An ancestry informative marker set for determining continental origin: validation and extension using human genome diversity panels

Case-control genetic studies of complex human diseases can be confounded by population stratification. This issue can be addressed using panels of ancestry informative markers (AIMs) that can provide substantial population substructure information. Previously, we described a panel of 128 SNP AIMs th...

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Published inBMC genetics Vol. 10; no. 1; p. 39
Main Authors Nassir, Rami, Kosoy, Roman, Tian, Chao, White, Phoebe A, Butler, Lesley M, Silva, Gabriel, Kittles, Rick, Alarcon-Riquelme, Marta E, Gregersen, Peter K, Belmont, John W, De La Vega, Francisco M, Seldin, Michael F
Format Journal Article
LanguageEnglish
Published England BioMed Central Ltd 24.07.2009
BioMed Central
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ISSN1471-2156
1471-2156
DOI10.1186/1471-2156-10-39

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Abstract Case-control genetic studies of complex human diseases can be confounded by population stratification. This issue can be addressed using panels of ancestry informative markers (AIMs) that can provide substantial population substructure information. Previously, we described a panel of 128 SNP AIMs that were designed as a tool for ascertaining the origins of subjects from Europe, Sub-Saharan Africa, Americas, and East Asia. In this study, genotypes from Human Genome Diversity Panel populations were used to further evaluate a 93 SNP AIM panel, a subset of the 128 AIMS set, for distinguishing continental origins. Using both model-based and relatively model-independent methods, we here confirm the ability of this AIM set to distinguish diverse population groups that were not previously evaluated. This study included multiple population groups from Oceana, South Asia, East Asia, Sub-Saharan Africa, North and South America, and Europe. In addition, the 93 AIM set provides population substructure information that can, for example, distinguish Arab and Ashkenazi from Northern European population groups and Pygmy from other Sub-Saharan African population groups. These data provide additional support for using the 93 AIM set to efficiently identify continental subject groups for genetic studies, to identify study population outliers, and to control for admixture in association studies.
AbstractList Case-control genetic studies of complex human diseases can be confounded by population stratification. This issue can be addressed using panels of ancestry informative markers (AIMs) that can provide substantial population substructure information. Previously, we described a panel of 128 SNP AIMs that were designed as a tool for ascertaining the origins of subjects from Europe, Sub-Saharan Africa, Americas, and East Asia. In this study, genotypes from Human Genome Diversity Panel populations were used to further evaluate a 93 SNP AIM panel, a subset of the 128 AIMS set, for distinguishing continental origins. Using both model-based and relatively model-independent methods, we here confirm the ability of this AIM set to distinguish diverse population groups that were not previously evaluated. This study included multiple population groups from Oceana, South Asia, East Asia, Sub-Saharan Africa, North and South America, and Europe. In addition, the 93 AIM set provides population substructure information that can, for example, distinguish Arab and Ashkenazi from Northern European population groups and Pygmy from other Sub-Saharan African population groups. These data provide additional support for using the 93 AIM set to efficiently identify continental subject groups for genetic studies, to identify study population outliers, and to control for admixture in association studies.
Abstract Background: Case-control genetic studies of complex human diseases can be confounded by population stratification. This issue can be addressed using panels of ancestry informative markers (AIMs) that can provide substantial population substructure information. Previously, we described a panel of 128 SNP AIMs that were designed as a tool for ascertaining the origins of subjects from Europe, Sub-Saharan Africa, Americas, and East Asia. Results: In this study, genotypes from Human Genome Diversity Panel populations were used to further evaluate a 93 SNP AIM panel, a subset of the 128 AIMS set, for distinguishing continental origins. Using both model-based and relatively model-independent methods, we here confirm the ability of this AIM set to distinguish diverse population groups that were not previously evaluated. This study included multiple population groups from Oceana, South Asia, East Asia, Sub-Saharan Africa, North and South America, and Europe. In addition, the 93 AIM set provides population substructure information that can, for example, distinguish Arab and Ashkenazi from Northern European population groups and Pygmy from other Sub-Saharan African population groups. Conclusion: These data provide additional support for using the 93 AIM set to efficiently identify continental subject groups for genetic studies, to identify study population outliers, and to control for admixture in association studies.
Background: Case-control genetic studies of complex human diseases can be confounded by population stratification. This issue can be addressed using panels of ancestry informative markers (AIMs) that can provide substantial population substructure information. Previously, we described a panel of 128 SNP AIMs that were designed as a tool for ascertaining the origins of subjects from Europe, Sub-Saharan Africa, Americas, and East Asia. Results: In this study, genotypes from Human Genome Diversity Panel populations were used to further evaluate a 93 SNP AIM panel, a subset of the 128 AIMS set, for distinguishing continental origins. Using both model-based and relatively model-independent methods, we here confirm the ability of this AIM set to distinguish diverse population groups that were not previously evaluated. This study included multiple population groups from Oceana, South Asia, East Asia, Sub-Saharan Africa, North and South America, and Europe. In addition, the 93 AIM set provides population substructure information that can, for example, distinguish Arab and Ashkenazi from Northern European population groups and Pygmy from other Sub-Saharan African population groups. Conclusion: These data provide additional support for using the 93 AIM set to efficiently identify continental subject groups for genetic studies, to identify study population outliers, and to control for admixture in association studies.
