Integrative Analysis of Epigenetic, Transcriptomic, and Metabolomic Responses to Arsenic Exposure Using Coupled Matrix Factorization
Sujit Silas Armstrong Suthahar, Patrick Allard

TL;DR
This study introduces a coupled matrix factorization framework to integrate epigenetic, transcriptomic, and metabolomic data, revealing coordinated molecular responses to arsenic exposure in stem cells.
Contribution
The paper presents a novel CMF-based method for joint analysis of multi-omics datasets, capturing interdependent molecular changes due to arsenic toxicity.
Findings
Identified shared molecular response components across omics layers.
Demonstrated the framework's effectiveness in analyzing arsenic-induced perturbations.
Showed potential for broader application in computational toxicology.
Abstract
Arsenic (As), a widespread environmental toxin, poses major health risks due to its inorganic forms (iAs), which are linked to cancer, cardiovascular disease, and endocrine disruption. Although its toxic effects have been extensively studied, the molecular mechanisms underlying arsenic-induced perturbations remain incompletely understood. This complexity arises from its ability to reprogram epigenetic landscapes, alter gene expression, and disrupt metabolic balance through interconnected regulatory networks. Existing studies often analyze epigenomic, transcriptomic, and metabolomic datasets independently, overlooking their interdependence. Here, we present a coupled matrix factorization (CMF) framework based on the PARAFAC2-AOADMM model for joint integration of DNA methylation (RRBS), RNA-seq, and metabolomics data from mouse embryonic stem cells (ESCs) and epiblast-like cells (EpiLCs)…
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Taxonomy
TopicsArsenic contamination and mitigation · Single-cell and spatial transcriptomics · Epigenetics and DNA Methylation
