Job ID = 5720231 sra ファイルのダウンロード中... Read layout: PAIRED fastq に変換中... spots read : 32,927,806 reads read : 65,855,612 reads written : 65,855,612 rm: cannot remove ‘[DSE]RR*’: No such file or directory 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: 00:00:00 Multiseed full-index search: 01:03:24 32927806 reads; of these: 32927806 (100.00%) were paired; of these: 17345589 (52.68%) aligned concordantly 0 times 11555056 (35.09%) aligned concordantly exactly 1 time 4027161 (12.23%) aligned concordantly >1 times ---- 17345589 pairs aligned concordantly 0 times; of these: 7734765 (44.59%) aligned discordantly 1 time ---- 9610824 pairs aligned 0 times concordantly or discordantly; of these: 19221648 mates make up the pairs; of these: 15366254 (79.94%) aligned 0 times 1124249 (5.85%) aligned exactly 1 time 2731145 (14.21%) aligned >1 times 76.67% overall alignment rate Time searching: 01:03:24 Overall time: 01:03:24 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 40 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] 4044098 / 22943411 = 0.1763 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/3.5.2/var/singularity/mnt/session/etc/resolv.conf [files]: /etc/resolv.conf doesn't exist in container INFO @ Thu, 16 Apr 2020 00:33:58: # Command line: callpeak -t /home/okishinya/chipatlas/results/ce10/SRX6619603/SRX6619603.bam -f BAM -g ce -n /home/okishinya/chipatlas/results/ce10/SRX6619603/SRX6619603.05 -q 1e-05 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/ce10/SRX6619603/SRX6619603.05 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/ce10/SRX6619603/SRX6619603.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 @ Thu, 16 Apr 2020 00:33:58: #1 read tag files... INFO @ Thu, 16 Apr 2020 00:33:58: #1 read treatment tags... INFO @ Thu, 16 Apr 2020 00:34:06: 1000000 INFO @ Thu, 16 Apr 2020 00:34:14: 2000000 INFO @ Thu, 16 Apr 2020 00:34:22: 3000000 WARNING: Skipping mount /opt/pkg/singularity/3.5.2/var/singularity/mnt/session/etc/resolv.conf [files]: /etc/resolv.conf doesn't exist in container INFO @ Thu, 16 Apr 2020 00:34:28: # Command line: callpeak -t /home/okishinya/chipatlas/results/ce10/SRX6619603/SRX6619603.bam -f BAM -g ce -n /home/okishinya/chipatlas/results/ce10/SRX6619603/SRX6619603.10 -q 1e-10 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/ce10/SRX6619603/SRX6619603.10 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/ce10/SRX6619603/SRX6619603.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 @ Thu, 16 Apr 2020 00:34:28: #1 read tag files... INFO @ Thu, 16 Apr 2020 00:34:28: #1 read treatment tags... INFO @ Thu, 16 Apr 2020 00:34:30: 4000000 INFO @ Thu, 16 Apr 2020 00:34:36: 1000000 INFO @ Thu, 16 Apr 2020 00:34:39: 5000000 INFO @ Thu, 16 Apr 2020 00:34:45: 2000000 INFO @ Thu, 16 Apr 2020 00:34:47: 6000000 INFO @ Thu, 16 Apr 2020 00:34:54: 3000000 INFO @ Thu, 16 Apr 2020 00:34:56: 7000000 BedGraph に変換中... WARNING: Skipping mount /opt/pkg/singularity/3.5.2/var/singularity/mnt/session/etc/resolv.conf [files]: /etc/resolv.conf doesn't exist in container INFO @ Thu, 16 Apr 2020 00:34:58: # Command line: callpeak -t /home/okishinya/chipatlas/results/ce10/SRX6619603/SRX6619603.bam -f BAM -g ce -n /home/okishinya/chipatlas/results/ce10/SRX6619603/SRX6619603.20 -q 1e-20 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/ce10/SRX6619603/SRX6619603.20 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/ce10/SRX6619603/SRX6619603.