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Gradient Projection for Sparse Reconstruction Method for Dynamic Fluorescence Molecular Tomography

机译:动态荧光分子断层扫描稀疏重建法的梯度投影

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Dynamic fluorescence molecular tomography (FMT) is a promising optical imaging technique for three-dimensionally demonstrating the metabolic process of fluorophore in small animals. Conventional FMT methods focus on reconstructing static distribution of fluorescent yield, and the reconstruction results may perform poorly if the boundary measurement data, acquired from time-varying fluorophore, were directly used in these methods. In this study, we apply joint l_1 and Laplacian manifold regularization model to dynamic FMT. The l_1-norm regularization method is used to deal with the ill-posedness of FMT, and the Laplacian manifold regularization is introduced to obtain spatial structure information of boundary measurements. Then, we use gradient projection for sparse reconstruction (GPSR) method to solve the joint regularization model. Since the boundary measurements are obtained from different time points, the input data is converted from a vector to a matrix, and each column of the matrix corresponds to a time point. Thus, a sequence of fluorophore concentration images, corresponding to different time points, can be reconstructed in one step. Numerical simulation experiments are performed and the results indicate that the proposed method can recover the dynamic fluorophore well.
机译:动态荧光分子断层扫描(FMT)是一个有前途的光学成像技术,用于三维地证明小动物中荧光团的代谢过程。传统的FMT方法专注于重建荧光产量的静态分布,并且如果在这些方法中直接使用从时变荧光团获得的边界测量数据,重建结果可能表现不佳。在这项研究中,我们将联合L_1和拉普拉斯歧管正则化模型应用于动态FMT。 L_1-NORM正则化方法用于处理FMT的不良姿势,并引入LAPPLIAN歧管正则化以获得边界测量的空间结构信息。然后,我们使用劣质重建(GPSR)方法来解决联合正则化模型的梯度投影。由于从不同的时间点获得边界测量,因此输入数据从向量转换为矩阵,并且矩阵的每列对应于时间点。因此,可以在一个步骤中重建一系列对应于不同时间点的荧光团浓度图像序列。进行数值模拟实验,结果表明所提出的方法可以恢复动态荧光团井。

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