annovar_annotate_region: Annotate variant regions

Description Usage Arguments Details Value

View source: R/annovar.R

Description

Annotate variant regions

Usage

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annovar_annotate_region(avinput.file, output.prefix,
  db.path = "/imbs/external_data/annotation_and_references/annovar/humandb",
  build = "hg19", exec = "annotate_variation.pl")

Arguments

avinput.file

[string]
The file name of the ANNOVAR input file.

output.prefix

[string]
The basename of the output files.

db.path

[string]
The path to the database files. Default is /imbs/external_data/annotation_and_references/annovar/humandb.

build

[string]
Human genome build code. Default is 'hg19'.

exec

[string]
Path to annotate_variation script.

Details

Use ANNOVAR to find if variants hit exons or hit intergenic regions, or hit introns, or hit a non-coding RNA genes.

Value

Captured system output as character vector.


imbs-hl/imbs documentation built on Sept. 6, 2019, 11:05 p.m.