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Decay of linkage disequilibrium within genes across HGDP-CEPH human samples: most population isolates do not show increased LD

BACKGROUND: It is well known that the pattern of linkage disequilibrium varies between human populations, with remarkable geographical stratification. Indirect association studies routinely exploit linkage disequilibrium around genes, particularly in isolated populations where it is assumed to be hi...

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Autores principales: Bosch, Elena, Laayouni, Hafid, Morcillo-Suarez, Carlos, Casals, Ferran, Moreno-Estrada, Andrés, Ferrer-Admetlla, Anna, Gardner, Michelle, Rosa, Araceli, Navarro, Arcadi, Comas, David, Graffelman, Jan, Calafell, Francesc, Bertranpetit, Jaume
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2723139/
https://www.ncbi.nlm.nih.gov/pubmed/19638193
http://dx.doi.org/10.1186/1471-2164-10-338
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author Bosch, Elena
Laayouni, Hafid
Morcillo-Suarez, Carlos
Casals, Ferran
Moreno-Estrada, Andrés
Ferrer-Admetlla, Anna
Gardner, Michelle
Rosa, Araceli
Navarro, Arcadi
Comas, David
Graffelman, Jan
Calafell, Francesc
Bertranpetit, Jaume
author_facet Bosch, Elena
Laayouni, Hafid
Morcillo-Suarez, Carlos
Casals, Ferran
Moreno-Estrada, Andrés
Ferrer-Admetlla, Anna
Gardner, Michelle
Rosa, Araceli
Navarro, Arcadi
Comas, David
Graffelman, Jan
Calafell, Francesc
Bertranpetit, Jaume
author_sort Bosch, Elena
collection PubMed
description BACKGROUND: It is well known that the pattern of linkage disequilibrium varies between human populations, with remarkable geographical stratification. Indirect association studies routinely exploit linkage disequilibrium around genes, particularly in isolated populations where it is assumed to be higher. Here, we explore both the amount and the decay of linkage disequilibrium with physical distance along 211 gene regions, most of them related to complex diseases, across 39 HGDP-CEPH population samples, focusing particularly on the populations defined as isolates. Within each gene region and population we use r(2 )between all possible single nucleotide polymorphism (SNP) pairs as a measure of linkage disequilibrium and focus on the proportion of SNP pairs with r(2 )greater than 0.8. RESULTS: Although the average r(2 )was found to be significantly different both between and within continental regions, a much higher proportion of r(2 )variance could be attributed to differences between continental regions (2.8% vs. 0.5%, respectively). Similarly, while the proportion of SNP pairs with r(2 )> 0.8 was significantly different across continents for all distance classes, it was generally much more homogenous within continents, except in the case of Africa and the Americas. The only isolated populations with consistently higher LD in all distance classes with respect to their continent are the Kalash (Central South Asia) and the Surui (America). Moreover, isolated populations showed only slightly higher proportions of SNP pairs with r(2 )> 0.8 per gene region than non-isolated populations in the same continent. Thus, the number of SNPs in isolated populations that need to be genotyped may be only slightly less than in non-isolates. CONCLUSION: The "isolated population" label by itself does not guarantee a greater genotyping efficiency in association studies, and properties other than increased linkage disequilibrium may make these populations interesting in genetic epidemiology.
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spelling pubmed-27231392009-08-08 Decay of linkage disequilibrium within genes across HGDP-CEPH human samples: most population isolates do not show increased LD Bosch, Elena Laayouni, Hafid Morcillo-Suarez, Carlos Casals, Ferran Moreno-Estrada, Andrés Ferrer-Admetlla, Anna Gardner, Michelle Rosa, Araceli Navarro, Arcadi Comas, David Graffelman, Jan Calafell, Francesc Bertranpetit, Jaume BMC Genomics Research Article BACKGROUND: It is well known that the pattern of linkage disequilibrium varies between human populations, with remarkable geographical stratification. Indirect association studies routinely exploit linkage disequilibrium around genes, particularly in isolated populations where it is assumed to be higher. Here, we explore both the amount and the decay of linkage disequilibrium with physical distance along 211 gene regions, most of them related to complex diseases, across 39 HGDP-CEPH population samples, focusing particularly on the populations defined as isolates. Within each gene region and population we use r(2 )between all possible single nucleotide polymorphism (SNP) pairs as a measure of linkage disequilibrium and focus on the proportion of SNP pairs with r(2 )greater than 0.8. RESULTS: Although the average r(2 )was found to be significantly different both between and within continental regions, a much higher proportion of r(2 )variance could be attributed to differences between continental regions (2.8% vs. 0.5%, respectively). Similarly, while the proportion of SNP pairs with r(2 )> 0.8 was significantly different across continents for all distance classes, it was generally much more homogenous within continents, except in the case of Africa and the Americas. The only isolated populations with consistently higher LD in all distance classes with respect to their continent are the Kalash (Central South Asia) and the Surui (America). Moreover, isolated populations showed only slightly higher proportions of SNP pairs with r(2 )> 0.8 per gene region than non-isolated populations in the same continent. Thus, the number of SNPs in isolated populations that need to be genotyped may be only slightly less than in non-isolates. CONCLUSION: The "isolated population" label by itself does not guarantee a greater genotyping efficiency in association studies, and properties other than increased linkage disequilibrium may make these populations interesting in genetic epidemiology. BioMed Central 2009-07-28 /pmc/articles/PMC2723139/ /pubmed/19638193 http://dx.doi.org/10.1186/1471-2164-10-338 Text en Copyright © 2009 Bosch et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Bosch, Elena
Laayouni, Hafid
Morcillo-Suarez, Carlos
Casals, Ferran
Moreno-Estrada, Andrés
Ferrer-Admetlla, Anna
Gardner, Michelle
Rosa, Araceli
Navarro, Arcadi
Comas, David
Graffelman, Jan
Calafell, Francesc
Bertranpetit, Jaume
Decay of linkage disequilibrium within genes across HGDP-CEPH human samples: most population isolates do not show increased LD
title Decay of linkage disequilibrium within genes across HGDP-CEPH human samples: most population isolates do not show increased LD
title_full Decay of linkage disequilibrium within genes across HGDP-CEPH human samples: most population isolates do not show increased LD
title_fullStr Decay of linkage disequilibrium within genes across HGDP-CEPH human samples: most population isolates do not show increased LD
title_full_unstemmed Decay of linkage disequilibrium within genes across HGDP-CEPH human samples: most population isolates do not show increased LD
title_short Decay of linkage disequilibrium within genes across HGDP-CEPH human samples: most population isolates do not show increased LD
title_sort decay of linkage disequilibrium within genes across hgdp-ceph human samples: most population isolates do not show increased ld
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2723139/
https://www.ncbi.nlm.nih.gov/pubmed/19638193
http://dx.doi.org/10.1186/1471-2164-10-338
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