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Dynamical cluster analysis for the detection of microglia activation

机译:微胶质植物激活检测的动态聚类分析

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Dynamical cluster analysis (DCA) was used to extract sets of representative time courses to detect brain lesions using positron emmision tomography (PET) data. DCA is an adaptive hard-clustering algorithm where the number of clusters k is not initially fixed but is dynamically changed by generation and fusion of clusters during runtime. We analyzed PET data sets of 9 patients applying DCA repeatedly. We compared the results that vary in the number of clusters even on the same data set. As validation measure we used the mean square quantization error (MSQE). We found that the MSQE was strictly correlated with k only on 4 of the 9 data sets. We propose DCA for extracting the reference time course required in reference tissue modeling [7]. In the case of one patient, we checked the ability of DCA to characterize directly the three most interesting regions, reference tissue, the veins and the lesion and how this ability relates to high validation scores. The characterisation of all three regions was not reproducible in all of the runs, however, runs rated high in validity by the MSQE were able to reproduce all the three regions.
机译:动态聚类分析(DCA)用于提取使用正电子Emmision断层扫描(PET)数据检测脑病变的代表时间课程。 DCA是自适应硬聚类算法,其中簇的数目k最初没有固定的,而是由生成和簇的融合在运行时期间被动态地改变。我们分析了9名患者的PET数据集反复应用DCA。我们比较了即使在相同的数据集上也可以在群集数量中变化的结果。作为验证度量,我们使用均线量化误差(MSQE)。我们发现MSQE仅与9个数据集中的4个严格相关。我们提出DCA用于提取参考组织建模所需的参考时间课程[7]。在一个患者的情况下,我们检查了DCA直接表征三个最有趣的区域,参考组织,静脉和病变以及这种能力如何与高验证分数相关的能力。所有这三个地区的表征是不是在所有试验的重复性,但是,额定运行高有效性由MSQE能够再现所有的三个区域。

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