After a description of our experimental method, we describe our experimental procedure, report our experimental results, and discuss their implications.
So, in the case of binary fingerprints, the only distinct profile similarity method we describe is BAYES method (Equation 24).
In addition to outlining the published ideas on this method, we describe several extensions: quantitative trait studies and case control studies with haplotypes and multiallelic markers.
The method we describe here is likely to be of general use in many Citrus cultivars to temporally control the activity of introduced transgenes.
The method we describe is based on a lactic acid polymer matrix with a predefined microstructure that is amenable to rapid prototyping and fabrication.
Using a modified broth microdilution method, we describe the in vitro sensitivity of two Australian isolates of B. dendrobatidis to six antimicrobial agents.
The method we describe exhibits the greatest improvement when only a small fraction of the total sapwood is measured, which is the typical scenario for most applications.
The method we describe in this section is based on the idea that notwithstanding this inherent computational hardness of the problem, it is reasonable to expect that if good n 1-sized and n 2-sized solutions are known, a (n 1+n 2 -sized solution better than one which would on average be obtained by a random draw can be hypothesized.
The method we describe now uses pair-wise sample compatibility to drive sample selection, that is, it builds an n r -sized solution by adding individual samples to the solution, the preference being guided by the previously included samples and their compatibility with the as of yet not selected samples.
The method we describe here could provide a quantitative means to select mice and rats with the highest levels of coat color chimerism.
The molecular modeling method we describe will prove useful to examine e. g. the variability of the recognition for the same p/MHC complex by different TCRs.
