MIDAA: deep archetypal analysis for interpretable multi-omic data integration based on biological principles

High-throughput multi-omic molecular profiling allows the probing of biological systems at unprecedented resolution. However, integrating and interpreting high-dimensional, sparse, and noisy multimodal datasets remains challenging. Deriving new biological insights with current methods is difficult because they are not rooted in biological principles but prioritise tasks like dimensionality reduction. Here, we introduce a framework that combines archetypal analysis, an approach grounded in biological principles, with deep learning. Using archetypes based on evolutionary trade-offs and Pareto optimality, MIDAA finds extreme data points that define the geometry of the latent space, preserving the complexity of biological interactions while retaining an interpretable output. We demonstrate that these extreme points represent cellular programmes reflecting the underlying biology. Moreover, we show that, compared to alternative methods, MIDAA can identify parsimonious, interpretable, and biologically relevant patterns from real and simulated multi-omics.

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Publication Details

Journal
Genome biology
Published
2025-04-08
DOI
https://doi.org/10.1186/s13059-025-03530-9
Citations
7
Primary Topic
Bioinformatics and Genomic Networks
Type
article
Field-Weighted Citation Impact
5.64

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article

MIDAA: deep archetypal analysis for interpretable multi-omic data integration based on biological principles

Giulio Caravagna, Andrea Sottoriva, Salvatore Milite
7 citations
Genome biology
Bioinformatics and Genomic Networks
5.64
article

MIDAA: deep archetypal analysis for interpretable multi-omic data integration based on biological principles

Giulio Caravagna, Andrea Sottoriva, Salvatore Milite
article en
7 citations

Abstract

High-throughput multi-omic molecular profiling allows the probing of biological systems at unprecedented resolution. However, integrating and interpreting high-dimensional, sparse, and noisy multimodal datasets remains challenging. Deriving new biological insights with current methods is difficult because they are not rooted in biological principles but prioritise tasks like dimensionality reduction. Here, we introduce a framework that combines archetypal analysis, an approach grounded in biological principles, with deep learning. Using archetypes based on evolutionary trade-offs and Pareto optimality, MIDAA finds extreme data points that define the geometry of the latent space, preserving the complexity of biological interactions while retaining an interpretable output. We demonstrate that these extreme points represent cellular programmes reflecting the underlying biology. Moreover, we show that, compared to alternative methods, MIDAA can identify parsimonious, interpretable, and biologically relevant patterns from real and simulated multi-omics.

Genome biologyVol. 26(1)
University of Trieste (IT), Human Technopole (IT)
Cancer Research UK, European Commission, Associazione Italiana per la Ricerca sul Cancro
Openalex Percentile: Top 4%
Bioinformatics and Genomic Networks
5.64
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MIDAA: deep archetypal analysis for interpretable multi-omic data integration based on biological principles — Giulio Caravagna, Andrea Sottoriva, et al. · Genome biology (2025) | TGRS Research Map | TGRS