Bayesian imaging inverse problems often require sampling from high-dimensional posterior distributions. While recent score-based and diffusion models provide expressive Bayesian priors, their sampling procedures remain inherently sequential and computationally expensive for large-scale imaging applications. We propose PiX-MC, a time-parallel posterior sampling framework based on proximal Langevin dynamics and Picard iteration. The proximal-likelihood formulation exploits the fact that many imaging likelihoods admit efficient, problem-specific proximal operators, while Picard refinement exposes parallelism across discretization nodes and naturally supports multi-GPU implementation. To further improve practical scalability and sampling performance, we develop multi-block and annealed variants of the proposed framework. We establish convergence guarantees under transparent assumptions, accommodating non-log-concave posteriors, imperfect learned score models, multi-block implementations, and annealing schedules. Experiments on a diverse collection of imaging inverse problems demonstrate that PiX-MC substantially reduces wall-clock time while preserving reconstruction quality. On a $512\times512\times80$ sparse-view computed tomography (CT) problem, annealed multi-block PiX-MC achieves up to a $50\times$ runtime speedup over the standard Langevin sampler using eight GPUs.
Andreas W. Aspe, Jonas Jalili Pedersen, Andreas Ohrt Johansen +4cs.CV cs.AI
This review provides an overview of recent advancements in automated segmentation methods on Computed Tomography (CT) for two types of cardiac fat: Epicardial adipose Tissue (EAT) and Pericardial Adipose Tissue (PAT). These fat deposits, separated by the pericardium, have been linked to various cardiovascular diseases, with EAT receiving the most research attention. Their complex anatomical context makes manual quantification highly time-consuming and prone to considerable inter-observer variability. Automated methods effectively address these complications, offering a more efficient and consistent solution. This study encompasses a broad range of methods, spanning AI as well as non-AI approaches. Additionally, it presents the remaining challenges, including the need for larger annotated public datasets and optimized attenuation thresholds for contrast-enhanced CT. It is demonstrated that automated methods are able to achieve segmentation results comparable to the quality of human annotation, proving their potential as a clinical tool for discovering new biomarkers and enhancing patient outcomes.
Quadratic unconstrained binary optimization (QUBO)-based quantum computed tomography (CT) casts reconstruction as a binary quadratic problem for quantum annealing and hybrid quantum--classical solvers. For grayscale CT, however, image encoding is constrained by the binary-variable budget: fixed global bit-plane encodings increase QUBO size and coupling complexity as gray-level precision improves, whereas low-bit encodings introduce quantization error. We propose a QUBO-based grayscale CT reconstruction framework that combines dynamic interval encoding with prior-balanced optimization. Each refinement round encodes active pixels only within local gray-level intervals around the current estimate, and a boundary-hit-guided update rule adaptively switches between search expansion and local refinement. To improve optimization stability, the method balances projection-domain data consistency and an edge-preserving quadratic prior before forming the final QUBO. Sparse-view and limited-angle fan-beam CT experiments show that the proposed method recovers structures and gray-level distributions more faithfully than the evaluated analytic, iterative, variational, and representation-based baselines. Expressivity analysis and ablation studies further indicate that the improvement mainly arises from effective gray-level representation through dynamic local encoding and more stable data-fidelity--prior coupling. Experiments on the D-Wave hybrid binary quadratic model (BQM) solver further demonstrate that the formulation is executable on a hardware-backed hybrid quantum--classical backend.
Sexual identification of decomposed cadavers challenges traditional methods dependent on visual anthropological analysis. This study evaluates state-of-the-art deep learning (including YOLO26, YOLO11, ConvNeXt-Tiny, EfficientNetV2, ViT-B16, VGG16, and ResNet50) with transfer learning to automatically determine biological sex from forensic computed tomography (CT) scans. We analyzed 141 autopsied cadavers from the Forensic Medical Institute of Goiânia-GO, including a broad age range and varying conditions of preservation. The three-dimensional reconstructions of the pelvis and skull were converted into standardized two-dimensional profile projections, contributing to the study of this new technical approach. Data augmentation techniques compensated for sample limitations. Two scenarios were validated: binary and quaternary classification (one class per sex vs. one class per anatomical region of each sex). The best-performing model achieved highly consistent results on the pelvis region and still satisfactory performance on the skull region, reaching an overall patient-level accuracy of 95.65%, recall of 92.86%, F1- score of 94.36%, and precision of 97.22%, maintaining consistent performance across the evaluated cases, including those with trauma-related artifacts. Results indicate the technical feasibility of the methodology, demonstrating that deep learning models can provide objective, high-speed skeletal analysis. Since the study was conducted using data from a single institution and a single computed tomography scanner, further validation across multiple centers and scanners is required to assess the generalizability of the proposed approach
Ziya Ata Yazıcı, N. Sinem Gezer, İlkay Öksüz +19cs.CV cs.AI
Accurate segmentation of hepatic and portal vessels in contrast-enhanced computed tomography angiography (CTA) remains challenging due to complex vascular topology, peripheral visibility limitations, and acquisition-induced ambiguities. While existing public datasets offer valuable benchmarks, few include clinically realistic annotation constraints. We introduce VEELA (Vessel Extraction and Extrication for Liver Analysis), a rigorously curated liver vessel dataset derived from 40 CTA scans inherited from the CHAOS grand-challenge cohort. All vessels were manually delineated slice-by-slice under multi-expert consensus, using a strict visibility-driven annotation policy and avoiding anatomically inferred interpolation. This design explicitly captures anatomical variability and imaging-related uncertainty. As a continuation of the CHAOS challenge, VEELA enables reproducible cross-benchmark evaluation while extending the scope to fine-grained hepatic and portal vessel segmentation. We further establish a standardized benchmarking framework and analyze complementary evaluation metrics, including topology-aware (clDice), overlap-based (IoU), boundary-sensitive (NSD), and geometry-aware (area, length) measures. Our results demonstrate that different metrics capture distinct aspects of vascular integrity, underscoring the necessity of multi-perspective evaluation for clinically meaningful vessel segmentation. VEELA is publicly released to facilitate reproducible research and support the development of robust vascular segmentation methods. Researchers can access the evaluation metrics, dataset, and submission platform at https://www.synapse.org/Synapse:syn65471967.