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

Compressive Sensing (CS) is an effective approach for fast Magnetic Resonance Imaging (MRI). It aims at reconstructing MR image from a small number of under-sampled data in k-space, and accelerating the data acquisition in MRI. To improve the current MRI system in reconstruction accuracy and computational speed, in this paper, we propose a novel deep architecture, dubbed ADMM-Net. ADMM-Net is defined over a data flow graph, which is derived from the iterative procedures in Alternating Direction Method of Multipliers (ADMM) algorithm for optimizing a CS-based MRI model. In the training phase, all parameters of the net, e.g., image transforms, shrinkage functions, etc., are discriminatively trained end-to-end using L-BFGS algorithm. In the testing phase, it has computational overhead similar to ADMM but uses optimized parameters learned from the training data for CS-based reconstruction task. Experiments on MRI image reconstruction under different sampling ratios in k-space demonstrate that it significantly improves the baseline ADMM algorithm and achieves high reconstruction accuracies with fast computational speed.

We demonstrate qualitatively and quantitatively that our proposed approach is able tomodel the appearance ofindividual strokes,aswell asthe compositional structure oflargerdiagram drawings.

Robotic systems are transforming image-guided interventions by enhancing accuracy and minimizing radiation exposure. A significant challenge in robotic assistance lies in surgical path planning, which often relies on the registration of intraoperative 2D images with preoperative 3D CT scans. This requirement can be burdensome and costly, particularly in procedures like vertebroplasty, where preoperative CT scans are not routinely performed. To address this issue, we introduce a differentiable rendering-based framework for 3D transpedicular path planning utilizing bi-planar 2D X-rays. Our method integrates differentiable rendering with a vertebral atlas generated through a Statistical Shape Model (SSM) and employs a learned similarity loss to refine the SSM shape and pose dynamically, independent of fixed imaging geometries. We evaluated our framework in two stages: first, through vertebral reconstruction from orthogonal X-rays for benchmarking, and second, via clinician-in-the-loop path planning using arbitrary-view X-rays. Our results indicate that our method outperformed a normalized cross-correlation baseline in reconstruction metrics (DICE: 0.75 vs. 0.65) and achieved comparable performance to the state-of-the-art model ReVerteR (DICE: 0.77), while maintaining generalization to arbitrary views. Success rates for bipedicular planning reached 82% with synthetic data and 75% with cadaver data, exceeding the 66% and 31% rates of a 2D-to-3D baseline, respectively. In conclusion, our framework facilitates versatile, CT-free 3D path planning for robot-assisted vertebroplasty, effectively accommodating real-world imaging diversity without the need for preoperative CT scans.

Wastewater-based genomic surveillance has emerged as a powerful tool for population-level viral monitoring, offering comprehensive insights into circulating viral variants across entire communities. However, this approach faces significant computational challenges stemming from high sequencing noise, low viral coverage, fragmented reads, and the complete absence of labeled variant annotations. Traditional reference-based variant calling pipelines struggle with novel mutations and require extensive computational resources. We present a comprehensive framework for unsupervised viral variant detection using Vector-Quantized Variational Autoencoders (VQ-VAE) that learns discrete codebooks of genomic patterns from k-mer tokenized sequences without requiring reference genomes or variant labels. Our approach extends the base VQ-VAE architecture with masked reconstruction pretraining for robustness to missing data and contrastive learning for highly discriminative embeddings. Evaluated on SARS-CoV-2 wastewater sequencing data comprising approximately 100,000 reads, our VQ-VAE achieves 99.52% mean token-level accuracy and 56.33% exact sequence match rate while maintaining 19.73% codebook utilization (101 of 512 codes active), demonstrating efficient discrete representation learning. Contrastive fine-tuning with different projection dimensions yields substantial clustering improvements: 64-dimensional embeddings achieve +35% Silhouette score improvement (0.31 to 0.42), while 128-dimensional embeddings achieve +42% improvement (0.31 to 0.44), clearly demonstrating the impact of embedding dimensionality on variant discrimination capability. Our reference-free framework provides a scalable, interpretable approach to genomic surveillance with direct applications to public health monitoring.

