Job ID = 5720406 sra ファイルのダウンロード中... Read layout: SINGLE fastq に変換中... spots read : 5,444,932 reads read : 5,444,932 reads written : 5,444,932 rm: cannot remove ‘[DSE]RR*’: No such file or directory rm: cannot remove ‘/home/okishinya/ncbi/public/sra/SRR5289672.sra.cache’: No such file or directory 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: 00:01:31 5444932 reads; of these: 5444932 (100.00%) were unpaired; of these: 2137389 (39.25%) aligned 0 times 2464414 (45.26%) aligned exactly 1 time 843129 (15.48%) aligned >1 times 60.75% overall alignment rate Time searching: 00:01:31 Overall time: 00:01:31 マッピングが完了しました。 samtools でBAM に変換中... [samopen] SAM header is present: 15 sequences. [bam_rmdupse_core] 671459 / 3307543 = 0.2030 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 @ Thu, 16 Apr 2020 00:23:30: # Command line: callpeak -t /home/okishinya/chipatlas/results/dm3/SRX2592395/SRX2592395.bam -f BAM -g dm -n /home/okishinya/chipatlas/results/dm3/SRX2592395/SRX2592395.05 -q 1e-05 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/dm3/SRX2592395/SRX2592395.05 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/dm3/SRX2592395/SRX2592395.bam'] # control file = None # effective genome size = 1.20e+08 # 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 @ Thu, 16 Apr 2020 00:23:30: #1 read tag files... INFO @ Thu, 16 Apr 2020 00:23:30: #1 read treatment tags... INFO @ Thu, 16 Apr 2020 00:23:36: 1000000 INFO @ Thu, 16 Apr 2020 00:23:42: 2000000 INFO @ Thu, 16 Apr 2020 00:23:46: #1 tag size is determined as 51 bps INFO @ Thu, 16 Apr 2020 00:23:46: #1 tag size = 51 INFO @ Thu, 16 Apr 2020 00:23:46: #1 total tags in treatment: 2636084 INFO @ Thu, 16 Apr 2020 00:23:46: #1 user defined the maximum tags... INFO @ Thu, 16 Apr 2020 00:23:46: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Thu, 16 Apr 2020 00:23:46: #1 tags after filtering in treatment: 2636084 INFO @ Thu, 16 Apr 2020 00:23:46: #1 Redundant rate of treatment: 0.00 INFO @ Thu, 16 Apr 2020 00:23:46: #1 finished! INFO @ Thu, 16 Apr 2020 00:23:46: #2 Build Peak Model... INFO @ Thu, 16 Apr 2020 00:23:46: #2 looking for paired plus/minus strand peaks... INFO @ Thu, 16 Apr 2020 00:23:47: #2 number of paired peaks: 784 WARNING @ Thu, 16 Apr 2020 00:23:47: Fewer paired peaks (784) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 784 pairs to build model! INFO @ Thu, 16 Apr 2020 00:23:47: start model_add_line... INFO @ Thu, 16 Apr 2020 00:23:47: start X-correlation... INFO @ Thu, 16 Apr 2020 00:23:47: end of X-cor INFO @ Thu, 16 Apr 2020 00:23:47: #2 finished! INFO @ Thu, 16 Apr 2020 00:23:47: #2 predicted fragment length is 53 bps INFO @ Thu, 16 Apr 2020 00:23:47: #2 alternative fragment length(s) may be 53 bps INFO @ Thu, 16 Apr 2020 00:23:47: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/dm3/SRX2592395/SRX2592395.05_model.r WARNING @ Thu, 16 Apr 2020 00:23:47: #2 Since the d (53) calculated from paired-peaks are smaller than 2*tag length, it may be influenced by unknown sequencing problem! WARNING @ Thu, 16 Apr 2020 00:23:47: #2 You may need to consider one of the other alternative d(s): 53 WARNING @ Thu, 16 Apr 2020 00:23:47: #2 You can restart the process with --nomodel --extsize XXX with your choice or an arbitrary number. Nontheless, MACS will continute computing. INFO @ Thu, 16 Apr 2020 00:23:47: #3 Call peaks... INFO @ Thu, 16 Apr 2020 00:23:47: #3 Pre-compute pvalue-qvalue table... INFO @ Thu, 16 Apr 2020 00:23:52: #3 Call peaks for each chromosome... INFO @ Thu, 16 Apr 2020 00:23:55: #4 Write output xls