首页> 外文会议>Conference on Imaging, Manipulation, and Analysis of Biomolecules, Cell, and Tissues; 20080121-23; San Jose,CA(US) >Data fitting and image fine-tuning approach to solve the inverse problem in fluorescence molecular imaging
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Data fitting and image fine-tuning approach to solve the inverse problem in fluorescence molecular imaging

机译:数据拟合和图像微调方法解决荧光分子成像中的逆问题

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One of the most challenging problems in medical imaging is to "see" a tumour embedded into tissue, which is a turbid medium, by using fluorescent probes for tumour labeling. This problem, despite the efforts made during the last years, has not been fully encountered yet, due to the non-linear nature of the inverse problem and the convergence failures of many optimization techniques. This paper describes a robust solution of the inverse problem, based on data fitting and image fine-tuning techniques. As a forward solver the coupled radiative transfer equation and diffusion approximation model is proposed and compromised via a finite element method, enhanced with adaptive multi-grids for faster and more accurate convergence. A database is constructed by application of the forward model on virtual tumours with known geometry, and thus fluorophore distribution, embedded into simulated tissues. The fitting procedure produces the best matching between the real and virtual data, and thus provides the initial estimation of the fluorophore distribution. Using this information, the coupled radiative transfer equation and diffusion approximation model has the required initial values for a computational reasonable and successful convergence during the image fine-tuning application.
机译:医学成像中最具挑战性的问题之一是通过使用荧光探针进行肿瘤标记来“看到”嵌入到混浊介质中的肿瘤。尽管反问问题的非线性性质和许多优化技术的收敛失败,但尽管在过去的几年中付出了很多努力,但这个问题尚未完全解决。本文介绍了基于数据拟合和图像微调技术的反问题的鲁棒解决方案。作为正向求解器,提出并耦合了辐射传递方程和扩散近似模型,并通过有限元方法加以折衷,并通过自适应多网格进行了增强,以实现更快,更准确的收敛。通过将正向模型应用于具有已知几何结构的虚拟肿瘤,从而将荧光团分布嵌入到模拟组织中,来构建数据库。拟合过程在真实数据和虚拟数据之间产生最佳匹配,从而提供了荧光团分布的初始估计。使用此信息,耦合的辐射传递方程和扩散近似模型具有在图像微调应用期间计算合理且成功收敛所需的初始值。

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