Prioritizing GWAS results: A review of statistical methods and recommendations for their application - PubMed (original) (raw)
Review
Prioritizing GWAS results: A review of statistical methods and recommendations for their application
Rita M Cantor et al. Am J Hum Genet. 2010 Jan.
Abstract
Genome-wide association studies (GWAS) have rapidly become a standard method for disease gene discovery. A substantial number of recent GWAS indicate that for most disorders, only a few common variants are implicated and the associated SNPs explain only a small fraction of the genetic risk. This review is written from the viewpoint that findings from the GWAS provide preliminary genetic information that is available for additional analysis by statistical procedures that accumulate evidence, and that these secondary analyses are very likely to provide valuable information that will help prioritize the strongest constellations of results. We review and discuss three analytic methods to combine preliminary GWAS statistics to identify genes, alleles, and pathways for deeper investigations. Meta-analysis seeks to pool information from multiple GWAS to increase the chances of finding true positives among the false positives and provides a way to combine associations across GWAS, even when the original data are unavailable. Testing for epistasis within a single GWAS study can identify the stronger results that are revealed when genes interact. Pathway analysis of GWAS results is used to prioritize genes and pathways within a biological context. Following a GWAS, association results can be assigned to pathways and tested in aggregate with computational tools and pathway databases. Reviews of published methods with recommendations for their application are provided within the framework for each approach.
2010 The American Society of Human Genetics. Published by Elsevier Inc.
Similar articles
- Epistasis network centrality analysis yields pathway replication across two GWAS cohorts for bipolar disorder.
Pandey A, Davis NA, White BC, Pajewski NM, Savitz J, Drevets WC, McKinney BA. Pandey A, et al. Transl Psychiatry. 2012 Aug 14;2(8):e154. doi: 10.1038/tp.2012.80. Transl Psychiatry. 2012. PMID: 22892719 Free PMC article. - Evaluation of PrediXcan for prioritizing GWAS associations and predicting gene expression.
Li B, Verma SS, Veturi YC, Verma A, Bradford Y, Haas DW, Ritchie MD. Li B, et al. Pac Symp Biocomput. 2018;23:448-459. Pac Symp Biocomput. 2018. PMID: 29218904 Free PMC article. - SMMB: a stochastic Markov blanket framework strategy for epistasis detection in GWAS.
Niel C, Sinoquet C, Dina C, Rocheleau G. Niel C, et al. Bioinformatics. 2018 Aug 15;34(16):2773-2780. doi: 10.1093/bioinformatics/bty154. Bioinformatics. 2018. PMID: 29547902 - Network.assisted analysis to prioritize GWAS results: principles, methods and perspectives.
Jia P, Zhao Z. Jia P, et al. Hum Genet. 2014 Feb;133(2):125-38. doi: 10.1007/s00439-013-1377-1. Hum Genet. 2014. PMID: 24122152 Free PMC article. Review. - Bioinformatics challenges for genome-wide association studies.
Moore JH, Asselbergs FW, Williams SM. Moore JH, et al. Bioinformatics. 2010 Feb 15;26(4):445-55. doi: 10.1093/bioinformatics/btp713. Epub 2010 Jan 6. Bioinformatics. 2010. PMID: 20053841 Free PMC article. Review.
Cited by
- Cancer pharmacogenomics: strategies and challenges.
Wheeler HE, Maitland ML, Dolan ME, Cox NJ, Ratain MJ. Wheeler HE, et al. Nat Rev Genet. 2013 Jan;14(1):23-34. doi: 10.1038/nrg3352. Epub 2012 Nov 27. Nat Rev Genet. 2013. PMID: 23183705 Free PMC article. Review. - Importance of different types of prior knowledge in selecting genome-wide findings for follow-up.
Minelli C, De Grandi A, Weichenberger CX, Gögele M, Modenese M, Attia J, Barrett JH, Boehnke M, Borsani G, Casari G, Fox CS, Freina T, Hicks AA, Marroni F, Parmigiani G, Pastore A, Pattaro C, Pfeufer A, Ruggeri F, Schwienbacher C, Taliun D, Pramstaller PP, Domingues FS, Thompson JR. Minelli C, et al. Genet Epidemiol. 2013 Feb;37(2):205-13. doi: 10.1002/gepi.21705. Genet Epidemiol. 2013. PMID: 23307621 Free PMC article. - Tree-based QTL mapping with expected local genetic relatedness matrices.
Link V, Schraiber JG, Fan C, Dinh B, Mancuso N, Chiang CWK, Edge MD. Link V, et al. Am J Hum Genet. 2023 Dec 7;110(12):2077-2091. doi: 10.1016/j.ajhg.2023.10.017. Am J Hum Genet. 2023. PMID: 38065072 Free PMC article. - Dissection of complex adult traits in a mouse synthetic population.
Burke DT, Kozloff KM, Chen S, West JL, Wilkowski JM, Goldstein SA, Miller RA, Galecki AT. Burke DT, et al. Genome Res. 2012 Aug;22(8):1549-57. doi: 10.1101/gr.135582.111. Epub 2012 May 15. Genome Res. 2012. PMID: 22588897 Free PMC article. - Parameters in dynamic models of complex traits are containers of missing heritability.
Wang Y, Gjuvsland AB, Vik JO, Smith NP, Hunter PJ, Omholt SW. Wang Y, et al. PLoS Comput Biol. 2012;8(4):e1002459. doi: 10.1371/journal.pcbi.1002459. Epub 2012 Apr 5. PLoS Comput Biol. 2012. PMID: 22496634 Free PMC article.
References
- Goldstein D.B. Common genetic variation and human traits. N. Engl. J. Med. 2009;360:1696–1698. - PubMed
- Halperin E., Eskin E. Haplotype reconstruction from genotype data using Imperfect Phylogeny. Bioinformatics. 2004;20:1842–1849. - PubMed
- Marchini J., Donnelly P., Cardon L.R. Genome-wide strategies for detecting multiple loci that influence complex diseases. Nat. Genet. 2005;37:413–417. - PubMed
Publication types
MeSH terms
Grants and funding
- HL28481/HL/NHLBI NIH HHS/United States
- MH59490/MH/NIMH NIH HHS/United States
- R01 MH059490/MH/NIMH NIH HHS/United States
- R37 MH059490/MH/NIMH NIH HHS/United States
- R01 GM053275/GM/NIGMS NIH HHS/United States
- GM53275/GM/NIGMS NIH HHS/United States
- P01 HL028481/HL/NHLBI NIH HHS/United States
LinkOut - more resources
Full Text Sources
Other Literature Sources