Job ID = 12264829 SRX = SRX7687152 Genome = ce10 sra ファイルのダウンロード中... Read layout: PAIRED fastq に変換中... Read 30680231 spots for SRR11034895/SRR11034895.sra Written 30680231 spots for SRR11034895/SRR11034895.sra fastq に変換しました。 bowtie でマッピング中... Your job 12265494 ("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: 00:50:12 30680231 reads; of these: 30680231 (100.00%) were paired; of these: 6619144 (21.57%) aligned concordantly 0 times 19699324 (64.21%) aligned concordantly exactly 1 time 4361763 (14.22%) aligned concordantly >1 times ---- 6619144 pairs aligned concordantly 0 times; of these: 4685278 (70.78%) aligned discordantly 1 time ---- 1933866 pairs aligned 0 times concordantly or discordantly; of these: 3867732 mates make up the pairs; of these: 1943832 (50.26%) aligned 0 times 712307 (18.42%) aligned exactly 1 time 1211593 (31.33%) aligned >1 times 96.83% overall alignment rate Time searching: 00:50:12 Overall time: 00:50:12 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] 8291006 / 28718515 = 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 07:06:47: # Command line: callpeak -t /home/okishinya/chipatlas/results/ce10/SRX7687152/SRX7687152.bam -f BAM -g ce -n /home/okishinya/chipatlas/results/ce10/SRX7687152/SRX7687152.05 -q 1e-05 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/ce10/SRX7687152/SRX7687152.05 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/ce10/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 07:06:47: #1 read tag files... INFO @ Sat, 03 Apr 2021 07:06:47: #1 read treatment tags... INFO @ Sat, 03 Apr 2021 07:06:56: 1000000 INFO @ Sat, 03 Apr 2021 07:07:04: 2000000 INFO @ Sat, 03 Apr 2021 07:07:12: 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 07:07:17: # Command line: callpeak -t /home/okishinya/chipatlas/results/ce10/SRX7687152/SRX7687152.bam -f BAM -g ce -n /home/okishinya/chipatlas/results/ce10/SRX7687152/SRX7687152.10 -q 1e-10 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/ce10/SRX7687152/SRX7687152.10 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/ce10/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 07:07:17: #1 read tag files... INFO @ Sat, 03 Apr 2021 07:07:17: #1 read treatment tags... INFO @ Sat, 03 Apr 2021 07:07:21: 4000000 INFO @ Sat, 03 Apr 2021 07:07:27: 1000000 INFO @ Sat, 03 Apr 2021 07:07:29: 5000000 INFO @ Sat, 03 Apr 2021 07:07:38: 2000000 INFO @ Sat, 03 Apr 2021 07:07:38: 6000000 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 07:07:46: 7000000 INFO @ Sat, 03 Apr 2021 07:07:47: # Command line: callpeak -t /home/okishinya/chipatlas/results/ce10/SRX7687152/SRX7687152.bam -f BAM -g ce -n /home/okishinya/chipatlas/results/ce10/SRX7687152/SRX7687152.20 -q 1e-20 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/ce10/SRX7687152/SRX7687152.20 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/ce10/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 07:07:47: #1 read tag files... INFO @ Sat, 03 Apr 2021 07:07:47: #1 read treatment tags... INFO @ Sat, 03 Apr 2021 07:07:47: 3000000 INFO @ Sat, 03 Apr 2021 07:07:55: 8000000 INFO @ Sat, 03 Apr 2021 07:07:58: 4000000 INFO @ Sat, 03 