Job ID = 6366189 SRX = SRX065714 Genome = ce11 sra ファイルのダウンロード中... Read layout: SINGLE fastq に変換中... 2020-06-15T22:46:37 prefetch.2.10.7: 1) Downloading 'SRR217420'... 2020-06-15T22:46:37 prefetch.2.10.7: Downloading via HTTPS... 2020-06-15T22:47:02 prefetch.2.10.7: HTTPS download succeed 2020-06-15T22:47:02 prefetch.2.10.7: 'SRR217420' is valid 2020-06-15T22:47:02 prefetch.2.10.7: 1) 'SRR217420' was downloaded successfully Read 2439120 spots for SRR217420/SRR217420.sra Written 2439120 spots for SRR217420/SRR217420.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: 00:00:15 2439120 reads; of these: 2439120 (100.00%) were unpaired; of these: 1445507 (59.26%) aligned 0 times 832410 (34.13%) aligned exactly 1 time 161203 (6.61%) aligned >1 times 40.74% overall alignment rate Time searching: 00:00:15 Overall time: 00:00:15 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] 64442 / 993613 = 0.0649 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 07:48:13: # Command line: callpeak -t /home/okishinya/chipatlas/results/ce11/SRX065714/SRX065714.bam -f BAM -g ce -n /home/okishinya/chipatlas/results/ce11/SRX065714/SRX065714.05 -q 1e-05 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/ce11/SRX065714/SRX065714.05 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/ce11/SRX065714/SRX065714.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 07:48:13: #1 read tag files... INFO @ Tue, 16 Jun 2020 07:48:13: #1 read treatment tags... INFO @ Tue, 16 Jun 2020 07:48:20: #1 tag size is determined as 32 bps INFO @ Tue, 16 Jun 2020 07:48:20: #1 tag size = 32 INFO @ Tue, 16 Jun 2020 07:48:20: #1 total tags in treatment: 929171 INFO @ Tue, 16 Jun 2020 07:48:20: #1 user defined the maximum tags... INFO @ Tue, 16 Jun 2020 07:48:20: #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 07:48:20: #1 tags after filtering in treatment: 929171 INFO @ Tue, 16 Jun 2020 07:48:20: #1 Redundant rate of treatment: 0.00 INFO @ Tue, 16 Jun 2020 07:48:20: #1 finished! INFO @ Tue, 16 Jun 2020 07:48:20: #2 Build Peak Model... INFO @ Tue, 16 Jun 2020 07:48:20: #2 looking for paired plus/minus strand peaks... INFO @ Tue, 16 Jun 2020 07:48:20: #2 number of paired peaks: 385 WARNING @ Tue, 16 Jun 2020 07:48:20: Fewer paired peaks (385) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 385 pairs to build model! INFO @ Tue, 16 Jun 2020 07:48:20: start model_add_line... INFO @ Tue, 16 Jun 2020 07:48:20: start X-correlation... INFO @ Tue, 16 Jun 2020 07:48:20: end of X-cor INFO @ Tue, 16 Jun 2020 07:48:20: #2 finished! INFO @ Tue, 16 Jun 2020 07:48:20: #2 predicted fragment length is 31 bps INFO @ Tue, 16 Jun 2020 07:48:20: #2 alternative fragment length(s) may be 31,91,146,207,277,372,445,544,570 bps INFO @ Tue, 16 Jun 2020 07:48:20: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/ce11/SRX065714/SRX065714.05_model.r WARNING @ Tue, 16 Jun 2020 07:48:20: #2 Since the d (31) calculated from paired-peaks are smaller than 2*tag length, it may be influenced by unknown sequencing problem! WARNING @ Tue, 16 Jun 2020 07:48:20: #2 You may need to consider one of the other alternative d(s): 31,91,146,207,277,372,445,544,570 WARNING @ Tue, 16 Jun 2020 07:48:20: #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 07:48:20: #3 Call peaks... INFO @ Tue, 16 Jun 2020 07:48:20: #3 Pre-compute pvalue-qvalue table... INFO @ Tue, 16 