Job ID = 14170079 SRX = SRX8556369 Genome = dm3 sra ファイルのダウンロード中... Read layout: PAIRED fastq に変換中... Read 24885068 spots for SRR12024925/SRR12024925.sra Written 24885068 spots for SRR12024925/SRR12024925.sra fastq に変換しました。 bowtie でマッピング中... Your job 14170665 ("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: 00:08:06 24885068 reads; of these: 24885068 (100.00%) were paired; of these: 24665424 (99.12%) aligned concordantly 0 times 128252 (0.52%) aligned concordantly exactly 1 time 91392 (0.37%) aligned concordantly >1 times ---- 24665424 pairs aligned concordantly 0 times; of these: 20434 (0.08%) aligned discordantly 1 time ---- 24644990 pairs aligned 0 times concordantly or discordantly; of these: 49289980 mates make up the pairs; of these: 49162695 (99.74%) aligned 0 times 40335 (0.08%) aligned exactly 1 time 86950 (0.18%) aligned >1 times 1.22% overall alignment rate Time searching: 00:08:06 Overall time: 00:08:06 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] 164764 / 236708 = 0.6961 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 05:16:59: # Command line: callpeak -t /home/okishinya/chipatlas/results/dm3/SRX8556369/SRX8556369.bam -f BAM -g dm -n /home/okishinya/chipatlas/results/dm3/SRX8556369/SRX8556369.05 -q 1e-05 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/dm3/SRX8556369/SRX8556369.05 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/dm3/SRX8556369/SRX8556369.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 05:16:59: #1 read tag files... INFO @ Sat, 11 Dec 2021 05:16:59: #1 read treatment tags... INFO @ Sat, 11 Dec 2021 05:17:02: #1 tag size is determined as 150 bps INFO @ Sat, 11 Dec 2021 05:17:02: #1 tag size = 150 INFO @ Sat, 11 Dec 2021 05:17:02: #1 total tags in treatment: 65200 INFO @ Sat, 11 Dec 2021 05:17:02: #1 user defined the maximum tags... INFO @ Sat, 11 Dec 2021 05:17:02: #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 05:17:02: #1 tags after filtering in treatment: 57745 INFO @ Sat, 11 Dec 2021 05:17:02: #1 Redundant rate of treatment: 0.11 INFO @ Sat, 11 Dec 2021 05:17:02: #1 finished! INFO @ Sat, 11 Dec 2021 05:17:02: #2 Build Peak Model... INFO @ Sat, 11 Dec 2021 05:17:02: #2 looking for paired plus/minus strand peaks... INFO @ Sat, 11 Dec 2021 05:17:02: #2 number of paired peaks: 2082 INFO @ Sat, 11 Dec 2021 05:17:02: start model_add_line... INFO @ Sat, 11 Dec 2021 05:17:02: start X-correlation... INFO @ Sat, 11 Dec 2021 05:17:02: end of X-cor INFO @ Sat, 11 Dec 2021 05:17:02: #2 finished! INFO @ Sat, 11 Dec 2021 05:17:02: #2 predicted fragment length is 169 bps INFO @ Sat, 11 Dec 2021 05:17:02: #2 alternative fragment length(s) may be 169 bps INFO @ Sat, 11 Dec 2021 05:17:02: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/dm3/SRX8556369/SRX8556369.05_model.r WARNING @ Sat, 11 Dec 2021 05:17:02: #2 Since the d (169) calculated from paired-peaks are smaller than 2*tag length, it may be influenced by unknown sequencing problem! WARNING @ Sat, 11 Dec 2021 05:17:02: #2 You may need to consider one of the other alternative d(s): 169 WARNING @ Sat, 11 Dec 2021 05:17:02: #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 05:17:02: #3 Call peaks... INFO @ Sat, 11 Dec 2021 05:17:02: #3 