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marker-assisted selection in wheat - ictsd

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Chapter 17 – Marker-<strong>assisted</strong> <strong>selection</strong> <strong>in</strong> fish and shellfish breed<strong>in</strong>g schemes 351Figure 5Relative efficiency of comb<strong>in</strong>ed GAS (for different family sizes [full-sibs]) and a known QTL,expla<strong>in</strong><strong>in</strong>g 10 percent of the genetic variance) versus an <strong>in</strong>dex us<strong>in</strong>g <strong>in</strong>formation from full-sibsonly for different values of the overall heritability (h²)80Relative efficiency of comb<strong>in</strong>ed MAS (full-sibs plus aQTL) versus full-sib <strong>in</strong>formation only(percentage)706050403020100.1 0.2 0.3 0.400 10 20 30 40 50Family sizeThe data were obta<strong>in</strong>ed from the ratio of square root of the variance of the <strong>in</strong>dices. Selection <strong>in</strong>dexformulae were derived from Lande and Thompson (1990).the same rate of <strong>in</strong>breed<strong>in</strong>g (Pong-Wonget al., 2002). This is because the accuracyof predict<strong>in</strong>g QTL effects us<strong>in</strong>g <strong>marker</strong>sis always smaller than when the QTLeffects are known, as <strong>in</strong> GAS schemes. Inreality, it is likely that MAS will be carriedout us<strong>in</strong>g <strong>in</strong>formation from many<strong>marker</strong>s to predict the allelic effects of morethan one QTL simultaneously whereas, <strong>in</strong>GAS schemes, only a limited number ofpolymorphisms are likely to be available.Therefore, on the whole, MAS schemesmay yield greater genetic response becausea greater proportion of the genetic variationis marked and used. Still, more <strong>marker</strong>genotyp<strong>in</strong>g is required for MAS schemes,which means that the additional proportionof the variance typed should pay for the<strong>in</strong>crease <strong>in</strong> the cost of many <strong>marker</strong>s typedsimultaneously.Due to the biology of many species<strong>in</strong> aquaculture, large family sizes can beused <strong>in</strong> a breed<strong>in</strong>g programme. Follow<strong>in</strong>gthe determ<strong>in</strong>istic model of Lande andThompson (1990), Figure 5 describes theeffect of family size and amount of polygenicvariation on the relative efficiency ofaccuracy estimates for an <strong>in</strong>dex us<strong>in</strong>g differentnumbers of full-sibs measured forthe trait, versus an <strong>in</strong>dex also <strong>in</strong>clud<strong>in</strong>g<strong>in</strong>formation on candidates for <strong>selection</strong> genotypedat loci targeted for GAS schemes (V.Mart<strong>in</strong>ez, unpublished results). For a s<strong>in</strong>gleQTL expla<strong>in</strong><strong>in</strong>g 10 percent of the geneticvariance, when the heritability is relativelylarge, family size has a small impact on theaccuracy. On the other hand, when the heritabilityof the trait is small, <strong>selection</strong> for aknown QTL has a major impact on relativeefficiency, particularly when the family size

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