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Chunk #35 — Discussion and prospects

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A second generation human haplotype map of over 3.1 million SNPs.
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The International HapMap Project has been instrumental in making well-powered, large-scale, genome-wide association studies a reality. It is now clear that the HapMap can be a useful resource for the design and analysis of disease association studies in populations across the world50-53. Furthermore, the decreasing costs and increasing SNP density of standard genotyping panels mean that the focus of attention in disease association studies is shifting from candidate gene approaches towards genome-wide analyses. Alongside developments in technology, new statistical methodologies aimed at improving aspects of analysis, such as genotype calling21,54, the identification of and correction for population stratification and relatedness55,56, and imputation of untyped variants21-23, are increasing the accuracy and reliability of genome-wide association studies.