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Unlocking Cross-Modal Biosignal Synthesis: A Temporally-Aware VAE-Diffusion Model

Chenyang Xu, Dezhen Wang, Hao Wang

ICML 2026 regular

Tóm tắt (nguồn: OpenReview · © tác giả)

Synthesizing authentic phonocardiograms (PCG) from ubiquitous electrocardiograms (ECG) is a critical task for accessible cardiac monitoring. Existing generative models, however, struggle to capture the heart's complex electromechanical coupling, failing to meet the dual requirements of temporal precision and physiological fidelity needed for clinically relevant waveform analysis. We introduce the Temporally-Aware VAE-Diffusion model, a synergistic hybrid architecture that resolves this trade-off. Our architecture enforces tight physiological coupling through an Enhanced Condition Fusion mechanism and explicitly models long-range cardiac dynamics via Temporal Attention Blocks. On the EPHNOGRAM benchmark, our model sets a new state-of-the-art, achieving a Pearson correlation of 0.910$\pm$0.008, 95.95\% S1 detection accuracy, and a precise 12.0 ms timing error, significantly outperforming leading diffusion and Transformer baselines. Crucially, our work provides a reproducible zero-shot transfer evaluation for ECG-to-PCG synthesis. Evaluated on the synchronized PhysioNet/CinC 2016 training-a/MITHSDB subset without target-domain training, our model preserves high waveform fidelity and clinically relevant timing structure under domain shift, including on pathological recordings. These results support cross-dataset robustness of the proposed synthesis framework, while downstream diagnostic validation remains an important direction for future work.

Từ khoá

Machine Learning Biosignal Synthesis VAE Diffusion Models Cross-Modal Learning

Metadata từ BioTender-max/icml2026-ai-bio (CC0-1.0). Phở không lưu trữ bản PDF; link trỏ về nguồn gốc.

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