Job ID = 14170087 SRX = SRX5007620 Genome = dm3 sra ファイルのダウンロード中... Read layout: SINGLE fastq に変換中... Read 5930350 spots for SRR8187835/SRR8187835.sra Written 5930350 spots for SRR8187835/SRR8187835.sra fastq に変換しました。 bowtie でマッピング中... Your job 14170660 ("srTdm6") has been submitted Time loading reference: 00:00:00 Time loading forward index: 00:00:00 Time loading mirror index: 00:00:00 Multiseed full-index search: 00:04:33 5930350 reads; of these: 5930350 (100.00%) were unpaired; of these: 1019884 (17.20%) aligned 0 times 4113210 (69.36%) aligned exactly 1 time 797256 (13.44%) aligned >1 times 82.80% overall alignment rate Time searching: 00:04:33 Overall time: 00:04:33 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] 3701783 / 4910466 = 0.7539 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, 11 Dec 2021 05:13:14: # Command line: callpeak -t /home/okishinya/chipatlas/results/dm3/SRX5007620/SRX5007620.bam -f BAM -g dm -n /home/okishinya/chipatlas/results/dm3/SRX5007620/SRX5007620.05 -q 1e-05 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/dm3/SRX5007620/SRX5007620.05 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/dm3/SRX5007620/SRX5007620.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 @ Sat, 11 Dec 2021 05:13:14: #1 read tag files... INFO @ Sat, 11 Dec 2021 05:13:14: #1 read treatment tags... INFO @ Sat, 11 Dec 2021 05:13:24: 1000000 INFO @ Sat, 11 Dec 2021 05:13:26: #1 tag size is determined as 151 bps INFO @ Sat, 11 Dec 2021 05:13:26: #1 tag size = 151 INFO @ Sat, 11 Dec 2021 05:13:26: #1 total tags in treatment: 1208683 INFO @ Sat, 11 Dec 2021 05:13:26: #1 user defined the maximum tags... INFO @ Sat, 11 Dec 2021 05:13:26: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Sat, 11 Dec 2021 05:13:26: #1 tags after filtering in treatment: 1208683 INFO @ Sat, 11 Dec 2021 05:13:26: #1 Redundant rate of treatment: 0.00 INFO @ Sat, 11 Dec 2021 05:13:26: #1 finished! INFO @ Sat, 11 Dec 2021 05:13:26: #2 Build Peak Model... INFO @ Sat, 11 Dec 2021 05:13:26: #2 looking for paired plus/minus strand peaks... INFO @ Sat, 11 Dec 2021 05:13:26: #2 number of paired peaks: 1315 INFO @ Sat, 11 Dec 2021 05:13:26: start model_add_line... INFO @ Sat, 11 Dec 2021 05:13:26: start X-correlation... INFO @ Sat, 11 Dec 2021 05:13:26: end of X-cor INFO @ Sat, 11 Dec 2021 05:13:26: #2 finished! INFO @ Sat, 11 Dec 2021 05:13:26: #2 predicted fragment length is 160 bps INFO @ Sat, 11 Dec 2021 05:13:26: #2 alternative fragment length(s) may be 160 bps INFO @ Sat, 11 Dec 2021 05:13:26: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/dm3/SRX5007620/SRX5007620.05_model.r WARNING @ Sat, 11 Dec 2021 05:13:26: #2 Since the d (160) calculated from paired-peaks are smaller than 2*tag length, it may be influenced by unknown sequencing problem! WARNING @ Sat, 11 Dec 2021 05:13:26: #2 You may need to consider one of the other alternative d(s): 160 WARNING @ Sat, 11 Dec 2021 05:13:26: #2 You can restart the process with --nomodel --extsize XXX with your choice or an arbitrary number. Nontheless, MACS will continute computing. INFO @ Sat, 11 Dec 2021 05:13:26: #3 Call peaks... INFO @ Sat, 11 Dec 2021 05:13:26: #3 Pre-compute pvalue-qvalue table... INFO @ Sat, 11 Dec 2021 05:13:29: #3 Call peaks for each chromosome... INFO @ Sat, 11 Dec 2021 05:13:31: #4 Write output xls