Job ID = 6367291 SRX = SRX331053 Genome = ce11 sra ファイルのダウンロード中... Read layout: SINGLE fastq に変換中... 2020-06-15T23:20:46 prefetch.2.10.7: 1) Downloading 'SRR947276'... 2020-06-15T23:20:46 prefetch.2.10.7: Downloading via HTTPS... 2020-06-15T23:21:07 prefetch.2.10.7: HTTPS download succeed 2020-06-15T23:21:08 prefetch.2.10.7: 'SRR947276' is valid 2020-06-15T23:21:08 prefetch.2.10.7: 1) 'SRR947276' was downloaded successfully Read 3927952 spots for SRR947276/SRR947276.sra Written 3927952 spots for SRR947276/SRR947276.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: 00:00:44 3927952 reads; of these: 3927952 (100.00%) were unpaired; of these: 147327 (3.75%) aligned 0 times 3161892 (80.50%) aligned exactly 1 time 618733 (15.75%) aligned >1 times 96.25% overall alignment rate Time searching: 00:00:44 Overall time: 00:00:44 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] 142300 / 3780625 = 0.0376 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 08:23:22: # Command line: callpeak -t /home/okishinya/chipatlas/results/ce11/SRX331053/SRX331053.bam -f BAM -g ce -n /home/okishinya/chipatlas/results/ce11/SRX331053/SRX331053.05 -q 1e-05 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/ce11/SRX331053/SRX331053.05 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/ce11/SRX331053/SRX331053.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 08:23:22: #1 read tag files... INFO @ Tue, 16 Jun 2020 08:23:22: #1 read treatment tags... INFO @ Tue, 16 Jun 2020 08:23:27: 1000000 INFO @ Tue, 16 Jun 2020 08:23:31: 2000000 INFO @ Tue, 16 Jun 2020 08:23:36: 3000000 INFO @ Tue, 16 Jun 2020 08:23:39: #1 tag size is determined as 32 bps INFO @ Tue, 16 Jun 2020 08:23:39: #1 tag size = 32 INFO @ Tue, 16 Jun 2020 08:23:39: #1 total tags in treatment: 3638325 INFO @ Tue, 16 Jun 2020 08:23:39: #1 user defined the maximum tags... INFO @ Tue, 16 Jun 2020 08:23:39: #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 08:23:39: #1 tags after filtering in treatment: 3638325 INFO @ Tue, 16 Jun 2020 08:23:39: #1 Redundant rate of treatment: 0.00 INFO @ Tue, 16 Jun 2020 08:23:39: #1 finished! INFO @ Tue, 16 Jun 2020 08:23:39: #2 Build Peak Model... INFO @ Tue, 16 Jun 2020 08:23:39: #2 looking for paired plus/minus strand peaks... INFO @ Tue, 16 Jun 2020 08:23:39: #2 number of paired peaks: 383 WARNING @ Tue, 16 Jun 2020 08:23:39: Fewer paired peaks (383) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 383 pairs to build model! INFO @ Tue, 16 Jun 2020 08:23:39: start model_add_line... INFO @ Tue, 16 Jun 2020 08:23:39: start X-correlation... INFO @ Tue, 16 Jun 2020 08:23:39: end of X-cor INFO @ Tue, 16 Jun 2020 08:23:39: #2 finished! INFO @ Tue, 16 Jun 2020 08:23:39: #2 predicted fragment length is 31 bps INFO @ Tue, 16 Jun 2020 08:23:39: #2 alternative fragment length(s) may be 31,451,467,590 bps INFO @ Tue, 16 Jun 2020 08:23:39: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/ce11/SRX331053/SRX331053.05_model.r WARNING @ Tue, 16 Jun 2020 08:23:39: #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 08:23:39: #2 You may need to consider one of the other alternative d(s): 31,451,467,590 WARNING @ Tue, 16 Jun 2020 08:23:39: #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 08:23:39: #3 Call peaks... INFO @ Tue, 16 Jun 2020 08:23:39: #3 Pre-compute pvalue-qvalue table... INFO @ Tue, 16 Jun 2020 08:23:47: #3 Call peaks for each chromosome... 