Your browser doesn't support javascript.
loading
Simultaneous SNP selection and adjustment for population structure in high dimensional prediction models.
Bhatnagar, Sahir R; Yang, Yi; Lu, Tianyuan; Schurr, Erwin; Loredo-Osti, J C; Forest, Marie; Oualkacha, Karim; Greenwood, Celia M T.
Afiliação
  • Bhatnagar SR; Department of Epidemiology, Biostatistics and Occupational Health, McGill University, Montréal, Québec, Canada.
  • Yang Y; Department of Diagnostic Radiology, McGill University, Montréal, Québec, Canada.
  • Lu T; Department of Mathematics and Statistics, McGill University, Montréal, Québec, Canada.
  • Schurr E; Quantitative Life Sciences, McGill University, Montréal, Québec, Canada.
  • Loredo-Osti JC; Lady Davis Institute, Jewish General Hospital, Montréal, Québec, Canada.
  • Forest M; Department of Medicine, McGill University, Montréal, Québec, Canada.
  • Oualkacha K; Department of Mathematics and Statistics, Memorial University, St. John's, Newfoundland and Labrador, Canada.
  • Greenwood CMT; École de Technologie Supérieure, Montréal, Québec, Canada.
PLoS Genet ; 16(5): e1008766, 2020 05.
Article em En | MEDLINE | ID: mdl-32365090
ABSTRACT
Complex traits are known to be influenced by a combination of environmental factors and rare and common genetic variants. However, detection of such multivariate associations can be compromised by low statistical power and confounding by population structure. Linear mixed effects models (LMM) can account for correlations due to relatedness but have not been applicable in high-dimensional (HD) settings where the number of fixed effect predictors greatly exceeds the number of samples. False positives or false negatives can result from two-stage approaches, where the residuals estimated from a null model adjusted for the subjects' relationship structure are subsequently used as the response in a standard penalized regression model. To overcome these challenges, we develop a general penalized LMM with a single random effect called ggmix for simultaneous SNP selection and adjustment for population structure in high dimensional prediction models. We develop a blockwise coordinate descent algorithm with automatic tuning parameter selection which is highly scalable, computationally efficient and has theoretical guarantees of convergence. Through simulations and three real data examples, we show that ggmix leads to more parsimonious models compared to the two-stage approach or principal component adjustment with better prediction accuracy. Our method performs well even in the presence of highly correlated markers, and when the causal SNPs are included in the kinship matrix. ggmix can be used to construct polygenic risk scores and select instrumental variables in Mendelian randomization studies. Our algorithms are available in an R package available on CRAN (https//cran.r-project.org/package=ggmix).
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Algoritmos / Polimorfismo de Nucleotídeo Único / Estudo de Associação Genômica Ampla / Modelos Genéticos Tipo de estudo: Clinical_trials / Evaluation_studies / Prognostic_studies / Risk_factors_studies Limite: Animals / Humans Idioma: En Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Algoritmos / Polimorfismo de Nucleotídeo Único / Estudo de Associação Genômica Ampla / Modelos Genéticos Tipo de estudo: Clinical_trials / Evaluation_studies / Prognostic_studies / Risk_factors_studies Limite: Animals / Humans Idioma: En Ano de publicação: 2020 Tipo de documento: Article