Abstract
The diagnosis of Myocardial Infarction (MI) can be enhanced through label-free biosensing techniques like Surface-Enhanced Resonance Raman Spectroscopy (SERRS). Machine learning is hindered by data scarcity, excessive dimensionality,
and class imbalance. This paper presents a scalable and interpretable pipeline for generating synthetic data for high-dimensional, low-sample-size (HDLSS) SERRS data. The method combines class-conditional Gaussian Mixture Models (GMMs), physiological renoising through Savitzky–Golay filtering and Gaussian noise, and manifold-constrained filtering using UMAP-KNN to maintain physiological validity. A composite score that integrates fidelity (Wasserstein), diversity (DTW), and generalisability (UMAP acceptance) is used to rank synthetic data configurations during generation. Experimental results indicate that classifiers trained over 5x-scaled synthetic data attain F1 scores of up to 82.35% and ROC AUC of 1.00, surpassing the performance of models trained solely on real data. This lightweight, modular approach offers a scalable alternative to
deep generative models in the context of clinical biosensing.
and class imbalance. This paper presents a scalable and interpretable pipeline for generating synthetic data for high-dimensional, low-sample-size (HDLSS) SERRS data. The method combines class-conditional Gaussian Mixture Models (GMMs), physiological renoising through Savitzky–Golay filtering and Gaussian noise, and manifold-constrained filtering using UMAP-KNN to maintain physiological validity. A composite score that integrates fidelity (Wasserstein), diversity (DTW), and generalisability (UMAP acceptance) is used to rank synthetic data configurations during generation. Experimental results indicate that classifiers trained over 5x-scaled synthetic data attain F1 scores of up to 82.35% and ROC AUC of 1.00, surpassing the performance of models trained solely on real data. This lightweight, modular approach offers a scalable alternative to
deep generative models in the context of clinical biosensing.
| Original language | English |
|---|---|
| Title of host publication | IEEE SENSORS Conference 2025 |
| Publisher | IEEE Xplore |
| Pages | 1-4 |
| Number of pages | 4 |
| ISBN (Electronic) | 979-8-3315-4467-6 |
| ISBN (Print) | 979-8-3315-4468-3 |
| DOIs | |
| Publication status | Published online - 19 Jan 2026 |
| Event | 2025 IEEE SENSORS - Vancouver, BC, Canada Duration: 19 Oct 2025 → 22 Oct 2025 |
Publication series
| Name | |
|---|---|
| ISSN (Print) | 1930-0395 |
| ISSN (Electronic) | 2168-9229 |
Conference
| Conference | 2025 IEEE SENSORS |
|---|---|
| Country/Territory | Canada |
| City | Vancouver, BC |
| Period | 19/10/25 → 22/10/25 |
Bibliographical note
Publisher Copyright:© 2025 IEEE.
Funding
This work has been supported by the Department for the Economy Northern Ireland under the US-Ireland R&D Partnership Programme (USI-207), and by the NSF’s Engineering Research Center for Precise Advanced Technologies and Health Systems for Underserved Populations (PATHS-UP), #1648451.
| Funders | Funder number |
|---|---|
| Department for the Economy | |
| US-IRELAND R&D Partnership Programme | USI-207 |
| NSF | 1648451 |
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
-
SDG 9 Industry, Innovation, and Infrastructure
-
SDG 12 Responsible Consumption and Production
Keywords
- Synthetic Data
- SERRS
- Gaussian mixture model
- Cardiac Troponin I
- High-dimensional Data
- point-of-care (PoC) diagnostics
- Gaussian Mixture Model
- Point-of-Care Diagnostics
- High-Dimensional Data
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