Job ID = 12265494 SRX = SRX7687152 Genome = ce11 sra ファイルのダウンロード中... Read layout: PAIRED fastq に変換中... 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: 00:00:01 Multiseed full-index search: 00:40:41 30680231 reads; of these: 30680231 (100.00%) were paired; of these: 6619095 (21.57%) aligned concordantly 0 times 19699231 (64.21%) aligned concordantly exactly 1 time 4361905 (14.22%) aligned concordantly >1 times ---- 6619095 pairs aligned concordantly 0 times; of these: 4685341 (70.79%) aligned discordantly 1 time ---- 1933754 pairs aligned 0 times concordantly or discordantly; of these: 3867508 mates make up the pairs; of these: 1943609 (50.25%) aligned 0 times 712267 (18.42%) aligned exactly 1 time 1211632 (31.33%) aligned >1 times 96.83% overall alignment rate Time searching: 00:40:42 Overall time: 00:40:42 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 28 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] 8291012 / 28718649 = 0.2887 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 08:11:34: # Command line: callpeak -t /home/okishinya/chipatlas/results/ce11/SRX7687152/SRX7687152.bam -f BAM -g ce -n /home/okishinya/chipatlas/results/ce11/SRX7687152/SRX7687152.05 -q 1e-05 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/ce11/SRX7687152/SRX7687152.05 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/ce11/SRX7687152/SRX7687152.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 08:11:34: #1 read tag files... INFO @ Sat, 03 Apr 2021 08:11:34: #1 read treatment tags... INFO @ Sat, 03 Apr 2021 08:11:40: 1000000 INFO @ Sat, 03 Apr 2021 08:11:45: 2000000 INFO @ Sat, 03 Apr 2021 08:11:51: 3000000 INFO @ Sat, 03 Apr 2021 08:11:57: 4000000 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 08:12:02: 5000000 INFO @ Sat, 03 Apr 2021 08:12:04: # Command line: callpeak -t /home/okishinya/chipatlas/results/ce11/SRX7687152/SRX7687152.bam -f BAM -g ce -n /home/okishinya/chipatlas/results/ce11/SRX7687152/SRX7687152.10 -q 1e-10 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/ce11/SRX7687152/SRX7687152.10 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/ce11/SRX7687152/SRX7687152.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 08:12:04: #1 read tag files... INFO @ Sat, 03 Apr 2021 08:12:04: #1 read treatment tags... INFO @ Sat, 03 Apr 2021 08:12:09: 6000000 INFO @ Sat, 03 Apr 2021 08:12:11: 1000000 INFO @ Sat, 03 Apr 2021 08:12:15: 7000000 INFO @ Sat, 03 Apr 2021 08:12:18: 2000000 INFO @ Sat, 03 Apr 2021 08:12:22: 8000000 INFO @ Sat, 03 Apr 2021 08:12:25: 3000000 INFO @ Sat, 03 Apr 2021 08:12:29: 9000000 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 08:12:32: 4000000 INFO @ Sat, 03 Apr 2021 08:12:34: # Command line: callpeak -t /home/okishinya/chipatlas/results/ce11/SRX7687152/SRX7687152.bam -f BAM -g ce -n /home/okishinya/chipatlas/results/ce11/SRX7687152/SRX7687152.20 -q 1e-20 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/ce11/SRX7687152/SRX7687152.20 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/ce11/SRX7687152/SRX7687152.