get_snv: Get single nucleotide variants (SNVs)
In Bio-Core/BioCore.Annotation: BioCore Variant Annotation Package
Description
Usage
Arguments
Value
Author(s)
Description
A method to filter mutations from ANNOVAR output. Limiting mutations to single nucleotide variants and removing indels.
Usage
1
Arguments
data
dataframe containing mutation output from the BioCore SNV pipeline
Value
Returns a dataframe with indels removed.
Author(s)
Richard J. de Borja
Bio-Core/BioCore.Annotation documentation built on Feb. 3, 2020, 6:01 p.m.
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Description Usage Arguments Value Author(s)
Description
A method to filter mutations from ANNOVAR output. Limiting mutations to single nucleotide variants and removing indels.
Usage
1 |
Arguments
data |
dataframe containing mutation output from the BioCore SNV pipeline |
Value
Returns a dataframe with indels removed.
Author(s)
Richard J. de Borja
R Package Documentation
Browse R Packages
We want your feedback!
Note that we can't provide technical support on individual packages. You should contact the package authors for that.
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