# Simulates BM evolution more quickly.
# A trend can be simulated by mu!=0.
# mu=0 is standard BM; mu<0 downward trend; mu>0 upward trend.
# Bounds can be simulated by bounds=c(>-Inf,<Inf).
# Written by Liam J. Revell 2011
fastBM<-function(tree,a=0,mu=0,sig2=1,bounds=c(-Inf,Inf),internal=FALSE,nsim=1){
# some minor error checking
if(class(tree)!="phylo") stop("tree object must be of class 'phylo.'")
if(bounds[2]<bounds[1]){
warning("bounds[2] must be > bounds[1]. Simulating without bounds.")
bounds<-c(-Inf,Inf)
}
if(bounds[1]==-Inf&&bounds[2]==Inf) no.bounds=TRUE
else no.bounds=FALSE
if(a<bounds[1]||a>bounds[2]){
warning("a must be bounds[1]<a<bounds[2]. Setting a to midpoint of bounds.")
a<-bounds[1]+(bounds[2]-bounds[1])/2
}
if(sig2<0){
warning("sig2 must be > 0. Setting sig2 to 1.0.")
sig2=1.0
}
# function for reflection off bounds
reflect<-function(yy,bounds){
while(yy<bounds[1]||yy>bounds[2]){
if(yy<bounds[1]) yy<-2*bounds[1]-yy
if(yy>bounds[2]) yy<-2*bounds[2]-yy
}
return(yy)
}
# how many species?
n<-length(tree$tip)
# first simulate changes along each branch
x<-matrix(data=rnorm(n=length(tree$edge.length)*nsim,mean=rep(mu*tree$edge.length,nsim),sd=rep(sqrt(sig2*tree$edge.length),nsim)),length(tree$edge.length),nsim)
# now add them up
y<-array(0,dim=c(nrow(tree$edge),ncol(tree$edge),nsim))
for(i in 1:nrow(x)){
if(tree$edge[i,1]==(n+1))
y[i,1,]<-a
else
y[i,1,]<-y[match(tree$edge[i,1],tree$edge[,2]),2,]
y[i,2,]<-y[i,1,]+x[i,]
if(!no.bounds) y[i,2,]<-apply(as.matrix(y[i,2,]),1,function(yy) reflect(yy,bounds))
}
rm(x); x<-matrix(data=rbind(y[1,1,],as.matrix(y[,2,])),length(tree$edge.length)+1,nsim)
rownames(x)<-c(n+1,tree$edge[,2])
x<-as.matrix(x[as.character(1:(n+tree$Nnode)),])
rownames(x)[1:n]<-tree$tip.label
# return simulated data
if(internal==TRUE)
return(x[1:nrow(x),]) # include internal nodes
else
return(x[1:length(tree$tip.label),]) # tip nodes only
}
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