ArticleComputational statistics & data analysis2020
Structured Analysis of the High-dimensional FMR Model.
Article in Computational statistics & data analysis, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.
What it found
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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.
The trial behind it
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
3 citing papers in PubMed.
- HETEROGENEITY ANALYSIS VIA INTEGRATING MULTI-SOURCES HIGH-DIMENSIONAL DATA WITH APPLICATIONS TO CANCER STUDIES.Statistica Sinica · 2023Article
- Histopathological imaging-based cancer heterogeneity analysis via penalized fusion with model averaging.Biometrics · 2021Article
- Vertical integration methods for gene expression data analysis.Briefings in bioinformatics · 2021Review
Corrections and comments
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Authors and funding
4 authors.
Funding
Abstract
The finite mixture of regression (FMR) model is a popular tool for accommodating data heterogeneity. In the analysis of FMR models with high-dimensional covariates, it is necessary to conduct regularized estimation and identify important covariates rather than noises. In the literature, there has been a lack of attention paid to the differences among important covariates, which can lead to the underlying structure of covariate effects. Specifically, important covariates can be classified into two types: those that behave the same in different subpopulations and those that behave differently. It is of interest to conduct structured analysis to identify such structures, which will enable researchers to better understand covariates and their associations with outcomes. Specifically, the FMR model with high-dimensional covariates is considered. A structured penalization approach is developed for regularized estimation, selection of important variables, and, equally importantly, identification of the underlying covariate effect structure. The proposed approach can be effectively realized, and its statistical properties are rigorously established. Simulation demonstrates its superiority over alternatives. In the analysis of cancer gene expression data, interesting models/structures missed by the existing analysis are identified.
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Registered trials
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