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The observed response to selection leads to an estimate of the narrow-sense heritability (called realized heritability). This is the principle underlying artificial selection or breeding. Example
Heritability is the proportion of variance caused by genetic factors of a specific trait in a population. [1] Falconer's formula is a mathematical formula that is used in twin studies to estimate the relative contribution of genetic vs. environmental factors to variation in a particular trait (that is, the heritability of the trait) based on ...
Broad-sense heritability, H 2 = V G /V P, Involves the proportion of phenotypic variation due to the effects of additive, dominance, and epistatic variance. Narrow-sense heritability, h 2 = V A /V P, refers to the proportion of phenotypic variation that is due to additive genetic values (V A). [6]
Narrow sense Heritability (h 2 or H N) focuses specifically on the ratio of additive variance (V A) to total phenotypic variance (V P), or: h 2 = V A / V P.. In the study of Heritability, Additive genetic effects are of particular interest in the fields of Conservation, and Artificial selection.
Narrow-sense heritability has been used also for predicting generally the results of artificial selection. In the latter case, however, the broadsense heritability may be more appropriate, as the whole attribute is being altered: not just adaptive capacity. Generally, advance from selection is more rapid the higher the heritability.
GCTA estimates are likewise sometimes misinterpreted as "lower bounds" on the narrow-sense heritability but this is also incorrect: first because GCTA estimates can be biased (including biased upwards) if the model assumptions are violated, and second because, by definition (and when model assumptions are met), GCTA can provide an unbiased ...
Selection coefficient, usually denoted by the letter s, is a measure used in population genetics to quantify the relative fitness of a genotype compared to other genotypes. . Selection coefficients are central to the quantitative description of evolution, since fitness differences determine the change in genotype frequencies attributable to selecti
(Using a Plomin example, [38] for two traits with heritabilities of 0.60 & 0.23, =, and phenotypic correlation of r=0.45 the bivariate heritability would be =, so of the observed phenotypic correlation, 0.28/0.45 = 62% of it is due to correlative genetic effects, which is to say nothing of trait mutability in and of itself.)