Job ID = 6367136 SRX = SRX277094 Genome = ce11 sra ファイルのダウンロード中... Read layout: SINGLE fastq に変換中... 2020-06-15T23:16:01 prefetch.2.10.7: 1) Downloading 'SRR849770'... 2020-06-15T23:16:01 prefetch.2.10.7: Downloading via HTTPS... 2020-06-15T23:16:23 prefetch.2.10.7: HTTPS download succeed 2020-06-15T23:16:23 prefetch.2.10.7: 'SRR849770' is valid 2020-06-15T23:16:23 prefetch.2.10.7: 1) 'SRR849770' was downloaded successfully Read 2675433 spots for SRR849770/SRR849770.sra Written 2675433 spots for SRR849770/SRR849770.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: 00:00:01 Multiseed full-index search: 00:00:26 2675433 reads; of these: 2675433 (100.00%) were unpaired; of these: 76216 (2.85%) aligned 0 times 2178763 (81.44%) aligned exactly 1 time 420454 (15.72%) aligned >1 times 97.15% overall alignment rate Time searching: 00:00:27 Overall time: 00:00:27 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] 78189 / 2599217 = 0.0301 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 08:18:00: # Command line: callpeak -t /home/okishinya/chipatlas/results/ce11/SRX277094/SRX277094.bam -f BAM -g ce -n /home/okishinya/chipatlas/results/ce11/SRX277094/SRX277094.05 -q 1e-05 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/ce11/SRX277094/SRX277094.05 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/ce11/SRX277094/SRX277094.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 08:18:00: #1 read tag files... INFO @ Tue, 16 Jun 2020 08:18:00: #1 read treatment tags... INFO @ Tue, 16 Jun 2020 08:18:05: 1000000 INFO @ Tue, 16 Jun 2020 08:18:11: 2000000 INFO @ Tue, 16 Jun 2020 08:18:14: #1 tag size is determined as 32 bps INFO @ Tue, 16 Jun 2020 08:18:14: #1 tag size = 32 INFO @ Tue, 16 Jun 2020 08:18:14: #1 total tags in treatment: 2521028 INFO @ Tue, 16 Jun 2020 08:18:14: #1 user defined the maximum tags... INFO @ Tue, 16 Jun 2020 08:18:14: #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 08:18:14: #1 tags after filtering in treatment: 2521028 INFO @ Tue, 16 Jun 2020 08:18:14: #1 Redundant rate of treatment: 0.00 INFO @ Tue, 16 Jun 2020 08:18:14: #1 finished! INFO @ Tue, 16 Jun 2020 08:18:14: #2 Build Peak Model... INFO @ Tue, 16 Jun 2020 08:18:14: #2 looking for paired plus/minus strand peaks... INFO @ Tue, 16 Jun 2020 08:18:14: #2 number of paired peaks: 352 WARNING @ Tue, 16 Jun 2020 08:18:14: Fewer paired peaks (352) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 352 pairs to build model! INFO @ Tue, 16 Jun 2020 08:18:14: start model_add_line... INFO @ Tue, 16 Jun 2020 08:18:14: start X-correlation... INFO @ Tue, 16 Jun 2020 08:18:14: end of X-cor INFO @ Tue, 16 Jun 2020 08:18:14: #2 finished! INFO @ Tue, 16 Jun 2020 08:18:14: #2 predicted fragment length is 32 bps INFO @ Tue, 16 Jun 2020 08:18:14: #2 alternative fragment length(s) may be 32,406,593 bps INFO @ Tue, 16 Jun 2020 08:18:14: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/ce11/SRX277094/SRX277094.05_model.r WARNING @ Tue, 16 Jun 2020 08:18:14: #2 Since the d (32) calculated from paired-peaks are smaller than 2*tag length, it may be influenced by unknown sequencing problem! WARNING @ Tue, 16 Jun 2020 08:18:14: #2 You may need to consider one of the other alternative d(s): 32,406,593 WARNING @ Tue, 16 Jun 2020 08:18:14: #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 08:18:14: #3 Call peaks... INFO @ Tue, 16 Jun 2020 08:18:14: #3 Pre-compute pvalue-qvalue table... INFO @ Tue, 16 Jun 2020 08:18:20: #3 Call peaks for each chromosome... INFO @ Tue, 16 Jun 2020 08:18:23: #4 Write output xls file... /home/okishinya/chipatlas/results/ce11/SRX277094/SRX277094.05_peaks.xls INFO @ Tue, 16 Jun 2020 08:18:23: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/ce11/SRX277094/SRX277094.05_peaks.narrowPeak INFO @ Tue, 16 Jun 2020 08:18:23: #4 Write summits bed file... /home/okishinya/chipatlas/results/ce11/SRX277094/SRX277094.05_summits.bed INFO @ Tue, 16 Jun 2020 08:18:23: Done! pass1 - making usageList (6 chroms): 1 millis pass2 - checking and writing primary data (242 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 08:18:30: # Command line: callpeak -t /home/okishinya/chipatlas/results/ce11/SRX277094/SRX277094.bam -f BAM -g ce -n /home/okishinya/chipatlas/results/ce11/SRX277094/SRX277094.10 -q 1e-10 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/ce11/SRX277094/SRX277094.10 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/ce11/SRX277094/SRX277094.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 08:18:30: #1 read tag files... INFO @ Tue, 16 Jun 2020 08:18:30: #1 read treatment tags... INFO @ Tue, 16 Jun 2020 08:18:35: 1000000 INFO @ Tue, 16 Jun 2020 08:18:41: 2000000 INFO @ Tue, 16 Jun 2020 08:18:44: #1 tag size is determined as 32 bps INFO @ Tue, 16 Jun 2020 08:18:44: #1 tag size = 32 INFO @ Tue, 16 Jun 2020 08:18:44: #1 total tags in treatment: 2521028 INFO @ Tue, 16 Jun 2020 08:18:44: #1 user defined the maximum tags... INFO @ Tue, 16 Jun 2020 08:18:44: #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 08:18:44: #1 tags after filtering in treatment: 2521028 INFO @ Tue, 16 Jun 2020 08:18:44: #1 Redundant rate of treatment: 0.00 INFO @ Tue, 16 Jun 2020 08:18:44: #1 finished! INFO @ Tue, 16 Jun 2020 08:18:44: #2 Build Peak Model... INFO @ Tue, 16 Jun 2020 08:18:44: #2 looking for paired plus/minus strand peaks... INFO @ Tue, 16 Jun 2020 08:18:44: #2 number of paired peaks: 352 WARNING @ Tue, 16 Jun 2020 08:18:44: Fewer paired peaks (352) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 352 pairs to build model! INFO @ Tue, 16 Jun 2020 08:18:44: start model_add_line... INFO @ Tue, 16 Jun 2020 08:18:44: start X-correlation... INFO @ Tue, 16 Jun 2020 08:18:44: end of X-cor INFO @ Tue, 16 Jun 2020 08:18:44: #2 finished! INFO @ Tue, 16 Jun 2020 08:18:44: #2 predicted fragment length is 32 bps INFO @ Tue, 16 Jun 2020 08:18:44: #2 alternative fragment length(s) may be 32,406,593 bps INFO @ Tue, 16 Jun 2020 08:18:44: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/ce11/SRX277094/SRX277094.10_model.r WARNING @ Tue, 16 Jun 2020 08:18:44: #2 Since the d (32) calculated from paired-peaks are smaller than 2*tag length, it may be influenced by unknown sequencing problem! WARNING @ Tue, 16 Jun 2020 08:18:44: #2 You may need to consider one of the other alternative d(s): 32,406,593 WARNING @ Tue, 16 Jun 2020 08:18:44: #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 08:18:44: #3 Call peaks... INFO @ Tue, 16 Jun 2020 08:18:44: #3 Pre-compute pvalue-qvalue table... INFO @ Tue, 16 Jun 2020 08:18:50: #3 Call peaks for each chromosome... INFO @ Tue, 16 Jun 2020 08:18:53: #4 Write output xls file... /home/okishinya/chipatlas/results/ce11/SRX277094/SRX277094.10_peaks.xls INFO @ Tue, 16 Jun 2020 08:18:53: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/ce11/SRX277094/SRX277094.10_peaks.narrowPeak INFO @ Tue, 16 Jun 