tigaR: integrative significance analysis of temporal differential gene expression induced by genomic abnormalities

• Published in: BMC bioinformatics 2014-10, Vol.15 (1), p.327-327, Article 327
• Main Authors: Miok, Viktorian, Wilting, Saskia M, van de Wiel, Mark A, Jaspers, Annelieke, van Noort, Paula I, Brakenhoff, Ruud H, Snijders, Peter J F, Steenbergen, Renske D M, van Wieringen, Wessel N
• Format: Article
• Language: English
• Subjects: Analysis; Bayes Theorem; Bayesian analysis; Carcinogens; Cell Line; Cervical cancer; Computer Simulation; Deoxyribonucleic acid; DNA; DNA - genetics; DNA microarrays; DNA, Complementary; Estimates; Gene Dosage; Gene expression; Gene Expression Regulation; Genes; Genetic aspects; Genome; Genomes; Genomics; Genomics - methods; Head & neck cancer; Host-Pathogen Interactions; Human papillomavirus 16; Human papillomavirus 16 - physiology; Human papillomavirus 18; Human papillomavirus 18 - physiology; Humans; Keratinocytes - metabolism; Keratinocytes - virology; Mathematical models; Medical research; Messenger RNA; Methodology; MicroRNAs; Models, Genetic; Papillomavirus Infections - genetics; Random variables; Reproduction; RNA sequencing; Statistical methods
• ISSN: 1471-2105; 1471-2105
• DOI: 10.1186/1471-2105-15-327

To determine which changes in the host cell genome are crucial for cervical carcinogenesis, a longitudinal in vitro model system of HPV-transformed keratinocytes was profiled in a genome-wide manner. Four cell lines affected with either HPV16 or HPV18 were assayed at 8 sequential time points for gene expression (mRNA) and gene copy number (DNA) using high-resolution microarrays. Available methods for temporal differential expression analysis are not designed for integrative genomic studies. Here, we present a method that allows for the identification of differential gene expression associated with DNA copy number changes over time. The temporal variation in gene expression is described by a generalized linear mixed model employing low-rank thin-plate splines. Model parameters are estimated with an empirical Bayes procedure, which exploits integrated nested Laplace approximation for fast computation. Iteratively, posteriors of hyperparameters and model parameters are estimated. The empirical Bayes procedure shrinks multiple dispersion-related parameters. Shrinkage leads to more stable estimates of the model parameters, better control of false positives and improvement of reproducibility. In addition, to make estimates of the DNA copy number more stable, model parameters are also estimated in a multivariate way using triplets of features, imposing a spatial prior for the copy number effect. With the proposed method for analysis of time-course multilevel molecular data, more profound insight may be gained through the identification of temporal differential expression induced by DNA copy number abnormalities. In particular, in the analysis of an integrative oncogenomics study with a time-course set-up our method finds genes previously reported to be involved in cervical carcinogenesis. Furthermore, the proposed method yields improvements in sensitivity, specificity and reproducibility compared to existing methods. Finally, the proposed method is able to handle count (RNAseq) data from time course experiments as is shown on a real data set.