'alignment.mle.remove'<-
function(path_raxml = "raxmlHPC", seqfiles, contreefile)
{
reftreefile = paste(seqfiles,".reftree",sep="")
contree = read.tree(contreefile)
spnames=contree$tip.label
for(i in 1:length(seqfiles))
{
genename=read.dna.seq(seqfiles[i],format="phylip")$name
delname=spnames[which(is.na(match(spnames,genename)==1))]
write.tree(drop.tip(contree,tip=delname),reftreefile[i])
}
for(i in 1:length(seqfiles))
{
command=paste(path_raxml," -s ",seqfiles[i]," -n ", seqfiles[i]," -mGTRGAMMA -p ",floor(runif(1)*3536219+45497),sep="")
try(system(command))
}
for(i in 1:length(seqfiles))
{
x=read.tree(reftreefile[i])
y=read.tree(paste("RAxML_bestTree.",seqfiles[i],sep=""))
ntip=length(x$tip.label)
w=order(x$edge[,2])
ref_length=(x$edge.length[w])[1:ntip]
ref_length=ref_length[order(x$tip.label)]
name = x$tip.label[order(x$tip.label)]
w=order(y$edge[,2])
fit_length=(y$edge.length[w])[1:ntip]
fit_length=fit_length[order(y$tip.label)]
ratio=fit_length[1:ntip]/ref_length[1:ntip]
if(length(which(ratio>5))>0)
{
data=read.dna.seq(seqfiles[i],format="phylip")
delseq=match(name[which(ratio>5)],data$name)
write.dna.seq(data$seq[-delseq,],data$name[-delseq],file=paste(seqfiles[i],".final",sep=""),format="phylip")
}else{
try(system(paste("cp ",seqfiles[i], " ", paste(seqfiles[i],".final",sep=""))))
}
}
}
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