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ReadAmplSeqs <-
function(flnm, type="DNA"){
## Read amplicon aligned sequences
## flnm: path to the fasta file that contains the reads.
## type: DNA for nucletide sequences or
## AA for amino acid sequences.
if(type!="AA" & type!= "DNA") stop("Check the type input \n")
# Load the reads as AAStringSet or DNAStringSet:
if (type == "AA") seqs <- readAAStringSet(flnm)
if (type == "DNA") seqs <- readDNAStringSet(flnm)
# Store in a different object the reported abundances.
nr <- vapply(names(seqs), function(str) strsplit(str, split="\\|")[[1]][2],
character(1))
nr <- as.numeric(nr)
nr[is.na(nr)] <- 1
# Return a list with two elements: the alignment and the frequency
return(list(nr=nr, hseqs=seqs))
}
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