Job ID = 1294360 sra ファイルのダウンロード中... Read layout: PAIRED fastq に変換中... 2019-06-02T21:52:56 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 ) 2019-06-02T21:55:14 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 : 24,675,815 reads read : 49,351,630 reads written : 49,351,630 rm: cannot remove ‘[DSE]RR*’: No such file or directory 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: 01:03:27 24675815 reads; of these: 24675815 (100.00%) were paired; of these: 1085954 (4.40%) aligned concordantly 0 times 16965061 (68.75%) aligned concordantly exactly 1 time 6624800 (26.85%) aligned concordantly >1 times ---- 1085954 pairs aligned concordantly 0 times; of these: 152320 (14.03%) aligned discordantly 1 time ---- 933634 pairs aligned 0 times concordantly or discordantly; of these: 1867268 mates make up the pairs; of these: 1082780 (57.99%) aligned 0 times 502967 (26.94%) aligned exactly 1 time 281521 (15.08%) aligned >1 times 97.81% overall alignment rate Time searching: 01:03:27 Overall time: 01:03:27 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] 777684 / 23715172 = 0.0328 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 @ Mon, 03 Jun 2019 08:29:25: # Command line: callpeak -t /home/okishinya/chipatlas/results/dm3/SRX2612525/SRX2612525.bam -f BAM -g dm -n /home/okishinya/chipatlas/results/dm3/SRX2612525/SRX2612525.20 -q 1e-20 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/dm3/SRX2612525/SRX2612525.20 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/dm3/SRX2612525/SRX2612525.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 @ Mon, 03 Jun 2019 08:29:25: #1 read tag files... INFO @ Mon, 03 Jun 2019 08:29:25: #1 read treatment tags... INFO @ Mon, 03 Jun 2019 08:29:25: # Command line: callpeak -t /home/okishinya/chipatlas/results/dm3/SRX2612525/SRX2612525.bam -f BAM -g dm -n /home/okishinya/chipatlas/results/dm3/SRX2612525/SRX2612525.05 -q 1e-05 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/dm3/SRX2612525/SRX2612525.05 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/dm3/SRX2612525/SRX2612525.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 @ Mon, 03 Jun 2019 08:29:25: #1 read tag files... INFO @ Mon, 03 Jun 2019 08:29:25: #1 read treatment tags... INFO @ Mon, 03 Jun 2019 08:29:25: # Command line: callpeak -t /home/okishinya/chipatlas/results/dm3/SRX2612525/SRX2612525.bam -f BAM -g dm -n /home/okishinya/chipatlas/results/dm3/SRX2612525/SRX2612525.10 -q 1e-10 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/dm3/SRX2612525/SRX2612525.10 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/dm3/SRX2612525/SRX2612525.