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A genomewide admixture map for latino populations

  • Alkes L. Price
  • , Nick Patterson
  • , Fuli Yu
  • , David R. Cox
  • , Alicja Waliszewska
  • , Gavin J. McDonald
  • , Arti Tandon
  • , Christine Schirmer
  • , Julie Neubauer
  • , Gabriel Bedoya
  • , Constanza Duque
  • , Alberto Villegas
  • , Maria Catira Bortolini
  • , Francisco M. Salzano
  • , Carla Gallo
  • , Guido Mazzotti
  • , Marcela Tello-Ruiz
  • , Laura Riba
  • , Carlos A. Aguilar-Salinas
  • , Samuel Canizales-Quinteros
  • Marta Menjivar, William Klitz, Brian Henderson, Christopher A. Haiman, Cheryl Winkler, Teresa Tusie-Luna, Andrés Ruiz-Linares, David Reich
  • Harvard Medical School
  • Massachusetts Institute of Technology
  • Perlegen Sciences, Inc.
  • Universidad de Antioquia
  • Universidade Federal do Rio Grande do Sul
  • Universidad Peruana Cayetano Heredia
  • Cold Spring Harbor Laboratory
  • UNAM
  • Instituto Nacional de Ciencias Médicas y Nutrición “Salvador Zubirán”
  • University of California, Berkeley
  • Public Health Institute
  • Keck School of Medicine of USC
  • Science Application International Corporation
  • University College London

Producción científica: Contribución a una revistaArtículorevisión exhaustiva

239 Citas (Scopus)

Resumen

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.

Idioma originalInglés
Páginas (desde-hasta)1024-1036
Número de páginas13
PublicaciónAmerican Journal of Human Genetics
Volumen80
N.º6
DOI
EstadoPublicada - 2007

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