scholarly journals Changes in Allele Frequencies When Different Genomic Coancestry Matrices Are Used for Maintaining Genetic Diversity

Genes ◽  
2021 ◽  
Vol 12 (5) ◽  
pp. 673
Author(s):  
Elisabeth Morales-González ◽  
Jesús Fernández ◽  
Ricardo Pong-Wong ◽  
Miguel Ángel Toro ◽  
Beatriz Villanueva

A main objective in conservation programs is to maintain genetic variability. This can be achieved using the Optimal Contributions (OC) method that optimizes the contributions of candidates to the next generation by minimizing the global coancestry. However, it has been argued that maintaining allele frequencies is also important. Different genomic coancestry matrices can be used on OC and the choice of the matrix will have an impact not only on the genetic variability maintained, but also on the change in allele frequencies. The objective of this study was to evaluate, through stochastic simulations, the genetic variability maintained and the trajectory of allele frequencies when using two different genomic coancestry matrices in OC to minimize the loss of diversity: (i) the matrix based on deviations of the observed number of alleles shared between two individuals from the expected numbers under Hardy–Weinberg equilibrium (θLH); and (ii) the matrix based on VanRaden’s genomic relationship matrix (θVR). The results indicate that the use of θLH resulted in a higher genetic variability than the use of θVR. However, the use of θVR maintained allele frequencies closer to those in the base population than the use of θLH.

2017 ◽  
Author(s):  
Yvonne C.J. Wientjes ◽  
Piter Bijma ◽  
Jérémie Vandenplas ◽  
Mario P.L. Calus

ABSTRACTDifferent methods are available to calculate multi-population genomic relationship matrices. Since those matrices differ in base population, it is anticipated that the method used to calculate the genomic relationship matrix affect the estimate of genetic variances, covariances and correlations. The aim of this paper is to define a multi-population genomic relationship matrix to estimate current genetic variances within and genetic correlations between populations. The genomic relationship matrix containing two populations consists of four blocks, one block for population 1, one block for population 2, and two blocks for relationships between the populations. It is known, based on literature, that current genetic variances are estimated when the current population is used as base population of the relationship matrix. In this paper, we theoretically derived the properties of the genomic relationship matrix to estimate genetic correlations and validated it using simulations. When the scaling factors of the genomic relationship matrix fulfill the property , the genetic correlation is estimated even though estimated variance components are not necessarily related to the current population. When this property is not met, the correlation based on estimated variance components should be multiplied by to rescale the genetic correlation. In this study we present a genomic relationship matrix which directly results in current genetic variances as well as genetic correlations between populations.


2019 ◽  
Vol 51 (1) ◽  
Author(s):  
Pascal Duenk ◽  
Mario P. L. Calus ◽  
Yvonne C. J. Wientjes ◽  
Vivian P. Breen ◽  
John M. Henshall ◽  
...  

Following publication of original article [1], we noticed that there was an error: Eq. (3) on page 5 is the genomic relationship matrix that


2018 ◽  
Vol 53 (6) ◽  
pp. 717-726 ◽  
Author(s):  
Michel Marques Farah ◽  
Marina Rufino Salinas Fortes ◽  
Matthew Kelly ◽  
Laercio Ribeiro Porto-Neto ◽  
Camila Tangari Meira ◽  
...  

Abstract: The objective of this work was to evaluate the effects of genomic information on the genetic evaluation of hip height in Brahman cattle using different matrices built from genomic and pedigree data. Hip height measurements from 1,695 animals, genotyped with high-density SNP chip or imputed from 50 K high-density SNP chip, were used. The numerator relationship matrix (NRM) was compared with the H matrix, which incorporated the NRM and genomic relationship (G) matrix simultaneously. The genotypes were used to estimate three versions of G: observed allele frequency (HGOF), average minor allele frequency (HGMF), and frequency of 0.5 for all markers (HG50). For matrix comparisons, animal data were either used in full or divided into calibration (80% older animals) and validation (20% younger animals) datasets. The accuracy values for the NRM, HGOF, and HG50 were 0.776, 0.813, and 0.594, respectively. The NRM and HGOF showed similar minor variances for diagonal and off-diagonal elements, as well as for estimated breeding values. The use of genomic information resulted in relationship estimates similar to those obtained based on pedigree; however, HGOF is the best option for estimating the genomic relationship matrix and results in a higher prediction accuracy. The ranking of the top 20% animals was very similar for all matrices, but the ranking within them varies depending on the method used.


