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The subject wore 57 markers, whose locations were determined based on an improved version of the Helen Hayes Hospital marker set.
Three independent experiments were conducted to determine the reliability, accuracy and minimal detectable difference of the marker set and model.
The change in marker sets from the initial exposure to a largely intracellular survival strategy may explain a corresponding shift in the marker sets observed in this study.
For example, one could envision partitioning a 100 marker set into three groups.
Figure 1 shows the sensitivity of each marker set for detecting population admixture.
It was therefore included in this study to provide a full characterisation of the entire moa microsatellite marker set.
The statistical approach to classifying marker sets demonstrated an ability to discriminate classes of exposure 75% of the time.
This "additional marker set" contained two more markers per chromosome than the original IM marker set.
However, no structuring was present in the 6R marker set.
Ambiguous genotypes were repeated using a different marker set.
Additionally, we compared the utility of the new marker set to that of the previously-developed conserved marker set [ 21].
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