#' GenomicRangeToGeneName
#'
#' Return information for all of the genes in a genomic region.
#'
#' @param seqnames A \code{chr} containing the sequence (\emph{i.e.}
#' chromosome) name. Must match the chromosome name in the MSUv7 GFF,
#' \emph{e.g.} chromosome 1 == \code{'Chr1'}
#' @param start A \code{numeric} containing the starting coordinate on
#' \code{seqnames}
#' @param end A \code{numeric} containing the end coordinat on \code{seqnames}
#' @return Returns a \code{data.table} of annotated genes found in the MSUv7
#' GFF between \code{start} and \code{end} on chromosome \code{seqnames}.
#'
#' @seealso \code{LocToGeneName} for a description of the returned
#' \code{data.table}.
#'
#' @import data.table
#'
#' @export
# seqnames <- "Chr1"
# start <- 34365
# end <- 55475
GenomicRangeToGeneName <- function(seqnames, start, end){
my_range <- GenomicRanges::GRanges(
seqnames = seqnames,
ranges = IRanges::IRanges(
start = start,
end = end
),
strand = "*",
seqinfo = GenomicRanges::seqinfo(gff.exons))
my_exons <- as.data.table(
GenomicRanges::findOverlaps(gff.exons, my_range))
my_hits <- as.data.table(
gff.exons[my_exons[, queryHits]]
)
my_hits[, parent_transcript := unlist(Parent)]
my_hits[, gene := gsub("\\..+$", "", parent_transcript)]
my_hits[, LocToGeneName(unique(gene))]
}
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