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Demographic processes such as bottlenecks might be sampled differently by markers with different mutation rates.
The G'ST estimate could control for differences between different markers with different heterozygosities [ 59].
Although great care should be taken when comparing levels of genetic structure between markers with different mutational properties [ 28, 29], this difference may suggest that estimates of genetic differentiation from a limited number of microsatellite loci may be even more inflated by hitch-hiking selection than previously assumed.
We would expect both clustering and FST patterns to be relatively robust to differences in mutation rates between the markers with different motif lengths (Haasl and Payseur 2011).
The availability of data on genetic markers with different modes of inheritance and rates of evolution allows to perform comparative analysis that shed further light on the genetic history of the Tyrolean Iceman.
In this study, we present a new objective method for measuring the eye colour on a continuous scale that allows researchers to associate genetic markers with different shades of eye colour.
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To gauge convergence, this procedure is repeated 5 times for each marker, with different random choices of initial conditions.
Because no allele size information was available for the new microsatellites, we initially multiplexed only three SSR markers (each marker with different fluorescence labels) for parental genotyping.
For each marker with different sensitivities and specificities plotted in ROC space, we quantify whether this could be explained by such threshold effect by estimating the (negative) correlation between sensitivity and specificity.
To ink over your drawing use a black pen or marker with different kinds of points so that there will be some variation of texture on your drawing.
In parallel, when comparing a similar number of markers but with different degrees of polymorphism (scenario 2 vs. 5, microsatellites vs. SNP) the biallelic markers yield worse performances.
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