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 08:12:34: #1 read tag files... INFO @ Sat, 03 Apr 2021 08:12:34: #1 read treatment tags... INFO @ Sat, 03 Apr 2021 08:12:36: 10000000 INFO @ Sat, 03 Apr 2021 08:12:39: 5000000 INFO @ Sat, 03 Apr 2021 08:12:41: 1000000 INFO @ Sat, 03 Apr 2021 08:12:43: 11000000 INFO @ Sat, 03 Apr 2021 08:12:47: 6000000 INFO @ Sat, 03 Apr 2021 08:12:49: 2000000 INFO @ Sat, 03 Apr 2021 08:12:50: 12000000 INFO @ Sat, 03 Apr 2021 08:12:54: 7000000 INFO @ Sat, 03 Apr 2021 08:12:57: 13000000 INFO @ Sat, 03 Apr 2021 08:12:57: 3000000 INFO @ Sat, 03 Apr 2021 08:13:01: 8000000 INFO @ Sat, 03 Apr 2021 08:13:04: 14000000 INFO @ Sat, 03 Apr 2021 08:13:05: 4000000 INFO @ Sat, 03 Apr 2021 08:13:08: 9000000 INFO @ Sat, 03 Apr 2021 08:13:11: 15000000 INFO @ Sat, 03 Apr 2021 08:13:13: 5000000 INFO @ Sat, 03 Apr 2021 08:13:15: 10000000 INFO @ Sat, 03 Apr 2021 08:13:18: 16000000 INFO @ Sat, 03 Apr 2021 08:13:21: 6000000 INFO @ Sat, 03 Apr 2021 08:13:22: 11000000 INFO @ Sat, 03 Apr 2021 08:13:25: 17000000 INFO @ Sat, 03 Apr 2021 08:13:28: 7000000 INFO @ Sat, 03 Apr 2021 08:13:29: 12000000 INFO @ Sat, 03 Apr 2021 08:13:32: 18000000 INFO @ Sat, 03 Apr 2021 08:13:36: 13000000 INFO @ Sat, 03 Apr 2021 08:13:36: 8000000 INFO @ Sat, 03 Apr 2021 08:13:39: 19000000 INFO @ Sat, 03 Apr 2021 08:13:43: 14000000 INFO @ Sat, 03 Apr 2021 08:13:44: 9000000 INFO @ Sat, 03 Apr 2021 08:13:46: 20000000 INFO @ Sat, 03 Apr 2021 08:13:50: 15000000 INFO @ Sat, 03 Apr 2021 08:13:52: 10000000 INFO @ Sat, 03 Apr 2021 08:13:53: 21000000 INFO @ Sat, 03 Apr 2021 08:13:57: 16000000 INFO @ Sat, 03 Apr 2021 08:14:00: 11000000 INFO @ Sat, 03 Apr 2021 08:14:00: 22000000 INFO @ Sat, 03 Apr 2021 08:14:04: 17000000 INFO @ Sat, 03 Apr 2021 08:14:07: 23000000 INFO @ Sat, 03 Apr 2021 08:14:07: 12000000 INFO @ Sat, 03 Apr 2021 08:14:11: 18000000 INFO @ Sat, 03 Apr 2021 08:14:13: 24000000 INFO @ Sat, 03 Apr 2021 08:14:15: 13000000 INFO @ Sat, 03 Apr 2021 08:14:18: 19000000 INFO @ Sat, 03 Apr 2021 08:14:20: 25000000 INFO @ Sat, 03 Apr 2021 08:14:23: 14000000 INFO @ Sat, 03 Apr 2021 08:14:25: 20000000 INFO @ Sat, 03 Apr 2021 08:14:27: 26000000 INFO @ Sat, 03 Apr 2021 08:14:30: 15000000 INFO @ Sat, 03 Apr 2021 08:14:32: 21000000 INFO @ Sat, 03 Apr 2021 08:14:34: 27000000 INFO @ Sat, 03 Apr 2021 08:14:38: 16000000 INFO @ Sat, 03 Apr 2021 08:14:39: 22000000 INFO @ Sat, 03 Apr 2021 08:14:41: 28000000 INFO @ Sat, 03 Apr 2021 08:14:46: 17000000 INFO @ Sat, 03 Apr 2021 08:14:46: 23000000 INFO @ Sat, 03 Apr 2021 08:14:48: 29000000 INFO @ Sat, 03 Apr 2021 08:14:53: 24000000 INFO @ Sat, 03 Apr 2021 08:14:53: 18000000 INFO @ Sat, 03 Apr 2021 08:14:55: 30000000 INFO @ Sat, 03 Apr 2021 08:15:00: 25000000 INFO @ Sat, 03 Apr 2021 08:15:01: 19000000 INFO @ Sat, 03 Apr 2021 08:15:02: 31000000 INFO @ Sat, 03 Apr 2021 08:15:07: 26000000 INFO @ Sat, 03 Apr 2021 08:15:09: 20000000 INFO @ Sat, 03 Apr 2021 08:15:09: 32000000 INFO @ Sat, 03 Apr 2021 08:15:14: 27000000 INFO @ Sat, 03 Apr 2021 08:15:16: 33000000 INFO @ Sat, 03 Apr 2021 08:15:16: 21000000 INFO @ Sat, 03 Apr 2021 08:15:21: 28000000 INFO @ Sat, 03 Apr 2021 08:15:23: 34000000 INFO @ Sat, 03 Apr 2021 08:15:24: 22000000 INFO @ Sat, 03 Apr 2021 08:15:27: 29000000 INFO @ Sat, 03 Apr 2021 08:15:30: 35000000 INFO @ Sat, 03 Apr 2021 08:15:32: 23000000 INFO @ Sat, 03 Apr 2021 08:15:34: 30000000 INFO @ Sat, 03 Apr 2021 08:15:37: 36000000 INFO @ Sat, 03 Apr 2021 08:15:39: 24000000 INFO @ Sat, 03 Apr 2021 08:15:41: 31000000 INFO @ Sat, 03 Apr 2021 08:15:45: 37000000 BedGraph に変換しました。 