Job ID = 6626413 SRX = SRX7262239 Genome = ce10 sra ファイルのダウンロード中... Read layout: SINGLE fastq に変換中... Read 4289752 spots for SRR10581862/SRR10581862.sra Written 4289752 spots for SRR10581862/SRR10581862.sra fastq に変換しました。 bowtie でマッピング中... Your job 6626511 ("srTce11") has been submitted Time loading reference: 00:00:00 Time loading forward index: 00:00:00 Time loading mirror index: 00:00:00 Multiseed full-index search: 00:01:05 4289752 reads; of these: 4289752 (100.00%) were unpaired; of these: 339457 (7.91%) aligned 0 times 3109948 (72.50%) aligned exactly 1 time 840347 (19.59%) aligned >1 times 92.09% overall alignment rate Time searching: 00:01:05 Overall time: 00:01:05 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] 980651 / 3950295 = 0.2482 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, 14 Jul 2020 07:02:10: # Command line: callpeak -t /home/okishinya/chipatlas/results/ce10/SRX7262239/SRX7262239.bam -f BAM -g ce -n /home/okishinya/chipatlas/results/ce10/SRX7262239/SRX7262239.05 -q 1e-05 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/ce10/SRX7262239/SRX7262239.05 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/ce10/SRX7262239/SRX7262239.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, 14 Jul 2020 07:02:10: #1 read tag files... INFO @ Tue, 14 Jul 2020 07:02:10: #1 read treatment tags... INFO @ Tue, 14 Jul 2020 07:02:17: 1000000 INFO @ Tue, 14 Jul 2020 07:02:24: 2000000 INFO @ Tue, 14 Jul 2020 07:02:30: #1 tag size is determined as 50 bps INFO @ Tue, 14 Jul 2020 07:02:30: #1 tag size = 50 INFO @ Tue, 14 Jul 2020 07:02:30: #1 total tags in treatment: 2969644 INFO @ Tue, 14 Jul 2020 07:02:30: #1 user defined the maximum tags... INFO @ Tue, 14 Jul 2020 07:02:30: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Tue, 14 Jul 2020 07:02:30: #1 tags after filtering in treatment: 2969644 INFO @ Tue, 14 Jul 2020 07:02:30: #1 Redundant rate of treatment: 0.00 INFO @ Tue, 14 Jul 2020 07:02:30: #1 finished! INFO @ Tue, 14 Jul 2020 07:02:30: #2 Build Peak Model... INFO @ Tue, 14 Jul 2020 07:02:30: #2 looking for paired plus/minus strand peaks... INFO @ Tue, 14 Jul 2020 07:02:30: #2 number of paired peaks: 553 WARNING @ Tue, 14 Jul 2020 07:02:30: Fewer paired peaks (553) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 553 pairs to build model! INFO @ Tue, 14 Jul 2020 07:02:30: start model_add_line... INFO @ Tue, 14 Jul 2020 07:02:30: start X-correlation... INFO @ Tue, 14 Jul 2020 07:02:30: end of X-cor INFO @ Tue, 14 Jul 2020 07:02:30: #2 finished! INFO @ Tue, 14 Jul 2020 07:02:30: #2 predicted fragment length is 48 bps INFO @ Tue, 14 Jul 2020 07:02:30: #2 alternative fragment length(s) may be 4,48,575 bps INFO @ Tue, 14 Jul 2020 07:02:30: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/ce10/SRX7262239/SRX7262239.05_model.r WARNING @ Tue, 14 Jul 2020 07:02:30: #2 Since the d (48) calculated from paired-peaks are smaller than 2*tag length, it may be influenced by unknown sequencing problem! WARNING @ Tue, 14 Jul 2020 07:02:30: #2 You may need to consider one of the other alternative d(s): 4,48,575 WARNING @ Tue, 14 Jul 2020 07:02:30: #2 You can restart the process with --nomodel --extsize XXX with your choice or an arbitrary number. Nontheless, MACS will continute computing. INFO @ Tue, 14 Jul 2020 07:02:30: #3 Call peaks... INFO @ Tue, 14 Jul 2020 07:02:30: #3 Pre-compute pvalue-qvalue table... INFO @ Tue, 14 Jul 2020 07:02:37: #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, 14 Jul 2020 07:02:40: #4 Write output xls