Spatial Adaptation Layer: Interpretable Domain Adaptation For Biosignal Sensor Array Applications

Biosignal acquisition is key for healthcare applications and wearable devices, with machine learning offering promising methods for processing signals like surface electromyography (sEMG) and electroencephalography (EEG). Despite high within-session performance, intersession performance is hindered by electrode shift, a known issue across modalities. Existing solutions often require large and expensive datasets and/or lack robustness and interpretability. Thus, we propose the Spatial Adaptation Layer (SAL), which can be prepended to any biosignal array model and learns a parametrized affine transformation at the input between two recording sessions. We also introduce learnable baseline normalization (LBN) to reduce baseline fluctuations. Tested on two HD-sEMG gesture recognition datasets, SAL and LBN outperform standard fine-tuning on regular arrays, achieving competitive performance even with a logistic regressor, with orders of magnitude less, physically interpretable parameters. Our ablation study shows that forearm circumferential translations account for the majority of performance improvements, in line with sEMG physiological expectations.

Tackling Electrode Shift In Gesture Recognition with HD-EMG Electrode Subsets

sEMG pattern recognition algorithms have been explored extensively in decoding movement intent, yet are known to be vulnerable to changing recording conditions, exhibiting significant drops in performance across subjects, and even across sessions. Multi-channel surface EMG, also referred to as high-density sEMG (HD-sEMG) systems, have been used to improve performance with the information collected through the use of additional electrodes. However, a lack of robustness is ever present due to limited datasets and the difficulties in addressing sources of variability, such as electrode placement. In this study, we propose training on a collection of input channel subsets and augmenting our training distribution with data from different electrode locations, simultaneously targeting electrode shift and reducing input dimensionality. Our method increases robustness against electrode shift and results in significantly higher intersession performance across subjects and classification algorithms.

It's easy to fool yourself: Case studies on identifying bias and confounding in bio-medical datasets

Confounding variables are a well known source of nuisance in biomedical studies. They present an even greater challenge when we combine them with black-box machine learning techniques that operate on raw data. This work presents two case studies. In one, we discovered biases arising from systematic errors in the data generation process. In the other, we found a spurious source of signal unrelated to the prediction task at hand. In both cases, our prediction models performed well but under careful examination hidden confounders and biases were revealed. These are cautionary tales on the limits of using machine learning techniques on raw data from scientific experiments.