MDiNE
MDiNE estimates and compares microbial co-occurrence networks from microbiome count data by modeling differences in precision matrices between groups defined by a binary covariate.
Key Features:
- Microbial Co-occurrence Network Estimation: Constructs co-occurrence networks of Operational Taxonomic Units (OTUs) using precision matrices derived from microbiome count data.
- Differential Network Analysis: Estimates differences between microbial networks corresponding to groups defined by a binary covariate through comparison of precision matrices.
- Multinomial Count Modeling: Models microbial taxon counts using a multinomial distribution influenced by latent Gaussian random variables.
- Sparse Precision Matrix Inference: Uses sparse precision matrices over latent variables to infer microbial interaction networks.
- Bayesian Inference via Hamiltonian Monte Carlo: Estimates model parameters and evaluates model fit using Hamiltonian Monte Carlo sampling.
Scientific Applications:
- Microbiome Network Analysis: Identifies interaction patterns among microbial taxa within microbial communities.
- Differential Microbial Network Studies: Detects changes in microbial co-occurrence networks between groups such as disease and control cohorts.
- Microbial Ecology and Disease Research: Investigates microbiome interaction structures associated with health conditions such as Crohn's disease.
Methodology:
MDiNE models microbial count data using a multinomial distribution influenced by latent Gaussian variables, estimates sparse precision matrices representing OTU co-occurrence networks, compares precision matrices between groups defined by a binary covariate, and performs parameter inference using Hamiltonian Monte Carlo.
Topics
Details
- Tool Type:
- command-line tool
- Programming Languages:
- R, C++
- Added:
- 1/14/2020
- Last Updated:
- 11/24/2024
Operations
Publications
McGregor K, Labbe A, Greenwood CMT. <tt>MDiNE</tt> : a model to estimate differential co-occurrence networks in microbiome studies. Bioinformatics. 2019;36(6):1840-1847. doi:10.1093/bioinformatics/btz824. PMID:31697315. PMCID:PMC7075537.