Privacy-Preserving Identification of Cancer Subtype-Specific Driver Genes Based on Multigenomics Data with Privatedriver.

IF 1.4 4区 生物学 Q4 BIOCHEMICAL RESEARCH METHODS Journal of Computational Biology Pub Date : 2024-02-01 Epub Date: 2024-01-25 DOI:10.1089/cmb.2023.0115
Junrong Song, Zhiming Song, Jinpeng Zhang, Yuanli Gong
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Abstract

Identifying cancer subtype-specific driver genes from a large number of irrelevant passengers is crucial for targeted therapy in cancer treatment. Recently, the rapid accumulation of large-scale cancer genomics data from multiple institutions has presented remarkable opportunities for identification of cancer subtype-specific driver genes. However, the insufficient subtype samples, privacy issues, and heterogenous of aberration events pose great challenges in precisely identifying cancer subtype-specific driver genes. To address this, we introduce privatedriver, the first model for identifying subtype-specific driver genes that integrates genomics data from multiple institutions in a data privacy-preserving collaboration manner. The process of identifying subtype-specific cancer driver genes using privatedriver involves the following two steps: genomics data integration and collaborative training. In the integration process, the aberration events from multiple genomics data sources are combined for each institution using the forward and backward propagation method of NetICS. In the collaborative training process, each institution utilizes the federated learning framework to upload encrypted model parameters instead of raw data of all institutions to train a global model by using the non-negative matrix factorization algorithm. We applied privatedriver on head and neck squamous cell and colon cancer from The Cancer Genome Atlas website and evaluated it with two benchmarks using macro-Fscore. The comparison analysis demonstrates that privatedriver achieves comparable results to centralized learning models and outperforms most other nonprivacy preserving models, all while ensuring the confidentiality of patient information. We also demonstrate that, for varying predicted driver gene distributions in subtype, our model fully considers the heterogeneity of subtype and identifies subtype-specific driver genes corresponding to the given prognosis and therapeutic effect. The success of privatedriver reveals the feasibility and effectiveness of identifying cancer subtype-specific driver genes in a data protection manner, providing new insights for future privacy-preserving driver gene identification studies.

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基于多基因组学数据的癌症亚型特异性驱动基因的隐私保护鉴定(Privatedriver)。
从大量无关基因中识别癌症亚型特异性驱动基因对于癌症治疗中的靶向治疗至关重要。最近,来自多个机构的大规模癌症基因组学数据的快速积累为鉴定癌症亚型特异性驱动基因提供了难得的机会。然而,亚型样本不足、隐私问题和畸变事件的异质性给精确鉴定癌症亚型特异性驱动基因带来了巨大挑战。为解决这一问题,我们引入了privatedriver,这是首个以数据隐私保护协作方式整合多个机构基因组学数据的亚型特异性驱动基因鉴定模型。使用 privatedriver 识别亚型特异性癌症驱动基因的过程包括以下两个步骤:基因组学数据整合和协作训练。在整合过程中,利用 NetICS 的前向和后向传播方法将来自多个基因组学数据源的畸变事件合并到每个机构。在协作训练过程中,各机构利用联合学习框架上传加密的模型参数,而不是所有机构的原始数据,通过非负矩阵因式分解算法训练全局模型。我们将privatedriver应用于癌症基因组图谱网站上的头颈部鳞状细胞癌和结肠癌,并用macro-Fscore与两个基准进行了评估。对比分析表明,privatedriver 在确保患者信息保密的前提下,取得了与集中式学习模型相当的结果,并优于大多数其他非隐私保护模型。我们还证明,对于亚型中不同的预测驱动基因分布,我们的模型充分考虑了亚型的异质性,并识别出与给定预后和治疗效果相对应的亚型特异性驱动基因。privatedriver 的成功揭示了以数据保护的方式识别癌症亚型特异性驱动基因的可行性和有效性,为未来保护隐私的驱动基因识别研究提供了新的启示。
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来源期刊
Journal of Computational Biology
Journal of Computational Biology 生物-计算机:跨学科应用
CiteScore
3.60
自引率
5.90%
发文量
113
审稿时长
6-12 weeks
期刊介绍: Journal of Computational Biology is the leading peer-reviewed journal in computational biology and bioinformatics, publishing in-depth statistical, mathematical, and computational analysis of methods, as well as their practical impact. Available only online, this is an essential journal for scientists and students who want to keep abreast of developments in bioinformatics. Journal of Computational Biology coverage includes: -Genomics -Mathematical modeling and simulation -Distributed and parallel biological computing -Designing biological databases -Pattern matching and pattern detection -Linking disparate databases and data -New tools for computational biology -Relational and object-oriented database technology for bioinformatics -Biological expert system design and use -Reasoning by analogy, hypothesis formation, and testing by machine -Management of biological databases
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