Summary
We propose a hierarchical Bayesian approach to infer the RNA synthesis, processing, and degradation rates from sequencing data. We parametrise kinetic rates with novel functional forms and estimate the parameters through a Dirichlet process defined at a low level of hierarchy. Despite the complexity of this approach, we manage to perform inference, clusterisation and model selection simultaneously. We apply our method to investigate transcriptional and post-transcriptional responses of murine fibroblasts to the activation of proto-oncogene MYC. We uncover a widespread choral regulation of the three rates, which was not previously observed in this biological system.
Competing Interest Statement
The authors have declared no competing interest.
Footnotes
Wrong references to tables fixed