BRACE: Taming Sharp Irregularities via Barycentric Rational Forecasting for Fast Diffusion Transformers Inference

Diffusion Transformers (DiTs) have demonstrated exceptional performance in high-fidelity image and video generation. To alleviate their massive computational overhead, temporal feature caching has been proposed to bypass redundant computations. However, existing cache-then-forecast methods driven by derivative-based polynomials often cause severe quality degradation under high acceleration due to unstable long-step predictions. To address this bottleneck, we propose Barycentric Rational Forecasting with Chebyshev Enhancement (BRACE). Motivated by the observation that DiT feature trajectories are globally smooth yet frequently exhibit sharp irregularities and local non-smoothness, BRACE shifts the paradigm from derivative-driven polynomial extrapolation to feature-driven rational forecasting. Specifically, it maintains a local sliding window to cache sparse historical features and leverages adapted Chebyshev weights to formulate a barycentric rational function, directly aggregating these raw features to ensure numerical stability. Extensive experiments demonstrate that BRACE achieves state-of-the-art quality-efficiency trade-offs across various DiT architectures with negligible computational overhead.

scGTN: Deep Siamese Graph Transformer Network for Single-cell RNA Sequencing Clustering

Single-cell RNA sequencing (scRNA-seq) serves a pivotal role in characterizing gene expression at the cellular level, enabling the identification of cell types and advancing the understanding of cellular heterogeneity. Despite the significant progress in scRNA-seq data clustering, we argue that current methods always ignore the sparsity and noise, as well as the complex intercellular structural information inherent in scRNA-seq data. Toward this end, in this paper, we propose a novel single-cell RNA-seq clustering framework via deep Siamese Graph Transformer Network (termed scGTN), which explicitly integrates gene expression profile and intercellular structural dependencies for cell clustering. In particular, we formulate scRNA-seq data as a graph and construct two augmented graph views that serve as dual views to capture complementary intercellular information. Then, a Siamese graph transformer network is employed to explicitly incorporate shortest-path information and node-wise distances for capturing richer structural relationships between cells. Finally, we employ an optimal transport strategy to guide the cell clustering in a self-supervised manner. Extensive experiments on multiple benchmark scRNA-seq datasets demonstrate that our scGTN consistently outperforms existing methods. Our code is available at https://github.com/W-RMSL/scGTN.