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The time scale of the evolution is scaled by a factor 1/D, which corresponds to set D=1.
Indeed, the ratios of the minima and the strength of the anisotropy can be controlled by the α i values from Eq. (6) and α 〈001〉, while γ 0 plays the role of a prefactor in Eq. (2), thus affecting only the absolute time scale of the evolution.
We present here a time scale of the evolution of the A3 loci, arising from their common origin with other cytidine deaminases.
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Furthermore, the software allows for the immediate and simultaneous visualization with the same temporal scales of the evolution of the current densities, membrane potentials, and gating variables.
These results suggest a time scale for the evolution of hotspots in primates.
We obtained a molecular time scale for the evolution of extant xenarthrans and other placental mammals.
The implicit time advancing is compared in terms of accuracy and computational time with the explicit approach for one-dimensional and two-dimensional sediment transport problems, characterized by different time scales for the evolution of the bed and of the water flow.
However, when scaled to the evolution of CCT8 sequences over the same periods of time, the substitution rate of CCT8L proteins was about 14-15 times higher than in CCT8 and 1.4-2.3 1.4-2.3igher timesin BBS proteins.
Large scale simulations of the evolution of representations of grain structures are presented in an accompanying paper.
In this paper, we present a complete analysis of all Haemagglutinin (HA) and Neuraminidase (NA) gene sequences available to allow large scale analyses of the evolution and epidemiology of type A influenza.
First, we aim to provide an updated time-scale for the evolution of the major passerine clades.
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