Job ID = 5720208 sra ファイルのダウンロード中... Read layout: PAIRED fastq に変換中... 2020-04-15T13:05:25 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 ) 2020-04-15T13:09:28 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 : 29,093,932 reads read : 58,187,864 reads written : 58,187,864 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: 00:50:26 29093932 reads; of these: 29093932 (100.00%) were paired; of these: 15637259 (53.75%) aligned concordantly 0 times 11247146 (38.66%) aligned concordantly exactly 1 time 2209527 (7.59%) aligned concordantly >1 times ---- 15637259 pairs aligned concordantly 0 times; of these: 7699221 (49.24%) aligned discordantly 1 time ---- 7938038 pairs aligned 0 times concordantly or discordantly; of these: 15876076 mates make up the pairs; of these: 13421227 (84.54%) aligned 0 times 963073 (6.07%) aligned exactly 1 time 1491776 (9.40%) aligned >1 times 76.93% overall alignment rate Time searching: 00:50:26 Overall time: 00:50:26 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 36 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] 2628670 / 20697652 = 0.1270 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 @ Wed, 15 Apr 2020 23:30:00: # Command line: callpeak -t /home/okishinya/chipatlas/results/ce10/SRX6619576/SRX6619576.bam -f BAM -g ce -n /home/okishinya/chipatlas/results/ce10/SRX6619576/SRX6619576.05 -q 1e-05 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/ce10/SRX6619576/SRX6619576.05 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/ce10/SRX6619576/SRX6619576.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 @ Wed, 15 Apr 2020 23:30:00: #1 read tag files... INFO @ Wed, 15 Apr 2020 23:30:00: #1 read treatment tags... INFO @ Wed, 15 Apr 2020 23:30:07: 1000000 INFO @ Wed, 15 Apr 2020 23:30:13: 2000000 INFO @ Wed, 15 Apr 2020 23:30:20: 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 @ Wed, 15 Apr 2020 23:30:26: 4000000 INFO @ Wed, 15 Apr 2020 23:30:29: # Command line: callpeak -t /home/okishinya/chipatlas/results/ce10/SRX6619576/SRX6619576.bam -f BAM -g ce -n /home/okishinya/chipatlas/results/ce10/SRX6619576/SRX6619576.10 -q 1e-10 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/ce10/SRX6619576/SRX6619576.10 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/ce10/SRX6619576/SRX6619576.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 @ Wed, 15 Apr 2020 23:30:29: #1 read tag files... INFO @ Wed, 15 Apr 2020 23:30:29: #1 read treatment tags... INFO @ Wed, 15 Apr 2020 23:30:33: 5000000 INFO @ Wed, 15 Apr 2020 23:30:36: 1000000 INFO @ Wed, 15 Apr 2020 23:30:40: 6000000 INFO @ Wed, 15 Apr 2020 23:30:43: 2000000 INFO @ Wed, 15 Apr 2020 23:30:47: 7000000 INFO @ Wed, 15 Apr 2020 23:30:50: 3000000 INFO @ Wed, 15 Apr 2020 23:30:54: 8000000 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 @ Wed, 15 Apr 2020 23:30:57: 4000000 INFO @ Wed, 15 Apr 2020 23:31:00: # Command line: callpeak -t /home/okishinya/chipatlas/results/ce10/SRX6619576/SRX6619576.bam -f BAM -g ce -n /home/okishinya/chipatlas/results/ce10/SRX6619576/SRX6619576.20 -q 1e-20 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/ce10/SRX6619576/SRX6619576.20 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/ce10/SRX6619576/SRX6619576.