ArticleGenetic epidemiology2010
Ordered subset analysis for case-control studies.
Article in Genetic epidemiology, 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.
- Finding associations in a heterogeneous setting: statistical test for aberration enrichment.Genome medicine · 2021Article
- JBASE: Joint Bayesian Analysis of Subphenotypes and Epistasis.Bioinformatics (Oxford, England) · 2016Article
- Ordered subset analysis of copy number variation association with age at onset of Alzheimer's disease.Journal of Alzheimer's disease : JAD · 2014Article
- The role of phenotype in gene discovery in the whole genome sequencing era.Human genetics · 2012Review
- TDT-HET: a new transmission disequilibrium test that incorporates locus heterogeneity into the analysis of family-based association data.BMC bioinformatics · 2012Article
Corrections and comments
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Authors and funding
3 authors.
Funding
Abstract
Genetic heterogeneity, which may manifest on a population level as different frequencies of a specific disease susceptibility allele in different subsets of patients, is a common problem for candidate gene and genome-wide association studies of complex human diseases. The ordered subset analysis (OSA) was originally developed as a method to reduce genetic heterogeneity in the context of family-based linkage studies. Here, we have extended a previously proposed method (OSACC) for applying the OSA methodology to case-control datasets. We have evaluated the type I error and power of different OSACC permutation tests with an extensive simulation study. Case-control datasets were generated under two different models by which continuous clinical or environmental covariates may influence the relationship between susceptibility genotypes and disease risk. Our results demonstrate that OSACC is more powerful under some disease models than the commonly used trend test and a previously proposed joint test of main genetic and gene-environment interaction effects. An additional unique benefit of OSACC is its ability to identify a more informative subset of cases that may be subjected to more detailed molecular analysis, such as DNA sequencing of selected genomic regions to detect functional variants in linkage disequilibrium with the associated polymorphism. The OSACC-identified covariate threshold may also improve the power of an additional dataset to replicate previously reported associations that may only be detectable in a fraction of the original and replication datasets. In summary, we have demonstrated that OSACC is a useful method for improving SNP association signals in genetically heterogeneous datasets.
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