Jun 2020 07:48:22: #3 Call peaks for each chromosome... INFO @ Tue, 16 Jun 2020 07:48:23: #4 Write output xls file... /home/okishinya/chipatlas/results/ce11/SRX065714/SRX065714.05_peaks.xls INFO @ Tue, 16 Jun 2020 07:48:23: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/ce11/SRX065714/SRX065714.05_peaks.narrowPeak INFO @ Tue, 16 Jun 2020 07:48:23: #4 Write summits bed file... /home/okishinya/chipatlas/results/ce11/SRX065714/SRX065714.05_summits.bed INFO @ Tue, 16 Jun 2020 07:48:23: Done! pass1 - making usageList (6 chroms): 1 millis pass2 - checking and writing primary data (93 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 07:48:43: # Command line: callpeak -t /home/okishinya/chipatlas/results/ce11/SRX065714/SRX065714.bam -f BAM -g ce -n /home/okishinya/chipatlas/results/ce11/SRX065714/SRX065714.10 -q 1e-10 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/ce11/SRX065714/SRX065714.10 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/ce11/SRX065714/SRX065714.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 07:48:43: #1 read tag files... INFO @ Tue, 16 Jun 2020 07:48:43: #1 read treatment tags... INFO @ Tue, 16 Jun 2020 07:48:50: #1 tag size is determined as 32 bps INFO @ Tue, 16 Jun 2020 07:48:50: #1 tag size = 32 INFO @ Tue, 16 Jun 2020 07:48:50: #1 total tags in treatment: 929171 INFO @ Tue, 16 Jun 2020 07:48:50: #1 user defined the maximum tags... INFO @ Tue, 16 Jun 2020 07:48:50: #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 07:48:50: #1 tags after filtering in treatment: 929171 INFO @ Tue, 16 Jun 2020 07:48:50: #1 Redundant rate of treatment: 0.00 INFO @ Tue, 16 Jun 2020 07:48:50: #1 finished! INFO @ Tue, 16 Jun 2020 07:48:50: #2 Build Peak Model... INFO @ Tue, 16 Jun 2020 07:48:50: #2 looking for paired plus/minus strand peaks... INFO @ Tue, 16 Jun 2020 07:48:50: #2 number of paired peaks: 385 WARNING @ Tue, 16 Jun 2020 07:48:50: Fewer paired peaks (385) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 385 pairs to build model! INFO @ Tue, 16 Jun 2020 07:48:50: start model_add_line... INFO @ Tue, 16 Jun 2020 07:48:50: start X-correlation... INFO @ Tue, 16 Jun 2020 07:48:50: end of X-cor INFO @ Tue, 16 Jun 2020 07:48:50: #2 finished! INFO @ Tue, 16 Jun 2020 07:48:50: #2 predicted fragment length is 31 bps INFO @ Tue, 16 Jun 2020 07:48:50: #2 alternative fragment length(s) may be 31,91,146,207,277,372,445,544,570 bps INFO @ Tue, 16 Jun 2020 07:48:50: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/ce11/SRX065714/SRX065714.10_model.r WARNING @ Tue, 16 Jun 2020 07:48:50: #2 Since the d (31) calculated from paired-peaks are smaller than 2*tag length, it may be influenced by unknown sequencing problem! WARNING @ Tue, 16 Jun 2020 07:48:50: #2 You may need to consider one of the other alternative d(s): 31,91,146,207,277,372,445,544,570 WARNING @ Tue, 16 Jun 2020 07:48:50: #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 07:48:50: #3 Call peaks... INFO @ Tue, 16 Jun 2020 07:48:50: #3 Pre-compute pvalue-qvalue table... INFO @ Tue, 16 Jun 2020 07:48:52: #3 Call peaks for each chromosome... INFO @ Tue, 16 Jun 2020 07:48:53: #4 Write output xls file... /home/okishinya/chipatlas/results/ce11/SRX065714/SRX065714.10_peaks.xls INFO @ Tue, 16 Jun 2020 07:48:53: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/ce11/SRX065714/SRX065714.10_peaks.narrowPeak INFO @ Tue, 16 Jun 2020 07:48:53: #4 Write summits bed file... /home/okishinya/chipatlas/results/ce11/SRX065714/SRX065714.10_summits.bed INFO @ Tue, 16 Jun 2020 07:48:53: Done! pass1 - making usageList (6 chroms): 1 millis pass2 - checking and writing primary data (29 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 07:49:13: # Command line: callpeak -t /home/okishinya/chipatlas/results/ce11/SRX065714/SRX065714.bam -f BAM -g ce -n /home/okishinya/chipatlas/results/ce11/SRX065714/SRX065714.20 -q 1e-20 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/ce11/SRX065714/SRX065714.20 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/ce11/SRX065714/SRX065714.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 07:49:13: #1 read tag files... INFO @ Tue, 16 Jun 2020 07:49:13: #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 07:49:19: #1 tag size is determined as 32 bps INFO @ Tue, 16 Jun 2020 07:49:19: #1 tag size = 32 INFO @ Tue, 16 Jun 2020 07:49:19: #1 total tags in treatment: 929171 INFO @ Tue, 16 Jun 2020 07:49:19: #1 user defined the maximum tags... INFO @ Tue, 16 Jun 2020 07:49:19: #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 07:49:19: #1 tags after filtering in treatment: 929171 INFO @ Tue, 16 Jun 2020 07:49:19: #1 Redundant rate of treatment: 0.00 INFO @ Tue, 16 Jun 2020 07:49:19: #1 finished! INFO @ Tue, 16 Jun 2020 07:49:19: #2 Build Peak Model... INFO @ Tue, 16 Jun 2020 07:49:19: #2 looking for paired plus/minus strand peaks... INFO @ Tue, 16 Jun 2020 07:49:19: #2 number of paired peaks: 385 WARNING @ Tue, 16 Jun 2020 07:49:19: Fewer paired peaks (385) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 385 pairs to build model! INFO @ Tue, 16 Jun 2020 07:49:19: start model_add_line... INFO @ Tue, 16 Jun 2020 07:49:19: start X-correlation... INFO @ Tue, 16 Jun 2020 07:49:19: end of X-cor INFO @ Tue, 16 Jun 2020 07:49:19: #2 finished! INFO @ Tue, 16 Jun 2020 07:49:19: #2 predicted fragment length is 31 bps INFO @ Tue, 16 Jun 2020 07:49:19: #2 alternative fragment length(s) may be 31,91,146,207,277,372,445,544,570 bps INFO @ Tue, 16 Jun 2020 07:49:19: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/ce11/SRX065714/SRX065714.20_model.r WARNING @ Tue, 16 Jun 2020 07:49:19: #2 Since the d (31) calculated from paired-peaks are smaller than 2*tag length, it may be influenced by unknown sequencing problem! WARNING @ Tue, 16 Jun 2020 07:49:19: #2 You may need to consider one of the other alternative d(s): 31,91,146,207,277,372,445,544,570 WARNING @ Tue, 16 Jun 2020 07:49:19: #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 07:49:19: #3 Call peaks... INFO @ Tue, 16 Jun 2020 07:49:19: #3 Pre-compute pvalue-qvalue table... INFO @ Tue, 16 Jun 2020 07:49:21: #3 Call peaks for each chromosome... INFO @ Tue, 16 Jun 2020 07:49:22: #4 Write output xls file... /home/okishinya/chipatlas/results/ce11/SRX065714/SRX065714.20_peaks.xls INFO @ Tue, 16 Jun 2020 07:49:22: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/ce11/SRX065714/SRX065714.20_peaks.narrowPeak INFO @ Tue, 16 Jun 2020 07:49:22: #4 Write summits bed file... /home/okishinya/chipatlas/results/ce11/SRX065714/SRX065714.20_summits.bed INFO @ Tue, 16 Jun 2020 07:49:22: Done! pass1 - making usageList (4 chroms): 0 millis pass2 - checking and writing primary data (7 records, 4 fields): 1 millis CompletedMACS2peakCalling