Job ID = 6366860 SRX = SRX235168 Genome = ce11 sra ファイルのダウンロード中... Read layout: SINGLE fastq に変換中... 2020-06-15T23:03:38 prefetch.2.10.7: 1) Downloading 'SRR708615'... 2020-06-15T23:03:38 prefetch.2.10.7: Downloading via HTTPS... 2020-06-15T23:03:53 prefetch.2.10.7: HTTPS download succeed 2020-06-15T23:03:53 prefetch.2.10.7: 'SRR708615' is valid 2020-06-15T23:03:53 prefetch.2.10.7: 1) 'SRR708615' was downloaded successfully Read 1161234 spots for SRR708615/SRR708615.sra Written 1161234 spots for SRR708615/SRR708615.sra 2020-06-15T23:04:07 prefetch.2.10.7: 1) Downloading 'SRR708616'... 2020-06-15T23:04:07 prefetch.2.10.7: Downloading via HTTPS... 2020-06-15T23:04:25 prefetch.2.10.7: HTTPS download succeed 2020-06-15T23:04:25 prefetch.2.10.7: 'SRR708616' is valid 2020-06-15T23:04:25 prefetch.2.10.7: 1) 'SRR708616' was downloaded successfully Read 1799780 spots for SRR708616/SRR708616.sra Written 1799780 spots for SRR708616/SRR708616.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: 00:00:20 2961014 reads; of these: 2961014 (100.00%) were unpaired; of these: 1362063 (46.00%) aligned 0 times 1324829 (44.74%) aligned exactly 1 time 274122 (9.26%) aligned >1 times 54.00% overall alignment rate Time searching: 00:00:20 Overall time: 00:00:20 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] 804086 / 1598951 = 0.5029 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 08:05:37: # Command line: callpeak -t /home/okishinya/chipatlas/results/ce11/SRX235168/SRX235168.bam -f BAM -g ce -n /home/okishinya/chipatlas/results/ce11/SRX235168/SRX235168.05 -q 1e-05 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/ce11/SRX235168/SRX235168.05 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/ce11/SRX235168/SRX235168.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 08:05:37: #1 read tag files... INFO @ Tue, 16 Jun 2020 08:05:37: #1 read treatment tags... INFO @ Tue, 16 Jun 2020 08:05:41: #1 tag size is determined as 32 bps INFO @ Tue, 16 Jun 2020 08:05:41: #1 tag size = 32 INFO @ Tue, 16 Jun 2020 08:05:41: #1 total tags in treatment: 794865 INFO @ Tue, 16 Jun 2020 08:05:41: #1 user defined the maximum tags... INFO @ Tue, 16 Jun 2020 08:05:41: #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 08:05:41: #1 tags after filtering in treatment: 794865 INFO @ Tue, 16 Jun 2020 08:05:41: #1 Redundant rate of treatment: 0.00 INFO @ Tue, 16 Jun 2020 08:05:41: #1 finished! INFO @ Tue, 16 Jun 2020 08:05:41: #2 Build Peak Model... INFO @ Tue, 16 Jun 2020 08:05:41: #2 looking for paired plus/minus strand peaks... INFO @ Tue, 16 Jun 2020 08:05:41: #2 number of paired peaks: 595 WARNING @ Tue, 16 Jun 2020 08:05:41: Fewer paired peaks (595) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 595 pairs to build model! INFO @ Tue, 16 Jun 2020 08:05:41: start model_add_line... INFO @ Tue, 16 Jun 2020 08:05:41: start X-correlation... INFO @ Tue, 16 Jun 2020 08:05:41: end of X-cor INFO @ Tue, 16 Jun 2020 08:05:41: #2 finished! INFO @ Tue, 16 Jun 2020 08:05:41: #2 predicted fragment length is 37 bps INFO @ Tue, 16 Jun 2020 08:05:41: #2 alternative fragment length(s) may be 37,57,83,110,531,557 bps INFO @ Tue, 16 Jun 2020 08:05:41: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/ce11/SRX235168/SRX235168.05_model.r WARNING @ Tue, 16 Jun 2020 08:05:41: #2 Since the d (37) calculated from paired-peaks are smaller than 2*tag length, it may be influenced by unknown sequencing problem! WARNING @ Tue, 16 Jun 2020 08:05:41: #2 You may need to