Nothing
fillX.G<-function(X.list, A, G, E1=0.005, E2=0.005, marker.type="MSW"){
mtype.numeric<-sum(c("MSC", "AFLP", "MSW", "SNP")%in%marker.type*c(1:4))
noff<-length(X.list$X)
ndam<-c(unlist(lapply(X.list$X,function(x){length(x$dam.id)})))
nsire<-c(unlist(lapply(X.list$X,function(x){length(x$sire.id)})))
offid<-as.numeric(names(X.list$X))-1
damid<-c(unlist(lapply(X.list$X,function(x){x$dam.id})))-1
sireid<-c(unlist(lapply(X.list$X,function(x){x$sire.id})))-1
nall<-sapply(A, length)
maxall<-max(nall)
nloci<-length(nall)
nind<-length(X.list$id)
A<-unlist(A)
if(any(A<1e-10)){
A[which(A<1e-10)]<-1e-8
}
if(is.null(E2)){
E1<-0.005
}
if(is.null(E2)){
E2<-0.005
}
G<-GtoC(G, (marker.type!="MSC" & marker.type!="MSW"))
X_design_G<-rep(0, sum(ndam*nsire))
output<-.C("fillXG",
as.integer(nind), # number of individuals sampled
as.integer(noff), # number of non-base (offspring) individuals
as.integer(ndam), # number of candidate dams per offspring
as.integer(nsire), # number of candidate sires per offspring
as.integer(nloci), # number of loci
as.integer(nall), # number of alleles per locus
as.integer(maxall), # number of alleles at most polymorhic locus
as.integer(offid), # offspring id
as.integer(damid), # candidate dam id's for each offspring
as.integer(sireid), # candidate sire id's for each offspring
as.double(X_design_G), # Mendelian transition probabilities dam and sire sampled
as.double(A), # starting allele frequencies
as.double(E1), # starting values of E1 and E2
as.double(E2),
as.integer(G), # starting true genotypes
as.integer(mtype.numeric)
)
startG<-1
startD<-1
startS<-1
for(i in 1:noff){
X.list$X[[i]]$G<-as.matrix(output[[11]][(startG-1)+1:(ndam[i]*nsire[i])])
startG<-startG+ndam[i]*nsire[i]
}
X.list
}
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