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Supersymmetry is a complex mathematical framework based on the theory of group transformations that was developed beginning in the early 1970s to understand at a more-fundamental level the burgeoning number of subatomic particles being produced in high-energy particle accelerator experiments.
Starting in the 1980s, Rinzel and Ermentrout [3, 4] pioneered a mathematical framework based on bifurcation theory that distinguishes type I and type II neural models.
The aim of this work is to propose a mathematical framework, based on population balance equations, to describe the simultaneous colloid aggregation and deposition.
In order to simplify the analysis, in this paper we propose a mathematical framework based on tropical algebra for circuit analysis.
The two sub-problems are considered within a unifying mathematical framework based on dynamic programming, in order to guarantee the optimality of the solution.
The mathematical framework based on the Baire partialquasi-metric space presents the advantage of providing the complexity of the algorithmsunder consideration through easier and fewer calculations than those given in theSchellekens methods.
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In our previous study, we reported a mathematical model based on population balance framework for a batch cooling sonocrystallization of l-asparagine monohydrate (LAM).
The mathematical framework is based on a combination of set theory, Boolean operators and automata unfolding.
This paper suggests an integrated mathematical framework developed based on the leader followers game for augmentation of transmission networks.
A large stumbling block is the utilization of the fairly extensive literature in social psychology related to risk avoidance, in formal mathematical decision frameworks based on probabilistic analysis.
In conclusion, a computer framework based on mathematical morphological analysis could be utilized as a reference for clinicians to quantify exudates and microaneurysms in NPDR, and larger exudate area and more aneurysm counts might help grading the NPDR, larger samples and prospective clinical trials are needed for further validation.
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