Uses a genome object to find context and add it to the variant table
Source:R/annotate_variants.R
add_flank_to_variants.Rd
Uses a genome object to find context and add it to the variant table
Usage
add_flank_to_variants(
musica,
g,
flank_start,
flank_end,
build_table = TRUE,
overwrite = FALSE
)
Arguments
- musica
Input samples
- g
A BSgenome object indicating which genome reference the variants and their coordinates were derived from.
- flank_start
Start of flank area to add, can be positive or negative
- flank_end
End of flank area to add, can be positive or negative
- build_table
Automatically build a table using the annotation and add
- overwrite
Overwrite existing count table
Examples
data(musica_sbs96_tiny)
g <- select_genome("19")
add_flank_to_variants(musica_sbs96_tiny, g, 1, 2)
add_flank_to_variants(musica_sbs96_tiny, g, -2, -1)