Evidence map›Paper›PMID 30507077›Full record

ArticleJournal of Zhejiang University. Science. B

An ensemble-based likelihood ratio approach for family-based genomic risk prediction.

Hui An, Chang-Shuai Wei, Oliver Wang, Da-Hui Wang, Liang-Wen Xu, Qing Lu, Cheng-Yin Ye

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Article in Journal of Zhejiang University. Science. B. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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5 · Who and what money

Authors and funding

7 authors.

Hui AnDepartment of Health Management, School of Medicine, Hangzhou Normal University, Hangzhou 310036, China.
Chang-Shuai WeiDepartment of Biostatistics and Epidemiology, University of North Texas Health Science Center, Fort Worth, TX 76107, USA.
Oliver WangHBI Solutions Inc, Palo Alto, CA 94301, USA.
Da-Hui WangDepartment of Health Management, School of Medicine, Hangzhou Normal University, Hangzhou 310036, China.
Liang-Wen XuDepartment of Preventive Medicine, School of Medicine, Hangzhou Normal University, Hangzhou 310036, China.
Qing LuDepartment of Epidemiology and Biostatistics, College of Human Medicine, Michigan State University, East Lansing, MI 48824, USA.
Cheng-Yin YeDepartment of Health Management, School of Medicine, Hangzhou Normal University, Hangzhou 310036, China.

Funding

Computational Efficient Statistical Tools for Analyzing Substance Dependence Sequencing DataR01DA043501 · NIDA · UNIVERSITY OF FLORIDA · PI LU, QING · 2017 to 2021
$2.1M
Gene-Gene/Gene-Environment Interactions Associated with Nicotine DependenceK01DA033346 · NIDA · MICHIGAN STATE UNIVERSITY · PI LU, QING · 2013 to 2017
$833k
NIDA NIH HHS K01 DA033346NIDA NIH HHS R01 DA043501
6 · The paper itself

Abstract

objectiveAs one of the most popular designs used in genetic research, family-based design has been well recognized for its advantages, such as robustness against population stratification and admixture. With vast amounts of genetic data collected from family-based studies, there is a great interest in studying the role of genetic markers from the aspect of risk prediction. This study aims to develop a new statistical approach for family-based risk prediction analysis with an improved prediction accuracy compared with existing methods based on family history.

methodsIn this study, we propose an ensemble-based likelihood ratio (ELR) approach, Fam-ELR, for family-based genomic risk prediction. Fam-ELR incorporates a clustered receiver operating characteristic (ROC) curve method to consider correlations among family samples, and uses a computationally efficient tree-assembling procedure for variable selection and model building.

resultsThrough simulations, Fam-ELR shows its robustness in various underlying disease models and pedigree structures, and attains better performance than two existing family-based risk prediction methods. In a real-data application to a family-based genome-wide dataset of conduct disorder, Fam-ELR demonstrates its ability to integrate potential risk predictors and interactions into the model for improved accuracy, especially on a genome-wide level.

conclusionsBy comparing existing approaches, such as genetic risk-score approach, Fam-ELR has the capacity of incorporating genetic variants with small or moderate marginal effects and their interactions into an improved risk prediction model. Therefore, it is a robust and useful approach for high-dimensional family-based risk prediction, especially on complex disease with unknown or less known disease etiology.

Indexed as

Genetic Predisposition to DiseaseGenome, HumanGenomicsArea Under CurveComputer SimulationConduct DisorderFamily HealthFemaleGenetic MarkersGenetic VariationGenome-Wide Association StudyHumansLikelihood FunctionsMaleModels, GeneticOdds RatioGenetic MarkersFamily-based study; Genetic risk prediction; High-dimensional data

Identifiers

PMID30507077
PMCPMC6305257

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