Article
A reference panel of 64,976 haplotypes for genotype imputation.
Nature genetics - 1 Oct 2016
McCarthy Shane, Das Sayantan, Kretzschmar Warren, Delaneau Olivier, Wood Andrew R, Teumer Alexander, Kang Hyun Min, Fuchsberger Christian, Danecek Petr, Sharp Kevin, Luo Yang, Sidore Carlo, Kwong Alan, Timpson Nicholas, Koskinen Seppo, Vrieze Scott, Scott Laura J, Zhang He, Mahajan Anubha, Veldink Jan, Peters Ulrike, Pato Carlos, van Duijn Cornelia M, Gillies Christopher E, Gandin Ilaria, Mezzavilla Massimo, Gilly Arthur, Cocca Massimiliano, Traglia Michela, Angius Andrea, Barrett Jeffrey C, Boomsma Dorrett, Branham Kari, Breen Gerome, Brummett Chad M, Busonero Fabio, Campbell Harry, Chan Andrew, Chen Sai, Chew Emily, Collins Francis S, Corbin Laura J, Smith George Davey, Dedoussis George, Dorr Marcus, Farmaki Aliki-Eleni, Ferrucci Luigi, Forer Lukas, Fraser Ross M, Gabriel Stacey, Levy Shawn, Groop Leif, Harrison Tabitha, Hattersley Andrew, Holmen Oddgeir L, Hveem Kristian, Kretzler Matthias, Lee James C, McGue Matt, Meitinger Thomas, Melzer David, Min Josine L, Mohlke Karen L, Vincent John B, Nauck Matthias, Nickerson Deborah, Palotie Aarno, Pato Michele, Pirastu Nicola, McInnis Melvin, Richards J Brent, Sala Cinzia, Salomaa Veikko, Schlessinger David, Schoenherr Sebastian, Slagboom P Eline, Small Kerrin, Spector Timothy, Stambolian Dwight, Tuke Marcus, Tuomilehto Jaakko, Van den Berg Leonard H, Van Rheenen Wouter, Volker Uwe, Wijmenga Cisca, Toniolo Daniela, Zeggini Eleftheria, Gasparini Paolo, Sampson Matthew G, Wilson James F, Frayling Timothy, de Bakker Paul I W, Swertz Morris A, McCarroll Steven, Kooperberg Charles, Dekker Annelot, Altshuler David, Willer Cristen, Iacono William, Ripatti Samuli, Soranzo Nicole, Walter Klaudia, Swaroop Anand, Cucca Francesco, Anderson Carl A, Myers Richard M, Boehnke Michael, McCarthy Mark I, Durbin Richard
Abstract excerpt
We describe a reference panel of 64,976 human haplotypes at 39,235,157 SNPs constructed using whole-genome sequence data from 20 studies of predominantly European ancestry. Using this resource leads to accurate genotype imputation at minor allele frequencies as low as 0.1% and a large increase in the number of SNPs tested in association studies, and it can help to discover and refine causal loci. We describe...