BigWig に変換中... INFO @ Sat, 03 Apr 2021 08:15:47: 25000000 INFO @ Sat, 03 Apr 2021 08:15:48: 32000000 INFO @ Sat, 03 Apr 2021 08:15:52: 38000000 INFO @ Sat, 03 Apr 2021 08:15:55: 26000000 INFO @ Sat, 03 Apr 2021 08:15:56: 33000000 INFO @ Sat, 03 Apr 2021 08:15:59: 39000000 INFO @ Sat, 03 Apr 2021 08:16:02: 27000000 INFO @ Sat, 03 Apr 2021 08:16:03: 34000000 INFO @ Sat, 03 Apr 2021 08:16:07: 40000000 INFO @ Sat, 03 Apr 2021 08:16:10: 28000000 INFO @ Sat, 03 Apr 2021 08:16:11: 35000000 INFO @ Sat, 03 Apr 2021 08:16:14: 41000000 INFO @ Sat, 03 Apr 2021 08:16:18: 29000000 INFO @ Sat, 03 Apr 2021 08:16:18: 36000000 INFO @ Sat, 03 Apr 2021 08:16:22: 42000000 INFO @ Sat, 03 Apr 2021 08:16:26: 37000000 INFO @ Sat, 03 Apr 2021 08:16:26: 30000000 INFO @ Sat, 03 Apr 2021 08:16:28: #1 tag size is determined as 75 bps INFO @ Sat, 03 Apr 2021 08:16:28: #1 tag size = 75 INFO @ Sat, 03 Apr 2021 08:16:28: #1 total tags in treatment: 16777542 INFO @ Sat, 03 Apr 2021 08:16:28: #1 user defined the maximum tags... INFO @ Sat, 03 Apr 2021 08:16:28: #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 08:16:28: #1 tags after filtering in treatment: 12108197 INFO @ Sat, 03 Apr 2021 08:16:28: #1 Redundant rate of treatment: 0.28 INFO @ Sat, 03 Apr 2021 08:16:28: #1 finished! INFO @ Sat, 03 Apr 2021 08:16:28: #2 Build Peak Model... INFO @ Sat, 03 Apr 2021 08:16:28: #2 looking for paired plus/minus strand peaks... INFO @ Sat, 03 Apr 2021 08:16:29: #2 number of paired peaks: 274 WARNING @ Sat, 03 Apr 2021 08:16:29: Fewer paired peaks (274) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 274 pairs to build model! INFO @ Sat, 03 Apr 2021 08:16:29: start model_add_line... INFO @ Sat, 03 Apr 2021 08:16:29: start X-correlation... INFO @ Sat, 03 Apr 2021 08:16:29: end of X-cor INFO @ Sat, 03 Apr 2021 08:16:29: #2 finished! INFO @ Sat, 03 Apr 2021 08:16:29: #2 predicted fragment length is 120 bps INFO @ Sat, 03 Apr 2021 08:16:29: #2 alternative fragment length(s) may be 3,120,144 bps INFO @ Sat, 03 Apr 2021 08:16:29: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/ce11/SRX7687152/SRX7687152.05_model.r WARNING @ Sat, 03 Apr 2021 08:16:29: #2 Since the d (120) calculated from paired-peaks are smaller than 2*tag length, it may be influenced by unknown sequencing problem! WARNING @ Sat, 03 Apr 2021 08:16:29: #2 You may need to consider one of the other alternative d(s): 3,120,144 WARNING @ Sat, 03 Apr 2021 08:16:29: #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 08:16:29: #3 Call peaks... INFO @ Sat, 03 Apr 2021 08:16:29: #3 Pre-compute pvalue-qvalue table... INFO @ Sat, 03 Apr 2021 08:16:33: 38000000 INFO @ Sat, 03 Apr 2021 08:16:33: 31000000 INFO @ Sat, 03 Apr 2021 08:16:40: 39000000 INFO @ Sat, 03 Apr 2021 08:16:41: 32000000 BigWig に変換しました。 