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首页> 外文期刊>Biomedical Optics Express >Improved sparse reconstruction for fluorescence molecular tomography with L1/2 regularization
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Improved sparse reconstruction for fluorescence molecular tomography with L1/2 regularization

机译:L 1/2 正则化的改进的稀疏重建荧光分子层析成像

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摘要

Fluorescence molecular tomography (FMT) is a promising imaging technique that allows in vivo visualization of molecular-level events associated with disease progression and treatment response. Accurate and efficient 3D reconstruction algorithms will facilitate the wide-use of FMT in preclinical research. Here, we utilize L1/2-norm regularization for improving FMT reconstruction. To efficiently solve the nonconvex L1/2-norm penalized problem, we transform it into a weighted L1-norm minimization problem and employ a homotopy-based iterative reweighting algorithm to recover small fluorescent targets. Both simulations on heterogeneous mouse model and in vivo experiments demonstrated that the proposed L1/2-norm method outperformed the comparative L1-norm reconstruction methods in terms of location accuracy, spatial resolution and quantitation of fluorescent yield. Furthermore, simulation analysis showed the robustness of the proposed method, under different levels of measurement noise and number of excitation sources.
机译:荧光分子层析成像(FMT)是一种很有前途的成像技术,可以在体内可视化与疾病进展和治疗反应相关的分子水平事件。准确高效的3D重建算法将有助于FMT在临床前研究中的广泛使用。在这里,我们利用L1 / 2范数正则化来改善FMT重建。为了有效地解决非凸L1 / 2范数的惩罚问题,我们将其转化为加权L1范数的最小化问题,并采用基于同伦的迭代重加权算法来恢复小的荧光目标。对异质小鼠模型的仿真和体内实验均表明,所提出的L1 / 2-范数方法在定位精度,空间分辨率和荧光产量的定量方面优于比较的L1-范数重构方法。此外,仿真分析显示了该方法在不同水平的测量噪声和激励源数量下的鲁棒性。

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