Detection of Piwi-interacting RNAs based on sequence features

被引:7
|
作者
Liu, Y. J. [1 ]
Zhang, J. Y. [1 ]
Li, A. M. [2 ]
Liu, Z. W. [1 ]
Zhang, Y. Y. [1 ]
Sun, X. H. [1 ]
机构
[1] Xidian Univ, Sch Comp Sci & Technol, Xian, Peoples R China
[2] Xian Univ Technol, Sch Comp Sci & Technol, Xian, Peoples R China
来源
GENETICS AND MOLECULAR RESEARCH | 2016年 / 15卷 / 02期
基金
高等学校博士学科点专项科研基金;
关键词
PiRNA; Detection; Weighted k-mer with wildcards; Weighted k-mer; MESSENGER-RNAS; PIRNAS; OLIGONUCLEOTIDES; PREDICTION; PROTEIN; TOOL;
D O I
10.4238/gmr.15028638
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Piwi-interacting RNAs (piRNAs) are a class of small non-coding RNAs. Distinguishing piRNAs from other non-coding RNAs is important because of their important role in the physiological regulation of spermatogenesis, genome protection from transposons, and regulation of mRNAs and long non-coding RNAs. Few computational studies have addressed piRNAs detection, and both effectiveness and efficiency of piRNA detection tools require improvement. In this study, a piRNA detection method based on sequence features and a support vector machine was developed. Four types of features are proposed: weighted k-mer, weighted k-mer with wildcards, position-specific base, and piRNA length. The piRNA sequences from human, mouse, rat, and drosophila were respectively used in this experiment. Compared to existing algorithms, the proposed method provides a better balance between precision and sensitivity (both are approximately 90%), and although these values were slightly slower than those obtained using the piRNA annotation approach, the proposed method was four-fold faster than piRPred and 229-fold faster than piRNA predictor.
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页数:13
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