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A mutation profile for top-k patient search exploiting Gene-Ontology and orthogonal non-negative matrix factorization

机译:利用基因本体和正交非负矩阵分解进行top-k患者搜索的突变谱

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摘要

>Motivation: As the quantity of genomic mutation data increases, the likelihood of finding patients with similar genomic profiles, for various disease inferences, increases. However, so does the difficulty in identifying them. Similarity search based on patient mutation profiles can solve various translational bioinformatics tasks, including prognostics and treatment efficacy predictions for better clinical decision making through large volume of data. However, this is a challenging problem due to heterogeneous and sparse characteristics of the mutation data as well as their high dimensionality.>Results: To solve this problem we introduce a compact representation and search strategy based on Gene-Ontology and orthogonal non-negative matrix factorization. Statistical significance between the identified cancer subtypes and their clinical features are computed for validation; results show that our method can identify and characterize clinically meaningful tumor subtypes comparable or better in most datasets than the recently introduced Network-Based Stratification method while enabling real-time search. To the best of our knowledge, this is the first attempt to simultaneously characterize and represent somatic mutational data for efficient search purposes.>Availability: The implementations are available at: .>Contact: or >Supplementary information: are available at Bioinformatics online.
机译:>动机:随着基因组突变数据量的增加,针对各种疾病推断,发现具有相似基因组特征的患者的可能性也随之增加。但是,识别它们的困难也是如此。基于患者突变谱的相似性搜索可以解决各种翻译生物信息学任务,包括预后和治疗效果预测,以便通过大量数据做出更好的临床决策。但是,由于突变数据的异质性和稀疏性以及其高维性,这是一个具有挑战性的问题。>结果:为解决此问题,我们引入了一种基于基因本体的紧凑表示和搜索策略和正交非负矩阵分解。计算确定的癌症亚型及其临床特征之间的统计显着性以进行验证;结果表明,与最近引入的基于网络的分层方法相比,我们的方法可以识别和表征在大多数数据集中具有相当或更好的临床意义的肿瘤亚型,同时能够进行实时搜索。据我们所知,这是同时表征和表示体细胞突变数据以进行有效搜索的首次尝试。>可用性:可通过以下网址获得实现:>联系方式:或>补充信息:可在线访问生物信息学。

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