Strategies for Genetic Studies of Complex Diseases
Author(s) -
Kai Wang,
Maja Bućan,
Struan F.A. Grant,
Gerard Schellenberg,
Hákon Hákonarson
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.2010.07.025
Subject(s) - genome wide association study , biology , international hapmap project , linkage disequilibrium , single nucleotide polymorphism , context (archaeology) , genetics , genetic association , computational biology , evolutionary biology , gene , genotype , paleontology
In a recent Essay published in Cell, McClellan and King discussed genetic heterogeneity and the potential role of rare genetic variants in complex human diseases (McClellan and King, 2010). These important issues, in particular the application of high-throughput sequencing techniques to discover disease genes, are highly relevant to genetics researchers. However, the authors allocated a substantial proportion of their efforts to being critical of the utility of genome-wide association studies (GWAS).
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