Job ID = 4178444 sra ファイルのダウンロード中... Read layout: PAIRED fastq に変換中... 2019-12-05T03:31:20 fasterq-dump.2.9.6 sys: timeout exhausted while reading file within network system module - mbedtls_ssl_read returned -76 ( NET - Reading information from the socket failed ) 2019-12-05T03:38:53 fasterq-dump.2.9.6 sys: timeout exhausted while reading file within network system module - mbedtls_ssl_read returned -76 ( NET - Reading information from the socket failed ) spots read : 21,992,818 reads read : 43,985,636 reads written : 43,985,636 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: 00:00:01 Multiseed full-index search: 02:02:08 21992818 reads; of these: 21992818 (100.00%) were paired; of these: 3220942 (14.65%) aligned concordantly 0 times 12170863 (55.34%) aligned concordantly exactly 1 time 6601013 (30.01%) aligned concordantly >1 times ---- 3220942 pairs aligned concordantly 0 times; of these: 1604955 (49.83%) aligned discordantly 1 time ---- 1615987 pairs aligned 0 times concordantly or discordantly; of these: 3231974 mates make up the pairs; of these: 1081493 (33.46%) aligned 0 times 727745 (22.52%) aligned exactly 1 time 1422736 (44.02%) aligned >1 times 97.54% overall alignment rate Time searching: 02:02:09 Overall time: 02:02:09 マッピングが完了しました。 samtools でBAM に変換中... [samopen] SAM header is present: 15 sequences. [bam_sort_core] merging from 20 files... [bam_rmdup_core] processing reference chr2L... [bam_rmdup_core] processing reference chr2LHet... [bam_rmdup_core] processing reference chr2R... [bam_rmdup_core] processing reference chr2RHet... [bam_rmdup_core] processing reference chr3L... [bam_rmdup_core] processing reference chr3LHet... [bam_rmdup_core] processing reference chr3R... [bam_rmdup_core] processing reference chr3RHet... [bam_rmdup_core] processing reference chr4... [bam_rmdup_core] processing reference chrM... [bam_rmdup_core] processing reference chrU... [bam_rmdup_core] processing reference chrUextra... [bam_rmdup_core] processing reference chrX... [bam_rmdup_core] processing reference chrXHet... [bam_rmdup_core] processing reference chrYHet... [bam_rmdup_core] 987218 / 20261238 = 0.0487 in library ' ' BAM に変換しました。 Bed ファイルを作成中... INFO @ Thu, 05 Dec 2019 15:20:13: # Command line: callpeak -t /home/okishinya/chipatlas/results/dm3/SRX4117268/SRX4117268.bam -f BAM -g dm -n /home/okishinya/chipatlas/results/dm3/SRX4117268/SRX4117268.05 -q 1e-05 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/dm3/SRX4117268/SRX4117268.05 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/dm3/SRX4117268/SRX4117268.bam'] # control file = None # effective genome size = 1.20e+08 # 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, 05 Dec 2019 15:20:13: #1 read tag files... INFO @ Thu, 05 Dec 2019 15:20:13: #1 read treatment tags... INFO @ Thu, 05 Dec 2019 15:20:22: 1000000 INFO @ Thu, 05 Dec 2019 15:20:31: 2000000 INFO @ Thu, 05 Dec 2019 15:20:39: 3000000 INFO @ Thu, 05 Dec 2019 15:20:43: # Command line: callpeak -t /home/okishinya/chipatlas/results/dm3/SRX4117268/SRX4117268.bam -f BAM -g dm -n /home/okishinya/chipatlas/results/dm3/SRX4117268/SRX4117268.10 -q 1e-10 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/dm3/SRX4117268/SRX4117268.10 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/dm3/SRX4117268/SRX4117268.bam'] # control file = None # effective genome size = 1.20e+08 # 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, 05 Dec 2019 15:20:43: #1 read tag files... INFO @ Thu, 05 Dec 2019 15:20:43: #1 read treatment tags... INFO @ Thu, 05 Dec 2019 15:20:48: 4000000 INFO @ Thu, 05 Dec 2019 15:20:53: 1000000 INFO @ Thu, 05 Dec 2019 15:20:58: 5000000 INFO @ Thu, 05 Dec 2019 15:21:02: 2000000 INFO @ Thu, 05 Dec 2019 15:21:07: 6000000 INFO @ Thu, 05 Dec 2019 15:21:11: 3000000 BedGraph に変換中... INFO @ Thu, 05 Dec 2019 15:21:13: # Command line: callpeak -t /home/okishinya/chipatlas/results/dm3/SRX4117268/SRX4117268.bam -f BAM -g dm -n /home/okishinya/chipatlas/results/dm3/SRX4117268/SRX4117268.20 -q 1e-20 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/dm3/SRX4117268/SRX4117268.20 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/dm3/SRX4117268/SRX4117268.bam'] # control file = None # effective genome size = 1.20e+08 # 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, 05 Dec 2019 15:21:13: #1 read tag files... INFO @ Thu, 05 Dec 2019 15:21:13: #1 read treatment tags... INFO @ Thu, 05 Dec 2019 15:21:16: 7000000 INFO @ Thu, 05 Dec 2019 15:21:20: 4000000 INFO @ Thu, 05 Dec 2019 15:21:26: 1000000 INFO @ Thu, 05 Dec 2019 15:21:26: 8000000 INFO @ Thu, 05 Dec 2019 15:21:30: 5000000 INFO @ Thu, 05 Dec 2019 15:21:36: 9000000 INFO @ Thu, 05 Dec 2019 15:21:37: 2000000 INFO @ Thu, 05 Dec 2019 15:21:39: 6000000 INFO @ Thu, 05 Dec 2019 15:21:45: 10000000 INFO @ Thu, 05 Dec 2019 15:21:48: 3000000 INFO @ Thu, 05 Dec 2019 15:21:48: 7000000 INFO @ Thu, 05 Dec 2019 15:21:55: 11000000 INFO @ Thu, 05 Dec 2019 15:21:58: 8000000 INFO @ Thu, 05 Dec 2019 15:21:58: 4000000 INFO @ Thu, 05 Dec 2019 15:22:05: 12000000 INFO @ Thu, 05 Dec 2019 15:22:08: 9000000 INFO @ Thu, 05 Dec 2019 15:22:09: 5000000 INFO @ Thu, 05 Dec 2019 15:22:14: 13000000 INFO @ Thu, 05 Dec 2019 15:22:17: 10000000 INFO @ Thu, 05 Dec 2019 15:22:20: 6000000 INFO @ Thu, 05 Dec 2019 15:22:24: 14000000 INFO @ Thu, 05 Dec 2019 15:22:27: 11000000 INFO @ Thu, 05 Dec 2019 15:22:31: 7000000 INFO @ Thu, 05 Dec 2019 15:22:34: 15000000 INFO @ Thu, 05 Dec 2019 15:22:36: 12000000 INFO @ Thu, 05 Dec 2019 15:22:43: 8000000 INFO @ Thu, 05 Dec 2019 15:22:44: 16000000 INFO @ Thu, 05 Dec 2019 15:22:46: 13000000 INFO @ Thu, 05 Dec 2019 15:22:53: 17000000 INFO @ Thu, 05 Dec 2019 15:22:54: 9000000 INFO @ Thu, 05 Dec 2019 