ORIGINAL RESEARCH article
Front. Cell Dev. Biol.
Sec. Cancer Cell Biology
This article is part of the Research TopicMulti-Omics Integration for Precision Oncology: Diagnostic and Prognostic BiomarkerView all 6 articles
Remics: A Redescription-based Framework for Multi-Omics Analysis
Provisionally accepted- 1IBM Research - Yorktown Heights, Yorktown Heights, United States
- 2DAIN Studios, Helsinki, Finland
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Abstract. Complex diseases such as cancer are characterized by their intricate etiology, arising from several molecular mechanisms that span multiple omic layers. To obtain insights on disease subtypes, associated biomarkers, and improve prognostic modeling, it is essential to integrate and interpret multi-omics data in a biologically meaningful way. We introduce Remics, a redescription-based framework for multi-omics integration inspired by higher-order statistical representations. Remics leverages higher-order cumulants to identify redescriptions, which are sets of multi-omics features that jointly capture equivalent biological variation across modalities. These feature groups are further analyzed through network representations, multi-omics risk scoring, and biomarker discovery to reveal molecular inter-actions underlying disease mechanisms. We applied Remics on simulated data as well as multi-omics data of six different cancer types from The Cancer Genome Atlas. We demonstrate that redescription-based integration uncovers functionally coherent cross-omics feature associations and compare them with state-of-the-art approaches. Our results highlight the potential of higher-order multi-omics statistical analysis to advance precision medicine through improved interpretability and discovery of novel molecular relationships.
Keywords: Biomarker Discovery, Data Mining, Disease Prediction, genetic epidemiology, multi-omics, networks, statistics
Received: 03 Nov 2025; Accepted: 02 Feb 2026.
Copyright: © 2026 Bose, Platt, Rhrissorrakrai, Burch, Guzmán Sáenz, Haiminen and Parida. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
* Correspondence: Aritra Bose
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