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 @ Thu, 16 Apr 2020 00:34:58: #1 read tag files... INFO @ Thu, 16 Apr 2020 00:34:58: #1 read treatment tags... INFO @ Thu, 16 Apr 2020 00:35:03: 4000000 INFO @ Thu, 16 Apr 2020 00:35:05: 8000000 INFO @ Thu, 16 Apr 2020 00:35:06: 1000000 INFO @ Thu, 16 Apr 2020 00:35:12: 5000000 INFO @ Thu, 16 Apr 2020 00:35:13: 9000000 INFO @ Thu, 16 Apr 2020 00:35:15: 2000000 INFO @ Thu, 16 Apr 2020 00:35:20: 6000000 INFO @ Thu, 16 Apr 2020 00:35:22: 10000000 INFO @ Thu, 16 Apr 2020 00:35:23: 3000000 INFO @ Thu, 16 Apr 2020 00:35:29: 7000000 INFO @ Thu, 16 Apr 2020 00:35:30: 11000000 INFO @ Thu, 16 Apr 2020 00:35:32: 4000000 INFO @ Thu, 16 Apr 2020 00:35:38: 8000000 INFO @ Thu, 16 Apr 2020 00:35:39: 12000000 INFO @ Thu, 16 Apr 2020 00:35:40: 5000000 INFO @ Thu, 16 Apr 2020 00:35:46: 9000000 INFO @ Thu, 16 Apr 2020 00:35:48: 13000000 INFO @ Thu, 16 Apr 2020 00:35:49: 6000000 INFO @ Thu, 16 Apr 2020 00:35:55: 10000000 INFO @ Thu, 16 Apr 2020 00:35:56: 14000000 INFO @ Thu, 16 Apr 2020 00:35:57: 7000000 INFO @ Thu, 16 Apr 2020 00:36:03: 11000000 INFO @ Thu, 16 Apr 2020 00:36:05: 15000000 INFO @ Thu, 16 Apr 2020 00:36:06: 8000000 INFO @ Thu, 16 Apr 2020 00:36:12: 12000000 INFO @ Thu, 16 Apr 2020 00:36:14: 16000000 INFO @ Thu, 16 Apr 2020 00:36:14: 9000000 INFO @ Thu, 16 Apr 2020 00:36:20: 13000000 INFO @ Thu, 16 Apr 2020 00:36:22: 17000000 INFO @ Thu, 16 Apr 2020 00:36:22: 10000000 INFO @ Thu, 16 Apr 2020 00:36:29: 14000000 INFO @ Thu, 16 Apr 2020 00:36:31: 11000000 INFO @ Thu, 16 Apr 2020 00:36:31: 18000000 INFO @ Thu, 16 Apr 2020 00:36:38: 15000000 INFO @ Thu, 16 Apr 2020 00:36:40: 12000000 INFO @ Thu, 16 Apr 2020 00:36:40: 19000000 INFO @ Thu, 16 Apr 2020 00:36:46: 16000000 INFO @ Thu, 16 Apr 2020 00:36:48: 13000000 INFO @ Thu, 16 Apr 2020 00:36:49: 20000000 INFO @ Thu, 16 Apr 2020 00:36:55: 17000000 INFO @ Thu, 16 Apr 2020 00:36:57: 14000000 INFO @ Thu, 16 Apr 2020 00:36:57: 21000000 INFO @ Thu, 16 Apr 2020 00:37:03: 18000000 INFO @ Thu, 16 Apr 2020 00:37:05: 15000000 INFO @ Thu, 16 Apr 2020 00:37:06: 22000000 INFO @ Thu, 16 Apr 2020 00:37:12: 19000000 INFO @ Thu, 16 Apr 2020 00:37:14: 16000000 INFO @ Thu, 16 Apr 2020 00:37:15: 23000000 INFO @ Thu, 16 Apr 2020 00:37:20: 20000000 INFO @ Thu, 16 Apr 2020 00:37:22: 17000000 INFO @ Thu, 16 Apr 2020 00:37:23: 24000000 INFO @ Thu, 16 Apr 2020 00:37:29: 21000000 INFO @ Thu, 16 Apr 2020 00:37:31: 18000000 INFO @ Thu, 16 Apr 2020 00:37:32: 25000000 INFO @ Thu, 16 Apr 2020 00:37:37: 22000000 INFO @ Thu, 16 Apr 2020 00:37:39: 26000000 INFO @ Thu, 16 Apr 2020 00:37:40: 19000000 INFO @ Thu, 16 Apr 2020 00:37:46: 23000000 INFO @ Thu, 16 Apr 2020 00:37:47: 27000000 INFO @ Thu, 16 Apr 2020 00:37:48: 20000000 INFO @ Thu, 16 Apr 2020 00:37:54: 24000000 INFO @ Thu, 16 Apr 2020 00:37:55: 28000000 INFO @ Thu, 16 Apr 2020 00:37:57: 21000000 INFO @ Thu, 16 Apr 2020 00:38:03: 25000000 INFO @ Thu, 16 Apr 2020 00:38:03: 29000000 INFO @ Thu, 16 Apr 2020 00:38:06: 22000000 INFO @ Thu, 16 Apr 2020 00:38:10: 26000000 INFO @ Thu, 16 Apr 2020 00:38:12: 30000000 INFO @ Thu, 16 Apr 2020 00:38:14: 23000000 INFO @ Thu, 16 Apr 2020 00:38:18: 27000000 INFO @ Thu, 