Literature DB >> 2253867

Search for faster methods of fitting the regressive models to quantitative traits.

F M Demenais1, C Murigande, G E Bonney.   

Abstract

The regressive models describe familial patterns of dependence of quantitative measures by specifying regression relationships among a person's phenotype and genotype and the phenotypes and genotypes of antecedents. When the number of sibs in the pattern of dependence increases, as in the class D regressive model, computation of the likelihood becomes time consuming, since the Elston-Stewart algorithm cannot be used generally. On the other hand, the simpler class A regressive model, which imposes a restriction on the sib-sib correlation, may lead to inference of a spurious major gene, as already observed in some instances. A simulation study is performed to explore the robustness of class A model with respect to false inference of a major gene and to search for faster methods of computing the likelihood under class D model. The class A model is not robust against the presence of a sib-sib correlation exceeding that specified by the model, unless tests on transmission probabilities are performed carefully: false detection of a major gene is reduced from a number of 26-30 to between 0 and 4 data sets out of 30 replicates after testing both the Mendelian transmission and the absence of transmission of a major effect against the general transmission model. Among various approximations of the likelihood formulation of the class D model, approximations 6 and 8 are found to work appropriately in terms of both the estimation of all parameters and hypothesis testing, for each generating model. These approximations lessen the computer time by allowing use of the Elston-Stewart algorithm.

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Year:  1990        PMID: 2253867     DOI: 10.1002/gepi.1370070503

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


  9 in total

1.  Regressive logistic models for familial diseases: a formulation assuming an underlying liability model.

Authors:  F M Demenais
Journal:  Am J Hum Genet       Date:  1991-10       Impact factor: 11.025

2.  Numerical comparison between powers of maximum likelihood and analysis of variance methods for QTL detection in progeny test designs: the case of monogenic inheritance.

Authors:  P Le Roy; J M Elsen
Journal:  Theor Appl Genet       Date:  1995-01       Impact factor: 5.699

3.  Methods for multiple-marker mapping of quantitative trait loci in half-sib populations.

Authors:  S A Knott; J M Elsen; C S Haley
Journal:  Theor Appl Genet       Date:  1996-07       Impact factor: 5.699

4.  The finite polygenic mixed model: An alternative formulation for the mixed model of inheritance.

Authors:  R L Fernando; C Stricker; R C Elston
Journal:  Theor Appl Genet       Date:  1994-07       Impact factor: 5.699

5.  Detection of a major gene for heterocellular hereditary persistence of fetal hemoglobin after accounting for genetic modifiers.

Authors:  S L Thein; M Sampietro; K Rohde; J Rochette; D J Weatherall; G M Lathrop; F Demenais
Journal:  Am J Hum Genet       Date:  1994-02       Impact factor: 11.025

6.  The transmission probability model is useful to prevent false inference.

Authors:  F Demenais; M Martinez; N Andrieu
Journal:  Am J Hum Genet       Date:  1993-02       Impact factor: 11.025

7.  Influence of genotype-dependent effects of covariates on the outcome of segregation analysis of the body mass index.

Authors:  I B Borecki; G E Bonney; T Rice; C Bouchard; D C Rao
Journal:  Am J Hum Genet       Date:  1993-09       Impact factor: 11.025

8.  Segregation analysis indicates a major gene in the control of interleukine-5 production in humans infected with Schistosoma mansoni.

Authors:  V Rodrigues; L Abel; K Piper; A J Dessein
Journal:  Am J Hum Genet       Date:  1996-08       Impact factor: 11.025

9.  Evidence for the segregation of a major gene in human susceptibility/resistance to infection by Schistosoma mansoni.

Authors:  L Abel; F Demenais; A Prata; A E Souza; A Dessein
Journal:  Am J Hum Genet       Date:  1991-05       Impact factor: 11.025

  9 in total

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