Job ID = 12265503 SRX = SRX7687148 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: 00:42:00 25143065 reads; of these: 25143065 (100.00%) were paired; of these: 5233549 (20.82%) aligned concordantly 0 times 14486576 (57.62%) aligned concordantly exactly 1 time 5422940 (21.57%) aligned concordantly >1 times ---- 5233549 pairs aligned concordantly 0 times; of these: 3930193 (75.10%) aligned discordantly 1 time ---- 1303356 pairs aligned 0 times concordantly or discordantly; of these: 2606712 mates make up the pairs; of these: 937887 (35.98%) aligned 0 times 623457 (23.92%) aligned exactly 1 time 1045368 (40.10%) aligned >1 times 98.13% overall alignment rate Time searching: 00:42:01 Overall time: 00:42:01 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] 4257346 / 23806168 = 0.1788 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 08:14:51: # Command line: callpeak -t /home/okishinya/chipatlas/results/ce11/SRX7687148/SRX7687148.bam -f BAM -g ce -n /home/okishinya/chipatlas/results/ce11/SRX7687148/SRX7687148.05 -q 1e-05 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/ce11/SRX7687148/SRX7687148.05 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/ce11/SRX7687148/SRX7687148.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 08:14:51: #1 read tag files... INFO @ Sat, 03 Apr 2021 08:14:51: #1 read treatment tags... INFO @ Sat, 03 Apr 2021 08:14:58: 1000000 INFO @ Sat, 03 Apr 2021 08:15:05: 2000000 INFO @ Sat, 03 Apr 2021 08:15:12: 3000000 INFO @ Sat, 03 Apr 2021 08:15:18: 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 08:15:21: # Command line: callpeak -t /home/okishinya/chipatlas/results/ce11/SRX7687148/SRX7687148.bam -f BAM -g ce -n /home/okishinya/chipatlas/results/ce11/SRX7687148/SRX7687148.10 -q 1e-10 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/ce11/SRX7687148/SRX7687148.10 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/ce11/SRX7687148/SRX7687148.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 08:15:21: #1 read tag files... INFO @ Sat, 03 Apr 2021 08:15:21: #1 read treatment tags... INFO @ Sat, 03 Apr 2021 08:15:26: 5000000 INFO @ Sat, 03 Apr 2021 08:15:30: 1000000 INFO @ Sat, 03 Apr 2021 08:15:35: 6000000 INFO @ Sat, 03 Apr 2021 08:15:40: 2000000 INFO @ Sat, 03 Apr 2021 08:15:44: 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 08:15:49: 3000000 INFO @ Sat, 03 Apr 2021 08:15:50: # Command line: callpeak -t /home/okishinya/chipatlas/results/ce11/SRX7687148/SRX7687148.bam -f BAM -g ce -n /home/okishinya/chipatlas/results/ce11/SRX7687148/SRX7687148.20 -q 1e-20 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/ce11/SRX7687148/SRX7687148.20 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/ce11/SRX7687148/SRX7687148.