Job ID = 1292441 sra ファイルのダウンロード中... Read layout: PAIRED fastq に変換中... spots read : 12,405,203 reads read : 24,810,406 reads written : 24,810,406 spots read : 12,280,355 reads read : 24,560,710 reads written : 24,560,710 rm: cannot remove ‘fastqDump_tmp*’: 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: 00:23:40 24685558 reads; of these: 24685558 (100.00%) were paired; of these: 3861435 (15.64%) aligned concordantly 0 times 17780369 (72.03%) aligned concordantly exactly 1 time 3043754 (12.33%) aligned concordantly >1 times ---- 3861435 pairs aligned concordantly 0 times; of these: 1084022 (28.07%) aligned discordantly 1 time ---- 2777413 pairs aligned 0 times concordantly or discordantly; of these: 5554826 mates make up the pairs; of these: 4447205 (80.06%) aligned 0 times 663002 (11.94%) aligned exactly 1 time 444619 (8.00%) aligned >1 times 90.99% overall alignment rate Time searching: 00:23:40 Overall time: 00:23:40 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 20 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] 558790 / 21788990 = 0.0256 in library ' ' BAM に変換しました。 Bed ファイルを作成中... BedGraph に変換中... INFO @ Sun, 02 Jun 2019 19:29:39: # Command line: callpeak -t /home/okishinya/chipatlas/results/ce10/SRX4419820/SRX4419820.bam -f BAM -g ce -n /home/okishinya/chipatlas/results/ce10/SRX4419820/SRX4419820.20 -q 1e-20 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/ce10/SRX4419820/SRX4419820.20 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/ce10/SRX4419820/SRX4419820.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 @ Sun, 02 Jun 2019 19:29:39: #1 read tag files... INFO @ Sun, 02 Jun 2019 19:29:39: #1 read treatment tags... INFO @ Sun, 02 Jun 2019 19:29:39: # Command line: callpeak -t /home/okishinya/chipatlas/results/ce10/SRX4419820/SRX4419820.bam -f BAM -g ce -n /home/okishinya/chipatlas/results/ce10/SRX4419820/SRX4419820.10 -q 1e-10 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/ce10/SRX4419820/SRX4419820.10 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/ce10/SRX4419820/SRX4419820.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 @ Sun, 02 Jun 2019 19:29:39: #1 read tag files... INFO @ Sun, 02 Jun 2019 19:29:39: #1 read treatment tags... INFO @ Sun, 02 Jun 2019 19:29:39: # Command line: callpeak -t /home/okishinya/chipatlas/results/ce10/SRX4419820/SRX4419820.bam -f BAM -g ce -n /home/okishinya/chipatlas/results/ce10/SRX4419820/SRX4419820.05 -q 1e-05 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/ce10/SRX4419820/SRX4419820.05 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/ce10/SRX4419820/SRX4419820.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 @ Sun, 02 Jun 2019 19:29:39: #1 read tag files... INFO @ Sun, 02 Jun 2019 19:29:39: #1 read treatment tags... INFO @ Sun, 02 Jun 2019 19:29:47: 1000000 INFO @ Sun, 02 Jun 2019 19:29:47: 1000000 INFO @ Sun, 02 Jun 2019 19:29:48: 1000000 INFO @ Sun, 02 Jun 2019 19:29:54: 2000000 INFO @ Sun, 02 Jun 2019 19:29:55: 2000000 INFO @ Sun, 02 Jun 2019 19:29:57: 2000000 INFO @ Sun, 02 Jun 2019 19:30:02: 3000000 INFO @ Sun, 02 Jun 2019 19:30:05: 3000000 INFO @ Sun, 02 Jun 2019 19:30:07: 3000000 INFO @ Sun, 02 Jun 2019 19:30:10: 4000000 INFO @ Sun, 02 Jun 2019 19:30:14: 4000000 INFO @ Sun, 02 Jun 2019 