Description Usage Arguments Details Value References See Also
View source: R/12_variant.annotation.R
A wrapper function to run table_annovar.pl in ANNOVAR
1 | table.annovar(fn.annovar, output.dir, sample.name, annovar.db, ref="hg38", protocol="refGene,cytoBand,genomicSuperDups,esp6500siv2_all,1000g2015aug_all,exac03,avsnp147,ljb26_all,cosmic70", protocol.type="g,r,r,f,f,f,f,f,f", nastring=".", run.cmd=TRUE, mc.cores=1)
|
fns.annovar |
Path to annovar files |
output.dir |
Output directory |
sample.name |
A character vector for the sample names |
annovar.db.dir |
Path to directory with ANNOVAR database |
ref |
A parameter value for -buildver in ANNOVAR. Specify the genome build version (default: hg38) |
protocol |
A parameter value for -protocol in ANNOVAR Database names in ANNOVAR (default: "refGene,cytoBand,genomicSuperDups,esp6500siv2_all,1000g2015aug_all,exac03,avsnp147,ljb26_all,cosmic70") |
protocol.type |
A parameter value for -operation in ANNOVAR. Strings separated by commas that specify the types of operation for each protocol (g: genome, r: region, f: filter, default="g,r,r,f,f,f,f,f,f") |
nastring |
A parameter value for -nastring in ANNOVAR. Strings to display when a score is not available (default: ".") |
run.cmd |
Whether to execute the command line (default=TRUE) |
mc.cores |
The number of cores to use. Must be at least one(default=1), and parallelization requires at least two cores. |
This function takes an input variant file (such as a VCF file) and generate a tab-delimited output file with many columns, each representing one set of annotations. Additionally, if the input is a VCF file, the program also generates a new output VCF file with the INFO field filled with annotation information.
CSV files from annovar format
ANNOVAR: functional annotation of genetic variants from high-throughput sequencing data
http://annovar.openbioinformatics.org/en/latest/user-guide/
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