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 08:15:50: #1 read tag files... INFO @ Sat, 03 Apr 2021 08:15:50: #1 read treatment tags... INFO @ Sat, 03 Apr 2021 08:15:53: 8000000 INFO @ Sat, 03 Apr 2021 08:15:59: 4000000 INFO @ Sat, 03 Apr 2021 08:16:00: 1000000 INFO @ Sat, 03 Apr 2021 08:16:02: 9000000 INFO @ Sat, 03 Apr 2021 08:16:09: 5000000 INFO @ Sat, 03 Apr 2021 08:16:11: 2000000 INFO @ Sat, 03 Apr 2021 08:16:11: 10000000 INFO @ Sat, 03 Apr 2021 08:16:20: 6000000 INFO @ Sat, 03 Apr 2021 08:16:20: 11000000 INFO @ Sat, 03 Apr 2021 08:16:21: 3000000 INFO @ Sat, 03 Apr 2021 08:16:29: 12000000 INFO @ Sat, 03 Apr 2021 08:16:30: 4000000 INFO @ Sat, 03 Apr 2021 08:16:31: 7000000 INFO @ Sat, 03 Apr 2021 08:16:38: 13000000 INFO @ Sat, 03 Apr 2021 08:16:40: 5000000 INFO @ Sat, 03 Apr 2021 08:16:41: 8000000 INFO @ Sat, 03 Apr 2021 08:16:47: 14000000 INFO @ Sat, 03 Apr 2021 08:16:50: 6000000 INFO @ Sat, 03 Apr 2021 08:16:52: 9000000 INFO @ Sat, 03 Apr 2021 08:16:56: 15000000 INFO @ Sat, 03 Apr 2021 08:17:00: 7000000 INFO @ Sat, 03 Apr 2021 08:17:01: 10000000 INFO @ Sat, 03 Apr 2021 08:17:05: 16000000 INFO @ Sat, 03 Apr 2021 08:17:09: 8000000 INFO @ Sat, 03 Apr 2021 08:17:11: 11000000 INFO @ Sat, 03 Apr 2021 08:17:14: 17000000 INFO @ Sat, 03 Apr 2021 08:17:19: 9000000 INFO @ Sat, 03 Apr 2021 08:17:20: 12000000 INFO @ Sat, 03 Apr 2021 08:17:23: 18000000 INFO @ Sat, 03 Apr 2021 08:17:28: 10000000 INFO @ Sat, 03 Apr 2021 08:17:30: 13000000 INFO @ Sat, 03 Apr 2021 08:17:32: 19000000 INFO @ Sat, 03 Apr 2021 08:17:38: 11000000 INFO @ Sat, 03 Apr 2021 08:17:39: 14000000 INFO @ Sat, 03 Apr 2021 08:17:42: 20000000 INFO @ Sat, 03 Apr 2021 08:17:48: 12000000 INFO @ Sat, 03 Apr 2021 08:17:48: 15000000 INFO @ Sat, 03 Apr 2021 08:17:51: 21000000 INFO @ Sat, 03 Apr 2021 08:17:58: 13000000 INFO @ Sat, 03 Apr 2021 08:17:58: 16000000 INFO @ Sat, 03 Apr 2021 08:18:00: 22000000 INFO @ Sat, 03 Apr 2021 08:18:07: 17000000 INFO @ Sat, 03 Apr 2021 08:18:07: 14000000 INFO @ Sat, 03 Apr 2021 08:18:09: 23000000 INFO @ Sat, 03 Apr 2021 08:18:16: 18000000 INFO @ Sat, 03 Apr 2021 08:18:17: 15000000 INFO @ Sat, 03 Apr 2021 08:18:18: 24000000 INFO @ Sat, 03 Apr 2021 08:18:25: 19000000 INFO @ Sat, 03 Apr 2021 08:18:26: 16000000 INFO @ Sat, 03 Apr 2021 08:18:27: 25000000 INFO @ Sat, 03 Apr 2021 08:18:35: 20000000 INFO @ Sat, 03 Apr 2021 08:18:36: 17000000 INFO @ Sat, 03 Apr 2021 08:18:37: 26000000 INFO @ Sat, 03 Apr 2021 08:18:44: 21000000 INFO @ Sat, 03 Apr 2021 08:18:46: 27000000 INFO @ Sat, 03 Apr 2021 08:18:47: 18000000 INFO @ Sat, 03 Apr 2021 08:18:53: 22000000 INFO @ Sat, 03 Apr 2021 08:18:55: 28000000 BedGraph に変換しました。 BigWig に変換中... INFO @ Sat, 03 Apr 2021 08:18:57: 19000000 INFO @ Sat, 03 Apr 2021 08:19:02: 23000000 INFO @ Sat, 03 Apr 2021 08:19:04: 29000000 INFO @ Sat, 03 Apr 2021 08:19:07: 20000000 INFO @ Sat, 03 Apr 2021 08:19:11: 24000000 INFO @ Sat, 03 Apr 2021 08:19:13: 30000000 INFO @ Sat, 03 Apr 2021 08:19:17: 21000000 INFO @ Sat, 03 Apr 2021 08:19:20: 25000000 INFO @ Sat, 03 Apr 2021 08:19:22: 31000000 INFO @ Sat, 03 Apr 2021 08:19:27: 22000000 INFO @ Sat, 03 Apr 2021 08:19:29: 26000000 INFO @ Sat, 03 Apr 2021 08:19:31: 32000000 INFO @ Sat, 03 Apr 2021 08:19:37: 23000000 INFO @ Sat, 03 Apr 2021 08:19:38: 27000000 INFO @ Sat, 03 Apr 2021 08:19:40: 33000000 INFO @ Sat, 03 Apr 2021 08:19:47: 24000000 INFO @ Sat, 03 Apr 2021 08:19:48: 28000000 INFO @ Sat, 03 Apr 2021 08:19:49: 34000000 BigWig に変換しました。 