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Estimating Realized Heritability in Panmictic Populations
M. Lstibůrek, V. Bittner, GR. Hodge, J. Picek, TFC. Mackay,
Language English Country United States
Document type Journal Article, Research Support, Non-U.S. Gov't
NLK
Free Medical Journals
from 1916 to 6 months ago
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from 1916 to 1 year ago
Europe PubMed Central
from 1916 to 1 year ago
ProQuest Central
from 2004-10-01 to 2020-12-31
Open Access Digital Library
from 1916-01-01
Open Access Digital Library
from 1916-01-01
Medline Complete (EBSCOhost)
from 1996-01-01 to 1 year ago
Health & Medicine (ProQuest)
from 2004-10-01 to 2020-12-31
Family Health Database (ProQuest)
from 2004-10-01 to 2020-12-31
Public Health Database (ProQuest)
from 2004-10-01 to 2020-12-31
- MeSH
- Algorithms MeSH
- Phenotype MeSH
- Quantitative Trait, Heritable MeSH
- Humans MeSH
- Models, Genetic * MeSH
- Computer Simulation MeSH
- Genetics, Population * MeSH
- Pedigree MeSH
- Selection, Genetic MeSH
- Body Height MeSH
- Inheritance Patterns * MeSH
- Check Tag
- Humans MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
Narrow sense heritability [Formula: see text] is a key concept in quantitative genetics, as it expresses the proportion of the observed phenotypic variation that is transmissible from parents to offspring. [Formula: see text] determines the resemblance among relatives, and the rate of response to artificial and natural selection. Classical methods for estimating [Formula: see text] use random samples of individuals with known relatedness, as well as response to artificial selection, when it is called realized heritability. Here, we present a method for estimating realized [Formula: see text] based on a simple assessment of a random-mating population with no artificial manipulation of the population structure, and derive SE of the estimates. This method can be applied to arbitrary phenotypic segments of the population (for example, the top-ranking p parents and offspring), rather than random samples. It can thus be applied to nonpedigreed random mating populations, where relatedness is determined from molecular markers in the p selected parents and offspring, thus substantially saving on genotyping costs. Further, we assessed the method by stochastic simulations, and, as expected from the mathematical derivation, it provides unbiased estimates of [Formula: see text] We compared our approach to the regression and maximum-likelihood approaches utilizing Galton's dataset on human heights, and all three methods provided identical results.
References provided by Crossref.org
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