Job ID = 6367096 SRX = SRX277053 Genome = ce11 sra ファイルのダウンロード中... Read layout: SINGLE fastq に変換中... 2020-06-15T23:08:31 prefetch.2.10.7: 1) Downloading 'SRR849729'... 2020-06-15T23:08:31 prefetch.2.10.7: Downloading via HTTPS... 2020-06-15T23:08:59 prefetch.2.10.7: HTTPS download succeed 2020-06-15T23:08:59 prefetch.2.10.7: 'SRR849729' is valid 2020-06-15T23:08:59 prefetch.2.10.7: 1) 'SRR849729' was downloaded successfully Read 4935314 spots for SRR849729/SRR849729.sra Written 4935314 spots for SRR849729/SRR849729.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: 00:00:45 4935314 reads; of these: 4935314 (100.00%) were unpaired; of these: 283272 (5.74%) aligned 0 times 3901821 (79.06%) aligned exactly 1 time 750221 (15.20%) aligned >1 times 94.26% overall alignment rate Time searching: 00:00:45 Overall time: 00:00:45 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] 269314 / 4652042 = 0.0579 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 08:11:17: # Command line: callpeak -t /home/okishinya/chipatlas/results/ce11/SRX277053/SRX277053.bam -f BAM -g ce -n /home/okishinya/chipatlas/results/ce11/SRX277053/SRX277053.05 -q 1e-05 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/ce11/SRX277053/SRX277053.05 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/ce11/SRX277053/SRX277053.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 08:11:17: #1 read tag files... INFO @ Tue, 16 Jun 2020 08:11:17: #1 read treatment tags... INFO @ Tue, 16 Jun 2020 08:11:22: 1000000 INFO @ Tue, 16 Jun 2020 08:11:27: 2000000 INFO @ Tue, 16 Jun 2020 08:11:33: 3000000 INFO @ Tue, 16 Jun 2020 08:11:38: 4000000 INFO @ Tue, 16 Jun 2020 08:11:40: #1 tag size is determined as 32 bps INFO @ Tue, 16 Jun 2020 08:11:40: #1 tag size = 32 INFO @ Tue, 16 Jun 2020 08:11:40: #1 total tags in treatment: 4382728 INFO @ Tue, 16 Jun 2020 08:11:40: #1 user defined the maximum tags... INFO @ Tue, 16 Jun 2020 08:11:40: #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 08:11:40: #1 tags after filtering in treatment: 4382728 INFO @ Tue, 16 Jun 2020 08:11:40: #1 Redundant rate of treatment: 0.00 INFO @ Tue, 16 Jun 2020 08:11:40: #1 finished! INFO @ Tue, 16 Jun 2020 08:11:40: #2 Build Peak Model... INFO @ Tue, 16 Jun 2020 08:11:40: #2 looking for paired plus/minus strand peaks... INFO @ Tue, 16 Jun 2020 08:11:40: #2 number of paired peaks: 468 WARNING @ Tue, 16 Jun 2020 08:11:40: Fewer paired peaks (468) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 468 pairs to build model! INFO @ Tue, 16 Jun 2020 08:11:40: start model_add_line... INFO @ Tue, 16 Jun 2020 08:11:40: start X-correlation... INFO @ Tue, 16 Jun 2020 08:11:40: end of X-cor INFO @ Tue, 16 Jun 2020 08:11:40: #2 finished! INFO @ Tue, 16 Jun 2020 08:11:40: #2 predicted fragment length is 35 bps INFO @ Tue, 16 Jun 2020 08:11:40: #2 alternative fragment length(s) may be 3,35,533,567 bps INFO @ Tue, 16 Jun 2020 08:11:40: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/ce11/SRX277053/SRX277053.05_model.r WARNING @ Tue, 16 Jun 2020 08:11:40: #2 Since the d (35) calculated from paired-peaks are smaller than 2*tag length, it may be influenced by unknown sequencing problem! WARNING @ Tue, 16 Jun 2020 08:11:40: #2 You may need to consider one of the other alternative d(s): 3,35,533,567 WARNING @ Tue, 16 Jun 2020 08:11:40: #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 08:11:40: #3 Call peaks... INFO @ Tue, 16 Jun 2020 08:11:40: #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 @ Tue, 16 Jun 2020 08:11:47: # Command line: callpeak -t /home/okishinya/chipatlas/results/ce11/SRX277053/SRX277053.bam -f BAM -g ce -n /home/okishinya/chipatlas/results/ce11/SRX277053/SRX277053.10 -q 1e-10 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/ce11/SRX277053/SRX277053.10 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/ce11/SRX277053/SRX277053.