🍩 Database of Original & Non-Theoretical Uses of Topology
(found 3 matches in 0.001314s)
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The Geometry of Synchronization Problems and Learning Group Actions (2019)
Tingran Gao, Jacek Brodzki, Sayan MukherjeeAbstract
We develop a geometric framework, based on the classical theory of fibre bundles, to characterize the cohomological nature of a large class of synchronization-type problems in the context of graph inference and combinatorial optimization. We identify each synchronization problem in topological group G on connected graph ΓΓ\Gamma with a flat principal G-bundle over ΓΓ\Gamma , thus establishing a classification result for synchronization problems using the representation variety of the fundamental group of ΓΓ\Gamma into G. We then develop a twisted Hodge theory on flat vector bundles associated with these flat principal G-bundles, and provide a geometric realization of the graph connection Laplacian as the lowest-degree Hodge Laplacian in the twisted de Rham–Hodge cochain complex. Motivated by these geometric intuitions, we propose to study the problem of learning group actions—partitioning a collection of objects based on the local synchronizability of pairwise correspondence relations—and provide a heuristic synchronization-based algorithm for solving this type of problems. We demonstrate the efficacy of this algorithm on simulated and real datasets. -
Improved Understanding of Aqueous Solubility Modeling Through Topological Data Analysis (2018)
Mariam Pirashvili, Lee Steinberg, Francisco Belchi Guillamon, Mahesan Niranjan, Jeremy G. Frey, Jacek BrodzkiAbstract
Topological data analysis is a family of recent mathematical techniques seeking to understand the ‘shape’ of data, and has been used to understand the structure of the descriptor space produced from a standard chemical informatics software from the point of view of solubility. We have used the mapper algorithm, a TDA method that creates low-dimensional representations of data, to create a network visualization of the solubility space. While descriptors with clear chemical implications are prominent features in this space, reflecting their importance to the chemical properties, an unexpected and interesting correlation between chlorine content and rings and their implication for solubility prediction is revealed. A parallel representation of the chemical space was generated using persistent homology applied to molecular graphs. Links between this chemical space and the descriptor space were shown to be in agreement with chemical heuristics. The use of persistent homology on molecular graphs, extended by the use of norms on the associated persistence landscapes allow the conversion of discrete shape descriptors to continuous ones, and a perspective of the application of these descriptors to quantitative structure property relations is presented.