#' Read Beatson bed formatted RNA-Seq file
#'
#' \code{read_rna_beatson} reads a file containing promoter annotation data
#' together with gene expression levels from RNA-Seq experiments using the
#' \code{\link[data.table]{fread}} function.
#'
#' @inheritParams read_bs_encode_haib
#'
#' @return A \code{\link[GenomicRanges]{GRanges}} object if \code{is_GRanges} is
#' TRUE, otherwise a \code{\link[data.table]{data.table}} object.
#'
#' The GRanges object contains three additional metadata columns: \itemize{
#' \item \code{id}: IDs of each gene promoter. \item
#' \code{gene_name}: Gene name. \item \code{gene_fpkm}: Expression level in
#' FPKM. } These columns can be accessed as follows:
#' \code{granges_object$id}
#'
#' @author C.A.Kapourani \email{C.A.Kapourani@@ed.ac.uk}
#'
#'
#' @export
read_rna_beatson <- function(file, chr_discarded = NULL, is_GRanges = TRUE){
message("Reading file ", file, " ...")
rna_data <- data.table::fread(input = file,
sep = "\t",
header = TRUE,
col.names = c("chr", "start", "end", "strand",
"gene_name", "id",
"gene_fpkm"))
# Remove selected chromosomes -------------------------------
rna_data <- .discard_chr(x = rna_data, chr_discarded = chr_discarded)
# Sorting data -----------------------------------------------
# With order priority: 1. chr, 2. start, 3. strand
message("Sorting RNA-Seq data ...")
rna_data <- rna_data[order(rna_data$chr, rna_data$start, rna_data$strand)]
if (is_GRanges){
# Create a GRanges object -----------------------------------
message("Creating GRanges object ...")
rna_data <- GenomicRanges::GRanges(seqnames = rna_data$chr,
strand = rna_data$strand,
ranges = IRanges::IRanges(start = rna_data$start,
end = rna_data$end),
id = rna_data$id,
gene_name = rna_data$gene_name,
gene_fpkm = rna_data$gene_fpkm)
}
message("Finished reading RNA-Seq file!\n")
return(rna_data)
}
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