A genomewide admixture mapping panel for hispanic/latino populations

被引:176
作者
Mao, Xianyun
Bigham, Abigail W.
Mei, Rui
Gutierrez, Gerardo
Weiss, Ken M.
Brutsaert, Tom D.
Leon-Velarde, Fabiola
Moore, Lorna G.
Vargas, Enrique
McKeigue, Paul M.
Shriver, Mark D.
Parra, Esteban J.
机构
[1] Penn State Univ, Dept Anthropol, University Pk, PA 16801 USA
[2] Affymetrix, Santa Clara, CA USA
[3] SUNY Albany, Dept Anthropol, Albany, NY 12222 USA
[4] Univ Peruana Cayetano Heredia, Dept Ciencias Biol & Fisiol, Lima, Peru
[5] Univ Colorado, Dept Hlth Behav Sci, Denver, CO 80202 USA
[6] Univ Colorado, Dept Anthropol, Denver, CO 80202 USA
[7] Univ Colorado, Hlth Sci Ctr, Denver, CO USA
[8] Univ Mayor San Andres, Inst Boliviano Biol Altura, La Paz, Bolivia
[9] Univ Coll Dublin, Conway Inst, Dublin 2, Ireland
[10] Univ Toronto, Dept Anthropol, Mississauga, ON L5L 1C6, Canada
关键词
D O I
10.1086/518564
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Admixture mapping ( AM) is a promising method for the identification of genetic risk factors for complex traits and diseases showing prevalence differences among populations. Efficient application of this method requires the use of a genomewide panel of ancestry-informative markers (AIMs) to infer the population of origin of chromosomal regions in admixed individuals. Genomewide AM panels with markers showing high frequency differences between West African and European populations are already available for disease-gene discovery in African Americans. However, no such a map is yet available for Hispanic/Latino populations, which are the result of two-way admixture between Native American and European populations or of three-way admixture of Native American, European, and West African populations. Here, we report a genomewide AM panel with 2,120 AIMs showing high frequency differences between Native American and European populations. The average intermarker genetic distance is similar to 1.7 cM. The panel was identified by genotyping, with the Affymetrix GeneChip Human Mapping 500K array, a population sample with European ancestry, a Mesoamerican sample comprising Maya and Nahua from Mexico, and a South American sample comprising Aymara/Quechua from Bolivia and Quechua from Peru. The main criteria for marker selection were both high information content for Native American/European ancestry (measured as the standardized variance of the allele frequencies, also known as "f value") and small frequency differences between the Mesoamerican and South American samples. This genomewide AM panel will make it possible to apply AM approaches in many admixed populations throughout the Americas.
引用
收藏
页码:1171 / 1178
页数:8
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