Search arXivSearch

arXiv · 2306.08610

Image Reconstruction Using a Mixture Score Function (MSF)

Abstract

Computed tomography (CT) reconstructs volumetric images using X-ray projection data acquired from multiple angles around an object. For low-dose or sparse-view CT scans, the classic image reconstruction algorithms often produce severe noise and artifacts. To address this issue, we develop a novel iterative image reconstruction method based on maximum a posteriori (MAP) estimation. In the MAP framework, the score function, i.e., the gradient of the logarithmic probability density distribution, plays a crucial role as an image prior in the iterative image reconstruction process. By leveraging the Gaussian mixture model, we derive a novel score matching formula to establish an advanced score function (ADSF) through deep learning. Integrating the new ADSF into the image reconstruction process, a new ADSF iterative reconstruction method is developed to improve image reconstruction quality. The convergence of the ADSF iterative reconstruction algorithm is proven through mathematical analysis. The performance of the ADSF reconstruction method is also evaluated on both public medical image datasets and clinical raw CT datasets. Our results show that the ADSF reconstruction method can achieve better denoising and deblurring effects than the state-of-the-art reconstruction methods, showing excellent generalizability and stability.

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

Wenxiang Cong, Wenjun Xia, Ge Wang. 2024-02-29. Image Reconstruction Using a Mixture Score Function (MSF). https://arxiv.org/abs/2306.08610

Cite the original work for its findings. Save a collection to share your selection of sources.

KEEP EXPLORING

Related papers

Prediction of biological radiation effects based on ionization clusters (nanodosimetry)

This article reviews approaches that link the formation of ionization clusters in nanometric volumes to radiobiological effectiveness. The corresponding models were developed as the field of nanodosimetry developed. Some address early biological radiation effects, such as DNA damage, while most aim to predict cell survival or inactivation. The models also differ in the nanodosimetric quantities considered, with many based on the probability distribution of ionization cluster formation in a single target. Some models account for the synergistic effects of pairs of ionization clusters formed in different targets. Several models feature macroscopic aggregation frameworks based on particle fluence, which are proposed for use in radiotherapy treatment planning, particularly in ion-beam radiotherapy. The models are presented here using harmonized terminology and notation for nanodosimetric quantities. An extension of the conceptual framework of nanodosimetry is also discussed. This extension transitions from a target-centered description to a track-centered description. It also introduces nanodosimetry-based analogs of dosimetric concepts, such as dose and linear energy transfer. This paper traces and summarizes the historical development of nanodosimetry-based biological effect models and discusses conceptual aspects of the models to reveal their underlying assumptions and the extent to which they are mechanistic or merely elucidate correlations. Eventually, an attempt is made to identify the key open questions in this field that still need to be addressed.

physics.med-ph

Contextual Cellular Growth (ConCeG) of neural cells for realistic grey matter tissue generation for diffusion MRI simulations

Accurate interpretation of diffusion magnetic resonance imaging (dMRI) signals in grey matter (GM) remains challenging due to the complex, heterogeneous, and densely packed cellular environment. Numerical phantoms provide a controlled framework for investigating the relationship between microstructure and diffusion signals, yet existing approaches often lack the morphological realism and multi-cellular organisation required to faithfully represent GM tissue. In this work, we introduce Contextual Cellular Growth (ConCeG), a generative framework for creating individual cells or constructing dense, three-dimensional, multi-cellular GM substrates informed by real neuronal and glial morphologies. The method combines topological neuron synthesis with a spatially constrained growth network, allowing for the controlled generation of heterogeneous cellular environments with realistic intra- and extracellular compartments. Synthetic cells are generated using morphological and topological characteristics derived from biological reconstructions. We validate the framework through comparisons of structural features with real cellular data, demonstrating strong agreement in branch order, length, angle, and tortuosity distributions. Power spectrum analysis further shows that both intracellular compartments reproduce the spatial correlations observed in biological tissue. Together, these results show ConCeG provides a biologically grounded framework for generating grey matter substrates suitable for large scale diffusion MRI simulation.

physics.med-ph

Magnetic Field of Firing Neuron in Humans: Measurable by Quantum Sensing MRI?

Firing neurons generate action potentials that propagate along axons to transmit signals supporting cognitive functions. These electrical currents generate magnetic fields, yet direct detection of these neuronal magnetic fields by MRI remains elusive. This Mini Review investigates why this goal has been proven difficult to achieve and whether an emerging approach, quantum sensing MRI, can overcome the challenge.

physics.med-ph