file... /home/okishinya/chipatlas/results/dm3/SRX2592395/SRX2592395.05_peaks.xls INFO @ Thu, 16 Apr 2020 00:23:55: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/dm3/SRX2592395/SRX2592395.05_peaks.narrowPeak INFO @ Thu, 16 Apr 2020 00:23:55: #4 Write summits bed file... /home/okishinya/chipatlas/results/dm3/SRX2592395/SRX2592395.05_summits.bed INFO @ Thu, 16 Apr 2020 00:23:55: Done! pass1 - making usageList (12 chroms): 1 millis pass2 - checking and writing primary data (1101 records, 4 fields): 2 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 @ Thu, 16 Apr 2020 00:24:00: # Command line: callpeak -t /home/okishinya/chipatlas/results/dm3/SRX2592395/SRX2592395.bam -f BAM -g dm -n /home/okishinya/chipatlas/results/dm3/SRX2592395/SRX2592395.10 -q 1e-10 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/dm3/SRX2592395/SRX2592395.10 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/dm3/SRX2592395/SRX2592395.bam'] # control file = None # effective genome size = 1.20e+08 # 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 @ Thu, 16 Apr 2020 00:24:00: #1 read tag files... INFO @ Thu, 16 Apr 2020 00:24:00: #1 read treatment tags... INFO @ Thu, 16 Apr 2020 00:24:07: 1000000 INFO @ Thu, 16 Apr 2020 00:24:13: 2000000 INFO @ Thu, 16 Apr 2020 00:24:17: #1 tag size is determined as 51 bps INFO @ Thu, 16 Apr 2020 00:24:17: #1 tag size = 51 INFO @ Thu, 16 Apr 2020 00:24:17: #1 total tags in treatment: 2636084 INFO @ Thu, 16 Apr 2020 00:24:17: #1 user defined the maximum tags... INFO @ Thu, 16 Apr 2020 00:24:17: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Thu, 16 Apr 2020 00:24:17: #1 tags after filtering in treatment: 2636084 INFO @ Thu, 16 Apr 2020 00:24:17: #1 Redundant rate of treatment: 0.00 INFO @ Thu, 16 Apr 2020 00:24:17: #1 finished! INFO @ Thu, 16 Apr 2020 00:24:17: #2 Build Peak Model... INFO @ Thu, 16 Apr 2020 00:24:17: #2 looking for paired plus/minus strand peaks... INFO @ Thu, 16 Apr 2020 00:24:17: #2 number of paired peaks: 784 WARNING @ Thu, 16 Apr 2020 00:24:17: Fewer paired peaks (784) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 784 pairs to build model! INFO @ Thu, 16 Apr 2020 00:24:17: start model_add_line... INFO @ Thu, 16 Apr 2020 00:24:17: start X-correlation... INFO @ Thu, 16 Apr 2020 00:24:17: end of X-cor INFO @ Thu, 16 Apr 2020 00:24:17: #2 finished! INFO @ Thu, 16 Apr 2020 00:24:17: #2 predicted fragment length is 53 bps INFO @ Thu, 16 Apr 2020 00:24:17: #2 alternative fragment length(s) may be 53 bps INFO @ Thu, 16 Apr 2020 00:24:17: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/dm3/SRX2592395/SRX2592395.10_model.r WARNING @ Thu, 16 Apr 2020 00:24:17: #2 Since the d (53) calculated from paired-peaks are smaller than 2*tag length, it may be influenced by unknown sequencing problem! WARNING @ Thu, 16 Apr 2020 00:24:17: #2 You may need to consider one of the other alternative d(s): 53 WARNING @ Thu, 16 Apr 2020 00:24:17: #2 You can restart the process with --nomodel --extsize XXX with your choice or an arbitrary number. Nontheless, MACS will continute computing. INFO @ Thu, 16 Apr 2020 00:24:17: #3 Call peaks... INFO @ Thu, 16 Apr 2020 00:24:17: #3 Pre-compute pvalue-qvalue table... INFO @ Thu, 16 Apr 2020 00:24:23: #3 Call peaks for each chromosome... INFO @ Thu, 16 Apr 2020 00:24:26: #4 Write output xls file... /home/okishinya/chipatlas/results/dm3/SRX2592395/SRX2592395.10_peaks.xls INFO @ Thu, 16 Apr 2020 00:24:26: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/dm3/SRX2592395/SRX2592395.10_peaks.narrowPeak INFO @ Thu, 16 Apr 2020 00:24:26: #4 Write summits bed file... /home/okishinya/chipatlas/results/dm3/SRX2592395/SRX2592395.10_summits.bed