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Extended Finite Element Method with Simplified Spherical Harmonics Approximation for the Forward Model of Optical Molecular Imaging

机译:具有简化球形谐波的光学分子成像前向模型的扩展有限元方法

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An extended finite element method (XFEM) for the forward model of 3D optical molecular imaging is developed with simplified spherical harmonics approximation (SPN). In XFEM scheme ofSPNequations, the signed distance function is employed to accurately represent the internal tissue boundary, and then it is used to construct the enriched basis function of the finite element scheme. Therefore, the finite element calculation can be carried out without the time-consuming internal boundary mesh generation. Moreover, the required overly fine mesh conforming to the complex tissue boundary which leads to excess time cost can be avoided. XFEM conveniences its application to tissues with complex internal structure and improves the computational efficiency. Phantom and digital mouse experiments were carried out to validate the efficiency of the proposed method. Compared with standard finite element method and classical Monte Carlo (MC) method, the validation results show the merits and potential of the XFEM for optical imaging.
机译:用简化的球形谐波近似(SPN)开发了用于3D光学分子成像的前向模型的扩展有限元方法(XFEM)。在XFEM方案的XFEM方案中,采用符号距离功能来精确地表示内部组织边界,然后用于构建有限元方案的富集基函数。因此,可以在没有耗时的内部边界网格生成的情况下执行有限元计算。此外,可以避免符合复杂组织边界的所需的过细网格,这可以避免导致过量的时间成本。 XFEM将其应用于具有复杂内部结构的组织,提高了计算效率。进行幻影和数字鼠标实验以验证所提出的方法的效率。与标准有限元方法和经典蒙特卡罗(MC)方法相比,验证结果显示了光学成像的XFEM的优点和潜力。

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