Workflow of FamSeq.

Abstract

<p>We use a pedigree file and a file that includes the likelihood () as the input to estimate the posterior probability () for each variant genotype. (E-S: Elston-Stewart algorithm; BN: Bayesian network method; BN-GPU: The computer needs a GPU card installed to run the GPU version of the Bayesian network method; MCMC: Markov chain Monte Carlo method; VCF: variant call format.)</p