Uncovering robust patterns of microRNA co-expression across cancers using Bayesian Relevance Networks

PLoS One. 2017 Aug 17;12(8):e0183103. doi: 10.1371/journal.pone.0183103. eCollection 2017.

Abstract

Co-expression networks have long been used as a tool for investigating the molecular circuitry governing biological systems. However, most algorithms for constructing co-expression networks were developed in the microarray era, before high-throughput sequencing-with its unique statistical properties-became the norm for expression measurement. Here we develop Bayesian Relevance Networks, an algorithm that uses Bayesian reasoning about expression levels to account for the differing levels of uncertainty in expression measurements between highly- and lowly-expressed entities, and between samples with different sequencing depths. It combines data from groups of samples (e.g., replicates) to estimate group expression levels and confidence ranges. It then computes uncertainty-moderated estimates of cross-group correlations between entities, and uses permutation testing to assess their statistical significance. Using large scale miRNA data from The Cancer Genome Atlas, we show that our Bayesian update of the classical Relevance Networks algorithm provides improved reproducibility in co-expression estimates and lower false discovery rates in the resulting co-expression networks. Software is available at www.perkinslab.ca.

MeSH terms

  • Algorithms
  • Bayes Theorem*
  • Humans
  • MicroRNAs / genetics*
  • Neoplasms / genetics*

Substances

  • MicroRNAs

Grants and funding

This work was supported by grant 328154 to TJP from the Natural Sciences and Engineering Research Council of Canada. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.