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DISEASE-RELATED CONCEPT MINING BY KNOWLEDGE-BASED TWO-DIMENSIONAL GENE MAPPING

机译:基于知识的二维基因映射的疾病相关概念挖掘

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There is a strong need to systematically organize and comprehend the rapidly expanding stores of biomedical knowledge to formulate hypotheses on disease mechanisms. However, no method is available that automatically structuralizes fragmentary knowledge along with domain-specific expressions for a large-scale integration. A method presented here, cross-subspace analysis (CSA), produces a holistic view of over 3,000 human genes with a two-dimensional (2D) arrangement. The genes are plotted in relation to functions determined by machine learning from the occurrence patterns of various biomedical terms in MEDLINE abstracts. By focusing on the 2D distributions of gene plots that share the same biomedical concepts, as defined by databases such as Gene Ontology, relevant biomedical concepts can be computationally extracted. In an analysis where myocardial infarction and ischemic stroke were taken as examples, we found valid relations with lifestyle, diet-related metabolism, and host immune responses, allof which are known risk factors for the diseases. These results demonstrate that systematizing accumulated gene knowledge can lead to hypothesis generation and knowledge discovery, regardless of the area of inquiry or discipline.
机译:迫切需要系统地组织和理解迅速扩展的生物医学知识储备,以提出关于疾病机理的假设。但是,没有一种方法可以自动将片段性知识以及特定于域的表达式进行结构化以进行大规模集成。这里介绍的一种方法,跨子空间分析(CSA),可以产生二维(2D)排列的3,000多种人类基因的整体视图。根据MEDLINE摘要中各种生物医学术语的发生模式通过机器学习确定的功能,对基因作图。通过关注共享相同生物医学概念的基因图的2D分布(如基因本体论等数据库所定义),可以通过计算提取相关的生物医学概念。在以心肌梗塞和缺血性中风为例的分析中,我们发现与生活方式,饮食相关的代谢和宿主免疫反应之间存在有效的关系,所有这些都是已知的疾病危险因素。这些结果表明,系统化积累的基因知识可以导致假设的产生和知识发现,而不管研究或学科领域如何。

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