PASCL:基于路径的稀疏深度聚类识别未知癌症亚型

Tejaswini Mallavarapu, Jie Hao, Youngsoon Kim, J. Oh, Mingon Kang
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引用次数: 2

摘要

癌症是一种异质性疾病,它有几个亚型,可以通过分子、组织病理学和临床分期来区分。准确诊断癌症亚型对于识别不同的疾病状态和开发有效的个性化治疗至关重要。许多无监督机器学习技术已被应用于肿瘤样本的基因组数据,其中形成了与患者生存等临床结果相关的患者集群。然而,基于数据之间距离(或相似度)的聚类方法往往不能聚类生物数据,因为它们的非线性。在本文中,我们开发了一种基于路径的稀疏深度聚类(PASCL)方法来识别癌症亚型。PASCL结合了来自通路数据库的先前生物学知识,构建了一个健壮的、生物可解释的模型。我们通过比较几种最先进的聚类方法来评估PASCL的性能。PASCL在logrank检验中优于p值最低的对标方法,并对其突出性能进行统计评价。PASCL不仅提供了一种利用高维非线性基因组数据有效识别亚型的解决方案,而且还在途径水平上对模型进行了生物学解释。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
PASCL: Pathway-based Sparse Deep Clustering for Identifying Unknown Cancer Subtypes
Cancer is a heterogeneous disease which has several subtypes that can be distinguished by molecular, histopathological, and clinical stages. Accurate diagnosis of cancer subtypes is vital to identify distinct disease states and develop effective personalized therapies. A number of unsupervised machine learning techniques have been applied to genomic data of the tumor samples, where clusters of patients were formed to be associated with a clinical outcome such as the survival of patients. However, clustering methods based on distance (or similarity) between data often fail to cluster biological data, due to their nonlinearity. In this paper, we develop a PAthway-based Sparse deep CLustering (PASCL) method for the identification of cancer subtypes. PASCL incorporates prior biological knowledge from pathway databases to build a robust and biological interpretable model. We evaluated the performance of PASCL by comparing with several state-of-the-art clustering methods. PASCL outperformed the benchmarking methods with lowest p-value in logrank test, and its outstanding performance is statistically assessed. PASCL provides a solution not only to effectively identify subtypes using high-dimensional nonlinear genomic data, but also to biologically interpret the model at a pathway level.
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