RNA的持续同源性分析

Q2 Mathematics
A. Mamuye, M. Rucco, L. Tesei, E. Merelli
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引用次数: 8

摘要

摘要近年来,拓扑数据分析已被用于从生物分子中提取有意义的信息。本文介绍了拓扑数据分析工具持久同源性(persistent homology)在计算RNA折叠空间持久特征(环)中的应用。RNA折叠空间的支架是一个复图,通过团和Vietoris-Rips复合体的概念,将复图补全为简单复合体,从中提取全局特征。所得到的简单复合体是用拓扑不变量来表征的,例如在任何维度上的孔数,即贝蒂数。我们的方法发现了持久的结构特征,这是RNA折叠空间可以减少的最小组件集。由于这一发现,在数据挖掘方面可以被认为是空间维数的减少,因此有可能提取出对理解RNA折叠机制至关重要的新见解,以实现最佳二级结构。该结构由RNA折叠空间还原过程中发现的组分组成,其特点是自由能最小。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Persistent Homology Analysis of RNA
Abstract Topological data analysis has been recently used to extract meaningful information frombiomolecules. Here we introduce the application of persistent homology, a topological data analysis tool, for computing persistent features (loops) of the RNA folding space. The scaffold of the RNA folding space is a complex graph from which the global features are extracted by completing the graph to a simplicial complex via the notion of clique and Vietoris-Rips complexes. The resulting simplicial complexes are characterised in terms of topological invariants, such as the number of holes in any dimension, i.e. Betti numbers. Our approach discovers persistent structural features, which are the set of smallest components to which the RNA folding space can be reduced. Thanks to this discovery, which in terms of data mining can be considered as a space dimension reduction, it is possible to extract a new insight that is crucial for understanding the mechanism of the RNA folding towards the optimal secondary structure. This structure is composed by the components discovered during the reduction step of the RNA folding space and is characterized by minimum free energy.
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来源期刊
Computational and Mathematical Biophysics
Computational and Mathematical Biophysics Mathematics-Mathematical Physics
CiteScore
2.50
自引率
0.00%
发文量
8
审稿时长
30 weeks
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