Job ID = 6366008 SRX = SRX044021 Genome = ce11 sra ファイルのダウンロード中... Read layout: SINGLE fastq に変換中... 2020-06-15T22:35:06 prefetch.2.10.7: 1) Downloading 'SRR107603'... 2020-06-15T22:35:06 prefetch.2.10.7: Downloading via HTTPS... 2020-06-15T22:36:36 prefetch.2.10.7: HTTPS download succeed 2020-06-15T22:36:36 prefetch.2.10.7: 'SRR107603' is valid 2020-06-15T22:36:36 prefetch.2.10.7: 1) 'SRR107603' was downloaded successfully Read 14244415 spots for SRR107603/SRR107603.sra Written 14244415 spots for SRR107603/SRR107603.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 14244415 reads; of these: 14244415 (100.00%) were unpaired; of these: 13244478 (92.98%) aligned 0 times 847675 (5.95%) aligned exactly 1 time 152262 (1.07%) aligned >1 times 7.02% 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] 24133 / 999937 = 0.0241 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 07:38:46: # Command line: callpeak -t /home/okishinya/chipatlas/results/ce11/SRX044021/SRX044021.bam -f BAM -g ce -n /home/okishinya/chipatlas/results/ce11/SRX044021/SRX044021.05 -q 1e-05 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/ce11/SRX044021/SRX044021.05 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/ce11/SRX044021/SRX044021.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 07:38:46: #1 read tag files... INFO @ Tue, 16 Jun 2020 07:38:46: #1 read treatment tags... INFO @ Tue, 16 Jun 2020 07:38:52: #1 tag size is determined as 34 bps INFO @ Tue, 16 Jun 2020 07:38:52: #1 tag size = 34 INFO @ Tue, 16 Jun 2020 07:38:52: #1 total tags in treatment: 975804 INFO @ Tue, 16 Jun 2020 07:38:52: #1 user defined the maximum tags... INFO @ Tue, 16 Jun 2020 07:38:52: #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 07:38:52: #1 tags after filtering in treatment: 975804 INFO @ Tue, 16 Jun 2020 07:38:52: #1 Redundant rate of treatment: 0.00 INFO @ Tue, 16 Jun 2020 07:38:52: #1 finished! INFO @ Tue, 16 Jun 2020 07:38:52: #2 Build Peak Model... INFO @ Tue, 16 Jun 2020 07:38:52: #2 looking for paired plus/minus strand peaks... INFO @ Tue, 16 Jun 2020 07:38:52: #2 number of paired peaks: 313 WARNING @ Tue, 16 Jun 2020 07:38:52: Fewer paired peaks (313) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 313 pairs to build model! INFO @ Tue, 16 Jun 2020 07:38:52: start model_add_line... INFO @ Tue, 16 Jun 2020 07:38:52: start X-correlation... INFO @ Tue, 16 Jun 2020 07:38:52: end of X-cor INFO @ Tue, 16 Jun 2020 07:38:52: #2 finished! INFO @ Tue, 16 Jun 2020 07:38:52: #2 predicted fragment length is 101 bps INFO @ Tue, 16 Jun 2020 07:38:52: #2 alternative fragment length(s) may be 35,101,152,568 bps INFO @ Tue, 16 Jun 2020 07:38:52: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/ce11/SRX044021/SRX044021.05_model.r INFO @ Tue, 16 Jun 2020 07:38:52: #3 Call peaks... INFO @ Tue, 16 Jun 2020 07:38:52: #3 Pre-compute pvalue-qvalue table... INFO @ Tue, 16 Jun 2020 07:38:54: #3 Call peaks for each chromosome... INFO @ Tue, 16 Jun 2020 07:38:56: #4 Write output xls file... /home/okishinya/chipatlas/results/ce11/SRX044021/SRX044021.05_peaks.xls INFO @ Tue, 16 Jun 2020 07:38:56: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/ce11/SRX044021/SRX044021.05_peaks.narrowPeak INFO @ Tue, 16 Jun 2020 07:38:56: #4 Write summits bed file... /home/okishinya/chipatlas/results/ce11/SRX044021/SRX044021.05_summits.bed INFO @ Tue, 16 Jun 2020 07:38:56: Done! pass1 - making usageList (7 chroms): 0 millis pass2 - checking and writing primary data (111 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 07:39:16: # Command line: callpeak -t /home/okishinya/chipatlas/results/ce11/SRX044021/SRX044021.bam -f BAM -g ce -n /home/okishinya/chipatlas/results/ce11/SRX044021/SRX044021.10 -q 1e-10 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/ce11/SRX044021/SRX044021.10 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/ce11/SRX044021/SRX044021.