Compressive Sensing (CS) is an effective approach for fast Magnetic Resonance Imaging (MRI). It aims at reconstructing MR image from a small number of under-sampled data in k-space, and accelerating the data acquisition in MRI. To improve the current MRI system in reconstruction accuracy and computational speed, in this paper, we propose a novel deep architecture, dubbed ADMM-Net. ADMM-Net is defined over a data flow graph, which is derived from the iterative procedures in Alternating Direction Method of Multipliers (ADMM) algorithm for optimizing a CS-based MRI model. In the training phase, all parameters of the net, e.g., image transforms, shrinkage functions, etc., are discriminatively trained end-to-end using L-BFGS algorithm. In the testing phase, it has computational overhead similar to ADMM but uses optimized parameters learned from the training data for CS-based reconstruction task. Experiments on MRI image reconstruction under different sampling ratios in k-space demonstrate that it significantly improves the baseline ADMM algorithm and achieves high reconstruction accuracies with fast computational speed.

At the same time, the use of deep learning as the basis for neural decoding has received less widespread attention.

This study investigates embedding reconstruction attacks in large language models (LLMs) applied to genomic sequences, with a specific focus on how fine-tuning affects vulnerability to these attacks. Building upon Pan et al.'s seminal work demonstrating that embeddings from pretrained language models can leak sensitive information, we conduct a comprehensive analysis using the HS3D genomic dataset to determine whether task-specific optimization strengthens or weakens privacy protections. Our research extends Pan et al.'s work in three significant dimensions. First, we apply their reconstruction attack pipeline to pretrained and fine-tuned model embeddings, addressing a critical gap in their methodology that did not specify embedding types. Second, we implement specialized tokenization mechanisms tailored specifically for DNA sequences, enhancing the model's ability to process genomic data, as these models are pretrained on natural language and not DNA. Third, we perform a detailed comparative analysis examining position-specific, nucleotide-type, and privacy changes between pretrained and fine-tuned embeddings. We assess embeddings vulnerabilities across different types and dimensions, providing deeper insights into how task adaptation shifts privacy risks throughout genomic sequences. Our findings show a clear distinction in reconstruction vulnerability between pretrained and fine-tuned embeddings. Notably, fine-tuning strengthens resistance to reconstruction attacks in multiple architectures -- XLNet (+19.8\%), GPT-2 (+9.8\%), and BERT (+7.8\%) -- pointing to task-specific optimization as a potential privacy enhancement mechanism. These results highlight the need for advanced protective mechanisms for language models processing sensitive genomic data, while highlighting fine-tuning as a potential privacy-enhancing technique worth further exploration.

Dynamic Bayesian networks (DBNs) are increasingly used in healthcare due to their ability to model complex temporal relationships in patient data while maintaining interpretability, an essential feature for clinical decision-making. However, existing approaches to handling missing data in longitudinal clinical datasets are largely derived from static Bayesian networks literature, failing to properly account for the temporal nature of the data. This gap limits the ability to quantify uncertainty over time, which is particularly critical in settings such as intensive care, where understanding the temporal dynamics is fundamental for model trustworthiness and applicability across diverse patient groups. Despite the potential of DBNs, a full Bayesian framework that integrates missing data handling remains underdeveloped. In this work, we propose a novel Gibbs sampling-based method for learning DBNs from incomplete data. Our method treats each missing value as an unknown parameter following a Gaussian distribution. At each iteration, the unobserved values are sampled from their full conditional distributions, allowing for principled imputation and uncertainty estimation. We evaluate our method on both simulated datasets and real-world intensive care data from critically ill patients. Compared to standard model-agnostic techniques such as MICE, our Bayesian approach demonstrates superior reconstruction accuracy and convergence properties. These results highlight the clinical relevance of incorporating full Bayesian inference in temporal models, providing more reliable imputations and offering deeper insight into model behavior. Our approach supports safer and more informed clinical decision-making, particularly in settings where missing data are frequent and potentially impactful.