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IDENTIFICATION OF RIBOSOME BINDING SITES IN ESCHERICHIA COLI USING NEURAL NETWORK MODELS

机译:神经网络模型识别大肠埃希氏菌中的核糖体结合位点

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This study investigated the use of neural networks in the identification of Escherichia coil ribosome binding sites. The recognition of these sites based on primary sequence data is difficult due to the multiple determinants that define them. Additionally, secondary structure plays a significant role in the determination of the site and this information is difficult to include in the models. Efforts to solve this problem have so far yielded poor results. A new compilation of E.coli ribosome binding sites was generated for this study. Feedforward backpropagation networks were applied to their identification. Perceptrons were also applied, since they have been the previous best method since 1982. Evaluation of performance for all the neural networks and perceptrons was determined by ROC analysis. The neural network provided significant improvement in the recognition of these sites when compared with the previous best method, finding less than half the number of false positives when both models were adjusted to find an equal number of actual sites. The best neural network used an input window of 101 nucleotides and a single hidden layer of 9 units. Both the neural network and the perceptron trained on the new compilation performed better than the original perceptron published by Stormo et al. in 1982.
机译:这项研究调查了神经网络在鉴定大肠埃希氏菌核糖体结合位点中的用途。由于定义这些位点的多个决定因素,因此很难根据一级序列数据识别这些位点。此外,二级结构在确定站点中起着重要作用,并且该信息很难包含在模型中。迄今为止,解决该问题的努力均产生了不良结果。这项研究产生了大肠杆菌核糖体结合位点的新汇编。前馈反向传播网络被应用于它们的识别。自从1982年以来,感知器一直是最好的方法,因此也应用了感知器。通过ROC分析确定了所有神经网络和感知器的性能评估。与以前的最佳方法相比,神经网络在识别这些位点方面提供了显着的改进,当对两个模型进行调整以找到相等数量的实际位点时,发现的假阳性数不到一半。最好的神经网络使用101个核苷酸的输入窗口和9个单位的单个隐藏层。在新的编译中训练的神经网络和感知器都比Stormo等人发表的原始感知器表现更好。 1982年。

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