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Frequency difference based DNA encoding methods in human splice site recognition

机译:基于频率差异的DNA编码方法在人类剪接位点识别中的应用

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Identifying structure of genes in Human genomes highly depends upon accurate recognition of boundaries between exons and introns, i.e. splice sites. Hence, development of new methods for effective detection of splice sites is essential. DNA encoding approaches are used for feature extraction from gene sequences, while machine learning methods are used for classification of splice sites using those extracted features. This paper presents a new DNA encoding method based on triplet nucleotide encoding with the frequency difference between true and false splice site sequences (TN-FDTF). Then, Support Vector Machine (SVM), Artificial Neural Network (NN), Random Forest (RF) and AdaBoost classifiers are used for prediction of splice sites. The performance of the proposed method was assessed on Homo Sapiens Splice Site Dataset (HS3D) using 10 fold cross validation. The results showed that the AdaBoost outperformed all the considered classifiers. In addition, the proposed method achieved higher prediction accuracy than most of the current existing state of the art methods. It is believed that the proposed method can help to achieve better results in Human splice site recognition and eukaryotic gene detection.
机译:鉴定人类基因组中基因的结构高度依赖于外显子与内含子之间边界的准确识别,即剪接位点。因此,开发有效检测剪接位点的新方法至关重要。 DNA编码方法用于从基因序列中提取特征,而机器学习方法用于使用那些提取的特征对剪接位点进行分类。本文提出了一种新的基于三重核苷酸编码的DNA编码方法,该编码方法具有正确和错误的剪接位点序列(TN-FDTF)之间的频率差。然后,将支持向量机(SVM),人工神经网络(NN),随机森林(RF)和AdaBoost分类器用于预测剪接位点。在Homo Sapiens拼接位点数据集(HS3D)上使用10倍交叉验证评估了所提出方法的性能。结果表明,AdaBoost的性能优于所有考虑的分类器。另外,与大多数当前现有的现有技术水平方法相比,所提出的方法实现了更高的预测精度。相信提出的方法可以帮助在人类剪接位点识别和真核基因检测中获得更好的结果。

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