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Comparisons of human and rodent genomes, thought to have split ∼100 MYA [78], yield many novel regulatory elements, while extending divergence to mammals and birds (∼310 MYA [79] [80]) causes a precipitous drop off in the ability to detect motifs [81] [82].
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Later, (L^{p} -estimates were extended to divergence form eL^{p} -estimatess were discontinuous coextendedto by divergencen [34].
In 2012, Shen and Chen [13] defined a stochastic integral with respect to sub-fractional Brownian motion (S^{H}) with index (H in 0, 1/2)) that extends the divergence integral from Malliavin calculus, and established versions of the formulas of Itô and Tanaka that hold for all (Hin 0, 1/2)).
Several recent whole-genome scans indicate that MYH9 has been the subject of natural selection during different periods of human evolution, starting from the time of human-primate divergence, and extending to the more recent local adaptations in modern populations.
Differentiating (sigma _{D_{beta }}) with respect to A v and setting it to 0, the interpolated amplitude extended using β divergence is obtained as A_{mathrm{v} beta} = left{begin{array}{ll} exp left left 1-alpha right) left left 1-alpha log A_{2} right) & (beta=1), logt(left(1-A_{ha right) A_{1}^{beta-1} + alpha A_{2}^{beta-1} right)^{frac{1}{beta-1}} & (text{otherwise}).
That divergence extends to which cases the court is willing to hear, says law professor Alan Morrison.
Comparison of restriction digest optical maps for the two mating-type chromosomes shows that divergence extends over 90% of the chromosome lengths, flanked at either end by two pseudoautosomal regions.
This structural divergence extends into the first eIF3k TPR-like repeat: Rpn12 repeat 2 has a much longer first helix (α3), and eIF3k a longer loop linking the helices so that the second helices of each are displaced relative to the other (compare Figures 2A and 2B).
Patterns of divergence between sibling species, extending the time scale of analysis, showed remarkable heterogeneity among functional regions of gambicin across all three species pairs, with over ten fold reduced divergence in coding as opposed to NC regions.
These three methods differ for the stringency of repeat masking (divergence < 10% vs. no divergence threshold) and the possibility of extending the alignment through masked sequence to reach the alignment length threshold (lowercase vs. N masking).
A μTAS can deliver significantly larger beam angular divergence at the sample and detector, thus extending the accessible resolution-intensity range, whether using flat or curved monochromating crystals.
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