Pre-compute pvalue-qvalue table... INFO @ Sat, 11 Dec 2021 05:17:02: #3 Call peaks for each chromosome... INFO @ Sat, 11 Dec 2021 05:17:02: #4 Write output xls file... /home/okishinya/chipatlas/results/dm3/SRX8556369/SRX8556369.05_peaks.xls INFO @ Sat, 11 Dec 2021 05:17:02: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/dm3/SRX8556369/SRX8556369.05_peaks.narrowPeak INFO @ Sat, 11 Dec 2021 05:17:02: #4 Write summits bed file... /home/okishinya/chipatlas/results/dm3/SRX8556369/SRX8556369.05_summits.bed INFO @ Sat, 11 Dec 2021 05:17:02: Done! pass1 - making usageList (5 chroms): 1 millis pass2 - checking and writing primary data (143 records, 4 fields): 1 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 05:17:29: # Command line: callpeak -t /home/okishinya/chipatlas/results/dm3/SRX8556369/SRX8556369.bam -f BAM -g dm -n /home/okishinya/chipatlas/results/dm3/SRX8556369/SRX8556369.10 -q 1e-10 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/dm3/SRX8556369/SRX8556369.10 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/dm3/SRX8556369/SRX8556369.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 05:17:29: #1 read tag files... INFO @ Sat, 11 Dec 2021 05:17:29: #1 read treatment tags... INFO @ Sat, 11 Dec 2021 05:17:32: #1 tag size is determined as 150 bps INFO @ Sat, 11 Dec 2021 05:17:32: #1 tag size = 150 INFO @ Sat, 11 Dec 2021 05:17:32: #1 total tags in treatment: 65200 INFO @ Sat, 11 Dec 2021 05:17:32: #1 user defined the maximum tags... INFO @ Sat, 11 Dec 2021 05:17:32: #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 05:17:32: #1 tags after filtering in treatment: 57745 INFO @ Sat, 11 Dec 2021 05:17:32: #1 Redundant rate of treatment: 0.11 INFO @ Sat, 11 Dec 2021 05:17:32: #1 finished! INFO @ Sat, 11 Dec 2021 05:17:32: #2 Build Peak Model... INFO @ Sat, 11 Dec 2021 05:17:32: #2 looking for paired plus/minus strand peaks... INFO @ Sat, 11 Dec 2021 05:17:32: #2 number of paired peaks: 2082 INFO @ Sat, 11 Dec 2021 05:17:32: start model_add_line... INFO @ Sat, 11 Dec 2021 05:17:32: start X-correlation... INFO @ Sat, 11 Dec 2021 05:17:32: end of X-cor INFO @ Sat, 11 Dec 2021 05:17:32: #2 finished! INFO @ Sat, 11 Dec 2021 05:17:32: #2 predicted fragment length is 169 bps INFO @ Sat, 11 Dec 2021 05:17:32: #2 alternative fragment length(s) may be 169 bps INFO @ Sat, 11 Dec 2021 05:17:32: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/dm3/SRX8556369/SRX8556369.10_model.r WARNING @ Sat, 11 Dec 2021 05:17:32: #2 Since the d (169) calculated from paired-peaks are smaller than 2*tag length, it may be influenced by unknown sequencing problem! WARNING @ Sat, 11 Dec 2021 05:17:32: #2 You may need to consider one of the other alternative d(s): 169 WARNING @ Sat, 11 Dec 2021 05:17:32: #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 05:17:32: #3 Call peaks... INFO @ Sat, 11 Dec 2021 05:17:32: #3 Pre-compute pvalue-qvalue table... INFO @ Sat, 11 Dec 2021 05:17:32: #3 Call peaks for each chromosome... INFO @ Sat, 11 Dec 2021 05:17:33: #4 Write output xls file... /home/okishinya/chipatlas/results/dm3/SRX8556369/SRX8556369.10_peaks.xls INFO @ Sat, 11 Dec 2021 05:17:33: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/dm3/SRX8556369/SRX8556369.10_peaks.narrowPeak