In particular we investigate the behaviour of the expected homozygosity (the probability that two randomly sampled genes are identical) in the transient and stationary phases, and how appropriate the Balding-Nichols model is for modelling allele frequency changes at different evolutionary time scales.
We find that the Balding-Nichols model is adequate for the pure drift model (no mutation), but the model is not sufficiently flexible for more general mutation structures. We suggest a new hierarchical Beta approximation for the Wright-Fisher model with a mutation model on the nucleotide level that distinguishes between transitions and transversions.