Yu Wang

Zhenchao Tang, Fang Wang, Haohuai He et al.

Effective post-training is essential to align Large Language Models (LLMs) with specialized biomedical knowledge to accelerate life science research. However, current approaches face significant limitations. First, biomedical reasoning involves intricate mechanisms often represented by sparse textual data. Standard Supervised Fine-Tuning (SFT) tends to overfit to surface-level instruction patterns without effectively internalizing this fragmented scientific knowledge. Second, Reinforcement Learning (RL) is impractical for this domain, as defining meaningful rewards often necessitates prohibitive experimental validation (e.g., wet-lab verification of drug responses), rendering real-time feedback unfeasible. We propose Balanced Fine-Tuning (BFT), an efficient post-training method designed to learn complex reasoning from sparse data without external reward signals. BFT operates through a two-layer weighting mechanism: 1. At the token level, it scales loss via prediction probabilities to stabilize gradients and prevent overfitting; 2. At the sample level, it uses "minimum group confidence" to adaptively enhance the learning of hard samples. Experiments demonstrate that BFT significantly outperforms SFT. In medical tasks, it enables LLMs to acquire knowledge that SFT misses. In biological tasks, BFT-based LLMs surpass GeneAgent (an accurate agent for biology analysis) in biological process reasoning. Moreover, the text embeddings generated by BFT can be directly applied to downstream tasks, such as gene interaction and single-cell perturbation response prediction. These results indicate that BFT facilitates broad applications of LLMs in biomedical research.

Enshu Liu, Xuefei Ning, Huazhong Yang et al.

Recent years have witnessed the rapid progress and broad application of diffusion probabilistic models (DPMs). Sampling from DPMs can be viewed as solving an ordinary differential equation (ODE). Despite the promising performance, the generation of DPMs usually consumes much time due to the large number of function evaluations (NFE). Though recent works have accelerated the sampling to around 20 steps with high-order solvers, the sample quality with less than 10 NFE can still be improved. In this paper, we propose a unified sampling framework (USF) to study the optional strategies for solver. Under this framework, we further reveal that taking different solving strategies at different timesteps may help further decrease the truncation error, and a carefully designed \emph{solver schedule} has the potential to improve the sample quality by a large margin. Therefore, we propose a new sampling framework based on the exponential integral formulation that allows free choices of solver strategy at each step and design specific decisions for the framework. Moreover, we propose $S^3$, a predictor-based search method that automatically optimizes the solver schedule to get a better time-quality trade-off of sampling. We demonstrate that $S^3$ can find outstanding solver schedules which outperform the state-of-the-art sampling methods on CIFAR-10, CelebA, ImageNet, and LSUN-Bedroom datasets. Specifically, we achieve 2.69 FID with 10 NFE and 6.86 FID with 5 NFE on CIFAR-10 dataset, outperforming the SOTA method significantly. We further apply $S^3$ to Stable-Diffusion model and get an acceleration ratio of 2$\times$, showing the feasibility of sampling in very few steps without retraining the neural network.