Job ID = 6365930 SRX = SRX043863 Genome = ce11 sra ファイルのダウンロード中... Read layout: SINGLE fastq に変換中... 2020-06-15T22:20:59 prefetch.2.10.7: 1) Downloading 'SRR107324'... 2020-06-15T22:20:59 prefetch.2.10.7: Downloading via HTTPS... 2020-06-15T22:21:32 prefetch.2.10.7: HTTPS download succeed 2020-06-15T22:21:33 prefetch.2.10.7: 'SRR107324' is valid 2020-06-15T22:21:33 prefetch.2.10.7: 1) 'SRR107324' was downloaded successfully Read 4304838 spots for SRR107324/SRR107324.sra Written 4304838 spots for SRR107324/SRR107324.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: 00:00:43 4304838 reads; of these: 4304838 (100.00%) were unpaired; of these: 1154148 (26.81%) aligned 0 times 2682021 (62.30%) aligned exactly 1 time 468669 (10.89%) aligned >1 times 73.19% overall alignment rate Time searching: 00:00:43 Overall time: 00:00:43 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] 289438 / 3150690 = 0.0919 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 07:23:47: # Command line: callpeak -t /home/okishinya/chipatlas/results/ce11/SRX043863/SRX043863.bam -f BAM -g ce -n /home/okishinya/chipatlas/results/ce11/SRX043863/SRX043863.05 -q 1e-05 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/ce11/SRX043863/SRX043863.05 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/ce11/SRX043863/SRX043863.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 07:23:47: #1 read tag files... INFO @ Tue, 16 Jun 2020 07:23:47: #1 read treatment tags... INFO @ Tue, 16 Jun 2020 07:23:52: 1000000 INFO @ Tue, 16 Jun 2020 07:23:58: 2000000 INFO @ Tue, 16 Jun 2020 07:24:03: #1 tag size is determined as 34 bps INFO @ Tue, 16 Jun 2020 07:24:03: #1 tag size = 34 INFO @ Tue, 16 Jun 2020 07:24:03: #1 total tags in treatment: 2861252 INFO @ Tue, 16 Jun 2020 07:24:03: #1 user defined the maximum tags... INFO @ Tue, 16 Jun 2020 07:24:03: #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 07:24:03: #1 tags after filtering in treatment: 2861252 INFO @ Tue, 16 Jun 2020 07:24:03: #1 Redundant rate of treatment: 0.00 INFO @ Tue, 16 Jun 2020 07:24:03: #1 finished! INFO @ Tue, 16 Jun 2020 07:24:03: #2 Build Peak Model... INFO @ Tue, 16 Jun 2020 07:24:03: #2 looking for paired plus/minus strand peaks... INFO @ Tue, 16 Jun 2020 07:24:03: #2 number of paired peaks: 295 WARNING @ Tue, 16 Jun 2020 07:24:03: Fewer paired peaks (295) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 295 pairs to build model! INFO @ Tue, 16 Jun 2020 07:24:03: start model_add_line... INFO @ Tue, 16 Jun 2020 07:24:03: start X-correlation... INFO @ Tue, 16 Jun 2020 07:24:03: end of X-cor INFO @ Tue, 16 Jun 2020 07:24:03: #2 finished! INFO @ Tue, 16 Jun 2020 07:24:03: #2 predicted fragment length is 36 bps INFO @ Tue, 16 Jun 2020 07:24:03: #2 alternative fragment length(s) may be 2,36,73,527,562,582 bps INFO @ Tue, 16 Jun 2020 07:24:03: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/ce11/SRX043863/SRX043863.05_model.r WARNING @ Tue, 16 Jun 2020 07:24:03: #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 07:24:03: #2 You may need to consider one of the other alternative d(s): 2,36,73,527,562,582 WARNING @ Tue, 16 Jun 2020 07:24:03: #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 07:24:03: #3 Call peaks... INFO @ Tue, 16 Jun 2020 07:24:03: #3 Pre-compute pvalue-qvalue table... INFO @ Tue, 16 Jun 2020 