16 Apr 2020 00:38:19: 31000000 INFO @ Thu, 16 Apr 2020 00:38:23: 24000000 INFO @ Thu, 16 Apr 2020 00:38:26: 28000000 INFO @ Thu, 16 Apr 2020 00:38:27: 32000000 INFO @ Thu, 16 Apr 2020 00:38:32: 25000000 INFO @ Thu, 16 Apr 2020 00:38:35: 29000000 INFO @ Thu, 16 Apr 2020 00:38:35: 33000000 INFO @ Thu, 16 Apr 2020 00:38:39: 26000000 INFO @ Thu, 16 Apr 2020 00:38:43: 30000000 INFO @ Thu, 16 Apr 2020 00:38:43: 34000000 INFO @ Thu, 16 Apr 2020 00:38:47: 27000000 INFO @ Thu, 16 Apr 2020 00:38:50: 31000000 INFO @ Thu, 16 Apr 2020 00:38:51: 35000000 INFO @ Thu, 16 Apr 2020 00:38:55: 28000000 INFO @ Thu, 16 Apr 2020 00:38:58: 32000000 INFO @ Thu, 16 Apr 2020 00:39:00: 36000000 INFO @ Thu, 16 Apr 2020 00:39:04: 29000000 INFO @ Thu, 16 Apr 2020 00:39:06: 33000000 INFO @ Thu, 16 Apr 2020 00:39:08: 37000000 INFO @ Thu, 16 Apr 2020 00:39:12: 30000000 INFO @ Thu, 16 Apr 2020 00:39:15: 34000000 INFO @ Thu, 16 Apr 2020 00:39:16: 38000000 INFO @ Thu, 16 Apr 2020 00:39:19: 31000000 INFO @ Thu, 16 Apr 2020 00:39:23: 35000000 INFO @ Thu, 16 Apr 2020 00:39:24: 39000000 INFO @ Thu, 16 Apr 2020 00:39:27: 32000000 INFO @ Thu, 16 Apr 2020 00:39:31: 36000000 INFO @ Thu, 16 Apr 2020 00:39:33: 40000000 INFO @ Thu, 16 Apr 2020 00:39:36: 33000000 INFO @ Thu, 16 Apr 2020 00:39:39: 37000000 INFO @ Thu, 16 Apr 2020 00:39:41: 41000000 INFO @ Thu, 16 Apr 2020 00:39:45: 34000000 INFO @ Thu, 16 Apr 2020 00:39:48: 38000000 INFO @ Thu, 16 Apr 2020 00:39:49: 42000000 INFO @ Thu, 16 Apr 2020 00:39:53: #1 tag size is determined as 150 bps INFO @ Thu, 16 Apr 2020 00:39:53: #1 tag size = 150 INFO @ Thu, 16 Apr 2020 00:39:53: #1 total tags in treatment: 12568150 INFO @ Thu, 16 Apr 2020 00:39:53: #1 user defined the maximum tags... INFO @ Thu, 16 Apr 2020 00:39:53: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Thu, 16 Apr 2020 00:39:53: #1 tags after filtering in treatment: 9802218 INFO @ Thu, 16 Apr 2020 00:39:53: #1 Redundant rate of treatment: 0.22 INFO @ Thu, 16 Apr 2020 00:39:53: #1 finished! INFO @ Thu, 16 Apr 2020 00:39:53: #2 Build Peak Model... INFO @ Thu, 16 Apr 2020 00:39:53: #2 looking for paired plus/minus strand peaks... INFO @ Thu, 16 Apr 2020 00:39:53: 35000000 INFO @ Thu, 16 Apr 2020 00:39:54: #2 number of paired peaks: 413 WARNING @ Thu, 16 Apr 2020 00:39:54: Fewer paired peaks (413) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 413 pairs to build model! INFO @ Thu, 16 Apr 2020 00:39:54: start model_add_line... INFO @ Thu, 16 Apr 2020 00:39:54: start X-correlation... INFO @ Thu, 16 Apr 2020 00:39:54: end of X-cor INFO @ Thu, 16 Apr 2020 00:39:54: #2 finished! INFO @ Thu, 16 Apr 2020 00:39:54: #2 predicted fragment length is 215 bps INFO @ Thu, 16 Apr 2020 00:39:54: #2 alternative fragment length(s) may be 4,215 bps INFO @ Thu, 16 Apr 2020 00:39:54: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/ce10/SRX6619603/SRX6619603.05_model.r WARNING @ Thu, 16 Apr 2020 00:39:54: #2 Since the d (215) calculated from paired-peaks are smaller than 2*tag length, it may be influenced by unknown sequencing problem! WARNING @ Thu, 16 Apr 2020 00:39:54: #2 You may need to consider one of the other alternative d(s): 4,215 WARNING @ Thu, 16 Apr 2020 00:39:54: #2 You can restart the process with --nomodel --extsize XXX with your choice or an arbitrary number. Nontheless, MACS