Nothing
Collapse <-
function(seqs){
## Collapse reads into haplotypes and frequencies
## seqs: a DNAStringSet with raw reads
# Read and sort the sequences.
seqso<-seqs
sqtbl <- sort(table(as.character(seqso)), decreasing=TRUE)
seqso <- names(sqtbl)
names(seqso) <- seq_len(length(seqso))
# Store the abundances
nr <- as.integer(sqtbl)
# Create an DNAStringSet or AAStringSet
if(is(seqs, "DNAStringSet")) seqso <- DNAStringSet(seqso)
if(is(seqs, "AAStringSet")) seqso <- AAStringSet(seqso)
# Return a list of two elements with the alignment
# and the abundances.
return(list(nr=nr, hseqs=seqso))
}
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