INFO @ Sat, 03 Apr 2021 08:16:47: 40000000 INFO @ Sat, 03 Apr 2021 08:16:50: 33000000 INFO @ Sat, 03 Apr 2021 08:16:54: 41000000 INFO @ Sat, 03 Apr 2021 08:16:55: #3 Call peaks for each chromosome... INFO @ Sat, 03 Apr 2021 08:16:58: 34000000 INFO @ Sat, 03 Apr 2021 08:17:01: 42000000 INFO @ Sat, 03 Apr 2021 08:17:06: 35000000 INFO @ Sat, 03 Apr 2021 08:17:07: #1 tag size is determined as 75 bps INFO @ Sat, 03 Apr 2021 08:17:07: #1 tag size = 75 INFO @ Sat, 03 Apr 2021 08:17:07: #1 total tags in treatment: 16777542 INFO @ Sat, 03 Apr 2021 08:17:07: #1 user defined the maximum tags... INFO @ Sat, 03 Apr 2021 08:17:07: #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 08:17:07: #1 tags after filtering in treatment: 12108197 INFO @ Sat, 03 Apr 2021 08:17:07: #1 Redundant rate of treatment: 0.28 INFO @ Sat, 03 Apr 2021 08:17:07: #1 finished! INFO @ Sat, 03 Apr 2021 08:17:07: #2 Build Peak Model... INFO @ Sat, 03 Apr 2021 08:17:07: #2 looking for paired plus/minus strand peaks... INFO @ Sat, 03 Apr 2021 08:17:08: #4 Write output xls file... /home/okishinya/chipatlas/results/ce11/SRX7687152/SRX7687152.05_peaks.xls INFO @ Sat, 03 Apr 2021 08:17:08: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/ce11/SRX7687152/SRX7687152.05_peaks.narrowPeak INFO @ Sat, 03 Apr 2021 08:17:08: #4 Write summits bed file... /home/okishinya/chipatlas/results/ce11/SRX7687152/SRX7687152.05_summits.bed INFO @ Sat, 03 Apr 2021 08:17:08: Done! pass1 - making usageList (7 chroms): 1 millis pass2 - checking and writing primary data (476 records, 4 fields): 1 millis CompletedMACS2peakCalling INFO @ Sat, 03 Apr 2021 08:17:08: #2 number of paired peaks: 274 WARNING @ Sat, 03 Apr 2021 08:17:08: Fewer paired peaks (274) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 274 pairs to build model! INFO @ Sat, 03 Apr 2021 08:17:08: start model_add_line... INFO @ Sat, 03 Apr 2021 08:17:08: start X-correlation... INFO @ Sat, 03 Apr 2021 08:17:08: end of X-cor INFO @ Sat, 03 Apr 2021 08:17:08: #2 finished! INFO @ Sat, 03 Apr 2021 08:17:08: #2 predicted fragment length is 120 bps INFO @ Sat, 03 Apr 2021 08:17:08: #2 alternative fragment length(s) may be 3,120,144 bps INFO @ Sat, 03 Apr 2021 08:17:08: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/ce11/SRX7687152/SRX7687152.10_model.r WARNING @ Sat, 03 Apr 2021 08:17:08: #2 Since the d (120) calculated from paired-peaks are smaller than 2*tag length, it may be influenced by unknown sequencing problem! WARNING @ Sat, 03 Apr 2021 08:17:08: #2 You may need to consider one of the other alternative d(s): 3,120,144 WARNING @ Sat, 03 Apr 2021 08:17:08: #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 08:17:08: #3 Call peaks... INFO @ Sat, 03 Apr 2021 08:17:08: #3 Pre-compute pvalue-qvalue table... INFO @ Sat, 03 Apr 2021 08:17:13: 36000000 INFO @ Sat, 03 Apr 2021 08:17:21: 37000000 INFO @ Sat, 03 Apr 2021 08:17:28: 38000000 INFO @ Sat, 03 Apr 2021 08:17:34: #3 Call peaks for each chromosome... INFO @ Sat, 03 Apr 2021 08:17:35: 39000000 INFO @ Sat, 03 Apr 2021 08:17:42: 40000000 INFO @ Sat, 03 Apr 2021 08:17:47: #4 Write output xls