var_plot_1000g: Compute and Plot Aggregate Allele Frequencies for 1000...

Description Usage Arguments

Description

This function takes a merged ClinVar-sequencing dataset and returns an ancestry-stratified plot of allele frequencies

Usage

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var_plot_1000g(vcf)
var_plot_1000g(vcf, fraction = FALSE)

Arguments

vcf

data.frame; clinvaR-processed VCF from 1000 Genomes. Defaults to importing from genes (if present).

fraction

logical; if TRUE, plots fraction with a finding. If FALSE, plots total counts.


jamesdiao/clinvaR documentation built on May 18, 2019, 11:19 a.m.