Single-step genomic predictions for crossbred Holstein and Jersey cattle using metafounders

I Ampofo1, G Vargas2, D Gonzalez-Peña2

  • 1Zoetis Genetics, Kalamazoo, MI 49007; Department of Animal Science, University of Connecticut, Storrs, CT 06269.

Journal of Dairy Science
|September 20, 2025
PubMed
Summary

Incorporating metafounders (MF) in single-step genomic best linear unbiased prediction (ssGBLUP) models improves genetic predictions for crossbred cattle, especially for low heritability traits. However, careful tailoring is needed to avoid overfitting in high heritability traits.

Related Concept Videos

Pedigree Analysis01:35

Pedigree Analysis

Overview
88.7K
Monohybrid Crosses01:20

Monohybrid Crosses

Overview
238.6K
Hardy-Weinberg Principle01:49

Hardy-Weinberg Principle

Diploid organisms have two alleles of each gene, one from each parent, in their somatic cells. Therefore, each individual contributes two alleles to the gene pool of the population. The gene pool of a population is the sum of every allele of all genes within that population and has some degree of variation. Genetic variation is typically expressed as a relative frequency, which is the percentage of the total population that has a given allele, genotype or phenotype.
75.8K
Dihybrid Crosses01:18

Dihybrid Crosses

Overview
80.7K
Heritability01:06

Heritability

Heritability is a statistical concept that measures the degree to which genetic differences among individuals contribute to trait variations within a population. It is a fundamental idea in genetics, often prone to misinterpretation. Heritability is expressed as a percentage, reflecting the proportion of variation in a specific trait across a population that can be linked to genetic differences. However, it's important to understand that heritability does not determine how "genetic"...
555
Single Nucleotide Polymorphisms-SNPs01:05

Single Nucleotide Polymorphisms-SNPs

A single nucleotide polymorphism or SNP is a single nucleotide variation at a specific genomic position in a large population. It is the most prevalent type of sequence variation found in the human genome. Point mutations that occur in more than 1% of the population qualify as SNPs. These are present once every 1000 nucleotides on an average in the human genome. Replacement of a purine with another purine (A/G) or a pyrimidine with another pyrimidine (C/T) is known as a transition. In contrast,...
17.8K