Job ID = 5720942 sra ファイルのダウンロード中... Read layout: SINGLE fastq に変換中... spots read : 5,668,271 reads read : 5,668,271 reads written : 5,668,271 rm: cannot remove ‘[DSE]RR*’: 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: 00:01:16 5668271 reads; of these: 5668271 (100.00%) were unpaired; of these: 2531076 (44.65%) aligned 0 times 2205080 (38.90%) aligned exactly 1 time 932115 (16.44%) aligned >1 times 55.35% overall alignment rate Time searching: 00:01:16 Overall time: 00:01:16 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] 565211 / 3137195 = 0.1802 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 03:25:28: # Command line: callpeak -t /home/okishinya/chipatlas/results/dm3/SRX6386741/SRX6386741.bam -f BAM -g dm -n /home/okishinya/chipatlas/results/dm3/SRX6386741/SRX6386741.05 -q 1e-05 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/dm3/SRX6386741/SRX6386741.05 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/dm3/SRX6386741/SRX6386741.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 03:25:28: #1 read tag files... INFO @ Thu, 16 Apr 2020 03:25:28: #1 read treatment tags... INFO @ Thu, 16 Apr 2020 03:25:33: 1000000 INFO @ Thu, 16 Apr 2020 03:25:38: 2000000 INFO @ Thu, 16 Apr 2020 03:25:40: #1 tag size is determined as 51 bps INFO @ Thu, 16 Apr 2020 03:25:40: #1 tag size = 51 INFO @ Thu, 16 Apr 2020 03:25:40: #1 total tags in treatment: 2571984 INFO @ Thu, 16 Apr 2020 03:25:40: #1 user defined the maximum tags... INFO @ Thu, 16 Apr 2020 03:25:40: #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 03:25:40: #1 tags after filtering in treatment: 2571984 INFO @ Thu, 16 Apr 2020 03:25:40: #1 Redundant rate of treatment: 0.00 INFO @ Thu, 16 Apr 2020 03:25:40: #1 finished! INFO @ Thu, 16 Apr 2020 03:25:40: #2 Build Peak Model... INFO @ Thu, 16 Apr 2020 03:25:40: #2 looking for paired plus/minus strand peaks... INFO @ Thu, 16 Apr 2020 03:25:41: #2 number of paired peaks: 181 WARNING @ Thu, 16 Apr 2020 03:25:41: Fewer paired peaks (181) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 181 pairs to build model! INFO @ Thu, 16 Apr 2020 03:25:41: start model_add_line... INFO @ Thu, 16 Apr 2020 03:25:41: start X-correlation... INFO @ Thu, 16 Apr 2020 03:25:41: end of X-cor INFO @ Thu, 16 Apr 2020 03:25:41: #2 finished! INFO @ Thu, 16 Apr 2020 03:25:41: #2 predicted fragment length is 54 bps INFO @ Thu, 16 Apr 2020 03:25:41: #2 alternative fragment length(s) may be 54 bps INFO @ Thu, 16 Apr 2020 03:25:41: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/dm3/SRX6386741/SRX6386741.05_model.r WARNING @ Thu, 16 Apr 2020 03:25:41: #2 Since the d (54) calculated from paired-peaks are smaller than 2*tag length, it may be influenced by unknown sequencing problem! WARNING @ Thu, 16 Apr 2020 03:25:41: #2 You may need to consider one of the other alternative d(s): 54 WARNING @ Thu, 16 Apr 2020 03:25:41: #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 03:25:41: #3 Call peaks... INFO @ Thu, 16 Apr 2020 03:25:41: #3 Pre-compute pvalue-qvalue table... INFO @ Thu, 16 Apr 2020 03:25:46: #3 Call peaks for each chromosome... INFO @ Thu, 16 Apr 2020 03:25:49: #4 Write output xls file... /home/okishinya/chipatlas/results/dm3/SRX6386741/SRX6386741.05_peaks.xls INFO @ Thu, 16 Apr 2020 