Genetic variability of milk components based on mid-infrared spectral data.Soyeurt, Hélène ; ; Gengler, Nicolas ![]() in Journal of Dairy Science (2010), 93(4), 1722-1728 The aim of this study was to estimate the genetic parameters of the mid-infrared (MIR) milk spectrum represented by 1,060 data points per sample. The dimensionality of traits was reduced by principal ... [more ▼] The aim of this study was to estimate the genetic parameters of the mid-infrared (MIR) milk spectrum represented by 1,060 data points per sample. The dimensionality of traits was reduced by principal components analysis. Therefore, 46 principal components describing 99.03% of the phenotypic variability were used to create 46 new traits. Variance components were estimated using canonical transformation. Heritability ranged from 0 to 0.35. Twenty-five out of 46 studied traits showed a permanent environment variance greater than genetic variance. Eight traits showed heritability greater than 0.10. Variances of original spectral traits were obtained by back transformation. Heritabilities for each spectral data points ranged from 0.003 to 0.42. In particular, 3 MIR regions showing moderate to high heritability estimates were of potential genetic interest. Heritabilities for specific wave numbers, linked with common milk traits (e.g., lipids, lactose), were similar to those estimated for these traits. This research confirms the genetic variability of the MIR milk spectrum and, therefore, the genetic variation of milk components. The objective of this study was to better understand the genetics of milk composition and, maybe in the future, to select animals to improve milk quality. [less ▲] Detailed reference viewed: 26 (5 ULg)![]() BLUPF90 and related programs (BGF90); ; et al in Proceedings from the 7th World Congress on Genetics Applied to Livestock Production (2002) Detailed reference viewed: 148 (1 ULg)![]() On the value of incorporating dominance effects in genetic evaluation of dairy cattle.Druet, Tom ; ; et alin Proceedings of the 7th World Congress on Genetics Applied to LivestockProduction, Montpellier, France, August, 2002. Session 1 (2002) Detailed reference viewed: 15 (2 ULg)![]() Estimation of genetic covariances with Method RDruet, Tom ; ; et alin Journal of Animal Science (2001), 79(3), 605-615 Method R is a simple and computationally inexpensive method for estimating (co)variances. The objective of the study was to investigate properties of Method R for estimation of (co)variance components ... [more ▼] Method R is a simple and computationally inexpensive method for estimating (co)variances. The objective of the study was to investigate properties of Method R for estimation of (co)variance components with emphasis on covariance estimation. Theoretical Method R formulas were developed for simplified single-variate and bivariate models. In single-trait models, the curve of the regression of Method R was continuous and monotonic and its slope depended on the amount of information on each animal and on the variance ratio. The curve became steeper as the number of records per animal decreased. For covariance, the curve of the regression was monotonic but not continuous. However, a regression coefficient of 1 still corresponded to the correct covariance. Similar curves were observed in analyses of simulated data sets. Because of the observed discontinuity, algorithms implementing Method R that require a continuous regression curve would not work in models with: covariances. An alternative algorithm was based on a transformation matrix obtained by multiplying a matrix of numerators with the inverse of a matrix of denominators of the regression factors. Such an algorithm converged reliably for all models tested. Method R can be modified to estimate covariances in models too large for other methods. [less ▲] Detailed reference viewed: 57 (27 ULg) Estimation of additive and nonadditive genetic variances in Hereford, Gelbvieh, and Charolais by Method R.; ; et al in Journal of Animal Science (2001), 79(12), 2997-3001 Parameters for direct and maternal dominance were estimated in models that included non-additive genetic effects. The analyses used weaning weight records adjusted for age of dam from populations of ... [more ▼] Parameters for direct and maternal dominance were estimated in models that included non-additive genetic effects. The analyses used weaning weight records adjusted for age of dam from populations of Canadian Hereford (n = 467,814), American Gelbvieh (n = 501,552), and American