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Network clustering: probing biological heterogeneity by sparse graphical models

机译:网络聚类:通过稀疏图形模型探索生物异质性

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Motivation: Networks and pathways are important in describing the collective biological function of molecular players such as genes or proteins. In many areas of biology, for example in cancer studies, available data may harbour undiscovered subtypes which differ in terms of network phenotype. That is, samples may be heterogeneous with respect to underlying molecular networks. This motivates a need for unsupervised methods capable of discovering such subtypes and elucidating the corresponding network structures.Results: We exploit recent results in sparse graphical model learning to put forward a 'network clustering' approach in which data are partitioned into subsets that show evidence of underlying, subset-level network structure. This allows us to simultaneously learn subset-specific networks and corresponding subset membership under challenging small-sample conditions. We illustrate this approach on synthetic and proteomic data.
机译:动机:网络和途径对于描述分子参与者(如基因或蛋白质)的集体生物学功能很重要。在生物学的许多领域,例如在癌症研究中,可用数据可能包含未发现的亚型,这些亚型的网络表型有所不同。也就是说,样品相对于基础分子网络可能是异质的。因此,我们需要能够发现此类亚型并阐明相应网络结构的无监督方法。结果:我们利用稀疏图形模型学习中的最新结果提出了一种“网络聚类”方法,其中将数据划分为子集,以显示证据。基础的子集级网络结构。这使我们能够在具有挑战性的小样本条件下同时学习特定于子集的网络和相应的子集成员身份。我们在合成和蛋白质组学数据上说明了这种方法。

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