特征(语言学)
DNA
算法
点式的
计算机科学
DNA甲基化
范畴变量
计算生物学
代表(政治)
人工智能
模式识别(心理学)
作者
Mingzhao Wang,Juanying Xie,Philip W. Grant,Shengquan Xu
标识
DOI:10.1016/j.ins.2022.05.060
摘要
• The bidirectional dinucleotide and trinucleotide Position-Specific Propensities (PSP) are developed. • The parameter ξ is introduced to represent the interval between the current nucleotide and its forward or backward dinucleotide. • The Pointwise Joint Mutual Information (PJMI) theory is proposed. • The feature representation algorithm referred to PSP-PJMI is proposed. • The 4mC-BiNP model is developed for identifying DNA 4mC sites. • The PSP-PJMI algorithm can also extract features from RNA sequences to identify RNA methylation sites. Identifying DNA N4-methylcytosine (4mC) sites is an essential step to study the biological functional mechanism. Feature representation is the primary step to identify 4mC sites due to its influencing the performance of the downstream 4mC site predictive model. Extracting numerical features having strong categorical information from DNA sequences is the key issue to build a 4mC predictive model having good performance. Therefore, a feature representation algorithm referred to as PSP-PJMI is proposed in this paper. It first proposes Pointwise Joint Mutual Information (PJMI), then the bidirectional k -nucleotide Position-Specific Propensities (PSP), so that the PSP-PJMI feature representation algorithm is developed. The parameter ξ is used to indicate the interval from the current nucleotide to the forward or backward dinucleotide in the bidirectional trinucleotide PSP, so that the position information of nucleotides is extracted from a DNA sequence as far as possible. The features corresponding to various ξ are concatenated to comprise the high dimensional feature vector having rich categorical information. The 4mC-BiNP model for identifying DNA 4mC sites is constructed using SVM and the extracted features. The experimental results of 10-fold cross validation test, cross-species validation test, and independent test on 6 species datasets show that the proposed PSP-PJMI algorithm can extract features having richer categorical information than the available feature representation algorithms can do. The 4mC-BiNP model is superior to the state-of-the-art predictive models for identifying DNA 4mC sites. Furthermore, the PSP-PJMI algorithm can be used to extract features for identifying other DNA methylation sites, and also be used for RNA sequences to predict RNA methylation sites.
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