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This research establishes a clear path to quantum advantage in Topological Data Analysis by leveraging Mayer homology, which naturally handles exponentially large Betti numbers that stymied previous approaches. The authors demonstrate that existing classical dequantization methods fail against these specific structural barriers, offering a distinct computational edge for applications in genomics and drug discovery with feasible resource estimates.
Quantum Advantage in Topological Data Analysis via Mayer Homology
arXiv:2609.28058v1 Announce Type: new Abstract: Prior work has explored quantum algorithms for topological data analysis (TDA), revealing the possibility of exponential quantum speedups in estimating the ratios of Betti numbers to the dimension of the combinatorial Laplacian. However, this quantity is only non-vanishing and efficient-to-quantumly-estimate when Betti numbers are exponentially large, a case for which concrete examples are rarely known. Furthermore, certain randomized classical algorithms are sometimes efficient in this regime. Thus, the prospect of achieving quantum advantage in conventional TDA appears fairly narrow. Here, we address these challenges to the quantum advantage in TDA by developing quantum algorithms for Mayer homology, which generalize simplicial homology to $N$-nilpotent boundary operators ($\partial^N =0$) and have recently been successfully applied to real-world TDA contexts. We introduce an efficient quantum algorithm for estimating Mayer Betti numbers and their persistent counterparts. We then prove that for high-order simplices, Mayer Betti numbers are often exponentially large in the dense regime, which ameliorates the normalization bottleneck of conventional quantum TDA. In the same regime, we argue that existing dequantization algorithms developed for conventional TDA, when applied to Mayer homology, generally lose theoretical guaranties, facing certain structural barriers that prevent their practical utilities. We also provide logical resource estimates revealing that a quantum computer with roughly a few hundred qubits and sixty million Toffoli gates could solve Mayer homology problems beyond the capabilities of known classical approaches. Finally, we discuss real-world applications of Mayer homology in genomics, supersymmetry, drug discovery, and neuroscience, revealing the potential of our quantum algorithm to deliver real-world impacts via Mayer homology.
Abstract:Prior work has explored quantum algorithms for topological data analysis (TDA), revealing the possibility of exponential quantum speedups in estimating the ratios of Betti numbers to the dimension of the combinatorial Laplacian. However, this quantity is only non-vanishing and efficient-to-quantumly-estimate when Betti numbers are exponentially large, a case for which concrete examples are rarely known. Furthermore, certain randomized classical algorithms are sometimes efficient in this regime. Thus, the prospect of achieving quantum advantage in conventional TDA appears fairly narrow. Here, we address these challenges to the quantum advantage in TDA by developing quantum algorithms for Mayer homology, which generalize simplicial homology to $N$-nilpotent boundary operators ($\partial^N =0$) and have recently been successfully applied to real-world TDA contexts. We introduce an efficient quantum algorithm for estimating Mayer Betti numbers and their persistent counterparts. We then prove that for high-order simplices, Mayer Betti numbers are often exponentially large in the dense regime, which ameliorates the normalization bottleneck of conventional quantum TDA. In the same regime, we argue that existing dequantization algorithms developed for conventional TDA, when applied to Mayer homology, generally lose theoretical guaranties, facing certain structural barriers that prevent their practical utilities. We also provide logical resource estimates revealing that a quantum computer with roughly a few hundred qubits and sixty million Toffoli gates could solve Mayer homology problems beyond the capabilities of known classical approaches. Finally, we discuss real-world applications of Mayer homology in genomics, supersymmetry, drug discovery, and neuroscience, revealing the potential of our quantum algorithm to deliver real-world impacts via Mayer homology.
arXiv:2609.28058 [quant-ph]
(or arXiv:2609.28058v1 [quant-ph] for this version)
https://doi.org/10.48550/arXiv.2609.28058 Focus to learn more arXiv-issued DOI via DataCite (pending registration)
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