This function takes a merged ClinVar-sequencing dataset and returns an ancestry-stratified plot of allele frequencies
1 2 | var_plot_1000g(vcf)
var_plot_1000g(vcf, fraction = FALSE)
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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. |
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