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#' Simple simulation
#'
#' Simulate counts from a simple negative binomial distribution without
#' simulated library sizes, differential expression etc.
#'
#' @param params SimpleParams object containing simulation parameters.
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#' @param verbose logical. Whether to print progress messages
#' @param ... any additional parameter settings to override what is provided in
#'        \code{params}.
#'
#' @details
#' Gene means are simulated from a gamma distribution with
#' \code{shape = mean.shape} and \code{rate = mean.rate}. Counts are then
#' simulated from a negative binomial distribution with \code{mu = means} and
#' \code{size = 1 / counts.disp}. See \code{\link{SimpleParams}} for more
#' details of the parameters.
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#'
#' @return SCESet containing simulated counts
#' @examples
#' sim <- simpleSimulate()
#' # Override default parameters
#' sim <- simpleSimulate(nGenes = 1000, nCells = 50)
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#' @export
#' @importFrom stats rgamma rnbinom
simpleSimulate <- function(params = newSimpleParams(), verbose = TRUE, ...) {
    checkmate::assertClass(params, "SimpleParams")
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    params <- setParams(params, ...)

    # Set random seed
    seed <- getParam(params, "seed")
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    set.seed(seed)

    # Get the parameters we are going to use
    nCells <- getParam(params, "nCells")
    nGenes <- getParam(params, "nGenes")
    mean.shape <- getParam(params, "mean.shape")
    mean.rate <- getParam(params, "mean.rate")
    count.disp <- getParam(params, "count.disp")
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    if (verbose) {message("Simulating means...")}
    means <- rgamma(nGenes, shape = mean.shape, rate = mean.rate)

    if (verbose) {message("Simulating counts...")}
    counts <- matrix(rnbinom(nGenes * nCells, mu = means,
                             size = 1 / count.disp),
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                     nrow = nGenes, ncol = nCells)

    if (verbose) {message("Creating final SCESet...")}
    cell.names <- paste0("Cell", 1:nCells)
    gene.names <- paste0("Gene", 1:nGenes)

    rownames(counts) <- gene.names
    colnames(counts) <- cell.names
    phenos <- new("AnnotatedDataFrame", data = data.frame(Cell = cell.names))
    rownames(phenos) <- cell.names
    features <- new("AnnotatedDataFrame",
                    data = data.frame(Gene = gene.names, GeneMean = means))
    rownames(features) <- gene.names
    sim <- newSCESet(countData = counts, phenoData = phenos,
                     featureData = features)

    return(sim)
}