Job ID = 6367447 SRX = SRX331205 Genome = ce11 sra ファイルのダウンロード中... Read layout: SINGLE fastq に変換中... 2020-06-15T23:22:01 prefetch.2.10.7: 1) Downloading 'SRR947437'... 2020-06-15T23:22:01 prefetch.2.10.7: Downloading via HTTPS... 2020-06-15T23:22:29 prefetch.2.10.7: HTTPS download succeed 2020-06-15T23:22:29 prefetch.2.10.7: 'SRR947437' is valid 2020-06-15T23:22:29 prefetch.2.10.7: 1) 'SRR947437' was downloaded successfully Read 6032643 spots for SRR947437/SRR947437.sra Written 6032643 spots for SRR947437/SRR947437.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: 00:00:31 6032643 reads; of these: 6032643 (100.00%) were unpaired; of these: 4506074 (74.69%) aligned 0 times 1284253 (21.29%) aligned exactly 1 time 242316 (4.02%) aligned >1 times 25.31% overall alignment rate Time searching: 00:00:31 Overall time: 00:00:31 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] 57286 / 1526569 = 0.0375 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 08:24:04: # Command line: callpeak -t /home/okishinya/chipatlas/results/ce11/SRX331205/SRX331205.bam -f BAM -g ce -n /home/okishinya/chipatlas/results/ce11/SRX331205/SRX331205.05 -q 1e-05 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/ce11/SRX331205/SRX331205.05 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/ce11/SRX331205/SRX331205.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 08:24:04: #1 read tag files... INFO @ Tue, 16 Jun 2020 08:24:04: #1 read treatment tags... INFO @ Tue, 16 Jun 2020 08:24:09: 1000000 INFO @ Tue, 16 Jun 2020 08:24:11: #1 tag size is determined as 32 bps INFO @ Tue, 16 Jun 2020 08:24:11: #1 tag size = 32 INFO @ Tue, 16 Jun 2020 08:24:11: #1 total tags in treatment: 1469283 INFO @ Tue, 16 Jun 2020 08:24:11: #1 user defined the maximum tags... INFO @ Tue, 16 Jun 2020 08:24:11: #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 08:24:12: #1 tags after filtering in treatment: 1469283 INFO @ Tue, 16 Jun 2020 08:24:12: #1 Redundant rate of treatment: 0.00 INFO @ Tue, 16 Jun 2020 08:24:12: #1 finished! INFO @ Tue, 16 Jun 2020 08:24:12: #2 Build Peak Model... INFO @ Tue, 16 Jun 2020 08:24:12: #2 looking for paired plus/minus strand peaks... INFO @ Tue, 16 Jun 2020 08:24:12: #2 number of paired peaks: 406 WARNING @ Tue, 16 Jun 2020 08:24:12: Fewer paired peaks (406) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 406 pairs to build model! INFO @ Tue, 16 Jun 2020 08:24:12: start model_add_line... INFO @ Tue, 16 Jun 2020 08:24:12: start X-correlation... INFO @ Tue, 16 Jun 2020 08:24:12: end of X-cor INFO @ Tue, 16 Jun 2020 08:24:12: #2 finished! INFO @ Tue, 16 Jun 2020 08:24:12: #2 predicted fragment length is 36 bps INFO @ Tue, 16 Jun 2020 08:24:12: #2 alternative fragment length(s) may be 36,56,196,407,551,590 bps INFO @ Tue, 16 Jun 2020 08:24:12: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/ce11/SRX331205/SRX331205.05_model.r WARNING @ Tue, 16 Jun 2020 08:24:12: #2 Since the d (36) calculated from paired-peaks are smaller than 2*tag length, it may be influenced by unknown sequencing problem! WARNING @ Tue, 16 Jun 2020 08:24:12: #2 You may need to consider one of the other alternative d(s): 36,56,196,407,551,590 WARNING @ Tue, 16 Jun 2020 08:24:12: #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 08:24:12: #3 Call peaks... INFO @ Tue, 16 Jun 2020 08:24:12: #3 Pre-compute pvalue-qvalue table... INFO @ Tue, 16 Jun 2020 08:24:15: #3 Call peaks for each chromosome... INFO @ Tue, 16 Jun 2020 08:24:16: #4 Write output xls file... /home/okishinya/chipatlas/results/ce11/SRX331205/SRX331205.05_peaks.xls INFO @ Tue, 16 Jun 2020 08:24:16: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/ce11/SRX331205/SRX331205.05_peaks.narrowPeak INFO @ Tue, 16 Jun 2020 08:24:16: #4 Write summits bed file... /home/okishinya/chipatlas/results/ce11/SRX331205/SRX331205.05_summits.bed INFO @ Tue, 16 Jun 2020 08:24:16: Done! pass1 - making usageList (6 chroms): 0 millis pass2 - checking and writing primary data (168 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 08:24:34: # Command line: callpeak -t /home/okishinya/chipatlas/results/ce11/SRX331205/SRX331205.bam -f BAM -g ce -n /home/okishinya/chipatlas/results/ce11/SRX331205/SRX331205.10 -q 1e-10 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/ce11/SRX331205/SRX331205.10 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/ce11/SRX331205/SRX331205.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 08:24:34: #1 read tag files... INFO @ Tue, 16 Jun 2020 08:24:34: #1 read treatment tags... INFO @ Tue, 16 Jun 2020 08:24:39: 1000000 INFO @ Tue, 16 Jun 2020 08:24:42: #1 tag size is determined as 32 bps INFO @ Tue, 16 Jun 2020 08:24:42: #1 tag size = 32 INFO @ Tue, 16 Jun 2020 08:24:42: #1 total tags in treatment: 1469283 INFO @ Tue, 16 Jun 2020 08:24:42: #1 user defined the maximum tags... INFO @ Tue, 16 Jun 2020 08:24:42: #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 08:24:42: #1 tags after filtering in treatment: 1469283 INFO @ Tue, 16 Jun 2020 08:24:42: #1 Redundant rate of treatment: 0.00 INFO @ Tue, 16 Jun 2020 08:24:42: #1 finished! INFO @ Tue, 16 Jun 2020 08:24:42: #2 Build Peak Model... INFO @ Tue, 16 Jun 2020 08:24:42: #2 looking for paired plus/minus strand peaks... INFO @ Tue, 16 Jun 2020 08:24:42: #2 number of paired peaks: 406 WARNING @ Tue, 16 Jun 2020 08:24:42: Fewer paired peaks (406) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 406 pairs to build model! INFO @ Tue, 16 Jun 2020 08:24:42: start model_add_line... INFO @ Tue, 16 Jun 2020 08:24:42: start X-correlation... INFO @ Tue, 16 Jun 2020 08:24:42: end of X-cor INFO @ Tue, 16 Jun 2020 08:24:42: #2 finished! INFO @ Tue, 16 Jun 2020 08:24:42: #2 predicted fragment length is 36 bps INFO @ Tue, 16 Jun 2020 08:24:42: #2 alternative fragment length(s) may be 36,56,196,407,551,590 bps INFO @ Tue, 16 Jun 2020 08:24:42: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/ce11/SRX331205/SRX331205.10_model.r WARNING @ Tue, 16 Jun 2020 08:24:42: #2 Since the d (36) calculated from paired-peaks are smaller than 2*tag length, it may be influenced by unknown sequencing problem! WARNING @ Tue, 16 Jun 2020 08:24:42: #2 You may need to consider one of the other alternative d(s): 36,56,196,407,551,590 WARNING @ Tue, 16 Jun 2020 08:24:42: #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 08:24:42: #3 Call peaks... INFO @ Tue, 16 Jun 2020 08:24:42: #3 Pre-compute pvalue-qvalue table... INFO @ Tue, 16 Jun 2020 08:24:45: #3 Call peaks for each chromosome... INFO @ Tue, 16 Jun 2020 08:24:46: #4 Write output xls file... /home/okishinya/chipatlas/results/ce11/SRX331205/SRX331205.10_peaks.xls INFO @ Tue, 16 Jun 2020 08:24:46: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/ce11/SRX331205/SRX331205.10_peaks.narrowPeak INFO @ Tue, 16 Jun 2020 08:24:46: #4 Write summits bed file... /home/okishinya/chipatlas/results/ce11/SRX331205/SRX331205.10_summits.bed INFO @ Tue, 16 Jun 2020 08:24:46: Done! pass1 - making usageList (6 chroms): 0 millis pass2 - checking and writing primary data (75 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 08:25:04: # Command line: callpeak -t /home/okishinya/chipatlas/results/ce11/SRX331205/SRX331205.bam -f BAM -g ce -n /home/okishinya/chipatlas/results/ce11/SRX331205/SRX331205.20 -q 1e-20 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/ce11/SRX331205/SRX331205.20 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/ce11/SRX331205/SRX331205.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 08:25:04: #1 read tag files... INFO @ Tue, 16 Jun 2020 08:25:04: #1 read treatment tags... BedGraph に変換しました。 BigWig に変換中... INFO @ Tue, 16 Jun 2020 08:25:10: 1000000 BigWig に変換しました。 INFO @ Tue, 16 Jun 2020 08:25:13: #1 tag size is determined as 32 bps INFO @ Tue, 16 Jun 2020 08:25:13: #1 tag size = 32 INFO @ Tue, 16 Jun 2020 08:25:13: #1 total tags in treatment: 1469283 INFO @ Tue, 16 Jun 2020 08:25:13: #1 user defined the maximum tags... INFO @ Tue, 16 Jun 2020 08:25:13: #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 08:25:13: #1 tags after filtering in treatment: 1469283 INFO @ Tue, 16 Jun 2020 08:25:13: #1 Redundant rate of treatment: 0.00 INFO @ Tue, 16 Jun 2020 08:25:13: #1 finished! INFO @ Tue, 16 Jun 2020 08:25:13: #2 Build Peak Model... INFO @ Tue, 16 Jun 2020 08:25:13: #2 looking for paired plus/minus strand peaks... INFO @ Tue, 16 Jun 2020 08:25:13: #2 number of paired peaks: 406 WARNING @ Tue, 16 Jun 2020 08:25:13: Fewer paired peaks (406) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 406 pairs to build model! INFO @ Tue, 16 Jun 2020 08:25:13: start model_add_line... INFO @ Tue, 16 Jun 2020 08:25:13: start X-correlation... INFO @ Tue, 16 Jun 2020 08:25:13: end of X-cor INFO @ Tue, 16 Jun 2020 08:25:13: #2 finished! INFO @ Tue, 16 Jun 2020 08:25:13: #2 predicted fragment length is 36 bps INFO @ Tue, 16 Jun 2020 08:25:13: #2 alternative fragment length(s) may be 36,56,196,407,551,590 bps INFO @ Tue, 16 Jun 2020 08:25:13: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/ce11/SRX331205/SRX331205.20_model.r WARNING @ Tue, 16 Jun 2020 08:25:13: #2 Since the d (36) calculated from paired-peaks are smaller than 2*tag length, it may be influenced by unknown sequencing problem! WARNING @ Tue, 16 Jun 2020 08:25:13: #2 You may need to consider one of the other alternative d(s): 36,56,196,407,551,590 WARNING @ Tue, 16 Jun 2020 08:25:13: #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 08:25:13: #3 Call peaks... INFO @ Tue, 16 Jun 2020 08:25:13: #3 Pre-compute pvalue-qvalue table... INFO @ Tue, 16 Jun 2020 08:25:16: #3 Call peaks for each chromosome... INFO @ Tue, 16 Jun 2020 08:25:18: #4 Write output xls file... /home/okishinya/chipatlas/results/ce11/SRX331205/SRX331205.20_peaks.xls INFO @ Tue, 16 Jun 2020 08:25:18: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/ce11/SRX331205/SRX331205.20_peaks.narrowPeak INFO @ Tue, 16 Jun 2020 08:25:18: #4 Write summits bed file... /home/okishinya/chipatlas/results/ce11/SRX331205/SRX331205.20_summits.bed INFO @ Tue, 16 Jun 2020 08:25:18: Done! pass1 - making usageList (6 chroms): 0 millis pass2 - checking and writing primary data (28 records, 4 fields): 1 millis CompletedMACS2peakCalling