Job ID = 12264824 SRX = SRX7687147 Genome = ce10 sra ファイルのダウンロード中... Read layout: PAIRED fastq に変換中... Read 27191206 spots for SRR11034890/SRR11034890.sra Written 27191206 spots for SRR11034890/SRR11034890.sra fastq に変換しました。 bowtie でマッピング中... Your job 12265511 ("srTce11") 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: 00:56:00 27191206 reads; of these: 27191206 (100.00%) were paired; of these: 5585219 (20.54%) aligned concordantly 0 times 16249320 (59.76%) aligned concordantly exactly 1 time 5356667 (19.70%) aligned concordantly >1 times ---- 5585219 pairs aligned concordantly 0 times; of these: 4164640 (74.57%) aligned discordantly 1 time ---- 1420579 pairs aligned 0 times concordantly or discordantly; of these: 2841158 mates make up the pairs; of these: 1099478 (38.70%) aligned 0 times 633243 (22.29%) aligned exactly 1 time 1108437 (39.01%) aligned >1 times 97.98% overall alignment rate Time searching: 00:56:00 Overall time: 00:56:00 マッピングが完了しました。 samtools でBAM に変換中... [samopen] SAM header is present: 7 sequences. [bam_sort_core] merging from 24 files... [bam_rmdup_core] processing reference chrI... [bam_rmdup_core] processing reference chrII... [bam_rmdup_core] processing reference chrIII... [bam_rmdup_core] processing reference chrIV... [bam_rmdup_core] processing reference chrV... [bam_rmdup_core] processing reference chrX... [bam_rmdup_core] processing reference chrM... [bam_rmdup_core] 5739625 / 25738075 = 0.2230 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/3.7.1/var/singularity/mnt/session/etc/resolv.conf [files]: /etc/resolv.conf doesn't exist in container INFO @ Sat, 03 Apr 2021 07:09:49: # Command line: callpeak -t /home/okishinya/chipatlas/results/ce10/SRX7687147/SRX7687147.bam -f BAM -g ce -n /home/okishinya/chipatlas/results/ce10/SRX7687147/SRX7687147.05 -q 1e-05 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/ce10/SRX7687147/SRX7687147.05 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/ce10/SRX7687147/SRX7687147.bam'] # control file = None # effective genome size = 9.00e+07 # 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, 03 Apr 2021 07:09:49: #1 read tag files... INFO @ Sat, 03 Apr 2021 07:09:49: #1 read treatment tags... INFO @ Sat, 03 Apr 2021 07:09:56: 1000000 INFO @ Sat, 03 Apr 2021 07:10:04: 2000000 INFO @ Sat, 03 Apr 2021 07:10:12: 3000000 WARNING: Skipping mount /opt/pkg/singularity/3.7.1/var/singularity/mnt/session/etc/resolv.conf [files]: /etc/resolv.conf doesn't exist in container INFO @ Sat, 03 Apr 2021 07:10:19: # Command line: callpeak -t /home/okishinya/chipatlas/results/ce10/SRX7687147/SRX7687147.bam -f BAM -g ce -n /home/okishinya/chipatlas/results/ce10/SRX7687147/SRX7687147.10 -q 1e-10 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/ce10/SRX7687147/SRX7687147.10 