Literature DB >> 19639555

Genetic composition of Brazilian population samples based on a set of twenty-eight ancestry informative SNPs.

Tulio C Lins1, Rodrigo G Vieira, Breno S Abreu, Dario Grattapaglia, Rinaldo W Pereira.   

Abstract

Ancestry informative SNPs can be useful to estimate individual and population biogeographical ancestry. Brazilian population is characterized by a genetic background of three parental populations (European, African, and Brazilian Native Amerindians) with a wide degree and diverse patterns of admixture. In this work we analyzed the information content of 28 ancestry-informative SNPs into multiplexed panels using three parental population sources (African, Amerindian, and European) to infer the genetic admixture in an urban sample of the five Brazilian geopolitical regions. The SNPs assigned apart the parental populations from each other and thus can be applied for ancestry estimation in a three hybrid admixed population. Data was used to infer genetic ancestry in Brazilians with an admixture model. Pairwise estimates of F(st) among the five Brazilian geopolitical regions suggested little genetic differentiation only between the South and the remaining regions. Estimates of ancestry results are consistent with the heterogeneous genetic profile of Brazilian population, with a major contribution of European ancestry (0.771) followed by African (0.143) and Amerindian contributions (0.085). The described multiplexed SNP panels can be useful tool for bioanthropological studies but it can be mainly valuable to control for spurious results in genetic association studies in admixed populations. (c) 2009 Wiley-Liss, Inc.

Mesh:

Year:  2010        PMID: 19639555     DOI: 10.1002/ajhb.20976

Source DB:  PubMed          Journal:  Am J Hum Biol        ISSN: 1042-0533            Impact factor:   1.937


  59 in total

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Journal:  J Clin Immunol       Date:  2012-03-09       Impact factor: 8.317

2.  Studies with Wnt genes and nonsyndromic cleft lip and palate.

Authors:  Renato Menezes; Ariadne Letra; Ana H Kim; Erika C Küchler; Alicia Day; Patricia N Tannure; Luise Gomes da Motta; Katiucia B S Paiva; Jose M Granjeiro; Alexandre R Vieira
Journal:  Birth Defects Res A Clin Mol Teratol       Date:  2010-10-01

3.  Evaluation of the association between polymorphisms at the DRD2 locus and stuttering.

Authors:  Changsoo Kang; Bianca Santos Domingues; Eduardo Sainz; Carlos Eduardo Frigério Domingues; Dennis Drayna; Danilo Moretti-Ferreira
Journal:  J Hum Genet       Date:  2011-03-10       Impact factor: 3.172

4.  FOXP3 immunoregulatory gene variants are independent predictors of human papillomavirus infection and cervical cancer precursor lesions.

Authors:  Fernando Cezar-Dos-Santos; Rodolfo Sanches Ferreira; Nádia Calvo Martins Okuyama; Kleber Paiva Trugilo; Michelle Mota Sena; Érica Romão Pereira; Ana Paula Lombardi Pereira; Maria Angelica Ehara Watanabe; Karen Brajão de Oliveira
Journal:  J Cancer Res Clin Oncol       Date:  2019-06-08       Impact factor: 4.553

5.  Common NOD2/CARD15 and TLR4 Polymorphisms Are Associated with Crohn's Disease Phenotypes in Southeastern Brazilians.

Authors:  Yolanda F M Tolentino; Paula Peruzzi Elia; Homero Soares Fogaça; Antonio José V Carneiro; Cyrla Zaltman; Rodrigo Moura-Neto; Ronir Raggio Luiz; Maria da Gloria C Carvalho; Heitor S de Souza
Journal:  Dig Dis Sci       Date:  2016-04-23       Impact factor: 3.199

Review 6.  Forensically relevant SNaPshot® assays for human DNA SNP analysis: a review.

Authors:  Bhavik Mehta; Runa Daniel; Chris Phillips; Dennis McNevin
Journal:  Int J Legal Med       Date:  2016-11-14       Impact factor: 2.686

7.  Validating GWAS Variants from Microglial Genes Implicated in Alzheimer's Disease.

Authors:  Lígia Ramos Dos Santos; Lúcia Helena Sagrillo Pimassoni; Geralda Gillian Silva Sena; Daniela Camporez; Luciano Belcavello; Maíra Trancozo; Renato Lírio Morelato; Flavia Imbroisi Valle Errera; Maria Rita Passos Bueno; Flavia de Paula
Journal:  J Mol Neurosci       Date:  2017-05-05       Impact factor: 3.444

8.  Drug metabolism and transport gene polymorphisms and efavirenz adverse effects in Brazilian HIV-positive individuals.

Authors:  Tailah Bernardo de Almeida; Marcelo Costa Velho Mendes de Azevedo; Jorge Francisco da Cunha Pinto; Fernando Rafael de Almeida Ferry; Guilherme Almeida Rosa da Silva; Izana Junqueira de Castro; Paxton Baker; Amilcar Tanuri; David W Haas; Cynthia C Cardoso
Journal:  J Antimicrob Chemother       Date:  2018-09-01       Impact factor: 5.790

9.  Haplotype Study in SCA10 Families Provides Further Evidence for a Common Ancestral Origin of the Mutation.

Authors:  Giovana B Bampi; Rafael Bisso-Machado; Tábita Hünemeier; Tailise C Gheno; Gabriel V Furtado; Diego Veliz-Otani; Mario Cornejo-Olivas; Pillar Mazzeti; Maria Cátira Bortolini; Laura B Jardim; Maria Luiza Saraiva-Pereira
Journal:  Neuromolecular Med       Date:  2017-09-13       Impact factor: 3.843

10.  The PTPN22 1858T allele but not variants in the proximal promoter region of IL-21 gene is associated with the susceptibility to type 1 diabetes and the presence of autoantibodies in a Brazilian cohort.

Authors:  D T O Mainardi-Novo; A S Santos; R T Fukui; M Gamberini; M R S Correia; M O Ruiz; C L P Mangueira; S R Matioli; D M Vasconcelos; M E R Silva
Journal:  Clin Exp Immunol       Date:  2013-04       Impact factor: 4.330

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