Job ID = 6455025 SRX = SRX2642376 Genome = dm6 sra ファイルのダウンロード中... Read layout: SINGLE fastq に変換中... 2020-06-21T09:29:14 prefetch.2.10.7: 1) Downloading 'SRR5345716'... 2020-06-21T09:29:14 prefetch.2.10.7: Downloading via HTTPS... 2020-06-21T09:30:09 prefetch.2.10.7: HTTPS download succeed 2020-06-21T09:30:09 prefetch.2.10.7: 'SRR5345716' is valid 2020-06-21T09:30:09 prefetch.2.10.7: 1) 'SRR5345716' was downloaded successfully 2020-06-21T09:30:09 prefetch.2.10.7: 'SRR5345716' has 0 unresolved dependencies Read 3342843 spots for SRR5345716/SRR5345716.sra Written 3342843 spots for SRR5345716/SRR5345716.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: 00:01:35 3342843 reads; of these: 3342843 (100.00%) were unpaired; of these: 506778 (15.16%) aligned 0 times 2044882 (61.17%) aligned exactly 1 time 791183 (23.67%) aligned >1 times 84.84% overall alignment rate Time searching: 00:01:35 Overall time: 00:01:35 マッピングが完了しました。 samtools でBAM に変換中... [samopen] SAM header is present: 1870 sequences. [bam_rmdupse_core] 183747 / 2836065 = 0.0648 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 @ Sun, 21 Jun 2020 18:33:35: # Command line: callpeak -t /home/okishinya/chipatlas/results/dm6/SRX2642376/SRX2642376.bam -f BAM -g dm -n /home/okishinya/chipatlas/results/dm6/SRX2642376/SRX2642376.05 -q 1e-05 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/dm6/SRX2642376/SRX2642376.05 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/dm6/SRX2642376/SRX2642376.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 @ Sun, 21 Jun 2020 18:33:35: #1 read tag files... INFO @ Sun, 21 Jun 2020 18:33:35: #1 read treatment tags... INFO @ Sun, 21 Jun 2020 18:33:42: 1000000 INFO @ Sun, 21 Jun 2020 18:33:50: 2000000 INFO @ Sun, 21 Jun 2020 18:33:55: #1 tag size is determined as 100 bps INFO @ Sun, 21 Jun 2020 18:33:55: #1 tag size = 100 INFO @ Sun, 21 Jun 2020 18:33:55: #1 total tags in treatment: 2652318 INFO @ Sun, 21 Jun 2020 18:33:55: #1 user defined the maximum tags... INFO @ Sun, 21 Jun 2020 18:33:55: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Sun, 21 Jun 2020 18:33:56: #1 tags after filtering in treatment: 2652274 INFO @ Sun, 21 Jun 2020 18:33:56: #1 Redundant rate of treatment: 0.00 INFO @ Sun, 21 Jun 2020 18:33:56: #1 finished! INFO @ Sun, 21 Jun 2020 18:33:56: #2 Build Peak Model... INFO @ Sun, 21 Jun 2020 18:33:56: #2 looking for paired plus/minus strand peaks... INFO @ Sun, 21 Jun 2020 18:33:56: #2 number of paired peaks: 747 WARNING @ Sun, 21 Jun 2020 18:33:56: Fewer paired peaks (747) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 747 pairs to build model! INFO @ Sun, 21 Jun 2020 18:33:56: start model_add_line... INFO @ Sun, 21 Jun 2020 18:33:56: start X-correlation... INFO @ Sun, 21 Jun 2020 18:33:56: end of X-cor INFO @ Sun, 21 Jun 2020 18:33:56: #2 finished! INFO @ Sun, 21 Jun 2020 18:33:56: #2 predicted fragment length is 105 bps INFO @ Sun, 21 Jun 2020 18:33:56: #2 alternative fragment length(s) may be 105,555 bps INFO @ Sun, 21 Jun 2020 18:33:56: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/dm6/SRX2642376/SRX2642376.05_model.r WARNING @ Sun, 21 Jun 2020 18:33:56: #2 Since the d (105) calculated from paired-peaks are smaller than 2*tag length, it may be influenced by unknown sequencing problem! WARNING @ Sun, 21 Jun 2020 18:33:56: #2 You may need to consider one of the other alternative d(s): 105,555 WARNING @ Sun, 21 Jun 2020 18:33:56: #2 You can restart the process with --nomodel --extsize XXX with your choice or an arbitrary number. Nontheless, MACS will continute computing. INFO @ Sun, 21 Jun 2020 18:33:56: #3 Call peaks... INFO @ Sun, 21 Jun 2020 18:33:56: #3 Pre-compute pvalue-qvalue table... INFO @ Sun, 21 Jun 2020 18:34:02: #3 Call peaks for each chromosome... 