file... /home/okishinya/chipatlas/results/dm3/SRX5007620/SRX5007620.05_peaks.xls INFO @ Sat, 11 Dec 2021 05:13:31: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/dm3/SRX5007620/SRX5007620.05_peaks.narrowPeak INFO @ Sat, 11 Dec 2021 05:13:31: #4 Write summits bed file... /home/okishinya/chipatlas/results/dm3/SRX5007620/SRX5007620.05_summits.bed INFO @ Sat, 11 Dec 2021 05:13:31: Done! pass1 - making usageList (14 chroms): 1 millis pass2 - checking and writing primary data (877 records, 4 fields): 3 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, 11 Dec 2021 05:13:44: # Command line: callpeak -t /home/okishinya/chipatlas/results/dm3/SRX5007620/SRX5007620.bam -f BAM -g dm -n /home/okishinya/chipatlas/results/dm3/SRX5007620/SRX5007620.10 -q 1e-10 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/dm3/SRX5007620/SRX5007620.10 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/dm3/SRX5007620/SRX5007620.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 @ Sat, 11 Dec 2021 05:13:44: #1 read tag files... INFO @ Sat, 11 Dec 2021 05:13:44: #1 read treatment tags... INFO @ Sat, 11 Dec 2021 05:13:53: 1000000 INFO @ Sat, 11 Dec 2021 05:13:55: #1 tag size is determined as 151 bps INFO @ Sat, 11 Dec 2021 05:13:55: #1 tag size = 151 INFO @ Sat, 11 Dec 2021 05:13:55: #1 total tags in treatment: 1208683 INFO @ Sat, 11 Dec 2021 05:13:55: #1 user defined the maximum tags... INFO @ Sat, 11 Dec 2021 05:13:55: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Sat, 11 Dec 2021 05:13:55: #1 tags after filtering in treatment: 1208683 INFO @ Sat, 11 Dec 2021 05:13:55: #1 Redundant rate of treatment: 0.00 INFO @ Sat, 11 Dec 2021 05:13:55: #1 finished! INFO @ Sat, 11 Dec 2021 05:13:55: #2 Build Peak Model... INFO @ Sat, 11 Dec 2021 05:13:55: #2 looking for paired plus/minus strand peaks... INFO @ Sat, 11 Dec 2021 05:13:55: #2 number of paired peaks: 1315 INFO @ Sat, 11 Dec 2021 05:13:55: start model_add_line... INFO @ Sat, 11 Dec 2021 05:13:55: start X-correlation... INFO @ Sat, 11 Dec 2021 05:13:55: end of X-cor INFO @ Sat, 11 Dec 2021 05:13:55: #2 finished! INFO @ Sat, 11 Dec 2021 05:13:55: #2 predicted fragment length is 160 bps INFO @ Sat, 11 Dec 2021 05:13:55: #2 alternative fragment length(s) may be 160 bps INFO @ Sat, 11 Dec 2021 05:13:55: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/dm3/SRX5007620/SRX5007620.10_model.r WARNING @ Sat, 11 Dec 2021 05:13:55: #2 Since the d (160) calculated from paired-peaks are smaller than 2*tag length, it may be influenced by unknown sequencing problem! WARNING @ Sat, 11 Dec 2021 05:13:55: #2 You may need to consider one of the other alternative d(s): 160 WARNING @ Sat, 11 Dec 2021 05:13:55: #2 You can restart the process with --nomodel --extsize XXX with your choice or an arbitrary number. Nontheless, MACS will continute computing. INFO @ Sat, 11 Dec 2021 05:13:55: #3 Call peaks... INFO @ Sat, 11 Dec 2021 05:13:55: #3 Pre-compute pvalue-qvalue table... INFO @ Sat, 11 Dec 2021 05:13:59: #3 Call peaks for each chromosome... INFO @ Sat, 11 Dec 2021 05:14:00: #4 Write output xls file... /home/okishinya/chipatlas/results/dm3/SRX5007620/SRX5007620.10_peaks.xls INFO @ Sat, 11 Dec 2021 05:14:00: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/dm3/SRX5007620/SRX5007620.10_peaks.narrowPeak INFO @ Sat, 11 Dec 2021 05:14:00: #4 Write summits bed