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Alternative explanations for the sex-specific genetic differentiation would be differential viability, lifespan or hatching rate between sexes, which can lead to the allele frequency difference between females and males detected by FST (see [ 8, 29]).
We do not know whether such fractions have been seen in other data sets or whether other factors, e.g. differential viability of the organisms, may have caused the observed values of r>1/2 in those older studies.
Remarkably, the system was capable of discriminating between wild-type and mutant animals based on the differential viability of just six mechanosensory neurons.
Such differential viability may also explain the low rate of outcrossed mating, if few Rosetteless haploids survived to mate with Isolate B haploids.
We model this within the context of zygotic differential viability, as shown in (Lorieux et al. 1995b; Wu et al. 2007).
Importantly, however, this does not mean that the differences between outgrowth potential are due to differential viability between the cells [ 11].
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Thus, differential progeny viability was not dependent upon a particular selective environment, or particular genetic components possessed by the progenitors.
Differential progeny viability that was consistent with ecological speciation was observed in almost all comparisons made at the level of lineage class as female (Fig. 4).
Furthermore, for the case of differential zygotic viability, T has been modeled and solved for an F2 (Zhu et al. 2007).
Finally, given the metabolic parameters were performed in the peri-infarct region of the heart, differential cell viability may be of modest concern.
Here we build upon existing genetic models of differential zygotic viability to model a heterozygote fitness term and calculate expected genotypic proportions in recombinant inbred populations propagated by selfing.
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