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Cerebrovascular network registration via an efficient attributed graph matching technique

机译:通过有效的归属图形匹配技术进行脑血管网络注册

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摘要

Registration of vascular networks is an indispensable element of prognostic and diagnostic studies that require structural analysis and comparison over time, among different samples, and to a gold standard. However, vascular networks manifest low spatial texture and sparse structural content so that even small variations in their location can make the intensity-based registration inefficient and prone to errors. Motivated by geometrical graph-based models developed in our prior work, we use the shape information in the graph topology sense to enhance the registration performance. An efficient feature-based registration is presented that seeks correspondence of the bifurcations and branches in a graph matching scheme. Since the graph matching is originally posed a NP-hard quadratic assignment problem (QAP) in the literature, we have designed a node signature that incorporates edge correspondences indirectly. This allows removing the quadratic term in the QAP to recast the problem as a linear assignment problem (LAP) to relieve the computational burden. The LAP is efficiently solvable and is scalable to data with graph representation of larger size. The performance is tested and validated using clinical 3-D angiography images of the human cerebrovasculature as well as synthetic datasets. This method proves to be robust in the face of different structural and algorithm's parameters. Quality of inter-subject and multimodal matching of clinical data has also been confirmed. (C) 2018 Elsevier B.V. All rights reserved.
机译:血管网络的登记是预后和诊断研究的不可或缺的元素,需要在不同样品中随时间进行结构分析和比较,以及金标准。然而,血管网络表现出低空间纹理和稀疏结构内容,使其位置的甚至小的变化可以使基于强度的配准效率低,并且容易出错。基于几何图形的模型在我们的前工作中开发,我们使用图形拓扑意义上的形状信息来增强注册性能。提出了一种有效的基于特征的注册,其寻求分叉和分支在图形匹配方案中的对应关系。由于图形匹配最初在文献中构成了NP硬二次分配问题(QAP),因此我们设计了一个节点签名,它间接地包含边缘对应。这允许删除QAP中的二次术语,以重新删除问题作为线性分配问题(LAP)以减轻计算负担。 LAP有效可解决,可扩展到具有更大尺寸的图表表示的数据。使用人脑血管结构的临床3-D血管造影图像以及合成数据集进行测试和验证性能。在不同的结构和算法的参数面前,该方法被证明是坚固的。还确认了临床数据的受试者间和多模式匹配的质量。 (c)2018 Elsevier B.v.保留所有权利。

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