We propose the position-based scaled gradient (PSG) that scales the gradient depending on the position of a weight vector to make it more compression-friendly. First, we theoretically show that applying PSG to the standard gradient descent (GD), which is called PSGD, is equivalent to the GD in the warped weight space, a space made by warping the original weight space via an appropriately designed invertible function. Second, we empirically show that PSG acting as a regularizer to a weight vector is favorable for model compression domains such as quantization and pruning. PSG reduces the gap between the weight distributions of a full-precision model and its compressed counterpart. This enables the versatile deployment of a model either as an uncompressed mode or as a compressed mode depending on the availability of resources. The experimental results on CIFAR-10/100 and ImageNet datasets show the effectiveness of the proposed PSG in both domains of pruning and quantization even for extremely low bits. The code is released in Github.

Study Objectives: Wrist accelerometry is widely used for inferring sleep-wake state. Previous works demonstrated poor wake detection, without cross-device generalizability and validation in different age range and sleep disorders. We developed a robust deep learning model for to detect sleep-wakefulness from triaxial accelerometry and evaluated its validity across three devices and in a large adult population spanning a wide range of ages with and without sleep disorders. Methods: We collected wrist accelerometry simultaneous to polysomnography (PSG) in 453 adults undergoing clinical sleep testing at a tertiary care sleep laboratory, using three devices. We extracted features in 30-second epochs and trained a 3-class model to detect wake, sleep, and sleep with arousals, which was then collapsed into wake vs. sleep using a decision tree. To enhance wake detection, the model was specifically trained on randomly selected subjects with low sleep efficiency and/or high arousal index from one device recording and then tested on the remaining recordings. Results: The model showed high performance with F1 Score of 0.86, sensitivity (sleep) of 0.87, and specificity (wakefulness) of 0.78, and significant and moderate correlation to PSG in predicting total sleep time (R=0.69) and sleep efficiency (R=0.63). Model performance was robust to the presence of sleep disorders, including sleep apnea and periodic limb movements in sleep, and was consistent across all three models of accelerometer. Conclusions: We present a deep model to detect sleep-wakefulness from actigraphy in adults with relative robustness to the presence of sleep disorders and generalizability across diverse commonly used wrist accelerometers.

Polysomnography signals are highly heterogeneous, varying in modality composition (e.g., EEG, EOG, ECG), channel availability (e.g., frontal, occipital EEG), and acquisition protocols across datasets and clinical sites. Most existing models that process polysomnography data rely on a fixed subset of modalities or channels and therefore neglect to fully exploit its inherently multimodal nature. We address this limitation by introducing NAP (Neural Aggregator of Predictions), an attention-based model which learns to combine multiple prediction streams using a tri-axial attention mechanism that captures temporal, spatial, and predictor-level dependencies. NAP is trained to adapt to different input dimensions. By aggregating outputs from frozen, pretrained single-channel models, NAP consistently outperforms individual predictors and simple ensembles, achieving state-of-the-art zero-shot generalization across multiple datasets. While demonstrated in the context of automated sleep staging from polysomnography, the proposed approach could be extended to other multimodal physiological applications.

Neural Information Processing Systems http://nips.cc/

We propose the position-based scaled gradient (PSG) that scales the gradient depending on the position of a weight vector to make it more compression-friendly. First, we theoretically show that applying PSG to the standard gradient descent (GD), which is called PSGD, is equivalent to the GD in the warped weight space, a space made by warping the original weight space via an appropriately designed invertible function. Second, we empirically show that PSG acting as a regularizer to a weight vector is favorable for model compression domains such as quantization and pruning. PSG reduces the gap between the weight distributions of a full-precision model and its compressed counterpart. This enables the versatile deployment of a model either as an uncompressed mode or as a compressed mode depending on the availability of resources.

Manual scoring of polysomnography (PSG) is a time intensive task, prone to inter scorer variability that can impact diagnostic reliability. This study investigates the integration of decision support systems (DSS) into PSG scoring workflows, focusing on their effects on accuracy, scoring time, and potential biases toward recommendations from artificial intelligence (AI) compared to human generated recommendations. Using a novel online scoring platform, we conducted a repeated measures study with sleep technologists, who scored traditional and self applied PSGs. Participants were occasionally presented with recommendations labeled as either human or AI generated. We found that traditional PSGs tended to be scored slightly more accurately than self applied PSGs, but this difference was not statistically significant. Correct recommendations significantly improved scoring accuracy for both PSG types, while incorrect recommendations reduced accuracy. No significant bias was observed toward or against AI generated recommendations compared to human generated recommendations. These findings highlight the potential of AI to enhance PSG scoring reliability. However, ensuring the accuracy of AI outputs is critical to maximizing its benefits. Future research should explore the long term impacts of DSS on scoring workflows and strategies for integrating AI in clinical practice.

Pediatric sleep is an important but often overlooked area in health informatics. We present PedSleepMAE, a generative model that fully leverages multimodal pediatric sleep signals including multichannel EEGs, respiratory signals, EOGs and EMG. This masked autoencoder-based model performs comparably to supervised learning models in sleep scoring and in the detection of apnea, hypopnea, EEG arousal and oxygen desaturation. Its embeddings are also shown to capture subtle differences in sleep signals coming from a rare genetic disorder. Furthermore, PedSleepMAE generates realistic signals that can be used for sleep segment retrieval, outlier detection, and missing channel imputation. This is the first general-purpose generative model trained on multiple types of pediatric sleep signals.

Federated learning (FL) is a decentralized AI mechanism suitable for a large number of devices like in smart IoT. A major challenge of FL is the non-IID dataset problem, originating from the heterogeneous data collected by FL participants, leading to performance deterioration of the trained global model. There have been various attempts to rectify non-IID dataset, mostly focusing on manipulating the collected data. This paper, however, proposes a novel approach to ensure data IIDness by properly clustering and grouping mobile IoT nodes exploiting their geographical characteristics, so that each FL group can achieve IID dataset. We first provide an experimental evidence for the independence and identicalness features of IoT data according to the inter-device distance, and then propose Dynamic Clustering and Partial-Steady Grouping algorithms that partition FL participants to achieve near-IIDness in their dataset while considering device mobility. Our mechanism significantly outperforms benchmark grouping algorithms at least by 110 times in terms of the joint cost between the number of dropout devices and the evenness in per-group device count, with a mild increase in the number of groups only by up to 0.93 groups.