Rare variant genotype imputation with thousands of study-specific whole-genome sequences: implications for cost-effective study designs
Giorgio Pistis(San Raffaele University of Rome), Serena Sanna(University Medical Center Groningen), Maristella Steri(Institute of Genetic and Biomedical Research), Maria Francesca Urru(Sardegna Ricerche (Italy)), William G. Iacono(University of Minnesota), Fabio Busonero(Institute of Genetic and Biomedical Research), Marco Marcelli(Baylor College of Medicine), Scott Vrieze(University of Colorado Boulder), Carlo Sidore(University of Michigan), Andrea Angius(Institute of Genetic and Biomedical Research), Andrea Maschio(Institute of Genetic and Biomedical Research), Antonella Mulas(Institute of Genetic and Biomedical Research), Christine Brennan(University of Michigan), Francesco Cucca(University of Sassari), Maristella Pitzalis(Institute of Genetic and Biomedical Research), Matt McGue(University of Minnesota), Fabrice Danjou(Institute of Genetic and Biomedical Research), Sandra Lai(Ospedale Microcitemico), Gonçalo R. Abecasis(Regeneron (United States)), David Schlessinger(National Institute on Aging), Chris M. Jones(Sardegna Ricerche (Italy)), Eleonora Porcu(Edinburgh Royal Infirmary), Robert H. Lyons(University of Michigan–Ann Arbor), Magdalena Żołędziewska(Institute of Genetic and Biomedical Research), Michael B. Miller(University of Minnesota), Hyun Min Kang(Regeneron (United States))
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