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Genetic basis of common human disease: insight into the role of nonsynonymous SNPs from genome-wide association studies
2011
Genome Biology
Genome Biology 2011, 12(Suppl 1):I18 Deep exome resequencing is a powerful approach for delineating patterns of protein-coding variation among genes, pathways, individuals and populations. We analyzed exome data from 2,440 individuals of European and African ancestry as part of the National Heart, Lung, and Blood Institute's Exome Project, the aim of which is to discover novel genes and mechanisms that contribute to heart, lung and blood disorders. Each exome was sequenced to a mean coverage of
doi:10.1186/gb-2011-12-s1-p10
fatcat:2c4ketwxg5bt7ge3pk3xfdwfae