Nothing
SortByMutations <-
function(bseqs, nr){
## Sort haplotypes by differences and abundances
## seqs: a DNAStringSet with haplotypes
## w: a vector of haplotype counts
if(!is(bseqs, "DNAStringSet") & !is(bseqs, "AAStringSet"))
stop("The input object must be DNAStringSet or AAStringSet\n")
if(length(bseqs) != length(nr))
stop("The input objects must have the same length \n")
# Compute the differences between the master and the haplotypes.
master <- bseqs[which.max(nr)]
psa <- pairwiseAlignment(pattern=bseqs, subject=master)
nm <- nmismatch(psa)
tnm <- table(nm)
# Order the sequences by the number of mutations
o <- order(nm)
bseqs <- bseqs[o]
nr <- nr[o]
nm <- nm[o]
# Number of order inside each number of mutations
isq <- unlist(sapply(seq_len(length(tnm)), function(i) seq_len(tnm[i])))
# Order by descendent frequency for each number of mutations
for(i in as.integer(names(tnm))){
idx <- which(nm == i)
o <- order(nr[idx], decreasing=TRUE)
bseqs[idx] <- bseqs[idx[o]]
nr[idx] <- nr[idx[o]]
}
# Compute relative frequency
frq <- round(nr/sum(nr)*100,2)
# Set a name to each haplotype
nms <- paste("Hpl", nm, sprintf("%04d",isq), sep="_")
names(bseqs) <- nms
return(list(bseqs=bseqs, nr=nr, nm=nm))
}
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