Literature DB >> 21108625

Correction for multiplicity in genetic association studies of triads: the permutational TDT.

James F Troendle1, James L Mills.   

Abstract

New technology for large-scale genotyping has created new challenges for statistical analysis. Correcting for multiple comparison without discarding true positive results and extending methods to triad studies are among the important problems facing statisticians. We present a one-sample permutation test for testing transmission disequilibrium hypotheses in triad studies, and show how this test can be used for multiple single nucleotide polymorphism (SNP) testing. The resulting multiple comparison procedure is shown in the case of the transmission disequilibrium test to control the familywise error. Furthermore, this procedure can handle multiple possible modes of risk inheritance per SNP. The resulting permutational procedure is shown through simulation of SNP data to be more powerful than the Bonferroni procedure when the SNPs are in linkage disequilibrium. Moreover, permutations implicitly avoid any multiple comparison correction penalties when the SNP has a rare allele. The method is illustrated by analyzing a large candidate gene study of neural tube defects and an independent study of oral clefts, where the smallest adjusted p-values using the permutation procedure are approximately half those of the Bonferroni procedure. We conclude that permutation tests are more powerful for identifying disease-associated SNPs in candidate gene studies and are useful for analysis of triad studies. No claim to original US government works Annals of Human Genetics
© 2010 Blackwell Publishing Ltd/University College London.

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Year:  2010        PMID: 21108625      PMCID: PMC3117224          DOI: 10.1111/j.1469-1809.2010.00626.x

Source DB:  PubMed          Journal:  Ann Hum Genet        ISSN: 0003-4800            Impact factor:   1.670


  6 in total

1.  Simple formulas for gauging the potential impacts of population stratification bias.

Authors:  Wen-Chung Lee; Liang-Yi Wang
Journal:  Am J Epidemiol       Date:  2007-09-19       Impact factor: 4.897

2.  Genotype relative risks: methods for design and analysis of candidate-gene association studies.

Authors:  D J Schaid; S S Sommer
Journal:  Am J Hum Genet       Date:  1993-11       Impact factor: 11.025

3.  Testing reported associations of genetic risk factors for oral clefts in a large Irish study population.

Authors:  Tonia C Carter; Anne M Molloy; Faith Pangilinan; James F Troendle; Peadar N Kirke; Mary R Conley; David J A Orr; Michael Earley; Eamon McKiernan; Ena C Lynn; Anne Doyle; John M Scott; Lawrence C Brody; James L Mills
Journal:  Birth Defects Res A Clin Mol Teratol       Date:  2010-02

4.  Multiple testing with minimal assumptions.

Authors:  Peter H Westfall; James F Troendle
Journal:  Biom J       Date:  2008-10       Impact factor: 2.207

5.  Transmission test for linkage disequilibrium: the insulin gene region and insulin-dependent diabetes mellitus (IDDM).

Authors:  R S Spielman; R E McGinnis; W J Ewens
Journal:  Am J Hum Genet       Date:  1993-03       Impact factor: 11.025

6.  Rapid and accurate multiple testing correction and power estimation for millions of correlated markers.

Authors:  Buhm Han; Hyun Min Kang; Eleazar Eskin
Journal:  PLoS Genet       Date:  2009-04-17       Impact factor: 5.917

  6 in total
  2 in total

1.  Genotyping of a tri-allelic polymorphism by a novel melting curve assay in MTHFD1L: an association study of nonsyndromic Cleft in Ireland.

Authors:  Stefano Minguzzi; Anne M Molloy; Kirke Peadar; James Mills; John M Scott; James Troendle; Faith Pangilinan; Lawrence Brody; Anne Parle-McDermott
Journal:  BMC Med Genet       Date:  2012-04-20       Impact factor: 2.103

2.  Evaluation of common genetic variants in 82 candidate genes as risk factors for neural tube defects.

Authors:  Faith Pangilinan; Anne M Molloy; James L Mills; James F Troendle; Anne Parle-McDermott; Caroline Signore; Valerie B O'Leary; Peter Chines; Jessica M Seay; Kerry Geiler-Samerotte; Adam Mitchell; Julia E VanderMeer; Kristine M Krebs; Angelica Sanchez; Joshua Cornman-Homonoff; Nicole Stone; Mary Conley; Peadar N Kirke; Barry Shane; John M Scott; Lawrence C Brody
Journal:  BMC Med Genet       Date:  2012-08-02       Impact factor: 2.103

  2 in total

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