19:30:16: 4000000 INFO @ Sun, 02 Jun 2019 19:30:18: 5000000 INFO @ Sun, 02 Jun 2019 19:30:23: 5000000 INFO @ Sun, 02 Jun 2019 19:30:26: 5000000 INFO @ Sun, 02 Jun 2019 19:30:26: 6000000 INFO @ Sun, 02 Jun 2019 19:30:32: 6000000 INFO @ Sun, 02 Jun 2019 19:30:34: 7000000 INFO @ Sun, 02 Jun 2019 19:30:35: 6000000 INFO @ Sun, 02 Jun 2019 19:30:40: 7000000 INFO @ Sun, 02 Jun 2019 19:30:41: 8000000 INFO @ Sun, 02 Jun 2019 19:30:44: 7000000 INFO @ Sun, 02 Jun 2019 19:30:48: 8000000 INFO @ Sun, 02 Jun 2019 19:30:49: 9000000 INFO @ Sun, 02 Jun 2019 19:30:53: 8000000 INFO @ Sun, 02 Jun 2019 19:30:56: 9000000 INFO @ Sun, 02 Jun 2019 19:30:56: 10000000 INFO @ Sun, 02 Jun 2019 19:31:02: 9000000 INFO @ Sun, 02 Jun 2019 19:31:04: 11000000 INFO @ Sun, 02 Jun 2019 19:31:04: 10000000 INFO @ Sun, 02 Jun 2019 19:31:11: 12000000 INFO @ Sun, 02 Jun 2019 19:31:11: 10000000 INFO @ Sun, 02 Jun 2019 19:31:11: 11000000 INFO @ Sun, 02 Jun 2019 19:31:18: 13000000 INFO @ Sun, 02 Jun 2019 19:31:19: 12000000 INFO @ Sun, 02 Jun 2019 19:31:20: 11000000 INFO @ Sun, 02 Jun 2019 19:31:26: 14000000 INFO @ Sun, 02 Jun 2019 19:31:27: 13000000 INFO @ Sun, 02 Jun 2019 19:31:29: 12000000 INFO @ Sun, 02 Jun 2019 19:31:33: 15000000 INFO @ Sun, 02 Jun 2019 19:31:35: 14000000 INFO @ Sun, 02 Jun 2019 19:31:38: 13000000 INFO @ Sun, 02 Jun 2019 19:31:41: 16000000 INFO @ Sun, 02 Jun 2019 19:31:43: 15000000 INFO @ Sun, 02 Jun 2019 19:31:46: 14000000 INFO @ Sun, 02 Jun 2019 19:31:48: 17000000 INFO @ Sun, 02 Jun 2019 19:31:51: 16000000 INFO @ Sun, 02 Jun 2019 19:31:56: 15000000 INFO @ Sun, 02 Jun 2019 19:31:56: 18000000 INFO @ Sun, 02 Jun 2019 19:31:59: 17000000 INFO @ Sun, 02 Jun 2019 19:32:03: 19000000 INFO @ Sun, 02 Jun 2019 19:32:05: 16000000 INFO @ Sun, 02 Jun 2019 19:32:07: 18000000 INFO @ Sun, 02 Jun 2019 19:32:10: 20000000 INFO @ Sun, 02 Jun 2019 19:32:14: 19000000 INFO @ Sun, 02 Jun 2019 19:32:15: 17000000 INFO @ Sun, 02 Jun 2019 19:32:18: 21000000 INFO @ Sun, 02 Jun 2019 19:32:22: 20000000 INFO @ Sun, 02 Jun 2019 19:32:25: 18000000 INFO @ Sun, 02 Jun 2019 19:32:25: 22000000 INFO @ Sun, 02 Jun 2019 19:32:30: 21000000 INFO @ Sun, 02 Jun 2019 19:32:33: 23000000 INFO @ Sun, 02 Jun 2019 19:32:34: 19000000 INFO @ Sun, 02 Jun 2019 19:32:38: 22000000 INFO @ Sun, 02 Jun 2019 19:32:40: 24000000 INFO @ Sun, 02 Jun 2019 19:32:44: 20000000 INFO @ Sun, 02 Jun 2019 19:32:45: 23000000 INFO @ Sun, 02 Jun 2019 19:32:47: 25000000 INFO @ Sun, 02 Jun 2019 19:32:53: 24000000 INFO @ Sun, 02 Jun 2019 19:32:53: 21000000 INFO @ Sun, 02 Jun 2019 19:32:55: 26000000 INFO @ Sun, 02 Jun 2019 19:33:01: 25000000 INFO @ Sun, 02 Jun 2019 19:33:02: 27000000 INFO @ Sun, 02 Jun 2019 19:33:03: 22000000 INFO @ Sun, 02 Jun 2019 19:33:09: 26000000 INFO @ Sun, 02 Jun 2019 19:33:09: 28000000 INFO @ Sun, 02 Jun 2019 19:33:13: 23000000 INFO @ Sun, 02 Jun 2019 19:33:17: 27000000 INFO @ Sun, 02 Jun 2019 19:33:17: 29000000 INFO @ Sun, 02 Jun 2019 19:33:22: 24000000 INFO @ Sun, 02 Jun 2019 19:33:24: 30000000 INFO @ Sun, 02 Jun 2019 19:33:24: 28000000 INFO @ Sun, 02 Jun 2019 19:33:32: 31000000 INFO @ Sun, 02 Jun 2019 19:33:32: 25000000 INFO @ Sun, 02 Jun 2019 19:33:32: 29000000 INFO @ Sun, 02 Jun 2019 19:33:39: 32000000 INFO @ Sun, 02 Jun 2019 19:33:40: 30000000 INFO @ Sun, 02 Jun 2019 19:33:41: 26000000 