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Uncertainty quantification in variable selection for genetic fine-mapping using bayesian neural networks

In this paper, we propose a new approach for variable selection using a collection of Bayesian neural networks with a focus on quantifying uncertainty over which variables are selected. Motivated by fine-mapping applications in statistical genetics, we refer to our framework as an “ensemble of singl...

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Detalles Bibliográficos
Autores principales: Cheng, Wei, Ramachandran, Sohini, Crawford, Lorin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9234235/
https://www.ncbi.nlm.nih.gov/pubmed/35769876
http://dx.doi.org/10.1016/j.isci.2022.104553
Descripción
Sumario:In this paper, we propose a new approach for variable selection using a collection of Bayesian neural networks with a focus on quantifying uncertainty over which variables are selected. Motivated by fine-mapping applications in statistical genetics, we refer to our framework as an “ensemble of single-effect neural networks” (ESNN) which generalizes the “sum of single effects” regression framework by both accounting for nonlinear structure in genotypic data (e.g., dominance effects) and having the capability to model discrete phenotypes (e.g., case-control studies). Through extensive simulations, we demonstrate our method’s ability to produce calibrated posterior summaries such as credible sets and posterior inclusion probabilities, particularly for traits with genetic architectures that have significant proportions of non-additive variation driven by correlated variants. Lastly, we use real data to demonstrate that the ESNN framework improves upon the state of the art for identifying true effect variables underlying various complex traits.