Return a consensus sequence from set of aligned sequences,
introducing IUPAC ambiguity codes where necessary.
Usage
createConsensus(x, ignore.gaps = FALSE)
Arguments
x
a '>gtypes object with aligned sequences or a list of
aligned DNA sequences.
ignore.gaps
logical. Ignore gaps at a site when creating consensus.
If TRUE, then bases with a gap are removed before consensus is
calculated. If FALSE and a gap is present, then the result is a gap.