ArticleBioinformatics (Oxford, England)2019
GWASinlps: non-local prior based iterative SNP selection tool for genome-wide association studies.
Article in Bioinformatics (Oxford, England), 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.
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Who cites it
8 citing papers in PubMed.
- BG2: Bayesian variable selection in generalized linear mixed models with nonlocal priors for non-Gaussian GWAS data.BMC bioinformatics · 2023Article
- Genetic fine-mapping from summary data using a nonlocal prior improves the detection of multiple causal variants.Bioinformatics (Oxford, England) · 2023Article
- BGWAS: Bayesian variable selection in linear mixed models with nonlocal priors for genome-wide association studies.BMC bioinformatics · 2023Article
- BICOSS: Bayesian iterative conditional stochastic search for GWAS.BMC bioinformatics · 2022Article
- Hybrid of Restricted and Penalized Maximum Likelihood Method for Efficient Genome-Wide Association Study.Genes · 2020Article
- Views on GWAS statistical analysis.Bioinformation · 2020Article
- Bayesian GWAS with Structured and Non-Local Priors.Bioinformatics (Oxford, England) · 2020Article
- Model-based clustering for identifying disease-associated SNPs in case-control genome-wide association studies.Scientific reports · 2019Article
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Authors and funding
7 authors.
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Abstract
Motivation: Multiple marker analysis of the genome-wide association study (GWAS) data has gained ample attention in recent years. However, because of the ultra high-dimensionality of GWAS data, such analysis is challenging. Frequently used penalized regression methods often lead to large number of false positives, whereas Bayesian methods are computationally very expensive. Motivated to ameliorate these issues simultaneously, we consider the novel approach of using non-local priors in an iterative variable selection framework. Results: We develop a variable selection method, named, iterative non-local prior based selection for GWAS, or GWASinlps, that combines, in an iterative variable selection framework, the computational efficiency of the screen-and-select approach based on some association learning and the parsimonious uncertainty quantification provided by the use of non-local priors. The hallmark of our method is the introduction of 'structured screen-and-select' strategy, that considers hierarchical screening, which is not only based on response-predictor associations, but also based on response-response associations and concatenates variable selection within that hierarchy. Extensive simulation studies with single nucleotide polymorphisms having realistic linkage disequilibrium structures demonstrate the advantages of our computationally efficient method compared to several frequentist and Bayesian variable selection methods, in terms of true positive rate, false discovery rate, mean squared error and effect size estimation error. Further, we provide empirical power analysis useful for study design. Finally, a real GWAS data application was considered with human height as phenotype. Availability and implementation: An R-package for implementing the GWASinlps method is available at https://cran.r-project.org/web/packages/GWASinlps/index.html. Supplementary information: Supplementary data are available at Bioinformatics online.
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