LGMay 28

EMAG: Differentiable 4D Gaussian Mixture Splatting for EEG Spatial Super-Resolution

arXiv:2605.2973111.5
Predicted impact top 45% in LG · last 90 daysOriginality Incremental advance
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For EEG researchers and clinicians, EMAG provides a cost-effective way to achieve high-resolution EEG without expensive hardware, with interpretable source visualization.

EMAG introduces a differentiable framework that reconstructs high-density EEG signals from sparse low-density electrodes by modeling brain sources as anisotropic 4D Gaussians, outperforming state-of-the-art methods on three benchmarks at most super-resolution factors.

High-density electroencephalography (HD-EEG) enables fine-grained measurement of cortical activity but requires expensive hardware and lengthy setup times, limiting its clinical and research accessibility. We propose EMAG (EEG Mixture of Anisotropic Gaussians), a differentiable framework that reconstructs HD-EEG signals from a sparse subset of low-density (LD) electrodes by representing brain electrical sources as a mixture of anisotropic 4D space-time Gaussians. EMAG places a mixture of multiple Gaussians at each point of a spherical brain grid, each parameterized by a full 4 x 4 precision matrix, enabling anisotropic spatial spreads and explicit coupling between spatial and temporal dimensions. The forward model renders scalp EEG via differentiable Gaussian field contributions at electrode locations, enabling end-to-end training without explicit source localization supervision. We evaluate EMAG on three public EEG benchmarks (Localize-MI, SEED, and SEED-IV) at super-resolution factors of 2x through 8/16x. EMAG outperforms the current state-of-the-art EEG super-resolution method at most super-resolution factors on three standard benchmarks (Localize-MI, SEED, SEED-IV). The explicit Gaussian parameterization further enables direct visualization and interpretability of learned brain source configurations, potentially opening avenues for clinical and neuroscientific applications, such as source localization or biomarker discovery.

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