Job ID = 14520688 SRX = SRX8866055 Genome = sacCer3 sra ファイルのダウンロード中... Read layout: SINGLE fastq に変換中... Read 1958913 spots for SRR12366842/SRR12366842.sra Written 1958913 spots for SRR12366842/SRR12366842.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: 00:00:12 1958913 reads; of these: 1958913 (100.00%) were unpaired; of these: 395021 (20.17%) aligned 0 times 1364709 (69.67%) aligned exactly 1 time 199183 (10.17%) aligned >1 times 79.83% overall alignment rate Time searching: 00:00:12 Overall time: 00:00:12 マッピングが完了しました。 samtools でBAM に変換中... [samopen] SAM header is present: 17 sequences. [bam_rmdupse_core] 429447 / 1563892 = 0.2746 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/3.8.3/var/singularity/mnt/session/etc/resolv.conf [files]: /etc/resolv.conf doesn't exist in container INFO @ Sat, 15 Jan 2022 19:38:03: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/SRX8866055/SRX8866055.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/SRX8866055/SRX8866055.05 -q 1e-05 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/SRX8866055/SRX8866055.05 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/SRX8866055/SRX8866055.bam'] # control file = None # effective genome size = 1.21e+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 @ Sat, 15 Jan 2022 19:38:03: #1 read tag files... INFO @ Sat, 15 Jan 2022 19:38:03: #1 read treatment tags... INFO @ Sat, 15 Jan 2022 19:38:07: 1000000 INFO @ Sat, 15 Jan 2022 19:38:08: #1 tag size is determined as 50 bps INFO @ Sat, 15 Jan 2022 19:38:08: #1 tag size = 50 INFO @ Sat, 15 Jan 2022 19:38:08: #1 total tags in treatment: 1134445 INFO @ Sat, 15 Jan 2022 19:38:08: #1 user defined the maximum tags... INFO @ Sat, 15 Jan 2022 19:38:08: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Sat, 15 Jan 2022 19:38:08: #1 tags after filtering in treatment: 1134445 INFO @ Sat, 15 Jan 2022 19:38:08: #1 Redundant rate of treatment: 0.00 INFO @ Sat, 15 Jan 2022 19:38:08: #1 finished! INFO @ Sat, 15 Jan 2022 19:38:08: #2 Build Peak Model... INFO @ Sat, 15 Jan 2022 19:38:08: #2 looking for paired plus/minus strand peaks... INFO @ Sat, 15 Jan 2022 19:38:08: #2 number of paired peaks: 400 WARNING @ Sat, 15 Jan 2022 19:38:08: Fewer paired peaks (400) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 400 pairs to build model! INFO @ Sat, 15 Jan 2022 19:38:08: start model_add_line... INFO @ Sat, 15 Jan 2022 19:38:08: start X-correlation... INFO @ Sat, 15 Jan 2022 19:38:08: end of X-cor INFO @ Sat, 15 Jan 2022 19:38:08: #2 finished! INFO @ Sat, 15 Jan 2022 19:38:08: #2 predicted fragment length is 115 bps INFO @ Sat, 15 Jan 2022 19:38:08: #2 alternative fragment length(s) may be 115 bps INFO @ Sat, 15 Jan 2022 19:38:08: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/sacCer3/SRX8866055/SRX8866055.05_model.r INFO @ Sat, 15 Jan 2022 19:38:08: #3 Call peaks... INFO @ Sat, 15 Jan 2022 19:38:08: #3 Pre-compute pvalue-qvalue table... INFO @ Sat, 15 Jan 2022 19:38:11: #3 Call peaks for each chromosome... INFO @ Sat, 15 Jan 2022 19:38:12: #4 Write output xls file... /home/okishinya/chipatlas/results/sacCer3/SRX8866055/SRX8866055.05_peaks.xls INFO @ Sat, 15 Jan 2022 