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Check nucleotide sites for low frequency substitutions.
lowFreqSubs(x, min.freq = 3, motif.length = 10, ...)
a DNAbin object.
DNAbin
minimum frequency of base to be flagged.
length of motif around low frequency base to output.
arguments passed from other functions (ignored).
data.frame listing id, site number, and motif around low frequency base call.
# NOT RUN { data(dolph.haps) library(ape) lowFreqSubs(as.DNAbin(dolph.haps)) # }
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