| Literature DB >> 19924719 |
Lisa J Martin1, Guimin Gao, Guolian Kang, Yixin Fang, Jessica G Woo.
Abstract
Genome-wide association studies employ hundreds of thousands of statistical tests to determine which regions of the genome may likely harbor disease-causing alleles. Such large-scale testing simultaneously requires stringent control over type I error and maintenance of sufficient power to detect true associations. These contradictory goals have led some researchers beyond Bonferroni correction of P-values to an exploration of methods to improve the detection of a few true effects in the presence of many unassociated loci. This article reviews how Genetic Analysis Workshop 16 Group 5 investigators proposed to adjust for multiple tests while simultaneously using information about the structure of the genome to improve the detection of true positives. (c) 2009 Wiley-Liss, Inc.Entities:
Mesh:
Year: 2009 PMID: 19924719 PMCID: PMC2908259 DOI: 10.1002/gepi.20469
Source DB: PubMed Journal: Genet Epidemiol ISSN: 0741-0395 Impact factor: 2.135