07:24:09: #3 Call peaks for each chromosome... INFO @ Tue, 16 Jun 2020 07:24:13: #4 Write output xls file... /home/okishinya/chipatlas/results/ce11/SRX043863/SRX043863.05_peaks.xls INFO @ Tue, 16 Jun 2020 07:24:13: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/ce11/SRX043863/SRX043863.05_peaks.narrowPeak INFO @ Tue, 16 Jun 2020 07:24:13: #4 Write summits bed file... /home/okishinya/chipatlas/results/ce11/SRX043863/SRX043863.05_summits.bed INFO @ Tue, 16 Jun 2020 07:24:13: Done! pass1 - making usageList (6 chroms): 0 millis pass2 - checking and writing primary data (231 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 07:24:17: # Command line: callpeak -t /home/okishinya/chipatlas/results/ce11/SRX043863/SRX043863.bam -f BAM -g ce -n /home/okishinya/chipatlas/results/ce11/SRX043863/SRX043863.10 -q 1e-10 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/ce11/SRX043863/SRX043863.10 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/ce11/SRX043863/SRX043863.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 07:24:17: #1 read tag files... INFO @ Tue, 16 Jun 2020 07:24:17: #1 read treatment tags... INFO @ Tue, 16 Jun 2020 07:24:22: 1000000 INFO @ Tue, 16 Jun 2020 07:24:28: 2000000 INFO @ Tue, 16 Jun 2020 07:24:33: #1 tag size is determined as 34 bps INFO @ Tue, 16 Jun 2020 07:24:33: #1 tag size = 34 INFO @ Tue, 16 Jun 2020 07:24:33: #1 total tags in treatment: 2861252 INFO @ Tue, 16 Jun 2020 07:24:33: #1 user defined the maximum tags... INFO @ Tue, 16 Jun 2020 07:24:33: #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 07:24:33: #1 tags after filtering in treatment: 2861252 INFO @ Tue, 16 Jun 2020 07:24:33: #1 Redundant rate of treatment: 0.00 INFO @ Tue, 16 Jun 2020 07:24:33: #1 finished! INFO @ Tue, 16 Jun 2020 07:24:33: #2 Build Peak Model... INFO @ Tue, 16 Jun 2020 07:24:33: #2 looking for paired plus/minus strand peaks... INFO @ Tue, 16 Jun 2020 07:24:34: #2 number of paired peaks: 295 WARNING @ Tue, 16 Jun 2020 07:24:34: Fewer paired peaks (295) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 295 pairs to build model! INFO @ Tue, 16 Jun 2020 07:24:34: start model_add_line... INFO @ Tue, 16 Jun 2020 07:24:34: start X-correlation... INFO @ Tue, 16 Jun 2020 07:24:34: end of X-cor INFO @ Tue, 16 Jun 2020 07:24:34: #2 finished! INFO @ Tue, 16 Jun 2020 07:24:34: #2 predicted fragment length is 36 bps INFO @ Tue, 16 Jun 2020 07:24:34: #2 alternative fragment length(s) may be 2,36,73,527,562,582 bps INFO @ Tue, 16 Jun 2020 07:24:34: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/ce11/SRX043863/SRX043863.10_model.r WARNING @ Tue, 16 Jun 2020 07:24:34: #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 07:24:34: #2 You may need to consider one of the other alternative d(s): 2,36,73,527,562,582 WARNING @ Tue, 16 Jun 2020 07:24:34: #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 07:24:34: #3 Call peaks... INFO @ Tue, 16 Jun 2020 07:24:34: #3 Pre-compute pvalue-qvalue table... INFO @ Tue, 16 Jun 2020 07:24:40: #3 Call peaks for each chromosome... INFO @ Tue, 16 Jun 2020 07:24:43: #4 Write output xls file... /home/okishinya/chipatlas/results/ce11/SRX043863/SRX043863.10_peaks.xls INFO @ Tue, 16 Jun 2020 07:24:43: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/ce11/SRX043863/SRX043863.10_peaks.narrowPeak INFO @ Tue, 16 Jun 2020 07:24:43: #4 Write summits bed file... /home/okishinya/chipatlas/results/ce11/SRX043863/SRX043863.10_summits.bed INFO @ Tue, 16 Jun 2020 07:24:43: Done! pass1 - making usageList (6 chroms): 1 millis pass2 - checking and writing primary data (86 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 07:24:47: # Command line: callpeak -t /home/okishinya/chipatlas/results/ce11/SRX043863/SRX043863.bam -f BAM -g ce -n /home/okishinya/chipatlas/results/ce11/SRX043863/SRX043863.20 -q 1e-20 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/ce11/SRX043863/SRX043863.20 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/ce11/SRX043863/SRX043863.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 07:24:47: #1 read tag files... INFO @ Tue, 16 Jun 2020 07:24:47: #1 read treatment tags... INFO @ Tue, 16 Jun 2020 07:24:53: 1000000 INFO @ Tue, 16 Jun 2020 07:24:59: 2000000 BedGraph に変換しました。 BigWig に変換中... INFO @ Tue, 16 Jun 2020 07:25:04: #1 tag size is determined as 34 bps INFO @ Tue, 16 Jun 2020 07:25:04: #1 tag size = 34 INFO @ Tue, 16 Jun 2020 07:25:04: #1 total tags in treatment: 2861252 INFO @ Tue, 16 Jun 2020 07:25:04: #1 user defined the maximum tags... INFO @ Tue, 16 Jun 2020 07:25:04: #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 07:25:04: #1 tags after filtering in treatment: 2861252 INFO @ Tue, 16 Jun 2020 07:25:04: #1 Redundant rate of treatment: 0.00 INFO @ Tue, 16 Jun 2020 07:25:04: #1 finished! INFO @ Tue, 16 Jun 2020 07:25:04: #2 Build Peak Model... INFO @ Tue, 16 Jun 2020 07:25:04: #2 looking for paired plus/minus strand peaks... INFO @ Tue, 16 Jun 2020 07:25:04: #2 number of paired peaks: 295 WARNING @ Tue, 16 Jun 2020 07:25:04: Fewer paired peaks (295) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 295 pairs to build model! INFO @ Tue, 16 Jun 2020 07:25:04: start model_add_line... INFO @ Tue, 16 Jun 2020 07:25:04: start X-correlation... INFO @ Tue, 16 Jun 2020 07:25:04: end of X-cor INFO @ Tue, 16 Jun 2020 07:25:04: #2 finished! INFO @ Tue, 16 Jun 2020 07:25:04: #2 predicted fragment length is 36 bps INFO @ Tue, 16 Jun 2020 07:25:04: #2 alternative fragment length(s) may be 2,36,73,527,562,582 bps INFO @ Tue, 16 Jun 2020 07:25:04: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/ce11/SRX043863/SRX043863.20_model.r WARNING @ Tue, 16 Jun 2020 07:25:04: #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 07:25:04: #2 You may need to consider one of the other alternative d(s): 2,36,73,527,562,582 WARNING @ Tue, 16 Jun 2020 07:25:04: #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 07:25:04: #3 Call peaks... INFO @ Tue, 16 Jun 2020 07:25:04: #3 Pre-compute pvalue-qvalue table... BigWig に変換しました。 INFO @ Tue, 16 Jun 2020 07:25:11: #3 Call peaks for each chromosome... INFO @ Tue, 16 Jun 2020 07:25:14: #4 Write output xls file... /home/okishinya/chipatlas/results/ce11/SRX043863/SRX043863.20_peaks.xls INFO @ Tue, 16 Jun 2020 07:25:14: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/ce11/SRX043863/SRX043863.20_peaks.narrowPeak INFO @ Tue, 16 Jun 2020 07:25:14: #4 Write summits bed file... /home/okishinya/chipatlas/results/ce11/SRX043863/SRX043863.20_summits.bed INFO @ Tue, 16 Jun 2020 07:25:14: Done! pass1 - making usageList (6 chroms): 0 millis pass2 - checking and writing primary data (11 records, 4 fields): 1 millis CompletedMACS2peakCalling