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An Improved Method for Splice Site Prediction in DNA Sequences Using Support Vector Machines

机译:使用支持向量机的DNA序列剪接位点预测的一种改进方法

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摘要

A vast amount of sequence data has been generated due to advancements in DNA sequencing technology. This exponential increase requires new and efficient methods for the analysis of DNA sequence data. Predicting genes in this newly sequenced data is an important and essential step towards genome annotation. Genome annotation helps in determining function of these genes. Accurate splice site prediction in DNA sequences leads to correct gene structure prediction in eukaryotes and it requires effective modelling of regions surrounding these sites. A large number of methods for splice site prediction are available in literature but very few of them are suitable to be incorporated as gene prediction module because of their complexity. In this paper, a splice site prediction method based on second order markov model and support vector machine is developed. This method shows improvement over most of the existing splice site predictors in use today. The experimental results suggest that second order markov model is an effective pre-processing approach. This approach when combined with support vector machine provides better classification accuracy in predicting splice sites.
机译:由于DNA测序技术的进步,已经产生了大量的序列数据。这种指数级增长需要新的有效方法来分析DNA序列数据。在此新测序数据中预测基因是迈向基因组注释的重要且必不可少的步骤。基因组注释有助于确定这些基因的功能。 DNA序列中正确的剪接位点预测可导致真核生物中正确的基因结构预测,并且需要对这些位点周围的区域进行有效建模。文献中有许多用于剪接位点预测的方法,但是由于它们的复杂性,很少有适合用作基因预测模块的方法。本文提出了一种基于二阶马尔可夫模型和支持向量机的剪接位点预测方法。该方法显示出对当今使用的大多数现有剪接位点预测器的改进。实验结果表明,二阶马尔可夫模型是一种有效的预处理方法。与支持向量机结合使用时,此方法可在预测剪接位点时提供更好的分类准确性。

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