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 @ Mon, 03 Jun 2019 08:29:25: #1 read tag files... INFO @ Mon, 03 Jun 2019 08:29:25: #1 read treatment tags... INFO @ Mon, 03 Jun 2019 08:29:32: 1000000 INFO @ Mon, 03 Jun 2019 08:29:33: 1000000 INFO @ Mon, 03 Jun 2019 08:29:34: 1000000 INFO @ Mon, 03 Jun 2019 08:29:38: 2000000 INFO @ Mon, 03 Jun 2019 08:29:42: 2000000 INFO @ Mon, 03 Jun 2019 08:29:44: 2000000 INFO @ Mon, 03 Jun 2019 08:29:45: 3000000 INFO @ Mon, 03 Jun 2019 08:29:50: 3000000 INFO @ Mon, 03 Jun 2019 08:29:51: 4000000 INFO @ Mon, 03 Jun 2019 08:29:53: 3000000 INFO @ Mon, 03 Jun 2019 08:29:58: 5000000 INFO @ Mon, 03 Jun 2019 08:29:59: 4000000 INFO @ Mon, 03 Jun 2019 08:30:03: 4000000 INFO @ Mon, 03 Jun 2019 08:30:04: 6000000 INFO @ Mon, 03 Jun 2019 08:30:07: 5000000 INFO @ Mon, 03 Jun 2019 08:30:10: 7000000 INFO @ Mon, 03 Jun 2019 08:30:13: 5000000 INFO @ Mon, 03 Jun 2019 08:30:15: 6000000 INFO @ Mon, 03 Jun 2019 08:30:16: 8000000 INFO @ Mon, 03 Jun 2019 08:30:22: 6000000 INFO @ Mon, 03 Jun 2019 08:30:23: 9000000 INFO @ Mon, 03 Jun 2019 08:30:24: 7000000 INFO @ Mon, 03 Jun 2019 08:30:29: 10000000 INFO @ Mon, 03 Jun 2019 08:30:32: 8000000 INFO @ Mon, 03 Jun 2019 08:30:32: 7000000 INFO @ Mon, 03 Jun 2019 08:30:35: 11000000 INFO @ Mon, 03 Jun 2019 08:30:40: 9000000 INFO @ Mon, 03 Jun 2019 08:30:42: 8000000 INFO @ Mon, 03 Jun 2019 08:30:42: 12000000 INFO @ Mon, 03 Jun 2019 08:30:46: 10000000 INFO @ Mon, 03 Jun 2019 08:30:48: 13000000 INFO @ Mon, 03 Jun 2019 08:30:51: 9000000 INFO @ Mon, 03 Jun 2019 08:30:54: 11000000 INFO @ Mon, 03 Jun 2019 08:30:54: 14000000 INFO @ Mon, 03 Jun 2019 08:31:00: 15000000 INFO @ Mon, 03 Jun 2019 08:31:01: 10000000 INFO @ Mon, 03 Jun 2019 08:31:02: 12000000 INFO @ Mon, 03 Jun 2019 08:31:07: 16000000 INFO @ Mon, 03 Jun 2019 08:31:10: 11000000 INFO @ Mon, 03 Jun 2019 08:31:11: 13000000 INFO @ Mon, 03 Jun 2019 08:31:13: 17000000 INFO @ Mon, 03 Jun 2019 08:31:19: 14000000 INFO @ Mon, 03 Jun 2019 08:31:19: 18000000 INFO @ Mon, 03 Jun 2019 08:31:19: 12000000 INFO @ Mon, 03 Jun 2019 08:31:25: 19000000 INFO @ Mon, 03 Jun 2019 08:31:27: 15000000 INFO @ Mon, 03 Jun 2019 08:31:29: 13000000 INFO @ Mon, 03 Jun 2019 08:31:32: 20000000 INFO @ Mon, 03 Jun 2019 08:31:35: 16000000 INFO @ Mon, 03 Jun 2019 08:31:38: 21000000 INFO @ Mon, 03 Jun 2019 08:31:38: 14000000 INFO @ Mon, 03 Jun 2019 08:31:44: 17000000 INFO @ Mon, 03 Jun 2019 08:31:44: 22000000 INFO @ Mon, 03 Jun 2019 08:31:48: 15000000 INFO @ Mon, 03 Jun 2019 08:31:50: 23000000 INFO @ Mon, 03 Jun 2019 08:31:52: 18000000 INFO @ Mon, 03 Jun 2019 08:31:56: 24000000 INFO @ Mon, 03 Jun 2019 08:31:57: 16000000 INFO @ Mon, 03 Jun 2019 08:32:00: 19000000 INFO @ Mon, 03 Jun 2019 08:32:03: 25000000 INFO @ Mon, 03 Jun 2019 08:32:06: 17000000 INFO @ Mon, 03 Jun 2019 08:32:08: 20000000 INFO @ Mon, 03 Jun 2019 08:32:09: 26000000 INFO @ Mon, 03 Jun 2019 08:32:15: 27000000 INFO @ Mon, 03 Jun 2019 08:32:16: 18000000 INFO @ Mon, 03 Jun 2019 08:32:16: 21000000 INFO @ Mon, 03 Jun 2019 08:32:22: 28000000 INFO @ Mon, 03 Jun 2019 08:32:25: 22000000 INFO @ Mon, 03 Jun 2019 08:32:25: 19000000 INFO @ Mon, 03 Jun 2019 08:32:28: 29000000 INFO @ Mon, 03 Jun 2019 08:32:33: 23000000 INFO @ Mon, 03 Jun 2019 08:32:34: 30000000 INFO @ Mon, 03 Jun 2019 08:32:35: 20000000 INFO @ Mon, 03 Jun 2019 08:32:41: 31000000 INFO @ Mon, 03 Jun 2019 08:32:41: 24000000 INFO @ Mon, 03 Jun 2019 08:32:44: 21000000 INFO @ Mon, 03 Jun 2019 08:32:47: 32000000 INFO @ Mon, 03 Jun 2019 08:32:49: 