Founder population-specific HapMap panel increases power in GWA studies through improved imputation accuracy and CNV tagging
Ida Surakka, Kati Kristiansson, Verneri Anttila, Michael Inouye, Chris Barnes, Loukas Moutsianas, Veikko Salomaa, Mark Daly, Aarno Palotie, Leena Peltonen, Samuli Ripatti
Genome Research | COLD SPRING HARBOR LAB PRESS, PUBLICATIONS DEPT | Published : 2010
Awarded by Wellcome Trust
Awarded by Center of Excellence for Complex Disease Genetics of the Academy of Finland
Awarded by Academy of Finland
This work was supported by the Wellcome Trust (WT089062/Z/09/Z, WT089061/Z/09/Z). L.P., S.R., and A.P. are supported by the Center of Excellence for Complex Disease Genetics of the Academy of Finland (grant nos. 213506 and 129680). L.P. is supported by the Biocentrum Helsinki Foundation and The Nordic Center of Excellence in Disease Genetics. V.S. is supported by the Academy of Finland (grant no. 129494), the Finnish Foundation for Cardiovascular Research, and the Sigrid Juselius Foundation. K.K. is supported by the Academy of Finland (grant no. 125973) and the Orion-Farmos Research Foundation. L.M. is supported by the EPSRC. V.A. is supported by the Finnish Cultural Foundation. We thank Peter Wagner for language revision of this manuscript.