15:22:55: 14000000 INFO @ Thu, 05 Dec 2019 15:23:03: 18000000 INFO @ Thu, 05 Dec 2019 15:23:05: 10000000 INFO @ Thu, 05 Dec 2019 15:23:05: 15000000 INFO @ Thu, 05 Dec 2019 15:23:13: 19000000 INFO @ Thu, 05 Dec 2019 15:23:15: 16000000 INFO @ Thu, 05 Dec 2019 15:23:16: 11000000 INFO @ Thu, 05 Dec 2019 15:23:23: 20000000 INFO @ Thu, 05 Dec 2019 15:23:25: 17000000 INFO @ Thu, 05 Dec 2019 15:23:27: 12000000 INFO @ Thu, 05 Dec 2019 15:23:33: 21000000 INFO @ Thu, 05 Dec 2019 15:23:35: 18000000 INFO @ Thu, 05 Dec 2019 15:23:38: 13000000 INFO @ Thu, 05 Dec 2019 15:23:43: 22000000 INFO @ Thu, 05 Dec 2019 15:23:45: 19000000 INFO @ Thu, 05 Dec 2019 15:23:49: 14000000 INFO @ Thu, 05 Dec 2019 15:23:53: 23000000 INFO @ Thu, 05 Dec 2019 15:23:55: 20000000 INFO @ Thu, 05 Dec 2019 15:24:00: 15000000 INFO @ Thu, 05 Dec 2019 15:24:03: 24000000 INFO @ Thu, 05 Dec 2019 15:24:04: 21000000 INFO @ Thu, 05 Dec 2019 15:24:11: 16000000 INFO @ Thu, 05 Dec 2019 15:24:13: 25000000 INFO @ Thu, 05 Dec 2019 15:24:14: 22000000 INFO @ Thu, 05 Dec 2019 15:24:23: 17000000 INFO @ Thu, 05 Dec 2019 15:24:23: 26000000 INFO @ Thu, 05 Dec 2019 15:24:24: 23000000 INFO @ Thu, 05 Dec 2019 15:24:33: 27000000 INFO @ Thu, 05 Dec 2019 15:24:34: 18000000 INFO @ Thu, 05 Dec 2019 15:24:34: 24000000 INFO @ Thu, 05 Dec 2019 15:24:43: 28000000 INFO @ Thu, 05 Dec 2019 15:24:44: 25000000 INFO @ Thu, 05 Dec 2019 15:24:45: 19000000 INFO @ Thu, 05 Dec 2019 15:24:53: 29000000 INFO @ Thu, 05 Dec 2019 15:24:54: 26000000 INFO @ Thu, 05 Dec 2019 15:24:57: 20000000 INFO @ Thu, 05 Dec 2019 15:25:04: 30000000 INFO @ Thu, 05 Dec 2019 15:25:04: 27000000 INFO @ Thu, 05 Dec 2019 15:25:09: 21000000 INFO @ Thu, 05 Dec 2019 15:25:14: 31000000 INFO @ Thu, 05 Dec 2019 15:25:15: 28000000 INFO @ Thu, 05 Dec 2019 15:25:20: 22000000 INFO @ Thu, 05 Dec 2019 15:25:24: 32000000 INFO @ Thu, 05 Dec 2019 15:25:24: 29000000 INFO @ Thu, 05 Dec 2019 15:25:31: 23000000 INFO @ Thu, 05 Dec 2019 15:25:34: 33000000 INFO @ Thu, 05 Dec 2019 15:25:34: 30000000 INFO @ Thu, 05 Dec 2019 15:25:43: 24000000 INFO @ Thu, 05 Dec 2019 15:25:44: 34000000 INFO @ Thu, 05 Dec 2019 15:25:44: 31000000 INFO @ Thu, 05 Dec 2019 15:25:53: 32000000 INFO @ Thu, 05 Dec 2019 15:25:54: 35000000 INFO @ Thu, 05 Dec 2019 15:25:54: 25000000 INFO @ Thu, 05 Dec 2019 15:26:03: 33000000 INFO @ Thu, 05 Dec 2019 15:26:04: 36000000 INFO @ Thu, 05 Dec 2019 15:26:05: 26000000 INFO @ Thu, 05 Dec 2019 15:26:13: 34000000 INFO @ Thu, 05 Dec 2019 15:26:14: 37000000 INFO @ Thu, 05 Dec 2019 15:26:17: 27000000 INFO @ Thu, 05 Dec 2019 15:26:24: 35000000 INFO @ Thu, 05 Dec 2019 15:26:24: 38000000 INFO @ Thu, 05 Dec 2019 15:26:28: 28000000 INFO @ Thu, 05 Dec 2019 15:26:34: 39000000 INFO @ Thu, 05 Dec 2019 15:26:34: 36000000 INFO @ Thu, 05 Dec 2019 15:26:40: 29000000 INFO @ Thu, 05 Dec 2019 15:26:43: 40000000 INFO @ Thu, 05 Dec 2019 15:26:44: 