INFO @ Sun, 02 Jun 2019 19:33:46: 33000000 INFO @ Sun, 02 Jun 2019 19:33:48: 31000000 INFO @ Sun, 02 Jun 2019 19:33:50: 27000000 INFO @ Sun, 02 Jun 2019 19:33:54: 34000000 INFO @ Sun, 02 Jun 2019 19:33:55: 32000000 INFO @ Sun, 02 Jun 2019 19:33:58: 28000000 INFO @ Sun, 02 Jun 2019 19:34:01: 35000000 INFO @ Sun, 02 Jun 2019 19:34:03: 33000000 INFO @ Sun, 02 Jun 2019 19:34:07: 29000000 INFO @ Sun, 02 Jun 2019 19:34:09: 36000000 INFO @ Sun, 02 Jun 2019 19:34:11: 34000000 INFO @ Sun, 02 Jun 2019 19:34:16: 30000000 INFO @ Sun, 02 Jun 2019 19:34:16: 37000000 INFO @ Sun, 02 Jun 2019 19:34:19: 35000000 INFO @ Sun, 02 Jun 2019 19:34:23: 38000000 INFO @ Sun, 02 Jun 2019 19:34:24: 31000000 INFO @ Sun, 02 Jun 2019 19:34:27: 36000000 INFO @ Sun, 02 Jun 2019 19:34:31: 39000000 INFO @ Sun, 02 Jun 2019 19:34:33: 32000000 INFO @ Sun, 02 Jun 2019 19:34:34: 37000000 INFO @ Sun, 02 Jun 2019 19:34:38: 40000000 INFO @ Sun, 02 Jun 2019 19:34:42: 33000000 INFO @ Sun, 02 Jun 2019 19:34:42: 38000000 INFO @ Sun, 02 Jun 2019 19:34:46: 41000000 INFO @ Sun, 02 Jun 2019 19:34:50: 39000000 INFO @ Sun, 02 Jun 2019 19:34:50: 34000000 INFO @ Sun, 02 Jun 2019 19:34:53: 42000000 INFO @ Sun, 02 Jun 2019 19:34:58: 40000000 INFO @ Sun, 02 Jun 2019 19:34:59: 35000000 INFO @ Sun, 02 Jun 2019 19:35:00: 43000000 INFO @ Sun, 02 Jun 2019 19:35:06: 41000000 INFO @ Sun, 02 Jun 2019 19:35:07: #1 tag size is determined as 50 bps INFO @ Sun, 02 Jun 2019 19:35:07: #1 tag size = 50 INFO @ Sun, 02 Jun 2019 19:35:07: #1 total tags in treatment: 20271287 INFO @ Sun, 02 Jun 2019 19:35:07: #1 user defined the maximum tags... INFO @ Sun, 02 Jun 2019 19:35:07: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Sun, 02 Jun 2019 19:35:07: #1 tags after filtering in treatment: 16404977 INFO @ Sun, 02 Jun 2019 19:35:07: #1 Redundant rate of treatment: 0.19 INFO @ Sun, 02 Jun 2019 19:35:07: #1 finished! INFO @ Sun, 02 Jun 2019 19:35:07: #2 Build Peak Model... INFO @ Sun, 02 Jun 2019 19:35:07: #2 looking for paired plus/minus strand peaks... INFO @ Sun, 02 Jun 2019 19:35:08: 36000000 INFO @ Sun, 02 Jun 2019 19:35:08: #2 number of paired peaks: 166 WARNING @ Sun, 02 Jun 2019 19:35:08: Fewer paired peaks (166) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 166 pairs to build model! INFO @ Sun, 02 Jun 2019 19:35:08: start model_add_line... INFO @ Sun, 02 Jun 2019 19:35:09: start X-correlation... INFO @ Sun, 02 Jun 2019 19:35:09: end of X-cor INFO @ Sun, 02 Jun 2019 19:35:09: #2 finished! INFO @ Sun, 02 Jun 2019 19:35:09: #2 predicted fragment length is 70 bps INFO @ Sun, 02 Jun 2019 19:35:09: #2 alternative fragment length(s) may be 3,55,70,106,126,148,203 bps INFO @ Sun, 02 Jun 2019 19:35:09: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/ce10/SRX4419820/SRX4419820.20_model.r WARNING @ Sun, 02 Jun 2019 19:35:09: #2 Since the d (70) calculated from paired-peaks are smaller than 2*tag length, it may be influenced by unknown sequencing problem! WARNING @ Sun, 02 Jun 2019 19:35:09: #2 You may need to consider one of the other alternative d(s): 3,55,70,106,126,148,203 WARNING @ Sun, 02 Jun 2019 19:35:09: #2 You can restart the process with --nomodel --extsize XXX with your choice or an arbitrary number. Nontheless, MACS will continute computing. INFO @ Sun, 02 Jun 