BACKGROUNDCase-control genetic studies of complex human diseases can be confounded by population stratification. This issue can be addressed using panels of ancestry informative markers (AIMs) that can provide substantial population substructure information. Previously, we described a panel of 128 SNP AIMs that were designed as a tool for ascertaining the origins of subjects from Europe, Sub-Saharan Africa, Americas, and East Asia.RESULTSIn this study, genotypes from Human Genome Diversity Panel populations were used to further evaluate a 93 SNP AIM panel, a subset of the 128 AIMS set, for distinguishing continental origins. Using both model-based and relatively model-independent methods, we here confirm the ability of this AIM set to distinguish diverse population groups that were not previously evaluated. This study included multiple population groups from Oceana, South Asia, East Asia, Sub-Saharan Africa, North and South America, and Europe. In addition, the 93 AIM set provides population substructure information that can, for example, distinguish Arab and Ashkenazi from Northern European population groups and Pygmy from other Sub-Saharan African population groups.CONCLUSIONThese data provide additional support for using the 93 AIM set to efficiently identify continental subject groups for genetic studies, to identify study population outliers, and to control for admixture in association studies.
Case-control genetic studies of complex human diseases can be confounded by population stratification. This issue can be addressed using panels of ancestry informative markers (AIMs) that can provide substantial population substructure information. Previously, we described a panel of 128 SNP AIMs that were designed as a tool for ascertaining the origins of subjects from Europe, Sub-Saharan Africa, Americas, and East Asia. In this study, genotypes from Human Genome Diversity Panel populations were used to further evaluate a 93 SNP AIM panel, a subset of the 128 AIMS set, for distinguishing continental origins. Using both model-based and relatively model-independent methods, we here confirm the ability of this AIM set to distinguish diverse population groups that were not previously evaluated. This study included multiple population groups from Oceana, South Asia, East Asia, Sub-Saharan Africa, North and South America, and Europe. In addition, the 93 AIM set provides population substructure information that can, for example, distinguish Arab and Ashkenazi from Northern European population groups and Pygmy from other Sub-Saharan African population groups. These data provide additional support for using the 93 AIM set to efficiently identify continental subject groups for genetic studies, to identify study population outliers, and to control for admixture in association studies.
ArticleNumber 39
Audience Academic
Author Seldin, Michael F
Kosoy, Roman
Belmont, John W
White, Phoebe A
Gregersen, Peter K
Alarcon-Riquelme, Marta E
Kittles, Rick
De La Vega, Francisco M
Silva, Gabriel
Tian, Chao
Butler, Lesley M
Nassir, Rami
AuthorAffiliation 5 Section of Genetic Medicine, Department of Medicine, University of Chicago, Chicago, Illinois 60637, USA
8 Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX 77030, USA
3 Department of Public Health Sciences, University of California Davis, Davis, CA 95616, USA
1 Rowe Program in Human Genetics, Departments of Biochemistry and Medicine, University of California Davis, Davis, CA 95616, USA
6 Department of Genetics and Pathology, Rudbeck Laboratory, Uppsala University, Uppsala, Sweden
4 Obras Sociales del Hermano Pedro, Antigua, Guatemala
2 Applied Biosystems, Foster City, CA 94404, USA
7 The Robert S. Boas Center for Genomics and Human Genetics, Feinstein Institute for Medical Research, North Shore LIJ Health System, Manhasset, NY 11030, USA
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BackLink https://www.ncbi.nlm.nih.gov/pubmed/19630973$$D View this record in MEDLINE/PubMed
https://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-128291$$DView record from Swedish Publication Index
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ContentType Journal Article
Copyright COPYRIGHT 2009 BioMed Central Ltd.
2009 Nassir et al; licensee BioMed Central Ltd. 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.
Copyright © 2009 Nassir et al; licensee BioMed Central Ltd. 2009 Nassir et al; licensee BioMed Central Ltd.
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Snippet Case-control genetic studies of complex human diseases can be confounded by population stratification. This issue can be addressed using panels of ancestry...
Background Case-control genetic studies of complex human diseases can be confounded by population stratification. This issue can be addressed using panels of...
Abstract Background: Case-control genetic studies of complex human diseases can be confounded by population stratification. This issue can be addressed using...
Background: Case-control genetic studies of complex human diseases can be confounded by population stratification. This issue can be addressed using panels of...
BACKGROUNDCase-control genetic studies of complex human diseases can be confounded by population stratification. This issue can be addressed using panels of...
BACKGROUND: Case-control genetic studies of complex human diseases can be confounded by population stratification. This issue can be addressed using panels of...
Abstract Background Case-control genetic studies of complex human diseases can be confounded by population stratification. This issue can be addressed using...
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SubjectTerms African Continental Ancestry Group - genetics
Asian Americans
Asian Continental Ancestry Group - genetics
Biologi
Biological diversity
Biology
Cluster Analysis
Data processing
European Continental Ancestry Group - genetics
Genetic Markers
Genetics
Genetics, Population
Genome, Human
Genomes
Genotype
Genotypes
Humans
Minority & ethnic groups
NATURAL SCIENCES
NATURVETENSKAP
Polymorphism, Single Nucleotide
Population genetics
Population studies
Principal Component Analysis
Single nucleotide polymorphisms
Single-nucleotide polymorphism
Studies
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Title An ancestry informative marker set for determining continental origin: validation and extension using human genome diversity panels
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