首页> 外文期刊>Journal of biomedical informatics. >Global mapping of gene/protein interactions in PubMed abstracts: a framework and an experiment with P53 interactions.
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Global mapping of gene/protein interactions in PubMed abstracts: a framework and an experiment with P53 interactions.

机译:PubMed摘要中基因/蛋白质相互作用的全球作图:P53相互作用的框架和实验。

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摘要

Gene/protein interactions provide critical information for a thorough understanding of cellular processes. Recently, considerable interest and effort has been focused on the construction and analysis of genome-wide gene networks. The large body of biomedical literature is an important source of gene/protein interaction information. Recent advances in text mining tools have made it possible to automatically extract such documented interactions from free-text literature. In this paper, we propose a comprehensive framework for constructing and analyzing large-scale gene functional networks based on the gene/protein interactions extracted from biomedical literature repositories using text mining tools. Our proposed framework consists of analyses of the network topology, network topology-gene function relationship, and temporal network evolution to distill valuable information embedded in the gene functional interactions in the literature. We demonstrate the application of the proposed framework using a testbed of P53-related PubMed abstracts, which shows that the literature-based P53 networks exhibit small-world and scale-free properties. We also found that high degree genes in the literature-based networks have a high probability of appearing in the manually curated database and genes in the same pathway tend to form local clusters in our literature-based networks. Temporal analysis showed that genes interacting with many other genes tend to be involved in a large number of newly discovered interactions.
机译:基因/蛋白质相互作用为全面了解细胞过程提供了关键信息。近来,相当大的兴趣和努力集中在全基因组基因网络的构建和分析上。大量的生物医学文献是基因/蛋白质相互作用信息的重要来源。文本挖掘工具的最新进展使从自由文本文献中自动提取此类已记录的交互成为可能。在本文中,我们基于使用文本挖掘工具从生物医学文献库中提取的基因/蛋白质相互作用,提出了一个用于构建和分析大规模基因功能网络的综合框架。我们提出的框架包括对网络拓扑,网络拓扑与基因功能的关系以及时间网络演化的分析,以从文献中提取出嵌入基因功能相互作用中的有价值的信息。我们使用与P53相关的PubMed摘要测试床演示了所提出框架的应用,这表明基于文献的P53网络展现出小世界和无标度的特性。我们还发现,基于文献的网络中的高度基因具有很高的可能性出现在手动管理的数据库中,并且同一途径中的基因倾向于在基于文献的网络中形成局部簇。时间分析表明,与许多其他基因相互作用的基因倾向于参与大量新发现的相互作用。

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