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Interestingly, computational studies showed that for both A3Es and A5Es the distribution of extensions, f(E), is markedly skewed toward short-range splice forms [ 18].
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The distribution of extension lengths implies that most gene boundaries are discordant between the two definitions.
Both transitions in each of the four SNARE complexes were binary, as indicated by the two peaks in the histogram distributions of extension.
The distribution of novel extensions is not substantially different from the global distribution, suggesting that many of these extensions are not phylogenetically conserved beyond melanogaster.
In order to compare these findings with A3E events, we obtained the distribution of short extensions and identified a similar, albeit distinctively different pattern (upper-right panel).
The probability distribution of molecular extension was determined as a function of time and strain rate.
Our results show that basin geometry is strongly dependent on the cumulative (and distribution) of lithospheric extension and the flexural rigidity of the lithosphere.
In this case, the animal involved will become sensitive to the ongoing dynamical state of its own body: the global bodily distribution of contraction-extension at any particular moment in time.
(B ) Histogram distributions of the extensions shown in A (symbols) and their best fits with double-Gaussian functions (lines).
Gray: global distribution of all potential extensions.
In order to allow an adequate distribution of the primer-extension products, non-homologous neutral sequences were incorporated at the 5′-ends of the minisequencing primers to adjust their lengths and obtain a more balanced base composition [ 36].
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