多分量异构信息数据的持久上同调。

IF 1.9 Q1 MATHEMATICS, APPLIED
SIAM journal on mathematics of data science Pub Date : 2020-01-01 Epub Date: 2020-05-19 DOI:10.1137/19m1272226
Zixuan Cang, Guo-Wei Wei
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引用次数: 12

摘要

持久同调是描述数据集在不同几何尺度上的拓扑结构的强大工具。当应用于分子结构的描述时,持续同源性可以捕捉分子结构的多尺度几何特征,揭示分子结构拓扑不变量的相互作用模式。然而,除了几何信息外,分子结构还有各种各样的非几何信息,如元素类型、原子部分电荷、原子对相互作用、静电势函数等,这些都不能用持久同源性来描述。虽然元素特定同调和静电持久同调可以将一些非几何信息编码为基于几何的拓扑不变量,但需要有一个数学范式来系统地将几何和非几何信息(即多组分异构信息)嵌入到统一的拓扑表示中。为此,我们提出了一个基于持久上同调的框架来丰富数据的表示。在我们的框架中,非几何信息既可以全局分布,也可以在几何意义上驻留在数据集上,并且可以在拓扑空间(即简单复合体)上适当地定义。利用所提出的基于持久上同源的框架,从数据集中提取丰富的条形码来表示异构信息。我们考虑了各种数据集来验证目前的公式,并说明了基于持久上同的提出的方法的实用性。研究发现,所提出的框架优于或至少与来自大量生物分子数据集的蛋白质-配体结合亲和力预测的最先进方法相匹配,而无需使用任何深度学习公式。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Persistent Cohomology for Data With Multicomponent Heterogeneous Information.

Persistent homology is a powerful tool for characterizing the topology of a data set at various geometric scales. When applied to the description of molecular structures, persistent homology can capture the multiscale geometric features and reveal certain interaction patterns in terms of topological invariants. However, in addition to the geometric information, there is a wide variety of nongeometric information of molecular structures, such as element types, atomic partial charges, atomic pairwise interactions, and electrostatic potential functions, that is not described by persistent homology. Although element-specific homology and electrostatic persistent homology can encode some nongeometric information into geometry based topological invariants, it is desirable to have a mathematical paradigm to systematically embed both geometric and nongeometric information, i.e., multicomponent heterogeneous information, into unified topological representations. To this end, we propose a persistent cohomology based framework for the enriched representation of data. In our framework, nongeometric information can either be distributed globally or reside locally on the datasets in the geometric sense and can be properly defined on topological spaces, i.e., simplicial complexes. Using the proposed persistent cohomology based framework, enriched barcodes are extracted from datasets to represent heterogeneous information. We consider a variety of datasets to validate the present formulation and illustrate the usefulness of the proposed method based on persistent cohomology. It is found that the proposed framework outperforms or at least matches the state-of-the-art methods in the protein-ligand binding affinity prediction from massive biomolecular datasets without resorting to any deep learning formulation.

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