This method builds a dataframe representing the mutation.
Details
The dataframe has the columns chr
, chr_pos
, ref
, alt
,
type
(i.e., "SNV
" and "indel
"), and cause
.
Examples
snv <- SNV("X", 20002, "T", "A")
snv$get_dataframe()
#> chr chr_pos allele ref alt type cause
#> 1 X 20002 random A T SNV <NA>