INFO @ Sat, 03 Apr 2021 08:19:57: 29000000 INFO @ Sat, 03 Apr 2021 08:19:57: 25000000 INFO @ Sat, 03 Apr 2021 08:19:58: 35000000 INFO @ Sat, 03 Apr 2021 08:20:06: 30000000 INFO @ Sat, 03 Apr 2021 08:20:07: 26000000 INFO @ Sat, 03 Apr 2021 08:20:08: 36000000 INFO @ Sat, 03 Apr 2021 08:20:15: 31000000 INFO @ Sat, 03 Apr 2021 08:20:17: 37000000 INFO @ Sat, 03 Apr 2021 08:20:18: 27000000 INFO @ Sat, 03 Apr 2021 08:20:24: 32000000 INFO @ Sat, 03 Apr 2021 08:20:26: 38000000 INFO @ Sat, 03 Apr 2021 08:20:28: 28000000 INFO @ Sat, 03 Apr 2021 08:20:34: 33000000 INFO @ Sat, 03 Apr 2021 08:20:35: 39000000 INFO @ Sat, 03 Apr 2021 08:20:39: 29000000 INFO @ Sat, 03 Apr 2021 08:20:43: 34000000 INFO @ Sat, 03 Apr 2021 08:20:44: 40000000 INFO @ Sat, 03 Apr 2021 08:20:49: 30000000 INFO @ Sat, 03 Apr 2021 08:20:51: #1 tag size is determined as 75 bps INFO @ Sat, 03 Apr 2021 08:20:51: #1 tag size = 75 INFO @ Sat, 03 Apr 2021 08:20:51: #1 total tags in treatment: 16003649 INFO @ Sat, 03 Apr 2021 08:20:51: #1 user defined the maximum tags... INFO @ Sat, 03 Apr 2021 08:20:51: #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 08:20:52: #1 tags after filtering in treatment: 11411903 INFO @ Sat, 03 Apr 2021 08:20:52: #1 Redundant rate of treatment: 0.29 INFO @ Sat, 03 Apr 2021 08:20:52: #1 finished! INFO @ Sat, 03 Apr 2021 08:20:52: #2 Build Peak Model... INFO @ Sat, 03 Apr 2021 08:20:52: #2 looking for paired plus/minus strand peaks... INFO @ Sat, 03 Apr 2021 08:20:52: 35000000 INFO @ Sat, 03 Apr 2021 08:20:52: #2 number of paired peaks: 406 WARNING @ Sat, 03 Apr 2021 08:20:52: Fewer paired peaks (406) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 406 pairs to build model! INFO @ Sat, 03 Apr 2021 08:20:52: start model_add_line... INFO @ Sat, 03 Apr 2021 08:20:53: start X-correlation... INFO @ Sat, 03 Apr 2021 08:20:53: end of X-cor INFO @ Sat, 03 Apr 2021 08:20:53: #2 finished! INFO @ Sat, 03 Apr 2021 08:20:53: #2 predicted fragment length is 115 bps INFO @ Sat, 03 Apr 2021 08:20:53: #2 alternative fragment length(s) may be 4,108,115,134 bps INFO @ Sat, 03 Apr 2021 08:20:53: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/ce11/SRX7687148/SRX7687148.05_model.r WARNING @ Sat, 03 Apr 2021 08:20:53: #2 Since the d (115) calculated from paired-peaks are smaller than 2*tag length, it may be influenced by unknown sequencing problem! WARNING @ Sat, 03 Apr 2021 08:20:53: #2 You may need to consider one of the other alternative d(s): 4,108,115,134 WARNING @ Sat, 03 Apr 2021 08:20:53: #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 08:20:53: #3 Call peaks... INFO @ Sat, 03 Apr 2021 08:20:53: #3 Pre-compute pvalue-qvalue table... INFO @ Sat, 03 Apr 2021 08:20:59: 31000000 INFO @ Sat, 03 Apr 2021 08:21:00: 36000000 INFO @ Sat, 03 Apr 2021 08:21:09: 37000000 INFO @ Sat, 03 Apr 2021 08:21:10: 32000000 INFO @ Sat, 03 Apr 2021 08:21:18: 38000000 INFO @ Sat, 03 Apr 2021 08:21:18: #3 Call peaks for each