So sánh phương pháp

	Nghiên cứu liên kết bộ gen trên toàn bộ bộ gen theo phương pháp Bayes	Phân tích làm giàu đường dẫn
Lĩnh vực	Tin sinh học	Tin sinh học
Họ	Process / pipeline	Process / pipeline
Năm ra đời	2007–2009 (formal statistical framework)	2003–2005
Người khởi xướng	Matthew Stephens, David J. Balding, Jon Wakefield (key formalizers ca. 2007–2009)	Mootha et al. (2003); systematised by Subramanian et al. (2005)
Loại	Statistical genetic association analysis	Statistical functional annotation method
Công trình gốc	Stephens, M., & Balding, D. J. (2009). Bayesian statistical methods for genetic association studies. Nature Reviews Genetics, 10(10), 681–690.	Subramanian, A., Tamayo, P., Mootha, V. K., Mukherjee, S., Ebert, B. L., Gillette, M. A., Paulovich, A., Pomeroy, S. L., Golub, T. R., Lander, E. S., & Mesirov, J. P. (2005). Gene set enrichment analysis: A knowledge-based approach for interpreting genome-wide expression profiles. Proceedings of the National Academy of Sciences, 102(43), 15545–15550.
Tên gọi khác	Bayesian GWAS, Bayesian genome-wide association analysis, Bayesian GWA study, BF-GWAS	PEA, overrepresentation analysis, ORA, functional enrichment analysis
Liên quan	5	6
Tóm tắt	Bayesian GWAS applies Bayesian statistical inference to genome-wide association studies, replacing classical p-value thresholds with Bayes factors and posterior probabilities. This framework naturally incorporates prior knowledge about effect sizes and variant frequencies, quantifies evidence for association on a continuous scale, and supports principled fine-mapping of causal variants within associated loci. It is widely used in complex trait genetics, population genomics, and translational research where uncertainty quantification and multi-variant modeling matter.	Pathway enrichment analysis (PEA) is a statistical approach that takes a list of genes or proteins of interest — typically derived from a differential expression or proteomics experiment — and identifies which pre-defined biological pathways or functional gene sets are represented more often than expected by chance. By mapping individual molecular changes onto curated pathway knowledge bases such as KEGG, Gene Ontology, or Reactome, PEA translates long gene lists into interpretable biological processes, making it a central tool in the post-analysis of high-throughput omics experiments.