seminars:stat:200423
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| + | Discrete data, for one example, the microbiome taxa count data | ||
| + | resulting from 16S rRNA sequencing, is routinely encountered in | ||
| + | bioinformatics. Taxa count data in microbiome studies are typically | ||
| + | high-dimensional, | ||
| + | therefore treated compositional. Analyzing compositional data presents many | ||
| + | challenges because they are restricted on a simplex. | ||
| + | logistic-normal multinomial model, one can map the relative abundance from | ||
| + | a simplex to a latent variable that exists on the real Euclidean space | ||
| + | using the additive log-ratio transformation. | ||
| + | latent variables brings in flexibility in modeling the data, it comes with | ||
| + | heavy computational cost when implemented relying on Bayesian techniques. | ||
| + | In this paper, we extend the logistic-normal multinomial transformation in | ||
| + | a finite mixture model framework to cluster microbiome data. Variational EM | ||
| + | based on the variational Gaussian approximations (VGA), where complex | ||
| + | posterior distributions are approximated using computationally convenient | ||
| + | Gaussian densities by minimizing the Kullback-Leibler (KL) divergence | ||
| + | between the true and the approximating densities of the posterior of the | ||
| + | latent variables, were utilized for parameter estimation. Adopting a | ||
| + | variational Gaussian approximation delivers accurate approximations of the | ||
| + | complex posterior while reducing computational overhead substantially. The | ||
| + | proposed method provides favorable clustering results and accurate | ||
| + | parameter recovery, which are illustrated using simulation and real data. | ||
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