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#' Cluster cytometry data using FlowSOM
#'
#' A function that cluster cytometry data using FlowSOM.
#' @param fcsFrame A flow frame.
#' @param excludeClusterParameters A vector specifying the name of markers not
#' to be used for clustering.
#' @param xdim An integer, defines the width of SOM
#' @param ydim An integer, defines the height of SOM
#' @param k An integer, defines the number of clusters to be identified by
#' flowSOM.
#' @param seed Set seed for reproducible results.
#' @return A list of clusters. Each cluster contains the ID of all cells that
#' belong to the cluster.
#' @examples
#' # Find fcs files
#' files=system.file("extdata",
#' "SDY420/ResultFiles/CyTOF_result",package="MetaCyto")
#' files=list.files(files,pattern="fcs$",full.names=TRUE)
#' # Preprocess
#' fcs = preprocessing(fcsFiles=files,assay ="CyTOF",b=1/8)
#' # cluster using flowSOM.MC
#' cluster_list=flowSOM.MC(fcsFrame=fcs,
#' excludeClusterParameters=c("Time","Cell_length"))
#' @importFrom FlowSOM ReadInput BuildSOM BuildMST metaClustering_consensus
#' @export
flowSOM.MC=function(fcsFrame,excludeClusterParameters,
xdim=10,ydim=10,k=40,seed = NULL){
set.seed(seed)
antibodies=markerFinder(fcsFrame)
excludeClusterParameters=toupper(excludeClusterParameters)
excludeClusterParameters=union(excludeClusterParameters,c("TIME","SAMPLE_ID"))
w=which(!antibodies%in%excludeClusterParameters)
fSOM <- FlowSOM::ReadInput(fcsFrame, transform = FALSE, scale = FALSE)
fSOM <- FlowSOM::BuildSOM(fSOM, colsToUse = w,
xdim = xdim, ydim = ydim)
fSOM <- FlowSOM::BuildMST(fSOM)
meta <- FlowSOM::metaClustering_consensus(fSOM$map$codes,k=k,seed = seed)
CL <- meta[fSOM$map$mapping[, 1]]
CL=lapply(unique(CL),function(x){which(CL==x)})
return(CL)
}
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