ArticleEuropean journal of human genetics : EJHG2010
An omnibus test for family-based association studies with multiple SNPs and multiple phenotypes.
Article in European journal of human genetics : EJHG, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.
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Who cites it
5 citing papers in PubMed, 9 citations in OpenAlex.
- Statistically efficient association analysis of quantitative traits with haplotypes and untyped SNPs in family studies.BMC genetics · 2020Article
- Identifying pleiotropic genes in genome-wide association studies from related subjects using the linear mixed model and Fisher combination function.BMC bioinformatics · 2017Article
- Family-based association analysis: a fast and efficient method of multivariate association analysis with multiple variants.BMC bioinformatics · 2015Article
- Detecting adaptive trait loci in nonmodel systems: divergence or admixture mapping?Molecular ecology · 2013Article
- Statistical challenges for genome-wide association studies of suicidality using family data.European psychiatry : the journal of the Association of European Psychiatrists · 2010Review
Corrections and comments
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Authors and funding
5 authors at 3 institutions in 1 country.
Funding
Abstract
We propose an omnibus family-based association test (MFBAT) that can be applied to multiple markers and multiple phenotypes and that has only one degree of freedom. The proposed test statistic extends current FBAT methodology to incorporate multiple markers as well as multiple phenotypes. Using simulation studies, power estimates for the proposed methodology are compared with the standard methodologies. On the basis of these simulations, we find that MFBAT substantially outperforms other methods, including haplotypic approaches and doing multiple tests with single single-nucleotide polymorphisms (SNPs) and single phenotypes. The practical relevance of the approach is illustrated by an application to asthma in which SNP/phenotype combinations are identified and reach overall significance that would not have been identified using other approaches. This methodology is directly applicable to cases in which there are multiple SNPs, such as candidate gene studies, cases in which there are multiple phenotypes, such as expression data, and cases in which there are multiple phenotypes and genotypes, such as genome-wide association studies that incorporate expression profiles as phenotypes. This program is available in the PBAT analysis package.
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Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.