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 in | BMC genetics Vol. 10; no. 1; p. 39 |
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Main Authors | , , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
England
BioMed Central Ltd
24.07.2009
BioMed Central BMC |
Subjects | |
Online Access | Get full text |
ISSN | 1471-2156 1471-2156 |
DOI | 10.1186/1471-2156-10-39 |
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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. |
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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 |
AuthorAffiliation_xml | – name: 3 Department of Public Health Sciences, University of California Davis, Davis, CA 95616, USA – name: 6 Department of Genetics and Pathology, Rudbeck Laboratory, Uppsala University, Uppsala, Sweden – name: 2 Applied Biosystems, Foster City, CA 94404, USA – name: 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 – name: 8 Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX 77030, USA – name: 1 Rowe Program in Human Genetics, Departments of Biochemistry and Medicine, University of California Davis, Davis, CA 95616, USA – name: 5 Section of Genetic Medicine, Department of Medicine, University of Chicago, Chicago, Illinois 60637, USA – name: 4 Obras Sociales del Hermano Pedro, Antigua, Guatemala |
Author_xml | – sequence: 1 givenname: Rami surname: Nassir fullname: Nassir, Rami – sequence: 2 givenname: Roman surname: Kosoy fullname: Kosoy, Roman – sequence: 3 givenname: Chao surname: Tian fullname: Tian, Chao – sequence: 4 givenname: Phoebe A surname: White fullname: White, Phoebe A – sequence: 5 givenname: Lesley M surname: Butler fullname: Butler, Lesley M – sequence: 6 givenname: Gabriel surname: Silva fullname: Silva, Gabriel – sequence: 7 givenname: Rick surname: Kittles fullname: Kittles, Rick – sequence: 8 givenname: Marta E surname: Alarcon-Riquelme fullname: Alarcon-Riquelme, Marta E – sequence: 9 givenname: Peter K surname: Gregersen fullname: Gregersen, Peter K – sequence: 10 givenname: John W surname: Belmont fullname: Belmont, John W – sequence: 11 givenname: Francisco M surname: De La Vega fullname: De La Vega, Francisco M – sequence: 12 givenname: Michael F surname: Seldin fullname: Seldin, Michael F |
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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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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