Job ID = 6367466 SRX = SRX331223 Genome = ce11 sra ファイルのダウンロード中... Read layout: SINGLE fastq に変換中... 2020-06-15T23:37:29 prefetch.2.10.7: 1) Downloading 'SRR947455'... 2020-06-15T23:37:29 prefetch.2.10.7: Downloading via HTTPS... 2020-06-15T23:38:40 prefetch.2.10.7: HTTPS download succeed 2020-06-15T23:38:41 prefetch.2.10.7: 'SRR947455' is valid 2020-06-15T23:38:41 prefetch.2.10.7: 1) 'SRR947455' was downloaded successfully Read 6105564 spots for SRR947455/SRR947455.sra Written 6105564 spots for SRR947455/SRR947455.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: 00:01:01 6105564 reads; of these: 6105564 (100.00%) were unpaired; of these: 62768 (1.03%) aligned 0 times 5030043 (82.38%) aligned exactly 1 time 1012753 (16.59%) aligned >1 times 98.97% overall alignment rate Time searching: 00:01:01 Overall time: 00:01:01 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_rmdupse_core] 384868 / 6042796 = 0.0637 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 08:41:41: # Command line: callpeak -t /home/okishinya/chipatlas/results/ce11/SRX331223/SRX331223.bam -f BAM -g ce -n /home/okishinya/chipatlas/results/ce11/SRX331223/SRX331223.05 -q 1e-05 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/ce11/SRX331223/SRX331223.05 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/ce11/SRX331223/SRX331223.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 08:41:41: #1 read tag files... INFO @ Tue, 16 Jun 2020 08:41:41: #1 read treatment tags... INFO @ Tue, 16 Jun 2020 08:41:48: 1000000 INFO @ Tue, 16 Jun 2020 08:41:55: 2000000 INFO @ Tue, 16 Jun 2020 08:42:02: 3000000 INFO @ Tue, 16 Jun 2020 08:42:09: 4000000 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 08:42:11: # Command line: callpeak -t /home/okishinya/chipatlas/results/ce11/SRX331223/SRX331223.bam -f BAM -g ce -n /home/okishinya/chipatlas/results/ce11/SRX331223/SRX331223.10 -q 1e-10 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/ce11/SRX331223/SRX331223.10 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/ce11/SRX331223/SRX331223.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 08:42:11: #1 read tag files... INFO @ Tue, 16 Jun 2020 08:42:11: #1 read treatment tags... INFO @ Tue, 16 Jun 2020 08:42:16: 5000000 INFO @ Tue, 16 Jun 2020 08:42:19: 1000000 INFO @ Tue, 16 Jun 2020 08:42:21: #1 tag size is determined as 32 bps INFO @ Tue, 16 Jun 2020 08:42:21: #1 tag size = 32 INFO @ Tue, 16 Jun 2020 08:42:21: #1 total tags in treatment: 5657928 INFO @ Tue, 16 Jun 2020 08:42:21: #1 user defined the maximum tags... INFO @ Tue, 16 Jun 2020 08:42:21: #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 08:42:21: #1 tags after filtering in treatment: 5657928 INFO @ Tue, 16 Jun 2020 08:42:21: #1 Redundant rate of treatment: 0.00 INFO @ Tue, 16 Jun 2020 08:42:21: #1 finished! INFO @ Tue, 16 Jun 2020 08:42:21: #2 Build Peak Model... INFO @ Tue, 16 Jun 2020 08:42:21: #2 looking for paired plus/minus strand peaks... INFO @ Tue, 16 Jun 2020 08:42:21: #2 number of paired peaks: 410 WARNING @ Tue, 16 Jun 2020 08:42:21: Fewer paired peaks (410) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 410 pairs to build model! INFO @ Tue, 16 Jun 2020 08:42:21: start model_add_line... INFO @ Tue, 16 Jun 2020 08:42:21: start X-correlation... INFO @ Tue, 16 Jun 2020 08:42:21: end of X-cor INFO @ Tue, 16 Jun 2020 08:42:21: #2 finished! INFO @ Tue, 16 Jun 2020 08:42:21: #2 predicted fragment length is 32 bps INFO @ Tue, 16 Jun 2020 08:42:21: #2 alternative fragment length(s) may be 2,32 bps INFO @ Tue, 16 Jun 2020 