Genetic parameter estimates for racing time by restricted maximum likelihood in the Thoroughbred horse of Japan

1995 ◽  
Vol 112 (1-6) ◽  
pp. 146-150 ◽  
Author(s):  
H. Oki ◽  
Y. Sasaki ◽  
R.L. Willham
2019 ◽  
Vol 11 (11) ◽  
pp. 303
Author(s):  
Hugo Zeni Neto ◽  
Renato Frederico dos Santos ◽  
Luiz Gustavo da Mata Borsuk ◽  
Henrique Sanches Angeli ◽  
Guilherme Souza Berton

Most sugarcane breeding programs tend to evaluate low heritability characteristics during the initial stages of genotype selection. Thus, family selection has been recently preferred. In this context, the aim of the present study was to select the best family among 78 sugarcane families, as well as estimate genetic values through the mixed models of restricted-maximum likelihood and best non-bias predictor (REML/BLUP) methodology, originating from the República Brasil 2005 (RB05) series. This strategy was deemed efficient, and 34 to 38 families were chosen from four evaluated characteristics underexplored by genetic researchers such as total plot mass (MTT), mean mass of one tiller in the plot (M1C), stature (EST), and mean number of canes per square meter (NCM). The family increments ranging from 6.02 to 82.11%, in the next genetic culture improvement program selection phases.


Methodology ◽  
2005 ◽  
Vol 1 (2) ◽  
pp. 81-85 ◽  
Author(s):  
Stefan C. Schmukle ◽  
Jochen Hardt

Abstract. Incremental fit indices (IFIs) are regularly used when assessing the fit of structural equation models. IFIs are based on the comparison of the fit of a target model with that of a null model. For maximum-likelihood estimation, IFIs are usually computed by using the χ2 statistics of the maximum-likelihood fitting function (ML-χ2). However, LISREL recently changed the computation of IFIs. Since version 8.52, IFIs reported by LISREL are based on the χ2 statistics of the reweighted least squares fitting function (RLS-χ2). Although both functions lead to the same maximum-likelihood parameter estimates, the two χ2 statistics reach different values. Because these differences are especially large for null models, IFIs are affected in particular. Consequently, RLS-χ2 based IFIs in combination with conventional cut-off values explored for ML-χ2 based IFIs may lead to a wrong acceptance of models. We demonstrate this point by a confirmatory factor analysis in a sample of 2449 subjects.


Genetics ◽  
1996 ◽  
Vol 143 (4) ◽  
pp. 1819-1829 ◽  
Author(s):  
G Thaller ◽  
L Dempfle ◽  
I Hoeschele

Abstract Maximum likelihood methodology was applied to determine the mode of inheritance of rare binary traits with data structures typical for swine populations. The genetic models considered included a monogenic, a digenic, a polygenic, and three mixed polygenic and major gene models. The main emphasis was on the detection of major genes acting on a polygenic background. Deterministic algorithms were employed to integrate and maximize likelihoods. A simulation study was conducted to evaluate model selection and parameter estimation. Three designs were simulated that differed in the number of sires/number of dams within sires (10/10, 30/30, 100/30). Major gene effects of at least one SD of the liability were detected with satisfactory power under the mixed model of inheritance, except for the smallest design. Parameter estimates were empirically unbiased with acceptable standard errors, except for the smallest design, and allowed to distinguish clearly between the genetic models. Distributions of the likelihood ratio statistic were evaluated empirically, because asymptotic theory did not hold. For each simulation model, the Average Information Criterion was computed for all models of analysis. The model with the smallest value was chosen as the best model and was equal to the true model in almost every case studied.


Genetics ◽  
1996 ◽  
Vol 143 (3) ◽  
pp. 1409-1416 ◽  
Author(s):  
Kenneth R Koots ◽  
John P Gibson

Abstract A data set of 1572 heritability estimates and 1015 pairs of genetic and phenotypic correlation estimates, constructed from a survey of published beef cattle genetic parameter estimates, provided a rare opportunity to study realized sampling variances of genetic parameter estimates. The distribution of both heritability estimates and genetic correlation estimates, when plotted against estimated accuracy, was consistent with random error variance being some three times the sampling variance predicted from standard formulae. This result was consistent with the observation that the variance of estimates of heritabilities and genetic correlations between populations were about four times the predicted sampling variance, suggesting few real differences in genetic parameters between populations. Except where there was a strong biological or statistical expectation of a difference, there was little evidence for differences between genetic and phenotypic correlations for most trait combinations or for differences in genetic correlations between populations. These results suggest that, even for controlled populations, estimating genetic parameters specific to a given population is less useful than commonly believed. A serendipitous discovery was that, in the standard formula for theoretical standard error of a genetic correlation estimate, the heritabilities refer to the estimated values and not, as seems generally assumed, the true population values.


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