| Literature DB >> 28557607 |
Yoonha Choi1, Marc Coram2, Jie Peng3, Hua Tang1.
Abstract
Constructing expression networks using transcriptomic data is an effective approach for studying gene regulation. A popular approach for constructing such a network is based on the Gaussian graphical model (GGM), in which an edge between a pair of genes indicates that the expression levels of these two genes are conditionally dependent, given the expression levels of all other genes. However, GGMs are not appropriate for non-Gaussian data, such as those generated in RNA-seq experiments. We propose a novel statistical framework that maximizes a penalized likelihood, in which the observed count data follow a Poisson log-normal distribution. To overcome the computational challenges, we use Laplace's method to approximate the likelihood and its gradients, and apply the alternating directions method of multipliers to find the penalized maximum likelihood estimates. The proposed method is evaluated and compared with GGMs using both simulated and real RNA-seq data. The proposed method shows improved performance in detecting edges that represent covarying pairs of genes, particularly for edges connecting low-abundant genes and edges around regulatory hubs.Entities:
Keywords: Gaussian graphical model; Poisson log-normal distribution; RNA-seq; alternating directions method of multipliers; penalized likelihood
Mesh:
Year: 2017 PMID: 28557607 PMCID: PMC5510689 DOI: 10.1089/cmb.2017.0053
Source DB: PubMed Journal: J Comput Biol ISSN: 1066-5277 Impact factor: 1.479