file... /home/okishinya/chipatlas/results/ce10/SRX7262239/SRX7262239.05_peaks.xls INFO @ Tue, 14 Jul 2020 07:02:40: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/ce10/SRX7262239/SRX7262239.05_peaks.narrowPeak INFO @ Tue, 14 Jul 2020 07:02:40: #4 Write summits bed file... /home/okishinya/chipatlas/results/ce10/SRX7262239/SRX7262239.05_summits.bed INFO @ Tue, 14 Jul 2020 07:02:40: Done! pass1 - making usageList (6 chroms): 1 millis pass2 - checking and writing primary data (523 records, 4 fields): 30 millis INFO @ Tue, 14 Jul 2020 07:02:40: # Command line: callpeak -t /home/okishinya/chipatlas/results/ce10/SRX7262239/SRX7262239.bam -f BAM -g ce -n /home/okishinya/chipatlas/results/ce10/SRX7262239/SRX7262239.10 -q 1e-10 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/ce10/SRX7262239/SRX7262239.10 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/ce10/SRX7262239/SRX7262239.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, 14 Jul 2020 07:02:40: #1 read tag files... INFO @ Tue, 14 Jul 2020 07:02:40: #1 read treatment tags... CompletedMACS2peakCalling INFO @ Tue, 14 Jul 2020 07:02:47: 1000000 INFO @ Tue, 14 Jul 2020 07:02:54: 2000000 INFO @ Tue, 14 Jul 2020 07:03:02: #1 tag size is determined as 50 bps INFO @ Tue, 14 Jul 2020 07:03:02: #1 tag size = 50 INFO @ Tue, 14 Jul 2020 07:03:02: #1 total tags in treatment: 2969644 INFO @ Tue, 14 Jul 2020 07:03:02: #1 user defined the maximum tags... INFO @ Tue, 14 Jul 2020 07:03:02: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Tue, 14 Jul 2020 07:03:02: #1 tags after filtering in treatment: 2969644 INFO @ Tue, 14 Jul 2020 07:03:02: #1 Redundant rate of treatment: 0.00 INFO @ Tue, 14 Jul 2020 07:03:02: #1 finished! INFO @ Tue, 14 Jul 2020 07:03:02: #2 Build Peak Model... INFO @ Tue, 14 Jul 2020 07:03:02: #2 looking for paired plus/minus strand peaks... INFO @ Tue, 14 Jul 2020 07:03:02: #2 number of paired peaks: 553 WARNING @ Tue, 14 Jul 2020 07:03:02: Fewer paired peaks (553) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 553 pairs to build model! INFO @ Tue, 14 Jul 2020 07:03:02: start model_add_line... INFO @ Tue, 14 Jul 2020 07:03:02: start X-correlation... INFO @ Tue, 14 Jul 2020 07:03:02: end of X-cor INFO @ Tue, 14 Jul 2020 07:03:02: #2 finished! INFO @ Tue, 14 Jul 2020 07:03:02: #2 predicted fragment length is 48 bps INFO @ Tue, 14 Jul 2020 07:03:02: #2 alternative fragment length(s) may be 4,48,575 bps INFO @ Tue, 14 Jul 2020 07:03:02: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/ce10/SRX7262239/SRX7262239.10_model.r WARNING @ Tue, 14 Jul 2020 07:03:02: #2 Since the d (48) calculated from paired-peaks are smaller than 2*tag length, it may be influenced by unknown sequencing problem! WARNING @ Tue, 14 Jul 2020 07:03:02: #2 You may need to consider one of the other alternative d(s): 4,48,575 WARNING @ Tue, 14 Jul 2020 07:03:02: #2 You can restart the process with --nomodel --extsize XXX with your choice or an arbitrary number. Nontheless, MACS will continute computing. INFO @ Tue, 14 Jul 2020 07:03:02: #3 Call peaks... INFO @ Tue, 14 Jul 2020 07:03:02: #3 Pre-compute pvalue-qvalue table... 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, 14 Jul 2020 07:03:08: #3 Call peaks for each chromosome... INFO @ Tue, 14 Jul 2020 07:03:10: # Command line: callpeak -t /home/okishinya/chipatlas/results/ce10/SRX7262239/SRX7262239.bam -f BAM -g ce -n /home/okishinya/chipatlas/results/ce10/SRX7262239/SRX7262239.20 -q 1e-20 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/ce10/SRX7262239/SRX7262239.20 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/ce10/SRX7262239/SRX7262239.