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/ce10/SRX7687147/SRX7687147.bam'] # control file = None # effective genome size = 9.00e+07 # 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, 03 Apr 2021 07:10:19: #1 read tag files... INFO @ Sat, 03 Apr 2021 07:10:19: #1 read treatment tags... INFO @ Sat, 03 Apr 2021 07:10:19: 4000000 INFO @ Sat, 03 Apr 2021 07:10:26: 1000000 INFO @ Sat, 03 Apr 2021 07:10:27: 5000000 INFO @ Sat, 03 Apr 2021 07:10:34: 2000000 INFO @ Sat, 03 Apr 2021 07:10:35: 6000000 INFO @ Sat, 03 Apr 2021 07:10:41: 3000000 INFO @ Sat, 03 Apr 2021 07:10:43: 7000000 BedGraph に変換中... WARNING: Skipping mount /opt/pkg/singularity/3.7.1/var/singularity/mnt/session/etc/resolv.conf [files]: /etc/resolv.conf doesn't exist in container INFO @ Sat, 03 Apr 2021 07:10:49: # Command line: callpeak -t /home/okishinya/chipatlas/results/ce10/SRX7687147/SRX7687147.bam -f BAM -g ce -n /home/okishinya/chipatlas/results/ce10/SRX7687147/SRX7687147.20 -q 1e-20 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/ce10/SRX7687147/SRX7687147.20 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/ce10/SRX7687147/SRX7687147.bam'] # control file = None # effective genome size = 9.00e+07 # 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, 03 Apr 2021 07:10:49: #1 read tag files... INFO @ Sat, 03 Apr 2021 07:10:49: #1 read treatment tags... INFO @ Sat, 03 Apr 2021 07:10:49: 4000000 INFO @ Sat, 03 Apr 2021 07:10:51: 8000000 INFO @ Sat, 03 Apr 2021 07:10:57: 1000000 INFO @ Sat, 03 Apr 2021 07:10:57: 5000000 INFO @ Sat, 03 Apr 2021 07:10:59: 9000000 INFO @ Sat, 03 Apr 2021 07:11:05: 6000000 INFO @ Sat, 03 Apr 2021 07:11:05: 2000000 INFO @ Sat, 03 Apr 2021 07:11:07: 10000000 INFO @ Sat, 03 Apr 2021 07:11:13: 7000000 INFO @ Sat, 03 Apr 2021 07:11:13: 3000000 INFO @ Sat, 03 Apr 2021 07:11:15: 11000000 INFO @ Sat, 03 Apr 2021 07:11:20: 8000000 INFO @ Sat, 03 Apr 2021 07:11:21: 4000000 INFO @ Sat, 03 Apr 2021 07:11:22: 12000000 INFO @ Sat, 03 Apr 2021 07:11:28: 9000000 INFO @ Sat, 03 Apr 2021 07:11:29: 5000000 INFO @ Sat, 03 Apr 2021 07:11:30: 13000000 INFO @ Sat, 03 Apr 2021 07:11:35: 10000000 INFO @ Sat, 03 Apr 2021 07:11:36: 6000000 INFO @ Sat, 03 Apr 2021 07:11:38: 14000000 INFO @ Sat, 03 Apr 2021 07:11:43: 11000000 INFO @ Sat, 03 Apr 2021 07:11:44: 7000000 INFO @ Sat, 03 Apr 2021 07:11:46: 15000000 INFO @ Sat, 03 Apr 2021 07:11:51: 12000000 INFO @ Sat, 03 Apr 2021 07:11:52: 8000000 INFO @ Sat, 03 Apr 2021 07:11:54: 16000000 INFO @ Sat, 03 Apr 2021 07:11:59: 13000000 INFO @ Sat, 03 Apr 2021 07:12:00: 9000000 INFO @ Sat, 03 Apr 2021 07:12:02: 17000000 INFO @ Sat, 03 Apr 2021 07:12:07: 14000000 INFO @ Sat, 03 Apr 2021 07:12:08: 10000000 INFO @ Sat, 03 Apr 2021 07:12:09: 18000000 INFO @ Sat, 03 Apr 2021 07:12:15: 15000000 INFO @ Sat, 03 Apr 2021 07:12:16: 11000000 INFO @ Sat, 03 Apr 2021 07:12:17: 19000000 INFO @ Sat, 03 Apr 2021 07:12:22: 16000000 INFO @ Sat, 03 Apr 2021 07:12:24: 12000000 INFO @ Sat, 03 Apr 2021 07:12:25: 20000000 INFO @ Sat, 03 Apr 2021 07:12:30: 17000000 INFO @ Sat, 03 Apr 2021 07:12:31: 13000000 INFO @ Sat, 03 Apr 2021 07:12:32: 21000000 INFO @ Sat, 03 Apr 2021 07:12:38: 18000000 INFO @ Sat, 03 Apr 2021 07:12:39: 14000000 INFO @ Sat, 03 Apr 2021 07:12:40: 22000000 INFO @ Sat, 03 Apr 2021 07:12:45: 19000000 INFO @ Sat, 03 Apr 2021 07:12:47: 15000000 INFO @ Sat, 03 Apr 2021 07:12:47: 23000000 INFO @ Sat, 03 Apr 2021 07:12:53: 20000000 INFO @ Sat, 03 Apr 2021 07:12:54: 16000000 INFO @ Sat, 03 Apr 2021 07:12:54: 24000000 INFO @ Sat, 03 Apr 2021 07:13:01: 21000000 INFO @ Sat, 03 Apr 2021 07:13:01: 25000000 INFO @ Sat, 03 Apr 2021 07:13:02: 17000000 INFO @ Sat, 03 Apr 2021 07:13:08: 22000000 INFO @ Sat, 03 Apr 2021 07:13:09: 26000000 INFO @ Sat, 03 Apr 2021 07:13:09: 18000000 INFO @ Sat, 03 Apr 2021 07:13:15: 23000000 INFO @ Sat, 03 Apr 2021 07:13:16: 27000000 INFO @ Sat, 03 Apr 2021 07:13:17: 19000000 INFO @ Sat, 03 Apr 2021 07:13:22: 24000000 INFO @ Sat, 03 Apr 2021 07:13:23: 28000000 INFO @ Sat, 03 Apr 2021 07:13:23: 20000000 INFO @ Sat, 03 Apr 2021 07:13:29: 29000000 INFO @ Sat, 03 Apr 2021 07:13:30: 25000000 INFO @ Sat, 03 Apr 2021 07:13:31: 21000000 INFO @ Sat, 03 Apr 2021 07:13:35: 30000000 INFO @ Sat, 03 Apr 2021 07:13:37: 26000000 INFO @ Sat, 03 Apr 2021 07:13:38: 22000000 INFO @ Sat, 03 Apr 2021 07:13:41: 31000000 INFO @ Sat, 03 Apr 2021 07:13:45: 27000000 INFO @ Sat, 03 Apr 2021 07:13:46: 23000000 INFO @ Sat, 03 Apr 2021 07:13:48: 32000000 INFO @ Sat, 03 Apr 2021 07:13:52: 28000000 INFO @ Sat, 03 Apr 2021 07:13:53: 24000000 INFO @ Sat, 03 Apr 2021 07:13:54: 33000000 INFO @ Sat, 03 Apr 2021 07:13:59: 29000000 INFO @ Sat, 03 Apr 2021 07:14:00: 34000000 INFO @ Sat, 03 Apr 2021 07:14:01: 25000000 INFO @ Sat, 03 Apr 2021 07:14:06: 35000000 INFO @ Sat, 03 Apr 2021 07:14:07: 30000000 BedGraph に変換しました。 BigWig に変換中... INFO @ Sat, 03 Apr 2021 07:14:08: 26000000 INFO @ Sat, 03 Apr 2021 07:14:12: 36000000 INFO @ Sat, 03 Apr 2021 07:14:14: 31000000 INFO @ Sat, 03 Apr 2021 07:14:15: 27000000 INFO @ Sat, 03 Apr 2021 07:14:19: 37000000 INFO @ Sat, 03 Apr 2021 07:14:22: 32000000 INFO @ Sat, 03 Apr 2021 07:14:23: 28000000 INFO @ Sat, 03 Apr 2021 07:14:26: 38000000 INFO @ Sat, 03 Apr 2021 07:14:29: 33000000 INFO @ Sat, 03 Apr 2021 07:14:30: 29000000 INFO @ Sat, 03 Apr 2021 07:14:33: 39000000 INFO @ Sat, 03 Apr 2021 07:14:36: 34000000 INFO @ Sat, 03 Apr 2021 07:14:37: 30000000 INFO @ Sat, 03 Apr 2021 07:14:40: 40000000 INFO @ Sat, 03 Apr 2021 07:14:44: 35000000 INFO @ Sat, 03 Apr 2021 07:14:44: 31000000 INFO @ Sat, 03 Apr 2021 07:14:48: 41000000 INFO @ Sat, 03 Apr 2021 07:14:51: 36000000 INFO @ Sat, 03 Apr 2021 07:14:51: 32000000 INFO @ Sat, 03 Apr 2021 07:14:53: #1 tag size