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 08:23:51: # Command line: callpeak -t /home/okishinya/chipatlas/results/ce11/SRX331053/SRX331053.bam -f BAM -g ce -n /home/okishinya/chipatlas/results/ce11/SRX331053/SRX331053.10 -q 1e-10 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/ce11/SRX331053/SRX331053.10 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/ce11/SRX331053/SRX331053.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 08:23:51: #1 read tag files... INFO @ Tue, 16 Jun 2020 08:23:51: #1 read treatment tags... INFO @ Tue, 16 Jun 2020 08:23:51: #4 Write output xls file... /home/okishinya/chipatlas/results/ce11/SRX331053/SRX331053.05_peaks.xls INFO @ Tue, 16 Jun 2020 08:23:51: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/ce11/SRX331053/SRX331053.05_peaks.narrowPeak INFO @ Tue, 16 Jun 2020 08:23:51: #4 Write summits bed file... /home/okishinya/chipatlas/results/ce11/SRX331053/SRX331053.05_summits.bed INFO @ Tue, 16 Jun 2020 08:23:52: Done! pass1 - making usageList (7 chroms): 1 millis pass2 - checking and writing primary data (349 records, 4 fields): 1 millis CompletedMACS2peakCalling INFO @ Tue, 16 Jun 2020 08:23:56: 1000000 INFO @ Tue, 16 Jun 2020 08:24:02: 2000000 INFO @ Tue, 16 Jun 2020 08:24:07: 3000000 INFO @ Tue, 16 Jun 2020 08:24:10: #1 tag size is determined as 32 bps INFO @ Tue, 16 Jun 2020 08:24:10: #1 tag size = 32 INFO @ Tue, 16 Jun 2020 08:24:10: #1 total tags in treatment: 3638325 INFO @ Tue, 16 Jun 2020 08:24:10: #1 user defined the maximum tags... INFO @ Tue, 16 Jun 2020 08:24:10: #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 08:24:10: #1 tags after filtering in treatment: 3638325 INFO @ Tue, 16 Jun 2020 08:24:10: #1 Redundant rate of treatment: 0.00 INFO @ Tue, 16 Jun 2020 08:24:10: #1 finished! INFO @ Tue, 16 Jun 2020 08:24:10: #2 Build Peak Model... INFO @ Tue, 16 Jun 2020 08:24:10: #2 looking for paired plus/minus strand peaks... INFO @ Tue, 16 Jun 2020 08:24:10: #2 number of paired peaks: 383 WARNING @ Tue, 16 Jun 2020 08:24:10: Fewer paired peaks (383) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 383 pairs to build model! INFO @ Tue, 16 Jun 2020 08:24:10: start model_add_line... INFO @ Tue, 16 Jun 2020 08:24:10: start X-correlation... INFO @ Tue, 16 Jun 2020 08:24:10: end of X-cor INFO @ Tue, 16 Jun 2020 08:24:10: #2 finished! INFO @ Tue, 16 Jun 2020 08:24:10: #2 predicted fragment length is 31 bps INFO @ Tue, 16 Jun 2020 08:24:10: #2 alternative fragment length(s) may be 31,451,467,590 bps INFO @ Tue, 16 Jun 2020 08:24:10: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/ce11/SRX331053/SRX331053.10_model.r WARNING @ Tue, 16 Jun 2020 08:24:10: #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 08:24:10: #2 You may need to consider one of the other alternative d(s): 31,451,467,590 WARNING @ Tue, 16 Jun 2020 08:24:10: #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 08:24:10: #3 Call peaks... INFO @ Tue, 16 Jun 2020 08:24:10: #3 Pre-compute pvalue-qvalue table... INFO @ Tue, 16 Jun 2020 08:24:18: #3 Call peaks for each chromosome... 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 08:24:21: # Command line: callpeak -t /home/okishinya/chipatlas/results/ce11/SRX331053/SRX331053.bam -f BAM -g ce -n /home/okishinya/chipatlas/results/ce11/SRX331053/SRX331053.20 -q 1e-20 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/ce11/SRX331053/SRX331053.20 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/ce11/SRX331053/SRX331053.