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This gives an approximation of the behavior of a mutant allele in a linked system under a deterministic scenario, making the assumption of constant linkage between consecutive sampling points.
Therefore, in animal half-sib designs, modelling linkage disequilibrium evolution using a Wright-Fisher model does not significantly improve the accuracy of the QTL location when compared to a simpler method assuming complete and constant linkage between the QTL and the marker alleles.
The conclusion of our study is that the probabilistic modelling of the linkage disequilibrium evolution using a Wright-Fisher model did not improve the accuracy of the QTL location when compared to a simple method using deterministic modelling that assumed complete and constant linkage between the QTL and the marker alleles.
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This study is being conducted in close collaboration with decision makers in order to allow constant linkages that are likely to favour the relevance and utilisation of research results.
K 1 = ∆T e/∆ δ│ (E^{prime}_{q})—change in electrical torque for a change in rotor angle with constant flux linkages in d-axis.
Stability constant, degree of linkage and related thermodynamic parameters (e.g. ΔG°, ΔH° and ΔS°) have been compared for the two complexation systems using Osada's methods.
Permanent magnet synchronous motors have quite limited field-weakening speed range due to the constant magnet flux linkage.
Constant velocity and determinate linkage kinematics are maintained by a spherical pantograph.
In the case of a slider-crank linkage a constant transmission ratio can be achieved with a properly designed circular guide-curve, which makes the slider-crank essentially equivalent to a four-bar.
Most probably, this is because, unlike multilocus model such as ours, those models assumed a constant genetic variance under linkage equilibrium (Huisman and Tufto 2012).
K 2 = ∆T e/∆ (E^{prime}_{q})│δ change in electrical torque for a change in d-axis flux linkages with constant rotor angle.
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