2006
DOI: 10.1016/j.biochi.2006.03.006
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An approach of encoding for prediction of splice sites using SVM

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Cited by 56 publications
(40 citation statements)
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“…One of the famous classification-based methods is support vector machine (SVM), which is an accurate and high-performance method [11]. Since the performance of the SVM-based methods largely depends on DNA encoding method, there are some works to effectively encode DNA for feature extraction [12], [13], [14], [15]. Another approach for prediction splice sites is statistical analysis, recently a statistical method is presented for the prediction of donor splice sites, which is based on dinucleotide dependencies at all possible positions [16].…”
Section: Introductionmentioning
confidence: 99%
“…One of the famous classification-based methods is support vector machine (SVM), which is an accurate and high-performance method [11]. Since the performance of the SVM-based methods largely depends on DNA encoding method, there are some works to effectively encode DNA for feature extraction [12], [13], [14], [15]. Another approach for prediction splice sites is statistical analysis, recently a statistical method is presented for the prediction of donor splice sites, which is based on dinucleotide dependencies at all possible positions [16].…”
Section: Introductionmentioning
confidence: 99%
“…Creating an optimized set of features that best represent the dataset has always remained a challenge for splice site prediction. The presence or absence of certain nucleotide sequences close to the splice sites were considered as features for splice site prediction for a long time [8,9,10,11,12,13,14]. Since all such features were not known, there have been constant efforts to improve or refine features as well as include more relevant features by taking into account recent experimental observations.…”
Section: Introductionmentioning
confidence: 99%
“…Shortly after its introduction, its performance has already either matched or outperformed that of traditional machine learning approaches (e.g., NN) for a wide range of applications including splice sites prediction [2]- [7]. Currently, the SVM approach mainly deals with numerical data (with the exception of special kernel functions), so the DNA sequences must be encoded beforehand in some way.…”
Section: Introductionmentioning
confidence: 99%