ArticleBioinformatics (Oxford, England)2020
BAGSE: a Bayesian hierarchical model approach for gene set enrichment analysis.
Article in Bioinformatics (Oxford, England), 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.
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Who cites it
3 citing papers in PubMed.
- Probabilistic integration of transcriptome-wide association studies and colocalization analysis identifies key molecular pathways of complex traits.American journal of human genetics · 2023Article
- TWO-SIGMA-G: a new competitive gene set testing framework for scRNA-seq data accounting for inter-gene and cell-cell correlation.Briefings in bioinformatics · 2022Article
- Overcoming false-positive gene-category enrichment in the analysis of spatially resolved transcriptomic brain atlas data.Nature communications · 2021Article
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Authors and funding
5 authors.
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Abstract
motivationGene set enrichment analysis has been shown to be effective in identifying relevant biological pathways underlying complex diseases. Existing approaches lack the ability to quantify the enrichment levels accurately, hence preventing the enrichment information to be further utilized in both upstream and downstream analyses. A modernized and rigorous approach for gene set enrichment analysis that emphasizes both hypothesis testing and enrichment estimation is much needed.
resultsWe propose a novel computational method, Bayesian Analysis of Gene Set Enrichment (BAGSE), for gene set enrichment analysis. BAGSE is built on a Bayesian hierarchical model and fully accounts for the uncertainty embedded in the association evidence of individual genes. We adopt an empirical Bayes inference framework to fit the proposed hierarchical model by implementing an efficient EM algorithm. Through simulation studies, we illustrate that BAGSE yields accurate enrichment quantification while achieving similar power as the state-of-the-art methods. Further simulation studies show that BAGSE can effectively utilize the enrichment information to improve the power in gene discovery. Finally, we demonstrate the application of BAGSE in analyzing real data from a differential expression experiment and a transcriptome-wide association study. Our results indicate that the proposed statistical framework is effective in aiding the discovery of potentially causal pathways and gene networks. AVAILABILITY AND IMPLEMENTATION: BAGSE is implemented using the C++ programing language and is freely available from https://github.com/xqwen/bagse/. Simulated and real data used in this paper are also available at the Github repository for reproducibility purposes. SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online.
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