37000000 INFO @ Thu, 05 Dec 2019 15:26:51: 30000000 INFO @ Thu, 05 Dec 2019 15:26:53: #1 tag size is determined as 99 bps INFO @ Thu, 05 Dec 2019 15:26:53: #1 tag size = 99 INFO @ Thu, 05 Dec 2019 15:26:53: #1 total tags in treatment: 17787990 INFO @ Thu, 05 Dec 2019 15:26:53: #1 user defined the maximum tags... INFO @ Thu, 05 Dec 2019 15:26:53: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Thu, 05 Dec 2019 15:26:53: #1 tags after filtering in treatment: 16208095 INFO @ Thu, 05 Dec 2019 15:26:53: #1 Redundant rate of treatment: 0.09 INFO @ Thu, 05 Dec 2019 15:26:53: #1 finished! INFO @ Thu, 05 Dec 2019 15:26:53: #2 Build Peak Model... INFO @ Thu, 05 Dec 2019 15:26:53: #2 looking for paired plus/minus strand peaks... INFO @ Thu, 05 Dec 2019 15:26:54: 38000000 INFO @ Thu, 05 Dec 2019 15:26:54: #2 number of paired peaks: 158 WARNING @ Thu, 05 Dec 2019 15:26:54: Fewer paired peaks (158) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 158 pairs to build model! INFO @ Thu, 05 Dec 2019 15:26:54: start model_add_line... INFO @ Thu, 05 Dec 2019 15:26:54: start X-correlation... INFO @ Thu, 05 Dec 2019 15:26:54: end of X-cor INFO @ Thu, 05 Dec 2019 15:26:54: #2 finished! INFO @ Thu, 05 Dec 2019 15:26:54: #2 predicted fragment length is 145 bps INFO @ Thu, 05 Dec 2019 15:26:54: #2 alternative fragment length(s) may be 145 bps INFO @ Thu, 05 Dec 2019 15:26:54: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/dm3/SRX4117268/SRX4117268.05_model.r WARNING @ Thu, 05 Dec 2019 15:26:54: #2 Since the d (145) calculated from paired-peaks are smaller than 2*tag length, it may be influenced by unknown sequencing problem! WARNING @ Thu, 05 Dec 2019 15:26:54: #2 You may need to consider one of the other alternative d(s): 145 WARNING @ Thu, 05 Dec 2019 15:26:54: #2 You can restart the process with --nomodel --extsize XXX with your choice or an arbitrary number. Nontheless, MACS will continute computing. INFO @ Thu, 05 Dec 2019 15:26:54: #3 Call peaks... INFO @ Thu, 05 Dec 2019 15:26:54: #3 Pre-compute pvalue-qvalue table... INFO @ Thu, 05 Dec 2019 15:27:03: 39000000 INFO @ Thu, 05 Dec 2019 15:27:03: 31000000 INFO @ Thu, 05 Dec 2019 15:27:12: 40000000 INFO @ Thu, 05 Dec 2019 15:27:15: 32000000 INFO @ Thu, 05 Dec 2019 15:27:21: #1 tag size is determined as 99 bps INFO @ Thu, 05 Dec 2019 15:27:21: #1 tag size = 99 INFO @ Thu, 05 Dec 2019 15:27:21: #1 total tags in treatment: 17787990 INFO @ Thu, 05 Dec 2019 15:27:21: #1 user defined the maximum tags... INFO @ Thu, 05 Dec 2019 15:27:21: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Thu, 05 Dec 2019 15:27:21: #1 tags after filtering in treatment: 16208095 INFO @ Thu, 05 Dec 2019 15:27:21: #1 Redundant rate of treatment: 0.09 INFO @ Thu, 05 Dec 2019 15:27:21: #1 finished! INFO @ Thu, 05 Dec 2019 15:27:21: #2 Build Peak Model... INFO @ Thu, 05 Dec 