Reconsideration of In-Silico siRNA Design Based on Feature Selection: A Cross-Platform Data Integration Perspective

被引:8
作者
Liu, Qi [1 ]
Zhou, Han [1 ]
Cui, Juan [2 ,3 ]
Cao, Zhiwei [1 ]
Xu, Ying [2 ,3 ,4 ]
机构
[1] Tongji Univ, Dept Bioinformat, Shanghai 200092, Peoples R China
[2] Univ Georgia, Dept Biochem & Mol Biol, Computat Syst Biol Lab, Athens, GA 30602 USA
[3] Univ Georgia, Inst Bioinformat, Athens, GA 30602 USA
[4] Jilin Univ, Coll Comp Sci & Technol, Changchun 130023, Peoples R China
来源
PLOS ONE | 2012年 / 7卷 / 05期
基金
中国国家自然科学基金;
关键词
DOUBLE-STRANDED-RNA; MESSENGER-RNA; RANK AGGREGATION; MONTE-CARLO; INTERFERENCE; PREDICTION; EFFICIENT; MODEL;
D O I
10.1371/journal.pone.0037879
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
RNA interference via exogenous short interference RNAs (siRNA) is increasingly more widely employed as a tool in gene function studies, drug target discovery and disease treatment. Currently there is a strong need for rational siRNA design to achieve more reliable and specific gene silencing; and to keep up with the increasing needs for a wider range of applications. While progress has been made in the ability to design siRNAs with specific targets, we are clearly at an infancy stage towards achieving rational design of siRNAs with high efficacy. Among the many obstacles to overcome, lack of general understanding of what sequence features of siRNAs may affect their silencing efficacy and of large-scale homogeneous data needed to carry out such association analyses represents two challenges. To address these issues, we investigated a feature-selection based in-silico siRNA design from a novel cross-platform data integration perspective. An integration analysis of 4,482 siRNAs from ten meta-datasets was conducted for ranking siRNA features, according to their possible importance to the silencing efficacy of siRNAs across heterogeneous data sources. Our ranking analysis revealed for the first time the most relevant features based on cross-platform experiments, which compares favorably with the traditional in-silico siRNA feature screening based on the small samples of individual platform data. We believe that our feature ranking analysis can offer more creditable suggestions to help improving the design of siRNA with specific silencing targets. Data and scripts are available at http://csbl.bmb.uga.edu/publications/materials/qiliu/siRNA.html.
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页数:10
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