Evidence map›Paper›PMID 37018147›Full record

ArticleBioinformatics (Oxford, England)2023

Finite mixtures of matrix variate Poisson-log normal distributions for three-way count data.

Anjali Silva, Xiaoke Qin, Steven J Rothstein, Paul D McNicholas, Sanjeena Subedi

Abstract read
In one paragraph

Article in Bioinformatics (Oxford, England), 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

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0cells of the map it votes in
2citing papers in PubMed
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3 · Its place in the literature

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2 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Anjali SilvaDepartment of Mathematics and Statistics, University of Guelph, Guelph, ON N1G 2W1, Canada.
Xiaoke QinSchool of Mathematics and Statistics, Carleton University, Ottawa, ON K1S 5B6, Canada.
Steven J RothsteinDepartment of Molecular and Cellular Biology, University of Guelph, Guelph, ON N1G 2W1, Canada.
Paul D McNicholasDepartment of Mathematics and Statistics, McMaster University, Hamilton, ON L8S 4L8, Canada.
Sanjeena SubediSchool of Mathematics and Statistics, Carleton University, Ottawa, ON K1S 5B6, Canada.ORCID 0000-0002-2462-7786

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

motivationThree-way data structures, characterized by three entities, the units, the variables and the occasions, are frequent in biological studies. In RNA sequencing, three-way data structures are obtained when high-throughput transcriptome sequencing data are collected for n genes across p conditions at r occasions. Matrix variate distributions offer a natural way to model three-way data and mixtures of matrix variate distributions can be used to cluster three-way data. Clustering of gene expression data is carried out as means of discovering gene co-expression networks.

resultsIn this work, a mixture of matrix variate Poisson-log normal distributions is proposed for clustering read counts from RNA sequencing. By considering the matrix variate structure, full information on the conditions and occasions of the RNA sequencing dataset is simultaneously considered, and the number of covariance parameters to be estimated is reduced. We propose three different frameworks for parameter estimation: a Markov chain Monte Carlo-based approach, a variational Gaussian approximation-based approach, and a hybrid approach. Various information criteria are used for model selection. The models are applied to both real and simulated data, and we demonstrate that the proposed approaches can recover the underlying cluster structure in both cases. In simulation studies where the true model parameters are known, our proposed approach shows good parameter recovery. AVAILABILITY AND IMPLEMENTATION: The GitHub R package for this work is available at https://github.com/anjalisilva/mixMVPLN and is released under the open source MIT license.

Indexed as

TranscriptomeComputer SimulationNormal DistributionSequence Analysis, RNAStatistical Distributions

Identifiers

PMID37018147
PMCPMC10159656

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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.