Moving target defenses based on dynamic platforms have been proposed as a way to make systems more resistant to attacks by changing the properties of the deployed platforms. Unfortunately, little work has been done on discerning effective strategies for the utilization of these systems, instead relying on two generally false premises: simple randomization leads to diversity and platforms are independent. In this paper, we study the strategic considerations of deploying a dynamic platform system by specifying a relevant threat model and applying game theory and statistical analysis to discover optimal usage strategies. We show that preferential selection of platforms based on optimizing platform diversity approaches the statistically optimal solution and significantly outperforms simple randomization strategies. Counter to popular belief, this deterministic strategy leverages fewer platforms than may be generally available, which increases system security.

Background: Clinical flow cytometry typically involves the sequential interpretation of two-dimensional histograms, usually culled from six or more cellular characteristics, following initial selection (gating) of cell populations based on a different subset of these characteristics. We examined the feasibility of instead treating gated n-parameter clinical flow cytometry data as objects embedded in n-dimensional space using principles of information geometry via a recently described method known as Fisher Information Non-parametric Embedding (FINE).Methods: After initial selection of relevant cell populations through an iterative gating strategy, we converted four color (six-parameter) clinical flow cytometry datasets into six-dimensional probability density functions, and calculated differences among these distributions using the Kullback-Leibler divergence (a measurement of relative distributional entropy shown to be an appropriate approximation of Fisher information distance in certain types of statistical manifolds). Neighborhood maps based on Kullback-Leibler divergences were projected onto two dimensional displays for comparison.Results: These methods resulted in the effective unsupervised clustering of cases of acute lymphoblastic leukemia from cases of expansion of physiologic B-cell precursors (hematogones) within a set of 54 patient samples.Conclusions: The treatment of flow cytometry datasets as objects embedded in high-dimensional space (as opposed to sequential two-dimensional analyses) harbors the potential for use as a decision-support tool in clinical practice or as a means for context-based archiving and searching of clinical flow cytometry data based on high-dimensional distribution patterns contained within stored list mode data. Additional studies will be needed to further test the effectiveness of this approach in clinical practice. q

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