Charolais (n = 314,552). Method R estimates of direct additive genetic, maternal additive genetic, permanent maternal environment, direct dominance, and maternal dominance variances as a proportion of the total variance were 23, 12, 13, 19, and 14% in Hereford; 27, 7, 10, 18, and 2% in Gelbvieh; and 34, 15, 15, 23, and 2% in Charolais. The correlations between direct and maternal additive genetic effects were -0.30, -0.23, and -0.47 in Hereford, Gelbvieh, and Charolais, respectively. The correlations between direct and maternal dominance were -0.38, -0.02, and -0.04 in Hereford, Gelbvieh, and Charolais, respectively. Estimates of inbreeding depression were -0.20, -0.18, and -0.13 kg per 1% of inbreeding for Hereford, Gelbvieh, and Charolais, respectively. Estimates of the maternal inbreeding depression were -0.01, -0.02, and -0.02 kg, respectively. The high ratio of direct dominance to additive genetic variances provided some evidence that direct dominance effects should be considered in beef cattle evaluation. However, maternal dominance effects seemed to be important only for Hereford cattle. [less ▲] Detailed reference viewed: 5 (0 ULg) Estimation of non-additive genetic variances and maternal inbreeding depression in Canadian Herefords; Druet, Tom ; et alin Abstracts from the 2000 ADSA/ASAS joint annual meeting (2000) Detailed reference viewed: 8 (1 ULg) Covariance estimation with Method-RDruet, Tom ; ; et alin Abstracts from the 2000 ADSA/ASAS joint annual meeting (2000) Detailed reference viewed: 5 (1 ULg)![]() Estimation of (co)variance function coefficients for test day yield with a expectation-maximization restricted maximum likelihood algorithmGengler, Nicolas ; ; et alin Journal of Dairy Science (1999), 82(8), 18491-184923 Detailed reference viewed: 11 (2 ULg) Studies on the value of incorporating the effect of dominance in genetic evaluations of dairy cattle, beef cattle and swine; ; et al in Biotechnologie, Agronomie, Société et Environnement = Biotechnology, Agronomy, Society and Environment [=BASE] (1998), 4 Nonadditive genetic effects are currently ignored in national genetic evaluations of farm animals because of ignorance of the level of dominance variance for traits of interest and the difficult ... [more ▼] Nonadditive genetic effects are currently ignored in national genetic evaluations of farm animals because of ignorance of the level of dominance variance for traits of interest and the difficult computational problems involved. Potential gains from including the effects of dominance in genetic evaluations include “purification” of additive values and availability of predictions of specific combining abilities for each pair of prospective parents. This study focused on making evaluation with dominance effects feasible computationally and on ascertaining benefits of such an evaluation for dairy cattle, beef cattle, and swine. Using iteration on data, computing costs for evaluation with dominance effects included costs could be less than twice expensive as with only an additive model. With Method Â, variance components could be estimated for problems involving up to 10 millions equations. Dominance effects accounted for up to 10% of phenotypic variance; estimates were larger for growth traits. As a percentage of additive variance, the estimate of dominance variance reached 78% for 21-d litter weight of swine and 47% for post weaning weight of beef cattle. When dominance effects are ignored, additive evaluations are “contaminated”; effects are greatest for evaluations of dams in a single large family. These changes in ranking were important for dairy cattle, especially for dams of full-sibs, but were less important for swine. Specific combining abilities cannot be included in sire evaluations and need to be computed separately for each set of parents. The predictions of specific combining abilities could be used in computerized mating programs via the Internet. Gains from including the dominance effect in genetic evaluations would be moderate but would outweigh expenditures to produce those evaluations. [less ▲] Detailed reference viewed: 26 (8 ULg)![]() Estimation of dominance variance in purebred Yorkshire swine; ; et al in Journal of Animal Science (1998), 76(2), 448-451 We used 179,485 Yorkshire reproductive and 239,354 Yorkshire growth records to estimate additive and dominance variances by Method Fraktur R. Estimates were obtained for number born alive (NBA), 21-d ... [more ▼] We used 179,485 Yorkshire reproductive and 239,354 Yorkshire growth records to