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This is significant, since it implies that cell shape/cell function relationships that are deduced from using engineered 2-D surfaces might not readily be applicable to cells in 3-D environments.
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Finally, the following expressions for the velocity field components on the boundary are deduced from (27) using the connection between the two systems of numbering, and returning to the global one: u ( x ¯ i ) = ∑ k = 1 3 N u i k f k, v ( x ¯ i ) = ∑ k = 1 3 N v i k f k, (31).
Normalized variances σX/⟨X⟩, σR/⟨ R⟩2 and σ P /⟨ P⟩2 are deduced from power spectra using the property.
Duplication and loss of genes are deduced from the tree using the criteria that duplications increase the number of paralogues in one clade, while gene losses were inferred by the absence of an ancestral gene in descendant clades.
The actual values of these adaptation parameters are deduced from the user profile, using inference rules.
Ensembl homologs (orthologs and paralogs) are deduced from the protein trees using the longest transcript of each gene.
Then the heat sources produced or absorbed by the material due to deformation processes are deduced from the temperature variations by using the heat diffusion equation.
The viscous Burgers and the nonlinear Schrodinger dynamic equations on a time-space scale are deduced from the Lax equation by using the Ablowitz-Kaup-Newel-Segur-Ladik method.
Secondary structures are deduced from the PDB (28) entry using the DSSP program (29).
Poleward boundaries of the auroral oval are deduced from the 427.8 nm and are checked using the electron precipitation data from the DMSP conjunctions.
AA sequence data was deduced from nt data using BioEdit [23], and were analysed using BioNumerics v3.5 (Applied Maths, Kortrijk, Belgium).
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