The key to the algorithm is the development of a sensitive domain boundary profile that can calibrate composite structural and sequence alignment information from the multiple threading templates for precise domain assignment.
At low NA and at depth within a tissue, nonlinear effects, such as self-focusing, result in focal plane jitter that make precise cutting adjacent to sensitive boundaries difficult.
These are (1) the ability to cut with a broad range of fluences without impacting the location of the focal plane, which is desirable given tissue differences (2) the use of beams which have longer working distances facilitating delivery, and (3) precise axial ablation with these beams enabling safer penetration up to sensitive boundaries or membranes.
DMRs act via long-range mechanisms, such as antisense RNA interference, and through methylation-sensitive boundary elements (CTCF) [30], [51], [52], [53].
Particular focus is placed on the tree-lines as these are regarded as climate-sensitive boundaries in the landscape.
A simple computational model, predicated on the premise that a rate-sensitive grain-boundary affected zone exists, is shown to explain the observed effect of grain size on the rate-dependent plastic response.
Compared with that of the 3DGN-assisted sample, the stability of thermal conductivity of the RGO nanosheets added composites under high temperature is better because of the more sensitive Kapitza boundary scattering (as a results of the more boundaries of the RGO nanosheets).
Compared with that of the 3DGN-assisted sample, the stability of thermal conductivity of the RGO nanosheets added composites under high temperature is better because of the more sensitive Kapitza boundary scattering (as a result of the more boundaries of the RGO nanosheets).
Resource heterogeneity and expected migration distance appear to be sensitive to boundary effects in small simulations, but approach an equilibrium value (and have lower variance) in simulations of >8,000 patches (Figures S7A and S7B).
