Job ID = 14170058 SRX = SRX8556363 Genome = dm3 sra ファイルのダウンロード中... Read layout: PAIRED fastq に変換中... Read 21672407 spots for SRR12024919/SRR12024919.sra Written 21672407 spots for SRR12024919/SRR12024919.sra fastq に変換しました。 bowtie でマッピング中... Your job 14170658 ("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: 00:10:43 21672407 reads; of these: 21672407 (100.00%) were paired; of these: 21048813 (97.12%) aligned concordantly 0 times 467223 (2.16%) aligned concordantly exactly 1 time 156371 (0.72%) aligned concordantly >1 times ---- 21048813 pairs aligned concordantly 0 times; of these: 110965 (0.53%) aligned discordantly 1 time ---- 20937848 pairs aligned 0 times concordantly or discordantly; of these: 41875696 mates make up the pairs; of these: 41623515 (99.40%) aligned 0 times 140326 (0.34%) aligned exactly 1 time 111855 (0.27%) aligned >1 times 3.97% overall alignment rate Time searching: 00:10:43 Overall time: 00:10:43 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_rmdup_core] processing reference chr2L... [bam_rmdup_core] processing reference chr2LHet... [bam_rmdup_core] processing reference chr2R... [bam_rmdup_core] processing reference chr2RHet... [bam_rmdup_core] processing reference chr3L... [bam_rmdup_core] processing reference chr3LHet... [bam_rmdup_core] processing reference chr3R... [bam_rmdup_core] processing reference chr3RHet... [bam_rmdup_core] processing reference chr4... [bam_rmdup_core] processing reference chrM... [bam_rmdup_core] processing reference chrU... [bam_rmdup_core] processing reference chrUextra... [bam_rmdup_core] processing reference chrX... [bam_rmdup_core] processing reference chrXHet... [bam_rmdup_core] processing reference chrYHet... [bam_rmdup_core] 408576 / 723151 = 0.5650 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 05:11:30: # Command line: callpeak -t /home/okishinya/chipatlas/results/dm3/SRX8556363/SRX8556363.bam -f BAM -g dm -n /home/okishinya/chipatlas/results/dm3/SRX8556363/SRX8556363.05 -q 1e-05 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/dm3/SRX8556363/SRX8556363.05 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/dm3/SRX8556363/SRX8556363.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 05:11:30: #1 read tag files... INFO @ Sat, 11 Dec 2021 05:11:30: #1 read treatment tags... INFO @ Sat, 11 Dec 2021 05:11:41: #1 tag size is determined as 150 bps INFO @ Sat, 11 Dec 2021 05:11:41: #1 tag size = 150 INFO @ Sat, 11 Dec 2021 05:11:41: #1 total tags in treatment: 265026 INFO @ Sat, 11 Dec 2021 05:11:41: #1 user defined the maximum tags... INFO @ Sat, 11 Dec 2021 05:11:41: #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 05:11:41: #1 tags after filtering in treatment: 245065 INFO @ Sat, 11 Dec 2021 05:11:41: #1 Redundant rate of treatment: 0.08 INFO @ Sat, 11 Dec 2021 05:11:41: #1 finished! INFO @ Sat, 11 Dec 2021 05:11:41: #2 Build Peak Model... INFO @ Sat, 11 Dec 2021 05:11:41: #2 looking for paired plus/minus strand peaks... INFO @ Sat, 11 Dec 2021 05:11:41: #2 number of paired peaks: 2402 INFO @ Sat, 11 Dec 2021 05:11:41: start model_add_line... INFO @ Sat, 11 Dec 2021 05:11:41: start X-correlation... INFO @ Sat, 11 Dec 2021 05:11:41: end of X-cor INFO @ Sat, 11 Dec 2021 05:11:41: #2 finished! INFO @ Sat, 11 Dec 2021 05:11:41: #2 predicted fragment length is 170 bps INFO @ Sat, 11 Dec 2021 05:11:41: #2 alternative fragment length(s) may be 170 bps INFO @ Sat, 11 Dec 2021 