2019 19:35:09: #3 Call peaks... INFO @ Sun, 02 Jun 2019 19:35:09: #3 Pre-compute pvalue-qvalue table... INFO @ Sun, 02 Jun 2019 19:35:14: 42000000 INFO @ Sun, 02 Jun 2019 19:35:16: 37000000 INFO @ Sun, 02 Jun 2019 19:35:21: 43000000 INFO @ Sun, 02 Jun 2019 19:35:25: 38000000 INFO @ Sun, 02 Jun 2019 19:35:28: #1 tag size is determined as 50 bps INFO @ Sun, 02 Jun 2019 19:35:28: #1 tag size = 50 INFO @ Sun, 02 Jun 2019 19:35:28: #1 total tags in treatment: 20271287 INFO @ Sun, 02 Jun 2019 19:35:28: #1 user defined the maximum tags... INFO @ Sun, 02 Jun 2019 19:35:28: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Sun, 02 Jun 2019 19:35:28: #1 tags after filtering in treatment: 16404977 INFO @ Sun, 02 Jun 2019 19:35:28: #1 Redundant rate of treatment: 0.19 INFO @ Sun, 02 Jun 2019 19:35:28: #1 finished! INFO @ Sun, 02 Jun 2019 19:35:28: #2 Build Peak Model... INFO @ Sun, 02 Jun 2019 19:35:28: #2 looking for paired plus/minus strand peaks... INFO @ Sun, 02 Jun 2019 19:35:30: #2 number of paired peaks: 166 WARNING @ Sun, 02 Jun 2019 19:35:30: Fewer paired peaks (166) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 166 pairs to build model! INFO @ Sun, 02 Jun 2019 19:35:30: start model_add_line... INFO @ Sun, 02 Jun 2019 19:35:30: start X-correlation... INFO @ Sun, 02 Jun 2019 19:35:30: end of X-cor INFO @ Sun, 02 Jun 2019 19:35:30: #2 finished! INFO @ Sun, 02 Jun 2019 19:35:30: #2 predicted fragment length is 70 bps INFO @ Sun, 02 Jun 2019 19:35:30: #2 alternative fragment length(s) may be 3,55,70,106,126,148,203 bps INFO @ Sun, 02 Jun 2019 19:35:30: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/ce10/SRX4419820/SRX4419820.05_model.r WARNING @ Sun, 02 Jun 2019 19:35:30: #2 Since the d (70) calculated from paired-peaks are smaller than 2*tag length, it may be influenced by unknown sequencing problem! WARNING @ Sun, 02 Jun 2019 19:35:30: #2 You may need to consider one of the other alternative d(s): 3,55,70,106,126,148,203 WARNING @ Sun, 02 Jun 2019 19:35:30: #2 You can restart the process with --nomodel --extsize XXX with your choice or an arbitrary number. Nontheless, MACS will continute computing. INFO @ Sun, 02 Jun 2019 19:35:30: #3 Call peaks... INFO @ Sun, 02 Jun 2019 19:35:30: #3 Pre-compute pvalue-qvalue table... INFO @ Sun, 02 Jun 2019 19:35:33: 39000000 INFO @ Sun, 02 Jun 2019 19:35:42: 40000000 INFO @ Sun, 02 Jun 2019 19:35:49: #3 Call peaks for each chromosome... INFO @ Sun, 02 Jun 2019 19:35:50: 41000000 INFO @ Sun, 02 Jun 2019 19:35:58: 42000000 INFO @ Sun, 02 Jun 2019 19:36:06: 43000000 INFO @ Sun, 02 Jun 2019 19:36:08: #4 Write output xls file... /home/okishinya/chipatlas/results/ce10/SRX4419820/SRX4419820.20_peaks.xls INFO @ Sun, 02 Jun 2019 19:36:08: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/ce10/SRX4419820/SRX4419820.20_peaks.narrowPeak INFO @ Sun, 02 Jun 2019 19:36:08: #4 Write summits bed file... /home/okishinya/chipatlas/results/ce10/SRX4419820/SRX4419820.20_summits.bed INFO @ Sun, 02 Jun 2019 19:36:08: Done! pass1 - making usageList (6 chroms): 1 millis pass2 - checking and writing primary data (111 records, 4 fields): 2 millis CompletedMACS2peakCalling INFO @ Sun, 02 Jun 2019 19:36:12: #3 Call peaks for each chromosome... INFO @ Sun, 02 Jun 2019 19:36:13: #1 tag