Apr 2021 07:07:59: 1000000 INFO @ Sat, 03 Apr 2021 07:08:04: 9000000 INFO @ Sat, 03 Apr 2021 07:08:10: 5000000 INFO @ Sat, 03 Apr 2021 07:08:11: 2000000 INFO @ Sat, 03 Apr 2021 07:08:12: 10000000 INFO @ Sat, 03 Apr 2021 07:08:21: 11000000 INFO @ Sat, 03 Apr 2021 07:08:22: 6000000 INFO @ Sat, 03 Apr 2021 07:08:22: 3000000 INFO @ Sat, 03 Apr 2021 07:08:30: 12000000 INFO @ Sat, 03 Apr 2021 07:08:34: 7000000 INFO @ Sat, 03 Apr 2021 07:08:34: 4000000 INFO @ Sat, 03 Apr 2021 07:08:39: 13000000 INFO @ Sat, 03 Apr 2021 07:08:45: 5000000 INFO @ Sat, 03 Apr 2021 07:08:45: 8000000 INFO @ Sat, 03 Apr 2021 07:08:47: 14000000 INFO @ Sat, 03 Apr 2021 07:08:56: 15000000 INFO @ Sat, 03 Apr 2021 07:08:56: 6000000 INFO @ Sat, 03 Apr 2021 07:08:57: 9000000 INFO @ Sat, 03 Apr 2021 07:09:05: 16000000 INFO @ Sat, 03 Apr 2021 07:09:08: 7000000 INFO @ Sat, 03 Apr 2021 07:09:09: 10000000 INFO @ Sat, 03 Apr 2021 07:09:14: 17000000 INFO @ Sat, 03 Apr 2021 07:09:20: 8000000 INFO @ Sat, 03 Apr 2021 07:09:21: 11000000 INFO @ Sat, 03 Apr 2021 07:09:24: 18000000 INFO @ Sat, 03 Apr 2021 07:09:32: 9000000 INFO @ Sat, 03 Apr 2021 07:09:33: 12000000 INFO @ Sat, 03 Apr 2021 07:09:33: 19000000 INFO @ Sat, 03 Apr 2021 07:09:43: 20000000 INFO @ Sat, 03 Apr 2021 07:09:44: 10000000 INFO @ Sat, 03 Apr 2021 07:09:45: 13000000 INFO @ Sat, 03 Apr 2021 07:09:52: 21000000 INFO @ Sat, 03 Apr 2021 07:09:56: 11000000 INFO @ Sat, 03 Apr 2021 07:09:56: 14000000 INFO @ Sat, 03 Apr 2021 07:10:01: 22000000 INFO @ Sat, 03 Apr 2021 07:10:07: 12000000 INFO @ Sat, 03 Apr 2021 07:10:08: 15000000 INFO @ Sat, 03 Apr 2021 07:10:10: 23000000 INFO @ Sat, 03 Apr 2021 07:10:19: 13000000 INFO @ Sat, 03 Apr 2021 07:10:19: 24000000 INFO @ Sat, 03 Apr 2021 07:10:21: 16000000 INFO @ Sat, 03 Apr 2021 07:10:28: 25000000 INFO @ Sat, 03 Apr 2021 07:10:30: 14000000 INFO @ Sat, 03 Apr 2021 07:10:32: 17000000 INFO @ Sat, 03 Apr 2021 07:10:37: 26000000 INFO @ Sat, 03 Apr 2021 07:10:42: 15000000 INFO @ Sat, 03 Apr 2021 07:10:44: 18000000 INFO @ Sat, 03 Apr 2021 07:10:46: 27000000 INFO @ Sat, 03 Apr 2021 07:10:54: 16000000 INFO @ Sat, 03 Apr 2021 07:10:55: 28000000 INFO @ Sat, 03 Apr 2021 07:10:56: 19000000 INFO @ Sat, 03 Apr 2021 07:11:04: 29000000 INFO @ Sat, 03 Apr 2021 07:11:06: 17000000 INFO @ Sat, 03 Apr 2021 07:11:08: 20000000 INFO @ Sat, 03 Apr 2021 07:11:12: 30000000 INFO @ Sat, 03 Apr 2021 07:11:18: 18000000 INFO @ Sat, 03 Apr 2021 07:11:20: 21000000 INFO @ Sat, 03 Apr 2021 07:11:21: 31000000 INFO @ Sat, 03 Apr 2021 07:11:30: 19000000 INFO @ Sat, 03 Apr 2021 07:11:32: 32000000 INFO @ Sat, 03 Apr 2021 07:11:32: 22000000 INFO @ Sat, 03 Apr 2021 07:11:42: 20000000 INFO @ Sat, 03 Apr 2021 07:11:42: 33000000 INFO @ Sat, 03 Apr 2021 07:11:44: 23000000 INFO @ Sat, 03 Apr 2021 07:11:52: 34000000 INFO @ Sat, 03 Apr 2021 07:11:54: 21000000 INFO @ Sat, 03 Apr 2021 07:11:55: 24000000 INFO @ Sat, 03 Apr 2021 07:12:02: 35000000 INFO @ Sat, 03 Apr 2021 07:12:06: 25000000 INFO @ Sat, 03 Apr 2021 07:12:07: 22000000 INFO @ Sat, 03 Apr 2021 07:12:12: 36000000 BedGraph に変換しました。 