| Literature DB >> 23735434 |
Abstract
In genomic analysis, there is growing interest in network structures that represent biochemistry interactions. Graph structured or constrained inference takes advantage of a known relational structure among variables to introduce smoothness and reduce complexity in modeling, especially for high-dimensional genomic data. There has been a lot of interest in its application in model regularization and selection. However, prior knowledge on the graphical structure among the variables can be limited and partial. Empirical data may suggest variations and modifications to such a graph, which could lead to new and interesting biological findings. In this paper, we propose a Bayesian random graph-constrained model, rGrace, an extension from the Grace model, to combine a priori network information with empirical evidence, for applications such as pathway analysis. Using both simulations and real data examples, we show that the new method, while leading to improved predictive performance, can identify discrepancy between data and a prior known graph structure and suggest modifications and updates.Mesh:
Year: 2013 PMID: 23735434 DOI: 10.1515/sagmb-2013-0011
Source DB: PubMed Journal: Stat Appl Genet Mol Biol ISSN: 1544-6115