is determined as 75 bps INFO @ Sat, 03 Apr 2021 07:14:53: #1 tag size = 75 INFO @ Sat, 03 Apr 2021 07:14:53: #1 total tags in treatment: 16447712 INFO @ Sat, 03 Apr 2021 07:14:53: #1 user defined the maximum tags... INFO @ Sat, 03 Apr 2021 07:14:53: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Sat, 03 Apr 2021 07:14:54: #1 tags after filtering in treatment: 11676400 INFO @ Sat, 03 Apr 2021 07:14:54: #1 Redundant rate of treatment: 0.29 INFO @ Sat, 03 Apr 2021 07:14:54: #1 finished! INFO @ Sat, 03 Apr 2021 07:14:54: #2 Build Peak Model... INFO @ Sat, 03 Apr 2021 07:14:54: #2 looking for paired plus/minus strand peaks... INFO @ Sat, 03 Apr 2021 07:14:54: #2 number of paired peaks: 381 WARNING @ Sat, 03 Apr 2021 07:14:54: Fewer paired peaks (381) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 381 pairs to build model! INFO @ Sat, 03 Apr 2021 07:14:54: start model_add_line... INFO @ Sat, 03 Apr 2021 07:14:55: start X-correlation... INFO @ Sat, 03 Apr 2021 07:14:55: end of X-cor INFO @ Sat, 03 Apr 2021 07:14:55: #2 finished! INFO @ Sat, 03 Apr 2021 07:14:55: #2 predicted fragment length is 135 bps INFO @ Sat, 03 Apr 2021 07:14:55: #2 alternative fragment length(s) may be 3,128,135 bps INFO @ Sat, 03 Apr 2021 07:14:55: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/ce10/SRX7687147/SRX7687147.05_model.r WARNING @ Sat, 03 Apr 2021 07:14:55: #2 Since the d (135) calculated from paired-peaks are smaller than 2*tag length, it may be influenced by unknown sequencing problem! WARNING @ Sat, 03 Apr 2021 07:14:55: #2 You may need to consider one of the other alternative d(s): 3,128,135 WARNING @ Sat, 03 Apr 2021 07:14:55: #2 You can restart the process with --nomodel --extsize XXX with your choice or an arbitrary number. Nontheless, MACS will continute computing. INFO @ Sat, 03 Apr 2021 07:14:55: #3 Call peaks... INFO @ Sat, 03 Apr 2021 07:14:55: #3 Pre-compute pvalue-qvalue table... INFO @ Sat, 03 Apr 2021 07:14:57: 37000000 INFO @ Sat, 03 Apr 2021 07:14:58: 33000000 INFO @ Sat, 03 Apr 2021 07:15:04: 38000000 INFO @ Sat, 03 Apr 2021 07:15:05: 34000000 INFO @ Sat, 03 Apr 2021 07:15:11: 39000000 INFO @ Sat, 03 Apr 2021 07:15:12: 35000000 INFO @ Sat, 03 Apr 2021 07:15:18: #3 Call peaks for each chromosome... BigWig に変換しました。 INFO @ Sat, 03 Apr 2021 07:15:18: 40000000 INFO @ Sat, 03 Apr 2021 07:15:19: 36000000 INFO @ Sat, 03 Apr 2021 07:15:26: 41000000 INFO @ Sat, 03 Apr 2021 07:15:26: 37000000 INFO @ Sat, 03 Apr 2021 07:15:29: #4 Write output xls file... /home/okishinya/chipatlas/results/ce10/SRX7687147/SRX7687147.05_peaks.xls INFO @ Sat, 03 Apr 2021 07:15:29: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/ce10/SRX7687147/SRX7687147.05_peaks.narrowPeak INFO @ Sat, 03 Apr 2021 07:15:29: #4 Write summits bed file... /home/okishinya/chipatlas/results/ce10/SRX7687147/SRX7687147.05_summits.bed