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PROBABILISTIC MODELING OF SYSTEMATIC ERRORS IN TWO-HYBRID EXPERIMENTS

机译:双杂交实验中系统误差的概率模型

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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:我们描述了一种新的概率方法来估算两种杂交(2H)实验中的误差。这种实验经常用于以高通量方式阐明蛋白质 - 蛋白质相互作用网络;然而,与这些重大挑战是它们相对较高的错误率,具体而言,具有高伪阳性率。我们描述了2H数据的全面错误模型,占随机和系统错误的占用。后者出现了2H实验方案的局限性:理论上,如果只有当测试真正互动的两种蛋白质时,才会激活2H实验的报告机制;在实践中,即使在没有真正的相互作用的情况下,也可以由一些蛋白质激活 - 或者通过它们自己或通过与其他蛋白质的混杂相互作用。我们描述了一种概率的关系模型,明确地模拟上述现象,并使用Markov链蒙特卡罗(MCMC)算法来计算观察到的2H交互的概率,以及单个蛋白质是自激活/混杂的概率。这是第一种方法,即明确地模拟蛋白质 - 蛋白质相互作用数据中系统误差;相比之下,此主题上的先前工作已为独立和随机的模型错误。通过在2H系统中明确地建模噪声源,我们发现我们能够更好地利用可用的实验数据。与Bader等人相比。估计2H预测相互作用的置信度的方法,所提出的方法总体上更好地进行了5-10%,特别是制定的预测精度高达76%。

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