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 @ Wed, 15 Apr 2020 23:31:00: #1 read tag files... INFO @ Wed, 15 Apr 2020 23:31:00: #1 read treatment tags... INFO @ Wed, 15 Apr 2020 23:31:01: 9000000 INFO @ Wed, 15 Apr 2020 23:31:04: 5000000 INFO @ Wed, 15 Apr 2020 23:31:07: 1000000 INFO @ Wed, 15 Apr 2020 23:31:08: 10000000 INFO @ Wed, 15 Apr 2020 23:31:11: 6000000 INFO @ Wed, 15 Apr 2020 23:31:14: 2000000 INFO @ Wed, 15 Apr 2020 23:31:14: 11000000 INFO @ Wed, 15 Apr 2020 23:31:18: 7000000 INFO @ Wed, 15 Apr 2020 23:31:21: 3000000 INFO @ Wed, 15 Apr 2020 23:31:21: 12000000 INFO @ Wed, 15 Apr 2020 23:31:25: 8000000 INFO @ Wed, 15 Apr 2020 23:31:28: 4000000 INFO @ Wed, 15 Apr 2020 23:31:28: 13000000 INFO @ Wed, 15 Apr 2020 23:31:32: 9000000 INFO @ Wed, 15 Apr 2020 23:31:35: 5000000 INFO @ Wed, 15 Apr 2020 23:31:35: 14000000 INFO @ Wed, 15 Apr 2020 23:31:39: 10000000 INFO @ Wed, 15 Apr 2020 23:31:42: 6000000 INFO @ Wed, 15 Apr 2020 23:31:42: 15000000 INFO @ Wed, 15 Apr 2020 23:31:46: 11000000 INFO @ Wed, 15 Apr 2020 23:31:49: 7000000 INFO @ Wed, 15 Apr 2020 23:31:50: 16000000 INFO @ Wed, 15 Apr 2020 23:31:53: 12000000 INFO @ Wed, 15 Apr 2020 23:31:56: 8000000 INFO @ Wed, 15 Apr 2020 23:31:57: 17000000 INFO @ Wed, 15 Apr 2020 23:32:01: 13000000 INFO @ Wed, 15 Apr 2020 23:32:03: 9000000 INFO @ Wed, 15 Apr 2020 23:32:04: 18000000 INFO @ Wed, 15 Apr 2020 23:32:08: 14000000 INFO @ Wed, 15 Apr 2020 23:32:10: 10000000 INFO @ Wed, 15 Apr 2020 23:32:11: 19000000 INFO @ Wed, 15 Apr 2020 23:32:15: 15000000 INFO @ Wed, 15 Apr 2020 23:32:17: 11000000 INFO @ Wed, 15 Apr 2020 23:32:18: 20000000 INFO @ Wed, 15 Apr 2020 23:32:22: 16000000 INFO @ Wed, 15 Apr 2020 23:32:24: 12000000 INFO @ Wed, 15 Apr 2020 23:32:25: 21000000 INFO @ Wed, 15 Apr 2020 23:32:29: 17000000 INFO @ Wed, 15 Apr 2020 23:32:31: 13000000 INFO @ Wed, 15 Apr 2020 23:32:32: 22000000 INFO @ Wed, 15 Apr 2020 23:32:36: 18000000 INFO @ Wed, 15 Apr 2020 23:32:37: 14000000 INFO @ Wed, 15 Apr 2020 23:32:39: 23000000 INFO @ Wed, 15 Apr 2020 23:32:43: 19000000 INFO @ Wed, 15 Apr 2020 23:32:44: 15000000 INFO @ Wed, 15 Apr 2020 23:32:47: 24000000 INFO @ Wed, 15 Apr 2020 23:32:51: 20000000 INFO @ Wed, 15 Apr 2020 23:32:51: 16000000 INFO @ Wed, 15 Apr 2020 23:32:54: 25000000 INFO @ Wed, 15 Apr 2020 23:32:58: 21000000 INFO @ Wed, 15 Apr 2020 23:32:58: 17000000 INFO @ Wed, 15 Apr 2020 23:33:01: 26000000 INFO @ Wed, 15 Apr 2020 23:33:05: 22000000 INFO @ Wed, 15 Apr 2020 23:33:05: 18000000 INFO @ Wed, 15 Apr 2020 23:33:08: 27000000 INFO @ Wed, 15 Apr 2020 23:33:12: 23000000 INFO @ Wed, 15 Apr 2020 23:33:12: 19000000 INFO @ Wed, 15 Apr 2020 23:33:14: 28000000 INFO @ Wed, 15 Apr 2020 23:33:19: 24000000 INFO @ Wed, 15 Apr 2020 23:33:19: 20000000 INFO @ Wed, 15 Apr 2020 23:33:21: 29000000 INFO @ Wed, 15 Apr 2020 23:33:26: 25000000 INFO @ Wed, 15 Apr 2020 23:33:26: 21000000 INFO @ Wed, 15 Apr 2020 23:33:28: 30000000 INFO @ Wed, 15 Apr 2020 23:33:33: 26000000 INFO @ Wed, 15 Apr 2020 23:33:33: 22000000 INFO @ Wed, 15 Apr 2020 23:33:35: 31000000 INFO @ Wed, 15 Apr 2020 23:33:40: 27000000 INFO @ Wed, 15 Apr 2020 23:33:41: 23000000 