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Efficient Test and Visualization of Multi-Set Intersections

机译:高套段的高效测试和可视化

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Identification of sets of objects with shared features is a common operation in all disciplines. Analysis of intersections among multiple sets is fundamental for in-depth understanding of their complex relationships. However, so far no method has been developed to assess statistical significance of intersections among three or more sets. Moreover, the state-of-the-art approaches for visualization of multi-set intersections are not scalable. Here, we first developed a theoretical framework for computing the statistical distributions of multi-set intersections based upon combinatorial theory, and then accordingly designed a procedure to efficiently calculate the exact probabilities of multi-set intersections. We further developed multiple efficient and scalable techniques to visualize multi-set intersections and the corresponding intersection statistics. We implemented both the theoretical framework and the visualization techniques in a unified R software package, SuperExactTest . We demonstrated the utility of SuperExactTest through an intensive simulation study and a comprehensive analysis of seven independently curated cancer gene sets as well as six disease or trait associated gene sets identified by genome-wide association studies. We expect SuperExactTest developed by this study will have a broad range of applications in scientific data analysis in many disciplines.
机译:具有共享功能的对象集的识别是所有学科的常见操作。多套之间交叉口的分析是对他们复杂关系的深入了解的基础。然而,到目前为止,没有开发任何方法来评估三个或更多套或更多套或更多套之间交叉口的统计显着性。此外,用于可视化多组交叉点的最先进的方法是不可扩展的。这里,首先开发了一种基于组合理论计算多组交叉口的统计分布的理论框架,然后设计了一种有效地计算多种交叉点的精确概率的过程。我们进一步开发了多种有效和可扩展的技术,可视化多种交叉点和相应的交叉统计。我们在统一的R软件包中实现了理论框架和可视化技术,超克XcExtTest。我们证明了通过密集的模拟研究的uperexacttest的效用,并综合分析了七种独立策划癌基因集以及基因组关联研究鉴定的六种疾病或性质相关基因集。我们预计本研究的超克赛将在许多学科中具有广泛的科学数据分析中的应用。

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