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Article: Mixture SNPs effect on phenotype in genome-wide association studies

TitleMixture SNPs effect on phenotype in genome-wide association studies
Authors
KeywordsGenome-wide association studies
Bayesian variable selection
Gibbs sampling
Issue Date2015
Citation
BMC Genomics, 2015, v. 16, n. 1, article no. 3 How to Cite?
Abstract© 2015 Wang et al.; licensee BioMed Central. Background: Recently mixed linear models are used to address the issue of "missing" heritability in traditional Genome-wide association studies (GWAS). The models assume that all single-nucleotide polymorphisms (SNPs) are associated with the phenotypes of interest. However, it is more common that only a small proportion of SNPs have significant effects on the phenotypes, while most SNPs have no or very small effects. To incorporate this feature, we propose an efficient Hierarchical Bayesian Model (HBM) that extends the existing mixed models to enforce automatic selection of significant SNPs. The HBM models the SNP effects using a mixture distribution of a point mass at zero and a normal distribution, where the point mass corresponds to those non-associative SNPs. Results: We estimate the HBM using Gibbs sampling. The estimation performance of our method is first demonstrated through two simulation studies. We make the simulation setups realistic by using parameters fitted on the Framingham Heart Study (FHS) data. The simulation studies show that our method can accurately estimate the proportion of SNPs associated with the simulated phenotype and identify these SNPs, as well as adapt to certain model mis-specification than the standard mixed models. In addition, we analyze data from the FHS and the Health and Retirement Study (HRS) to study the association between Body Mass Index (BMI) and SNPs on Chromosome 16, and replicate the identified genetic associations. The analysis of the FHS data identifies 0.3% SNPs on Chromosome 16 that affect BMI, including rs9939609 and rs9939973 on the FTO gene. These two SNPs are in strong linkage disequilibrium with rs1558902 (Rsq =0.901 for rs9939609 and Rsq =0.905 for rs9939973), which has been reported to be linked with obesity in previous GWAS. We then replicate the findings using the HRS data: the analysis finds 0.4% of SNPs associated with BMI on Chromosome 16. Furthermore, around 25% of the genes that are identified to be associated with BMI are common between the two studies. Conclusions: The results demonstrate that the HBM and the associated estimation algorithm offer a powerful tool for identifying significant genetic associations with phenotypes of interest, among a large number of SNPs that are common in modern genetics studies.
Persistent Identifierhttp://hdl.handle.net/10722/219784

 

DC FieldValueLanguage
dc.contributor.authorWang, Ling-
dc.contributor.authorShen, Haipeng-
dc.contributor.authorLiu, Hexuan-
dc.contributor.authorGuo, Guang-
dc.date.accessioned2015-09-23T02:57:57Z-
dc.date.available2015-09-23T02:57:57Z-
dc.date.issued2015-
dc.identifier.citationBMC Genomics, 2015, v. 16, n. 1, article no. 3-
dc.identifier.urihttp://hdl.handle.net/10722/219784-
dc.description.abstract© 2015 Wang et al.; licensee BioMed Central. Background: Recently mixed linear models are used to address the issue of "missing" heritability in traditional Genome-wide association studies (GWAS). The models assume that all single-nucleotide polymorphisms (SNPs) are associated with the phenotypes of interest. However, it is more common that only a small proportion of SNPs have significant effects on the phenotypes, while most SNPs have no or very small effects. To incorporate this feature, we propose an efficient Hierarchical Bayesian Model (HBM) that extends the existing mixed models to enforce automatic selection of significant SNPs. The HBM models the SNP effects using a mixture distribution of a point mass at zero and a normal distribution, where the point mass corresponds to those non-associative SNPs. Results: We estimate the HBM using Gibbs sampling. The estimation performance of our method is first demonstrated through two simulation studies. We make the simulation setups realistic by using parameters fitted on the Framingham Heart Study (FHS) data. The simulation studies show that our method can accurately estimate the proportion of SNPs associated with the simulated phenotype and identify these SNPs, as well as adapt to certain model mis-specification than the standard mixed models. In addition, we analyze data from the FHS and the Health and Retirement Study (HRS) to study the association between Body Mass Index (BMI) and SNPs on Chromosome 16, and replicate the identified genetic associations. The analysis of the FHS data identifies 0.3% SNPs on Chromosome 16 that affect BMI, including rs9939609 and rs9939973 on the FTO gene. These two SNPs are in strong linkage disequilibrium with rs1558902 (Rsq =0.901 for rs9939609 and Rsq =0.905 for rs9939973), which has been reported to be linked with obesity in previous GWAS. We then replicate the findings using the HRS data: the analysis finds 0.4% of SNPs associated with BMI on Chromosome 16. Furthermore, around 25% of the genes that are identified to be associated with BMI are common between the two studies. Conclusions: The results demonstrate that the HBM and the associated estimation algorithm offer a powerful tool for identifying significant genetic associations with phenotypes of interest, among a large number of SNPs that are common in modern genetics studies.-
dc.languageeng-
dc.relation.ispartofBMC Genomics-
dc.rightsCreative Commons: Attribution 3.0 Hong Kong License-
dc.subjectGenome-wide association studies-
dc.subjectBayesian variable selection-
dc.subjectGibbs sampling-
dc.titleMixture SNPs effect on phenotype in genome-wide association studies-
dc.typeArticle-
dc.description.naturepublished_or_final_version-
dc.identifier.doi10.1186/1471-2164-16-3-
dc.identifier.scopuseid_2-s2.0-84928721855-
dc.identifier.hkuros263849-
dc.identifier.volume16-
dc.identifier.issue1-
dc.identifier.spagearticle no. 3-
dc.identifier.epagearticle no. 3-
dc.identifier.eissn1471-2164-

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