Reverse engineering of gene regulatory networks

被引:71
作者
Cho, K.-H. [1 ]
Choo, S.-M.
Jung, S. H.
Kim, J.-R.
Choi, H.-S.
Kim, J.
机构
[1] Seoul Natl Univ, Coll Med, Seoul 110799, South Korea
[2] Univ Ulsan, Sch Elect Engn, Ulsan 680749, South Korea
[3] Hansung Univ, Dept Informat & Commun Engn, Seoul 136792, South Korea
[4] Seoul Natl Univ, Bio MAX Inst, Seoul 151818, South Korea
[5] Seoul Natl Univ, Interdisciplinary Program Bioinformat, Seoul 151747, South Korea
关键词
FUNCTIONAL INTERACTION STRUCTURE; PROBABILISTIC BOOLEAN NETWORKS; DYNAMIC BAYESIAN NETWORK; TIME-SERIES; TRANSCRIPTIONAL NETWORKS; MICROARRAY DATA; BINDING-SITES; CELL-CYCLE; IN-SILICO; EXPRESSION;
D O I
10.1049/iet-syb:20060075
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Systems biology is a multi-disciplinary approach to the study of the interactions of various cellular mechanisms and cellular components. Owing to the development of new technologies that simultaneously measure the expression of genetic information, systems biological studies involving gene interactions are increasingly prominent. In this regard, reconstructing gene regulatory networks (GRNs) forms the basis for the dynamical analysis of gene interactions and related effects on cellular control pathways. Various approaches of inferring GRNs from gene expression profiles and biological information, including machine learning approaches, have been reviewed, with a brief introduction of DNA microarray experiments as typical tools for measuring levels of messenger ribonucleic acid (mRNA) expression. In particular, the inference methods are classified according to the required input information, and the main idea of each method is elucidated by comparing its advantages and disadvantages with respect to the other methods. In addition, recent developments in this field are introduced and discussions on the challenges and opportunities for future research are provided.
引用
收藏
页码:149 / 163
页数:15
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