INFO @ Sat, 03 Apr 2021 07:15:29: Done! pass1 - making usageList (7 chroms): 0 millis pass2 - checking and writing primary data (520 records, 4 fields): 3 millis CompletedMACS2peakCalling INFO @ Sat, 03 Apr 2021 07:15:31: #1 tag size is determined as 75 bps INFO @ Sat, 03 Apr 2021 07:15:31: #1 tag size = 75 INFO @ Sat, 03 Apr 2021 07:15:31: #1 total tags in treatment: 16447712 INFO @ Sat, 03 Apr 2021 07:15:31: #1 user defined the maximum tags... INFO @ Sat, 03 Apr 2021 07:15:31: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Sat, 03 Apr 2021 07:15:31: #1 tags after filtering in treatment: 11676400 INFO @ Sat, 03 Apr 2021 07:15:31: #1 Redundant rate of treatment: 0.29 INFO @ Sat, 03 Apr 2021 07:15:31: #1 finished! INFO @ Sat, 03 Apr 2021 07:15:31: #2 Build Peak Model... INFO @ Sat, 03 Apr 2021 07:15:31: #2 looking for paired plus/minus strand peaks... INFO @ Sat, 03 Apr 2021 07:15:32: 38000000 INFO @ Sat, 03 Apr 2021 07:15:32: #2 number of paired peaks: 381 WARNING @ Sat, 03 Apr 2021 07:15:32: Fewer paired peaks (381) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 381 pairs to build model! INFO @ Sat, 03 Apr 2021 07:15:32: start model_add_line... INFO @ Sat, 03 Apr 2021 07:15:32: start X-correlation... INFO @ Sat, 03 Apr 2021 07:15:32: end of X-cor INFO @ Sat, 03 Apr 2021 07:15:32: #2 finished! INFO @ Sat, 03 Apr 2021 07:15:32: #2 predicted fragment length is 135 bps INFO @ Sat, 03 Apr 2021 07:15:32: #2 alternative fragment length(s) may be 3,128,135 bps INFO @ Sat, 03 Apr 2021 07:15:32: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/ce10/SRX7687147/SRX7687147.10_model.r WARNING @ Sat, 03 Apr 2021 07:15:32: #2 Since the d (135) calculated from paired-peaks are smaller than 2*tag length, it may be influenced by unknown sequencing problem! WARNING @ Sat, 03 Apr 2021 07:15:32: #2 You may need to consider one of the other alternative d(s): 3,128,135 WARNING @ Sat, 03 Apr 2021 07:15:32: #2 You can restart the process with --nomodel --extsize XXX with your choice or an arbitrary number. Nontheless, MACS will continute computing. INFO @ Sat, 03 Apr 2021 07:15:32: #3 Call peaks... INFO @ Sat, 03 Apr 2021 07:15:32: #3 Pre-compute pvalue-qvalue table... INFO @ Sat, 03 Apr 2021 07:15:37: 39000000 INFO @ Sat, 03 Apr 2021 07:15:42: 40000000 INFO @ Sat, 03 Apr 2021 07:15:47: 41000000 INFO @ Sat, 03 Apr 2021 07:15:52: #1 tag size is determined as 75 bps INFO @ Sat, 03 Apr 2021 07:15:52: #1 tag size = 75 INFO @ Sat, 03 Apr 2021 07:15:52: #1 total tags in treatment: 16447712 INFO @ Sat, 03 Apr 2021 07:15:52: #1 user defined the maximum tags... INFO @ Sat, 03 Apr 2021 07:15:52: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Sat, 03 Apr 2021 07:15:52: #1 tags after filtering in treatment: 11676400 INFO @ Sat, 03 Apr 2021 07:15:52: #1 Redundant rate of