Successes of Genome-wide Association Studies
Author(s) -
Robert J. Klein,
Xing Xu,
Semanti Mukherjee,
Jason Willis,
James E. Hayes
Publication year - 2010
Publication title -
cell
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 26.304
H-Index - 776
eISSN - 1097-4172
pISSN - 0092-8674
DOI - 10.1016/j.cell.2010.07.026
Subject(s) - genome wide association study , biology , missing heritability problem , linkage disequilibrium , genetic association , disease , genetics , population , heritability , population stratification , allele , computational biology , haplotype , genetic variants , single nucleotide polymorphism , genotype , gene , demography , medicine , pathology , sociology
In a recent Essay in Cell, McClellan and King argue that genomic resequencing rather than genome-wide association studies (GWAS) will be necessary to understand the genetic basis of common disease (McClellan and King, 2010). Like the authors, we too are excited about the potential for emerging sequencing technologies to facilitate discoveries that explain the missing heritability of common diseases. However, we disagree with the implication that GWAS have not been successful to date. Instead, we propose that insofar as the goal of these studies is to understand the etiology of heritable diseases, GWAS have provided numerous tantalizing clues for us biologists to decipher.
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