Genetic Value Analysis

The genetic value analysis proceeds according to the following steps:

  1. First, the average of all pairwise kinship coefficients are calculated for each living animal in the breeding colony relative to every other living animal in the colony according, to the algorithm of Lange (1997). The grand mean kinship in the breeding colony is then calculated from the distribution of individual mean kinships, along with other summary statistics describing this distribution.
  2. Second, measures of individual mean kinship for each animal are then calculated in terms of standard deviates from this grand mean kinship, as z = (x-μ)/σ, i.e., "z-scores", in which x is the estimate of individual mean kinship, μ is the grand mean kinship, and σ is the standard deviation of the distribution of all individual mean kinship values of living animals in the colony.

    These z-scores indicate the extent and direction to which each animal's individual mean kinship deviates from the grand mean kinship in the colony. An animal having a positive z-score has individual mean kinship that lies above the colony grand mean kinship, suggesting that this animal's genome is over-represented in the colony, making the animal of lesser genetic value than others with negative z-scores. Conversely, an animal having a negative z-score has individual mean kinship that lies below the grand mean kinship, suggesting that this animal's genome is underrepresented in the colony, making the animal of greater genetic value than animals with positive z-scores.

  3. Third, genome uniqueness values are calculated using a gene-drop simulation according to MacCluer et al. (1986) and Ballou & Lacy (1995), by assigning unique alleles to all pedigree founders, and simulating their segregation throughout the pedigree according to Mendelian rules. Genome uniqueness is a measure of the probability that an animal possesses founder alleles that are carried by at most x animals in all, counting the animal itself (the application offers 1-5, default 4), and thus are rare and at risk of being lost from the population. A range of 100 to 10,000 simulations may be selected. A minimum of 1,000 simulations is recommended, and 1,000 is the default. A genome uniqueness threshold value between 1 and 5 should also be selected, as desired.

    Because genome uniqueness is estimated from a finite number of gene-drop iterations, each value carries a sampling standard error (the guSE column), which shrinks roughly in proportion to one over the square root of the number of iterations; the default of 1,000 iterations gives a sampling error below one percentage point on the pedigrees we have examined. Keep two ideas separate: the standard error tells you how precise the genome uniqueness number is, while what actually decides which animals are selected for breeding is the order in which they are ranked. A small standard error does not by itself mean that order has settled. The gvaConvergence() function checks how many gene-drop iterations a given pedigree needs for the selection order to stop changing.

  4. Following the calculation of mean kinship, related z-scores, and genome uniqueness for all animals, animals are ranked from the highest genetic value (ranking = 1) to the lowest. The Ranking Scheme control offers two schemes:

    Under either scheme, the value column labels each animal High Value (imported animals and those above the high-uniqueness or low-kinship cutoff), Low Value (all others), or Undetermined. Animals labeled High Value are considered to be of high genetic value, while animals labeled Low Value are not recommended for breeding, but may be suitable for research assignment or sale. Low Value animals are not highlighted; read the value column.

    This ranking scheme follows Vinson & Raboin (2015).


Breeding Group Formation