# iModMix: integrative module analysis for multi-omics data

**Authors:** Isis Narváez-Bandera, Ashley Lui, Yonatan Ayalew Mekonnen, Vanessa Rubio, Augustine Takyi, Noah Sulman, Christopher Wilson, Hayley D Ackerman, Oscar E Ospina, Guillermo Gonzalez-Calderon, Elsa R Flores, Qian Li, Ann Chen, Brooke L Fridley, Paul A Stewart

PMC · DOI: 10.1093/bioinformatics/btag030 · 2026-01-19

## TL;DR

iModMix is a new tool that finds connections between different types of biological data without needing prior knowledge, helping researchers discover new multi-omics relationships.

## Contribution

iModMix introduces a biology-agnostic framework for integrative module analysis that works with unidentified metabolites and avoids reliance on pathway annotations.

## Key findings

- iModMix uses graphical lasso to build sparse networks from omics data, enabling data-driven module discovery.
- The framework supports horizontal integration of eigenfeatures across datasets while preserving omics-specific interpretability.
- iModMix is accessible via a user-friendly R Shiny app and a Bioconductor package for advanced users.

## Abstract

Integrative Module Analysis for Multi-omics Data (iModMix) is a biology-agnostic framework that enables the discovery of novel associations across any type of quantitative abundance data, including but not limited to transcriptomics, proteomics, and metabolomics. Instead of relying on pathway annotations or prior biological knowledge, iModMix constructs data-driven modules using graphical lasso to estimate sparse networks from omics features. These modules are summarized into eigenfeatures and correlated across datasets for horizontal integration, while preserving the distinct feature sets and interpretability of each omics type. iModMix operates directly on matrices containing expression or abundances for a wide range of features, including but not limited to genes, proteins, and metabolites. Because it does not rely on annotations (e.g., KEGG identifiers), it can seamlessly incorporate both identified and unidentified metabolites, addressing a key limitation of many existing metabolomics tools. iModMix is available as a user-friendly R Shiny application requiring no programming expertise (https://imodmix.moffitt.org), and as a Bioconductor R package for advanced users (https://bioconductor.org/packages/release/bioc/html/iModMix.html). The tool includes several public and in-house datasets to illustrate its utility in identifying novel multi-omics relationships in diverse biological contexts.

iModMix is freely available from Bioconductor (https://bioconductor.org/packages/release/bioc/html/iModMix.html), and the example dataset package (iModMixData) is also available from Bioconductor (https://bioconductor.org/packages/release/ data/experiment/html/iModMixData.html). The R package source code and Docker are available from GitHub: https://github.com/biodatalab/iModMix. Shiny application can be accessed at: https://imodmix.moffitt.org.

## Full-text entities

- **Diseases:** LUAD (MESH:D000077192), Cancer (MESH:D009369), clear cell renal cell carcinoma (MESH:D002292)
- **Species:** Mus musculus (house mouse, species) [taxon 10090]
- **Cell lines:** RC20 — Homo sapiens (Human), Embryonic stem cell (CVCL_Y642)

## Figures

1 figure with captions in the complete paper: https://tomesphere.com/paper/PMC12925246/full.md

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Source: https://tomesphere.com/paper/PMC12925246