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Robust transformed l1 metric for fluorescence molecular tomography

算法 稳健性(进化) 计算机科学 公制(单位) 数学 化学 生物化学 运营管理 经济 基因
作者
Yating Yuan,Huangjian Yi,Dizhen Kang,Jingjing Yu,Hongbo Guo,Xuelei He,Xiaowei He
出处
期刊:Computer Methods and Programs in Biomedicine [Elsevier]
卷期号:234: 107503-107503 被引量:5
标识
DOI:10.1016/j.cmpb.2023.107503
摘要

Fluorescence molecular tomography (FMT) is a non-invasive molecular imaging modality that can be used to observe the three-dimensional distribution of fluorescent probes in vivo. FMT is a promising imaging technique in clinical and preclinical research that has attracted significant attention. Numerous regularization based reconstruction algorithms have been proposed. However, traditional algorithms that use the squared l2-norm distance usually exaggerate the influence of noise and measurement and calculation errors, and their robustness cannot be guaranteed.In this study, we propose a novel robust transformed l1 (TL1) metric that interpolates l0 and l1 norms through a nonnegative parameter α∈(0,+∞). The TL1 metric looks like the lp-norm with p∈(0,1). These are markedly different because TL1 metric has two properties, boundedness and Lipschitz-continuity, which make the TL1 criterion suitable distance metric, particularly for robustness, owing to its stronger noise suppression. Subsequently, we apply the proposed metric to FMT and build a robust model to reduce the influence of noise. The nonconvexity of the proposed model made direct optimization difficult, and a continuous optimization method was developed to solve the model. The problem was converted into a difference in convex programming problem for the TL1 metric (DCATL1), and the corresponding algorithm converged linearly.Various numerical simulations and in vivo bead-implanted mouse experiments were conducted to verify the performance of the proposed method. The experimental results show that the DCATL1 algorithm is more robust than the state-of-the-art approaches and achieves better source localization and morphology recovery.The in vivo experiments showed that DCATL1 can be used to visualize the distribution of fluorescent probes inside biological tissues and promote preclinical application in small animals, demonstrating the feasibility and effectiveness of the proposed method.

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