ArticleMicrobiome2024
MIDASim: a fast and simple simulator for realistic microbiome data.
Article in Microbiome, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.
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19 citing papers in PubMed.
- Coenocline Simulation of Microbiome Samples: A Biologically Mechanistic Framework for Generating Ecologically Realistic Synthetic Datasets to Support Classification Method Evaluation.Pathogens (Basel, Switzerland) · 2026Article
- Joint-RPCA: domain-aware multi-omics integration for systems microbiology.Molecular systems biology · 2026Article
- DTH: a nonparametric test for homogeneity of multivariate dispersions.Bioinformatics (Oxford, England) · 2026Article
- Fast and reliable association discovery in large-scale microbiome studies and meta-analyses using PALM.bioRxiv : the preprint server for biology · 2026Article
- Ensemble test for microbiome data.Microbiome · 2026Article
- Identifying unmeasured heterogeneity in microbiome data via quantile thresholding (QuanT).Microbiome · 2026Article
- Decoding the reproductive microbiome: enabling clinical and biological insights through machine and deep learning.Frontiers in endocrinology · 2026Review
- Small-scale biogeography of biofilms and its implications for sequencing-based studies.ISME communications · 2026Article
- N2SIMBA: from Network topology to SIMulation of interactions and BActerial abundance, using microbial consumer resource model.Frontiers in bioinformatics · 2026Article
- CAFT: A Compositional Log-Linear Model for Microbiome Data with Zero Cells.bioRxiv : the preprint server for biology · 2025Article
- GIMIC: smoothed graph-image representation of microbiome samples induce an optimal distance.Genome biology · 2025Article
- Article
- PhyloMix: enhancing microbiome-trait association prediction through phylogeny-mixing augmentation.Bioinformatics (Oxford, England) · 2025Article
- Benchmarking Differential Abundance Tests for 16S microbiome sequencing data using simulated data based on experimental templates.PloS one · 2025Article
- Semisynthetic simulation for microbiome data analysis.Briefings in bioinformatics · 2024Review
- ADAPT: Analysis of Microbiome Differential Abundance by Pooling Tobit Models.Bioinformatics (Oxford, England) · 2024Article
- mbtransfer: Microbiome intervention analysis using transfer functions and mirror statistics.PLoS computational biology · 2024Article
- Interactions-based classification of a single microbial sample.Cell reports methods · 2024Article
- Deep learning in microbiome analysis: a comprehensive review of neural network models.Frontiers in microbiology · 2024Review
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Abstract
backgroundAdvances in sequencing technology has led to the discovery of associations between the human microbiota and many diseases, conditions, and traits. With the increasing availability of microbiome data, many statistical methods have been developed for studying these associations. The growing number of newly developed methods highlights the need for simple, rapid, and reliable methods to simulate realistic microbiome data, which is essential for validating and evaluating the performance of these methods. However, generating realistic microbiome data is challenging due to the complex nature of microbiome data, which feature correlation between taxa, sparsity, overdispersion, and compositionality. Current methods for simulating microbiome data are deficient in their ability to capture these important features of microbiome data, or can require exorbitant computational time.
methodsWe develop MIDASim (MIcrobiome DAta Simulator), a fast and simple approach for simulating realistic microbiome data that reproduces the distributional and correlation structure of a template microbiome dataset. MIDASim is a two-step approach. The first step generates correlated binary indicators that represent the presence-absence status of all taxa, and the second step generates relative abundances and counts for the taxa that are considered to be present in step 1, utilizing a Gaussian copula to account for the taxon-taxon correlations. In the second step, MIDASim can operate in both a nonparametric and parametric mode. In the nonparametric mode, the Gaussian copula uses the empirical distribution of relative abundances for the marginal distributions. In the parametric mode, a generalized gamma distribution is used in place of the empirical distribution.
resultsWe demonstrate improved performance of MIDASim relative to other existing methods using gut and vaginal data. MIDASim showed superior performance by PERMANOVA and in terms of alpha diversity and beta dispersion in either parametric or nonparametric mode. We also show how MIDASim in parametric mode can be used to assess the performance of methods for finding differentially abundant taxa in a compositional model.
conclusionsMIDASim is easy to implement, flexible and suitable for most microbiome data simulation situations. MIDASim has three major advantages. First, MIDASim performs better in reproducing the distributional features of real data compared to other methods, at both the presence-absence level and the relative-abundance level. MIDASim-simulated data are more similar to the template data than competing methods, as quantified using a variety of measures. Second, MIDASim makes few distributional assumptions for the relative abundances, and thus can easily accommodate complex distributional features in real data. Third, MIDASim is computationally efficient and can be used to simulate large microbiome datasets. Video Abstract.
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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.