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A rate allocation that maximizes the inner problem can be calculated directly for a given independently of and.
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Most genes are located on one strand, termed the major strand, and skew was calculated directly for these genes.
Assume that all nonsense mutations in each gene in our data set (Tn) is pathogenic, which was calculated directly for each human gene from the nucleotide sequence.
In a kind of experimental design, the transition rates can be calculated directly from the data for two successive time moments, but the age-stage-specific rates of reproduction still remain uncertain, adding more complexity to the calibration problem.
Therefore, as the initial size of the partitions should correspond to the maximum acceptable blocking probability, each S j 0 can be calculated directly from Equation (1) for the case of equality (i.e., P b,j(A j, m j ) = G j, ∀ j ∈ [1, (k − 1)]).
These solutions can either be calculated directly from the differential equation for the extremal solutions or they can be determined from h c by applying the conjugation mapping s ∗.
In this way, the new, inter-calibrated, Digital Numbers (DN) can be calculated directly from the old numbers, for each image, using the following equation: DN new = C 0 + C 1 ∗ DN old + C 2 ∗ DN old 2. (1).
It is shown that spectral information may be calculated directly from output probabilities and a method for estimating output probabilities from AND/OR graphs is presented.
From Table 2 and the results described in [21] we deduce the 6 most important parameters to be: 1. E d (and C v ); 2. E s0 (and C a,C e ); 3. p a (0) (and p e (0),p LV (0)); 4. A; 5. R LV ; 6. ω 0. The final parameter ω 0 is not estimated, since it may be calculated directly from the pressure signal (and similarly for ϕ).
It's a purely geometric quantity that can be calculated directly from a map.
Solid effluent flux can be calculated directly from this model.
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com