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 08:24:21: #1 read tag files... INFO @ Tue, 16 Jun 2020 08:24:21: #1 read treatment tags... INFO @ Tue, 16 Jun 2020 08:24:22: #4 Write output xls file... /home/okishinya/chipatlas/results/ce11/SRX331053/SRX331053.10_peaks.xls INFO @ Tue, 16 Jun 2020 08:24:22: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/ce11/SRX331053/SRX331053.10_peaks.narrowPeak INFO @ Tue, 16 Jun 2020 08:24:22: #4 Write summits bed file... /home/okishinya/chipatlas/results/ce11/SRX331053/SRX331053.10_summits.bed INFO @ Tue, 16 Jun 2020 08:24:22: Done! pass1 - making usageList (6 chroms): 0 millis pass2 - checking and writing primary data (166 records, 4 fields): 1 millis CompletedMACS2peakCalling INFO @ Tue, 16 Jun 2020 08:24:26: 1000000 INFO @ Tue, 16 Jun 2020 08:24:32: 2000000 BedGraph に変換しました。 BigWig に変換中... INFO @ Tue, 16 Jun 2020 08:24:37: 3000000 INFO @ Tue, 16 Jun 2020 08:24:41: #1 tag size is determined as 32 bps INFO @ Tue, 16 Jun 2020 08:24:41: #1 tag size = 32 INFO @ Tue, 16 Jun 2020 08:24:41: #1 total tags in treatment: 3638325 INFO @ Tue, 16 Jun 2020 08:24:41: #1 user defined the maximum tags... INFO @ Tue, 16 Jun 2020 08:24:41: #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 08:24:41: #1 tags after filtering in treatment: 3638325 INFO @ Tue, 16 Jun 2020 08:24:41: #1 Redundant rate of treatment: 0.00 INFO @ Tue, 16 Jun 2020 08:24:41: #1 finished! INFO @ Tue, 16 Jun 2020 08:24:41: #2 Build Peak Model... INFO @ Tue, 16 Jun 2020 08:24:41: #2 looking for paired plus/minus strand peaks... INFO @ Tue, 16 Jun 2020 08:24:41: #2 number of paired peaks: 383 WARNING @ Tue, 16 Jun 2020 08:24:41: Fewer paired peaks (383) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 383 pairs to build model! INFO @ Tue, 16 Jun 2020 08:24:41: start model_add_line... INFO @ Tue, 16 Jun 2020 08:24:41: start X-correlation... INFO @ Tue, 16 Jun 2020 08:24:41: end of X-cor INFO @ Tue, 16 Jun 2020 08:24:41: #2 finished! INFO @ Tue, 16 Jun 2020 08:24:41: #2 predicted fragment length is 31 bps INFO @ Tue, 16 Jun 2020 08:24:41: #2 alternative fragment length(s) may be 31,451,467,590 bps INFO @ Tue, 16 Jun 2020 08:24:41: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/ce11/SRX331053/SRX331053.20_model.r WARNING @ Tue, 16 Jun 2020 08:24:41: #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 08:24:41: #2 You may need to consider one of the other alternative d(s): 31,451,467,590 WARNING @ Tue, 16 Jun 2020 08:24:41: #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 08:24:41: #3 Call peaks... INFO @ Tue, 16 Jun 2020 08:24:41: #3 Pre-compute pvalue-qvalue table... BigWig に変換しました。 INFO @ Tue, 16 Jun 2020 08:24:49: #3 Call peaks for each chromosome... INFO @ Tue, 16 Jun 2020 08:24:53: #4 Write output xls file... /home/okishinya/chipatlas/results/ce11/SRX331053/SRX331053.20_peaks.xls INFO @ Tue, 16 Jun 2020 08:24:53: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/ce11/SRX331053/SRX331053.20_peaks.narrowPeak INFO @ Tue, 16 Jun 2020 08:24:53: #4 Write summits bed file... /home/okishinya/chipatlas/results/ce11/SRX331053/SRX331053.20_summits.bed INFO @ Tue, 16 Jun 2020 08:24:53: Done! pass1 - making usageList (6 chroms): 0 millis pass2 - checking and writing primary data (48 records, 4 fields): 1 millis CompletedMACS2peakCalling