# GENOME.class <- readData("\home\Alignments")
# GENOME.class
# GENOME.class <- F_ST.stats(GENOME.class)
# GENOME.class <- F_ST.stats(GENOME.class,list(1:4,5:10),subsites="syn")
# GENOME.class <- F_ST.stats(GENOME.class,list(c("seq1","seq5","seq3"),c("seq2","seq8")))
# show the result:
# get.F_ST(GENOME.class)
# get.F_ST(GENOME.class, pairwise=TRUE)
# get.diversity(GENOME.class, between=TRUE)
# GENOME.class@Pi --> population specific view
# GENOME.class@region.stats
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