estimate additive and dominance variances by Method Fraktur R. Estimates were obtained for number born alive (NBA), 21-d litter weight (LWT), days to 104.5 kg (DAYS), and backfat at 104.5 kg (BF). The single-trait models for NBA and LWT included the fixed effects of contemporary group and regression on inbreeding percentage and the random effects mate within contemporary group, animal permanent environment, animal additive, and parental dominance. The single-trait models for DAYS and BF included the fixed effects of contemporary group, sex, and regression on inbreeding percentage and the random effects litter of birth, dam permanent environment, animal additive, and parental dominance. Final estimates were obtained from six samples for each trait. Regression coefficients for 10% inbreeding were found to be -.23 for NBA, -.52 kg for LWT, 2.1 d for DAYS, and 0 mm for BF. Estimates of additive and dominance variances expressed as a percentage of phenotypic variances were, respectively, 8.8 +/- .5 and 2.2 +/- .7 for NBA, 8.1 +/- 1.1 and 6.3 +/- .9 for LWT, 33.2 +/- .4 and 10.3 +/- 1.5 for DAYS, and 43.6 +/- .9 and 4.8 +/- .7 for BF. The ratio of dominance to additive variances ranged from .78 to .11. [less ▲] Detailed reference viewed: 8 (0 ULg)![]() Estimation of the dominance variance for postweaning gain in the US Limousin populationGengler, Nicolas ; ; et alin Journal of Animal Science (1998), 76(10), 2515-2520 The objective of this study was to estimate the dominance variance for postweaning gain in Limousin cattle. Data included 215,326 records of postweaning gain from 205 to 365 d, provided by the North ... [more ▼] The objective of this study was to estimate the dominance variance for postweaning gain in Limousin cattle. Data included 215,326 records of postweaning gain from 205 to 365 d, provided by the North American Limousin Foundation. Parental dominance subclasses were formed and related using the method of Hoeschele and VanRaden. Variance components were estimated using Method R based on six samples of 50%. Fixed effects in the model included contemporary group apd covariates for inbreeding and breed composition (percentage Limousin). Heterozygosity was negatively correlated with breed composition (< -.99) and was therefore not included in the model. Two types of contemporary groups used as original groups from the National Cattle Evaluation were partially based on breed composition. Original contemporary groups that were too homogeneous for breed composition were replaced by herd-year-sex classes. Two models were used with the two data sets. Model 1 contained the fixed effects described above and an additive genetic effect. Model 2 Included a dominance effect in addition to the effects contained in Model 1. In total, four combinations of contemporary group x model were used. Dominance variance was computed as being four times the estimated parental subclass variance. Estimates for inbreeding depression and breed composition (percentage Limousin) were all small and not greatly affected by inclusion of dominance effects or changes in contemporary groups. Estimates of the additive variance (expressed as percentage of the phenotypic variance) were only slightly affected, with values between 20 and 21%. Dominance estimates were highly affected when passing from original (10%) and to alternative contemporary groups (18%). Such large values may indicate that dominance is important for postweaning gain. Results showed the advantage of an individual dominance approach based on sire-dam combinations; therefore, expected gains through the use of specific combination ability as a part of the mating selection criteria for growth might be high. [less ▲] Detailed reference viewed: 8 (2 ULg)![]() Influence of dominance relationships on the estimation of dominance variance with sire-dam subclass effectsGengler, Nicolas ; ; et alin Journal of Animal Science (1997), 75(11), 2885-2891 Two data sets from the USDA Livestock and Range Research Laboratory mere analyzed to study dominance variance and the influence of dominance relationships. The first consisted of 4,155 birth weight (3,884 ... [more ▼] Two data sets from the USDA Livestock and Range Research Laboratory mere analyzed to study dominance variance and the influence of dominance relationships. The first consisted of 4,155 birth weight (3,884 weaning weight) records of inbred USDA Line 1 Herefords. The second consisted of 8,065 birth weight (7,380 weaning weight) records from a line-cross experiment with five lines. Two models were