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 @ Sun, 21 Jun 2020 18:34:05: # Command line: callpeak -t /home/okishinya/chipatlas/results/dm6/SRX2642376/SRX2642376.bam -f BAM -g dm -n /home/okishinya/chipatlas/results/dm6/SRX2642376/SRX2642376.10 -q 1e-10 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/dm6/SRX2642376/SRX2642376.10 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/dm6/SRX2642376/SRX2642376.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 @ Sun, 21 Jun 2020 18:34:05: #1 read tag files... INFO @ Sun, 21 Jun 2020 18:34:05: #1 read treatment tags... INFO @ Sun, 21 Jun 2020 18:34:05: #4 Write output xls file... /home/okishinya/chipatlas/results/dm6/SRX2642376/SRX2642376.05_peaks.xls INFO @ Sun, 21 Jun 2020 18:34:05: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/dm6/SRX2642376/SRX2642376.05_peaks.narrowPeak INFO @ Sun, 21 Jun 2020 18:34:05: #4 Write summits bed file... /home/okishinya/chipatlas/results/dm6/SRX2642376/SRX2642376.05_summits.bed INFO @ Sun, 21 Jun 2020 18:34:05: Done! pass1 - making usageList (399 chroms): 1 millis pass2 - checking and writing primary data (724 records, 4 fields): 11 millis CompletedMACS2peakCalling INFO @ Sun, 21 Jun 2020 18:34:12: 1000000 INFO @ Sun, 21 Jun 2020 18:34:20: 2000000 INFO @ Sun, 21 Jun 2020 18:34:25: #1 tag size is determined as 100 bps INFO @ Sun, 21 Jun 2020 18:34:25: #1 tag size = 100 INFO @ Sun, 21 Jun 2020 18:34:25: #1 total tags in treatment: 2652318 INFO @ Sun, 21 Jun 2020 18:34:25: #1 user defined the maximum tags... INFO @ Sun, 21 Jun 2020 18:34:25: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Sun, 21 Jun 2020 18:34:25: #1 tags after filtering in treatment: 2652274 INFO @ Sun, 21 Jun 2020 18:34:25: #1 Redundant rate of treatment: 0.00 INFO @ Sun, 21 Jun 2020 18:34:25: #1 finished! INFO @ Sun, 21 Jun 2020 18:34:25: #2 Build Peak Model... INFO @ Sun, 21 Jun 2020 18:34:25: #2 looking for paired plus/minus strand peaks... INFO @ Sun, 21 Jun 2020 18:34:26: #2 number of paired peaks: 747 WARNING @ Sun, 21 Jun 2020 18:34:26: Fewer paired peaks (747) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 747 pairs to build model! INFO @ Sun, 21 Jun 2020 18:34:26: start model_add_line... INFO @ Sun, 21 Jun 2020 18:34:26: start X-correlation... INFO @ Sun, 21 Jun 2020 18:34:26: end of X-cor INFO @ Sun, 21 Jun 2020 18:34:26: #2 finished! INFO @ Sun, 21 Jun 2020 18:34:26: #2 predicted fragment length is 105 bps INFO @ Sun, 21 Jun 2020 18:34:26: #2 alternative fragment length(s) may be 105,555 bps INFO @ Sun, 21 Jun 2020 18:34:26: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/dm6/SRX2642376/SRX2642376.10_model.r WARNING @ Sun, 21 Jun 2020 18:34:26: #2 Since the d (105) calculated from paired-peaks are smaller than 2*tag length, it may be influenced by unknown sequencing problem! WARNING @ Sun, 21 Jun 2020 18:34:26: #2 You may need to consider one of the other alternative d(s): 105,555 WARNING @ Sun, 21 Jun 2020 18:34:26: #2 You can restart the process with --nomodel --extsize XXX with your choice or an arbitrary number. Nontheless, MACS will continute computing. INFO @ Sun, 21 Jun 2020 18:34:26: #3 Call peaks... INFO @ Sun, 21 Jun 2020 18:34:26: #3 Pre-compute pvalue-qvalue table... INFO @ Sun, 21 Jun 2020 18:34:32: #3 Call peaks for each chromosome... 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 @ Sun, 21 Jun 2020 18:34:35: # Command line: callpeak -t /home/okishinya/chipatlas/results/dm6/SRX2642376/SRX2642376.bam -f BAM -g dm -n /home/okishinya/chipatlas/results/dm6/SRX2642376/SRX2642376.20 -q 1e-20 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/dm6/SRX2642376/SRX2642376.20 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/dm6/SRX2642376/SRX2642376.