BigWig に変換中... INFO @ Sat, 03 Apr 2021 07:12:17: 26000000 INFO @ Sat, 03 Apr 2021 07:12:20: 23000000 INFO @ Sat, 03 Apr 2021 07:12:22: 37000000 INFO @ Sat, 03 Apr 2021 07:12:29: 27000000 INFO @ Sat, 03 Apr 2021 07:12:31: 24000000 INFO @ Sat, 03 Apr 2021 07:12:32: 38000000 INFO @ Sat, 03 Apr 2021 07:12:40: 28000000 INFO @ Sat, 03 Apr 2021 07:12:41: 39000000 INFO @ Sat, 03 Apr 2021 07:12:43: 25000000 INFO @ Sat, 03 Apr 2021 07:12:52: 40000000 INFO @ Sat, 03 Apr 2021 07:12:52: 29000000 INFO @ Sat, 03 Apr 2021 07:12:54: 26000000 INFO @ Sat, 03 Apr 2021 07:13:02: 41000000 INFO @ Sat, 03 Apr 2021 07:13:03: 30000000 INFO @ Sat, 03 Apr 2021 07:13:06: 27000000 INFO @ Sat, 03 Apr 2021 07:13:12: 42000000 INFO @ Sat, 03 Apr 2021 07:13:15: 31000000 INFO @ Sat, 03 Apr 2021 07:13:18: 28000000 INFO @ Sat, 03 Apr 2021 07:13:20: #1 tag size is determined as 75 bps INFO @ Sat, 03 Apr 2021 07:13:20: #1 tag size = 75 INFO @ Sat, 03 Apr 2021 07:13:20: #1 total tags in treatment: 16777482 INFO @ Sat, 03 Apr 2021 07:13:20: #1 user defined the maximum tags... INFO @ Sat, 03 Apr 2021 07:13:20: #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 07:13:20: #1 tags after filtering in treatment: 12108087 INFO @ Sat, 03 Apr 2021 07:13:20: #1 Redundant rate of treatment: 0.28 INFO @ Sat, 03 Apr 2021 07:13:20: #1 finished! INFO @ Sat, 03 Apr 2021 07:13:20: #2 Build Peak Model... INFO @ Sat, 03 Apr 2021 07:13:20: #2 looking for paired plus/minus strand peaks... INFO @ Sat, 03 Apr 2021 07:13:21: #2 number of paired peaks: 273 WARNING @ Sat, 03 Apr 2021 07:13:21: Fewer paired peaks (273) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 273 pairs to build model! INFO @ Sat, 03 Apr 2021 07:13:21: start model_add_line... INFO @ Sat, 03 Apr 2021 07:13:21: start X-correlation... INFO @ Sat, 03 Apr 2021 07:13:21: end of X-cor INFO @ Sat, 03 Apr 2021 07:13:21: #2 finished! INFO @ Sat, 03 Apr 2021 07:13:21: #2 predicted fragment length is 122 bps INFO @ Sat, 03 Apr 2021 07:13:21: #2 alternative fragment length(s) may be 3,122,143 bps INFO @ Sat, 03 Apr 2021 07:13:21: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/ce10/SRX7687152/SRX7687152.05_model.r WARNING @ Sat, 03 Apr 2021 07:13:21: #2 Since the d (122) calculated from paired-peaks are smaller than 2*tag length, it may be influenced by unknown sequencing problem! WARNING @ Sat, 03 Apr 2021 07:13:21: #2 You may need to consider one of the other alternative d(s): 3,122,143 WARNING @ Sat, 03 Apr 2021 07:13:21: #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 07:13:21: #3 Call peaks... INFO @ Sat, 03 Apr 2021 07:13:21: #3 Pre-compute pvalue-qvalue table... INFO @ Sat, 03 Apr 2021 07:13:29: 32000000 INFO @ Sat, 03 Apr 2021 07:13:30: 29000000 BigWig に変換しました。 INFO @ Sat, 03 Apr 2021 07:13:40: 33000000 INFO @ Sat, 03 Apr 2021 07:13:43: 30000000 INFO @ Sat, 03 Apr 2021 07:13:54: 34000000 INFO @ Sat, 03 Apr 2021 07:13:55: 31000000 INFO @ Sat, 03 Apr 2021 07:13:57: #3 Call peaks for each chromosome... INFO @ Sat, 03 Apr 2021 07:14:07: 32000000 INFO @ Sat, 03 Apr 2021 07:14:08: 35000000 INFO @ Sat, 03 Apr 2021 07:14:15: #4 Write output xls file... /home/okishinya/chipatlas/results/ce10/SRX7687152/SRX7687152.05_peaks.xls INFO @ Sat, 03 Apr 2021 