Abstract:Real-world multimodal systems routinely face missing-input scenarios, and in reality, robots lose audio in a factory or a clinical record omits lab tests at inference time. Standard fusion layers either preserve robustness or calibration but never both. We introduce Adaptive Entropy-Gated Contrastive Fusion (AECF), a single light-weight layer that (i) adapts its entropy coefficient per instance, (ii) enforces monotone calibration across all modality subsets, and (iii) drives a curriculum mask directly from training-time entropy. On AV-MNIST and MS-COCO, AECF improves masked-input mAP by +18 pp at a 50% drop rate while reducing ECE by up to 200%, yet adds 1% run-time. All back-bones remain frozen, making AECF an easy drop-in layer for robust, calibrated multimodal inference.
Abstract:Electroencephalographic (EEG) monitoring of neural activity is widely used for sleep disorder diagnostics and research. The standard of care is to manually classify 30-second epochs of EEG time-domain traces into 5 discrete sleep stages. Unfortunately, this scoring process is subjective and time-consuming, and the defined stages do not capture the heterogeneous landscape of healthy and clinical neural dynamics. This motivates the search for a data-driven and principled way to identify the number and composition of salient, reoccurring brain states present during sleep. To this end, we propose a Hierarchical Dirichlet Process Hidden Markov Model (HDP-HMM), combined with wide-sense stationary (WSS) time series spectral estimation to construct a generative model for personalized subject sleep states. In addition, we employ multitaper spectral estimation to further reduce the large variance of the spectral estimates inherent to finite-length EEG measurements. By applying our method to both simulated and human sleep data, we arrive at three main results: 1) a Bayesian nonparametric automated algorithm that recovers general temporal dynamics of sleep, 2) identification of subject-specific "microstates" within canonical sleep stages, and 3) discovery of stage-dependent sub-oscillations with shared spectral signatures across subjects.