Nothing
plotLGDistances.func <- function(object, allStrands, lg='all', labels=TRUE, state='all', alreadyOrdered=FALSE)
{
if(lg[1] == 'all')
{
linkageStrands <- data.frame(do.call(rbind, lapply(object, computeConsensus, allStrands)))
# rownames(linkageStrands) <- sapply(1:nrow(linkageStrands), function(x){paste('LG', x, ' (', length(object[[x]]), ')', sep='') })
}else{
linkageStrands <- allStrands[unlist(object[lg]),]
#For brevity, only report chromosome name, not split locations.
chrName <- as.character(matrix(unlist(strsplit(rownames(linkageStrands), ':')), ncol=2, byrow=TRUE)[,1])
chrName <- paste(chrName, '_', seq(1,nrow(linkageStrands)), sep='')
if(state == 'homo')
{
linkageStrands <- replace(linkageStrands, linkageStrands == 2, NA)
}else if(state == 'hetero'){
linkageStrands <- replace(linkageStrands, linkageStrands == 3, 1)
}
linkageStrands <- data.frame(linkageStrands)
linkageStrands <- data.frame(lapply(linkageStrands, function(x) factor(x, levels=c(1,2,3))))
rownames(linkageStrands) <- chrName
}
sim <- suppressWarnings(1-as.matrix(daisy(data.frame(linkageStrands))))
rownames(sim) <- rownames(linkageStrands)
colnames(sim) <- rownames(linkageStrands)
if(labels)
{
labRow=NULL
labCol=NULL
}else
{
labRow=rep('', nrow(sim))
labCol=rep('', ncol(sim))
}
labelScale <- min(1, 32/nrow(sim))
if(alreadyOrdered)
{
plotDen=FALSE
dend='none'
}else{
plotDen=TRUE
dend='both'
}
breaks <- (seq(0:11)-1)/11
cols <- colorRampPalette(c('#a50026','#ffffbf','#313695'))(11)
if(lg[1] == 'all')
{
chrLabels <- data.frame(1:length(object), names(object))
}else{
chrLabels <- melt(object[lg])
}
chrCols <- rainbow_hcl(length(unique(chrLabels[,2])), c=90, l=60)
names(chrCols) <- unique(chrLabels[,2])
rowCols <- chrCols[chrLabels[,2]]
colCols <- rowCols
heatmap.2(sim,
trace='none',
col=cols,
Rowv=plotDen,
Colv=plotDen,
dendrogram=dend,
labRow=labRow,
breaks=breaks,
labCol=labCol,
cexRow=labelScale,
cexCol=labelScale,
RowSideColors=rowCols,
ColSideColors=colCols,
main=paste('Distances of ', nrow(sim),' linkage groups', sep=''))
#legend("topright",
# legend=unique(names(rowCols)),
# fill=unique(rowCols),
# border=FALSE,
# bty="n",
# cex=0.7)
}
####################################################################################################
#' plotLGDistances -- plots a heatmap of the distances between linkage groups
#' @param object LinkageGroupList
#' @param allStrands StrandStateMatrix for all linkageGroups (usually reoriented by reorientStrandTable)
#' @param lg ='all' vector of integers to determine which linkage group(s) to plot. 'all' will calculate consensus
#' strand calls for all linkage groups and plot them side by side (default it 'all')
#' @param labels =TRUE if TRUE, contig names will be plotted on the axes
#' @param state string denoting whether only homozygous states should be used ('homo'; just WW vs CC), if a comparison should be made between
#' homozygous and heterozygous states only ('hetero'; just homo vs hetero), or if all three states ('all'; WW vs WC vs CC). Default is 'all'
#' @param alreadyOrdered if TRUE, the function will assume that the linkageGroupList is already ordered and not
#' create a dendrogram. Default is FALSE
#' @param ... additional parameters to pass to heatmap.2
#' @aliases plotLGDistances plotLGDistances,LinkageGroupList,LinkageGroupList-method
#' @example inst/examples/plotLGDistances.R
#' @return a heatplot of linkage group calls
#' @export
#' @importFrom cluster daisy
#' @importFrom gplots heatmap.2
#' @importFrom colorspace rainbow_hcl
#' @importFrom reshape2 melt
####################################################################################################
setMethod('plotLGDistances',
signature = signature(object='LinkageGroupList', allStrands = 'StrandStateMatrix'),
definition = plotLGDistances.func
)
Any scripts or data that you put into this service are public.
Add the following code to your website.
For more information on customizing the embed code, read Embedding Snippets.