03:25:49: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/dm3/SRX6386741/SRX6386741.05_peaks.narrowPeak INFO @ Thu, 16 Apr 2020 03:25:49: #4 Write summits bed file... /home/okishinya/chipatlas/results/dm3/SRX6386741/SRX6386741.05_summits.bed INFO @ Thu, 16 Apr 2020 03:25:49: Done! pass1 - making usageList (10 chroms): 0 millis pass2 - checking and writing primary data (568 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 03:25:58: # Command line: callpeak -t /home/okishinya/chipatlas/results/dm3/SRX6386741/SRX6386741.bam -f BAM -g dm -n /home/okishinya/chipatlas/results/dm3/SRX6386741/SRX6386741.10 -q 1e-10 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/dm3/SRX6386741/SRX6386741.10 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/dm3/SRX6386741/SRX6386741.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 03:25:58: #1 read tag files... INFO @ Thu, 16 Apr 2020 03:25:58: #1 read treatment tags... INFO @ Thu, 16 Apr 2020 03:26:03: 1000000 INFO @ Thu, 16 Apr 2020 03:26:08: 2000000 INFO @ Thu, 16 Apr 2020 03:26:11: #1 tag size is determined as 51 bps INFO @ Thu, 16 Apr 2020 03:26:11: #1 tag size = 51 INFO @ Thu, 16 Apr 2020 03:26:11: #1 total tags in treatment: 2571984 INFO @ Thu, 16 Apr 2020 03:26:11: #1 user defined the maximum tags... INFO @ Thu, 16 Apr 2020 03:26:11: #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 03:26:11: #1 tags after filtering in treatment: 2571984 INFO @ Thu, 16 Apr 2020 03:26:11: #1 Redundant rate of treatment: 0.00 INFO @ Thu, 16 Apr 2020 03:26:11: #1 finished! INFO @ Thu, 16 Apr 2020 03:26:11: #2 Build Peak Model... INFO @ Thu, 16 Apr 2020 03:26:11: #2 looking for paired plus/minus strand peaks... INFO @ Thu, 16 Apr 2020 03:26:11: #2 number of paired peaks: 181 WARNING @ Thu, 16 Apr 2020 03:26:11: Fewer paired peaks (181) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 181 pairs to build model! INFO @ Thu, 16 Apr 2020 03:26:11: start model_add_line... INFO @ Thu, 16 Apr 2020 03:26:11: start X-correlation... INFO @ Thu, 16 Apr 2020 03:26:11: end of X-cor INFO @ Thu, 16 Apr 2020 03:26:11: #2 finished! INFO @ Thu, 16 Apr 2020 03:26:11: #2 predicted fragment length is 54 bps INFO @ Thu, 16 Apr 2020 03:26:11: #2 alternative fragment length(s) may be 54 bps INFO @ Thu, 16 Apr 2020 03:26:11: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/dm3/SRX6386741/SRX6386741.10_model.r WARNING @ Thu, 16 Apr 2020 03:26:11: #2 Since the d (54) calculated from paired-peaks are smaller than 2*tag length, it may be influenced by unknown sequencing problem! WARNING @ Thu, 16 Apr 2020 03:26:11: #2 You may need to consider one of the other alternative d(s): 54 WARNING @ Thu, 16 Apr 2020 03:26:11: #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 03:26:11: #3 Call peaks... INFO @ Thu, 16 Apr 2020 03:26:11: #3 Pre-compute pvalue-qvalue table... INFO @ Thu, 16 Apr 2020 03:26:16: #3 Call peaks for each chromosome... INFO @ Thu, 16 Apr 2020 03:26:19: #4 Write output xls file... /home/okishinya/chipatlas/results/dm3/SRX6386741/SRX6386741.10_peaks.xls INFO @ Thu, 16 Apr 2020 03:26:19: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/dm3/SRX6386741/SRX6386741.10_peaks.narrowPeak INFO @ Thu, 16 Apr 2020 03:26:19: #4 Write summits bed file... /home/okishinya/chipatlas/results/dm3/SRX6386741/SRX6386741.10_summits.bed