (74.96%) aligned exactly 1 time 2459674 (17.84%) aligned >1 times 92.80% overall alignment rate Time searching: 00:04:30 Overall time: 00:04:30 マッピングが完了しました。 samtools でBAM に変換中... [samopen] SAM header is present: 7 sequences. [bam_sort_core] merging from 8 files... [bam_rmdupse_core] 10253030 / 12793191 = 0.8014 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, 16 Jun 2020 08:28:04: # Command line: callpeak -t /home/okishinya/chipatlas/results/ce11/SRX330986/SRX330986.bam -f BAM -g ce -n /home/okishinya/chipatlas/results/ce11/SRX330986/SRX330986.05 -q 1e-05 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/ce11/SRX330986/SRX330986.05 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/ce11/SRX330986/SRX330986.bam'] # control file = None # effective genome size = 9.00e+07 # 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, 16 Jun 2020 08:28:04: #1 read tag files... INFO @ Tue, 16 Jun 2020 08:28:04: #1 read treatment tags... INFO @ Tue, 16 Jun 2020 08:28:11: 1000000 INFO @ Tue, 16 Jun 2020 08:28:18: 2000000 INFO @ Tue, 16 Jun 2020 08:28:22: #1 tag size is determined as 76 bps INFO @ Tue, 16 Jun 2020 08:28:22: #1 tag size = 76 INFO @ Tue, 16 Jun 2020 08:28:22: #1 total tags in treatment: 2540161 INFO @ Tue, 16 Jun 2020 08:28:22: #1 user defined the maximum tags... INFO @ Tue, 16 Jun 2020 08:28:22: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Tue, 16 Jun 2020 08:28:22: #1 tags after filtering in treatment: 2540161 INFO @ Tue, 16 Jun 2020 08:28:22: #1 Redundant rate of treatment: 0.00 INFO @ Tue, 16 Jun 2020 08:28:22: #1 finished! INFO @ Tue, 16 Jun 2020 08:28:22: #2 Build Peak Model... INFO @ Tue, 16 Jun 2020 08:28:22: #2 looking for paired plus/minus strand peaks... INFO @ Tue, 16 Jun 2020 08:28:22: #2 number of paired peaks: 1483 INFO @ Tue, 16 Jun 2020 08:28:22: start model_add_line... INFO @ Tue, 16 Jun 2020 08:28:22: start X-correlation... INFO @ Tue, 16 Jun 2020 08:28:22: end of X-cor INFO @ Tue, 16 Jun 2020 08:28:22: #2 finished! INFO @ Tue, 16 Jun 2020 08:28:22: #2 predicted fragment length is 113 bps INFO @ Tue, 16 Jun 2020 08:28:22: #2 alternative fragment length(s) may be 113 bps INFO @ Tue, 16 Jun 2020 08:28:22: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/ce11/SRX330986/SRX330986.05_model.r WARNING @ Tue, 16 Jun 2020 08:28:22: #2 Since the d (113) calculated from paired-peaks are smaller than 2*tag length, it may be influenced by unknown sequencing problem! WARNING @ Tue, 16 Jun 2020 08:28:22: #2 You may need to consider one of the other alternative d(s): 113 WARNING @ Tue, 16 Jun 2020 08:28:22: #2 You can restart the process with --nomodel --extsize XXX with your choice or an arbitrary number. Nontheless, MACS will continute computing. INFO @ Tue, 16 Jun 2020 08:28:22: #3 Call peaks... INFO @ Tue, 16 Jun 2020 08:28:22: #3 Pre-compute pvalue-qvalue table... INFO @ Tue, 16 Jun 2020 08:28:28: #3 Call peaks for each chromosome... INFO @ Tue, 16 Jun 2020 08:28:31: #4 Write output xls file... /home/okishinya/chipatlas/results/ce11/SRX330986/SRX330986.05_peaks.xls INFO @ Tue, 16 Jun 2020 08:28:31: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/ce11/SRX330986/SRX330986.05_peaks.narrowPeak INFO @ Tue, 16 Jun 2020 08:28:31: #4 Write summits bed file... /home/okishinya/chipatlas/results/ce11/SRX330986/SRX330986.05_summits.bed