2020 ◽  
Vol 10 (6) ◽  
pp. 2069-2078 ◽  
Author(s):  
Christos Palaiokostas ◽  
Shannon M. Clarke ◽  
Henrik Jeuthe ◽  
Rudiger Brauning ◽  
Timothy P. Bilton ◽  
...  

Arctic charr (Salvelinus alpinus) is a species of high economic value for the aquaculture industry, and of high ecological value due to its Holarctic distribution in both marine and freshwater environments. Novel genome sequencing approaches enable the study of population and quantitative genetic parameters even on species with limited or no prior genomic resources. Low coverage genotyping by sequencing (GBS) was applied in a selected strain of Arctic charr in Sweden originating from a landlocked freshwater population. For the needs of the current study, animals from year classes 2013 (171 animals, parental population) and 2017 (759 animals; 13 full sib families) were used as a template for identifying genome wide single nucleotide polymorphisms (SNPs). GBS libraries were constructed using the PstI and MspI restriction enzymes. Approximately 14.5K SNPs passed quality control and were used for estimating a genomic relationship matrix. Thereafter a wide range of analyses were conducted in order to gain insights regarding genetic diversity and investigate the efficiency of the genomic information for parentage assignment and breeding value estimation. Heterozygosity estimates for both year classes suggested a slight excess of heterozygotes. Furthermore, FST estimates among the families of year class 2017 ranged between 0.009 – 0.066. Principal components analysis (PCA) and discriminant analysis of principal components (DAPC) were applied aiming to identify the existence of genetic clusters among the studied population. Results obtained were in accordance with pedigree records allowing the identification of individual families. Additionally, DNA parentage verification was performed, with results in accordance with the pedigree records with the exception of a putative dam where full sib genotypes suggested a potential recording error. Breeding value estimation for juvenile growth through the usage of the estimated genomic relationship matrix clearly outperformed the pedigree equivalent in terms of prediction accuracy (0.51 opposed to 0.31). Overall, low coverage GBS has proven to be a cost-effective genotyping platform that is expected to boost the selection efficiency of the Arctic charr breeding program.


Genetics ◽  
2020 ◽  
Vol 216 (3) ◽  
pp. 651-669
Author(s):  
Yong Jiang ◽  
Jochen C. Reif

The genomic relationship matrix plays a key role in the analysis of genetic diversity, genomic prediction, and genome-wide association studies. The epistatic genomic relationship matrix is a natural generalization of the classic genomic relationship matrix in the sense that it implicitly models the epistatic effects among all markers. Calculating the exact form of the epistatic relationship matrix requires high computational load, and is hence not feasible when the number of markers is large, or when high-degree of epistasis is in consideration. Currently, many studies use the Hadamard product of the classic genomic relationship matrix as an approximation. However, the quality of the approximation is difficult to investigate in the strict mathematical sense. In this study, we derived iterative formulas for the precise form of the epistatic genomic relationship matrix for arbitrary degree of epistasis including both additive and dominance interactions. The key to our theoretical results is the observation of an interesting link between the elements in the genomic relationship matrix and symmetric polynomials, which motivated the application of the corresponding mathematical theory. Based on the iterative formulas, efficient recursive algorithms were implemented. Compared with the approximation by the Hadamard product, our algorithms provided a complete solution to the problem of calculating the exact epistatic genomic relationship matrix. As an application, we showed that our new algorithms easily relieved the computational burden in a previous study on the approximation behavior of two limit models.


2018 ◽  
Vol 97 (1) ◽  
pp. 35-42 ◽  
Author(s):  
Kirsty Lee Moore ◽  
Conrad Vilela ◽  
Karolina Kaseja ◽  
Raphael Mrode ◽  
Mike Coffey

Sign in / Sign up

Export Citation Format

Share Document