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There are possible branches at each time sample.
(T^2) is equal to a scalar value for each time sample showing the distance away the main etch.
The most general case of this model is where the parameters are completely uncorrelated at each time sample.
In our approach, approximate linear models are extracted at each time sample by instantaneous linearization of nonlinear fuzzy model and adaptive GPC is used.
The advantage of GPC and other linear MBPC methods is in garanteed convergence within each time sample, but they are not able to deal with strong process nonlinearities.
Therefore, each time sample of x[ n] would be represented by M unknown coefficients; hence, it is not a practical approach.
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Each time samples were taken from healthy volunteers, a record of the amount of blood and date was written in a dedicated log book.
We repeated the simulation 1000 times, each time sampling and analyzing a single SNP.
Each time samples were washed around 100 times with glass Pasteur pipettes with long tip and centrifuged at the same conditions (1000× g, 10 min, 4 °C).
After an incubation of 20 min at 37°C each time, samples were purified using phenol (pH6.6): chloroform (1 1, v/v) and chloroform, followed by isopropanol precipitation.
The anode chamber was sparged with nitrogen gas to displace the oxygen present prior to closure and each time samples were taken.
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