Midparent

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In human genetics the midparent value of a trait is defined as the average of the trait value of the father and a scaled version of that of the mother. This value can be used in a study to analyze the data set without heeding sex effects. Studying quantitative traits in heritability studies may be complicated by sex differences observed for the trait.

Well-known examples include studies of humans' height, whose midparent value hmp is given by: [1]

where hf is the father's height, and hm the mother's.

The coefficient 1.08 serves as a scaling factor. After the 1.08 scaling, the mean of the mother's height is the same as that of the father's, and the variance is closer to the father's; in this way, sex difference can be ignored.

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<span class="mw-page-title-main">Inbreeding</span> Reproduction by closely related organisms

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Research on the heritability of IQ inquires into the degree of variation in IQ within a population that is due to genetic variation between individuals in that population. There has been significant controversy in the academic community about the heritability of IQ since research on the issue began in the late nineteenth century. Intelligence in the normal range is a polygenic trait, meaning that it is influenced by more than one gene, and in the case of intelligence at least 500 genes. Further, explaining the similarity in IQ of closely related persons requires careful study because environmental factors may be correlated with genetic factors.

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Population structure is the presence of a systematic difference in allele frequencies between subpopulations. In a randomly mating population, allele frequencies are expected to be roughly similar between groups. However, mating tends to be non-random to some degree, causing structure to arise. For example, a barrier like a river can separate two groups of the same species and make it difficult for potential mates to cross; if a mutation occurs, over many generations it can spread and become common in one subpopulation while being completely absent in the other.

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The missing heritability problem is the fact that single genetic variations cannot account for much of the heritability of diseases, behaviors, and other phenotypes. This is a problem that has significant implications for medicine, since a person's susceptibility to disease may depend more on the combined effect of all the genes in the background than on the disease genes in the foreground, or the role of genes may have been severely overestimated.

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References

  1. Vogel, Friedrich; Motulsky, Arno G. (1997). "Formal Genetics of Humans: Multifactorial Inheritance and Common Diseases". Human Genetics. Problems and Approaches. p. 207. doi:10.1007/978-3-662-03356-2_7. ISBN   978-3-662-03356-2.