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PROBABILISTIC MODELING OF SYSTEMATIC ERRORS IN TWO-HYBRID EXPERIMENTS

机译:两种混合实验中系统误差的概率建模

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We describe a novel probabilistic approach to estimating errors in two-hybrid (2H) experiments. Such experiments are frequently used to elucidate protein-protein interaction networks in a high-throughput fashion; however, a significant challenge with these is their relatively high error rate, specifically, a high false-positive rate. We describe a comprehensive error model for 2H data, accounting for both random and systematic errors. The latter arise from limitations of the 2H experimental protocol: in theory, the reporting mechanism of a 2H experiment should be activated if and only if the two proteins being tested truly interact; in practice, even in the absence of a true interaction, it may be activated by some proteins - either by themselves or through promiscuous interaction with other proteins. We describe a probabilistic relational model that explicitly models the above phenomenon and use Markov Chain Monte Carlo (MCMC) algorithms to compute both the probability of an observed 2H interaction being true as well as the probability of individual proteins being self-activating/promiscuous. This is the first approach that explicitly models systematic errors in protein-protein interaction data; in contrast, previous work on this topic has modeled errors as being independent and random. By explicitly modeling the sources of noise in 2H systems, we find that we are better able to make use of the available experimental data. In comparison with Bader et al.'s method for estimating confidence in 2H predicted interactions, the proposed method performed 5-10% better overall, and in particular regimes improved prediction accuracy by as much as 76%.
机译:我们描述了一种新颖的概率方法来估计两杂交(2H)实验中的错误。此类实验通常用于以高通量的方式阐明蛋白质-蛋白质相互作用网络。然而,这些方面的重大挑战是它们的相对较高的错误率,特别是较高的假阳性率。我们描述了2H数据的综合误差模型,考虑了随机误差和系统误差。后者是由2H实验方案的局限性引起的:理论上,仅当两个被测蛋白真正相互作用时,才应激活2H实验的报告机制。实际上,即使没有真正的相互作用,它也可能被某些蛋白质激活-本身或与其他蛋白质的混杂相互作用。我们描述了一个概率关系模型,该模型显式地对上述现象进行建模,并使用马尔可夫链蒙特卡洛(MCMC)算法来计算观察到的2H相互作用为真的概率以及单个蛋白质被自我激活/混杂的概率。这是第一个明确建模蛋白质-蛋白质相互作用数据中系统错误的方法。相反,以前有关该主题的工作将错误建模为独立且随机的。通过对2H系统中的噪声源进行显式建模,我们发现我们能够更好地利用可用的实验数据。与Bader等人的方法对2H预测的交互作用的置信度进行估算相比,所提出的方法的整体效果要好5-10%,特别是在某些情况下,其预测准确性提高了76%。

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