Flint Xiaofeng Fan, Cheston Tan, Yew-Soon Ong +1cs.AI cs.LG
Radiology reports describe findings and locations in free text, but downstream search and analysis require these relations in a fixed schema. Learning this extraction requires labels that are unevenly distributed across institutions: smaller hospitals have less local evidence, and pooling data may be infeasible. We introduce FedPref: frozen public language models propose alternative JSON extractions, local annotations rank them, and sites collaboratively train compact Qwen3-8B adapters while sharing only model updates. A heterogeneous teacher pool provides cross-model contrast when repeated single-model samples collapse. On development data from six simulated hospitals with unequal data volume and disease prevalence, FedPref improves client-mean F1 by 2.49 points and worst-site F1 by 9.10 points compared with training each site in isolation, with the largest gains at the sites holding the least data. Central training on the pooled preference-pair union is 2.66 points higher on client-mean F1. On a locked, 400-report manually validated gold test set, FedPref reaches 68.68 F1 and pooled training 71.67, preserving that same ordering. FedPref thus lets institutions with unequal, unpooled data benefit from collaboration without ever sharing reports or annotations.
Antibody expression ranking is a critical task in antibody design, yet its modelling is severely hindered by the scarcity of labeled experimental data. To address this, we propose a unified preference-based learning framework that integrates scarce quantitative expression data with large-scale weak positive supervision from immunization data. We adapt Direct Preference Optimization (DPO) to protein language models by introducing a union-masked log-likelihood approximation and IMGT-based alignment, enabling efficient training on variable-length sequences. Evaluating on a diverse internal dataset of 1254 labeled sequences and 4 million unlabeled camelid-derived antibodies, we show that our method consistently outperforms baselines on most metrics. Our results demonstrate that preference learning can effectively learn from weak supervision, providing a scalable solution for antibody expressibility optimization in data-constrained settings. Project page: https://kisoji-biotechnology-inc.github.io/Preference-Expression-Ranking/.
Prabhjot Singh, Abhishek Gupta, Chris Betz +4cs.LG cs.AI
We reframe clinician overrides of clinical AI recommendations as implicit preference data - the same signal structure exploited by reinforcement learning from human feedback (RLHF), but richer: the annotator is a domain expert, the alternatives carry real consequences, and downstream outcomes are observable. We present a formal framework extending standard preference learning with three contributions: a five-category override taxonomy mapping override types to distinct model update targets; a preference formulation conditioned on patient state s, organizational context c, and clinician capability kappa, where kappa decomposes into execution capability kappa-exec and alignment capability kappa-align; and a dual learning architecture that jointly trains a reward model and a capability model via alternating optimization, preventing a failure mode we term suppression bias-the systematic suppression of correct-but-difficult recommendations when clinician capability falls below the execution threshold. We argue that chronic disease management under outcome-based payment contracts produces override data with uniquely favorable properties-longitudinal density, concentrated decision space, outcome labels, and natural capability variation-and that training environments combining longitudinal outcome measurement with aligned financial incentives are a necessary condition for learning a reward model aligned with patient trajectory rather than with encounter economics. This framework emerged from operational work to improve clinician capability in a live value-based care deployment.