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#' Given an input of cytobands, it outputs a list of genes that are present in the cytoband regions
#' @export
#' @param folder.name Name of output folder
#' @param cyto.cin4heatmapObj Output of the cytoband T test results
#' @param genome.ucsc Reference sequence
#' @param gene.annotations Information about CDS start and end positions, Gene names
#' @return Output files: The genes names present in the cytoband regions
#' @seealso See accompanying vignette for an end-to-end tutorial
#' @description Once the user has a list of cytobands of interest, one downstream application could
#' be to find the list of genes present in the cytoband regions. This \code{extract.genes.in.cyto.regions}
#' function can be used for this purpose. The following steps should be run before this function can
#' be called:
#' #Step 1 : Run cytoband CIN - using \code{run.cin.chr()}
#' #Step 2: Plot cytoband level heatmap - using \code{comp.heatmap()}
#' #Step 3: Go through heatmaps as select one appropriate threshold. Load the file.
#' #Step 4: Perform T test to find differentially expressed cytobands - using \code{ttest.cyto.cin.heatmap()}
#' #Step 5: Call this funtion to extract genes located in cytoband regions
#' #More details and tutorial are given in the accompanying vignette
#' @examples
#' #For this example, we load example T test output object
#'data("cyto.cin4heatmap")
#'data("hg18.ucsctrack") #load Hg 18 reference annotation file
#'data("geneAnno") #load Gene annotations file
#'extract.genes.in.cyto.regions(cyto.cin4heatmapObj =cyto.cin4heatmap,
#'genome.ucsc = hg18.ucsctrack, gene.annotations = geneAnno)
#######################################################################################################
"extract.genes.in.cyto.regions" <- function(cyto.cin4heatmapObj = NULL,
genome.ucsc = NULL,
gene.annotations = NULL,
folder.name = "output_genename") {
#browser()
if (is.null(cyto.cin4heatmapObj) || is.null(genome.ucsc) || is.null(gene.annotations)) {
stop("One of the inputs is NULL. Please enter input in the correct format")
}
if(is.matrix(gene.annotations)) {
## convert reference GRanges object into required format
ref.info <- process.reference.genome(genome.ucsc)
ref <- ref.info$cytobands
cyto.list = rownames(cyto.cin4heatmapObj)
gene.chrs = gene.annotations[, 1]
gene.start = as.numeric(gene.annotations[, 3])
gene.end = as.numeric(gene.annotations[, 4])
mark = rep(FALSE, nrow(gene.annotations))
cytoband_genes <- {
}
for (i in 1:length(cyto.list)) {
info = strsplit(cyto.list[i], "_")[[1]] #KB changed - to _ , changed cyto.list[1] to cyto.list[i]
chr = paste(info[1], info[2], sep = "")
cyto = info[3]
idx = (ref[, 1] == chr) & (ref[, 4] == cyto)
cur.cyto.start = ref[idx, 2]
cur.cyto.end = ref[idx, 3]
idx.chr = (gene.annotations[, 1] == chr)
idx.start = gene.start >= cur.cyto.start
idx.end = gene.end <= cur.cyto.end
idx.genes = idx.chr & idx.start & idx.end
mark = mark | idx.genes # KB changed || to |
# added by KB
geneNames <- unlist(gene.annotations[idx.genes, 5])
tempM <- cbind(cyto.list[i], geneNames)
cytoband_genes <- rbind(cytoband_genes, tempM)
colnames(cytoband_genes) <- c("Cytoband", "geneNames")
}
# browser()
out.genes = gene.annotations[mark, ]
dir.create(folder.name, showWarnings = FALSE)
filename1 <- paste(folder.name, "/", "out.genes.csv", sep = "")
filename2 <- paste(folder.name, "/", "cytoband_genes.csv", sep = "")
filename3 <- paste(folder.name, "/", "cytoband_genes.Rdata", sep = "")
write.csv(out.genes, filename1, row.names = FALSE)
write.csv(cytoband_genes, filename2, row.names = FALSE)
save(cytoband_genes, file = filename3)
} else {
stop("Input 'gene.annotations' must be a matrix")
}
}
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