Evidence map›Paper›PMID 32334509›Full record

ArticleBMC bioinformatics2020

High dimensional model representation of log-likelihood ratio: binary classification with expression data.

Ali Foroughi Pour, Maciej Pietrzak, Lori A Dalton, Grzegorz A Rempała

Abstract read
In one paragraph

Article in BMC bioinformatics, 2020. 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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1citing papers in PubMed
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1 · What the graph read from it

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3 · Its place in the literature

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1 citing paper in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Ali Foroughi PourDepartment of Electrical and Computer Engineering, The Ohio State University, 205 Dreese laboratories, 2015 Neil Ave., Columbus, 43210, USA.
Maciej PietrzakDepartment of Biomedical Informatics, The Ohio State University, 1585 Neil Ave, Columbus, 43210, USA.
Lori A DaltonDepartment of Electrical and Computer Engineering, The Ohio State University, 205 Dreese laboratories, 2015 Neil Ave., Columbus, 43210, USA.
Grzegorz A RempałaDepartment of Mathematics, The Ohio State University, 100 Math Tower, 31 West 18th Ave., Columbus, 43210, USA. rempala.3@osu.edu.ORCID http://orcid.org/0000-0002-6307-4555

Funding

Directorate for Mathematical and Physical Sciences 1853587
6 · The paper itself

Abstract

backgroundBinary classification rules based on a small-sample of high-dimensional data (for instance, gene expression data) are ubiquitous in modern bioinformatics. Constructing such classifiers is challenging due to (a) the complex nature of underlying biological traits, such as gene interactions, and (b) the need for highly interpretable glass-box models. We use the theory of high dimensional model representation (HDMR) to build interpretable low dimensional approximations of the log-likelihood ratio accounting for the effects of each individual gene as well as gene-gene interactions. We propose two algorithms approximating the second order HDMR expansion, and a hypothesis test based on the HDMR formulation to identify significantly dysregulated pairwise interactions. The theory is seen as flexible and requiring only a mild set of assumptions.

resultsWe apply our approach to gene expression data from both synthetic and real (breast and lung cancer) datasets comparing it also against several popular state-of-the-art methods. The analyses suggest the proposed algorithms can be used to obtain interpretable prediction rules with high prediction accuracies and to successfully extract significantly dysregulated gene-gene interactions from the data. They also compare favorably against their competitors across multiple synthetic data scenarios.

conclusionThe proposed HDMR-based approach appears to produce a reliable classifier that additionally allows one to describe how individual genes or gene-gene interactions affect classification decisions. Both real and synthetic data analyses suggest that our methods can be used to identify gene networks with dysregulated pairwise interactions, and are therefore appropriate for differential networks analysis.

Indexed as

Models, TheoreticalAlgorithmsArea Under CurveBreast NeoplasmsDatabases, GeneticFemaleGene Expression Regulation, NeoplasticHumansLung NeoplasmsROC CurveClassificationDisease predictionExpression analysisHigh dimensional model representationLog-likelihood ratio

Identifiers

PMID32334509
PMCPMC7183128

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.