Jiaxin Liu

Zenan Huang, Yihong Zhuang, Guoshan Lu et al.

Reinforcement Learning from Verifiable Rewards (RLVR) has emerged as a powerful paradigm for enhancing Large Language Models (LLMs), exemplified by the success of OpenAI's o-series. In RLVR, rewards are derived from verifiable signals-such as passing unit tests in code generation or matching correct answers in mathematical reasoning. While effective, this requirement largely confines RLVR to domains with automatically checkable outcomes. To overcome this, we extend the RLVR paradigm to open-ended tasks by integrating rubric-based rewards, where carefully designed rubrics serve as structured, model-interpretable criteria for automatic scoring of subjective outputs. We construct, to our knowledge, the largest rubric reward system to date, with over 10,000 rubrics from humans, LLMs, or a hybrid human-LLM collaboration. Implementing rubric-based RL is challenging; we tackle these issues with a clear framework and present an open-sourced Qwen-30B-A3B model with notable gains: 1) With only 5K+ samples, our system improves by +5.2% on open-ended benchmarks (especially humanities), outperforming a 671B DeepSeek-V3 model by +2.4%, while preserving general and reasoning abilities. 2) Our method provides fine-grained stylistic control, using rubrics as anchors to mitigate the "AI-like" tone and produce more human-like, expressive responses. We share key lessons in rubric construction, data selection, and training, and discuss limitations and future releases.

Yiting Wei, Bingo Wing-Kuen Ling, Qing Liu et al.

Diabetes is a serious chronic metabolic disease. In the recent years, more and more consumer technology enterprises focusing on human health are committed to implementing accurate and non-invasive blood glucose algorithm in their products. However, due to the interference from the external environment, these wearable non-invasive methods yield the low estimation accuracy. To address this issue, this paper employs different models based on different ranges of the blood glucose values for performing the blood glucose estimation. First the photoplethysmograms (PPGs) are acquired and they are denoised via the bit plane singular spectrum analysis (SSA) method. Second, the features are extracted. For the data in the training set, first the features are averaged across the measurements in the feature domain via the optimization approach. Second, the random forest is employed to sort the importance of each feature. Third, the training set is divided into three subsets according to the reference blood glucose values. Fourth, the feature vectors and the corresponding blood glucose values in the same group are employed to build an individual model. Fifth, for each feature, the average of the feature values for all the measurements in the same subset is computed. For the data in the test set, first, the sum of the weighted distances between the test feature values and the average values obtained in the above is computed for each model. Here, the weights are defined based on the importance sorted by the random forest obtained in the above. The model corresponding to the smallest sum is assigned. Finally, the blood glucose value is estimated based on the corresponding model. Compared to the state of arts methods, our proposed method can effectively improve the estimation accuracy.