INFO @ Sat, 11 Dec 2021 05:17:33: #4 Write summits bed file... /home/okishinya/chipatlas/results/dm3/SRX8556369/SRX8556369.10_summits.bed INFO @ Sat, 11 Dec 2021 05:17:33: Done! pass1 - making usageList (5 chroms): 0 millis pass2 - checking and writing primary data (76 records, 4 fields): 1 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 05:17:59: # Command line: callpeak -t /home/okishinya/chipatlas/results/dm3/SRX8556369/SRX8556369.bam -f BAM -g dm -n /home/okishinya/chipatlas/results/dm3/SRX8556369/SRX8556369.20 -q 1e-20 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/dm3/SRX8556369/SRX8556369.20 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/dm3/SRX8556369/SRX8556369.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 05:17:59: #1 read tag files... INFO @ Sat, 11 Dec 2021 05:17:59: #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 05:18:02: #1 tag size is determined as 150 bps INFO @ Sat, 11 Dec 2021 05:18:02: #1 tag size = 150 INFO @ Sat, 11 Dec 2021 05:18:02: #1 total tags in treatment: 65200 INFO @ Sat, 11 Dec 2021 05:18:02: #1 user defined the maximum tags... INFO @ Sat, 11 Dec 2021 05:18:02: #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 05:18:02: #1 tags after filtering in treatment: 57745 INFO @ Sat, 11 Dec 2021 05:18:02: #1 Redundant rate of treatment: 0.11 INFO @ Sat, 11 Dec 2021 05:18:02: #1 finished! INFO @ Sat, 11 Dec 2021 05:18:02: #2 Build Peak Model... INFO @ Sat, 11 Dec 2021 05:18:02: #2 looking for paired plus/minus strand peaks... INFO @ Sat, 11 Dec 2021 05:18:02: #2 number of paired peaks: 2082 INFO @ Sat, 11 Dec 2021 05:18:02: start model_add_line... INFO @ Sat, 11 Dec 2021 05:18:02: start X-correlation... INFO @ Sat, 11 Dec 2021 05:18:02: end of X-cor INFO @ Sat, 11 Dec 2021 05:18:02: #2 finished! INFO @ Sat, 11 Dec 2021 05:18:02: #2 predicted fragment length is 169 bps INFO @ Sat, 11 Dec 2021 05:18:02: #2 alternative fragment length(s) may be 169 bps INFO @ Sat, 11 Dec 2021 05:18:02: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/dm3/SRX8556369/SRX8556369.20_model.r WARNING @ Sat, 11 Dec 2021 05:18:02: #2 Since the d (169) calculated from paired-peaks are smaller than 2*tag length, it may be influenced by unknown sequencing problem! WARNING @ Sat, 11 Dec 2021 05:18:02: #2 You may need to consider one of the other alternative d(s): 169 WARNING @ Sat, 11 Dec 2021 05:18:02: #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 05:18:02: #3 Call peaks... INFO @ Sat, 11 Dec 2021 05:18:02: #3 Pre-compute pvalue-qvalue table... INFO @ Sat, 11 Dec 2021 05:18:03: #3 Call peaks for each chromosome... INFO @ Sat, 11 Dec 2021 05:18:03: #4 Write output xls file... /home/okishinya/chipatlas/results/dm3/SRX8556369/SRX8556369.20_peaks.xls INFO @ Sat, 11 Dec 2021 05:18:03: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/dm3/SRX8556369/SRX8556369.20_peaks.narrowPeak INFO @ Sat, 11 Dec 2021 05:18:03: #4 Write summits bed file... /home/okishinya/chipatlas/results/dm3/SRX8556369/SRX8556369.20_summits.bed INFO @ Sat, 11 Dec 2021 05:18:03: Done! pass1 - making usageList (4 chroms): 0 millis pass2 - checking and writing primary data (30 records, 4 fields): 1 millis CompletedMACS2peakCalling