2020 08:18:53: #4 Write summits bed file... /home/okishinya/chipatlas/results/ce11/SRX277094/SRX277094.10_summits.bed INFO @ Tue, 16 Jun 2020 08:18:53: Done! pass1 - making usageList (6 chroms): 0 millis pass2 - checking and writing primary data (117 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 08:19:00: # Command line: callpeak -t /home/okishinya/chipatlas/results/ce11/SRX277094/SRX277094.bam -f BAM -g ce -n /home/okishinya/chipatlas/results/ce11/SRX277094/SRX277094.20 -q 1e-20 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/ce11/SRX277094/SRX277094.20 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/ce11/SRX277094/SRX277094.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 08:19:00: #1 read tag files... INFO @ Tue, 16 Jun 2020 08:19:00: #1 read treatment tags... INFO @ Tue, 16 Jun 2020 08:19:06: 1000000 BedGraph に変換しました。 BigWig に変換中... INFO @ Tue, 16 Jun 2020 08:19:13: 2000000 BigWig に変換しました。 INFO @ Tue, 16 Jun 2020 08:19:16: #1 tag size is determined as 32 bps INFO @ Tue, 16 Jun 2020 08:19:16: #1 tag size = 32 INFO @ Tue, 16 Jun 2020 08:19:16: #1 total tags in treatment: 2521028 INFO @ Tue, 16 Jun 2020 08:19:16: #1 user defined the maximum tags... INFO @ Tue, 16 Jun 2020 08:19:16: #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 08:19:16: #1 tags after filtering in treatment: 2521028 INFO @ Tue, 16 Jun 2020 08:19:16: #1 Redundant rate of treatment: 0.00 INFO @ Tue, 16 Jun 2020 08:19:16: #1 finished! INFO @ Tue, 16 Jun 2020 08:19:16: #2 Build Peak Model... INFO @ Tue, 16 Jun 2020 08:19:16: #2 looking for paired plus/minus strand peaks... INFO @ Tue, 16 Jun 2020 08:19:17: #2 number of paired peaks: 352 WARNING @ Tue, 16 Jun 2020 08:19:17: Fewer paired peaks (352) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 352 pairs to build model! INFO @ Tue, 16 Jun 2020 08:19:17: start model_add_line... INFO @ Tue, 16 Jun 2020 08:19:17: start X-correlation... INFO @ Tue, 16 Jun 2020 08:19:17: end of X-cor INFO @ Tue, 16 Jun 2020 08:19:17: #2 finished! INFO @ Tue, 16 Jun 2020 08:19:17: #2 predicted fragment length is 32 bps INFO @ Tue, 16 Jun 2020 08:19:17: #2 alternative fragment length(s) may be 32,406,593 bps INFO @ Tue, 16 Jun 2020 08:19:17: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/ce11/SRX277094/SRX277094.20_model.r WARNING @ Tue, 16 Jun 2020 08:19:17: #2 Since the d (32) calculated from paired-peaks are smaller than 2*tag length, it may be influenced by unknown sequencing problem! WARNING @ Tue, 16 Jun 2020 08:19:17: #2 You may need to consider one of the other alternative d(s): 32,406,593 WARNING @ Tue, 16 Jun 2020 08:19:17: #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 08:19:17: #3 Call peaks... INFO @ Tue, 16 Jun 2020 08:19:17: #3 Pre-compute pvalue-qvalue table... INFO @ Tue, 16 Jun 2020 08:19:23: #3 Call peaks for each chromosome... INFO @ Tue, 16 Jun 2020 08:19:26: #4 Write output xls file... /home/okishinya/chipatlas/results/ce11/SRX277094/SRX277094.20_peaks.xls INFO @ Tue, 16 Jun 2020 08:19:26: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/ce11/SRX277094/SRX277094.20_peaks.narrowPeak INFO @ Tue, 16 Jun 2020 08:19:26: #4 Write summits bed file... /home/okishinya/chipatlas/results/ce11/SRX277094/SRX277094.20_summits.bed INFO @ Tue, 16 Jun 2020 08:19:26: Done! pass1 - making usageList (6 chroms): 0 millis pass2 - checking and writing primary data (28 records, 4 fields): 1 millis CompletedMACS2peakCalling