Job ID = 6626368 SRX = SRX7262208 Genome = ce10 sra ファイルのダウンロード中... Read layout: SINGLE fastq に変換中... Read 7180962 spots for SRR10581831/SRR10581831.sra Written 7180962 spots for SRR10581831/SRR10581831.sra fastq に変換しました。 bowtie でマッピング中... Your job 6626427 ("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: 00:01:26 7180962 reads; of these: 7180962 (100.00%) were unpaired; of these: 1771295 (24.67%) aligned 0 times 4255448 (59.26%) aligned exactly 1 time 1154219 (16.07%) aligned >1 times 75.33% overall alignment rate Time searching: 00:01:26 Overall time: 00:01:26 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] 686072 / 5409667 = 0.1268 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 07:00:02: # Command line: callpeak -t /home/okishinya/chipatlas/results/ce10/SRX7262208/SRX7262208.bam -f BAM -g ce -n /home/okishinya/chipatlas/results/ce10/SRX7262208/SRX7262208.05 -q 1e-05 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/ce10/SRX7262208/SRX7262208.05 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/ce10/SRX7262208/SRX7262208.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 07:00:02: #1 read tag files... INFO @ Tue, 14 Jul 2020 07:00:02: #1 read treatment tags... INFO @ Tue, 14 Jul 2020 07:00:09: 1000000 INFO @ Tue, 14 Jul 2020 07:00:15: 2000000 INFO @ Tue, 14 Jul 2020 07:00:21: 3000000 INFO @ Tue, 14 Jul 2020 07:00:27: 4000000 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 07:00:32: #1 tag size is determined as 50 bps INFO @ Tue, 14 Jul 2020 07:00:32: #1 tag size = 50 INFO @ Tue, 14 Jul 2020 07:00:32: #1 total tags in treatment: 4723595 INFO @ Tue, 14 Jul 2020 07:00:32: #1 user defined the maximum tags... INFO @ Tue, 14 Jul 2020 07:00:32: #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 07:00:32: #1 tags after filtering in treatment: 4723595 INFO @ Tue, 14 Jul 2020 07:00:32: #1 Redundant rate of treatment: 0.00 INFO @ Tue, 14 Jul 2020 07:00:32: #1 finished! INFO @ Tue, 14 Jul 2020 07:00:32: #2 Build Peak Model... INFO @ Tue, 14 Jul 2020 07:00:32: #2 looking for paired plus/minus strand peaks... INFO @ Tue, 14 Jul 2020 07:00:32: #2 number of paired peaks: 619 WARNING @ Tue, 14 Jul 2020 07:00:32: Fewer paired peaks (619) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 619 pairs to build model! INFO @ Tue, 14 Jul 2020 07:00:32: start model_add_line... INFO @ Tue, 14 Jul 2020 07:00:32: start X-correlation... INFO @ Tue, 14 Jul 2020 07:00:32: end of X-cor INFO @ Tue, 14 Jul 2020 07:00:32: #2 finished! INFO @ Tue, 14 Jul 2020 07:00:32: #2 predicted fragment length is 50 bps INFO @ Tue, 14 Jul 2020 07:00:32: #2 alternative fragment length(s) may be 4,50,489 bps INFO @ Tue, 14 Jul 2020 07:00:32: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/ce10/SRX7262208/SRX7262208.05_model.r WARNING @ Tue, 14 Jul 2020 07:00:32: #2 Since the d (50) calculated from paired-peaks are smaller than 2*tag length, it may be influenced by unknown sequencing problem! WARNING @ Tue, 14 Jul 2020 07:00:32: #2 You may need to consider one of the other alternative d(s): 4,50,489 WARNING @ Tue, 14 Jul 2020 07:00:32: #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 07:00:32: #3 Call peaks... INFO @ Tue, 14 Jul 2020 07:00:32: #3 Pre-compute pvalue-qvalue table... INFO @ Tue, 14 Jul 2020 07:00:32: # Command line: callpeak -t /home/okishinya/chipatlas/results/ce10/SRX7262208/SRX7262208.bam -f BAM -g ce -n /home/okishinya/chipatlas/results/ce10/SRX7262208/SRX7262208.10 -q 1e-10 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/ce10/SRX7262208/SRX7262208.10 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/ce10/SRX7262208/SRX7262208.