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The proposed cover refinement method also does not significantly change the manifold elements at the vicinity of the crack tips.
The DG-Chimera method also does not require the use of fringe points to maintain the interior stencil across inter-grid boundaries.
The method also does not degrade substantially the order of the overall scheme despite the extra constraints of monotonicity and conservation.
This method also does not provide any insight into the relative temperature sensitivity of the degradation and thus a possible controlled temperature shelf-life, however defined.
Similar to the previous idea, this method also does not provide analytical insight and becomes tedious if not infeasible for correlated signals as well as large matrices.
When different commodities are continuously picked up, rather than pick up simultaneously to compare, this method also does not work well.
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The test method also did not sufficiently discriminate formulations with different in vivo absorption rates.
The combination method also did not perform as well as the disaggregation method in tree-level predictions.
However, this method also did not allow for multisample anti-aliasing, and was only compatible with Nvidia video cards, leaving ATI cards unable to run high dynamic range.
However, the more sensitive DBM method also did not detect hippocampal volume change.
To test a potential linear relation between BMI and As metabolites (%iAs, %MMA, %DMA, PMI, or SMI) we applied multiple linear regression analyses, adjusting for U-As, age, and SES; this method also did not show any significant association.
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