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 07:39:16: #1 read tag files... INFO @ Tue, 16 Jun 2020 07:39:16: #1 read treatment tags... INFO @ Tue, 16 Jun 2020 07:39:22: #1 tag size is determined as 34 bps INFO @ Tue, 16 Jun 2020 07:39:22: #1 tag size = 34 INFO @ Tue, 16 Jun 2020 07:39:22: #1 total tags in treatment: 975804 INFO @ Tue, 16 Jun 2020 07:39:22: #1 user defined the maximum tags... INFO @ Tue, 16 Jun 2020 07:39:22: #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 07:39:22: #1 tags after filtering in treatment: 975804 INFO @ Tue, 16 Jun 2020 07:39:22: #1 Redundant rate of treatment: 0.00 INFO @ Tue, 16 Jun 2020 07:39:22: #1 finished! INFO @ Tue, 16 Jun 2020 07:39:22: #2 Build Peak Model... INFO @ Tue, 16 Jun 2020 07:39:22: #2 looking for paired plus/minus strand peaks... INFO @ Tue, 16 Jun 2020 07:39:22: #2 number of paired peaks: 313 WARNING @ Tue, 16 Jun 2020 07:39:22: Fewer paired peaks (313) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 313 pairs to build model! INFO @ Tue, 16 Jun 2020 07:39:22: start model_add_line... INFO @ Tue, 16 Jun 2020 07:39:22: start X-correlation... INFO @ Tue, 16 Jun 2020 07:39:22: end of X-cor INFO @ Tue, 16 Jun 2020 07:39:22: #2 finished! INFO @ Tue, 16 Jun 2020 07:39:22: #2 predicted fragment length is 101 bps INFO @ Tue, 16 Jun 2020 07:39:22: #2 alternative fragment length(s) may be 35,101,152,568 bps INFO @ Tue, 16 Jun 2020 07:39:22: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/ce11/SRX044021/SRX044021.10_model.r INFO @ Tue, 16 Jun 2020 07:39:22: #3 Call peaks... INFO @ Tue, 16 Jun 2020 07:39:22: #3 Pre-compute pvalue-qvalue table... INFO @ Tue, 16 Jun 2020 07:39:25: #3 Call peaks for each chromosome... INFO @ Tue, 16 Jun 2020 07:39:26: #4 Write output xls file... /home/okishinya/chipatlas/results/ce11/SRX044021/SRX044021.10_peaks.xls INFO @ Tue, 16 Jun 2020 07:39:26: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/ce11/SRX044021/SRX044021.10_peaks.narrowPeak INFO @ Tue, 16 Jun 2020 07:39:26: #4 Write summits bed file... /home/okishinya/chipatlas/results/ce11/SRX044021/SRX044021.10_summits.bed INFO @ Tue, 16 Jun 2020 07:39:26: Done! pass1 - making usageList (7 chroms): 0 millis pass2 - checking and writing primary data (52 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 07:39:46: # Command line: callpeak -t /home/okishinya/chipatlas/results/ce11/SRX044021/SRX044021.bam -f BAM -g ce -n /home/okishinya/chipatlas/results/ce11/SRX044021/SRX044021.20 -q 1e-20 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/ce11/SRX044021/SRX044021.20 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/ce11/SRX044021/SRX044021.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 07:39:46: #1 read tag files... INFO @ Tue, 16 Jun 2020 07:39:46: #1 read treatment tags... BedGraph に変換しました。 BigWig に変換中... BigWig に変換しました。 INFO @ Tue, 16 Jun 2020 07:39:52: #1 tag size is determined as 34 bps INFO @ Tue, 16 Jun 2020 07:39:52: #1 tag size = 34 INFO @ Tue, 16 Jun 2020 07:39:52: #1 total tags in treatment: 975804 INFO @ Tue, 16 Jun 2020 07:39:52: #1 user defined the maximum tags... INFO @ Tue, 16 Jun 2020 07:39:52: #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 07:39:52: #1 tags after filtering in treatment: 975804 INFO @ Tue, 16 Jun 2020 07:39:52: #1 Redundant rate of treatment: 0.00 INFO @ Tue, 16 Jun 2020 07:39:52: #1 finished! INFO @ Tue, 16 Jun 2020 07:39:52: #2 Build Peak Model... INFO @ Tue, 16 Jun 2020 07:39:52: #2 looking for paired plus/minus strand peaks... INFO @ Tue, 16 Jun 2020 07:39:53: #2 number of paired peaks: 313 WARNING @ Tue, 16 Jun 2020 07:39:53: Fewer paired peaks (313) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 313 pairs to build model! INFO @ Tue, 16 Jun 2020 07:39:53: start model_add_line... INFO @ Tue, 16 Jun 2020 07:39:53: start X-correlation... INFO @ Tue, 16 Jun 2020 07:39:53: end of X-cor INFO @ Tue, 16 Jun 2020 07:39:53: #2 finished! INFO @ Tue, 16 Jun 2020 07:39:53: #2 predicted fragment length is 101 bps INFO @ Tue, 16 Jun 2020 07:39:53: #2 alternative fragment length(s) may be 35,101,152,568 bps INFO @ Tue, 16 Jun 2020 07:39:53: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/ce11/SRX044021/SRX044021.20_model.r INFO @ Tue, 16 Jun 2020 07:39:53: #3 Call peaks... INFO @ Tue, 16 Jun 2020 07:39:53: #3 Pre-compute pvalue-qvalue table... INFO @ Tue, 16 Jun 2020 07:39:55: #3 Call peaks for each chromosome... INFO @ Tue, 16 Jun 2020 07:39:56: #4 Write output xls file... /home/okishinya/chipatlas/results/ce11/SRX044021/SRX044021.20_peaks.xls INFO @ Tue, 16 Jun 2020 07:39:56: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/ce11/SRX044021/SRX044021.20_peaks.narrowPeak INFO @ Tue, 16 Jun 2020 07:39:56: #4 Write summits bed file... /home/okishinya/chipatlas/results/ce11/SRX044021/SRX044021.20_summits.bed INFO @ Tue, 16 Jun 2020 07:39:56: Done! pass1 - making usageList (7 chroms): 1 millis pass2 - checking and writing primary data (18 records, 4 fields): 0 millis CompletedMACS2peakCalling