X-Git-Url: https://git.donarmstrong.com/?p=ape.git;a=blobdiff_plain;f=R%2Fvcv.phylo.R;h=294b7673004dd2210bd2ddc8f9175379ec49827e;hp=2473280424f7545ba9ae08e8be20bf422c538958;hb=48681c35f7904c17b064de9c6bf96d84581e9e52;hpb=e9f75370481c37eb9d3d811ce7494f818b423136 diff --git a/R/vcv.phylo.R b/R/vcv.phylo.R index 2473280..294b767 100644 --- a/R/vcv.phylo.R +++ b/R/vcv.phylo.R @@ -1,8 +1,8 @@ -## vcv.phylo.R (2009-11-19) +## vcv.phylo.R (2012-02-09) ## Phylogenetic Variance-Covariance or Correlation Matrix -## Copyright 2002-2009 Emmanuel Paradis +## Copyright 2002-2012 Emmanuel Paradis ## This file is part of the R-package `ape'. ## See the file ../COPYING for licensing issues. @@ -12,39 +12,41 @@ vcv <- function(phy, ...) UseMethod("vcv") vcv.phylo <- function(phy, model = "Brownian", corr = FALSE, ...) { if (is.null(phy$edge.length)) - stop("the tree has no branch lengths") - - foo <- function(node, var, endofclade) { - ## First, get the extent of clade descending - ## from `node' in the matrix `edge': - from <- which(phy$edge[, 1] == node) - to <- c(from[-1] - 1, endofclade) - ## Get the #'s of the descendants of `node': - desc <- phy$edge[from, 2] - ## The variance of each of these is easy: - vcv[desc, desc] <<- var + phy$edge.length[from] - nd <- length(desc) - ## The variance of `node' is equal to the covariance of - ## each possible pair among its descendant clades. - for (i in 1:(nd - 1)) - for (j in (i + 1):nd) - for (k in phy$edge[from[i]:to[i], 2]) - for (l in phy$edge[from[j]:to[j], 2]) - vcv[k, l] <<- vcv[l, k] <<- var - for (i in 1:nd) { - if (desc[i] <= n) next - foo(desc[i], vcv[desc[i], desc[i]], to[i]) + stop("the tree has no branch lengths") + + pp <- prop.part(phy) + + phy <- reorder(phy, "pruningwise") + + n <- length(phy$tip.label) + e1 <- phy$edge[, 1] + e2 <- phy$edge[, 2] + EL <- phy$edge.length + + ## xx: vecteur donnant la distance d'un noeud + ## ou d'un tip à partir de la racine + ## (same than in is.ultrametric) + xx <- numeric(n + phy$Nnode) + + vcv <- matrix(0, n, n) + + ## the loop below starts from the bottom of the edge matrix, so + ## from the root + + for (i in length(e1):1) { + var.cur.node <- xx[e1[i]] + xx[e2[i]] <- var.cur.node + EL[i] # sets the variance + j <- i - 1L + while (e1[j] == e1[i] && j > 0) { + left <- if (e2[j] > n) pp[[e2[j] - n]] else e2[j] + right <- if (e2[i] > n) pp[[e2[i] - n]] else e2[i] + vcv[left, right] <- vcv[right, left] <- var.cur.node # sets the covariance + j <- j - 1L } } - phy <- reorder(phy) - n <- length(phy$tip.label) - n.node <- phy$Nnode - N <- n.node + n - vcv <- matrix(0, N, N) - foo(n + 1, 0, dim(phy$edge)[1]) + diag(vcv) <- xx[1:n] - vcv <- vcv[1:n, 1:n] if (corr) { ## This is inspired from the code of `cov2cor' (2005-09-08): M <- vcv @@ -52,7 +54,9 @@ vcv.phylo <- function(phy, model = "Brownian", corr = FALSE, ...) vcv[] <- Is * M * rep(Is, each = n) vcv[1 + 0:(n - 1)*(n + 1)] <- 1 } - rownames(vcv) <- colnames(vcv) <- phy$tip.label + + dimnames(vcv)[1:2] <- list(phy$tip.label) + vcv }