[R-sig-ME] Performing a single animal model that estimates additive genetic variation for many populations?
Pierre de Villemereuil
pierre.de.villemereuil at mailoo.org
Thu Jun 18 15:33:32 CEST 2015
Dear all,
A kind of "multi-population" animal model framework which accounts for inter-
population, as well as for intra-population genetic structure has been developed
by Ovaskainen /et al./:
Ovaskainen, O., Karhunen, M., Zheng, C., Arias, J. M. C. & Merilä, J. A new method to
uncover signatures of divergent and stabilizing selection in quantitative traits.
/Genetics/ *189,* 621–632 (2011).
Instead of assuming a homogeneous Va across population, but maybe having a
population×additive genetic interaction (i.e. a population-specific Va component)
would solve this issue?
Regards,Pierre
Le jeudi 18 juin 2015, 10:55:07 David Duffy a écrit :
> On Thu, 18 Jun 2015, Jackie Wood wrote:
> > I'm working on a manuscript which investigates the relationship of various
> > metrics of adaptive potential (additive genetic variation (VA),
> > heritability (h2), and mean-scaled evolvability (IA)) with population size
> > in a common garden experiment using a large number of wild, isolated
> > populations of a vertebrate fish. One comment/request we received on the
> > manuscript was whether we could fit a single animal model that includes
> > all
> > of our populations. That is, in addition to the standard terms to estimate
> > VA, whether we could also include population size and interactions with
> > population size such that we could examine whether VA (or h2 or IA) varies
> > among populations, and the magnitude of the interaction between population
> > and additive (and potentially maternal) effects.
>
> Yes ;) It is essentially a GxE term. Probably MCMCglmm would be easiest.
>
> | David Duffy (MBBS PhD)
> | email: David.Duffy at qimrberghofer.edu.au ph: INT+61+7+3362-0217 fax: -0101
> | Genetic Epidemiology, QIMR Berghofer Institute of Medical Research
> | 300 Herston Rd, Brisbane, Queensland 4006, Australia GPG 4D0B994A
>
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