#' Build metacell oblect
#' Wrapper that inits and builds metacell object from count matrix
#'
#' @param sc.counts single-cell count matrix (genes x cells)
#' @param proj.name project_name parameter in \link[metacell]
#' @param genes.to.use genes to use ti build metacell
#' @param mc.k.knn k in kNN single-cell network in metacell
#' @param MC.T_vm cutoff to select HVG in metacell
#' @param MC.folder folder to store metacell files
#' @param min_mc_size minimum size of metacell (used to vary graining level)
#' @param p_resamp
#'
#' @return metacell::scdb_mc - like output with some additional information stored as a list
#' @export
#'
build_MC <- function(
sc.counts,
proj.name,
genes.to.use = NULL, # NULL == all genes
mc.k.knn = 100,
MC.T_vm = 0.08,
MC.folder = "MC",
min_mc_size = 20,
p_resamp = 0.75, n_resamp = 500, mc.alpha = 2, mc.K = 30,
verbose = FALSE
){
SuperCellBM::init_mc(mc.dir = MC.folder)
mc.bknn <- SuperCellBM::mc_build_cgraph(
ge.mtrx = as.matrix(sc.counts),
genes.to.use = genes.to.use,
k.knn = mc.k.knn,
T_vm = MC.T_vm,
project_name = proj.name,
balanced.Knn = T,
return.igraph = F,
verbose = verbose)
mc <- mc_build_mc(mc.bknn, min_mc_size = min_mc_size, p_resamp = p_resamp,
n_resamp = n_resamp, mc.K = mc.K, mc.alpha = mc.alpha)
}
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