25000000 INFO @ Mon, 03 Jun 2019 08:32:53: 33000000 INFO @ Mon, 03 Jun 2019 08:32:54: 22000000 INFO @ Mon, 03 Jun 2019 08:32:58: 26000000 INFO @ Mon, 03 Jun 2019 08:33:00: 34000000 INFO @ Mon, 03 Jun 2019 08:33:03: 23000000 INFO @ Mon, 03 Jun 2019 08:33:06: 27000000 INFO @ Mon, 03 Jun 2019 08:33:07: 35000000 INFO @ Mon, 03 Jun 2019 08:33:13: 24000000 INFO @ Mon, 03 Jun 2019 08:33:13: 36000000 INFO @ Mon, 03 Jun 2019 08:33:14: 28000000 INFO @ Mon, 03 Jun 2019 08:33:20: 37000000 INFO @ Mon, 03 Jun 2019 08:33:22: 25000000 INFO @ Mon, 03 Jun 2019 08:33:23: 29000000 INFO @ Mon, 03 Jun 2019 08:33:26: 38000000 INFO @ Mon, 03 Jun 2019 08:33:31: 30000000 INFO @ Mon, 03 Jun 2019 08:33:32: 26000000 INFO @ Mon, 03 Jun 2019 08:33:32: 39000000 INFO @ Mon, 03 Jun 2019 08:33:38: 40000000 INFO @ Mon, 03 Jun 2019 08:33:39: 31000000 INFO @ Mon, 03 Jun 2019 08:33:41: 27000000 INFO @ Mon, 03 Jun 2019 08:33:45: 41000000 INFO @ Mon, 03 Jun 2019 08:33:47: 32000000 INFO @ Mon, 03 Jun 2019 08:33:50: 28000000 INFO @ Mon, 03 Jun 2019 08:33:51: 42000000 INFO @ Mon, 03 Jun 2019 08:33:55: 33000000 INFO @ Mon, 03 Jun 2019 08:33:58: 43000000 INFO @ Mon, 03 Jun 2019 08:34:00: 29000000 INFO @ Mon, 03 Jun 2019 08:34:03: 34000000 INFO @ Mon, 03 Jun 2019 08:34:04: 44000000 INFO @ Mon, 03 Jun 2019 08:34:08: 30000000 INFO @ Mon, 03 Jun 2019 08:34:10: 35000000 INFO @ Mon, 03 Jun 2019 08:34:10: 45000000 INFO @ Mon, 03 Jun 2019 08:34:16: 31000000 INFO @ Mon, 03 Jun 2019 08:34:17: 46000000 INFO @ Mon, 03 Jun 2019 08:34:17: 36000000 INFO @ Mon, 03 Jun 2019 08:34:21: #1 tag size is determined as 50 bps INFO @ Mon, 03 Jun 2019 08:34:21: #1 tag size = 50 INFO @ Mon, 03 Jun 2019 08:34:21: #1 total tags in treatment: 22812608 INFO @ Mon, 03 Jun 2019 08:34:21: #1 user defined the maximum tags... INFO @ Mon, 03 Jun 2019 08:34:21: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Mon, 03 Jun 2019 08:34:22: #1 tags after filtering in treatment: 20932442 INFO @ Mon, 03 Jun 2019 08:34:22: #1 Redundant rate of treatment: 0.08 INFO @ Mon, 03 Jun 2019 08:34:22: #1 finished! INFO @ Mon, 03 Jun 2019 08:34:22: #2 Build Peak Model... INFO @ Mon, 03 Jun 2019 08:34:22: #2 looking for paired plus/minus strand peaks... INFO @ Mon, 03 Jun 2019 08:34:24: 32000000 INFO @ Mon, 03 Jun 2019 08:34:24: #2 number of paired peaks: 400 WARNING @ Mon, 03 Jun 2019 08:34:24: Fewer paired peaks (400) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 400 pairs to build model! INFO @ Mon, 03 Jun 2019 08:34:24: start model_add_line... INFO @ Mon, 03 Jun 2019 08:34:24: start X-correlation... INFO @ Mon, 03 Jun 2019 08:34:24: end of X-cor INFO @ Mon, 03 Jun 2019 08:34:24: #2 finished! INFO @ Mon, 03 Jun 2019 08:34:24: #2 predicted fragment length is 156 bps INFO @ Mon, 03 Jun 2019 08:34:24: #2 alternative fragment length(s) may be 156 bps INFO @ Mon, 03 Jun 2019 08:34:24: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/dm3/SRX2612525/SRX2612525.05_model.r INFO @ Mon, 03 Jun 2019 08:34:24: #3 Call peaks... INFO @ Mon, 03 Jun 2019 08:34:24: #3 Pre-compute pvalue-qvalue