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Gene Prioritization Through Geometric-Inspired Kernel Data Fusion

机译:通过几何启发内核数据融合的基因优先级排序

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In biology there is often the need to discover the most promising genes, among a large list of candidate genes, to further investigate. While a single data source might not be effective enough, integrating several complementary genomic data sources leads to more accurate prediction. We propose a kernel-based gene prioritization framework using geometric kernel fusion which we have recently developed as a powerful tool for protein fold classification [1]. It has been shown that taking more involved geometry means of their corresponding kernel matrices is less sensitive in dealing with complementary and noisy kernel matrices compared to standard multiple kernel learning methods. Since genomic kernels often encodes the complementary characteristics of biological data, this leads us to research the application of geometric kernel fusion in the gene prioritization task. We utilize an unbiased and prospective benchmark based on the OMIM [2] associations. Experimental results on our prospective benchmark show that our model can improve the accuracy of the state-of-the-art gene prioritization model.
机译:在生物学中,通常需要发现最有前途的基因,在大型候选基因列表中,进一步调查。虽然单个数据源可能不够有效,但整合多个互补基因组数据源导致更准确的预测。我们提出了一种使用基于内核的基因优先级框架,使用几何核融合,我们最近开发为蛋白质折叠分类的强大工具[1]。已经表明,与标准多个内核学习方法相比处理互补和嘈杂的内核矩阵的涉及其相应的内核矩阵的更多涉及的几何方法在不太敏感。由于基因组内核经常编码生物数据的互补特征,因此我们导致我们研究几何核融合在基因优先级任务中的应用。我们利用基于OMIM [2]关联的无偏见和预期基准。我们的预期基准测试结果表明,我们的模型可以提高最先进的基因优先级模型的准确性。

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