Your browser doesn't support javascript.
loading
Probabilistic Estimation of Identity by Descent Segment Endpoints and Detection of Recent Selection.
Browning, Sharon R; Browning, Brian L.
Afiliação
  • Browning SR; Department of Biostatistics, University of Washington, Seattle, WA 98195, USA. Electronic address: sguy@uw.edu.
  • Browning BL; Department of Biostatistics, University of Washington, Seattle, WA 98195, USA; Department of Medicine, Division of Medical Genetics, University of Washington, Seattle, WA 98195, USA.
Am J Hum Genet ; 107(5): 895-910, 2020 11 05.
Article em En | MEDLINE | ID: mdl-33053335
ABSTRACT
Most methods for fast detection of identity by descent (IBD) segments report identity by state segments without any quantification of the uncertainty in the endpoints and lengths of the IBD segments. We present a method for determining the posterior probability distribution of IBD segment endpoints. Our approach accounts for genotype errors, recent mutations, and gene conversions which disrupt DNA sequence identity within IBD segments, and it can be applied to large cohorts with whole-genome sequence or SNP array data. We find that our method's estimates of uncertainty are well calibrated for homogeneous samples. We quantify endpoint uncertainty for 77.7 billion IBD segments from 408,883 individuals of white British ancestry in the UK Biobank, and we use these IBD segments to find regions showing evidence of recent natural selection. We show that many spurious selection signals are eliminated by the use of unbiased estimates of IBD segment endpoints and a pedigree-based genetic map. Eleven of the twelve regions with the greatest evidence for recent selection in our scan have been identified as selected in previous analyses using different approaches. Our computationally efficient method for quantifying IBD segment endpoint uncertainty is implemented in the open source ibd-ends software package.
Assuntos
Palavras-chave

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Genoma Humano / Modelos Estatísticos / Mapeamento Cromossômico / Polimorfismo de Nucleotídeo Único / Padrões de Herança / Identificação Biométrica Tipo de estudo: Diagnostic_studies / Risk_factors_studies Limite: Female / Humans / Male País como assunto: Europa Idioma: En Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Genoma Humano / Modelos Estatísticos / Mapeamento Cromossômico / Polimorfismo de Nucleotídeo Único / Padrões de Herança / Identificação Biométrica Tipo de estudo: Diagnostic_studies / Risk_factors_studies Limite: Female / Humans / Male País como assunto: Europa Idioma: En Ano de publicação: 2020 Tipo de documento: Article