19:38:12: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/sacCer3/SRX8866055/SRX8866055.05_peaks.narrowPeak INFO @ Sat, 15 Jan 2022 19:38:12: #4 Write summits bed file... /home/okishinya/chipatlas/results/sacCer3/SRX8866055/SRX8866055.05_summits.bed INFO @ Sat, 15 Jan 2022 19:38:12: Done! pass1 - making usageList (17 chroms): 1 millis pass2 - checking and writing primary data (1670 records, 4 fields): 4 millis CompletedMACS2peakCalling WARNING: Skipping mount /opt/pkg/singularity/3.8.3/var/singularity/mnt/session/etc/resolv.conf [files]: /etc/resolv.conf doesn't exist in container INFO @ Sat, 15 Jan 2022 19:38:33: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/SRX8866055/SRX8866055.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/SRX8866055/SRX8866055.10 -q 1e-10 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/SRX8866055/SRX8866055.10 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/SRX8866055/SRX8866055.bam'] # control file = None # effective genome size = 1.21e+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 @ Sat, 15 Jan 2022 19:38:33: #1 read tag files... INFO @ Sat, 15 Jan 2022 19:38:33: #1 read treatment tags... INFO @ Sat, 15 Jan 2022 19:38:38: 1000000 INFO @ Sat, 15 Jan 2022 19:38:39: #1 tag size is determined as 50 bps INFO @ Sat, 15 Jan 2022 19:38:39: #1 tag size = 50 INFO @ Sat, 15 Jan 2022 19:38:39: #1 total tags in treatment: 1134445 INFO @ Sat, 15 Jan 2022 19:38:39: #1 user defined the maximum tags... INFO @ Sat, 15 Jan 2022 19:38:39: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Sat, 15 Jan 2022 19:38:39: #1 tags after filtering in treatment: 1134445 INFO @ Sat, 15 Jan 2022 19:38:39: #1 Redundant rate of treatment: 0.00 INFO @ Sat, 15 Jan 2022 19:38:39: #1 finished! INFO @ Sat, 15 Jan 2022 19:38:39: #2 Build Peak Model... INFO @ Sat, 15 Jan 2022 19:38:39: #2 looking for paired plus/minus strand peaks... INFO @ Sat, 15 Jan 2022 19:38:39: #2 number of paired peaks: 400 WARNING @ Sat, 15 Jan 2022 19:38:39: Fewer paired peaks (400) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 400 pairs to build model! INFO @ Sat, 15 Jan 2022 19:38:39: start model_add_line... INFO @ Sat, 15 Jan 2022 19:38:39: start X-correlation... INFO @ Sat, 15 Jan 2022 19:38:39: end of X-cor INFO @ Sat, 15 Jan 2022 19:38:39: #2 finished! INFO @ Sat, 15 Jan 2022 19:38:39: #2 predicted fragment length is 115 bps INFO @ Sat, 15 Jan 2022 19:38:39: #2 alternative fragment length(s) may be 115 bps INFO @ Sat, 15 Jan 2022 19:38:39: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/sacCer3/SRX8866055/SRX8866055.10_model.r INFO @ Sat, 15 Jan 2022 19:38:39: #3 Call peaks... INFO @ Sat, 15 Jan 2022 19:38:39: #3 Pre-compute pvalue-qvalue table... INFO @ Sat, 15 Jan 2022 19:38:42: #3 Call peaks for each chromosome... INFO @ Sat, 15 Jan 2022 19:38:43: #4 Write output xls file... /home/okishinya/chipatlas/results/sacCer3/SRX8866055/SRX8866055.10_peaks.xls INFO @ Sat, 15 Jan 2022 19:38:43: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/sacCer3/SRX8866055/SRX8866055.10_peaks.narrowPeak INFO @ Sat, 15 Jan 2022 19:38:43: #4 Write summits bed file... /home/okishinya/chipatlas/results/sacCer3/SRX8866055/SRX8866055.10_summits.bed INFO @ Sat, 15 Jan 2022 19:38:43: Done! pass1 - making usageList (17 chroms): 1 millis pass2 - checking and writing primary data (982 records, 4 fields): 3 millis CompletedMACS2peakCalling BedGraph に変換中... WARNING: Skipping mount /opt/pkg/singularity/3.8.3/var/singularity/mnt/session/etc/resolv.conf [files]: /etc/resolv.conf doesn't exist in container INFO @ Sat, 15 Jan 2022 19:39:03: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/SRX8866055/SRX8866055.