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A Tool Preference Choice Method for RNA Secondary Structure Prediction by SVM with Statistical Tests

机译:统计支持向量机支持向量机预测RNA二级结构的工具偏好选择方法

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摘要

The Prediction of RNA secondary structures has drawn much attention from both biologists and computer scientists. Many useful tools have been developed for this purpose. These tools have their individual strengths and weaknesses. As a result, based on support vector machines (SVM), we propose a tool choice method which integrates three prediction tools: pknotsRG, RNAStructure, and NUPACK. Our method first extracts features from the target RNA sequence, and adopts two information-theoretic feature selection methods for feature ranking. We propose a method to combine feature selection and classifier fusion in an incremental manner. Our test data set contains 720 RNA sequences, where 225 pseudoknotted RNA sequences are obtained from PseudoBase, and 495 nested RNA sequences are obtained from RNA SSTRAND. The method serves as a preprocessing way in analyzing RNA sequences before the RNA secondary structure prediction tools are employed. In addition, the performance of various configurations is subject to statistical tests to examine their significance. The best base-pair accuracy achieved is 75.5%, which is obtained by the proposed incremental method, and is significantly higher than 68.8%, which is associated with the best predictor, pknotsRG.
机译:RNA二级结构的预测已引起生物学家和计算机科学家的广泛关注。为此已经开发了许多有用的工具。这些工具各有优缺点。因此,基于支持向量机(SVM),我们提出了一种工具选择方法,该方法集成了三个预测工具:pknotsRG,RNAStructure和NUPACK。我们的方法首先从目标RNA序列中提取特征,然后采用两种信息理论特征选择方法进行特征排名。我们提出了一种以增量方式将特征选择和分类器融合相结合的方法。我们的测试数据集包含720个RNA序列,其中从PseudoBase获得225个假结RNA序列,并从RNA SSTRAND获得495个嵌套RNA序列。该方法是在使用RNA二级结构预测工具之前分析RNA序列的预处理方法。另外,对各种配置的性能进行统计测试以检查其重要性。通过提出的增量方法获得的最佳碱基对准确性为75.5%,并且显着高于68.8%,这与最佳预测变量pknotsRG有关。

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