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Título : Magnitude and distribution of linkage disequilibrium in population isolates and implications for genome - wide association studies
Autor : Bedoya Berrio, Gabriel De Jesus
Ruiz Linares, Andrés
Service, Susan
Deyoung, Joseph
Karayiorgou, María
Pretoriuos, Herman
Bedoya, Gabriel
Ospina Duque, Jorge
Macedo, António
Palha, Joana Almeida
Heutink, Peter
Aulchenko, Yurii
Oostra, Ben
Van Duijn, Cornelia
Jarvelin, Marjo Riitta
Varilo, Teppo
Peddle, Lynette
Rahman, Proton
Murray, Sarah
Galver, Luana
Peltonen, Leena
Sabatti, Chiara
Collins, Andrew
Freimer, Nelson
metadata.dc.subject.*: Cromosomas Humanos Par 22
Chromosomes, Human, Pair 22
Genética de Población
Genetics, Population
Genoma Humano
Genome, Human
Desequilibrio de Ligamiento
Linkage Disequilibrium
Polimorfismo de Nucleótido Simple
Polymorphism, Single Nucleotide
Fecha de publicación : 2006
Editorial : Nature Research
Citación : Service S, DeYoung J, Karayiorgou M, Roos JL, Pretorious H, Bedoya G, Ospina J, Ruiz-Linares A, Macedo A, Palha JA, Heutink P, Aulchenko Y, Oostra B, van Duijn C, Jarvelin MR, Varilo T, Peddle L, Rahman P, Piras G, Monne M, Murray S, Galver L, Peltonen L, Sabatti C, Collins A, Freimer N. Magnitude and distribution of linkage disequilibrium in population isolates and implications for genome-wide association studies. Nat Genet. 2006 May;38(5):556-60. doi: 10.1038/ng1770. Epub 2006 Apr 2. PMID: 16582909.
Resumen : ABSTRACT: The genome-wide distribution of linkage disequilibrium (LD) determines the strategy for selecting markers for association studies, but it varies between populations. We assayed LD in large samples (200 individuals) from each of 11 well-described population isolates and an outbred European-derived sample, using SNP markers spaced across chromosome 22. Most isolates show substantially higher levels of LD than the outbred sample and many fewer regions of very low LD (termed 'holes'). Young isolates known to have had relatively few founders show particularly extensive LD with very few holes; these populations offer substantial advantages for genome-wide association mapping.
metadata.dc.identifier.eissn: 1546-1718
ISSN : 1061-4036
metadata.dc.identifier.doi: 10.1038/ng1770
Aparece en las colecciones: Artículos de Revista en Ciencias Médicas

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