arXiv:2603.17248v1 Announce Type: cross
Abstract: Reconstructing a 12-lead electrocardiogram (ECG) from a reduced lead set is an ill-posed inverse problem due to anatomical variability. Standard deep learning methods often ignore underlying cardiac pathology losing vital morphology in precordial leads. We propose Pathology-Aware Multi-View Contrastive Learning, a framework that regularizes the latent space through a pathological manifold. Our architecture integrates high-fidelity time-domain waveforms with pathology-aware embeddings learned via supervised contrastive alignment. By maximizing mutual information between latent representations and clinical labels, the framework learns to filter anatomical “nuisance” variables. On the PTB-XL dataset, our method achieves approx. 76% reduction in RMSE compared to state-of-the-art model in patient-independent setting. Cross-dataset evaluation on the PTB Diagnostic Database confirms superior generalization, bridging the gap between hardware portability and diagnostic-grade reconstruction.
Three immunoregulatory signatures define non-productive HIV infection in CD4+ T memory stem cells
The persistent HIV reservoir constitutes the main obstacle to curing HIV/AIDS disease. Our understanding of how non-productive HIV infections are established in primary human CD4+




