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TOPAS是一种基于网络的方法,用于自上而下地检测疾病模块。

TOPAS, a network-based approach to detect disease modules in a top-down fashion.

作者信息

Buzzao Davide, Castresana-Aguirre Miguel, Guala Dimitri, Sonnhammer Erik L L

机构信息

Department of Biochemistry and Biophysics, Stockholm University, Science for Life Laboratory, Box 1031, 171 21 Solna, Sweden.

K7 Department of Oncology-Pathology, Karolinska Institute, 171 77 Stockholm, Sweden.

出版信息

NAR Genom Bioinform. 2022 Nov 29;4(4):lqac093. doi: 10.1093/nargab/lqac093. eCollection 2022 Dec.

Abstract

A vast scenario of potential disease mechanisms and remedies is yet to be discovered. The field of Network Medicine has grown thanks to the massive amount of high-throughput data and the emerging evidence that disease-related proteins form 'disease modules'. Relying on prior disease knowledge, network-based disease module detection algorithms aim at connecting the list of known disease associated genes by exploiting interaction networks. Most existing methods extend disease modules by iteratively adding connector genes in a bottom-up fashion, while top-down approaches remain largely unexplored. We have created TOPAS, an iterative approach that aims at connecting the largest number of seed nodes in a top-down fashion through connectors that guarantee the highest flow of a Random Walk with Restart in a network of functional associations. We used a corpus of 382 manually selected functional gene sets to benchmark our algorithm against SCA, DIAMOnD, MaxLink and ROBUST across four interactomes. We demonstrate that TOPAS outperforms competing methods in terms of Seed Recovery Rate, Seed to Connector Ratio and consistency during module detection. We also show that TOPAS achieves competitive performance in terms of biological relevance of detected modules and scalability.

摘要

大量潜在的疾病机制和治疗方法仍有待发现。由于大量的高通量数据以及疾病相关蛋白质形成“疾病模块”的新证据,网络医学领域得以发展。基于先前的疾病知识,基于网络的疾病模块检测算法旨在通过利用相互作用网络来连接已知的疾病相关基因列表。大多数现有方法通过自下而上的方式迭代添加连接基因来扩展疾病模块,而自上而下的方法在很大程度上仍未得到探索。我们创建了TOPAS,这是一种迭代方法,旨在通过连接器以自上而下的方式连接最多数量的种子节点,这些连接器可确保在功能关联网络中随机游走重启的最大流量。我们使用了382个手动选择的功能基因集语料库,在四个相互作用组上针对SCA、DIAMOnD、MaxLink和ROBUST对我们的算法进行基准测试。我们证明,在种子恢复率、种子与连接器比率以及模块检测过程中的一致性方面,TOPAS优于竞争方法。我们还表明,在检测到的模块的生物学相关性和可扩展性方面,TOPAS具有竞争力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c675/9706483/9bff805072b3/lqac093fig1.jpg

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