INFO @ Thu, 16 Apr 2020 03:26:19: Done! pass1 - making usageList (10 chroms): 1 millis pass2 - checking and writing primary data (310 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 @ Thu, 16 Apr 2020 03:26:28: # Command line: callpeak -t /home/okishinya/chipatlas/results/dm3/SRX6386741/SRX6386741.bam -f BAM -g dm -n /home/okishinya/chipatlas/results/dm3/SRX6386741/SRX6386741.20 -q 1e-20 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/dm3/SRX6386741/SRX6386741.20 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/dm3/SRX6386741/SRX6386741.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 03:26:28: #1 read tag files... INFO @ Thu, 16 Apr 2020 03:26:28: #1 read treatment tags... INFO @ Thu, 16 Apr 2020 03:26:33: 1000000 INFO @ Thu, 16 Apr 2020 03:26:38: 2000000 INFO @ Thu, 16 Apr 2020 03:26:41: #1 tag size is determined as 51 bps INFO @ Thu, 16 Apr 2020 03:26:41: #1 tag size = 51 INFO @ Thu, 16 Apr 2020 03:26:41: #1 total tags in treatment: 2571984 INFO @ Thu, 16 Apr 2020 03:26:41: #1 user defined the maximum tags... INFO @ Thu, 16 Apr 2020 03:26:41: #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 03:26:41: #1 tags after filtering in treatment: 2571984 INFO @ Thu, 16 Apr 2020 03:26:41: #1 Redundant rate of treatment: 0.00 INFO @ Thu, 16 Apr 2020 03:26:41: #1 finished! INFO @ Thu, 16 Apr 2020 03:26:41: #2 Build Peak Model... INFO @ Thu, 16 Apr 2020 03:26:41: #2 looking for paired plus/minus strand peaks... INFO @ Thu, 16 Apr 2020 03:26:41: #2 number of paired peaks: 181 WARNING @ Thu, 16 Apr 2020 03:26:41: Fewer paired peaks (181) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 181 pairs to build model! INFO @ Thu, 16 Apr 2020 03:26:41: start model_add_line... INFO @ Thu, 16 Apr 2020 03:26:41: start X-correlation... INFO @ Thu, 16 Apr 2020 03:26:41: end of X-cor INFO @ Thu, 16 Apr 2020 03:26:41: #2 finished! INFO @ Thu, 16 Apr 2020 03:26:41: #2 predicted fragment length is 54 bps INFO @ Thu, 16 Apr 2020 03:26:41: #2 alternative fragment length(s) may be 54 bps INFO @ Thu, 16 Apr 2020 03:26:41: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/dm3/SRX6386741/SRX6386741.20_model.r WARNING @ Thu, 16 Apr 2020 03:26:41: #2 Since the d (54) calculated from paired-peaks are smaller than 2*tag length, it may be influenced by unknown sequencing problem! WARNING @ Thu, 16 Apr 2020 03:26:41: #2 You may need to consider one of the other alternative d(s): 54 WARNING @ Thu, 16 Apr 2020 03:26:41: #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 03:26:41: #3 Call peaks... INFO @ Thu, 16 Apr 2020 03:26:41: #3 Pre-compute pvalue-qvalue table... INFO @ Thu, 16 Apr 2020 03:26:46: #3 Call peaks for each chromosome... INFO @ Thu, 16 Apr 2020 03:26:49: #4 Write output xls file... /home/okishinya/chipatlas/results/dm3/SRX6386741/SRX6386741.20_peaks.xls INFO @ Thu, 16 Apr 2020 03:26:49: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/dm3/SRX6386741/SRX6386741.20_peaks.narrowPeak INFO @ Thu, 16 Apr 2020 03:26:49: #4 Write summits bed file... /home/okishinya/chipatlas/results/dm3/SRX6386741/SRX6386741.20_summits.bed INFO @ Thu, 16 Apr 2020 03:26:49: Done! pass1 - making usageList (7 chroms): 1 millis pass2 - checking and writing primary data (99 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。