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Following DE-pairing, the density of axons in supragranular layers projecting from the labeled neurons in the D2 column was higher in E- than in C-row columns.
As the choice of coprime pair increases, the density of differential array generated would decrease correspondingly, though the coprime sampling might still calculate the full coverage of all lag by satisfying the Property 4. Then the correlation estimates at that lag could be deteriorated offsetting from the real values.
We calculated the Pearson correlation coefficient r between the paired density profiles of the different elements.
Experimentally determined KIEs are paired with density function theory (DFT) to determine the TS structure of the enzymatic reaction, here applied to the deacetylation of OAADPr by MacroD1.
We also investigated the relationship between wobble base pairing, relative occupancy, and the density of large and small footprints.
We show that the time evolution of the wave function describing the macroscopic variations of the pair density in BCS theory can be approximated, in the dilute limit, by a time-dependent Gross Pitaevskii equation.
We demonstrated that by using several restriction enzymes paired with PstI we increase the density of markers across the wheat genome.
We obtain this term as the diagonal part of a pair interaction appearing in the density of a Gibbs measure derived from the Feynman Kac representation of the Hamiltonian.
The pair distribution function gives the density of points in the rectangle d X i × d X j on the plot (X i X j ).
where π N ′ N = g s [ f ( E N ′ ) − f ( E N ) ] ℏ Ω + E N ′ − E N + i δ (17). is the pair bubble (or density-density correlation function) in the absence of e-e coupling with g s = 2, counting for spin degeneracy, and f(E N ) = [ 1 + e ( E N − E F ) / k B T ] − 1 being the Fermi-Dirac function.
Other applications could be the investigation of consequences of mate choice or experiments manipulating the density of breeding pairs in a plot.
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