05:11:41: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/dm3/SRX8556363/SRX8556363.05_model.r WARNING @ Sat, 11 Dec 2021 05:11:41: #2 Since the d (170) calculated from paired-peaks are smaller than 2*tag length, it may be influenced by unknown sequencing problem! WARNING @ Sat, 11 Dec 2021 05:11:41: #2 You may need to consider one of the other alternative d(s): 170 WARNING @ Sat, 11 Dec 2021 05:11:41: #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 05:11:41: #3 Call peaks... INFO @ Sat, 11 Dec 2021 05:11:41: #3 Pre-compute pvalue-qvalue table... INFO @ Sat, 11 Dec 2021 05:11:42: #3 Call peaks for each chromosome... INFO @ Sat, 11 Dec 2021 05:11:42: #4 Write output xls file... /home/okishinya/chipatlas/results/dm3/SRX8556363/SRX8556363.05_peaks.xls INFO @ Sat, 11 Dec 2021 05:11:42: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/dm3/SRX8556363/SRX8556363.05_peaks.narrowPeak INFO @ Sat, 11 Dec 2021 05:11:42: #4 Write summits bed file... /home/okishinya/chipatlas/results/dm3/SRX8556363/SRX8556363.05_summits.bed INFO @ Sat, 11 Dec 2021 05:11:42: Done! pass1 - making usageList (12 chroms): 1 millis pass2 - checking and writing primary data (596 records, 4 fields): 4 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 05:12:01: # Command line: callpeak -t /home/okishinya/chipatlas/results/dm3/SRX8556363/SRX8556363.bam -f BAM -g dm -n /home/okishinya/chipatlas/results/dm3/SRX8556363/SRX8556363.10 -q 1e-10 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/dm3/SRX8556363/SRX8556363.10 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/dm3/SRX8556363/SRX8556363.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 05:12:01: #1 read tag files... INFO @ Sat, 11 Dec 2021 05:12:01: #1 read treatment tags... INFO @ Sat, 11 Dec 2021 05:12:11: #1 tag size is determined as 150 bps INFO @ Sat, 11 Dec 2021 05:12:11: #1 tag size = 150 INFO @ Sat, 11 Dec 2021 05:12:11: #1 total tags in treatment: 265026 INFO @ Sat, 11 Dec 2021 05:12:11: #1 user defined the maximum tags... INFO @ Sat, 11 Dec 2021 05:12:11: #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 05:12:11: #1 tags after filtering in treatment: 245065 INFO @ Sat, 11 Dec 2021 05:12:11: #1 Redundant rate of treatment: 0.08 INFO @ Sat, 11 Dec 2021 05:12:11: #1 finished! INFO @ Sat, 11 Dec 2021 05:12:11: #2 Build Peak Model... INFO @ Sat, 11 Dec 2021 05:12:11: #2 looking for paired plus/minus strand peaks... INFO @ Sat, 11 Dec 2021 05:12:12: #2 number of paired peaks: 2402 INFO @ Sat, 11 Dec 2021 05:12:12: start model_add_line... INFO @ Sat, 11 Dec 2021 05:12:12: start X-correlation... INFO @ Sat, 11 Dec 2021 05:12:12: end of X-cor INFO @ Sat, 11 Dec 2021 05:12:12: #2 finished! INFO @ Sat, 11 Dec 2021 05:12:12: #2 predicted fragment length is 170 bps INFO @ Sat, 11 Dec 2021 05:12:12: #2 alternative fragment length(s) may be 170 bps INFO @ Sat, 11 Dec 2021 05:12:12: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/dm3/SRX8556363/SRX8556363.10_model.r WARNING @ Sat, 11 Dec 2021 05:12:12: #2 Since the d (170) calculated from paired-peaks are smaller than 2*tag length, it may be influenced by unknown sequencing problem! WARNING @ Sat, 11 Dec 2021 05:12:12: #2 You may need to consider one of the other alternative d(s): 170 WARNING @ Sat, 11 Dec 2021 05:12:12: #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 05:12:12: #3 Call peaks... INFO @ Sat, 11 Dec 2021 05:12:12: #3 Pre-compute pvalue-qvalue table... INFO @ Sat, 11 Dec 2021 05:12:12: #3 Call peaks for each chromosome... INFO @ Sat, 11 Dec 2021 05:12:12: #4 Write output xls file... /home/okishinya/chipatlas/results/dm3/SRX8556363/SRX8556363.10_peaks.xls INFO @ Sat, 11 Dec 2021 05:12:12: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/dm3/SRX8556363/SRX8556363.10_peaks.narrowPeak INFO @ Sat, 11 Dec 2021 05:12:12: #4 Write summits bed file... /home/okishinya/chipatlas/results/dm3/SRX8556363/SRX8556363.10_summits.bed INFO @ Sat, 11 Dec 2021 05:12:12: Done! pass1 - making usageList (10 chroms): 0 millis pass2 - checking and writing primary data (298 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 05:12:30: # Command line: callpeak -t /home/okishinya/chipatlas/results/dm3/SRX8556363/SRX8556363.bam -f BAM -g dm -n /home/okishinya/chipatlas/results/dm3/SRX8556363/SRX8556363.20 -q 1e-20 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/dm3/SRX8556363/SRX8556363.20 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/dm3/SRX8556363/SRX8556363.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 05:12:30: #1 read tag files... INFO @ Sat, 11 Dec 2021 05:12:30: #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 @ Sat, 11 Dec 2021 05:12:41: #1 tag size is determined as 150 bps INFO @ Sat, 11 Dec 2021 05:12:41: #1 tag size = 150 INFO @ Sat, 11 Dec 2021 05:12:41: #1 total tags in treatment: 265026 INFO @ Sat, 11 Dec 2021 05:12:41: #1 user defined the maximum tags... INFO @ Sat, 11 Dec 2021 05:12:41: #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 05:12:41: #1 tags after filtering in treatment: 245065 INFO @ Sat, 11 Dec 2021 05:12:41: #1 Redundant rate of treatment: 0.08 INFO @ Sat, 11 Dec 2021 05:12:41: #1 finished! INFO @ Sat, 11 Dec 2021 05:12:41: #2 Build Peak Model... INFO @ Sat, 11 Dec 2021 05:12:41: #2 looking for paired plus/minus strand peaks... INFO @ Sat, 11 Dec 2021 05:12:42: #2 number of paired peaks: 2402 INFO @ Sat, 11 Dec 2021 05:12:42: start model_add_line... INFO @ Sat, 11 Dec 2021 05:12:42: start X-correlation... INFO @ Sat, 11 Dec 2021 05:12:42: end of X-cor INFO @ Sat, 11 Dec 2021 05:12:42: #2 finished! INFO @ Sat, 11 Dec 2021 05:12:42: #2 predicted fragment length is 170 bps INFO @ Sat, 11 Dec 2021 05:12:42: #2 alternative fragment length(s) may be 170 bps INFO @ Sat, 11 Dec 2021 05:12:42: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/dm3/SRX8556363/SRX8556363.20_model.r WARNING @ Sat, 11 Dec 2021 05:12:42: #2 Since the d (170) calculated from paired-peaks are smaller than 2*tag length, it may be influenced by unknown sequencing problem! WARNING @ Sat, 11 Dec 2021 05:12:42: #2 You may need to consider one of the other alternative d(s): 170 WARNING @ Sat, 11 Dec 2021 05:12:42: #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 05:12:42: #3 Call peaks... INFO @ Sat, 11 Dec 2021 05:12:42: #3 Pre-compute pvalue-qvalue table... INFO @ Sat, 11 Dec 2021 05:12:42: #3 Call peaks for each chromosome... INFO @ Sat, 11 Dec 2021 05:12:42: #4 Write output xls file... /home/okishinya/chipatlas/results/dm3/SRX8556363/SRX8556363.20_peaks.xls INFO @ Sat, 11 Dec 2021 05:12:42: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/dm3/SRX8556363/SRX8556363.20_peaks.narrowPeak INFO @ Sat, 11 Dec 2021 05:12:42: #4 Write summits bed file... /home/okishinya/chipatlas/results/dm3/SRX8556363/SRX8556363.20_summits.bed INFO @ Sat, 11 Dec 2021 05:12:42: Done! pass1 - making usageList (8 chroms): 1 millis pass2 - checking and writing primary data (128 records, 4 fields): 1 millis CompletedMACS2peakCalling