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D-DOIT introduces a training-free adaptation method for discrete diffusion models that leverages Doob's h-transform to guide sampling using reward values instead of gradients. This approach is particularly significant for applications like regulatory DNA design and protein inverse folding, where it outperforms existing baselines while avoiding the computational cost of full trajectory rollouts. The technique effectively bridges the gap between continuous and discrete diffusion by reweighting reverse transition probabilities to enhance sample quality in generative biology tasks.
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D-DOIT: Training-free Adaptation of Discrete Diffusion via Doob's h-Transform

arXiv3 min read

arXiv:2610.04938v1 Announce Type: cross Abstract: We propose D-DOIT (Discrete Doob-Oriented Inference-time Transformation), a training-free and efficient adaptation method for discrete diffusion models with generic rewards. D-DOIT formulates adaptation as sampling from a reward-tilted target distribution and realizes this transport through Doob's h-transform of the discrete diffusion reverse kernel, using only reward values rather than reward gradients. Unlike continuous diffusion, masked discrete diffusion samples categorical token-reveal transitions rather than continuous state updates. D-DOIT derives the corresponding discrete Doob's h-transform, which guides sampling by reweighting reverse transition probabilities instead of adding a drift correction. To make this transformation practical, D-DOIT avoids expensive future rollouts. At each guided step, D-DOIT samples candidate next states, uses the model prediction head to complete each candidate into a clean sequence, evaluates each completion with the reward oracle, and resamples the next state with probabilities proportional to the rewards. An optional late-stage best-of-K refinement further improves sample quality by branching trajectories only near the end of denoising, avoiding the $K$-fold cost over the full trajectory. Empirically, across regulatory DNA design and protein inverse folding benchmarks, D-DOIT outperforms training-free guidance baselines. It improves enhancer activity and cell-type specificity while preserving sequence naturalness, and achieves the highest success rate in protein inverse folding.

Abstract:We propose D-DOIT (Discrete Doob-Oriented Inference-time Transformation), a training-free and efficient adaptation method for discrete diffusion models with generic rewards. D-DOIT formulates adaptation as sampling from a reward-tilted target distribution and realizes this transport through Doob's h-transform of the discrete diffusion reverse kernel, using only reward values rather than reward gradients. Unlike continuous diffusion, masked discrete diffusion samples categorical token-reveal transitions rather than continuous state updates. D-DOIT derives the corresponding discrete Doob's h-transform, which guides sampling by reweighting reverse transition probabilities instead of adding a drift correction. To make this transformation practical, D-DOIT avoids expensive future rollouts. At each guided step, D-DOIT samples candidate next states, uses the model prediction head to complete each candidate into a clean sequence, evaluates each completion with the reward oracle, and resamples the next state with probabilities proportional to the rewards. An optional late-stage best-of-K refinement further improves sample quality by branching trajectories only near the end of denoising, avoiding the $K$-fold cost over the full trajectory. Empirically, across regulatory DNA design and protein inverse folding benchmarks, D-DOIT outperforms training-free guidance baselines. It improves enhancer activity and cell-type specificity while preserving sequence naturalness, and achieves the highest success rate in protein inverse folding.

Machine Learning (cs.LG); Artificial Intelligence (cs.AI)

arXiv:2610.04938 [cs.LG]

(or arXiv:2610.04938v1 [cs.LG] for this version)

https://doi.org/10.48550/arXiv.2610.04938 Focus to learn more arXiv-issued DOI via DataCite (pending registration)

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Full text under the publisher's open licence · 296 words

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