2019 15:27:21: #2 looking for paired plus/minus strand peaks... INFO @ Thu, 05 Dec 2019 15:27:22: #3 Call peaks for each chromosome... INFO @ Thu, 05 Dec 2019 15:27:22: #2 number of paired peaks: 158 WARNING @ Thu, 05 Dec 2019 15:27:22: Fewer paired peaks (158) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 158 pairs to build model! INFO @ Thu, 05 Dec 2019 15:27:22: start model_add_line... INFO @ Thu, 05 Dec 2019 15:27:22: start X-correlation... INFO @ Thu, 05 Dec 2019 15:27:22: end of X-cor INFO @ Thu, 05 Dec 2019 15:27:22: #2 finished! INFO @ Thu, 05 Dec 2019 15:27:22: #2 predicted fragment length is 145 bps INFO @ Thu, 05 Dec 2019 15:27:22: #2 alternative fragment length(s) may be 145 bps INFO @ Thu, 05 Dec 2019 15:27:22: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/dm3/SRX4117268/SRX4117268.10_model.r WARNING @ Thu, 05 Dec 2019 15:27:22: #2 Since the d (145) calculated from paired-peaks are smaller than 2*tag length, it may be influenced by unknown sequencing problem! WARNING @ Thu, 05 Dec 2019 15:27:22: #2 You may need to consider one of the other alternative d(s): 145 WARNING @ Thu, 05 Dec 2019 15:27:22: #2 You can restart the process with --nomodel --extsize XXX with your choice or an arbitrary number. Nontheless, MACS will continute computing. INFO @ Thu, 05 Dec 2019 15:27:22: #3 Call peaks... INFO @ Thu, 05 Dec 2019 15:27:22: #3 Pre-compute pvalue-qvalue table... INFO @ Thu, 05 Dec 2019 15:27:26: 33000000 INFO @ Thu, 05 Dec 2019 15:27:37: 34000000 INFO @ Thu, 05 Dec 2019 15:27:38: #4 Write output xls file... /home/okishinya/chipatlas/results/dm3/SRX4117268/SRX4117268.05_peaks.xls INFO @ Thu, 05 Dec 2019 15:27:38: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/dm3/SRX4117268/SRX4117268.05_peaks.narrowPeak INFO @ Thu, 05 Dec 2019 15:27:38: #4 Write summits bed file... /home/okishinya/chipatlas/results/dm3/SRX4117268/SRX4117268.05_summits.bed INFO @ Thu, 05 Dec 2019 15:27:38: Done! pass1 - making usageList (15 chroms): 1 millis pass2 - checking and writing primary data (4561 records, 4 fields): 21 millis CompletedMACS2peakCalling INFO @ Thu, 05 Dec 2019 15:27:49: 35000000 INFO @ Thu, 05 Dec 2019 15:27:49: #3 Call peaks for each chromosome... INFO @ Thu, 05 Dec 2019 15:28:00: 36000000 INFO @ Thu, 05 Dec 2019 15:28:06: #4 Write output xls file... /home/okishinya/chipatlas/results/dm3/SRX4117268/SRX4117268.10_peaks.xls INFO @ Thu, 05 Dec 2019 15:28:06: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/dm3/SRX4117268/SRX4117268.10_peaks.narrowPeak INFO @ Thu, 05 Dec 2019 15:28:06: #4 Write summits bed file... /home/okishinya/chipatlas/results/dm3/SRX4117268/SRX4117268.10_summits.bed INFO @ Thu, 05 Dec 2019 15:28:06: Done! pass1 - making usageList (14 chroms): 1 millis pass2 - checking and writing primary data (2279 records, 4 fields): 21 millis CompletedMACS2peakCalling