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/SRX8866055/SRX8866055.20 -q 1e-20 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/SRX8866055/SRX8866055.20 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/SRX8866055/SRX8866055.bam'] # control file = None # effective genome size = 1.21e+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 @ Sat, 15 Jan 2022 19:39:03: #1 read tag files... INFO @ Sat, 15 Jan 2022 19:39:03: #1 read treatment tags... BedGraph に変換しました。 BigWig に変換中... INFO @ Sat, 15 Jan 2022 19:39:07: 1000000 INFO @ Sat, 15 Jan 2022 19:39:08: #1 tag size is determined as 50 bps INFO @ Sat, 15 Jan 2022 19:39:08: #1 tag size = 50 INFO @ Sat, 15 Jan 2022 19:39:08: #1 total tags in treatment: 1134445 INFO @ Sat, 15 Jan 2022 19:39:08: #1 user defined the maximum tags... INFO @ Sat, 15 Jan 2022 19:39:08: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Sat, 15 Jan 2022 19:39:08: #1 tags after filtering in treatment: 1134445 INFO @ Sat, 15 Jan 2022 19:39:08: #1 Redundant rate of treatment: 0.00 INFO @ Sat, 15 Jan 2022 19:39:08: #1 finished! INFO @ Sat, 15 Jan 2022 19:39:08: #2 Build Peak Model... INFO @ Sat, 15 Jan 2022 19:39:08: #2 looking for paired plus/minus strand peaks... INFO @ Sat, 15 Jan 2022 19:39:08: #2 number of paired peaks: 400 WARNING @ Sat, 15 Jan 2022 19:39:08: Fewer paired peaks (400) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 400 pairs to build model! INFO @ Sat, 15 Jan 2022 19:39:08: start model_add_line... INFO @ Sat, 15 Jan 2022 19:39:08: start X-correlation... INFO @ Sat, 15 Jan 2022 19:39:08: end of X-cor INFO @ Sat, 15 Jan 2022 19:39:08: #2 finished! INFO @ Sat, 15 Jan 2022 19:39:08: #2 predicted fragment length is 115 bps INFO @ Sat, 15 Jan 2022 19:39:08: #2 alternative fragment length(s) may be 115 bps INFO @ Sat, 15 Jan 2022 19:39:08: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/sacCer3/SRX8866055/SRX8866055.20_model.r INFO @ Sat, 15 Jan 2022 19:39:08: #3 Call peaks... INFO @ Sat, 15 Jan 2022 19:39:08: #3 Pre-compute pvalue-qvalue table... BigWig に変換しました。 INFO @ Sat, 15 Jan 2022 19:39:11: #3 Call peaks for each chromosome... INFO @ Sat, 15 Jan 2022 19:39:12: #4 Write output xls file... /home/okishinya/chipatlas/results/sacCer3/SRX8866055/SRX8866055.20_peaks.xls INFO @ Sat, 15 Jan 2022 19:39:12: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/sacCer3/SRX8866055/SRX8866055.20_peaks.narrowPeak INFO @ Sat, 15 Jan 2022 19:39:12: #4 Write summits bed file... /home/okishinya/chipatlas/results/sacCer3/SRX8866055/SRX8866055.20_summits.bed INFO @ Sat, 15 Jan 2022 19:39:12: Done! pass1 - making usageList (17 chroms): 0 millis pass2 - checking and writing primary data (477 records, 4 fields): 2 millis CompletedMACS2peakCalling