file... /home/okishinya/chipatlas/results/ce11/SRX7687152/SRX7687152.10_peaks.xls INFO @ Sat, 03 Apr 2021 08:17:47: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/ce11/SRX7687152/SRX7687152.10_peaks.narrowPeak INFO @ Sat, 03 Apr 2021 08:17:47: #4 Write summits bed file... /home/okishinya/chipatlas/results/ce11/SRX7687152/SRX7687152.10_summits.bed INFO @ Sat, 03 Apr 2021 08:17:47: Done! pass1 - making usageList (7 chroms): 0 millis pass2 - checking and writing primary data (282 records, 4 fields): 2 millis CompletedMACS2peakCalling INFO @ Sat, 03 Apr 2021 08:17:50: 41000000 INFO @ Sat, 03 Apr 2021 08:17:57: 42000000 INFO @ Sat, 03 Apr 2021 08:18:03: #1 tag size is determined as 75 bps INFO @ Sat, 03 Apr 2021 08:18:03: #1 tag size = 75 INFO @ Sat, 03 Apr 2021 08:18:03: #1 total tags in treatment: 16777542 INFO @ Sat, 03 Apr 2021 08:18:03: #1 user defined the maximum tags... INFO @ Sat, 03 Apr 2021 08:18:03: #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 08:18:03: #1 tags after filtering in treatment: 12108197 INFO @ Sat, 03 Apr 2021 08:18:03: #1 Redundant rate of treatment: 0.28 INFO @ Sat, 03 Apr 2021 08:18:03: #1 finished! INFO @ Sat, 03 Apr 2021 08:18:03: #2 Build Peak Model... INFO @ Sat, 03 Apr 2021 08:18:03: #2 looking for paired plus/minus strand peaks... INFO @ Sat, 03 Apr 2021 08:18:04: #2 number of paired peaks: 274 WARNING @ Sat, 03 Apr 2021 08:18:04: Fewer paired peaks (274) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 274 pairs to build model! INFO @ Sat, 03 Apr 2021 08:18:04: start model_add_line... INFO @ Sat, 03 Apr 2021 08:18:04: start X-correlation... INFO @ Sat, 03 Apr 2021 08:18:04: end of X-cor INFO @ Sat, 03 Apr 2021 08:18:04: #2 finished! INFO @ Sat, 03 Apr 2021 08:18:04: #2 predicted fragment length is 120 bps INFO @ Sat, 03 Apr 2021 08:18:04: #2 alternative fragment length(s) may be 3,120,144 bps INFO @ Sat, 03 Apr 2021 08:18:04: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/ce11/SRX7687152/SRX7687152.20_model.r WARNING @ Sat, 03 Apr 2021 08:18:04: #2 Since the d (120) calculated from paired-peaks are smaller than 2*tag length, it may be influenced by unknown sequencing problem! WARNING @ Sat, 03 Apr 2021 08:18:04: #2 You may need to consider one of the other alternative d(s): 3,120,144 WARNING @ Sat, 03 Apr 2021 08:18:04: #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 08:18:04: #3 Call peaks... INFO @ Sat, 03 Apr 2021 08:18:04: #3 Pre-compute pvalue-qvalue table... INFO @ Sat, 03 Apr 2021 08:18:30: #3 Call peaks for each chromosome... INFO @ Sat, 03 Apr 2021 08:18:43: #4 Write output xls file... /home/okishinya/chipatlas/results/ce11/SRX7687152/SRX7687152.20_peaks.xls INFO @ Sat, 03 Apr 2021 08:18:43: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/ce11/SRX7687152/SRX7687152.20_peaks.narrowPeak INFO @ Sat, 03 Apr 2021 08:18:43: #4 Write summits bed file... /home/okishinya/chipatlas/results/ce11/SRX7687152/SRX7687152.20_summits.bed INFO @ Sat, 03 Apr 2021 08:18:43: Done! pass1 - making usageList (6 chroms): 0 millis pass2 - checking and writing primary data (139 records, 4 fields): 2 millis CompletedMACS2peakCalling