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 08:11:47: #1 read tag files... INFO @ Tue, 16 Jun 2020 08:11:47: #1 read treatment tags... INFO @ Tue, 16 Jun 2020 08:11:49: #3 Call peaks for each chromosome... INFO @ Tue, 16 Jun 2020 08:11:54: #4 Write output xls file... /home/okishinya/chipatlas/results/ce11/SRX277053/SRX277053.05_peaks.xls INFO @ Tue, 16 Jun 2020 08:11:54: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/ce11/SRX277053/SRX277053.05_peaks.narrowPeak INFO @ Tue, 16 Jun 2020 08:11:54: #4 Write summits bed file... /home/okishinya/chipatlas/results/ce11/SRX277053/SRX277053.05_summits.bed INFO @ Tue, 16 Jun 2020 08:11:54: Done! pass1 - making usageList (7 chroms): 0 millis pass2 - checking and writing primary data (436 records, 4 fields): 2 millis CompletedMACS2peakCalling INFO @ Tue, 16 Jun 2020 08:11:54: 1000000 INFO @ Tue, 16 Jun 2020 08:12:00: 2000000 INFO @ Tue, 16 Jun 2020 08:12:06: 3000000 INFO @ Tue, 16 Jun 2020 08:12:13: 4000000 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 08:12:15: #1 tag size is determined as 32 bps INFO @ Tue, 16 Jun 2020 08:12:15: #1 tag size = 32 INFO @ Tue, 16 Jun 2020 08:12:15: #1 total tags in treatment: 4382728 INFO @ Tue, 16 Jun 2020 08:12:15: #1 user defined the maximum tags... INFO @ Tue, 16 Jun 2020 08:12:15: #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 08:12:15: #1 tags after filtering in treatment: 4382728 INFO @ Tue, 16 Jun 2020 08:12:15: #1 Redundant rate of treatment: 0.00 INFO @ Tue, 16 Jun 2020 08:12:15: #1 finished! INFO @ Tue, 16 Jun 2020 08:12:15: #2 Build Peak Model... INFO @ Tue, 16 Jun 2020 08:12:15: #2 looking for paired plus/minus strand peaks... INFO @ Tue, 16 Jun 2020 08:12:15: #2 number of paired peaks: 468 WARNING @ Tue, 16 Jun 2020 08:12:15: Fewer paired peaks (468) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 468 pairs to build model! INFO @ Tue, 16 Jun 2020 08:12:15: start model_add_line... INFO @ Tue, 16 Jun 2020 08:12:15: start X-correlation... INFO @ Tue, 16 Jun 2020 08:12:15: end of X-cor INFO @ Tue, 16 Jun 2020 08:12:15: #2 finished! INFO @ Tue, 16 Jun 2020 08:12:15: #2 predicted fragment length is 35 bps INFO @ Tue, 16 Jun 2020 08:12:15: #2 alternative fragment length(s) may be 3,35,533,567 bps INFO @ Tue, 16 Jun 2020 08:12:15: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/ce11/SRX277053/SRX277053.10_model.r WARNING @ Tue, 16 Jun 2020 08:12:15: #2 Since the d (35) calculated from paired-peaks are smaller than 2*tag length, it may be influenced by unknown sequencing problem! WARNING @ Tue, 16 Jun 2020 08:12:15: #2 You may need to consider one of the other alternative d(s): 3,35,533,567 WARNING @ Tue, 16 Jun 2020 08:12:15: #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 08:12:15: #3 Call peaks... INFO @ Tue, 16 Jun 2020 08:12:15: #3 Pre-compute pvalue-qvalue table... INFO @ Tue, 16 Jun 2020 08:12:17: # Command line: callpeak -t /home/okishinya/chipatlas/results/ce11/SRX277053/SRX277053.bam -f BAM -g ce -n /home/okishinya/chipatlas/results/ce11/SRX277053/SRX277053.20 -q 1e-20 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/ce11/SRX277053/SRX277053.20 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/ce11/SRX277053/SRX277053.