ArticleBioinformatics (Oxford, England)2018
Temporal probabilistic modeling of bacterial compositions derived from 16S rRNA sequencing.
Article in Bioinformatics (Oxford, England), 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers, 1 of them a synthesis that pooled it.
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Who cites it
37 citing papers in PubMed, 1 synthesis or guideline pooled it.
- Deep learning in single-cell and spatial transcriptomics data analysis: advances and challenges from a data science perspective.Briefings in bioinformatics · 2025Pooled it
- LGTM: Gaussian process modulated neural topic modeling for longitudinal microbiome.Gut microbes · 2026Article
- Joint-RPCA: domain-aware multi-omics integration for systems microbiology.Molecular systems biology · 2026Article
- A Tree-Based Model for Addressing Sparsity and Taxa Covariance in Microbiome Compositional Count Data.Statistics in medicine · 2026Article
- Temporal network analysis in systems biology: concepts, inference, and validation.Frontiers in bioinformatics · 2026Review
- Deciphering gut microbial impact in coronary artery disease through multimodal computational approaches.BMC microbiology · 2025Article
- LorDist: a novel method for calculating the distance based on functional data analysis with application to longitudinal microbial data.Microbiology spectrum · 2025Article
- Incorporating scale uncertainty in microbiome and gene expression analysis as an extension of normalization.Genome biology · 2025Article
- Scalable Inference for Bayesian Multinomial Logistic-Normal Dynamic Linear Models.Proceedings of machine learning research · 2025Article
- Mixtures of logistic normal multinomial regression models for microbiome data.Journal of applied statistics · 2025Article
- TEMPTED: time-informed dimensionality reduction for longitudinal microbiome studies.Genome biology · 2024Article
- Microbiome time series data reveal predictable patterns of change.Microbiology spectrum · 2024Article
- Article
- Beyond Normalization: Incorporating Scale Uncertainty in Microbiome and Gene Expression Analysis.bioRxiv : the preprint server for biology · 2024Article
- Methodological Considerations in Longitudinal Analyses of Microbiome Data: A Comprehensive Review.Genes · 2023Review
- Principles and challenges of modeling temporal and spatial omics data.Nature methods · 2023Review
- Clustering microbiome data using mixtures of logistic normal multinomial models.Scientific reports · 2023Article
- A Comprehensive Insight of Current and Future Challenges in Large-Scale Soil Microbiome Analyses.Microbial ecology · 2023Review
- EMBED: Essential MicroBiomE Dynamics, a dimensionality reduction approach for longitudinal microbiome studies.NPJ systems biology and applications · 2023Article
- Article
Corrections and comments
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Authors and funding
3 authors.
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No grant is acknowledged in the PubMed record.
Abstract
Motivation: The number of microbial and metagenomic studies has increased drastically due to advancements in next-generation sequencing-based measurement techniques. Statistical analysis and the validity of conclusions drawn from (time series) 16S rRNA and other metagenomic sequencing data is hampered by the presence of significant amount of noise and missing data (sampling zeros). Accounting uncertainty in microbiome data is often challenging due to the difficulty of obtaining biological replicates. Additionally, the compositional nature of current amplicon and metagenomic data differs from many other biological data types adding another challenge to the data analysis. Results: To address these challenges in human microbiome research, we introduce a novel probabilistic approach to explicitly model overdispersion and sampling zeros by considering the temporal correlation between nearby time points using Gaussian Processes. The proposed Temporal Gaussian Process Model for Compositional Data Analysis (TGP-CODA) shows superior modeling performance compared to commonly used Dirichlet-multinomial, multinomial and non-parametric regression models on real and synthetic data. We demonstrate that the nonreplicative nature of human gut microbiota studies can be partially overcome by our method with proper experimental design of dense temporal sampling. We also show that different modeling approaches have a strong impact on ecological interpretation of the data, such as stationarity, persistence and environmental noise models. Availability and implementation: A Stan implementation of the proposed method is available under MIT license at https://github.com/tare/GPMicrobiome. Contact: taijo@flatironinstitute.org or rb113@nyu.edu. Supplementary information: Supplementary data are available at Bioinformatics online.
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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.