Inferring slowly-changing dynamic gene-regulatory networks

BMC Bioinformatics

Research

Ernst C Wit¹  Antonino Abbruzzo² 

[1] Johann Bernoulli Institute, University of Groningen, 9747, Nijenborgh 9, AG Groningen, Netherlands;SEAS - Dipartimento di Scienze Economiche Finanziarie e Statistiche, Università degli Studi di Palermo, Viale delle Scienze Ed., 13, 90128, Palermo, Italy;

关键词: gene-regulatory networks;    graphical models;    L;   

DOI  :  10.1186/1471-2105-16-S6-S5

来源: Springer

【 摘 要 】

Dynamic gene-regulatory networks are complex since the interaction patterns between their components mean that it is impossible to study parts of the network in separation. This holistic character of gene-regulatory networks poses a real challenge to any type of modelling. Graphical models are a class of models that connect the network with a conditional independence relationships between random variables. By interpreting these random variables as gene activities and the conditional independence relationships as functional non-relatedness, graphical models have been used to describe gene-regulatory networks. Whereas the literature has been focused on static networks, most time-course experiments are designed in order to tease out temporal changes in the underlying network. It is typically reasonable to assume that changes in genomic networks are few, because biological systems tend to be stable.We introduce a new model for estimating slow changes in dynamic gene-regulatory networks, which is suitable for high-dimensional data, e.g. time-course microarray data. Our aim is to estimate a dynamically changing genomic network based on temporal activity measurements of the genes in the network. Our method is based on the penalized likelihood with ℓ1-norm, that penalizes conditional dependencies between genes as well as differences between conditional independence elements across time points. We also present a heuristic search strategy to find optimal tuning parameters. We re-write the penalized maximum likelihood problem into a standard convex optimization problem subject to linear equality constraints. We show that our method performs well in simulation studies. Finally, we apply the proposed model to a time-course T-cell dataset.

【 授权许可】

CC BY   
© Wit and Abbruzzo; licensee BioMed Central Ltd. 2015