used. Both included fixed effects of year-sex of calf and age of dam, and covariates for calving date, inbreeding of animal, and inbreeding of dam. For the second set, additional covariates were line composition and heterozygosity coefficients. Random effects were direct and maternal additive genetic, maternal permanent environment, sire-dam subclass, and residual. Model 1 considered sire-dam subclasses unrelated. Model 2 related sire-dam subclasses with a parental dominance relationship matrix. Variance components were estimated using REML. Differences between estimates with Model 1 and 2 were unimportant except for dominance variance. For the first data set, estimates with Model 2 of relative genetic direct and maternal variances, direct-maternal correlation, permanent environment, and dominance variances for birth weight were .35, .13, -.02, .03, and .25, respectively, and they were .39, .11, .04, .06 and .14 for the second data set. For weaning weight, the first data set estimates were .20, .15, -.37, .19, and .11, respectively, and they were .16, .20, -.07, .18, and .18 for the second data set. Changes, decreases and increases, in estimates of dominance variances may be due to increased information from relationships and family types other than full-sibs. The assumption of unrelated sire-dam subclasses might not be appropriate for estimation of dominance variance in populations with many dominance relationships among siredam classes. [less ▲] Detailed reference viewed: 6 (0 ULg)![]() Relationships among estimates of inbreeding depression, dominance and additive variance for linear traits in Holsteins; ; Gengler, Nicolas ![]() in Genetics, Selection, Evolution [=GSE] (1997), 29(4), 319-326 Estimates of dominance and additive variances were obtained for 14 linear traits. The data included 600 678 first parity records on 14 linear traits in Holsteins. The model included management groups, age ... [more ▼] Estimates of dominance and additive variances were obtained for 14 linear traits. The data included 600 678 first parity records on 14 linear traits in Holsteins. The model included management groups, age at calving, additive and dominance effects, and regression on inbreeding percentage. The estimate of the dominance variance was 9.8% of the phenotypic variance for body depth: 8.0% for strength, 6.9% for stature, and was less than 5% for the remaining traits. The additive variance ranged from 12.2% for foot angle to 45.3% for stature. No clear relationship was found between the estimates of dominance and additive variance. larger negative estimates of the inbreeding depression were associated with higher estimates of the dominance variance. [less ▲] Detailed reference viewed: 35 (1 ULg)![]() Approximation of reliability for multiple-trait animal models with missing data by canonical transformationGengler, Nicolas ; in Journal of Dairy Science (1996), 79(2), 317-328 An algorithm for approximation of reliability for multiple traits by multiple diagonalization was modified to support missing data by weighting transformed contributions of records based on the pattern of ... [more ▼] An algorithm for approximation of reliability for multiple traits by multiple diagonalization was modified to support missing data by weighting transformed contributions of records based on the pattern of missing data. The accuracy of approximation was assessed with simulated and field data by comparing approximate reliabilities with those from direct inversion. Simulated data had several levels of missing data and covariances between traits; correlations were close to those for linear type traits of dairy cattle. Field data were 1) dairy records for milk, fat, and protein yields with 26% of the observations for fat and protein removed and 2) beef records for birth weight, weaning weight, and mean gain after weaning with 43% of observations missing. These files also contained empty fixed effect classes. The algorithm worked best for simulated data, and, when covariances between traits decreased, proportion of missing traits decreased and the number of empty fixed classes decreased. For dairy data, improvement over single-trait reliability occurred only for traits with missing data; for beef data, little or no improvement occurred. The method is useful with multiple diagonalization if the proportion of missing records or number of empty fixed effect classes or covariances between traits is moderate. [less ▲] Detailed reference viewed: 12 (0 ULg) |
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