首页> 外文会议>Conference on Neural Information Processing Systems(NIPS); 20061204-09; Vancouver and Whistler(CA) >Mutagenetic tree Fisher kernel improves prediction of HIV drug resistance from viral genotype
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Mutagenetic tree Fisher kernel improves prediction of HIV drug resistance from viral genotype

机译:诱变树费舍尔内核改善了病毒基因型对HIV耐药性的预测

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Starting with the work of Jaakkola and Haussler, a variety of approaches have been proposed for coupling domain-specific generative models with statistical learning methods. The link is established by a kernel function which provides a similarity measure based inherently on the underlying model. In computational biology, the full promise of this framework has rarely ever been exploited, as most kernels are derived from very generic models, such as sequence profiles or hidden Markov models. Here, we introduce the MTreeMix kernel, which is based on a generative model tailored to the underlying biological mechanism. Specifically, the kernel quantifies the similarity of evolutionary escape from antiviral drug pressure between two viral sequence samples. We compare this novel kernel to a standard, evolution-agnostic amino acid encoding in the prediction of HIV drug resistance from genotype, using support vector regression. The results show significant improvements in predictive performance across 17 anti-HIV drugs. Thus, in our study, the generative-discriminative paradigm is key to bridging the gap between population genetic modeling and clinical decision making.
机译:从Jaakkola和Haussler的工作开始,已经提出了多种方法来将特定于领域的生成模型与统计学习方法耦合在一起。该链接由内核函数建立,该内核函数固有地基于底层模型提供相似性度量。在计算生物学中,很少有人会充分利用这个框架的全部希望,因为大多数内核都来自非常通用的模型,例如序列配置文件或隐马尔可夫模型。在这里,我们介绍MTreeMix内核,该内核基于为基础生物学机制量身定制的生成模型。具体而言,内核量化了两个病毒序列样本之间从抗病毒药物压力进化逃逸的相似性。我们使用支持向量回归将这种新内核与标准的,与进化无关的氨基酸编码进行比较,从而从基因型预测HIV耐药性。结果显示,在17种抗HIV药物的预测性能上有显着改善。因此,在我们的研究中,生成歧视范式是弥合人口遗传建模与临床决策之间差距的关键。

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