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Clustering microarray-derived gene lists through implicit literature relationships

机译:通过隐式文献关系聚类微阵列来源的基因列表

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Motivation: Microarrays rapidly generate large quantities of gene expression information, but interpreting such data within a biological context is still relatively complex and laborious. New methods that can identify functionally related genes via shared literature concepts will be useful in addressing these needs.Results: We have developed a novel method that uses implicit literature relationships (concepts related via shared, intermediate concepts) to cluster related genes. Genes are evaluated for implicit connections within a network of biomedical objects (other genes, ontological concepts and diseases) that are connected via their co-occurrences in Medline titles and/or abstracts. On the basis of these implicit relationships, individual gene pairs are scored using a probability-based algorithm. Scores are generated for all pairwise combinations of genes, which are then clustered based on the scores. We applied this method to a test set composed of nine functional groups with known relationships. The method scored highly for all nine groups and significantly better than a benchmark co-occurrence-based method for six groups. We then applied this method to gene sets specific to two previously defined breast tumor subtypes. Analysis of the results recapitulated known biological relationships and identified novel pathway relationships unique to each tumor subtype. We demonstrate that this method provides a valuable new means of identifying and visualizing significantly related genes within gene lists via their implicit relationships in the literature.
机译:动机:微阵列快速产生大量基因表达信息,但是在生物学背景下解释此类数据仍然相对复杂且费力。可以通过共享文献概念识别功能相关基因的新方法将有助于解决这些需求。结果:我们开发了一种新方法,该方法使用隐式文献关系(通过共享,中间概念相关的概念)将相关基因聚类。通过在Medline标题和/或摘要中同时存在的生物医学对象(其他基因,本体论概念和疾病)网络中的基因进行隐式连接评估。基于这些隐式关系,使用基于概率的算法对单个基因对进行评分。为所有成对的基因组合生成分数,然后基于分数将其聚类。我们将此方法应用于由9个具有已知关系的功能组组成的测试集。该方法在所有九个组中得分很高,并且明显优于六个组中基于基准共现的方法。然后,我们将这种方法应用于特定于两个先前定义的乳腺肿瘤亚型的基因组。对结果的分析概括了已知的生物学关系,并确定了每种肿瘤亚型独有的新型途径关系。我们证明该方法提供了一种有价值的新手段,可以通过文献中的隐式关系来识别和可视化基因列表中的显着相关基因。

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