07:14:15: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/ce10/SRX7687152/SRX7687152.05_peaks.narrowPeak INFO @ Sat, 03 Apr 2021 07:14:15: #4 Write summits bed file... /home/okishinya/chipatlas/results/ce10/SRX7687152/SRX7687152.05_summits.bed INFO @ Sat, 03 Apr 2021 07:14:15: Done! pass1 - making usageList (7 chroms): 1 millis pass2 - checking and writing primary data (471 records, 4 fields): 5 millis CompletedMACS2peakCalling INFO @ Sat, 03 Apr 2021 07:14:17: 36000000 INFO @ Sat, 03 Apr 2021 07:14:19: 33000000 INFO @ Sat, 03 Apr 2021 07:14:28: 37000000 INFO @ Sat, 03 Apr 2021 07:14:32: 34000000 INFO @ Sat, 03 Apr 2021 07:14:38: 38000000 INFO @ Sat, 03 Apr 2021 07:14:44: 35000000 INFO @ Sat, 03 Apr 2021 07:14:48: 39000000 INFO @ Sat, 03 Apr 2021 07:14:57: 36000000 INFO @ Sat, 03 Apr 2021 07:14:57: 40000000 INFO @ Sat, 03 Apr 2021 07:15:07: 41000000 INFO @ Sat, 03 Apr 2021 07:15:10: 37000000 INFO @ Sat, 03 Apr 2021 07:15:17: 42000000 INFO @ Sat, 03 Apr 2021 07:15:23: 38000000 INFO @ Sat, 03 Apr 2021 07:15:24: #1 tag size is determined as 75 bps INFO @ Sat, 03 Apr 2021 07:15:24: #1 tag size = 75 INFO @ Sat, 03 Apr 2021 07:15:24: #1 total tags in treatment: 16777482 INFO @ Sat, 03 Apr 2021 07:15:24: #1 user defined the maximum tags... INFO @ Sat, 03 Apr 2021 07:15:24: #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 07:15:25: #1 tags after filtering in treatment: 12108087 INFO @ Sat, 03 Apr 2021 07:15:25: #1 Redundant rate of treatment: 0.28 INFO @ Sat, 03 Apr 2021 07:15:25: #1 finished! INFO @ Sat, 03 Apr 2021 07:15:25: #2 Build Peak Model... INFO @ Sat, 03 Apr 2021 07:15:25: #2 looking for paired plus/minus strand peaks... INFO @ Sat, 03 Apr 2021 07:15:26: #2 number of paired peaks: 273 WARNING @ Sat, 03 Apr 2021 07:15:26: Fewer paired peaks (273) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 273 pairs to build model! INFO @ Sat, 03 Apr 2021 07:15:26: start model_add_line... INFO @ Sat, 03 Apr 2021 07:15:26: start X-correlation... INFO @ Sat, 03 Apr 2021 07:15:26: end of X-cor INFO @ Sat, 03 Apr 2021 07:15:26: #2 finished! INFO @ Sat, 03 Apr 2021 07:15:26: #2 predicted fragment length is 122 bps INFO @ Sat, 03 Apr 2021 07:15:26: #2 alternative fragment length(s) may be 3,122,143 bps INFO @ Sat, 03 Apr 2021 07:15:26: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/ce10/SRX7687152/SRX7687152.10_model.r WARNING @ Sat, 03 Apr 2021 07:15:26: #2 Since the d (122) calculated from paired-peaks are smaller than 2*tag length, it may be influenced by unknown sequencing problem! WARNING @ Sat, 03 Apr 2021 07:15:26: #2 You may need to consider one of the other alternative d(s): 3,122,143 WARNING @ Sat, 03 Apr 2021 07:15:26: #2 You can restart the process with --nomodel --extsize XXX with your choice or an arbitrary number. Nontheless, MACS will continute computing. INFO @ Sat, 03 Apr 2021 07:15:26: #3 Call peaks... INFO @ Sat, 03 Apr 2021 07:15:26: #3 Pre-compute pvalue-qvalue table... INFO @ Sat, 03 Apr 2021 07:15:36: 39000000 INFO @ Sat, 03 Apr 2021 07:15:48: 40000000 INFO @ Sat, 03 Apr 2021 07:15:59: #3 Call peaks for each chromosome... INFO @ Sat, 03 Apr 2021 07:16:01: 41000000 INFO @ Sat, 03 Apr 2021 07:16:13: 42000000 INFO @ Sat, 03 Apr 2021 07:16:16: #4 Write output xls file... /home/okishinya/chipatlas/results/ce10/SRX7687152/SRX7687152.10_peaks.xls INFO @ Sat, 03 Apr 2021 07:16:16: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/ce10/SRX7687152/SRX7687152.10_peaks.narrowPeak INFO @ Sat, 03 Apr 2021 07:16:16: #4 Write summits bed file... /home/okishinya/chipatlas/results/ce10/SRX7687152/SRX7687152.10_summits.bed INFO @ Sat, 03 Apr 2021 07:16:16: Done! pass1 - making usageList (7 chroms): 1 millis pass2 - checking and writing primary data (281 records, 4 fields): 3 millis CompletedMACS2peakCalling INFO @ Sat, 03 Apr 2021 07:16:23: #1 tag size is determined as 75 bps INFO @ Sat, 03 Apr 2021 07:16:23: #1 tag size = 75 INFO @ Sat, 03 Apr 2021 07:16:23: #1 total tags in treatment: 16777482 INFO @ Sat, 03 Apr 2021 07:16:23: #1 user defined the maximum tags... INFO @ Sat, 03 Apr 2021 07:16:23: #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 07:16:23: #1 tags after filtering in treatment: 12108087 INFO @ Sat, 03 Apr 2021 07:16:23: #1 Redundant rate of treatment: 0.28 INFO @ Sat, 03 Apr 2021 07:16:23: #1 finished! INFO @ Sat, 03 Apr 2021 07:16:23: #2 Build Peak Model... INFO @ Sat, 03 Apr 2021 07:16:23: #2 looking for paired plus/minus strand peaks... INFO @ Sat, 03 Apr 2021 07:16:24: #2 number of paired peaks: 273 WARNING @ Sat, 03 Apr 2021 07:16:24: Fewer paired peaks (273) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 273 pairs to build model! INFO @ Sat, 03 Apr 2021 07:16:24: start model_add_line... INFO @ Sat, 03 Apr 2021 07:16:24: start X-correlation... INFO @ Sat, 03 Apr 2021 07:16:25: end of X-cor INFO @ Sat, 03 Apr 2021 07:16:25: #2 finished! INFO @ Sat, 03 Apr 2021 07:16:25: #2 predicted fragment length is 122 bps INFO @ Sat, 03 Apr 2021 07:16:25: #2 alternative fragment length(s) may be 3,122,143 bps INFO @ Sat, 03 Apr 2021 07:16:25: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/ce10/SRX7687152/SRX7687152.20_model.r WARNING @ Sat, 03 Apr 2021 07:16:25: #2 Since the d (122) calculated from paired-peaks are smaller than 2*tag length, it may be influenced by unknown sequencing problem! WARNING @ Sat, 03 Apr 2021 07:16:25: #2 You may need to consider one of the other alternative d(s): 3,122,143 WARNING @ Sat, 03 Apr 2021 07:16:25: #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 07:16:25: #3 Call peaks... INFO @ Sat, 03 Apr 2021 07:16:25: #3 Pre-compute pvalue-qvalue table... INFO @ Sat, 03 Apr 2021 07:17:00: #3 Call peaks for each chromosome... INFO @ Sat, 03 Apr 2021 07:17:19: #4 Write output xls file... /home/okishinya/chipatlas/results/ce10/SRX7687152/SRX7687152.20_peaks.xls INFO @ Sat, 03 Apr 2021 07:17:19: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/ce10/SRX7687152/SRX7687152.20_peaks.narrowPeak INFO @ Sat, 03 Apr 2021 07:17:19: #4 Write summits bed file... /home/okishinya/chipatlas/results/ce10/SRX7687152/SRX7687152.20_summits.bed INFO @ Sat, 03 Apr 2021 07:17:19: Done! pass1 - making usageList (6 chroms): 1 millis pass2 - checking and writing primary data (139 records, 4 fields): 2 millis CompletedMACS2peakCalling