Literature DB >> 7668300

Model-free linkage analysis using likelihoods.

D Curtis1, P C Sham.   

Abstract

Misspecification of transmission model parameters can produce artifactually negative lod scores at small recombination fractions and in multipoint analysis. To avoid this problem, we have tried to devise a test that aims to detect a genetic effect at a particular locus, rather than attempting to estimate the map position of a locus with specified effect. Maximizing likelihoods over transmission model parameters, as well as linkage parameters, can produce seriously biased parameter estimates and so yield tests that lack power for the detection of linkage. However, constraining the transmission model parameters to produce the correct population prevalence largely avoids this problem. For computational convenience, we recommend that the likelihoods under linkage and non-linkage are independently maximized over a limited set of transmission models, ranging from Mendelian dominant to null effect and from null effect to Mendelian recessive. In order to test for a genetic effect at a given map position, the likelihood under linkage is maximized over admixture, the proportion of families linked. Application to simulated data for a wide range of transmission models in both affected sib pairs and pedigrees demonstrates that the new method is well behaved under the null hypothesis and provides a powerful test for linkage when it is present. This test requires no specification of transmission model parameters, apart from an approximate estimate of the population prevalence. It can be applied equally to sib pairs and pedigrees, and, since it does not diminish the lod score at test positions very close to a marker, it is suitable for application to multipoint data.

Mesh:

Year:  1995        PMID: 7668300      PMCID: PMC1801268     

Source DB:  PubMed          Journal:  Am J Hum Genet        ISSN: 0002-9297            Impact factor:   11.025


  18 in total

1.  Sequential tests for the detection of linkage.

Authors:  N E MORTON
Journal:  Am J Hum Genet       Date:  1955-09       Impact factor: 11.025

2.  Model misspecification and multipoint linkage analysis.

Authors:  N Risch; L Giuffra
Journal:  Hum Hered       Date:  1992       Impact factor: 0.444

3.  A multisample bootstrap approach to the estimation of maximized-over-models lod score distributions.

Authors:  J D Terwilliger; J Ott
Journal:  Cytogenet Cell Genet       Date:  1992

4.  Distribution of the admixture test for the detection of linkage under heterogeneity.

Authors:  J J Faraway
Journal:  Genet Epidemiol       Date:  1993       Impact factor: 2.135

5.  Asymptotic properties of affected-sib-pair linkage analysis.

Authors:  P Holmans
Journal:  Am J Hum Genet       Date:  1993-02       Impact factor: 11.025

6.  Two-locus models of disease: comparison of likelihood and nonparametric linkage methods.

Authors:  L R Goldin; D E Weeks
Journal:  Am J Hum Genet       Date:  1993-10       Impact factor: 11.025

7.  Linkage detection by the Affected-Pedigree-Member method: what is really tested?

Authors:  M C Babron; M Martinez; C Bonaïti-Pellié; F Clerget-Darpoux
Journal:  Genet Epidemiol       Date:  1993       Impact factor: 2.135

8.  Joint linkage of multiple loci for a complex disorder.

Authors:  C J MacLean; P C Sham; K S Kendler
Journal:  Am J Hum Genet       Date:  1993-08       Impact factor: 11.025

9.  Using risk calculation to implement an extended relative pair analysis.

Authors:  D Curtis; P C Sham
Journal:  Ann Hum Genet       Date:  1994-05       Impact factor: 1.670

10.  The apolipoprotein E/CI/CII gene cluster and late-onset Alzheimer disease.

Authors:  C E Yu; H Payami; J M Olson; M Boehnke; E M Wijsman; H T Orr; W A Kukull; K A Goddard; E Nemens; J A White
Journal:  Am J Hum Genet       Date:  1994-04       Impact factor: 11.025

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  19 in total

1.  Power comparison of parametric and nonparametric linkage tests in small pedigrees.

Authors:  P C Sham; M W Lin; J H Zhao; D Curtis
Journal:  Am J Hum Genet       Date:  2000-04-11       Impact factor: 11.025

Review 2.  Linkage analysis in heterogeneous and complex traits.

Authors:  J Ott; A Bhat
Journal:  Eur Child Adolesc Psychiatry       Date:  1999       Impact factor: 4.785

3.  Genomewide genetic linkage analysis confirms the presence of susceptibility loci for schizophrenia, on chromosomes 1q32.2, 5q33.2, and 8p21-22 and provides support for linkage to schizophrenia, on chromosomes 11q23.3-24 and 20q12.1-11.23.

Authors:  H M Gurling; G Kalsi; J Brynjolfson; T Sigmundsson; R Sherrington; B S Mankoo; T Read; P Murphy; E Blaveri; A McQuillin; H Petursson; D Curtis
Journal:  Am J Hum Genet       Date:  2001-03       Impact factor: 11.025

4.  A second-generation genomewide screen for asthma-susceptibility alleles in a founder population.

Authors:  C Ober; A Tsalenko; R Parry; N J Cox
Journal:  Am J Hum Genet       Date:  2000-10-05       Impact factor: 11.025

5.  Linkage of tuberculosis to chromosome 2q35 loci, including NRAMP1, in a large aboriginal Canadian family.

Authors:  C M Greenwood; T M Fujiwara; L J Boothroyd; M A Miller; D Frappier; E A Fanning; E Schurr; K Morgan
Journal:  Am J Hum Genet       Date:  2000-07-05       Impact factor: 11.025

6.  Genomewide linkage scan for opioid dependence and related traits.

Authors:  Joel Gelernter; Carolien Panhuysen; Marsha Wilcox; Victor Hesselbrock; Bruce Rounsaville; James Poling; Roger Weiss; Susan Sonne; Hongyu Zhao; Lindsay Farrer; Henry R Kranzler
Journal:  Am J Hum Genet       Date:  2006-03-16       Impact factor: 11.025

7.  Affecteds-only linkage methods are not a panacea.

Authors:  D A Greenberg; S E Hodge; V J Vieland; M A Spence
Journal:  Am J Hum Genet       Date:  1996-04       Impact factor: 11.025

8.  Genome scanning for linkage: an overview.

Authors:  A S Whittemore
Journal:  Am J Hum Genet       Date:  1996-09       Impact factor: 11.025

9.  The problem of ascertainment for linkage analysis.

Authors:  V J Vieland; S E Hodge
Journal:  Am J Hum Genet       Date:  1996-05       Impact factor: 11.025

10.  Identification of genetic loci for basal cell nevus syndrome and inflammatory bowel disease in a single large pedigree.

Authors:  Carolien I Panhuysen; Amir Karban; Alisa Knodle Manning; Theodore M Bayless; Richard H Duerr; Joan E Bailey-Wilson; Ervin H Epstein; Steven R Brant
Journal:  Hum Genet       Date:  2006-05-30       Impact factor: 4.132

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