chromosome... INFO @ Sat, 03 Apr 2021 08:21:20: 33000000 INFO @ Sat, 03 Apr 2021 08:21:26: 39000000 INFO @ Sat, 03 Apr 2021 08:21:30: 34000000 INFO @ Sat, 03 Apr 2021 08:21:31: #4 Write output xls file... /home/okishinya/chipatlas/results/ce11/SRX7687148/SRX7687148.05_peaks.xls INFO @ Sat, 03 Apr 2021 08:21:31: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/ce11/SRX7687148/SRX7687148.05_peaks.narrowPeak INFO @ Sat, 03 Apr 2021 08:21:31: #4 Write summits bed file... /home/okishinya/chipatlas/results/ce11/SRX7687148/SRX7687148.05_summits.bed INFO @ Sat, 03 Apr 2021 08:21:31: Done! pass1 - making usageList (7 chroms): 2 millis pass2 - checking and writing primary data (518 records, 4 fields): 2 millis CompletedMACS2peakCalling INFO @ Sat, 03 Apr 2021 08:21:35: 40000000 INFO @ Sat, 03 Apr 2021 08:21:39: 35000000 INFO @ Sat, 03 Apr 2021 08:21:42: #1 tag size is determined as 75 bps INFO @ Sat, 03 Apr 2021 08:21:42: #1 tag size = 75 INFO @ Sat, 03 Apr 2021 08:21:42: #1 total tags in treatment: 16003649 INFO @ Sat, 03 Apr 2021 08:21:42: #1 user defined the maximum tags... INFO @ Sat, 03 Apr 2021 08:21:42: #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 08:21:43: #1 tags after filtering in treatment: 11411903 INFO @ Sat, 03 Apr 2021 08:21:43: #1 Redundant rate of treatment: 0.29 INFO @ Sat, 03 Apr 2021 08:21:43: #1 finished! INFO @ Sat, 03 Apr 2021 08:21:43: #2 Build Peak Model... INFO @ Sat, 03 Apr 2021 08:21:43: #2 looking for paired plus/minus strand peaks... INFO @ Sat, 03 Apr 2021 08:21:43: #2 number of paired peaks: 406 WARNING @ Sat, 03 Apr 2021 08:21:43: Fewer paired peaks (406) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 406 pairs to build model! INFO @ Sat, 03 Apr 2021 08:21:43: start model_add_line... INFO @ Sat, 03 Apr 2021 08:21:44: start X-correlation... INFO @ Sat, 03 Apr 2021 08:21:44: end of X-cor INFO @ Sat, 03 Apr 2021 08:21:44: #2 finished! INFO @ Sat, 03 Apr 2021 08:21:44: #2 predicted fragment length is 115 bps INFO @ Sat, 03 Apr 2021 08:21:44: #2 alternative fragment length(s) may be 4,108,115,134 bps INFO @ Sat, 03 Apr 2021 08:21:44: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/ce11/SRX7687148/SRX7687148.10_model.r WARNING @ Sat, 03 Apr 2021 08:21:44: #2 Since the d (115) calculated from paired-peaks are smaller than 2*tag length, it may be influenced by unknown sequencing problem! WARNING @ Sat, 03 Apr 2021 08:21:44: #2 You may need to consider one of the other alternative d(s): 4,108,115,134 WARNING @ Sat, 03 Apr 2021 08:21:44: #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 08:21:44: #3 Call peaks... INFO @ Sat, 03 Apr 2021 08:21:44: #3 Pre-compute pvalue-qvalue table... INFO @ Sat, 03 Apr 2021 08:21:48: 36000000 INFO @ Sat, 03 Apr 2021 08:21:56: 37000000 INFO @ Sat, 03 Apr 2021 08:22:04: 38000000 INFO @ Sat, 03 Apr 2021 08:22:09: #3 Call peaks for each chromosome... INFO @ Sat, 03 Apr 2021 08:22:13: 39000000 INFO @ Sat, 03 Apr 2021 08:22:21: 40000000 INFO @ Sat, 03 Apr 2021 08:22:21: #4 Write output xls