ArticleBiometrics2016
Detection of gene-gene interactions using multistage sparse and low-rank regression.
Article in Biometrics, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 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.
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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
5 citing papers in PubMed.
- Article
- A Bayesian approach to differential edges with probabilistic interactions: applications in association and classification.Bioinformatics advances · 2023Article
- Sparse and Low-rank Tensor Estimation via Cubic Sketchings.IEEE transactions on information theory · 2020Article
- Robust semiparametric gene-environment interaction analysis using sparse boosting.Statistics in medicine · 2019Article
- Efficient Signal Inclusion With Genomic Applications.Journal of the American Statistical Association · 2019Article
Corrections and comments
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Authors and funding
6 authors.
Funding
Abstract
Finding an efficient and computationally feasible approach to deal with the curse of high-dimensionality is a daunting challenge faced by modern biological science. The problem becomes even more severe when the interactions are the research focus. To improve the performance of statistical analyses, we propose a sparse and low-rank (SLR) screening based on the combination of a low-rank interaction model and the Lasso screening. SLR models the interaction effects using a low-rank matrix to achieve parsimonious parametrization. The low-rank model increases the efficiency of statistical inference and, hence, SLR screening is able to more accurately detect gene-gene interactions than conventional methods. Incorporation of SLR screening into the Screen-and-Clean approach (Wasserman and Roeder, 2009; Wu et al., 2010) is also discussed, which suffers less penalty from Boferroni correction, and is able to assign p-values for the identified variables in high-dimensional model. We apply the proposed screening procedure to the Warfarin dosage study and the CoLaus study. The results suggest that the new procedure can identify main and interaction effects that would have been omitted by conventional screening methods.
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Registered trials
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