Literature DB >> 11246457

Power of variance component linkage analysis to detect quantitative trait loci.

J T Williams1, J Blangero.   

Abstract

Expressions are derived for the sample size required to achieve a given power in variance component linkage analysis of a quantitative trait in unascertained samples. For simplicity an additive model, comprising effects due to a single QTL, residual additive genetic factors, and individual-specific random environmental variation, is considered. Equations are given relating sample size to trait heritability for sibpairs, sib trios, nuclear families having two and three sibs, and arbitrary relative pairs. The effects of nonzero residual additive genetic variance and parental information are discussed, and a scale relationship for sample sizes with sibships and nuclear families is derived. For larger sampling structures such as extended pedigrees the inheritance space is randomly sampled and the relevant equations are solved numerically. Comparative power curves are presented for sibships of size 2-4 and for an extended pedigree of 48 individuals. Simulation results for sibpairs confirm the validity of the theoretical results.

Mesh:

Year:  1999        PMID: 11246457     DOI: 10.1017/S0003480099007848

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


  41 in total

1.  Testing for genetic linkage in families by a variance-components approach in the presence of genomic imprinting.

Authors:  Sanjay Shete; Christopher I Amos
Journal:  Am J Hum Genet       Date:  2002-02-08       Impact factor: 11.025

2.  Large upward bias in estimation of locus-specific effects from genomewide scans.

Authors:  H H Göring; J D Terwilliger; J Blangero
Journal:  Am J Hum Genet       Date:  2001-10-09       Impact factor: 11.025

3.  Theoretical and empirical power of regression and maximum-likelihood methods to map quantitative trait loci in general pedigrees.

Authors:  Xijiang Yu; Sara A Knott; Peter M Visscher
Journal:  Am J Hum Genet       Date:  2004-05-19       Impact factor: 11.025

4.  Guidelines for genotyping in genomewide linkage studies: single-nucleotide-polymorphism maps versus microsatellite maps.

Authors:  David M Evans; Lon R Cardon
Journal:  Am J Hum Genet       Date:  2004-08-13       Impact factor: 11.025

5.  Mapping quantitative traits with random and with ascertained sibships.

Authors:  Jie Peng; D Siegmund
Journal:  Proc Natl Acad Sci U S A       Date:  2004-04-14       Impact factor: 11.205

6.  A genomewide search using an original pairwise sampling approach for large genealogies identifies a new locus for total and low-density lipoprotein cholesterol in two genetically differentiated isolates of Sardinia.

Authors:  Mario Falchi; Paola Forabosco; Evelina Mocci; Cesare Cappio Borlino; Andrea Picciau; Emanuela Virdis; Ivana Persico; Debora Parracciani; Andrea Angius; Mario Pirastu
Journal:  Am J Hum Genet       Date:  2004-10-11       Impact factor: 11.025

Review 7.  Genomic similarity and kernel methods I: advancements by building on mathematical and statistical foundations.

Authors:  Daniel J Schaid
Journal:  Hum Hered       Date:  2010-07-03       Impact factor: 0.444

8.  Contribution of Inbred Singletons to Variance Component Estimation of Heritability and Linkage.

Authors:  Lucy Blondell; August Blackburn; Mark Z Kos; John Blangero; Harald H H Göring
Journal:  Hum Hered       Date:  2018-11-02       Impact factor: 0.444

9.  Shared genetic factors influence risk for bipolar disorder and alcohol use disorders.

Authors:  N Carmiol; J M Peralta; L Almasy; J Contreras; A Pacheco; M A Escamilla; E E M Knowles; H Raventós; D C Glahn
Journal:  Eur Psychiatry       Date:  2013-12-08       Impact factor: 5.361

Review 10.  Human QTL linkage mapping.

Authors:  Laura Almasy; John Blangero
Journal:  Genetica       Date:  2008-07-31       Impact factor: 1.082

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