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##' @title Export network for Cytoscape
##' @description Export nodes and edges of ce network for
##' \strong{Cytoscape} visualization
##' @param ceNetwork a dataframe generated from \code{\link{gdcCEAnalysis}}
##' @param net one of \code{'nodes'} and \code{'edges'}
##' @return A dataframe of nodes or edges
##' @export
##' @author Ruidong Li and Han Qu
##' @examples
##' ####### ceRNA network analysis #######
##' ceOutput <- data.frame(lncRNAs=c('ENSG00000242125','ENSG00000242125',
##' 'ENSG00000245532'),
##' Genes=c('ENSG00000043355','ENSG00000109586',
##' 'ENSG00000144355'),
##' miRNAs=c('hsa-miR-340-5p','hsa-miR-340-5p',
##' 'hsa-miR-320b,hsa-miR-320d,
##' hsa-miR-320c,hsa-miR-320a'),
##' Counts=c(1,1,4), stringsAsFactors=FALSE)
##' ####### Export edges #######
##' edges <- gdcExportNetwork(ceNetwork=ceOutput, net='edges')
##'
##' ####### Export nodes #######
##' \dontrun{nodes <- gdcExportNetwork(ceNetwork=ceOutput, net='nodes')}
gdcExportNetwork <- function(ceNetwork, net) {
mirs <- unlist(strsplit(ceNetwork$miRNAs, ',', fixed=TRUE))
fromNode <- rep(c(ceNetwork$lncRNAs,ceNetwork$Genes),
times=rep(as.numeric(ceNetwork$Counts),2))
toNode <- rep(mirs, 2)
altNode1Name <- ensembl2symbolFun(fromNode)
edges <- data.frame(fromNode, toNode, altNode1Name,
stringsAsFactors = FALSE)
#filter <- duplicated(edges)
#edges <- edges[-filter,]
edges <- unique(edges)
nodeTable1 <- table(edges$fromNode)
nodeTable2 <- table(edges$toNode)
symbol <- c(ensembl2symbolFun(names(nodeTable1)), names(nodeTable2))
type <- c(ifelse(names(nodeTable1) %in% ceNetwork$lncRNAs, 'lnc', 'pc'),
rep('mir', length(nodeTable2)))
nodes <- data.frame(gene=c(names(nodeTable1), names(nodeTable2)),
symbol, type, numInteractions=as.numeric(c(nodeTable1, nodeTable2)))
if (net=='nodes') {
return (nodes)
} else if (net=='edges') {
return (edges)
}
}
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