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A shortcut for multiple testing on the directed acyclic graph of gene ontology

机译:对基因本体的有向无环图进行多重测试的捷径

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Background Gene set testing has become an important analysis technique in high throughput microarray and next generation sequencing studies for uncovering patterns of differential expression of various biological processes. Often, the large number of gene sets that are tested simultaneously require some sort of multiplicity correction to account for the multiplicity effect. This work provides a substantial computational improvement to an existing familywise error rate controlling multiplicity approach (the Focus Level method) for gene set testing in high throughput microarray and next generation sequencing studies using Gene Ontology graphs, which we call the Short Focus Level. Results The Short Focus Level procedure, which performs a shortcut of the full Focus Level procedure, is achieved by extending the reach of graphical weighted Bonferroni testing to closed testing situations where restricted hypotheses are present, such as in the Gene Ontology graphs. The Short Focus Level multiplicity adjustment can perform the full top-down approach of the original Focus Level procedure, overcoming a significant disadvantage of the otherwise powerful Focus Level multiplicity adjustment. The computational and power differences of the Short Focus Level procedure as compared to the original Focus Level procedure are demonstrated both through simulation and using real data. Conclusions The Short Focus Level procedure shows a significant increase in computation speed over the original Focus Level procedure (as much as ~15,000 times faster). The Short Focus Level should be used in place of the Focus Level procedure whenever the logical assumptions of the Gene Ontology graph structure are appropriate for the study objectives and when either no a priori focus level of interest can be specified or the focus level is selected at a higher level of the graph, where the Focus Level procedure is computationally intractable.
机译:背景基因集测试已成为高通量微阵列和下一代测序研究中的重要分析技术,用于揭示各种生物过程差异表达的模式。通常,同时测试的大量基因集需要某种形式的多重性校正才能解决多重性效应。这项工作对现有的家庭错误率控制多重性方法(“聚焦水平”方法)进行了实质性的计算改进,用于高通量微阵列中的基因组测试以及使用基因本体图的下一代测序研究(我们称为“短聚焦水平”)。结果通过将图形加权Bonferroni测试的作用范围扩展到存在受限假设的封闭测试情况(例如在Gene Ontology图中),可以实现“短焦点水平”过程,该过程是完整“焦点水平”过程的快捷方式。短聚焦级别多重性调整可以执行原始聚焦级别过程的完全自上而下的方法,克服了原本强大的聚焦级别多重性调整的显着缺点。通过仿真和使用实际数据,都证明了“短聚焦级别”过程与原始“聚焦级别”过程相比的计算和功效差异。结论短聚焦级别过程显示出比原始聚焦级别过程显着提高的计算速度(快约15,000倍)。只要基因本体图结构的逻辑假设适合研究目标,或者无法指定先验关注重点或在以下情况下选择关注重点时,应使用“简短关注重点”代替“关注重点”程序。图表的更高级别,其中“聚焦级别”过程在计算上难以处理。

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