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Yanruisheng Shao

Publications and source records attributed to Yanruisheng Shao.

2 recordsLinked to original sources

Heuristics are Not Enough: Calibrated and Corrected Caching for Video Diffusion Acceleration

Feature caching has become a mainstream training-free strategy for accelerating video diffusion models by reusing intermediate outputs across denoising steps. However, existing adaptive methods rely on heuristic difference measures misaligned with actual generation quality, employ a single global threshold that ignores heterogeneous phase dynamics, and never validate their budget estimates against true approximation error, allowing systematic bias to propagate uncorrected. We propose \textbf{AlignCache}, a closed-loop caching framework that directly aligns scheduling decisions with their true influence on the final generated video through three tightly coupled components: (1) phase-adaptive budget routing that partitions the denoising trajectory into structurally distinct phases, each governed by an independent threshold and a staleness-aware guard; (2) closed-loop threshold calibration that exploits counterfactual error measurement at the classifier-free guided output level to adjust decision boundaries online via an EMA feedback loop; and (3) momentum-augmented draft synthesis combining direction-magnitude gated residual extrapolation with anchor-guided unconditional correction. By transforming scheduling from a static risk accumulator into a feedback-driven, self-correcting controller, AlignCache consistently achieves superior acceleration-quality trade-offs across state-of-the-art video generation models. Our code is available at https://github.com/jiangjyjy/AlignCache.

cs.CV↗

DS-ProGen: A Dual-Structure Deep Language Model for Functional Protein Design

Inverse Protein Folding (IPF) is a critical subtask in the field of protein design, aiming to engineer amino acid sequences capable of folding correctly into a specified three-dimensional (3D) conformation. Although substantial progress has been achieved in recent years, existing methods generally rely on either backbone coordinates or molecular surface features alone, which restricts their ability to fully capture the complex chemical and geometric constraints necessary for precise sequence prediction. To address this limitation, we present DS-ProGen, a dual-structure deep language model for functional protein design, which integrates both backbone geometry and surface-level representations. By incorporating backbone coordinates as well as surface chemical and geometric descriptors into a next-amino-acid prediction paradigm, DS-ProGen is able to generate functionally relevant and structurally stable sequences while satisfying both global and local conformational constraints. On the PRIDE dataset, DS-ProGen attains the current state-of-the-art recovery rate of 61.47%, demonstrating the synergistic advantage of multi-modal structural encoding in protein design. Furthermore, DS-ProGen excels in predicting interactions with a variety of biological partners, including ligands, ions, and RNA, confirming its robust functional retention capabilities.

cs.CL↗