INFO @ Thu, 16 Apr 2020 00:24:26: Done! pass1 - making usageList (9 chroms): 0 millis pass2 - checking and writing primary data (903 records, 4 fields): 2 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 @ Thu, 16 Apr 2020 00:24:30: # Command line: callpeak -t /home/okishinya/chipatlas/results/dm3/SRX2592395/SRX2592395.bam -f BAM -g dm -n /home/okishinya/chipatlas/results/dm3/SRX2592395/SRX2592395.20 -q 1e-20 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/dm3/SRX2592395/SRX2592395.20 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/dm3/SRX2592395/SRX2592395.bam'] # control file = None # effective genome size = 1.20e+08 # 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 @ Thu, 16 Apr 2020 00:24:30: #1 read tag files... INFO @ Thu, 16 Apr 2020 00:24:30: #1 read treatment tags... INFO @ Thu, 16 Apr 2020 00:24:36: 1000000 INFO @ Thu, 16 Apr 2020 00:24:41: 2000000 INFO @ Thu, 16 Apr 2020 00:24:44: #1 tag size is determined as 51 bps INFO @ Thu, 16 Apr 2020 00:24:44: #1 tag size = 51 INFO @ Thu, 16 Apr 2020 00:24:44: #1 total tags in treatment: 2636084 INFO @ Thu, 16 Apr 2020 00:24:44: #1 user defined the maximum tags... INFO @ Thu, 16 Apr 2020 00:24:44: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Thu, 16 Apr 2020 00:24:44: #1 tags after filtering in treatment: 2636084 INFO @ Thu, 16 Apr 2020 00:24:44: #1 Redundant rate of treatment: 0.00 INFO @ Thu, 16 Apr 2020 00:24:44: #1 finished! INFO @ Thu, 16 Apr 2020 00:24:44: #2 Build Peak Model... INFO @ Thu, 16 Apr 2020 00:24:44: #2 looking for paired plus/minus strand peaks... INFO @ Thu, 16 Apr 2020 00:24:44: #2 number of paired peaks: 784 WARNING @ Thu, 16 Apr 2020 00:24:44: Fewer paired peaks (784) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 784 pairs to build model! INFO @ Thu, 16 Apr 2020 00:24:44: start model_add_line... INFO @ Thu, 16 Apr 2020 00:24:44: start X-correlation... INFO @ Thu, 16 Apr 2020 00:24:44: end of X-cor INFO @ Thu, 16 Apr 2020 00:24:44: #2 finished! INFO @ Thu, 16 Apr 2020 00:24:44: #2 predicted fragment length is 53 bps INFO @ Thu, 16 Apr 2020 00:24:44: #2 alternative fragment length(s) may be 53 bps INFO @ Thu, 16 Apr 2020 00:24:44: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/dm3/SRX2592395/SRX2592395.20_model.r WARNING @ Thu, 16 Apr 2020 00:24:44: #2 Since the d (53) calculated from paired-peaks are smaller than 2*tag length, it may be influenced by unknown sequencing problem! WARNING @ Thu, 16 Apr 2020 00:24:44: #2 You may need to consider one of the other alternative d(s): 53 WARNING @ Thu, 16 Apr 2020 00:24:44: #2 You can restart the process with --nomodel --extsize XXX with your choice or an arbitrary number. Nontheless, MACS will continute computing. INFO @ Thu, 16 Apr 2020 00:24:44: #3 Call peaks... INFO @ Thu, 16 Apr 2020 00:24:44: #3 Pre-compute pvalue-qvalue table... INFO @ Thu, 16 Apr 2020 00:24:50: #3 Call peaks for each chromosome... INFO @ Thu, 16 Apr 2020 00:24:53: #4 Write output xls file... /home/okishinya/chipatlas/results/dm3/SRX2592395/SRX2592395.20_peaks.xls INFO @ Thu, 16 Apr 2020 00:24:53: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/dm3/SRX2592395/SRX2592395.20_peaks.narrowPeak INFO @ Thu, 16 Apr 2020 00:24:53: #4 Write summits bed file... /home/okishinya/chipatlas/results/dm3/SRX2592395/SRX2592395.20_summits.bed INFO @ Thu, 16 Apr 2020 00:24:53: Done! pass1 - making usageList (8 chroms): 0 millis pass2 - checking and writing primary data (679 records, 4 fields): 1 millis CompletedMACS2peakCalling BedGraph に変換しました。 BigWig に変換中... BigWig に変換しました。