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We just remind that for I b < 0, Eq. (27) has two equilibria: a stable attractor and a nonstable equilibrium.
In Fig. 4, we represented the evolution in time of the characteristics in the case I b < 0. For I b = 0, the equation has one equilibrium, which is a saddle node, while for the case I b > 0, (27) has no equilibrium.
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The average packet sizes for I-, B-, and P-frames are 956, 179, and 624 bytes, respectively.
The standard deviations for plasma, σ i b, and for urine, σ i u, are fitted investigation-specifically by simulated annealing [ 28] before starting the MCMC sampling process.
It is shown that the solid line is higher than the dotted line which indicates that the subinterval for i = B − m/8 + 1, …, B, …, B + m/8 will be larger resulting from their higher final frequency counts.
As f′(x i ) increases for i = B − δ + 1, …, B, …, B + δ, the inequality c ' x i − c ' x i − 1 c ' x I − 1 > c x i − c x i − 1 c x I − 1 can be obtained.
Calculate d i( a, b) = g i(a) – g i(b) for each two time alternatives; 7.
Let ω i(c, X) be the maximum value of ω ˜ i b, π for b, π ∈ Δ i, c, X, and let φ i(c, X) be the (b, π) obtaining this maximum, concluding the recursive step.
We define similar sets A i, B i for the rows W i and W i + N in the evolved genotype, representing the inputs to the paralogous genes.
For each P(ψ i )≥α i in ϕ, substitute a new atomic proposition B i for ψ i to construct Ψ. Let Γ be assignment P≥1, where γ is the conjunction of the clauses corresponding to (ψ i )⇔B i, (¬ψ i ∨B i )∧(ψ i ∨¬B i ), for all B i introduced.
We decrease the λ i 's for i ∈ B k with different speed.
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com