McKeigue Paul M
Conway Institute, University College Dublin, Belfield, Dublin 4, Ireland.
Am J Hum Genet. 2005 Jan;76(1):1-7. doi: 10.1086/426949. Epub 2004 Nov 11.
Admixture mapping extends to human populations the principles that underlie linkage analysis of an experimental cross. For detecting genes that contribute to ethnic variation in disease risk, admixture mapping has greater statistical power than family-linkage studies. In comparison with association studies, admixture mapping requires far fewer markers to search the genome and is less affected by allelic heterogeneity. Statistical-analysis programs for admixture mapping are now available, and a genomewide panel of markers for admixture mapping in populations formed by West African-European admixture has been assembled. Some of the remaining technical challenges include the ability to ensure that the statistical methods are robust and to develop marker panels for other admixed populations. Where admixed populations and panels of markers informative for ancestry are available, admixture mapping can be applied to localize genes that contribute to ethnic variation in any measurable trait.
混合映射将实验杂交连锁分析的基本原理扩展到了人类群体。对于检测导致疾病风险存在种族差异的基因,混合映射比家系连锁研究具有更强的统计效力。与关联研究相比,混合映射在全基因组搜索中所需的标记物要少得多,并且受等位基因异质性的影响较小。目前已有用于混合映射的统计分析程序,并且已经构建了一个全基因组范围的标记物面板,用于西非 - 欧洲混合形成的群体中的混合映射。剩下的一些技术挑战包括确保统计方法稳健的能力,以及为其他混合群体开发标记物面板。在有混合群体和对祖先有信息价值的标记物面板的情况下,混合映射可用于定位导致任何可测量性状出现种族差异的基因。