INFO @ Wed, 15 Apr 2020 23:33:42: 32000000 INFO @ Wed, 15 Apr 2020 23:33:46: 28000000 INFO @ Wed, 15 Apr 2020 23:33:48: 24000000 INFO @ Wed, 15 Apr 2020 23:33:49: 33000000 INFO @ Wed, 15 Apr 2020 23:33:53: 29000000 INFO @ Wed, 15 Apr 2020 23:33:55: 25000000 INFO @ Wed, 15 Apr 2020 23:33:56: 34000000 INFO @ Wed, 15 Apr 2020 23:34:00: 30000000 INFO @ Wed, 15 Apr 2020 23:34:02: 26000000 INFO @ Wed, 15 Apr 2020 23:34:03: 35000000 INFO @ Wed, 15 Apr 2020 23:34:07: 31000000 INFO @ Wed, 15 Apr 2020 23:34:09: 27000000 INFO @ Wed, 15 Apr 2020 23:34:10: 36000000 INFO @ Wed, 15 Apr 2020 23:34:14: 32000000 INFO @ Wed, 15 Apr 2020 23:34:15: 28000000 INFO @ Wed, 15 Apr 2020 23:34:17: 37000000 INFO @ Wed, 15 Apr 2020 23:34:21: 33000000 INFO @ Wed, 15 Apr 2020 23:34:22: 29000000 INFO @ Wed, 15 Apr 2020 23:34:23: 38000000 INFO @ Wed, 15 Apr 2020 23:34:28: 34000000 INFO @ Wed, 15 Apr 2020 23:34:29: 30000000 INFO @ Wed, 15 Apr 2020 23:34:30: 39000000 INFO @ Wed, 15 Apr 2020 23:34:34: #1 tag size is determined as 150 bps INFO @ Wed, 15 Apr 2020 23:34:34: #1 tag size = 150 INFO @ Wed, 15 Apr 2020 23:34:34: #1 total tags in treatment: 11652694 INFO @ Wed, 15 Apr 2020 23:34:34: #1 user defined the maximum tags... INFO @ Wed, 15 Apr 2020 23:34:34: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Wed, 15 Apr 2020 23:34:34: #1 tags after filtering in treatment: 10204543 INFO @ Wed, 15 Apr 2020 23:34:34: #1 Redundant rate of treatment: 0.12 INFO @ Wed, 15 Apr 2020 23:34:34: #1 finished! INFO @ Wed, 15 Apr 2020 23:34:34: #2 Build Peak Model... INFO @ Wed, 15 Apr 2020 23:34:34: #2 looking for paired plus/minus strand peaks... INFO @ Wed, 15 Apr 2020 23:34:35: #2 number of paired peaks: 319 WARNING @ Wed, 15 Apr 2020 23:34:35: Fewer paired peaks (319) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 319 pairs to build model! INFO @ Wed, 15 Apr 2020 23:34:35: start model_add_line... INFO @ Wed, 15 Apr 2020 23:34:35: start X-correlation... INFO @ Wed, 15 Apr 2020 23:34:35: end of X-cor INFO @ Wed, 15 Apr 2020 23:34:35: #2 finished! INFO @ Wed, 15 Apr 2020 23:34:35: #2 predicted fragment length is 206 bps INFO @ Wed, 15 Apr 2020 23:34:35: #2 alternative fragment length(s) may be 206 bps INFO @ Wed, 15 Apr 2020 23:34:35: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/ce10/SRX6619576/SRX6619576.05_model.r WARNING @ Wed, 15 Apr 2020 23:34:35: #2 Since the d (206) calculated from paired-peaks are smaller than 2*tag length, it may be influenced by unknown sequencing problem! WARNING @ Wed, 15 Apr 2020 23:34:35: #2 You may need to consider one of the other alternative d(s): 206 WARNING @ Wed, 15 Apr 2020 23:34:35: #2 You can restart the process with --nomodel --extsize XXX with your choice or an arbitrary number. Nontheless, MACS will continute computing. INFO @ Wed, 15 Apr 2020 23:34:35: #3 Call peaks... INFO @ Wed, 15 Apr 2020 23:34:35: #3 Pre-compute pvalue-qvalue table... INFO @ Wed, 15 Apr 2020 23:34:35: 35000000 INFO @ Wed, 15 Apr 2020 23:34:36: 31000000 INFO @ Wed, 15 Apr 2020 23:34:42: 36000000 INFO @ Wed, 15 Apr 2020 23:34:43: 32000000 INFO @ Wed, 15 Apr 2020 23:34:49: 37000000 INFO @ Wed, 15 Apr 2020 23:34:50: 33000000 INFO @ Wed, 