Measuring and using admixture to study the genetics of complex diseases

<p>Abstract</p> <p>Admixture is an important evolutionary force that can and should be used in efforts to apply genomic data and technology to the study of complex disease genetics. Admixture linkage disequilibrium (ALD) is created by the process of admixture and, in recently admix...

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Main Authors: Halder Indrani, Shriver Mark D
Format: Article
Language:English
Published: BMC 2003-11-01
Series:Human Genomics
Subjects:
Online Access:http://www.humgenomics.com/content/1/1/52
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spelling doaj-7eda5f623a08462295477b9a763e91682020-11-24T23:53:12ZengBMCHuman Genomics1479-73642003-11-0111526210.1186/1479-7364-1-1-52Measuring and using admixture to study the genetics of complex diseasesHalder IndraniShriver Mark D<p>Abstract</p> <p>Admixture is an important evolutionary force that can and should be used in efforts to apply genomic data and technology to the study of complex disease genetics. Admixture linkage disequilibrium (ALD) is created by the process of admixture and, in recently admixed populations, extends for substantial distances (of the order of 10 to 20 cM). The amount of ALD generated depends on the level of admixture, ancestry information content of markers and the admixture dynamics of the population, and thus influences admixture mapping (AM). The authors discuss different models of admixture and how these can have an impact on the success of AM studies. Selection of markers is important, since markers informative for parental population ancestry are required and these are uncommon. Rarely does the process of admixture result in a population that is uniform for individual admixture levels, but instead there is substantial population stratification. This stratification can be understood as variation in individual admixtures and can be both a source of statistical power for ancestry-phenotype correlation studies as well as a confounder in causing false-positives in gene association studies. Methods to detect and control for stratification in case/control and AM studies are reviewed, along with recent studies showing individual ancestry-phenotype correlations. Using skin pigmentation as a model phenotype, implications of AM in complex disease gene mapping studies are discussed. Finally, the article discusses some limitations of this approach that should be considered when designing an effective AM study.</p> http://www.humgenomics.com/content/1/1/52complex diseasesadmixture linkage disequilibrium (ALD)admixture mapping (AM)biogeographical ancestry (BGA)structurephenotype-ancestry correlation
collection DOAJ
language English
format Article
sources DOAJ
author Halder Indrani
Shriver Mark D
spellingShingle Halder Indrani
Shriver Mark D
Measuring and using admixture to study the genetics of complex diseases
Human Genomics
complex diseases
admixture linkage disequilibrium (ALD)
admixture mapping (AM)
biogeographical ancestry (BGA)
structure
phenotype-ancestry correlation
author_facet Halder Indrani
Shriver Mark D
author_sort Halder Indrani
title Measuring and using admixture to study the genetics of complex diseases
title_short Measuring and using admixture to study the genetics of complex diseases
title_full Measuring and using admixture to study the genetics of complex diseases
title_fullStr Measuring and using admixture to study the genetics of complex diseases
title_full_unstemmed Measuring and using admixture to study the genetics of complex diseases
title_sort measuring and using admixture to study the genetics of complex diseases
publisher BMC
series Human Genomics
issn 1479-7364
publishDate 2003-11-01
description <p>Abstract</p> <p>Admixture is an important evolutionary force that can and should be used in efforts to apply genomic data and technology to the study of complex disease genetics. Admixture linkage disequilibrium (ALD) is created by the process of admixture and, in recently admixed populations, extends for substantial distances (of the order of 10 to 20 cM). The amount of ALD generated depends on the level of admixture, ancestry information content of markers and the admixture dynamics of the population, and thus influences admixture mapping (AM). The authors discuss different models of admixture and how these can have an impact on the success of AM studies. Selection of markers is important, since markers informative for parental population ancestry are required and these are uncommon. Rarely does the process of admixture result in a population that is uniform for individual admixture levels, but instead there is substantial population stratification. This stratification can be understood as variation in individual admixtures and can be both a source of statistical power for ancestry-phenotype correlation studies as well as a confounder in causing false-positives in gene association studies. Methods to detect and control for stratification in case/control and AM studies are reviewed, along with recent studies showing individual ancestry-phenotype correlations. Using skin pigmentation as a model phenotype, implications of AM in complex disease gene mapping studies are discussed. Finally, the article discusses some limitations of this approach that should be considered when designing an effective AM study.</p>
topic complex diseases
admixture linkage disequilibrium (ALD)
admixture mapping (AM)
biogeographical ancestry (BGA)
structure
phenotype-ancestry correlation
url http://www.humgenomics.com/content/1/1/52
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