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Persistent spectral graph

机译:持久频谱图

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摘要

Persistent homology is constrained to purely topological persistence, while multiscale graphs account only for geometric information. This work introduces persistent spectral theory to create a unified low-dimensional multiscale paradigm for revealing topological persistence and extracting geometric shapes from high-dimensional datasets. For a point-cloud dataset, a filtration procedure is used to generate a sequence of chain complexes and associated families of simplicial complexes and chains, from which we construct persistent combinatorial Laplacian matrices. We show that a full set of topological persistence can be completely recovered from the harmonic persistent spectra, that is, the spectra that have zero eigenvalues, of the persistent combinatorial Laplacian matrices. However, non-harmonic spectra of the Laplacian matrices induced by the filtration offer another powerful tool for data analysis, modeling, and prediction. In this work, fullerene stability is predicted by using both harmonic spectra and non-harmonic persistent spectra, while the latter spectra are successfully devised to analyze the structure of fullerenes and model protein flexibility, which cannot be straightforwardly extracted from the current persistent homology. The proposed method is found to provide excellent predictions of the protein B-factors for which current popular biophysical models break down.
机译:持续同源性被限制为纯粹的拓扑持久性,而多尺度图仅用于几何信息。这项工作介绍了持久的频谱理论,以创建统一的低维模式范式,用于揭示拓扑持久性并从高维数据集中提取几何形状。对于点云数据集,过滤过程用于生成一系列链复合物和外部复合物和链的相关系列,从中构建持久组合拉普拉斯矩阵。我们表明,可以从谐波持久谱中完全恢复全套拓扑持久性,即持久组合拉普拉斯基质的谐波持久谱,即具有零特征值的光谱。然而,过滤引起的Laplacian基质的非谐波谱提供了用于数据分析,建模和预测的另一个强大的工具。在这项工作中,通过使用谐波谱和非谐波持久谱来预测富勒烯稳定性,而后者谱成功设计以分析富勒烯和模型蛋白质柔性的结构,从电流持续同源性中不能直接地提取。发现所提出的方法提供了对蛋白质B因子的优异预测,目前流行的生物物理模型分解。

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