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      Exomic variants of an elderly cohort of Brazilians in the ABraOM database : NASLAVSKY et al.

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          Healthy life expectancy for 187 countries, 1990–2010: a systematic analysis for the Global Burden Disease Study 2010

          The Lancet, 380(9859), 2144-2162
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            Ancestry informative marker sets for determining continental origin and admixture proportions in common populations in America.

            To provide a resource for assessing continental ancestry in a wide variety of genetic studies, we identified, validated, and characterized a set of 128 ancestry informative markers (AIMs). The markers were chosen for informativeness, genome-wide distribution, and genotype reproducibility on two platforms (TaqMan assays and Illumina arrays). We analyzed genotyping data from 825 subjects with diverse ancestry, including European, East Asian, Amerindian, African, South Asian, Mexican, and Puerto Rican. A comprehensive set of 128 AIMs and subsets as small as 24 AIMs are shown to be useful tools for ascertaining the origin of subjects from particular continents, and to correct for population stratification in admixed population sample sets. Our findings provide general guidelines for the application of specific AIM subsets as a resource for wide application. We conclude that investigators can use TaqMan assays for the selected AIMs as a simple and cost efficient tool to control for differences in continental ancestry when conducting association studies in ethnically diverse populations. Copyright 2008 Wiley-Liss, Inc.
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              Next generation disparities in human genomics: concerns and remedies.

              Studies of human genetics, particularly genome-wide association studies (GWAS), have concentrated heavily on European populations, with individuals of African ancestry rarely represented. Reasons for this include the distribution of biomedical funding and the increased population structure and reduced linkage disequilibrium in African populations. Currently, few GWAS findings have clinical utility and, therefore, the field has not yet contributed to health-care disparities. As human genomics research progresses towards the whole-genome sequencing era, however, more clinically relevant results are likely to be discovered. As we discuss here, to avoid the genetics community contributing to healthcare disparities, it is important to adopt measures to ensure that populations of diverse ancestry are included in genomic studies, and that no major population groups are excluded.
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                Author and article information

                Journal
                Human Mutation
                Human Mutation
                Wiley-Blackwell
                10597794
                July 2017
                July 03 2017
                : 38
                : 7
                : 751-763
                Article
                10.1002/humu.23220
                28332257
                0564e6cf-f6ee-4ed6-87ad-c4a42cb1bf8d
                © 2017

                http://doi.wiley.com/10.1002/tdm_license_1.1

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