gene.variants.fmi: Apply NLP to genomic reports to extract gene variants (CNVs)...

Description Usage Arguments Value

View source: R/gene.variants.fmi.R

Description

'gene.variants.fmi()' provides natural language processing tools to abstract gene variants data from foundation medicine genomic reports

Usage

1
gene.variants.fmi(data = dplyr::tibble(Results = readr::clipboard()))

Arguments

data

The data frame of the genomic report of interest. This can be copied to the Clipboard from the EHR report by "selecting all" and then "copy". That is the default. If you don't use the clipboard function, you can use a data frame of the text file. The single column data frame should be labeled "Results". Required.

Value

a data frame with two columns: variables (the redcap variable names) and results (the data to be imported in to redcap)


TheMillerLab/genetex documentation built on Dec. 18, 2021, 4:09 p.m.