Title
A genomewide admixture map for latino populations
Date Issued
01 January 2007
Access level
open access
Resource Type
journal article
Author(s)
Price A.L.
Patterson N.
Yu F.
Cox D.R.
Waliszewska A.
McDonald G.J.
Tandon A.
Schirmer C.
Neubauer J.
Bedoya G.
Duque C.
Villegas A.
Bortolini M.C.
Salzano F.M.
Tello-Ruiz M.
Riba L.
Aguilar-Salinas C.A.
Canizales-Quinteros S.
Menjivar M.
Klitz W.
Henderson B.
Haiman C.A.
Winkler C.
Tusie-Luna T.
Ruiz-Linares A.
Reich D.
Publisher(s)
Cell Press
Abstract
Admixture mapping is an economical and powerful approach for localizing disease genes in populations of recently mixed ancestry and has proven successful in African Americans. The method holds equal promise for Latinos, who typically inherit a mix of European, Native American, and African ancestry. However, admixture mapping in Latinos has not been practical because of the lack of a map of ancestry-informative markers validated in Native American and other populations. To address this, we screened multiple databases, containing millions of markers, to identify 4,186 markers that were putatively informative for determining the ancestry of chromosomal segments in Latino populations. We experimentally validated each of these markers in at least 232 new Latino, European, Native American, and African samples, and we selected a subset of 1,649 markers to form an admixture map. An advantage of our strategy is that we focused our map on markers distinguishing Native American from other ancestries and restricted it to markers with very similar frequencies in Europeans and Africans, which decreased the number of markers needed and minimized the possibility of false disease associations. We evaluated the effectiveness of our map for localizing disease genes in four Latino populations from both North and South America. © 2007 by The American Society of Human Genetics. All rights reserved.
Start page
1024
End page
1036
Volume
80
Issue
6
Language
English
OCDE Knowledge area
Genética humana Antropología
Scopus EID
2-s2.0-34250894969
PubMed ID
Source
American Journal of Human Genetics
ISSN of the container
00029297
Sponsor(s)
We thank Itsik Peer for assistance with the MEC 100K data, The Broad Institute Center for Genotyping and Analysis, George Ayodo and Courtney Montague for assistance with genotyping, Andrew Kirby for assistance with figure 5 , and Maribel Rodriguez, Phabiola Herrera, Giovanni Poletti, Sijia Wang, and David E. Ruiz for assistance with DNA samples. A.L.P. is supported by a Ruth Kirschstein K-08 award from the National Institutes of Health (NIH). A.V. is supported by Colciencias grant 111504012986. M.C.B. and F.M.S. are supported by the Institutos do Milenio and Apoio a Nucleos de Excelencia Programs, Conselho Nacional de Desenvolvimento Cientifico e Tecnologico, and Fundacao de Amparo a Pesquisa do Estado do Rio Grande do Sul. D.R. is supported by a Burroughs Wellcome Career Development Award in the Biomedical Sciences. Support for this project was provided by the Broad-Novartis-Lund Type 2 Diabetes Initiative, discretionary funding from Harvard Medical School (to D.R.), NIH grants NS043538 (to A.R.-L.) and DK073818 (to D.R.), and federal funds from the National Cancer Institute, NIH, under contract N01-CO-12400. C.W. is supported by the Intramural Research Program of the Center for Cancer Research, National Cancer Institute, NIH, but the content of this publication does not necessarily reflect the views or policies of the Department of Health and Human Services, nor does mention of trade names, commercial products, or organizations imply endorsement by the U.S. Government. The Broad Institute Center for Genotyping and Analysis is supported by National Center for Research Resources grant U54 RR020278-01.
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