Lu Zhang

Xutian Li, Yifeng Zhu, Xianlin Zhao et al.

Large language models (LLMs) are increasingly used for software evolution, yet most interaction paradigms remain code-centric and require manual context management and prompt iteration. We present FeatX, a feature-oriented tool for editing software by editing features. Given an existing repository, FeatX extracts a hierarchical epic-feature structure with explicit feature-to-code mappings, then invokes a three-stage Evolution Agent to translate feature edits into code patches. The workflow is exposed through four coordinated panels. Across a controlled user study and replay experiments on 38 real-world feature-editing commits, FeatX significantly reduces cognitive load and improves usability compared with vanilla ChatGPT. It also achieves a 42.6\% relative improvement in function-level modification localization F1 over strong LLM baselines, at substantially lower cost (\$0.07 in total). The tool and collected dataset are available at https://github.com/a496263365/FeatX/tree/demo, with a demonstration video at https://youtu.be/OZqKZ4Ii-yM.

Davy Guan, Lu Zhang, Asiri Wijesinghe et al.

Predicting biomolecular properties from limited labeled data is a central bottleneck in protein engineering and small-molecule design. As strong pretrained encoders now supply rich fixed-length representations, the difficulty has shifted from representation learning to building a data-efficient predictor for the few-shot regime. Tabular foundation models such as TabPFN3 and TabICL are unlikely candidates for this role: they are in-context learners pretrained on synthetic tables drawn from random causal graphs, a generative prior with no obvious correspondence to the processes that produce protein sequences or molecular graphs. That this tabular, causal inductive bias should transfer to biomolecular data at all is unintuitive, yet we find it does. Treating each method as a predictor-representation pair, we evaluate across two domains. Over a fixed ESMC representation, tabular in-context learning is consistently competitive for protein fitness regression on ProteinGym and a diverse esterase dataset. For small-molecule classification with ECFP/RDKit descriptors, no single pairing dominates across TDC ADMET, MoleculeNet, FS-Mol, and DrugOOD; representation choice becomes a primary determinant, as expected when the predictor's own prior is indifferent to molecular structure. We conclude that tabular foundation models are strong performers on biomolecular prediction tasks, but that their performance depends strongly on the sequence or molecular representation used.