Job ID = 6366432 SRX = SRX146489 Genome = ce11 sra ファイルのダウンロード中... Read layout: SINGLE fastq に変換中... 2020-06-15T23:13:16 prefetch.2.10.7: 1) Downloading 'SRR494654'... 2020-06-15T23:13:16 prefetch.2.10.7: Downloading via HTTPS... 2020-06-15T23:13:39 prefetch.2.10.7: HTTPS download succeed 2020-06-15T23:13:39 prefetch.2.10.7: 'SRR494654' is valid 2020-06-15T23:13:39 prefetch.2.10.7: 1) 'SRR494654' was downloaded successfully Read 3730166 spots for SRR494654/SRR494654.sra Written 3730166 spots for SRR494654/SRR494654.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: 00:00:21 3730166 reads; of these: 3730166 (100.00%) were unpaired; of these: 2491243 (66.79%) aligned 0 times 1023331 (27.43%) aligned exactly 1 time 215592 (5.78%) aligned >1 times 33.21% overall alignment rate Time searching: 00:00:21 Overall time: 00:00:21 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] 85531 / 1238923 = 0.0690 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 08:14:56: # Command line: callpeak -t /home/okishinya/chipatlas/results/ce11/SRX146489/SRX146489.bam -f BAM -g ce -n /home/okishinya/chipatlas/results/ce11/SRX146489/SRX146489.05 -q 1e-05 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/ce11/SRX146489/SRX146489.05 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/ce11/SRX146489/SRX146489.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 08:14:56: #1 read tag files... INFO @ Tue, 16 Jun 2020 08:14:56: #1 read treatment tags... INFO @ Tue, 16 Jun 2020 08:15:00: 1000000 INFO @ Tue, 16 Jun 2020 08:15:01: #1 tag size is determined as 32 bps INFO @ Tue, 16 Jun 2020 08:15:01: #1 tag size = 32 INFO @ Tue, 16 Jun 2020 08:15:01: #1 total tags in treatment: 1153392 INFO @ Tue, 16 Jun 2020 08:15:01: #1 user defined the maximum tags... INFO @ Tue, 16 Jun 2020 08:15:01: #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 08:15:01: #1 tags after filtering in treatment: 1153392 INFO @ Tue, 16 Jun 2020 08:15:01: #1 Redundant rate of treatment: 0.00 INFO @ Tue, 16 Jun 2020 08:15:01: #1 finished! INFO @ Tue, 16 Jun 2020 08:15:01: #2 Build Peak Model... INFO @ Tue, 16 Jun 2020 08:15:01: #2 looking for paired plus/minus strand peaks... INFO @ Tue, 16 Jun 2020 08:15:01: #2 number of paired peaks: 441 WARNING @ Tue, 16 Jun 2020 08:15:01: Fewer paired peaks (441) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 441 pairs to build model! INFO @ Tue, 16 Jun 2020 08:15:01: start model_add_line... INFO @ Tue, 16 Jun 2020 08:15:01: start X-correlation... INFO @ Tue, 16 Jun 2020 08:15:01: end of X-cor INFO @ Tue, 16 Jun 2020 08:15:01: #2 finished! INFO @ Tue, 16 Jun 2020 08:15:01: #2 predicted fragment length is 34 bps INFO @ Tue, 16 Jun 2020 08:15:01: #2 alternative fragment length(s) may be 34,512,569 bps INFO @ Tue, 16 Jun 2020 08:15:01: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/ce11/SRX146489/SRX146489.05_model.r WARNING @ Tue, 16 Jun 2020 08:15:01: #2 Since the d (34) calculated from paired-peaks are smaller than 2*tag length, it may be influenced by unknown sequencing problem! WARNING @ Tue, 16 Jun 2020 08:15:01: #2 You may need to consider one of the other alternative d(s): 34,512,569 WARNING @ Tue, 16 Jun 2020 08:15:01: #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 08:15:01: #3 Call peaks... INFO @ Tue, 16 Jun 2020 08:15:01: #3 Pre-compute pvalue-qvalue table... INFO @ Tue, 16 Jun 2020 08:15:04: #3 Call peaks for each chromosome... INFO @ Tue, 16 Jun 2020 08:15:05: #4 Write output xls file... /home/okishinya/chipatlas/results/ce11/SRX146489/SRX146489.05_peaks.xls INFO @ Tue, 16 Jun 2020 08:15:05: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/ce11/SRX146489/SRX146489.05_peaks.narrowPeak INFO @ Tue, 16 Jun 2020 08:15:05: #4 Write summits bed file... /home/okishinya/chipatlas/results/ce11/SRX146489/SRX146489.05_summits.bed INFO @ Tue, 16 Jun 2020 08:15:05: Done! pass1 - making usageList (6 chroms): 0 millis pass2 - checking and writing primary data (199 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 08:15:26: # Command line: callpeak -t /home/okishinya/chipatlas/results/ce11/SRX146489/SRX146489.bam -f BAM -g ce -n /home/okishinya/chipatlas/results/ce11/SRX146489/SRX146489.10 -q 1e-10 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/ce11/SRX146489/SRX146489.10 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/ce11/SRX146489/SRX146489.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 08:15:26: #1 read tag files... INFO @ Tue, 16 Jun 2020 08:15:26: #1 read treatment tags... INFO @ Tue, 16 Jun 2020 08:15:30: 1000000 INFO @ Tue, 16 Jun 2020 08:15:31: #1 tag size is determined as 32 bps INFO @ Tue, 16 Jun 2020 08:15:31: #1 tag size = 32 INFO @ Tue, 16 Jun 2020 08:15:31: #1 total tags in treatment: 1153392 INFO @ Tue, 16 Jun 2020 08:15:31: #1 user defined the maximum tags... INFO @ Tue, 16 Jun 2020 08:15:31: #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 08:15:31: #1 tags after filtering in treatment: 1153392 INFO @ Tue, 16 Jun 2020 08:15:31: #1 Redundant rate of treatment: 0.00 INFO @ Tue, 16 Jun 2020 08:15:31: #1 finished! INFO @ Tue, 16 Jun 2020 08:15:31: #2 Build Peak Model... INFO @ Tue, 16 Jun 2020 08:15:31: #2 looking for paired plus/minus strand peaks... INFO @ Tue, 16 Jun 2020 08:15:31: #2 number of paired peaks: 441 WARNING @ Tue, 16 Jun 2020 08:15:31: Fewer paired peaks (441) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 441 pairs to build model! INFO @ Tue, 16 Jun 2020 08:15:31: start model_add_line... INFO @ Tue, 16 Jun 2020 08:15:31: start X-correlation... INFO @ Tue, 16 Jun 2020 08:15:31: end of X-cor INFO @ Tue, 16 Jun 2020 08:15:31: #2 finished! INFO @ Tue, 16 Jun 2020 08:15:31: #2 predicted fragment length is 34 bps INFO @ Tue, 16 Jun 2020 08:15:31: #2 alternative fragment length(s) may be 34,512,569 bps INFO @ Tue, 16 Jun 2020 08:15:31: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/ce11/SRX146489/SRX146489.10_model.r WARNING @ Tue, 16 Jun 2020 08:15:31: #2 Since the d (34) calculated from paired-peaks are smaller than 2*tag length, it may be influenced by unknown sequencing problem! WARNING @ Tue, 16 Jun 2020 08:15:31: #2 You may need to consider one of the other alternative d(s): 34,512,569 WARNING @ Tue, 16 Jun 2020 08:15:31: #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 08:15:31: #3 Call peaks... INFO @ Tue, 16 Jun 2020 08:15:31: #3 Pre-compute pvalue-qvalue table... INFO @ Tue, 16 Jun 2020 08:15:34: #3 Call peaks for each chromosome... INFO @ Tue, 16 Jun 2020 08:15:35: #4 Write output xls file... /home/okishinya/chipatlas/results/ce11/SRX146489/SRX146489.10_peaks.xls INFO @ Tue, 16 Jun 2020 08:15:35: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/ce11/SRX146489/SRX146489.10_peaks.narrowPeak INFO @ Tue, 16 Jun 2020 08:15:35: #4 Write summits bed file... /home/okishinya/chipatlas/results/ce11/SRX146489/SRX146489.10_summits.bed INFO @ Tue, 16 Jun 2020 08:15:35: Done! pass1 - making usageList (6 chroms): 0 millis pass2 - checking and writing primary data (88 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 08:15:56: # Command line: callpeak -t /home/okishinya/chipatlas/results/ce11/SRX146489/SRX146489.bam -f BAM -g ce -n /home/okishinya/chipatlas/results/ce11/SRX146489/SRX146489.20 -q 1e-20 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/ce11/SRX146489/SRX146489.20 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/ce11/SRX146489/SRX146489.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 08:15:56: #1 read tag files... INFO @ Tue, 16 Jun 2020 08:15:56: #1 read treatment tags... BedGraph に変換しました。 BigWig に変換中... INFO @ Tue, 16 Jun 2020 08:16:00: 1000000 INFO @ Tue, 16 Jun 2020 08:16:01: #1 tag size is determined as 32 bps INFO @ Tue, 16 Jun 2020 08:16:01: #1 tag size = 32 INFO @ Tue, 16 Jun 2020 08:16:01: #1 total tags in treatment: 1153392 INFO @ Tue, 16 Jun 2020 08:16:01: #1 user defined the maximum tags... INFO @ Tue, 16 Jun 2020 08:16:01: #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 08:16:01: #1 tags after filtering in treatment: 1153392 INFO @ Tue, 16 Jun 2020 08:16:01: #1 Redundant rate of treatment: 0.00 INFO @ Tue, 16 Jun 2020 08:16:01: #1 finished! INFO @ Tue, 16 Jun 2020 08:16:01: #2 Build Peak Model... INFO @ Tue, 16 Jun 2020 08:16:01: #2 looking for paired plus/minus strand peaks... INFO @ Tue, 16 Jun 2020 08:16:01: #2 number of paired peaks: 441 WARNING @ Tue, 16 Jun 2020 08:16:01: Fewer paired peaks (441) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 441 pairs to build model! INFO @ Tue, 16 Jun 2020 08:16:01: start model_add_line... INFO @ Tue, 16 Jun 2020 08:16:01: start X-correlation... INFO @ Tue, 16 Jun 2020 08:16:01: end of X-cor INFO @ Tue, 16 Jun 2020 08:16:01: #2 finished! INFO @ Tue, 16 Jun 2020 08:16:01: #2 predicted fragment length is 34 bps INFO @ Tue, 16 Jun 2020 08:16:01: #2 alternative fragment length(s) may be 34,512,569 bps INFO @ Tue, 16 Jun 2020 08:16:01: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/ce11/SRX146489/SRX146489.20_model.r WARNING @ Tue, 16 Jun 2020 08:16:01: #2 Since the d (34) calculated from paired-peaks are smaller than 2*tag length, it may be influenced by unknown sequencing problem! WARNING @ Tue, 16 Jun 2020 08:16:01: #2 You may need to consider one of the other alternative d(s): 34,512,569 WARNING @ Tue, 16 Jun 2020 08:16:01: #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 08:16:01: #3 Call peaks... INFO @ Tue, 16 Jun 2020 08:16:01: #3 Pre-compute pvalue-qvalue table... BigWig に変換しました。 INFO @ Tue, 16 Jun 2020 08:16:04: #3 Call peaks for each chromosome... INFO @ Tue, 16 Jun 2020 08:16:05: #4 Write output xls file... /home/okishinya/chipatlas/results/ce11/SRX146489/SRX146489.20_peaks.xls INFO @ Tue, 16 Jun 2020 08:16:05: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/ce11/SRX146489/SRX146489.20_peaks.narrowPeak INFO @ Tue, 16 Jun 2020 08:16:05: #4 Write summits bed file... /home/okishinya/chipatlas/results/ce11/SRX146489/SRX146489.20_summits.bed INFO @ Tue, 16 Jun 2020 08:16:05: Done! pass1 - making usageList (6 chroms): 1 millis pass2 - checking and writing primary data (13 records, 4 fields): 0 millis CompletedMACS2peakCalling