15 Apr 2020 23:34:55: 38000000 INFO @ Wed, 15 Apr 2020 23:34:56: #3 Call peaks for each chromosome... INFO @ Wed, 15 Apr 2020 23:34:57: 34000000 INFO @ Wed, 15 Apr 2020 23:35:02: 39000000 INFO @ Wed, 15 Apr 2020 23:35:04: 35000000 INFO @ Wed, 15 Apr 2020 23:35:05: #4 Write output xls file... /home/okishinya/chipatlas/results/ce10/SRX6619576/SRX6619576.05_peaks.xls INFO @ Wed, 15 Apr 2020 23:35:05: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/ce10/SRX6619576/SRX6619576.05_peaks.narrowPeak INFO @ Wed, 15 Apr 2020 23:35:05: #4 Write summits bed file... /home/okishinya/chipatlas/results/ce10/SRX6619576/SRX6619576.05_summits.bed INFO @ Wed, 15 Apr 2020 23:35:05: Done! INFO @ Wed, 15 Apr 2020 23:35:06: #1 tag size is determined as 150 bps INFO @ Wed, 15 Apr 2020 23:35:06: #1 tag size = 150 INFO @ Wed, 15 Apr 2020 23:35:06: #1 total tags in treatment: 11652694 INFO @ Wed, 15 Apr 2020 23:35:06: #1 user defined the maximum tags... INFO @ Wed, 15 Apr 2020 23:35:06: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Wed, 15 Apr 2020 23:35:06: #1 tags after filtering in treatment: 10204543 INFO @ Wed, 15 Apr 2020 23:35:06: #1 Redundant rate of treatment: 0.12 INFO @ Wed, 15 Apr 2020 23:35:06: #1 finished! INFO @ Wed, 15 Apr 2020 23:35:06: #2 Build Peak Model... INFO @ Wed, 15 Apr 2020 23:35:06: #2 looking for paired plus/minus strand peaks... INFO @ Wed, 15 Apr 2020 23:35:07: #2 number of paired peaks: 319 WARNING @ Wed, 15 Apr 2020 23:35:07: Fewer paired peaks (319) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 319 pairs to build model! INFO @ Wed, 15 Apr 2020 23:35:07: start model_add_line... INFO @ Wed, 15 Apr 2020 23:35:07: start X-correlation... INFO @ Wed, 15 Apr 2020 23:35:07: end of X-cor INFO @ Wed, 15 Apr 2020 23:35:07: #2 finished! INFO @ Wed, 15 Apr 2020 23:35:07: #2 predicted fragment length is 206 bps INFO @ Wed, 15 Apr 2020 23:35:07: #2 alternative fragment length(s) may be 206 bps INFO @ Wed, 15 Apr 2020 23:35:07: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/ce10/SRX6619576/SRX6619576.10_model.r WARNING @ Wed, 15 Apr 2020 23:35:07: #2 Since the d (206) calculated from paired-peaks are smaller than 2*tag length, it may be influenced by unknown sequencing problem! WARNING @ Wed, 15 Apr 2020 23:35:07: #2 You may need to consider one of the other alternative d(s): 206 WARNING @ Wed, 15 Apr 2020 23:35:07: #2 You can restart the process with --nomodel --extsize XXX with your choice or an arbitrary number. Nontheless, MACS will continute computing. INFO @ Wed, 15 Apr 2020 23:35:07: #3 Call peaks... INFO @ Wed, 15 Apr 2020 23:35:07: #3 Pre-compute pvalue-qvalue table... pass1 - making usageList (7 chroms): 0 millis pass2 - checking and writing primary data (466 records, 4 fields): 3 millis CompletedMACS2peakCalling INFO @ Wed, 15 Apr 2020 23:35:11: 36000000 INFO @ Wed, 15 Apr 2020 23:35:18: 37000000 INFO @ Wed, 15 Apr 2020 23:35:24: 38000000 INFO @ Wed, 15 Apr 2020 23:35:27: #3 Call peaks for each chromosome... INFO @ Wed, 15 Apr 2020 23:35:31: 39000000 INFO @ Wed, 15 Apr 2020 23:35:34: #1 tag size is determined as 150 bps INFO @ Wed, 15 Apr 2020 23:35:34: #1 tag size = 150 INFO @ Wed, 15 Apr 