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Bridge Matching Sampler: Scalable Sampling via Generalized Fixed-Point Diffusion Matching

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Sampling from unnormalized densities using diffusion models has emerged as a powerful paradigm. However, while recent approaches that use least-squares `matching' objectives have improved scalability, they often necessitate significant trade-offs, such as restricting prior distributions or relying on unstable optimization schemes. By generalizing these methods as special forms of fixed-point iterations rooted in Nelson's relation, we develop a new method that addresses these limitations, called Bridge Matching Sampler (BMS). Our approach enables learning a stochastic transport map between arbitrary prior and target distributions with a single, scalable, and stable objective. Furthermore, we introduce a damped variant of this iteration that incorporates a regularization term to mitigate mode collapse and further stabilize training. Empirically, we demonstrate that our method enables sampling at unprecedented scales while preserving mode diversity, achieving state-of-the-art results on complex synthetic densities and high-dimensional molecular benchmarks.

Denis Blessing, Lorenz Richter, Julius Berner, Egor Malitskiy, Gerhard Neumann• 2026

Related benchmarks

TaskDatasetResultRank
n-body particle system samplingDW-4 d = 8
W2 Distance0.38
20
n-body particle system samplingLJ-13 (d = 39)
W2 Distance1.54
13
n-body particle system samplingLJ-55 d = 165
W23.8
10
Molecular conformation samplingAlanine Dipeptide (ALA2) d = 66
DJS (phi, psi)0.068
4
Molecular conformation samplingTetrapeptide ALA4 (d = 126)
(phi, psi)-DJS0.228
4
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