#' Plot allelic ratio result as forest
#'
#' Draw a forest plot to visualized cell type specific
#' allelic ratio estimator and confidence interval.
#' It is based on the \pkg{forestplot}-package`s \code{forestplot} function.
#'
#' @param sce A SingleCellExperiment containing colData
#' allelic ratio estimator in the third column
#' and last two column is the confidence interval.
#' @param genepoi the gene position index or gene name vector that want to be plotted.
#' Ordered by increased cell type svalue.
#' Default is the top 40 genes that has minimum svalue in any cell type
#' or all genes if number of genes smaller than 40.
#' @param ctpoi the cell type position index that want to be plotted.
#' @param showtext indicate whether show the svalue information along the forestplot.
#' @param xticks argument as described in \code{\link[forestplot]{forestplot}}
#' @param boxsize Override the default box size based on precision
#' @param xlab x-axis label. Default is "Allelic Ratio"
#' @param col Set the colors for all the elements. See
#' \code{\link[forestplot]{fpColors}} for details
#' @param grid If you want a discrete gray dashed grid
#' at the level of the ticks
#' you can set this parameter to TRUE.
#' If you set the parameter to a vector of values lines will be drawn at the
#' corresponding positions.
#' If you want to specify the \code{\link[grid]{gpar}} of the lines
#' then either directly pass a \code{\link[grid]{gpar}} object
#' or set the gp attribute e.g.
#' \code{attr(line_vector, "gp") <- }
#' \code{\link[grid]{gpar}}\code{(lty=2, col = "red")}
#' @param ... Passsed on the other argument in
#' \code{\link[forestplot]{forestplot}}.
#'
#' @return generates a forest plot
#'
#' @seealso \code{\link[forestplot]{forestplot}},
#' \code{\link[forestplot]{fpColors}},
#' \code{\link[forestplot]{fpShapesGp}}, \code{\link[forestplot]{fpLegend}}
#'
#' @examples
#' sce <- makeSimulatedData()
#' sce <- preprocess(sce)
#' sce <- geneCluster(sce, G = 1:4)
#' sce_sub <- wilcoxExt(sce, genecluster = 1)
#' sce_sub <- allelicRatio(sce_sub)
#' makeForest(sce_sub, showtext = TRUE)
#'
#' # if want to change some properties, like ticks position
#' library(forestplot)
#' xticks <- seq(from = 0, to = 1, by = 0.25)
#' xtlab <- rep(c(TRUE, FALSE), length.out = length(xticks))
#' attr(xticks, "labels") <- xtlab
#' genepoi <- paste0("gene", seq_len(5))
#' ctpoi <- c(1, 3)
#' makeForest(sce_sub, genepoi, ctpoi,
#' xticks = xticks,
#' col = fpColors(box = c("blue", "red", "black", "darkgreen"))
#' )
#' @import grid
#' @import forestplot
#' @importFrom utils head
#'
#' @export
makeForest <- function(sce, genepoi, ctpoi = seq_len(nlevels(sce$x)), showtext = FALSE, xticks, boxsize = .25,
xlab = "Allelic Ratio", col,
grid = structure(seq(0.1, 0.9, 0.1),
gp = gpar(lty = 2, col = "#CCCCFF")
), ...) {
qual_col_pals <- brewer.pal.info[brewer.pal.info$category == "qual", ]
col_vector <- unlist(mapply(brewer.pal, qual_col_pals$maxcolors, rownames(qual_col_pals)))
if (missing(xticks)) {
xticks <- seq(from = 0, to = 1, by = 0.1)
xtlab <- rep(c(TRUE, FALSE, TRUE, FALSE, FALSE), length.out = length(xticks))
attr(xticks, "labels") <- xtlab
}
if (missing(col)) {
col <- fpColors(box = col_vector[seq_len(length(ctpoi))])
}
ar <- rowData(sce)[, c(grep("svalue", colnames(rowData(sce)), value = TRUE))] %>% `colnames<-`(levels(sce$x))
if (showtext) {
forest_text <- data.frame(`Gene` = rownames(sce), ar[, ctpoi])
} else {
forest_text <- data.frame(Gene = rownames(sce)) %>% `rownames<-`(rownames(ar))
}
if (missing(genepoi)) {
smin <- apply(apply(ar, 2, as.numeric), 1, min)
genepoi <- head(order(smin), min(40, nrow(sce)))
}
forest_text <- rbind(colnames(forest_text), forest_text[genepoi, ] %>% as.data.frame())
message("svalue shown in columns per cell type")
forestplot::forestplot(forest_text,
is.summary = c(TRUE, rep(FALSE, nrow(forest_text) - 1)),
hrzl_lines = list("2" = gpar(lty = 2)),
line.margin = .1, # We need to add this to avoid crowding
legend = levels(sce$x)[ctpoi], grid = grid,
txt_gp = fpTxtGp(
label = list(gpar(cex = 0.8), gpar(cex = 0.8, col = "#703C3C")),
ticks = gpar(cex = 0.9), xlab = gpar(cex = 0.9)
),
boxsize = boxsize, graphwidth = unit(15, "cm"),
mean = rbind(rep(NA, length(ctpoi)), rowData(sce)[genepoi, c(grep("ar_", colnames(rowData(sce)), value = TRUE))[ctpoi]] %>% as.matrix()),
lower = rbind(rep(NA, length(ctpoi)), rowData(sce)[genepoi, c(grep("lower_", colnames(rowData(sce)), value = TRUE))[ctpoi]] %>% as.matrix()),
upper = rbind(rep(NA, length(ctpoi)), rowData(sce)[genepoi, c(grep("upper_", colnames(rowData(sce)), value = TRUE))[ctpoi]] %>% as.matrix()),
clip = c(0.01, 1), xticks = xticks, ref = 0.5,
col = col, xlab = xlab
)
}
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