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.

PMID: 31697315
PMCID: PMC7075537
Funding: - McGill University Faculty of Medicine’s Cameron-Davis and Davis Fellowship: Gerald Clavet Fellowship - CIHR: MOP-130344