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 @ Sun, 21 Jun 2020 18:34:35: #1 read tag files... INFO @ Sun, 21 Jun 2020 18:34:35: #1 read treatment tags... INFO @ Sun, 21 Jun 2020 18:34:35: #4 Write output xls file... /home/okishinya/chipatlas/results/dm6/SRX2642376/SRX2642376.10_peaks.xls INFO @ Sun, 21 Jun 2020 18:34:35: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/dm6/SRX2642376/SRX2642376.10_peaks.narrowPeak INFO @ Sun, 21 Jun 2020 18:34:35: #4 Write summits bed file... /home/okishinya/chipatlas/results/dm6/SRX2642376/SRX2642376.10_summits.bed INFO @ Sun, 21 Jun 2020 18:34:35: Done! pass1 - making usageList (225 chroms): 1 millis pass2 - checking and writing primary data (364 records, 4 fields): 8 millis CompletedMACS2peakCalling INFO @ Sun, 21 Jun 2020 18:34:42: 1000000 BedGraph に変換しました。 BigWig に変換中... INFO @ Sun, 21 Jun 2020 18:34:50: 2000000 INFO @ Sun, 21 Jun 2020 18:34:55: #1 tag size is determined as 100 bps INFO @ Sun, 21 Jun 2020 18:34:55: #1 tag size = 100 INFO @ Sun, 21 Jun 2020 18:34:55: #1 total tags in treatment: 2652318 INFO @ Sun, 21 Jun 2020 18:34:55: #1 user defined the maximum tags... INFO @ Sun, 21 Jun 2020 18:34:55: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Sun, 21 Jun 2020 18:34:56: #1 tags after filtering in treatment: 2652274 INFO @ Sun, 21 Jun 2020 18:34:56: #1 Redundant rate of treatment: 0.00 INFO @ Sun, 21 Jun 2020 18:34:56: #1 finished! INFO @ Sun, 21 Jun 2020 18:34:56: #2 Build Peak Model... INFO @ Sun, 21 Jun 2020 18:34:56: #2 looking for paired plus/minus strand peaks... BigWig に変換しました。 INFO @ Sun, 21 Jun 2020 18:34:56: #2 number of paired peaks: 747 WARNING @ Sun, 21 Jun 2020 18:34:56: Fewer paired peaks (747) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 747 pairs to build model! INFO @ Sun, 21 Jun 2020 18:34:56: start model_add_line... INFO @ Sun, 21 Jun 2020 18:34:56: start X-correlation... INFO @ Sun, 21 Jun 2020 18:34:56: end of X-cor INFO @ Sun, 21 Jun 2020 18:34:56: #2 finished! INFO @ Sun, 21 Jun 2020 18:34:56: #2 predicted fragment length is 105 bps INFO @ Sun, 21 Jun 2020 18:34:56: #2 alternative fragment length(s) may be 105,555 bps INFO @ Sun, 21 Jun 2020 18:34:56: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/dm6/SRX2642376/SRX2642376.20_model.r WARNING @ Sun, 21 Jun 2020 18:34:56: #2 Since the d (105) calculated from paired-peaks are smaller than 2*tag length, it may be influenced by unknown sequencing problem! WARNING @ Sun, 21 Jun 2020 18:34:56: #2 You may need to consider one of the other alternative d(s): 105,555 WARNING @ Sun, 21 Jun 2020 18:34:56: #2 You can restart the process with --nomodel --extsize XXX with your choice or an arbitrary number. Nontheless, MACS will continute computing. INFO @ Sun, 21 Jun 2020 18:34:56: #3 Call peaks... INFO @ Sun, 21 Jun 2020 18:34:56: #3 Pre-compute pvalue-qvalue table... INFO @ Sun, 21 Jun 2020 18:35:02: #3 Call peaks for each chromosome... INFO @ Sun, 21 Jun 2020 18:35:05: #4 Write output xls file... /home/okishinya/chipatlas/results/dm6/SRX2642376/SRX2642376.20_peaks.xls INFO @ Sun, 21 Jun 2020 18:35:06: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/dm6/SRX2642376/SRX2642376.20_peaks.narrowPeak INFO @ Sun, 21 Jun 2020 18:35:06: #4 Write summits bed file... /home/okishinya/chipatlas/results/dm6/SRX2642376/SRX2642376.20_summits.bed INFO @ Sun, 21 Jun 2020 18:35:06: Done! pass1 - making usageList (121 chroms): 1 millis pass2 - checking and writing primary data (187 records, 4 fields): 5 millis CompletedMACS2peakCalling