Validity of tagging SNPs across populations for association studies

13Citations
Citations of this article
21Readers
Mendeley users who have this article in their library.
Get full text

Abstract

Recent advances in high throughput genotyping technologies will allow large-scale association studies to disentangle the genetic basis of human common diseases. Currently, a large-scale genotyping effort is being carried out by the HapMap project and the outcome of this project is expected to help researchers in their efforts to understand how genetic variation influences susceptibility to disease. However, there is some controversy on whether this huge public effort will be of value for those populations not studied in the HapMap project. Here, we present simulation results based on the empirical distribution of linkage disequilibrium (LD) on a large chromosomal region (10 Mb) on human chromosome 201,2 for two European and two Asian populations. These results show that statistical power to detect associations does not depend on the population were SNP tagging was performed. © 2006 Nature Publishing Group. All rights reserved.

Author supplied keywords

Cite

CITATION STYLE

APA

Tenesa, A., & Dunlop, M. G. (2006). Validity of tagging SNPs across populations for association studies. European Journal of Human Genetics, 14(3), 357–363. https://doi.org/10.1038/sj.ejhg.5201554

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free