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There were several traits for which we found no significant dominance component, resulting in equal broad and narrow heritability estimates.
However, the additive variance becomes zero in a model that also fits a dominance component.
The additive component accounted for 73.7% of the variance and the dominance component for 19.7% of the variance.
Tmet appears to have a strong dominance component to the variation observed (Table 2, Additional file 4).
The moderating effects of marital status and number of siblings on the dominance component were marginally significant (p < .05 but p > .01).01
The BCMA QTL has an R=0.804, with the additive component accounting for 69.1% of the variance and the dominance component accounting for 11.3% of the variance.
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Heritable variances were partitioned into additive and dominance components.
Variance due to dominance was not significant but was difficult to assess because of the high sampling correlation between additive and dominance components.
Both additive and dominance components were found significant in controlling the biochemical traits; the predominance of the additive effect was observed in capsaicinoids and dominance was observed for carotenoids.
Using a recently developed method, we estimate the additive and dominance components of variance or, equivalently, the narrow and broad sense heritabilities of several traits in the Hutterites, a founder population with extensive genealogical records.
Alternatively, we may extend to a multiple regression approach to dissect the genotypic value into additive and dominance components.
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