Uncovering robust patterns of microRNA co-expression across cancers using Bayesian Relevance Networks
Author(s) -
Parameswaran Ramachandran,
Daniel SánchezTaltavull,
Theodore J. Perkins
Publication year - 2017
Publication title -
plos one
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.99
H-Index - 332
ISSN - 1932-6203
DOI - 10.1371/journal.pone.0183103
Subject(s) - bayesian probability , relevance (law) , computational biology , dna microarray , expression (computer science) , data mining , computer science , false discovery rate , permutation (music) , bayesian network , gene expression profiling , biology , bioinformatics , gene expression , artificial intelligence , genetics , gene , acoustics , law , programming language , physics , political science
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 .
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