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 07:00:32: #1 read tag files... INFO @ Tue, 14 Jul 2020 07:00:32: #1 read treatment tags... INFO @ Tue, 14 Jul 2020 07:00:40: 1000000 INFO @ Tue, 14 Jul 2020 07:00:43: #3 Call peaks for each chromosome... INFO @ Tue, 14 Jul 2020 07:00:48: 2000000 INFO @ Tue, 14 Jul 2020 07:00:48: #4 Write output xls file... /home/okishinya/chipatlas/results/ce10/SRX7262208/SRX7262208.05_peaks.xls INFO @ Tue, 14 Jul 2020 07:00:49: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/ce10/SRX7262208/SRX7262208.05_peaks.narrowPeak INFO @ Tue, 14 Jul 2020 07:00:49: #4 Write summits bed file... /home/okishinya/chipatlas/results/ce10/SRX7262208/SRX7262208.05_summits.bed INFO @ Tue, 14 Jul 2020 07:00:49: Done! pass1 - making usageList (6 chroms): 1 millis pass2 - checking and writing primary data (530 records, 4 fields): 24 millis CompletedMACS2peakCalling INFO @ Tue, 14 Jul 2020 07:00:55: 3000000 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 07:01:02: # Command line: callpeak -t /home/okishinya/chipatlas/results/ce10/SRX7262208/SRX7262208.bam -f BAM -g ce -n /home/okishinya/chipatlas/results/ce10/SRX7262208/SRX7262208.20 -q 1e-20 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/ce10/SRX7262208/SRX7262208.20 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/ce10/SRX7262208/SRX7262208.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 07:01:02: #1 read tag files... INFO @ Tue, 14 Jul 2020 07:01:02: #1 read treatment tags... INFO @ Tue, 14 Jul 2020 07:01:03: 4000000 INFO @ Tue, 14 Jul 2020 07:01:09: #1 tag size is determined as 50 bps INFO @ Tue, 14 Jul 2020 07:01:09: #1 tag size = 50 INFO @ Tue, 14 Jul 2020 07:01:09: #1 total tags in treatment: 4723595 INFO @ Tue, 14 Jul 2020 07:01:09: #1 user defined the maximum tags... INFO @ Tue, 14 Jul 2020 07:01:09: #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 07:01:09: #1 tags after filtering in treatment: 4723595 INFO @ Tue, 14 Jul 2020 07:01:09: #1 Redundant rate of treatment: 0.00 INFO @ Tue, 14 Jul 2020 07:01:09: #1 finished! INFO @ Tue, 14 Jul 2020 07:01:09: #2 Build Peak Model... INFO @ Tue, 14 Jul 2020 07:01:09: #2 looking for paired plus/minus strand peaks... INFO @ Tue, 14 Jul 2020 07:01:09: #2 number of paired peaks: 619 WARNING @ Tue, 14 Jul 2020 07:01:09: Fewer paired peaks (619) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 619 pairs to build model! INFO @ Tue, 14 Jul 2020 07:01:09: start model_add_line... INFO @ Tue, 14 Jul 2020 07:01:09: start X-correlation... INFO @ Tue, 14 Jul 2020 07:01:09: end of X-cor INFO @ Tue, 14 Jul 2020 07:01:09: #2 finished! INFO @ Tue, 14 Jul 2020 07:01:09: #2 predicted fragment length is 50 bps INFO @ Tue, 14 Jul 2020 07:01:09: #2 alternative fragment length(s) may be 4,50,489 bps INFO @ Tue, 14 Jul 2020 07:01:09: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/ce10/SRX7262208/SRX7262208.10_model.r WARNING @ Tue, 14 Jul 2020 07:01:09: #2 Since the d (50) calculated from paired-peaks are smaller than 2*tag length, it may be influenced by unknown sequencing problem! WARNING @ Tue, 14 Jul 2020 07:01:09: #2 You may need to consider one of the other alternative d(s): 4,50,489 WARNING @ Tue, 14 Jul 2020 07:01:09: #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 07:01:09: #3 Call peaks... INFO @ Tue, 14 Jul 2020 07:01:09: #3 Pre-compute pvalue-qvalue table... INFO @ Tue, 14 Jul 2020 07:01:10: 1000000 INFO @ Tue, 14 Jul 2020 07:01:18: 2000000 INFO @ Tue, 14 Jul 2020 07:01:21: #3 Call peaks for each chromosome... BedGraph に変換しました。 