file... /home/okishinya/chipatlas/results/ce11/SRX7687148/SRX7687148.10_peaks.xls INFO @ Sat, 03 Apr 2021 08:22:21: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/ce11/SRX7687148/SRX7687148.10_peaks.narrowPeak INFO @ Sat, 03 Apr 2021 08:22:21: #4 Write summits bed file... /home/okishinya/chipatlas/results/ce11/SRX7687148/SRX7687148.10_summits.bed INFO @ Sat, 03 Apr 2021 08:22:21: Done! pass1 - making usageList (7 chroms): 1 millis pass2 - checking and writing primary data (339 records, 4 fields): 1 millis CompletedMACS2peakCalling INFO @ Sat, 03 Apr 2021 08:22:28: #1 tag size is determined as 75 bps INFO @ Sat, 03 Apr 2021 08:22:28: #1 tag size = 75 INFO @ Sat, 03 Apr 2021 08:22:28: #1 total tags in treatment: 16003649 INFO @ Sat, 03 Apr 2021 08:22:28: #1 user defined the maximum tags... INFO @ Sat, 03 Apr 2021 08:22:28: #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 08:22:28: #1 tags after filtering in treatment: 11411903 INFO @ Sat, 03 Apr 2021 08:22:28: #1 Redundant rate of treatment: 0.29 INFO @ Sat, 03 Apr 2021 08:22:28: #1 finished! INFO @ Sat, 03 Apr 2021 08:22:28: #2 Build Peak Model... INFO @ Sat, 03 Apr 2021 08:22:28: #2 looking for paired plus/minus strand peaks... INFO @ Sat, 03 Apr 2021 08:22:29: #2 number of paired peaks: 406 WARNING @ Sat, 03 Apr 2021 08:22:29: Fewer paired peaks (406) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 406 pairs to build model! INFO @ Sat, 03 Apr 2021 08:22:29: start model_add_line... INFO @ Sat, 03 Apr 2021 08:22:29: start X-correlation... INFO @ Sat, 03 Apr 2021 08:22:29: end of X-cor INFO @ Sat, 03 Apr 2021 08:22:29: #2 finished! INFO @ Sat, 03 Apr 2021 08:22:29: #2 predicted fragment length is 115 bps INFO @ Sat, 03 Apr 2021 08:22:29: #2 alternative fragment length(s) may be 4,108,115,134 bps INFO @ Sat, 03 Apr 2021 08:22:29: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/ce11/SRX7687148/SRX7687148.20_model.r WARNING @ Sat, 03 Apr 2021 08:22:29: #2 Since the d (115) calculated from paired-peaks are smaller than 2*tag length, it may be influenced by unknown sequencing problem! WARNING @ Sat, 03 Apr 2021 08:22:29: #2 You may need to consider one of the other alternative d(s): 4,108,115,134 WARNING @ Sat, 03 Apr 2021 08:22:29: #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 08:22:29: #3 Call peaks... INFO @ Sat, 03 Apr 2021 08:22:29: #3 Pre-compute pvalue-qvalue table... INFO @ Sat, 03 Apr 2021 08:22:54: #3 Call peaks for each chromosome... INFO @ Sat, 03 Apr 2021 08:23:07: #4 Write output xls file... /home/okishinya/chipatlas/results/ce11/SRX7687148/SRX7687148.20_peaks.xls INFO @ Sat, 03 Apr 2021 08:23:07: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/ce11/SRX7687148/SRX7687148.20_peaks.narrowPeak INFO @ Sat, 03 Apr 2021 08:23:07: #4 Write summits bed file... /home/okishinya/chipatlas/results/ce11/SRX7687148/SRX7687148.20_summits.bed INFO @ Sat, 03 Apr 2021 08:23:07: Done! pass1 - making usageList (6 chroms): 1 millis pass2 - checking and writing primary data (170 records, 4 fields): 1 millis CompletedMACS2peakCalling