BAARC: Uncertainty-Driven Adaptive Partial Spectral Measurement to Full Reconstruction for Material Classification

Machine-learning models for spectroscopy usually treat a spectrum as a fixed-grid intensity vector, leaving the physical coordinate implicit in the array index. Such models are tied to a single sampling grid, spectral range and resolution, which limits their use when measurement conditions change. Here we represent each spectral point as a pair of intensity and wavenumber and compute Transformer positional encodings from the wavenumber itself. On Raman spectra of three bacterial species and their synthetic mixtures, this representation remained robust to noise, sparser sampling and partial spectral coverage across convolutional, residual and Transformer networks. In controlled comparisons, wavenumber-based encoding outperformed index-based and learned encodings under partial observation and retained its performance on sampling grids never seen during training, where index-based encoding degraded. These findings were reproduced on a public 30-isolate bacterial benchmark. Explicit physical coordinates offer a simple route to robust spectral analysis under variable measurement conditions.

Antimicrobial resistance is expected to claim 10 million lives per year by 2050, and resource-limited regions are most affected. Raman spectroscopy is a novel pathogen diagnostic approach promising rapid and portable antibiotic resistance testing within a few hours, compared to days when using gold standard methods. However, current algorithms for Raman spectra analysis 1) are unable to generalize well on limited datasets across diverse patient populations and 2) require increased complexity due to the necessity of non-trivial pre-processing steps, such as feature extraction, which are essential to mitigate the low-quality nature of Raman spectral data. In this work, we address these limitations using Sharpness-Aware Minimization (SAM) to enhance model generalization across a diverse array of hyperparameters in clinical bacterial isolate classification tasks. We demonstrate that SAM achieves accuracy improvements of up to 10.5% on a single split, and an increase in average accuracy of 2.7% across all splits in spectral classification tasks over the traditional optimizer, Adam. These results display the capability of SAM to advance the clinical application of AI-powered Raman spectroscopy tools.

Machine learning (ML) has transformed many scientific fields, yet key applications still lack standardized benchmarks. Raman spectroscopy, a widely used technique for non-invasive molecular analysis, is one such field where progress is limited by fragmented datasets, inconsistent evaluation, and models that fail to capture the structure of spectral data. We introduce RamanBench, the first large-scale, fully reproducible benchmark for ML on Raman spectroscopy, consisting of streamlined data access (https://pypi.org/project/raman-data/), evaluation protocols and code (https://pypi.org/project/raman-bench/), as well as a live leaderboard (https://huggingface.co/spaces/HTW-KI-Werkstatt/RamanBench). It unifies 77 datasets (including 17 first released with this benchmark) across four domains, comprising 325,862 spectra and spanning classification and regression tasks under diverse experimental conditions. We benchmark 28 models under a standardized protocol, including classical methods (e.g., PLS), Raman-specific (e.g., RamanNet), tabular foundation models (TFMs; e.g., TabPFN), and time-series approaches (e.g., ROCKET). TFMs consistently outperform domain-specific and gradient boosting baselines, while time-series models remain competitive. However, no single method dominates across these heterogeneous datasets, revealing that Raman spectroscopy remains an open challenge for machine learning. Therefore, we invite the community to contribute new approaches to our living benchmark, with the potential to accelerate advances in critical applications such as medical diagnostics, biological research, and materials science.