2020 23:35:34: #1 total tags in treatment: 11652694 INFO @ Wed, 15 Apr 2020 23:35:34: #1 user defined the maximum tags... INFO @ Wed, 15 Apr 2020 23:35:34: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Wed, 15 Apr 2020 23:35:34: #1 tags after filtering in treatment: 10204543 INFO @ Wed, 15 Apr 2020 23:35:34: #1 Redundant rate of treatment: 0.12 INFO @ Wed, 15 Apr 2020 23:35:34: #1 finished! INFO @ Wed, 15 Apr 2020 23:35:34: #2 Build Peak Model... INFO @ Wed, 15 Apr 2020 23:35:34: #2 looking for paired plus/minus strand peaks... INFO @ Wed, 15 Apr 2020 23:35:35: #2 number of paired peaks: 319 WARNING @ Wed, 15 Apr 2020 23:35:35: Fewer paired peaks (319) than 1000! Model may not be build well! Lower your MFOLD parameter may erase this warning. Now I will use 319 pairs to build model! INFO @ Wed, 15 Apr 2020 23:35:35: start model_add_line... INFO @ Wed, 15 Apr 2020 23:35:35: start X-correlation... INFO @ Wed, 15 Apr 2020 23:35:35: end of X-cor INFO @ Wed, 15 Apr 2020 23:35:35: #2 finished! INFO @ Wed, 15 Apr 2020 23:35:35: #2 predicted fragment length is 206 bps INFO @ Wed, 15 Apr 2020 23:35:35: #2 alternative fragment length(s) may be 206 bps INFO @ Wed, 15 Apr 2020 23:35:35: #2.2 Generate R script for model : /home/okishinya/chipatlas/results/ce10/SRX6619576/SRX6619576.20_model.r WARNING @ Wed, 15 Apr 2020 23:35:35: #2 Since the d (206) calculated from paired-peaks are smaller than 2*tag length, it may be influenced by unknown sequencing problem! WARNING @ Wed, 15 Apr 2020 23:35:35: #2 You may need to consider one of the other alternative d(s): 206 WARNING @ Wed, 15 Apr 2020 23:35:35: #2 You can restart the process with --nomodel --extsize XXX with your choice or an arbitrary number. Nontheless, MACS will continute computing. INFO @ Wed, 15 Apr 2020 23:35:35: #3 Call peaks... INFO @ Wed, 15 Apr 2020 23:35:35: #3 Pre-compute pvalue-qvalue table... INFO @ Wed, 15 Apr 2020 23:35:37: #4 Write output xls file... /home/okishinya/chipatlas/results/ce10/SRX6619576/SRX6619576.10_peaks.xls INFO @ Wed, 15 Apr 2020 23:35:37: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/ce10/SRX6619576/SRX6619576.10_peaks.narrowPeak INFO @ Wed, 15 Apr 2020 23:35:37: #4 Write summits bed file... /home/okishinya/chipatlas/results/ce10/SRX6619576/SRX6619576.10_summits.bed INFO @ Wed, 15 Apr 2020 23:35:37: Done! pass1 - making usageList (7 chroms): 0 millis pass2 - checking and writing primary data (321 records, 4 fields): 2 millis CompletedMACS2peakCalling INFO @ Wed, 15 Apr 2020 23:35:56: #3 Call peaks for each chromosome... INFO @ Wed, 15 Apr 2020 23:36:05: #4 Write output xls file... /home/okishinya/chipatlas/results/ce10/SRX6619576/SRX6619576.20_peaks.xls INFO @ Wed, 15 Apr 2020 23:36:05: #4 Write peak in narrowPeak format file... /home/okishinya/chipatlas/results/ce10/SRX6619576/SRX6619576.20_peaks.narrowPeak INFO @ Wed, 15 Apr 2020 23:36:05: #4 Write summits bed file... /home/okishinya/chipatlas/results/ce10/SRX6619576/SRX6619576.20_summits.bed INFO @ Wed, 15 Apr 2020 23:36:05: Done! pass1 - making usageList (6 chroms): 0 millis pass2 - checking and writing primary data (212 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。