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Function that expands biomarker evidence items with variant annotations

Usage

expand_biomarker_items(
  callset = NULL,
  variant_origin = "somatic",
  target_genes = NULL
)

Arguments

callset

list object with 'variant' and 'biomarker_evidence' data frames

variant_origin

'somatic' or 'germline'

target_genes

data frame with target genes of interest