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Testing for goodness rather than lack of fit of an X-chromosomal SNP to the Hardy-Weinberg model.
Wellek, Stefan; Ziegler, Andreas.
Affiliation
  • Wellek S; Department of Biostatistics, CIMH Mannheim, Mannheim Medical School of the University of Heidelberg, Mannheim, Germany.
  • Ziegler A; Department of Medical Biostatistics, Epidemiology & Informatics, University Medical Center of the Johannes Gutenberg University Mainz, Mainz, Germany.
PLoS One ; 14(2): e0212344, 2019.
Article in En | MEDLINE | ID: mdl-30789927
The problem of checking the genotype distribution obtained for some diallelic marker for compatibility with the Hardy-Weinberg equilibrium (HWE) condition arises also for loci on the X chromosome. The possible genotypes depend on the sex of the individual in this case: for females, the genotype distribution is trinomial, as in the case of an autosomal locus, whereas a binomial proportion is observed for males. Like in genetic association studies with autosomal SNPs, interest is typically in establishing approximate compatibility of the observed genotype frequencies with HWE. This requires to replace traditional methods tailored for detecting lack of fit to the model with an equivalence testing procedure to be derived by treating approximate compatibility with the model as the alternative hypothesis. The test constructed here is based on an upper confidence bound and a simple to interpret combined measure of distance between true and HWE conforming genotype distributions in female and male subjects. A particular focus of the paper is on the derivation of the asymptotic distribution of the test statistic under null alternatives which is not of the usual Gaussian form. A closed sample size formula is also provided and shown to behave satisfactorily in terms of the approximation error.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Venous Thrombosis / Polymorphism, Single Nucleotide / Chromosomes, Human, X / Models, Genetic Type of study: Risk_factors_studies Limits: Humans Language: En Journal: PLoS One Journal subject: CIENCIA / MEDICINA Year: 2019 Document type: Article Affiliation country: Alemania Country of publication: Estados Unidos

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Venous Thrombosis / Polymorphism, Single Nucleotide / Chromosomes, Human, X / Models, Genetic Type of study: Risk_factors_studies Limits: Humans Language: En Journal: PLoS One Journal subject: CIENCIA / MEDICINA Year: 2019 Document type: Article Affiliation country: Alemania Country of publication: Estados Unidos