We propose a novel variational method for solving the sub-graph isomorphism problem on a gatebased quantum computer. The method relies (1) on a new representation of the adjacency matrices of the underlying graphs, which requires a number of qubits that scales logarithmically with the number of vertices of the graphs; and (2) on a new Ansatz that can efficiently probe the permutation space. Simulations are then presented to showcase the approach on graphs up to 16 vertices, whereas, given the logarithmic scaling, the approach could be applied to realistic sub-graph isomorphism problem instances in the medium term.
We propose a novel variational method for solving the sub-graph isomorphism problem on a gate-based quantum computer. The method relies (1) on a new representation of the adjacency matrices of the underlying graphs, which requires a number of qubits that scales logarithmically with the number of vertices of the graphs; and (2) on a new Ansatz that can efficiently probe the permutation space. Simulations are then presented to showcase the approach on graphs up to 16 vertices, whereas, given the logarithmic scaling, the approach could be applied to realistic sub-graph isomorphism problem instances in the medium term.
Optimal Transport (OT) has fueled machine learning (ML) applications across many domains. In cases where paired data measurements (µ, ν) are coupled to a context variable p i , one may aspire to learn a global transportation map that can be parameterized through a potentially unseen context. Existing approaches utilize Neural OT and largely rely on Brenier's theorem. Here, we propose a first-of-its-kind quantum computing formulation for amortized optimization of contextualized transportation plans. We exploit a direct link between doubly stochastic matrices and unitary operators thus finding a natural connection between OT and quantum computation. We verify our method on synthetic and real data, by predicting variations in cell type distributions parameterized through drug dosage as context. Our comparisons to several baselines reveal that our method can capture dose-induced variations in cell distributions, even to some extent when dosages are extrapolated and sometimes with performance similar to the best classical models. In summary, this is a first step toward learning to predict contextualized transportation plans through quantum. 1 We use "contextual" rather than "conditional" to differentiate from OT on conditional probabilities (Tabak et al., 2021)
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