BigWig に変換中... INFO @ Tue, 14 Jul 2020 07:01:26: 3000000 INFO @ Tue, 14 Jul 2020 07:01:26: #4 Write output xls file... /home/okishinya/chipatlas/results/ce10/SRX7262208/SRX7262208.10_peaks.xls INFO @ Tue, 14 Jul 2020 07:01:26: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/ce10/SRX7262208/SRX7262208.10_peaks.narrowPeak INFO @ Tue, 14 Jul 2020 07:01:26: #4 Write summits bed file... /home/okishinya/chipatlas/results/ce10/SRX7262208/SRX7262208.10_summits.bed INFO @ Tue, 14 Jul 2020 07:01:26: Done! pass1 - making usageList (6 chroms): 1 millis pass2 - checking and writing primary data (338 records, 4 fields): 1 millis CompletedMACS2peakCalling INFO @ Tue, 14 Jul 2020 07:01:33: 4000000 BigWig に変換しました。 INFO @ Tue, 14 Jul 2020 07:01:38: #1 tag size is determined as 50 bps INFO @ Tue, 14 Jul 2020 07:01:38: #1 tag size = 50 INFO @ Tue, 14 Jul 2020 07:01:38: #1 total tags in treatment: 4723595 INFO @ Tue, 14 Jul 2020 07:01:38: #1 user defined the maximum tags... INFO @ Tue, 14 Jul 2020 07:01:38: #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 07:01:39: #1 tags after filtering in treatment: 4723595 INFO @ Tue, 14 Jul 2020 07:01:39: #1 Redundant rate of treatment: 0.00 INFO @ Tue, 14 Jul 2020 07:01:39: #1 finished! INFO @ Tue, 14 Jul 2020 07:01:39: #2 Build Peak Model... INFO @ Tue, 14 Jul 2020 07:01:39: #2 looking for paired plus/minus strand peaks... INFO @ Tue, 14 Jul 2020 07:01:39: #2 number of paired peaks: 619 WARNING @ Tue, 14 Jul 2020 07:01:39: Fewer paired peaks (619) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 619 pairs to build model! INFO @ Tue, 14 Jul 2020 07:01:39: start model_add_line... INFO @ Tue, 14 Jul 2020 07:01:39: start X-correlation... INFO @ Tue, 14 Jul 2020 07:01:39: end of X-cor INFO @ Tue, 14 Jul 2020 07:01:39: #2 finished! INFO @ Tue, 14 Jul 2020 07:01:39: #2 predicted fragment length is 50 bps INFO @ Tue, 14 Jul 2020 07:01:39: #2 alternative fragment length(s) may be 4,50,489 bps INFO @ Tue, 14 Jul 2020 07:01:39: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/ce10/SRX7262208/SRX7262208.20_model.r WARNING @ Tue, 14 Jul 2020 07:01:39: #2 Since the d (50) calculated from paired-peaks are smaller than 2*tag length, it may be influenced by unknown sequencing problem! WARNING @ Tue, 14 Jul 2020 07:01:39: #2 You may need to consider one of the other alternative d(s): 4,50,489 WARNING @ Tue, 14 Jul 2020 07:01:39: #2 You can restart the process with --nomodel --extsize XXX with your choice or an arbitrary number. Nontheless, MACS will continute computing. INFO @ Tue, 14 Jul 2020 07:01:39: #3 Call peaks... INFO @ Tue, 14 Jul 2020 07:01:39: #3 Pre-compute pvalue-qvalue table... INFO @ Tue, 14 Jul 2020 07:01:50: #3 Call peaks for each chromosome... INFO @ Tue, 14 Jul 2020 07:01:56: #4 Write output xls file... /home/okishinya/chipatlas/results/ce10/SRX7262208/SRX7262208.20_peaks.xls INFO @ Tue, 14 Jul 2020 07:01:56: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/ce10/SRX7262208/SRX7262208.20_peaks.narrowPeak INFO @ Tue, 14 Jul 2020 07:01:56: #4 Write summits bed file... /home/okishinya/chipatlas/results/ce10/SRX7262208/SRX7262208.20_summits.bed INFO @ Tue, 14 Jul 2020 07:01:56: Done! pass1 - making usageList (6 chroms): 1 millis pass2 - checking and writing primary data (135 records, 4 fields): 21 millis CompletedMACS2peakCalling