treatment: 0.29 INFO @ Sat, 03 Apr 2021 07:15:52: #1 finished! INFO @ Sat, 03 Apr 2021 07:15:52: #2 Build Peak Model... INFO @ Sat, 03 Apr 2021 07:15:52: #2 looking for paired plus/minus strand peaks... INFO @ Sat, 03 Apr 2021 07:15:53: #2 number of paired peaks: 381 WARNING @ Sat, 03 Apr 2021 07:15:53: Fewer paired peaks (381) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 381 pairs to build model! INFO @ Sat, 03 Apr 2021 07:15:53: start model_add_line... INFO @ Sat, 03 Apr 2021 07:15:53: start X-correlation... INFO @ Sat, 03 Apr 2021 07:15:53: end of X-cor INFO @ Sat, 03 Apr 2021 07:15:53: #2 finished! INFO @ Sat, 03 Apr 2021 07:15:53: #2 predicted fragment length is 135 bps INFO @ Sat, 03 Apr 2021 07:15:53: #2 alternative fragment length(s) may be 3,128,135 bps INFO @ Sat, 03 Apr 2021 07:15:53: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/ce10/SRX7687147/SRX7687147.20_model.r WARNING @ Sat, 03 Apr 2021 07:15:53: #2 Since the d (135) calculated from paired-peaks are smaller than 2*tag length, it may be influenced by unknown sequencing problem! WARNING @ Sat, 03 Apr 2021 07:15:53: #2 You may need to consider one of the other alternative d(s): 3,128,135 WARNING @ Sat, 03 Apr 2021 07:15:53: #2 You can restart the process with --nomodel --extsize XXX with your choice or an arbitrary number. Nontheless, MACS will continute computing. INFO @ Sat, 03 Apr 2021 07:15:53: #3 Call peaks... INFO @ Sat, 03 Apr 2021 07:15:53: #3 Pre-compute pvalue-qvalue table... INFO @ Sat, 03 Apr 2021 07:15:54: #3 Call peaks for each chromosome... INFO @ Sat, 03 Apr 2021 07:16:04: #4 Write output xls file... /home/okishinya/chipatlas/results/ce10/SRX7687147/SRX7687147.10_peaks.xls INFO @ Sat, 03 Apr 2021 07:16:04: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/ce10/SRX7687147/SRX7687147.10_peaks.narrowPeak INFO @ Sat, 03 Apr 2021 07:16:04: #4 Write summits bed file... /home/okishinya/chipatlas/results/ce10/SRX7687147/SRX7687147.10_summits.bed INFO @ Sat, 03 Apr 2021 07:16:04: Done! pass1 - making usageList (7 chroms): 1 millis pass2 - checking and writing primary data (340 records, 4 fields): 2 millis CompletedMACS2peakCalling INFO @ Sat, 03 Apr 2021 07:16:15: #3 Call peaks for each chromosome... INFO @ Sat, 03 Apr 2021 07:16:25: #4 Write output xls file... /home/okishinya/chipatlas/results/ce10/SRX7687147/SRX7687147.20_peaks.xls INFO @ Sat, 03 Apr 2021 07:16:25: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/ce10/SRX7687147/SRX7687147.20_peaks.narrowPeak INFO @ Sat, 03 Apr 2021 07:16:25: #4 Write summits bed file... /home/okishinya/chipatlas/results/ce10/SRX7687147/SRX7687147.20_summits.bed INFO @ Sat, 03 Apr 2021 07:16:25: Done! pass1 - making usageList (6 chroms): 1 millis pass2 - checking and writing primary data (180 records, 4 fields): 1 millis CompletedMACS2peakCalling