will continute computing. INFO @ Thu, 16 Apr 2020 00:39:54: #3 Call peaks... INFO @ Thu, 16 Apr 2020 00:39:54: #3 Pre-compute pvalue-qvalue table... INFO @ Thu, 16 Apr 2020 00:39:56: 39000000 INFO @ Thu, 16 Apr 2020 00:40:02: 36000000 INFO @ Thu, 16 Apr 2020 00:40:04: 40000000 INFO @ Thu, 16 Apr 2020 00:40:10: 37000000 INFO @ Thu, 16 Apr 2020 00:40:13: 41000000 INFO @ Thu, 16 Apr 2020 00:40:15: #3 Call peaks for each chromosome... INFO @ Thu, 16 Apr 2020 00:40:18: 38000000 INFO @ Thu, 16 Apr 2020 00:40:21: 42000000 INFO @ Thu, 16 Apr 2020 00:40:24: #1 tag size is determined as 150 bps INFO @ Thu, 16 Apr 2020 00:40:24: #1 tag size = 150 INFO @ Thu, 16 Apr 2020 00:40:24: #1 total tags in treatment: 12568150 INFO @ Thu, 16 Apr 2020 00:40:24: #1 user defined the maximum tags... INFO @ Thu, 16 Apr 2020 00:40:24: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Thu, 16 Apr 2020 00:40:25: #1 tags after filtering in treatment: 9802218 INFO @ Thu, 16 Apr 2020 00:40:25: #1 Redundant rate of treatment: 0.22 INFO @ Thu, 16 Apr 2020 00:40:25: #1 finished! INFO @ Thu, 16 Apr 2020 00:40:25: #2 Build Peak Model... INFO @ Thu, 16 Apr 2020 00:40:25: #2 looking for paired plus/minus strand peaks... INFO @ Thu, 16 Apr 2020 00:40:25: #2 number of paired peaks: 413 WARNING @ Thu, 16 Apr 2020 00:40:25: Fewer paired peaks (413) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 413 pairs to build model! INFO @ Thu, 16 Apr 2020 00:40:25: start model_add_line... INFO @ Thu, 16 Apr 2020 00:40:25: start X-correlation... INFO @ Thu, 16 Apr 2020 00:40:25: end of X-cor INFO @ Thu, 16 Apr 2020 00:40:25: #2 finished! INFO @ Thu, 16 Apr 2020 00:40:25: #2 predicted fragment length is 215 bps INFO @ Thu, 16 Apr 2020 00:40:25: #2 alternative fragment length(s) may be 4,215 bps INFO @ Thu, 16 Apr 2020 00:40:25: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/ce10/SRX6619603/SRX6619603.10_model.r WARNING @ Thu, 16 Apr 2020 00:40:25: #2 Since the d (215) calculated from paired-peaks are smaller than 2*tag length, it may be influenced by unknown sequencing problem! WARNING @ Thu, 16 Apr 2020 00:40:25: #2 You may need to consider one of the other alternative d(s): 4,215 WARNING @ Thu, 16 Apr 2020 00:40:25: #2 You can restart the process with --nomodel --extsize XXX with your choice or an arbitrary number. Nontheless, MACS will continute computing. INFO @ Thu, 16 Apr 2020 00:40:25: #3 Call peaks... INFO @ Thu, 16 Apr 2020 00:40:25: #3 Pre-compute pvalue-qvalue table... INFO @ Thu, 16 Apr 2020 00:40:25: #4 Write output xls file... /home/okishinya/chipatlas/results/ce10/SRX6619603/SRX6619603.05_peaks.xls INFO @ Thu, 16 Apr 2020 00:40:25: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/ce10/SRX6619603/SRX6619603.05_peaks.narrowPeak INFO @ Thu, 16 Apr 2020 00:40:25: #4 Write summits bed file... /home/okishinya/chipatlas/results/ce10/SRX6619603/SRX6619603.05_summits.bed INFO @ Thu, 16 Apr 2020 00:40:25: Done! pass1 - making usageList (6 chroms): 0 millis pass2 - checking and writing primary data (768 records, 4 fields): 2 millis CompletedMACS2peakCalling INFO @ Thu, 16 Apr 2020 00:40:27: 39000000 INFO @ Thu, 16 Apr 2020 00:40:35: 40000000 INFO @ Thu, 16 Apr 2020 00:40:43: 41000000 INFO @ Thu, 16 Apr 2020 00:40:47: #3 Call peaks for each chromosome... INFO @ Thu, 16 