08:42:21: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/ce11/SRX331223/SRX331223.05_model.r WARNING @ Tue, 16 Jun 2020 08:42:21: #2 Since the d (32) calculated from paired-peaks are smaller than 2*tag length, it may be influenced by unknown sequencing problem! WARNING @ Tue, 16 Jun 2020 08:42:21: #2 You may need to consider one of the other alternative d(s): 2,32 WARNING @ Tue, 16 Jun 2020 08:42:21: #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 08:42:21: #3 Call peaks... INFO @ Tue, 16 Jun 2020 08:42:21: #3 Pre-compute pvalue-qvalue table... INFO @ Tue, 16 Jun 2020 08:42:27: 2000000 INFO @ Tue, 16 Jun 2020 08:42:33: #3 Call peaks for each chromosome... INFO @ Tue, 16 Jun 2020 08:42:35: 3000000 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 08:42:40: #4 Write output xls file... /home/okishinya/chipatlas/results/ce11/SRX331223/SRX331223.05_peaks.xls INFO @ Tue, 16 Jun 2020 08:42:40: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/ce11/SRX331223/SRX331223.05_peaks.narrowPeak INFO @ Tue, 16 Jun 2020 08:42:40: #4 Write summits bed file... /home/okishinya/chipatlas/results/ce11/SRX331223/SRX331223.05_summits.bed INFO @ Tue, 16 Jun 2020 08:42:40: Done! pass1 - making usageList (6 chroms): 0 millis pass2 - checking and writing primary data (470 records, 4 fields): 2 millis CompletedMACS2peakCalling INFO @ Tue, 16 Jun 2020 08:42:41: # Command line: callpeak -t /home/okishinya/chipatlas/results/ce11/SRX331223/SRX331223.bam -f BAM -g ce -n /home/okishinya/chipatlas/results/ce11/SRX331223/SRX331223.20 -q 1e-20 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/ce11/SRX331223/SRX331223.20 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/ce11/SRX331223/SRX331223.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 08:42:41: #1 read tag files... INFO @ Tue, 16 Jun 2020 08:42:41: #1 read treatment tags... INFO @ Tue, 16 Jun 2020 08:42:42: 4000000 INFO @ Tue, 16 Jun 2020 08:42:48: 1000000 INFO @ Tue, 16 Jun 2020 08:42:50: 5000000 INFO @ Tue, 16 Jun 2020 08:42:55: #1 tag size is determined as 32 bps INFO @ Tue, 16 Jun 2020 08:42:55: #1 tag size = 32 INFO @ Tue, 16 Jun 2020 08:42:55: #1 total tags in treatment: 5657928 INFO @ Tue, 16 Jun 2020 08:42:55: #1 user defined the maximum tags... INFO @ Tue, 16 Jun 2020 08:42:55: #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 08:42:55: #1 tags after filtering in treatment: 5657928 INFO @ Tue, 16 Jun 2020 08:42:55: #1 Redundant rate of treatment: 0.00 INFO @ Tue, 16 Jun 2020 08:42:55: #1 finished! INFO @ Tue, 16 Jun 2020 08:42:55: #2 Build Peak Model... INFO @ Tue, 16 Jun 2020 08:42:55: #2 looking for paired plus/minus strand peaks... INFO @ Tue, 16 Jun 2020 08:42:55: 2000000 INFO @ Tue, 16 Jun 2020 08:42:55: #2 number of paired peaks: 410 WARNING @ Tue, 16 Jun 2020 08:42:55: Fewer paired peaks (410) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 410 pairs to build model! INFO @ Tue, 16 Jun 2020 08:42:55: start model_add_line... INFO @ Tue, 16 Jun 2020 08:42:55: start X-correlation... INFO @ Tue, 16 Jun 2020 08:42:55: end of X-cor INFO @ Tue, 16 Jun 2020 08:42:55: #2 finished! INFO @ Tue, 16 Jun 2020 08:42:55: #2 predicted fragment length is 32 bps INFO @ Tue, 16 Jun 2020 08:42:55: #2 alternative fragment length(s) may be 2,32 bps INFO @ Tue, 16 Jun 2020 08:42:55: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/ce11/SRX331223/SRX331223.10_model.r WARNING @ Tue, 16 Jun 2020 08:42:55: #2 Since the d (32) calculated from paired-peaks are smaller than 2*tag length, it may be influenced by unknown sequencing problem! WARNING @ Tue, 16 Jun 2020 08:42:55: #2 You may need to consider one of the other alternative d(s): 2,32 WARNING @ Tue, 16 Jun 2020 08:42:55: #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 08:42:55: #3 Call peaks... INFO @ Tue, 16 Jun 2020 08:42:55: #3 Pre-compute pvalue-qvalue table... INFO @ Tue, 16 Jun 2020 08:43:01: 3000000 INFO @ Tue, 16 Jun 2020 08:43:07: 4000000 INFO @ Tue, 16 Jun 2020 08:43:08: #3 Call peaks for each chromosome... BedGraph に変換しました。 