size is determined as 50 bps INFO @ Sun, 02 Jun 2019 19:36:13: #1 tag size = 50 INFO @ Sun, 02 Jun 2019 19:36:13: #1 total tags in treatment: 20271287 INFO @ Sun, 02 Jun 2019 19:36:13: #1 user defined the maximum tags... INFO @ Sun, 02 Jun 2019 19:36:13: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Sun, 02 Jun 2019 19:36:14: #1 tags after filtering in treatment: 16404977 INFO @ Sun, 02 Jun 2019 19:36:14: #1 Redundant rate of treatment: 0.19 INFO @ Sun, 02 Jun 2019 19:36:14: #1 finished! INFO @ Sun, 02 Jun 2019 19:36:14: #2 Build Peak Model... INFO @ Sun, 02 Jun 2019 19:36:14: #2 looking for paired plus/minus strand peaks... INFO @ Sun, 02 Jun 2019 19:36:15: #2 number of paired peaks: 166 WARNING @ Sun, 02 Jun 2019 19:36:15: Fewer paired peaks (166) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 166 pairs to build model! INFO @ Sun, 02 Jun 2019 19:36:15: start model_add_line... INFO @ Sun, 02 Jun 2019 19:36:15: start X-correlation... INFO @ Sun, 02 Jun 2019 19:36:15: end of X-cor INFO @ Sun, 02 Jun 2019 19:36:15: #2 finished! INFO @ Sun, 02 Jun 2019 19:36:15: #2 predicted fragment length is 70 bps INFO @ Sun, 02 Jun 2019 19:36:15: #2 alternative fragment length(s) may be 3,55,70,106,126,148,203 bps INFO @ Sun, 02 Jun 2019 19:36:15: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/ce10/SRX4419820/SRX4419820.10_model.r WARNING @ Sun, 02 Jun 2019 19:36:15: #2 Since the d (70) calculated from paired-peaks are smaller than 2*tag length, it may be influenced by unknown sequencing problem! WARNING @ Sun, 02 Jun 2019 19:36:15: #2 You may need to consider one of the other alternative d(s): 3,55,70,106,126,148,203 WARNING @ Sun, 02 Jun 2019 19:36:15: #2 You can restart the process with --nomodel --extsize XXX with your choice or an arbitrary number. Nontheless, MACS will continute computing. INFO @ Sun, 02 Jun 2019 19:36:15: #3 Call peaks... INFO @ Sun, 02 Jun 2019 19:36:15: #3 Pre-compute pvalue-qvalue table... INFO @ Sun, 02 Jun 2019 19:36:31: #4 Write output xls file... /home/okishinya/chipatlas/results/ce10/SRX4419820/SRX4419820.05_peaks.xls INFO @ Sun, 02 Jun 2019 19:36:31: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/ce10/SRX4419820/SRX4419820.05_peaks.narrowPeak INFO @ Sun, 02 Jun 2019 19:36:31: #4 Write summits bed file... /home/okishinya/chipatlas/results/ce10/SRX4419820/SRX4419820.05_summits.bed INFO @ Sun, 02 Jun 2019 19:36:31: Done! pass1 - making usageList (6 chroms): 1 millis pass2 - checking and writing primary data (524 records, 4 fields): 2 millis CompletedMACS2peakCalling INFO @ Sun, 02 Jun 2019 19:36:56: #3 Call peaks for each chromosome... INFO @ Sun, 02 Jun 2019 19:37:15: #4 Write output xls file... /home/okishinya/chipatlas/results/ce10/SRX4419820/SRX4419820.10_peaks.xls INFO @ Sun, 02 Jun 2019 19:37:15: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/ce10/SRX4419820/SRX4419820.10_peaks.narrowPeak INFO @ Sun, 02 Jun 2019 19:37:15: #4 Write summits bed file... /home/okishinya/chipatlas/results/ce10/SRX4419820/SRX4419820.10_summits.bed INFO @ Sun, 02 Jun 2019 19:37:15: Done! pass1 - making usageList (6 chroms): 1 millis pass2 - checking and writing primary data (246 records, 4 fields): 1 millis CompletedMACS2peakCalling BedGraph に変換しました。 BigWig に変換中... BigWig に変換しました。