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, 14 Jul 2020 07:03:10: #1 read tag files... INFO @ Tue, 14 Jul 2020 07:03:10: #1 read treatment tags... INFO @ Tue, 14 Jul 2020 07:03:12: #4 Write output xls file... /home/okishinya/chipatlas/results/ce10/SRX7262239/SRX7262239.10_peaks.xls INFO @ Tue, 14 Jul 2020 07:03:12: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/ce10/SRX7262239/SRX7262239.10_peaks.narrowPeak INFO @ Tue, 14 Jul 2020 07:03:12: #4 Write summits bed file... /home/okishinya/chipatlas/results/ce10/SRX7262239/SRX7262239.10_summits.bed INFO @ Tue, 14 Jul 2020 07:03:12: Done! pass1 - making usageList (6 chroms): 0 millis pass2 - checking and writing primary data (314 records, 4 fields): 15 millis CompletedMACS2peakCalling INFO @ Tue, 14 Jul 2020 07:03:17: 1000000 BedGraph に変換しました。 BigWig に変換中... INFO @ Tue, 14 Jul 2020 07:03:23: 2000000 INFO @ Tue, 14 Jul 2020 07:03:30: #1 tag size is determined as 50 bps INFO @ Tue, 14 Jul 2020 07:03:30: #1 tag size = 50 INFO @ Tue, 14 Jul 2020 07:03:30: #1 total tags in treatment: 2969644 INFO @ Tue, 14 Jul 2020 07:03:30: #1 user defined the maximum tags... INFO @ Tue, 14 Jul 2020 07:03:30: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Tue, 14 Jul 2020 07:03:30: #1 tags after filtering in treatment: 2969644 INFO @ Tue, 14 Jul 2020 07:03:30: #1 Redundant rate of treatment: 0.00 INFO @ Tue, 14 Jul 2020 07:03:30: #1 finished! INFO @ Tue, 14 Jul 2020 07:03:30: #2 Build Peak Model... INFO @ Tue, 14 Jul 2020 07:03:30: #2 looking for paired plus/minus strand peaks... BigWig に変換しました。 INFO @ Tue, 14 Jul 2020 07:03:30: #2 number of paired peaks: 553 WARNING @ Tue, 14 Jul 2020 07:03:30: Fewer paired peaks (553) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 553 pairs to build model! INFO @ Tue, 14 Jul 2020 07:03:30: start model_add_line... INFO @ Tue, 14 Jul 2020 07:03:30: start X-correlation... INFO @ Tue, 14 Jul 2020 07:03:30: end of X-cor INFO @ Tue, 14 Jul 2020 07:03:30: #2 finished! INFO @ Tue, 14 Jul 2020 07:03:30: #2 predicted fragment length is 48 bps INFO @ Tue, 14 Jul 2020 07:03:30: #2 alternative fragment length(s) may be 4,48,575 bps INFO @ Tue, 14 Jul 2020 07:03:30: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/ce10/SRX7262239/SRX7262239.20_model.r WARNING @ Tue, 14 Jul 2020 07:03:30: #2 Since the d (48) calculated from paired-peaks are smaller than 2*tag length, it may be influenced by unknown sequencing problem! WARNING @ Tue, 14 Jul 2020 07:03:30: #2 You may need to consider one of the other alternative d(s): 4,48,575 WARNING @ Tue, 14 Jul 2020 07:03:30: #2 You can restart the process with --nomodel --extsize XXX with your choice or an arbitrary number. Nontheless, MACS will continute computing. INFO @ Tue, 14 Jul 2020 07:03:30: #3 Call peaks... INFO @ Tue, 14 Jul 2020 07:03:30: #3 Pre-compute pvalue-qvalue table... INFO @ Tue, 14 Jul 2020 07:03:37: #3 Call peaks for each chromosome... INFO @ Tue, 14 Jul 2020 07:03:41: #4 Write output xls file... /home/okishinya/chipatlas/results/ce10/SRX7262239/SRX7262239.20_peaks.xls INFO @ Tue, 14 Jul 2020 07:03:41: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/ce10/SRX7262239/SRX7262239.20_peaks.narrowPeak INFO @ Tue, 14 Jul 2020 07:03:41: #4 Write summits bed file... /home/okishinya/chipatlas/results/ce10/SRX7262239/SRX7262239.20_summits.bed INFO @ Tue, 14 Jul 2020 07:03:41: Done! pass1 - making usageList (6 chroms): 1 millis pass2 - checking and writing primary data (124 records, 4 fields): 17 millis CompletedMACS2peakCalling