Literature DB >> 7607416

Guess LOD approach: sufficient conditions for robustness.

J A Williamson1, C I Amos.   

Abstract

Analysis of genetic linkage between a disease and a marker locus requires specifying a genetic model describing both the inheritance pattern and the gene frequencies of the marker and trait loci. Misspecification of the genetic model is likely for etiologically complex diseases. In previous work we have shown through analytic studies that misspecifying the genetic model for disease inheritance does not lead to excess false-positive evidence for genetic linkage provided the genetic marker alleles of all pedigree members are known, or can be inferred without bias from the data. Here, under various selection or ascertainment schemes we extend these previous results to situations in which the genetic model for the marker locus may be incorrect. We provide sufficient conditions for the asymptotic unbiased estimation of the recombination fraction under the null hypothesis of no linkage, and also conditions for the limiting distribution of the likelihood ratio test for no linkage to be chi-squared. Through simulation studies we document some situations under which asymptotic bias can result when the genetic model is misspecified. Among those situations under which an excess of false-positive evidence for genetic linkage can be generated, the most common is failure to provide accurate estimates of the marker allele frequencies. We show that in most cases false-positive evidence for genetic linkage is unlikely to result solely from the misspecification of the genetic model for disease or trait inheritance.

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Year:  1995        PMID: 7607416     DOI: 10.1002/gepi.1370120205

Source DB:  PubMed          Journal:  Genet Epidemiol        ISSN: 0741-0395            Impact factor:   2.135


  7 in total

1.  Ignoring linkage disequilibrium among tightly linked markers induces false-positive evidence of linkage for affected sib pair analysis.

Authors:  Qiqing Huang; Sanjay Shete; Christopher I Amos
Journal:  Am J Hum Genet       Date:  2004-10-18       Impact factor: 11.025

2.  A follow-up report of a genome search for affective disorder predisposition loci in the Old Order Amish.

Authors:  M C LaBuda; M Maldonado; D Marshall; K Otten; D S Gerhard
Journal:  Am J Hum Genet       Date:  1996-12       Impact factor: 11.025

3.  Linkage mapping in experimental crosses: the robustness of single-gene models.

Authors:  F A Wright; A Kong
Journal:  Genetics       Date:  1997-05       Impact factor: 4.562

4.  Estimation of effects of quantitative trait loci in large complex pedigrees.

Authors:  T H Meuwissen; M E Goddard
Journal:  Genetics       Date:  1997-05       Impact factor: 4.562

5.  Identification of rare variants from exome sequence in a large pedigree with autism.

Authors:  E E Marchani; N H Chapman; C Y K Cheung; K Ankenman; I B Stanaway; H H Coon; D Nickerson; R Bernier; Z Brkanac; E M Wijsman
Journal:  Hum Hered       Date:  2013-04-11       Impact factor: 0.444

6.  Age-related macular degeneration--a genome scan in extended families.

Authors:  Jacek Majewski; Dennis W Schultz; Richard G Weleber; Mitchell B Schain; Albert O Edwards; Tara C Matise; Ted S Acott; Jurg Ott; Michael L Klein
Journal:  Am J Hum Genet       Date:  2003-07-25       Impact factor: 11.025

7.  Examining the effect of linkage disequilibrium on multipoint linkage analysis.

Authors:  Qiqing Huang; Sanjay Shete; Michael Swartz; Christopher I Amos
Journal:  BMC Genet       Date:  2005-12-30       Impact factor: 2.797

  7 in total

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