For each prototype, we defined a random direction in our parametric shape space and selected two shapes along this dimension, equally distant from the prototype in the positive and negative direction (Fig. 1d).
In the mixture prior, given dω and a set of prototypes, we define the posterior loss as And similarly define as the parameters that minimize this loss: This minimization problem can be solved by running P (the number of prototypes) minimization problems, one per prototype.
For the design of our TrustCAM prototype system, we define the following goals.
We define a prototype as compatible with a farm type if the prototype is not likely to increase the constraints of a farm of that type (CI = 1).
We define what a prototype is, then outline the design challenges.
To demonstrate the first functionality, we define in our prototype some locations and associated these locations with mobile applications.
Using sequence analysis and conservation we define the acyltransferase domain prototyped by the fungal Cas1p proteins, identify its active site residues and unify them to the superfamily of classical 10TM acyltransferases (e.g. oatA).
We define here that two clusters are k-means neighbors if k-means can move prototypes from a cluster to its neighbor.
Define prototype cell classes (Fig. 6 ): We next define prototype cell classes.