file... /home/okishinya/chipatlas/results/dm3/SRX5007620/SRX5007620.10_summits.bed INFO @ Sat, 11 Dec 2021 05:14:00: Done! pass1 - making usageList (13 chroms): 0 millis pass2 - checking and writing primary data (434 records, 4 fields): 2 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, 11 Dec 2021 05:14:14: # Command line: callpeak -t /home/okishinya/chipatlas/results/dm3/SRX5007620/SRX5007620.bam -f BAM -g dm -n /home/okishinya/chipatlas/results/dm3/SRX5007620/SRX5007620.20 -q 1e-20 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/dm3/SRX5007620/SRX5007620.20 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/dm3/SRX5007620/SRX5007620.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 @ Sat, 11 Dec 2021 05:14:14: #1 read tag files... INFO @ Sat, 11 Dec 2021 05:14:14: #1 read treatment tags... BedGraph に変換しました。 BigWig に変換中... INFO @ Sat, 11 Dec 2021 05:14:24: 1000000 BigWig に変換しました。 INFO @ Sat, 11 Dec 2021 05:14:26: #1 tag size is determined as 151 bps INFO @ Sat, 11 Dec 2021 05:14:26: #1 tag size = 151 INFO @ Sat, 11 Dec 2021 05:14:26: #1 total tags in treatment: 1208683 INFO @ Sat, 11 Dec 2021 05:14:26: #1 user defined the maximum tags... INFO @ Sat, 11 Dec 2021 05:14:26: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Sat, 11 Dec 2021 05:14:26: #1 tags after filtering in treatment: 1208683 INFO @ Sat, 11 Dec 2021 05:14:26: #1 Redundant rate of treatment: 0.00 INFO @ Sat, 11 Dec 2021 05:14:26: #1 finished! INFO @ Sat, 11 Dec 2021 05:14:26: #2 Build Peak Model... INFO @ Sat, 11 Dec 2021 05:14:26: #2 looking for paired plus/minus strand peaks... INFO @ Sat, 11 Dec 2021 05:14:26: #2 number of paired peaks: 1315 INFO @ Sat, 11 Dec 2021 05:14:26: start model_add_line... INFO @ Sat, 11 Dec 2021 05:14:26: start X-correlation... INFO @ Sat, 11 Dec 2021 05:14:26: end of X-cor INFO @ Sat, 11 Dec 2021 05:14:26: #2 finished! INFO @ Sat, 11 Dec 2021 05:14:26: #2 predicted fragment length is 160 bps INFO @ Sat, 11 Dec 2021 05:14:26: #2 alternative fragment length(s) may be 160 bps INFO @ Sat, 11 Dec 2021 05:14:26: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/dm3/SRX5007620/SRX5007620.20_model.r WARNING @ Sat, 11 Dec 2021 05:14:26: #2 Since the d (160) calculated from paired-peaks are smaller than 2*tag length, it may be influenced by unknown sequencing problem! WARNING @ Sat, 11 Dec 2021 05:14:26: #2 You may need to consider one of the other alternative d(s): 160 WARNING @ Sat, 11 Dec 2021 05:14:26: #2 You can restart the process with --nomodel --extsize XXX with your choice or an arbitrary number. Nontheless, MACS will continute computing. INFO @ Sat, 11 Dec 2021 05:14:26: #3 Call peaks... INFO @ Sat, 11 Dec 2021 05:14:26: #3 Pre-compute pvalue-qvalue table... INFO @ Sat, 11 Dec 2021 05:14:30: #3 Call peaks for each chromosome... INFO @ Sat, 11 Dec 2021 05:14:31: #4 Write output xls file... /home/okishinya/chipatlas/results/dm3/SRX5007620/SRX5007620.20_peaks.xls INFO @ Sat, 11 Dec 2021 05:14:31: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/dm3/SRX5007620/SRX5007620.20_peaks.narrowPeak INFO @ Sat, 11 Dec 2021 05:14:31: #4 Write summits bed file... /home/okishinya/chipatlas/results/dm3/SRX5007620/SRX5007620.20_summits.bed INFO @ Sat, 11 Dec 2021 05:14:31: Done! pass1 - making usageList (11 chroms): 0 millis pass2 - checking and writing primary data (177 records, 4 fields): 2 millis CompletedMACS2peakCalling