ArticleBioinformatics (Oxford, England)2019
Clustering of temporal gene expression data with mixtures of mixed effects models with a penalized likelihood.
Article in Bioinformatics (Oxford, England), 2019. 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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Who cites it
2 citing papers in PubMed.
- Multivariate Poisson lognormal distribution for modeling counts from modern biological data: An overview.Computational and structural biotechnology journal · 2025Article
- Temporal and Quantitative Transcriptomic Differences Define Sexual Dimorphism in Murine Postnatal Bone Aging.JBMR plus · 2022Article
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Authors and funding
4 authors.
Funding
Abstract
motivationClustering algorithms like K-Means and standard Gaussian mixture models (GMM) fail to account for the structure of variability of replicated data or repeated measures over time. Additionally, a priori cluster number assumptions add an additional complexity to the process. Current methods to optimize cluster labels and number can be inaccurate or computationally intensive for temporal gene expression data with this additional variability.
resultsAn extension to a model-based clustering algorithm is proposed using mixtures of mixed effects polynomial regression models and the EM algorithm with an entropy penalized log-likelihood function (EPEM). The EPEM is used to cluster temporal gene expression data with this additional variability. The addition of random effects in our model decreased the misclassification error when compared to mixtures of fixed effects models or other methods such as K-Means and GMM. Applying our method to microarray data from a fracture healing study revealed distinct temporal patterns of gene expression. AVAILABILITY AND IMPLEMENTATION: https://github.com/darlenelu72/EPEM-GMM. SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online.
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