INFO @ Thu, 05 Dec 2019 15:28:11: 37000000 INFO @ Thu, 05 Dec 2019 15:28:22: 38000000 INFO @ Thu, 05 Dec 2019 15:28:33: 39000000 INFO @ Thu, 05 Dec 2019 15:28:44: 40000000 INFO @ Thu, 05 Dec 2019 15:28:54: #1 tag size is determined as 99 bps INFO @ Thu, 05 Dec 2019 15:28:54: #1 tag size = 99 INFO @ Thu, 05 Dec 2019 15:28:54: #1 total tags in treatment: 17787990 INFO @ Thu, 05 Dec 2019 15:28:54: #1 user defined the maximum tags... INFO @ Thu, 05 Dec 2019 15:28:54: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Thu, 05 Dec 2019 15:28:54: #1 tags after filtering in treatment: 16208095 INFO @ Thu, 05 Dec 2019 15:28:54: #1 Redundant rate of treatment: 0.09 INFO @ Thu, 05 Dec 2019 15:28:54: #1 finished! INFO @ Thu, 05 Dec 2019 15:28:54: #2 Build Peak Model... INFO @ Thu, 05 Dec 2019 15:28:54: #2 looking for paired plus/minus strand peaks... INFO @ Thu, 05 Dec 2019 15:28:55: #2 number of paired peaks: 158 WARNING @ Thu, 05 Dec 2019 15:28:55: Fewer paired peaks (158) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 158 pairs to build model! INFO @ Thu, 05 Dec 2019 15:28:55: start model_add_line... INFO @ Thu, 05 Dec 2019 15:28:55: start X-correlation... INFO @ Thu, 05 Dec 2019 15:28:55: end of X-cor INFO @ Thu, 05 Dec 2019 15:28:55: #2 finished! INFO @ Thu, 05 Dec 2019 15:28:55: #2 predicted fragment length is 145 bps INFO @ Thu, 05 Dec 2019 15:28:55: #2 alternative fragment length(s) may be 145 bps INFO @ Thu, 05 Dec 2019 15:28:55: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/dm3/SRX4117268/SRX4117268.20_model.r WARNING @ Thu, 05 Dec 2019 15:28:55: #2 Since the d (145) calculated from paired-peaks are smaller than 2*tag length, it may be influenced by unknown sequencing problem! WARNING @ Thu, 05 Dec 2019 15:28:55: #2 You may need to consider one of the other alternative d(s): 145 WARNING @ Thu, 05 Dec 2019 15:28:55: #2 You can restart the process with --nomodel --extsize XXX with your choice or an arbitrary number. Nontheless, MACS will continute computing. INFO @ Thu, 05 Dec 2019 15:28:55: #3 Call peaks... INFO @ Thu, 05 Dec 2019 15:28:55: #3 Pre-compute pvalue-qvalue table... INFO @ Thu, 05 Dec 2019 15:29:22: #3 Call peaks for each chromosome... INFO @ Thu, 05 Dec 2019 15:29:38: #4 Write output xls file... /home/okishinya/chipatlas/results/dm3/SRX4117268/SRX4117268.20_peaks.xls INFO @ Thu, 05 Dec 2019 15:29:38: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/dm3/SRX4117268/SRX4117268.20_peaks.narrowPeak INFO @ Thu, 05 Dec 2019 15:29:38: #4 Write summits bed file... /home/okishinya/chipatlas/results/dm3/SRX4117268/SRX4117268.20_summits.bed INFO @ Thu, 05 Dec 2019 15:29:38: Done! pass1 - making usageList (12 chroms): 1 millis pass2 - checking and writing primary data (908 records, 4 fields): 3 millis CompletedMACS2peakCalling BedGraph に変換しました。 BigWig に変換中... BigWig に変換しました。