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 08:12:17: #1 read tag files... INFO @ Tue, 16 Jun 2020 08:12:17: #1 read treatment tags... INFO @ Tue, 16 Jun 2020 08:12:22: 1000000 INFO @ Tue, 16 Jun 2020 08:12:24: #3 Call peaks for each chromosome... INFO @ Tue, 16 Jun 2020 08:12:27: 2000000 INFO @ Tue, 16 Jun 2020 08:12:28: #4 Write output xls file... /home/okishinya/chipatlas/results/ce11/SRX277053/SRX277053.10_peaks.xls INFO @ Tue, 16 Jun 2020 08:12:28: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/ce11/SRX277053/SRX277053.10_peaks.narrowPeak INFO @ Tue, 16 Jun 2020 08:12:28: #4 Write summits bed file... /home/okishinya/chipatlas/results/ce11/SRX277053/SRX277053.10_summits.bed INFO @ Tue, 16 Jun 2020 08:12:28: Done! pass1 - making usageList (6 chroms): 0 millis pass2 - checking and writing primary data (202 records, 4 fields): 1 millis CompletedMACS2peakCalling INFO @ Tue, 16 Jun 2020 08:12:32: 3000000 BedGraph に変換しました。 BigWig に変換中... INFO @ Tue, 16 Jun 2020 08:12:38: 4000000 INFO @ Tue, 16 Jun 2020 08:12:39: #1 tag size is determined as 32 bps INFO @ Tue, 16 Jun 2020 08:12:39: #1 tag size = 32 INFO @ Tue, 16 Jun 2020 08:12:39: #1 total tags in treatment: 4382728 INFO @ Tue, 16 Jun 2020 08:12:39: #1 user defined the maximum tags... INFO @ Tue, 16 Jun 2020 08:12:39: #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 08:12:40: #1 tags after filtering in treatment: 4382728 INFO @ Tue, 16 Jun 2020 08:12:40: #1 Redundant rate of treatment: 0.00 INFO @ Tue, 16 Jun 2020 08:12:40: #1 finished! INFO @ Tue, 16 Jun 2020 08:12:40: #2 Build Peak Model... INFO @ Tue, 16 Jun 2020 08:12:40: #2 looking for paired plus/minus strand peaks... INFO @ Tue, 16 Jun 2020 08:12:40: #2 number of paired peaks: 468 WARNING @ Tue, 16 Jun 2020 08:12:40: Fewer paired peaks (468) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 468 pairs to build model! INFO @ Tue, 16 Jun 2020 08:12:40: start model_add_line... INFO @ Tue, 16 Jun 2020 08:12:40: start X-correlation... INFO @ Tue, 16 Jun 2020 08:12:40: end of X-cor INFO @ Tue, 16 Jun 2020 08:12:40: #2 finished! INFO @ Tue, 16 Jun 2020 08:12:40: #2 predicted fragment length is 35 bps INFO @ Tue, 16 Jun 2020 08:12:40: #2 alternative fragment length(s) may be 3,35,533,567 bps INFO @ Tue, 16 Jun 2020 08:12:40: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/ce11/SRX277053/SRX277053.20_model.r WARNING @ Tue, 16 Jun 2020 08:12:40: #2 Since the d (35) calculated from paired-peaks are smaller than 2*tag length, it may be influenced by unknown sequencing problem! WARNING @ Tue, 16 Jun 2020 08:12:40: #2 You may need to consider one of the other alternative d(s): 3,35,533,567 WARNING @ Tue, 16 Jun 2020 08:12:40: #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 08:12:40: #3 Call peaks... INFO @ Tue, 16 Jun 2020 08:12:40: #3 Pre-compute pvalue-qvalue table... BigWig に変換しました。 INFO @ Tue, 16 Jun 2020 08:12:49: #3 Call peaks for each chromosome... INFO @ Tue, 16 Jun 2020 08:12:53: #4 Write output xls file... /home/okishinya/chipatlas/results/ce11/SRX277053/SRX277053.20_peaks.xls INFO @ Tue, 16 Jun 2020 08:12:53: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/ce11/SRX277053/SRX277053.20_peaks.narrowPeak INFO @ Tue, 16 Jun 2020 08:12:53: #4 Write summits bed file... /home/okishinya/chipatlas/results/ce11/SRX277053/SRX277053.20_summits.bed INFO @ Tue, 16 Jun 2020 08:12:53: Done! pass1 - making usageList (6 chroms): 1 millis pass2 - checking and writing primary data (61 records, 4 fields): 1 millis CompletedMACS2peakCalling