BigWig に変換中... INFO @ Tue, 16 Jun 2020 08:43:13: 5000000 INFO @ Tue, 16 Jun 2020 08:43:14: #4 Write output xls file... /home/okishinya/chipatlas/results/ce11/SRX331223/SRX331223.10_peaks.xls INFO @ Tue, 16 Jun 2020 08:43:14: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/ce11/SRX331223/SRX331223.10_peaks.narrowPeak INFO @ Tue, 16 Jun 2020 08:43:14: #4 Write summits bed file... /home/okishinya/chipatlas/results/ce11/SRX331223/SRX331223.10_summits.bed INFO @ Tue, 16 Jun 2020 08:43:14: Done! pass1 - making usageList (6 chroms): 0 millis pass2 - checking and writing primary data (228 records, 4 fields): 2 millis CompletedMACS2peakCalling INFO @ Tue, 16 Jun 2020 08:43:16: #1 tag size is determined as 32 bps INFO @ Tue, 16 Jun 2020 08:43:16: #1 tag size = 32 INFO @ Tue, 16 Jun 2020 08:43:16: #1 total tags in treatment: 5657928 INFO @ Tue, 16 Jun 2020 08:43:16: #1 user defined the maximum tags... INFO @ Tue, 16 Jun 2020 08:43:16: #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 08:43:17: #1 tags after filtering in treatment: 5657928 INFO @ Tue, 16 Jun 2020 08:43:17: #1 Redundant rate of treatment: 0.00 INFO @ Tue, 16 Jun 2020 08:43:17: #1 finished! INFO @ Tue, 16 Jun 2020 08:43:17: #2 Build Peak Model... INFO @ Tue, 16 Jun 2020 08:43:17: #2 looking for paired plus/minus strand peaks... INFO @ Tue, 16 Jun 2020 08:43:17: #2 number of paired peaks: 410 WARNING @ Tue, 16 Jun 2020 08:43:17: Fewer paired peaks (410) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 410 pairs to build model! INFO @ Tue, 16 Jun 2020 08:43:17: start model_add_line... INFO @ Tue, 16 Jun 2020 08:43:17: start X-correlation... INFO @ Tue, 16 Jun 2020 08:43:17: end of X-cor INFO @ Tue, 16 Jun 2020 08:43:17: #2 finished! INFO @ Tue, 16 Jun 2020 08:43:17: #2 predicted fragment length is 32 bps INFO @ Tue, 16 Jun 2020 08:43:17: #2 alternative fragment length(s) may be 2,32 bps INFO @ Tue, 16 Jun 2020 08:43:17: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/ce11/SRX331223/SRX331223.20_model.r WARNING @ Tue, 16 Jun 2020 08:43:17: #2 Since the d (32) calculated from paired-peaks are smaller than 2*tag length, it may be influenced by unknown sequencing problem! WARNING @ Tue, 16 Jun 2020 08:43:17: #2 You may need to consider one of the other alternative d(s): 2,32 WARNING @ Tue, 16 Jun 2020 08:43:17: #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 08:43:17: #3 Call peaks... INFO @ Tue, 16 Jun 2020 08:43:17: #3 Pre-compute pvalue-qvalue table... BigWig に変換しました。 INFO @ Tue, 16 Jun 2020 08:43:29: #3 Call peaks for each chromosome... INFO @ Tue, 16 Jun 2020 08:43:35: #4 Write output xls file... /home/okishinya/chipatlas/results/ce11/SRX331223/SRX331223.20_peaks.xls INFO @ Tue, 16 Jun 2020 08:43:35: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/ce11/SRX331223/SRX331223.20_peaks.narrowPeak INFO @ Tue, 16 Jun 2020 08:43:35: #4 Write summits bed file... /home/okishinya/chipatlas/results/ce11/SRX331223/SRX331223.20_summits.bed INFO @ Tue, 16 Jun 2020 08:43:35: Done! pass1 - making usageList (6 chroms): 1 millis pass2 - checking and writing primary data (78 records, 4 fields): 1 millis CompletedMACS2peakCalling