INFO @ Tue, 16 Jun 2020 08:28:31: Done! pass1 - making usageList (7 chroms): 1 millis pass2 - checking and writing primary data (2090 records, 4 fields): 3 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, 16 Jun 2020 08:28:34: # Command line: callpeak -t /home/okishinya/chipatlas/results/ce11/SRX330986/SRX330986.bam -f BAM -g ce -n /home/okishinya/chipatlas/results/ce11/SRX330986/SRX330986.10 -q 1e-10 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/ce11/SRX330986/SRX330986.10 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/ce11/SRX330986/SRX330986.bam'] # control file = None # effective genome size = 9.00e+07 # 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, 16 Jun 2020 08:28:34: #1 read tag files... INFO @ Tue, 16 Jun 2020 08:28:34: #1 read treatment tags... INFO @ Tue, 16 Jun 2020 08:28:40: 1000000 INFO @ Tue, 16 Jun 2020 08:28:46: 2000000 INFO @ Tue, 16 Jun 2020 08:28:49: #1 tag size is determined as 76 bps INFO @ Tue, 16 Jun 2020 08:28:49: #1 tag size = 76 INFO @ Tue, 16 Jun 2020 08:28:49: #1 total tags in treatment: 2540161 INFO @ Tue, 16 Jun 2020 08:28:49: #1 user defined the maximum tags... INFO @ Tue, 16 Jun 2020 08:28:49: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Tue, 16 Jun 2020 08:28:49: #1 tags after filtering in treatment: 2540161 INFO @ Tue, 16 Jun 2020 08:28:49: #1 Redundant rate of treatment: 0.00 INFO @ Tue, 16 Jun 2020 08:28:49: #1 finished! INFO @ Tue, 16 Jun 2020 08:28:49: #2 Build Peak Model... INFO @ Tue, 16 Jun 2020 08:28:49: #2 looking for paired plus/minus strand peaks... INFO @ Tue, 16 Jun 2020 08:28:49: #2 number of paired peaks: 1483 INFO @ Tue, 16 Jun 2020 08:28:49: start model_add_line... INFO @ Tue, 16 Jun 2020 08:28:49: start X-correlation... INFO @ Tue, 16 Jun 2020 08:28:49: end of X-cor INFO @ Tue, 16 Jun 2020 08:28:49: #2 finished! INFO @ Tue, 16 Jun 2020 08:28:49: #2 predicted fragment length is 113 bps INFO @ Tue, 16 Jun 2020 08:28:49: #2 alternative fragment length(s) may be 113 bps INFO @ Tue, 16 Jun 2020 08:28:49: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/ce11/SRX330986/SRX330986.10_model.r WARNING @ Tue, 16 Jun 2020 08:28:49: #2 Since the d (113) calculated from paired-peaks are smaller than 2*tag length, it may be influenced by unknown sequencing problem! WARNING @ Tue, 16 Jun 2020 08:28:49: #2 You may need to consider one of the other alternative d(s): 113 WARNING @ Tue, 16 Jun 2020 08:28:49: #2 You can restart the process with --nomodel --extsize XXX with your choice or an arbitrary number. Nontheless, MACS will continute computing. INFO @ Tue, 16 Jun 2020 08:28:49: #3 Call peaks... INFO @ Tue, 16 Jun 2020 08:28:49: #3 Pre-compute pvalue-qvalue table... INFO @ Tue, 16 Jun 2020 08:28:55: #3 Call peaks for each chromosome... INFO @ Tue, 16 Jun 2020 08:28:58: #4 Write output xls file... /home/okishinya/chipatlas/results/ce11/SRX330986/SRX330986.10_peaks.xls INFO @ Tue, 16 Jun 2020 08:28:58: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/ce11/SRX330986/SRX330986.10_peaks.narrowPeak INFO @ Tue, 16 Jun 2020 08:28:58: #4 Write summits bed file... /home/okishinya/chipatlas/results/ce11/SRX330986/SRX330986.10_summits.bed INFO @ Tue, 16 Jun 2020 08:28:58: Done! pass1 - making usageList (6 chroms): 1 millis pass2 - checking