Approximate inference of gene regulatory network models from RNA-Seq time series data
1Department of Computer Science, University of Reading, Reading, UK. t.thorne@reading.ac.uk.
BMC Bioinformatics
|April 13, 2018
Summary
This study introduces a new model for RNA-Seq time series data, improving gene regulatory network inference. The method accurately identifies gene interactions by modeling count data distributions.
Area of Science:
- Bioinformatics
- Computational Biology
- Genomics
Background:
- RNA-Seq data presents challenges for gene regulatory network inference due to its count-based nature.
- Existing methods struggle with the statistical properties of RNA sequencing measurements.
Purpose of the Study:
- To develop a novel model for inferring gene regulatory network structures from RNA-Seq time series data.
- To address the limitations of current methods by explicitly modeling RNA-Seq data distributions.
Main Methods:
- Utilized a negative binomial distribution to model RNA-Seq count observations.
- Employed sparse regression with a horseshoe prior for learning dynamic Bayesian networks.
- Applied variational inference for efficient estimation of model parameters.
Main Results:
- The proposed method demonstrated improved performance in learning directed gene networks compared to other sparse regression techniques on synthetic data.
- Successfully applied to human neuronal stem cell differentiation data to infer gene interactions.
Conclusions:
- The model enhances gene regulatory network inference from RNA-Seq time series by accurately capturing data distributions.
- Approximate inference enables rapid network structure learning with modest computational resources.
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