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A new decoding algorithm for hidden Markov models improves the prediction of the topology of all-beta membrane proteins

机译:隐马尔可夫模型的新解码算法改进了全β膜蛋白拓扑结构的预测

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摘要

Background Structure prediction of membrane proteins is still a challenging computational problem. Hidden Markov models (HMM) have been successfully applied to the problem of predicting membrane protein topology. In a predictive task, the HMM is endowed with a decoding algorithm in order to assign the most probable state path, and in turn the labels, to an unknown sequence. The Viterbi and the posterior decoding algorithms are the most common. The former is very efficient when one path dominates, while the latter, even though does not guarantee to preserve the HMM grammar, is more effective when several concurring paths have similar probabilities. A third good alternative is 1-best, which was shown to perform equal or better than Viterbi. Results In this paper we introduce the posterior-Viterbi (PV) a new decoding which combines the posterior and Viterbi algorithms. PV is a two step process: first the posterior probability of each state is computed and then the best posterior allowed path through the model is evaluated by a Viterbi algorithm. Conclusion We show that PV decoding performs better than other algorithms when tested on the problem of the prediction of the topology of beta-barrel membrane proteins.
机译:膜蛋白的背景结构预测仍然是一个具有挑战性的计算问题。隐马尔可夫模型(HMM)已成功地应用于预测膜蛋白拓扑的问题。在预测性任务中,HMM具有解码算法,以便将最可能的状态路径分配给未知序列,进而将标签分配给未知序列。最常见的是维特比和后验解码算法。前者在一条路径占主导地位时非常有效,而后者虽然不能保证保留HMM语法,但在多个并发路径具有相似概率时则更为有效。第三个好的选择是1最佳,它的表现与Viterbi相等或更好。结果在本文中,我们介绍了后验维特比(PV)的新解码,该算法结合了后验和维特比算法。 PV是一个分为两个步骤的过程:首先计算每个状态的后验概率,然后通过维特比算法评估通过模型的最佳后验允许路径。结论我们证明,在对β-桶状膜蛋白拓扑结构的预测问题进行测试时,PV解码的性能优于其他算法。

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