Machine translation systems are periodically upgraded to stronger models, but the available preference signal is human post-edits of an older system’s outputs, which the newer model may already surpass. Moreover, collecting fresh post-edits for every new model is prohibitively expensive. We call this the Stale Preference problem. Standard DPO can fail in this setting: it may increase the likelihood of inferior post-edits, erode the model’s existing quality, and fail to provide the per-token control needed to correct localized errors. We introduce StalePO, an objective derived from three requirements this regime imposes. Likelihood movement must be downward on both responses, the policy must be anchored to its own base response, and the KL constraint must apply at the token level. These requirements are jointly necessary. In ablations, each mechanism in isolation leaves the model’s performance indistinguishable from the base model, and only their combination converts stale feedback into gains. On English-to-Hindi and English-to-Turkish localization data, StalePO improves the fraction of segments passing all LLM-as-judge MQM quality checks by 14.9 and 4.6 percentage points, respectively, with gains concentrated on style and fluency. A human evaluation under the same framework confirms these gains on English-to-Hindi, raising the fraction of segments passing all seven human checks by 13.8 percentage points.

Large-scale machine-translation (MT) systems are typically evaluated on random samples from a corpus whose distributional composition is an artifact of how it was assembled. Such a sample inherits the phenomena the collection happens to contain rather than the full space a system must handle, spanning rule-governed conventions (terminology, punctuation, currency formatting) and context-dependent phenomena (tone, honorifics, document-level coherence), and thus provides no coverage guarantee for assessing robustness. We propose TACTICS (Taxonomy-Aware Coverage-opTimized Intelligent Corpus Sampling), which recasts coverage as an explicit objective. TACTICS induces a hierarchical taxonomy from a locale style guide, classifies segments against it, and selects a fixed-budget subset jointly optimizing coverage of rare categories, document-level coherence, and distributional fidelity to the full corpus. Applied to MT evaluation across four translation directions, TACTICS improves coverage of rare categories over lexical and embedding-based selection. By targeting the phenomena that separate systems, TACTICS makes a fixed evaluation budget go further, recovering the true system ranking from far fewer segments than random sampling wherever a real quality gap exists and never signaling a difference where none exists.

Bi-encoder architectures for biomedical entity linking learn flat embedding spaces that ignore ontology structure. HiCo-EL encodes hierarchical knowledge into bi-encoder representations through hierarchical contrastive pretraining. The core idea is within-space hierarchical multi-label contrastive learning (HMLC): contrastive losses applied independently within each encoder space, preserving cross-space compatibility for retrieval. Our formulation drops the monotonicity constraints of prior HMLC work, handles variable-depth hierarchy paths, and adds depth-weighted alignment between encoder spaces. Treating each entity as a leaf node unifies coarse type structure with fine-grained entity discrimination. On MedMentions and NCBI Disease, HiCo-EL outperforms ArboEL by +3.7% and +1.8% Recall@1 respectively. The gains reveal a key insight: breadth amplifies, depth generalizes—broad hierarchies help common entities most (+6.3% R@1), while deep hierarchies benefit unseen entities (+9.6% R@1 zero-shot).

Biomedical entity linking (BioEL) is the process of connecting entities referenced in documents to entries in biomedical databases such as the Unified Medical Language System (UMLS) or Medical Subject Headings (MeSH). The study objective was to comprehensively evaluate nine recent state-of-the-art biomedical entity linking models under a unified framework. We compare these models along axes of (1) accuracy, (2) speed, (3) ease of use, (4) generalization, and (5) adaptability to new ontologies and datasets. We additionally quantify the impact of various preprocessing choices such as abbreviation detection. Systematic evaluation reveals several notable gaps in current methods. In particular, current methods struggle to correctly link genes and proteins and often have difficulty effectively incorporating context into linking decisions. To expedite future development and baseline testing, we release our unified evaluation framework and all included models on GitHub at https://github.com/davidkartchner/biomedical-entity-linking