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AdaBoost Based Multi-Instance Transfer Learning for Predicting Proteome-Wide Interactions between Salmonella and Human Proteins

机译:基于AdaBoost的多实例转移学习可预测沙门氏菌和人类蛋白之间的蛋白质组间相互作用

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摘要

Pathogen-host protein-protein interaction (PPI) plays an important role in revealing the underlying pathogenesis of viruses and bacteria. The need of rapidly mapping proteome-wide pathogen-host interactome opens avenues for and imposes burdens on computational modeling. For Salmonella typhimurium, only 62 interactions with human proteins are reported to date, and the computational modeling based on such a small training data is prone to yield model overfitting. In this work, we propose a multi-instance transfer learning method to reconstruct the proteome-wide Salmonella-human PPI networks, wherein the training data is augmented by homolog knowledge transfer in the form of independent homolog instances. We use AdaBoost instance reweighting to counteract the noise from homolog instances, and deliberately design three experimental settings to validate the assumption that the homolog instances are effective to address the problems of data scarcity and data unavailability. The experimental results show that the proposed method outperforms the existing models and some predictions are validated by the findings from recent literature. Lastly, we conduct gene ontology based clustering analysis of the predicted networks to provide insights into the pathogenesis of Salmonella.
机译:病原体-宿主蛋白-蛋白相互作用(PPI)在揭示病毒和细菌的潜在发病机理中起着重要作用。快速绘制全蛋白组病原体-宿主相互作用组的图谱为计算建模开辟了道路,并给计算模型带来了负担。对于鼠伤寒沙门氏菌,迄今仅报道了与人蛋白质的62种相互作用,并且基于如此小的训练数据的计算模型易于产生模型过度拟合。在这项工作中,我们提出了一种多实例转移学习方法来重建整个蛋白质组学范围的沙门氏菌-人类PPI网络,其中训练数据通过以独立同源实例的形式进行同源知识转移而得以增强。我们使用AdaBoost实例重加权来抵消同源实例的噪声,并故意设计三个实验设置,以验证假设同源实例有效解决数据稀缺和数据不可用的问题。实验结果表明,所提出的方法优于现有模型,并且通过最近文献的发现验证了一些预测。最后,我们对预测的网络进行基于基因本体的聚类分析,以提供对沙门氏菌发病机理的见解。

著录项

  • 期刊名称 PLoS Clinical Trials
  • 作者

    Suyu Mei; Hao Zhu;

  • 作者单位
  • 年(卷),期 2010(9),10
  • 年度 2010
  • 页码 e110488
  • 总页数 12
  • 原文格式 PDF
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