Genetic network inference: from co-expression clustering to reverse engineering

被引:643
作者
D'haeseleer, P [1 ]
Liang, SD
Somogyi, R
机构
[1] Univ New Mexico, Dept Comp Sci, Albuquerque, NM 87131 USA
[2] NASA, Ames Res Ctr, Moffett Field, CA 94035 USA
[3] Incyte Pharmaceut, Palo Alto, CA 94304 USA
基金
美国国家科学基金会; 美国国家航空航天局;
关键词
D O I
10.1093/bioinformatics/16.8.707
中图分类号
Q5 [生物化学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
摘要
Motivation: Advances in molecular biological, analytical and computational technologies are enabling us to systematically investigate the complex molecular processes underlying biological systems. In particular; using high-throughput gene expression assays, we are able to measure the output of the gene regulatory network. We aim here to review dntamining and modeling approaches for conceptualizing and unraveling the functional relationships implicit in these datasets. Clustering of co-expression profiles allows us to infer shared regulatory inputs and functional pathways. We discuss various aspects of clustering, ranging from distance measures to clustering algorithms and multiple-cluster memberships. More advanced analysis aims to infer causal connections between genes directly, i.e. who is regulating whom and how. We discuss several approaches to the problem of reverse engineering of genetic networks, from discrete Boolean networks, to continuous linear and non-linear models. We conclude that the combination of predictive modeling with systematic experimental verification will be required to gain a deeper insight into living organisms, therapeutic targeting and bioengineering.
引用
收藏
页码:707 / 726
页数:20
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