Apr 2020 00:40:51: 42000000 INFO @ Thu, 16 Apr 2020 00:40:55: #1 tag size is determined as 150 bps INFO @ Thu, 16 Apr 2020 00:40:55: #1 tag size = 150 INFO @ Thu, 16 Apr 2020 00:40:55: #1 total tags in treatment: 12568150 INFO @ Thu, 16 Apr 2020 00:40:55: #1 user defined the maximum tags... INFO @ Thu, 16 Apr 2020 00:40:55: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Thu, 16 Apr 2020 00:40:55: #1 tags after filtering in treatment: 9802218 INFO @ Thu, 16 Apr 2020 00:40:55: #1 Redundant rate of treatment: 0.22 INFO @ Thu, 16 Apr 2020 00:40:55: #1 finished! INFO @ Thu, 16 Apr 2020 00:40:55: #2 Build Peak Model... INFO @ Thu, 16 Apr 2020 00:40:55: #2 looking for paired plus/minus strand peaks... INFO @ Thu, 16 Apr 2020 00:40:56: #2 number of paired peaks: 413 WARNING @ Thu, 16 Apr 2020 00:40:56: Fewer paired peaks (413) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 413 pairs to build model! INFO @ Thu, 16 Apr 2020 00:40:56: start model_add_line... INFO @ Thu, 16 Apr 2020 00:40:56: start X-correlation... INFO @ Thu, 16 Apr 2020 00:40:56: end of X-cor INFO @ Thu, 16 Apr 2020 00:40:56: #2 finished! INFO @ Thu, 16 Apr 2020 00:40:56: #2 predicted fragment length is 215 bps INFO @ Thu, 16 Apr 2020 00:40:56: #2 alternative fragment length(s) may be 4,215 bps INFO @ Thu, 16 Apr 2020 00:40:56: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/ce10/SRX6619603/SRX6619603.20_model.r WARNING @ Thu, 16 Apr 2020 00:40:56: #2 Since the d (215) calculated from paired-peaks are smaller than 2*tag length, it may be influenced by unknown sequencing problem! WARNING @ Thu, 16 Apr 2020 00:40:56: #2 You may need to consider one of the other alternative d(s): 4,215 WARNING @ Thu, 16 Apr 2020 00:40:56: #2 You can restart the process with --nomodel --extsize XXX with your choice or an arbitrary number. Nontheless, MACS will continute computing. INFO @ Thu, 16 Apr 2020 00:40:56: #3 Call peaks... INFO @ Thu, 16 Apr 2020 00:40:56: #3 Pre-compute pvalue-qvalue table... INFO @ Thu, 16 Apr 2020 00:40:57: #4 Write output xls file... /home/okishinya/chipatlas/results/ce10/SRX6619603/SRX6619603.10_peaks.xls INFO @ Thu, 16 Apr 2020 00:40:57: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/ce10/SRX6619603/SRX6619603.10_peaks.narrowPeak INFO @ Thu, 16 Apr 2020 00:40:57: #4 Write summits bed file... /home/okishinya/chipatlas/results/ce10/SRX6619603/SRX6619603.10_summits.bed INFO @ Thu, 16 Apr 2020 00:40:57: Done! pass1 - making usageList (6 chroms): 0 millis pass2 - checking and writing primary data (380 records, 4 fields): 2 millis CompletedMACS2peakCalling INFO @ Thu, 16 Apr 2020 00:41:17: #3 Call peaks for each chromosome... BedGraph に変換しました。 BigWig に変換中... INFO @ Thu, 16 Apr 2020 00:41:27: #4 Write output xls file... /home/okishinya/chipatlas/results/ce10/SRX6619603/SRX6619603.20_peaks.xls INFO @ Thu, 16 Apr 2020 00:41:27: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/ce10/SRX6619603/SRX6619603.20_peaks.narrowPeak INFO @ Thu, 16 Apr 2020 00:41:27: #4 Write summits bed file... /home/okishinya/chipatlas/results/ce10/SRX6619603/SRX6619603.20_summits.bed INFO @ Thu, 16 Apr 2020 00:41:27: Done! pass1 - making usageList (6 chroms): 1 millis pass2 - checking and writing primary data (217 records, 4 fields): 1 millis CompletedMACS2peakCalling BigWig に変換しました。