Job ID = 4289152 sra ファイルのダウンロード中... Read layout: SINGLE fastq に変換中... spots read : 10,699,720 reads read : 21,399,440 reads written : 10,699,720 reads 0-length : 10,699,720 spots read : 10,706,152 reads read : 21,412,304 reads written : 10,706,152 reads 0-length : 10,706,152 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: 00:02:49 21405872 reads; of these: 21405872 (100.00%) were unpaired; of these: 13318754 (62.22%) aligned 0 times 5134866 (23.99%) aligned exactly 1 time 2952252 (13.79%) aligned >1 times 37.78% overall alignment rate Time searching: 00:02:49 Overall time: 00:02:49 マッピングが完了しました。 samtools でBAM に変換中... [samopen] SAM header is present: 17 sequences. [bam_rmdupse_core] 3419830 / 8087118 = 0.4229 in library ' ' BAM に変換しました。 Bed ファイルを作成中... INFO @ Tue, 10 Dec 2019 13:51:17: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/SRX6616767/SRX6616767.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/SRX6616767/SRX6616767.05 -q 1e-05 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/SRX6616767/SRX6616767.05 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/SRX6616767/SRX6616767.bam'] # control file = None # effective genome size = 1.21e+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 @ Tue, 10 Dec 2019 13:51:17: #1 read tag files... INFO @ Tue, 10 Dec 2019 13:51:17: #1 read treatment tags... INFO @ Tue, 10 Dec 2019 13:51:24: 1000000 INFO @ Tue, 10 Dec 2019 13:51:31: 2000000 INFO @ Tue, 10 Dec 2019 13:51:38: 3000000 INFO @ Tue, 10 Dec 2019 13:51:45: 4000000 INFO @ Tue, 10 Dec 2019 13:51:46: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/SRX6616767/SRX6616767.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/SRX6616767/SRX6616767.10 -q 1e-10 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/SRX6616767/SRX6616767.10 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/SRX6616767/SRX6616767.bam'] # control file = None # effective genome size = 1.21e+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 @ Tue, 10 Dec 2019 13:51:46: #1 read tag files... INFO @ Tue, 10 Dec 2019 13:51:46: #1 read treatment tags... INFO @ Tue, 10 Dec 2019 13:51:49: #1 tag size is determined as 50 bps INFO @ Tue, 10 Dec 2019 13:51:49: #1 tag size = 50 INFO @ Tue, 10 Dec 2019 13:51:49: #1 total tags in treatment: 4667288 INFO @ Tue, 10 Dec 2019 13:51:49: #1 user defined the maximum tags... INFO @ Tue, 10 Dec 2019 13:51:49: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Tue, 10 Dec 2019 13:51:49: #1 tags after filtering in treatment: 4667288 INFO @ Tue, 10 Dec 2019 13:51:49: #1 Redundant rate of treatment: 0.00 INFO @ Tue, 10 Dec 2019 13:51:49: #1 finished! INFO @ Tue, 10 Dec 2019 13:51:49: #2 Build Peak Model... INFO @ Tue, 10 Dec 2019 13:51:49: #2 looking for paired plus/minus strand peaks... INFO @ Tue, 10 Dec 2019 13:51:50: #2 number of paired peaks: 30 WARNING @ Tue, 10 Dec 2019 13:51:50: Too few paired peaks (30) so I can not build the model! Broader your MFOLD range parameter may erase this error. If it still can't build the model, we suggest to use --nomodel and --extsize 147 or other fixed number instead. WARNING @ Tue, 10 Dec 2019 13:51:50: Process for pairing-model is terminated! cut: /home/okishinya/chipatlas/results/sacCer3/SRX6616767/SRX6616767.05_peaks.narrowPeak: No such file or directory pass1 - making usageList (0 chroms): 2 millis needLargeMem: trying to allocate 0 bytes (limit: 17179869184) rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX6616767/SRX6616767.05_model.r’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX6616767/SRX6616767.05_*.xls’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX6616767/SRX6616767.05_peaks.narrowPeak’: No such file or directory CompletedMACS2peakCalling INFO @ Tue, 10 Dec 2019 13:51:53: 1000000 INFO @ Tue, 10 Dec 2019 13:52:00: 2000000 INFO @ Tue, 10 Dec 2019 13:52:06: 3000000 BedGraph に変換中... INFO @ Tue, 10 Dec 2019 13:52:13: 4000000 INFO @ Tue, 10 Dec 2019 13:52:15: # Command line: callpeak -t /home/okishinya/chipatlas/results/sacCer3/SRX6616767/SRX6616767.bam -f BAM -g 12100000 -n /home/okishinya/chipatlas/results/sacCer3/SRX6616767/SRX6616767.20 -q 1e-20 # ARGUMENTS LIST: # name = /home/okishinya/chipatlas/results/sacCer3/SRX6616767/SRX6616767.20 # format = BAM # ChIP-seq file = ['/home/okishinya/chipatlas/results/sacCer3/SRX6616767/SRX6616767.bam'] # control file = None # effective genome size = 1.21e+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 @ Tue, 10 Dec 2019 13:52:15: #1 read tag files... INFO @ Tue, 10 Dec 2019 13:52:15: #1 read treatment tags... INFO @ Tue, 10 Dec 2019 13:52:18: #1 tag size is determined as 50 bps INFO @ Tue, 10 Dec 2019 13:52:18: #1 tag size = 50 INFO @ Tue, 10 Dec 2019 13:52:18: #1 total tags in treatment: 4667288 INFO @ Tue, 10 Dec 2019 13:52:18: #1 user defined the maximum tags... INFO @ Tue, 10 Dec 2019 13:52:18: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Tue, 10 Dec 2019 13:52:18: #1 tags after filtering in treatment: 4667288 INFO @ Tue, 10 Dec 2019 13:52:18: #1 Redundant rate of treatment: 0.00 INFO @ Tue, 10 Dec 2019 13:52:18: #1 finished! INFO @ Tue, 10 Dec 2019 13:52:18: #2 Build Peak Model... INFO @ Tue, 10 Dec 2019 13:52:18: #2 looking for paired plus/minus strand peaks... INFO @ Tue, 10 Dec 2019 13:52:18: #2 number of paired peaks: 30 WARNING @ Tue, 10 Dec 2019 13:52:18: Too few paired peaks (30) so I can not build the model! Broader your MFOLD range parameter may erase this error. If it still can't build the model, we suggest to use --nomodel and --extsize 147 or other fixed number instead. WARNING @ Tue, 10 Dec 2019 13:52:18: Process for pairing-model is terminated! cut: /home/okishinya/chipatlas/results/sacCer3/SRX6616767/SRX6616767.10_peaks.narrowPeak: No such file or directory pass1 - making usageList (0 chroms): 1 millis needLargeMem: trying to allocate 0 bytes (limit: 17179869184) rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX6616767/SRX6616767.10_model.r’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX6616767/SRX6616767.10_*.xls’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX6616767/SRX6616767.10_peaks.narrowPeak’: No such file or directory CompletedMACS2peakCalling INFO @ Tue, 10 Dec 2019 13:52:23: 1000000 INFO @ Tue, 10 Dec 2019 13:52:31: 2000000 INFO @ Tue, 10 Dec 2019 13:52:41: 3000000 INFO @ Tue, 10 Dec 2019 13:52:48: 4000000 INFO @ Tue, 10 Dec 2019 13:52:53: #1 tag size is determined as 50 bps INFO @ Tue, 10 Dec 2019 13:52:53: #1 tag size = 50 INFO @ Tue, 10 Dec 2019 13:52:53: #1 total tags in treatment: 4667288 INFO @ Tue, 10 Dec 2019 13:52:53: #1 user defined the maximum tags... INFO @ Tue, 10 Dec 2019 13:52:53: #1 filter out redundant tags at the same location and the same strand by allowing at most 1 tag(s) INFO @ Tue, 10 Dec 2019 13:52:53: #1 tags after filtering in treatment: 4667288 INFO @ Tue, 10 Dec 2019 13:52:53: #1 Redundant rate of treatment: 0.00 INFO @ Tue, 10 Dec 2019 13:52:53: #1 finished! INFO @ Tue, 10 Dec 2019 13:52:53: #2 Build Peak Model... INFO @ Tue, 10 Dec 2019 13:52:53: #2 looking for paired plus/minus strand peaks... INFO @ Tue, 10 Dec 2019 13:52:53: #2 number of paired peaks: 30 WARNING @ Tue, 10 Dec 2019 13:52:53: Too few paired peaks (30) so I can not build the model! Broader your MFOLD range parameter may erase this error. If it still can't build the model, we suggest to use --nomodel and --extsize 147 or other fixed number instead. WARNING @ Tue, 10 Dec 2019 13:52:53: Process for pairing-model is terminated! cut: /home/okishinya/chipatlas/results/sacCer3/SRX6616767/SRX6616767.20_peaks.narrowPeak: No such file or directory pass1 - making usageList (0 chroms): 1 millis needLargeMem: trying to allocate 0 bytes (limit: 17179869184) rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX6616767/SRX6616767.20_model.r’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX6616767/SRX6616767.20_*.xls’: No such file or directory rm: cannot remove ‘/home/okishinya/chipatlas/results/sacCer3/SRX6616767/SRX6616767.20_peaks.narrowPeak’: No such file or directory CompletedMACS2peakCalling BedGraph に変換しました。 BigWig に変換中... BigWig に変換しました。