ArticleBiometrics2019
A hybrid omnibus test for generalized semiparametric single-index models with high-dimensional covariate sets.
Article in Biometrics, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
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Who cites it
1 citing paper in PubMed.
- Flexible Bayesian Inference for Identifying Significantly Correlated Multiple Pathway Sets.Statistics in medicine · 2026Article
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Authors and funding
3 authors.
Funding
Abstract
Numerous statistical methods have been developed for analyzing high-dimensional data. These methods often focus on variable selection approaches but are limited for the purpose of testing with high-dimensional data. They are often required to have explicit-likelihood functions. In this article, we propose a "hybrid omnibus test" for high-dicmensional data testing purpose with much weaker requirements. Our hybrid omnibus test is developed under a semiparametric framework where a likelihood function is no longer necessary. Our test is a version of a frequentist-Bayesian hybrid score-type test for a generalized partially linear single-index model, which has a link function being a function of a set of variables through a generalized partially linear single index. We propose an efficient score based on estimating equations, define local tests, and then construct our hybrid omnibus test using local tests. We compare our approach with an empirical-likelihood ratio test and Bayesian inference based on Bayes factors, using simulation studies. Our simulation results suggest that our approach outperforms the others, in terms of type I error, power, and computational cost in both the low- and high-dimensional cases. The advantage of our approach is demonstrated by applying it to genetic pathway data for type II diabetes mellitus.
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