中间性中心性
中心性
计算机科学
网络分析
节点(物理)
计算生物学
脆弱性(计算)
交互网络
R包
聚类系数
生物网络
聚类分析
钥匙(锁)
数据挖掘
人工智能
生物
基因
数学
遗传学
计算机安全
工程类
物理
结构工程
计算科学
量子力学
组合数学
作者
Swapnil Kumar,Grace Pauline,Vaibhav Vindal
标识
DOI:10.1080/07391102.2024.2303607
摘要
In biological network analysis, identifying key molecules plays a decisive role in the development of potential diagnostic and therapeutic candidates. Among various approaches of network analysis, network vulnerability analysis is quite important, as it assesses significant associations between topological properties and the functional essentiality of a network. Similarly, some node centralities are also used to screen out key molecules. Among these node centralities, escape velocity centrality (EVC), and its extended version (EVC+) outperform others, viz., Degree, Betweenness, and Clustering coefficient. Keeping this in mind, we aimed to develop a first-of-its-kind R package named NetVA, which analyzes networks to identify key molecular players (individual proteins and protein pairs/triplets) through network vulnerability and EVC+-based approaches. To demonstrate the application and relevance of our package in network analysis, previously published and publicly available protein–protein interactions (PPIs) data of human breast cancer were analyzed. This resulted in identifying some most important proteins. These included essential proteins, non-essential proteins, hubs, and bottlenecks, which play vital roles in breast cancer development. Thus, the NetVA package, available at https://github.com/kr-swapnil/NetVA with a detailed tutorial to download and use, assists in predicting potential candidates for therapeutic and diagnostic purposes by exploring various topological features of a disease-specific PPIs network.
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