table... INFO @ Mon, 03 Jun 2019 08:34:25: 37000000 INFO @ Mon, 03 Jun 2019 08:34:32: 33000000 INFO @ Mon, 03 Jun 2019 08:34:32: 38000000 INFO @ Mon, 03 Jun 2019 08:34:39: 34000000 INFO @ Mon, 03 Jun 2019 08:34:40: 39000000 INFO @ Mon, 03 Jun 2019 08:34:47: 35000000 INFO @ Mon, 03 Jun 2019 08:34:47: 40000000 INFO @ Mon, 03 Jun 2019 08:34:55: 36000000 INFO @ Mon, 03 Jun 2019 08:34:56: 41000000 INFO @ Mon, 03 Jun 2019 08:35:03: 37000000 INFO @ Mon, 03 Jun 2019 08:35:04: 42000000 INFO @ Mon, 03 Jun 2019 08:35:12: 38000000 INFO @ Mon, 03 Jun 2019 08:35:13: 43000000 INFO @ Mon, 03 Jun 2019 08:35:20: #3 Call peaks for each chromosome... INFO @ Mon, 03 Jun 2019 08:35:21: 39000000 INFO @ Mon, 03 Jun 2019 08:35:22: 44000000 INFO @ Mon, 03 Jun 2019 08:35:30: 40000000 INFO @ Mon, 03 Jun 2019 08:35:31: 45000000 INFO @ Mon, 03 Jun 2019 08:35:39: 41000000 INFO @ Mon, 03 Jun 2019 08:35:40: 46000000 INFO @ Mon, 03 Jun 2019 08:35:46: #4 Write output xls file... /home/okishinya/chipatlas/results/dm3/SRX2612525/SRX2612525.05_peaks.xls INFO @ Mon, 03 Jun 2019 08:35:46: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/dm3/SRX2612525/SRX2612525.05_peaks.narrowPeak INFO @ Mon, 03 Jun 2019 08:35:46: #4 Write summits bed file... /home/okishinya/chipatlas/results/dm3/SRX2612525/SRX2612525.05_summits.bed INFO @ Mon, 03 Jun 2019 08:35:46: Done! pass1 - making usageList (15 chroms): 2 millis pass2 - checking and writing primary data (2915 records, 4 fields): 8 millis CompletedMACS2peakCalling INFO @ Mon, 03 Jun 2019 08:35:47: #1 tag size is determined as 50 bps INFO @ Mon, 03 Jun 2019 08:35:47: #1 tag size = 50 INFO @ Mon, 03 Jun 2019 08:35:47: #1 total tags in treatment: 22812608 INFO @ Mon, 03 Jun 2019 08:35:47: #1 user defined the maximum tags... INFO @ Mon, 03 Jun 2019 08:35:47: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Mon, 03 Jun 2019 08:35:48: #1 tags after filtering in treatment: 20932442 INFO @ Mon, 03 Jun 2019 08:35:48: #1 Redundant rate of treatment: 0.08 INFO @ Mon, 03 Jun 2019 08:35:48: #1 finished! INFO @ Mon, 03 Jun 2019 08:35:48: #2 Build Peak Model... INFO @ Mon, 03 Jun 2019 08:35:48: #2 looking for paired plus/minus strand peaks... INFO @ Mon, 03 Jun 2019 08:35:48: 42000000 INFO @ Mon, 03 Jun 2019 08:35:49: #2 number of paired peaks: 400 WARNING @ Mon, 03 Jun 2019 08:35:49: Fewer paired peaks (400) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 400 pairs to build model! INFO @ Mon, 03 Jun 2019 08:35:49: start model_add_line... INFO @ Mon, 03 Jun 2019 08:35:50: start X-correlation... INFO @ Mon, 03 Jun 2019 08:35:50: end of X-cor INFO @ Mon, 03 Jun 2019 08:35:50: #2 finished! INFO @ Mon, 03 Jun 2019 08:35:50: #2 predicted fragment length is 156 bps INFO @ Mon, 03 Jun 2019 08:35:50: #2 alternative fragment length(s) may be 156 bps INFO @ Mon, 03 Jun 2019 08:35:50: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/dm3/SRX2612525/SRX2612525.20_model.r INFO @ Mon, 03 Jun 2019 08:35:50: #3 Call peaks... INFO @ Mon, 03 Jun 2019 08:35:50: #3 Pre-compute pvalue-qvalue table... INFO @ Mon, 03 Jun 2019 08:35:56: 43000000 INFO @ Mon, 03 Jun 2019 08:36:04: 44000000 INFO @ Mon, 03 Jun 2019 08:36:12: 45000000 INFO @ Mon, 03 Jun 2019 08:36:20: 46000000 INFO @ Mon, 03 Jun 2019 08:36:26: #1 tag size is determined as 50 bps INFO @ Mon, 03 Jun 2019 08:36:26: #1 tag size = 50 INFO @ Mon, 03 Jun 2019 08:36:26: #1 total tags in treatment: 22812608 INFO @ Mon, 03 Jun 2019 08:36:26: #1 user defined the maximum tags... INFO @ Mon, 03 Jun 2019 08:36:26: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Mon, 03 Jun 2019 08:36:26: #1 tags after filtering in treatment: 20932442 INFO @ Mon, 03 Jun 2019 08:36:26: #1 Redundant rate of treatment: 0.08 INFO @ Mon, 03 Jun 2019 08:36:26: #1 finished! INFO @ Mon, 03 Jun 2019 08:36:26: #2 Build Peak Model... INFO @ Mon, 03 Jun 2019 08:36:26: #2 looking for paired plus/minus strand peaks... INFO @ Mon, 03 Jun 2019 08:36:28: #2 number of paired peaks: 400 WARNING @ Mon, 03 Jun 2019 08:36:28: Fewer paired peaks (400) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 400 pairs to build model! INFO @ Mon, 03 Jun 2019 08:36:28: start model_add_line... INFO @ Mon, 03 Jun 2019 08:36:28: start X-correlation... INFO @ Mon, 03 Jun 2019 08:36:28: end of X-cor INFO @ Mon, 03 Jun 2019 08:36:28: #2 finished! INFO @ Mon, 03 Jun 2019 08:36:28: #2 predicted fragment length is 156 bps INFO @ Mon, 03 Jun 2019 08:36:28: #2 alternative fragment length(s) may be 156 bps INFO @ Mon, 03 Jun 2019 08:36:28: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/dm3/SRX2612525/SRX2612525.10_model.r INFO @ Mon, 03 Jun 2019 08:36:28: #3 Call peaks... INFO @ Mon, 03 Jun 2019 08:36:28: #3 Pre-compute pvalue-qvalue table... INFO @ Mon, 03 Jun 2019 08:36:47: #3 Call peaks for each chromosome... INFO @ Mon, 03 Jun 2019 08:37:12: #4 Write output xls file... /home/okishinya/chipatlas/results/dm3/SRX2612525/SRX2612525.20_peaks.xls INFO @ Mon, 03 Jun 2019 08:37:12: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/dm3/SRX2612525/SRX2612525.20_peaks.narrowPeak INFO @ Mon, 03 Jun 2019 08:37:12: #4 Write summits bed file... /home/okishinya/chipatlas/results/dm3/SRX2612525/SRX2612525.20_summits.bed INFO @ Mon, 03 Jun 2019 08:37:13: Done! pass1 - making usageList (14 chroms): 2 millis pass2 - checking and writing primary data (1084 records, 4 fields): 5 millis CompletedMACS2peakCalling INFO @ Mon, 03 Jun 2019 08:37:25: #3 Call peaks for each chromosome... INFO @ Mon, 03 Jun 2019 08:37:50: #4 Write output xls file... /home/okishinya/chipatlas/results/dm3/SRX2612525/SRX2612525.10_peaks.xls INFO @ Mon, 03 Jun 2019 08:37:50: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/dm3/SRX2612525/SRX2612525.10_peaks.narrowPeak INFO @ Mon, 03 Jun 2019 08:37:50: #4 Write summits bed file... /home/okishinya/chipatlas/results/dm3/SRX2612525/SRX2612525.10_summits.bed INFO @ Mon, 03 Jun 2019 08:37:50: Done! pass1 - making usageList (15 chroms): 1 millis pass2 - checking and writing primary data (1841 records, 4 fields): 5 millis CompletedMACS2peakCalling BedGraph に変換しました。 BigWig に変換中... BigWig に変換しました。