and writing primary data (1337 records, 4 fields): 2 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, 16 Jun 2020 08:29:04: # Command line: callpeak -t /home/okishinya/chipatlas/results/ce11/SRX330986/SRX330986.bam -f BAM -g ce -n /home/okishinya/chipatlas/results/ce11/SRX330986/SRX330986.20 -q 1e-20 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/ce11/SRX330986/SRX330986.20 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/ce11/SRX330986/SRX330986.bam'] # control file = None # effective genome size = 9.00e+07 # 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, 16 Jun 2020 08:29:04: #1 read tag files... INFO @ Tue, 16 Jun 2020 08:29:04: #1 read treatment tags... INFO @ Tue, 16 Jun 2020 08:29:10: 1000000 BedGraph に変換しました。 BigWig に変換中... INFO @ Tue, 16 Jun 2020 08:29:16: 2000000 INFO @ Tue, 16 Jun 2020 08:29:19: #1 tag size is determined as 76 bps INFO @ Tue, 16 Jun 2020 08:29:19: #1 tag size = 76 INFO @ Tue, 16 Jun 2020 08:29:19: #1 total tags in treatment: 2540161 INFO @ Tue, 16 Jun 2020 08:29:19: #1 user defined the maximum tags... INFO @ Tue, 16 Jun 2020 08:29:19: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Tue, 16 Jun 2020 08:29:19: #1 tags after filtering in treatment: 2540161 INFO @ Tue, 16 Jun 2020 08:29:19: #1 Redundant rate of treatment: 0.00 INFO @ Tue, 16 Jun 2020 08:29:19: #1 finished! INFO @ Tue, 16 Jun 2020 08:29:19: #2 Build Peak Model... INFO @ Tue, 16 Jun 2020 08:29:19: #2 looking for paired plus/minus strand peaks... INFO @ Tue, 16 Jun 2020 08:29:19: #2 number of paired peaks: 1483 INFO @ Tue, 16 Jun 2020 08:29:19: start model_add_line... INFO @ Tue, 16 Jun 2020 08:29:19: start X-correlation... INFO @ Tue, 16 Jun 2020 08:29:19: end of X-cor INFO @ Tue, 16 Jun 2020 08:29:19: #2 finished! INFO @ Tue, 16 Jun 2020 08:29:19: #2 predicted fragment length is 113 bps INFO @ Tue, 16 Jun 2020 08:29:19: #2 alternative fragment length(s) may be 113 bps INFO @ Tue, 16 Jun 2020 08:29:19: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/ce11/SRX330986/SRX330986.20_model.r WARNING @ Tue, 16 Jun 2020 08:29:19: #2 Since the d (113) calculated from paired-peaks are smaller than 2*tag length, it may be influenced by unknown sequencing problem! WARNING @ Tue, 16 Jun 2020 08:29:19: #2 You may need to consider one of the other alternative d(s): 113 WARNING @ Tue, 16 Jun 2020 08:29:19: #2 You can restart the process with --nomodel --extsize XXX with your choice or an arbitrary number. Nontheless, MACS will continute computing. INFO @ Tue, 16 Jun 2020 08:29:19: #3 Call peaks... INFO @ Tue, 16 Jun 2020 08:29:19: #3 Pre-compute pvalue-qvalue table... BigWig に変換しました。 INFO @ Tue, 16 Jun 2020 08:29:25: #3 Call peaks for each chromosome... INFO @ Tue, 16 Jun 2020 08:29:28: #4 Write output xls file... /home/okishinya/chipatlas/results/ce11/SRX330986/SRX330986.20_peaks.xls INFO @ Tue, 16 Jun 2020 08:29:28: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/ce11/SRX330986/SRX330986.20_peaks.narrowPeak INFO @ Tue, 16 Jun 2020 08:29:28: #4 Write summits bed file... /home/okishinya/chipatlas/results/ce11/SRX330986/SRX330986.20_summits.bed INFO @ Tue, 16 Jun 2020 08:29:28: Done! pass1 - making usageList (6 chroms): 1 millis pass2 - checking and writing primary data (752 records, 4 fields): 2 millis CompletedMACS2peakCalling