consider one of the other alternative d(s): 37,57,83,110,531,557 WARNING @ Tue, 16 Jun 2020 08:05:41: #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 08:05:41: #3 Call peaks... INFO @ Tue, 16 Jun 2020 08:05:41: #3 Pre-compute pvalue-qvalue table... INFO @ Tue, 16 Jun 2020 08:05:43: #3 Call peaks for each chromosome... INFO @ Tue, 16 Jun 2020 08:05:44: #4 Write output xls file... /home/okishinya/chipatlas/results/ce11/SRX235168/SRX235168.05_peaks.xls INFO @ Tue, 16 Jun 2020 08:05:44: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/ce11/SRX235168/SRX235168.05_peaks.narrowPeak INFO @ Tue, 16 Jun 2020 08:05:44: #4 Write summits bed file... /home/okishinya/chipatlas/results/ce11/SRX235168/SRX235168.05_summits.bed INFO @ Tue, 16 Jun 2020 08:05:44: Done! pass1 - making usageList (6 chroms): 1 millis pass2 - checking and writing primary data (167 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, 16 Jun 2020 08:06:10: # Command line: callpeak -t /home/okishinya/chipatlas/results/ce11/SRX235168/SRX235168.bam -f BAM -g ce -n /home/okishinya/chipatlas/results/ce11/SRX235168/SRX235168.10 -q 1e-10 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/ce11/SRX235168/SRX235168.10 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/ce11/SRX235168/SRX235168.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 08:06:10: #1 read tag files... INFO @ Tue, 16 Jun 2020 08:06:10: #1 read treatment tags... INFO @ Tue, 16 Jun 2020 08:06:15: #1 tag size is determined as 32 bps INFO @ Tue, 16 Jun 2020 08:06:15: #1 tag size = 32 INFO @ Tue, 16 Jun 2020 08:06:15: #1 total tags in treatment: 794865 INFO @ Tue, 16 Jun 2020 08:06:15: #1 user defined the maximum tags... INFO @ Tue, 16 Jun 2020 08:06:15: #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 08:06:15: #1 tags after filtering in treatment: 794865 INFO @ Tue, 16 Jun 2020 08:06:15: #1 Redundant rate of treatment: 0.00 INFO @ Tue, 16 Jun 2020 08:06:15: #1 finished! INFO @ Tue, 16 Jun 2020 08:06:15: #2 Build Peak Model... INFO @ Tue, 16 Jun 2020 08:06:15: #2 looking for paired plus/minus strand peaks... INFO @ Tue, 16 Jun 2020 08:06:15: #2 number of paired peaks: 595 WARNING @ Tue, 16 Jun 2020 08:06:15: Fewer paired peaks (595) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 595 pairs to build model! INFO @ Tue, 16 Jun 2020 08:06:15: start model_add_line... INFO @ Tue, 16 Jun 2020 08:06:15: start X-correlation... INFO @ Tue, 16 Jun 2020 08:06:15: end of X-cor INFO @ Tue, 16 Jun 2020 08:06:15: #2 finished! INFO @ Tue, 16 Jun 2020 08:06:15: #2 predicted fragment length is 37 bps INFO @ Tue, 16 Jun 2020 08:06:15: #2 alternative fragment length(s) may be 37,57,83,110,531,557 bps INFO @ Tue, 16 Jun 2020 08:06:15: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/ce11/SRX235168/SRX235168.10_model.r WARNING @ Tue, 16 Jun 2020 08:06:15: #2 Since the d (37) calculated from paired-peaks are smaller than 2*tag length, it may be influenced by unknown sequencing problem! WARNING @ Tue, 16 Jun 2020 08:06:15: #2 You may need to consider one of the other alternative d(s): 37,57,83,110,531,557 WARNING @ Tue, 16 Jun 2020 08:06:15: #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 08:06:15: #3 Call peaks... INFO @ Tue, 16 Jun 2020 08:06:15: #3 Pre-compute pvalue-qvalue table... INFO @ Tue, 16 Jun 2020 08:06:17: #3 Call peaks for each chromosome... INFO @ Tue, 16 Jun 2020 08:06:18: #4 Write output xls file... /home/okishinya/chipatlas/results/ce11/SRX235168/SRX235168.10_peaks.xls INFO @ Tue, 16 Jun 2020 08:06:18: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/ce11/SRX235168/SRX235168.10_peaks.narrowPeak INFO @ Tue, 16 Jun 2020 08:06:18: #4 Write summits bed file... /home/okishinya/chipatlas/results/ce11/SRX235168/SRX235168.10_summits.bed INFO @ Tue, 16 Jun 2020 08:06:18: Done! pass1 - making usageList (6 chroms): 1 millis pass2 - checking and writing primary data (46 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, 16 Jun 2020 08:06:37: # Command line: callpeak -t /home/okishinya/chipatlas/results/ce11/SRX235168/SRX235168.bam -f BAM -g ce -n /home/okishinya/chipatlas/results/ce11/SRX235168/SRX235168.20 -q 1e-20 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/ce11/SRX235168/SRX235168.20 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/ce11/SRX235168/SRX235168.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 08:06:37: #1 read tag files... INFO @ Tue, 16 Jun 2020 08:06:37: #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, 16 Jun 2020 08:06:41: #1 tag size is determined as 32 bps INFO @ Tue, 16 Jun 2020 08:06:41: #1 tag size = 32 INFO @ Tue, 16 Jun 2020 08:06:41: #1 total tags in treatment: 794865 INFO @ Tue, 16 Jun 2020 08:06:41: #1 user defined the maximum tags... INFO @ Tue, 16 Jun 2020 08:06:41: #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 08:06:41: #1 tags after filtering in treatment: 794865 INFO @ Tue, 16 Jun 2020 08:06:41: #1 Redundant rate of treatment: 0.00 INFO @ Tue, 16 Jun 2020 08:06:41: #1 finished! INFO @ Tue, 16 Jun 2020 08:06:41: #2 Build Peak Model... INFO @ Tue, 16 Jun 2020 08:06:41: #2 looking for paired plus/minus strand peaks... INFO @ Tue, 16 Jun 2020 08:06:41: #2 number of paired peaks: 595 WARNING @ Tue, 16 Jun 2020 08:06:41: Fewer paired peaks (595) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 595 pairs to build model! INFO @ Tue, 16 Jun 2020 08:06:41: start model_add_line... INFO @ Tue, 16 Jun 2020 08:06:41: start X-correlation... INFO @ Tue, 16 Jun 2020 08:06:41: end of X-cor INFO @ Tue, 16 Jun 2020 08:06:41: #2 finished! INFO @ Tue, 16 Jun 2020 08:06:41: #2 predicted fragment length is 37 bps INFO @ Tue, 16 Jun 2020 08:06:41: #2 alternative fragment length(s) may be 37,57,83,110,531,557 bps INFO @ Tue, 16 Jun 2020 08:06:41: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/ce11/SRX235168/SRX235168.20_model.r WARNING @ Tue, 16 Jun 2020 08:06:41: #2 Since the d (37) calculated from paired-peaks are smaller than 2*tag length, it may be influenced by unknown sequencing problem! WARNING @ Tue, 16 Jun 2020 08:06:41: #2 You may need to consider one of the other alternative d(s): 37,57,83,110,531,557 WARNING @ Tue, 16 Jun 2020 08:06:41: #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 08:06:41: #3 Call peaks... INFO @ Tue, 16 Jun 2020 08:06:41: #3 Pre-compute pvalue-qvalue table... INFO @ Tue, 16 Jun 2020 08:06:43: #3 Call peaks for each chromosome... INFO @ Tue, 16 Jun 2020 08:06:44: #4 Write output xls file... /home/okishinya/chipatlas/results/ce11/SRX235168/SRX235168.20_peaks.xls INFO @ Tue, 16 Jun 2020 08:06:44: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/ce11/SRX235168/SRX235168.20_peaks.narrowPeak INFO @ Tue, 16 Jun 2020 08:06:44: #4 Write summits bed file... /home/okishinya/chipatlas/results/ce11/SRX235168/SRX235168.20_summits.bed INFO @ Tue, 16 Jun 2020 08:06:44: Done! pass1 - making usageList (5 chroms): 1 millis pass2 - checking and writing primary data (8 records, 4 fields): 3 millis CompletedMACS2peakCalling