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Related Concept Videos

Incomplete Dominance01:43

Incomplete Dominance

Gregor Mendel's work (1822 - 1884) was primarily focused on pea plants. Through his initial experiments, he determined that every gene in a diploid cell has two variants called alleles inherited from each parent. He suggested that amongst these two alleles, one allele is dominant in character and the other recessive. The combination of alleles determines the phenotype of a gene in an organism.
Polygenic Traits01:18

Polygenic Traits

When more than one gene is responsible for a given phenotype, the trait is considered polygenic. Human height is a polygenic trait. Studies have uncovered hundreds of loci that influence height, and there are believed to be many more. Due to the high number of genes involved, as well as environmental and nutritional factors, height varies significantly within a given population. The distribution of height forms a bell-shaped curve, with relatively few individuals in the population at the...
Polygenic Traits01:18

Polygenic Traits

When more than one gene is responsible for a given phenotype, the trait is considered polygenic. Human height is a polygenic trait. Studies have uncovered hundreds of loci that influence height, and there are believed to be many more. Due to the high number of genes involved, as well as environmental and nutritional factors, height varies significantly within a given population. The distribution of height forms a bell-shaped curve, with relatively few individuals in the population at the...
X-linked Traits01:19

X-linked Traits

In most mammalian species, females have two X sex chromosomes and males have an X and Y. As a result, mutations on the X chromosome in females may be masked by the presence of a normal allele on the second X. In contrast, a mutation on the X chromosome in males more often causes observable biological defects, as there is no normal X to compensate. Trait variations arising from mutations on the X chromosome are called “X-linked”.
X-linked Traits01:19

X-linked Traits

In most mammalian species, females have two X sex chromosomes and males have an X and Y. As a result, mutations on the X chromosome in females may be masked by the presence of a normal allele on the second X. In contrast, a mutation on the X chromosome in males more often causes observable biological defects, as there is no normal X to compensate. Trait variations arising from mutations on the X chromosome are called “X-linked”.
Multiple Allele Traits01:49

Multiple Allele Traits

The Concept of Multiple Allelism

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Exploring the Longissimus Muscle: Unraveling its Correlation with Meat Quality in Bos indicus and Crossbred Bulls
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Understanding and predicting complex traits: knowledge from cattle.

Kathryn E Kemper1, Mike E Goddard

  • 1Agriculture and Food Systems, University of Melbourne, Parkville, VIC 3010, Australia. kathryn.kemper@dpi.vic.gov.au

Human Molecular Genetics
|August 18, 2012
PubMed
Summary
This summary is machine-generated.

Predicting cattle genetic value using genomic markers requires approximately 2500 animals. Genomic prediction accuracy for cattle is 0.65, influenced by effective population size and marker linkage disequilibrium.

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Area of Science:

  • Animal Genetics
  • Quantitative Genetics
  • Genomic Prediction

Background:

  • Complex traits in cattle are influenced by numerous genetic loci, most with small effects.
  • Recent selection can lead to moderate-to-large effect loci with low allele frequencies.
  • Genomic markers capture substantial, but not all, additive genetic variance due to incomplete linkage disequilibrium.

Purpose of the Study:

  • To evaluate the accuracy of genomic prediction for cattle genetic values.
  • To determine the sample size required for accurate genomic prediction in cattle.
  • To compare genomic prediction requirements between cattle and humans.

Main Methods:

  • Utilized statistical models incorporating all genomic markers with random marker effects.
  • Assessed the impact of effective population size on prediction accuracy.
  • Calculated the number of animals needed for a prediction accuracy of 0.65 in cattle.

Main Results:

  • An effective population size of approximately 100 in cattle allows for a prediction accuracy of 0.65 with around 2500 animals.
  • Humans, with a larger effective population size (10,000-15,000), require over 145,000 records for similar accuracy.
  • Current genomic markers may not capture all genetic variance due to low-frequency causal variants.

Conclusions:

  • Genomic prediction is a powerful tool for cattle breeding, requiring manageable sample sizes.
  • Effective population size significantly influences the data requirements for accurate genomic prediction.
  • Future advancements, like genotyping causal polymorphisms via genome sequencing, may further enhance prediction accuracy.