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Mining complex genotypic features for predicting HIV-1 drug resistance

机译:挖掘复杂的基因型特征以预测HIV-1耐药性

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Motivation: Human immunodeficiency virus type 1 (HIV-1) evolves in human body, and its exposure to a drug often causes mutations that enhance the resistance against the drug. To design an effective pharmacotherapy for an individual patient, it is important to accurately predict the drug resistance based on genotype data. Notably, the resistance is not just the simple sum of the effects of all mutations. Structural biological studies suggest that the association of mutations is crucial: even if mutations A or B alone do not affect the resistance, a significant change might happen when the two mutations occur together. Linear regression methods cannot take the associations into account, while decision tree methods can reveal only limited associations. Kernel methods and neural networks implicitly use all possible associations for prediction, but cannot select salient associations explicitly.Results: Our method, itemset boosting, performs linear regression in the complete space of power sets of mutations. It implements a forward feature selection procedure where, in each iteration, one mutation combination is found by an efficient branch-and-bound search. This method uses all possible combinations, and salient associations are explicitly shown. In experiments, our method worked particularly well for predicting the resistance of nucleotide reverse transcriptase inhibitors (NRTIs). Furthermore, it successfully recovered many mutation associations known in biological literature.
机译:动机:1型人类免疫缺陷病毒(HIV-1)在人体中进化,暴露于药物中通常会引起突变,从而增强对药物的抵抗力。为了为单个患者设计有效的药物疗法,重要的是基于基因型数据准确预测耐药性。值得注意的是,抗性不仅仅是所有突变作用的简单总和。结构生物学研究表明,突变的关联至关重要:即使仅突变A或B都不影响抗药性,但当两个突变同时出现时,可能会发生重大变化。线性回归方法不能考虑关联,而决策树方法只能揭示有限的关联。内核方法和神经网络隐式地使用所有可能的关联进行预测,但不能显式选择显着关联。结果:我们的方法(项集增强)在完整的突变幂集空间中执行线性回归。它实现了前向特征选择过程,其中在每次迭代中,通过有效的分支定界搜索找到一个突变组合。此方法使用所有可能的组合,显式显示显着关联。在实验中,我们的方法在预测核苷酸逆转录酶抑制剂(NRTIs)的耐药性方面特别有效。此外,它成功地恢复了生物学文献中已知的许多突变关联。

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