arXiv subjects

Tianfan Fu

Publications and source records attributed to Tianfan Fu.

At least 19 recordsLinked to original sources

arXiv2026

PACT: Certifying What Is Written in Parallel Decoding of Diffusion Language Models

Parallel decoding speeds up masked diffusion language models by writing several tokens per forward pass. Published commit rules choose these tokens by testing the predicted distributions. Under sampling the written tokens are drawn, and these tests do not see them. We find that answer quality follows the reliability of the tokens actually written. An answer's log probability splits into this reliability and the dependence within each step. We propose PACT, a training-free commit rule that draws the tokens first, certifies the set it will write and spaces the positions of each step apart. This certificate holds at every temperature, and we show that no rule with the same guarantee commits more positions. Experiments use four models of the LLaDA and Dream families and HumanEval, MBPP, GSM8K, MATH500 and IFEval benchmarks. PACT reaches the quality of published commit rules with fewer forward passes. Spacing removes positions from each step, yet it usually lowers the total cost because later steps then write more tokens. At the same speed, published decoders also write a word twice in a row far more often than PACT. These results suggest that commit rules should certify the tokens they write. Code is available at https://github.com/LiZaiyuan0619/PACT.

cs.CL↗

arXiv2026

ProteoCraft: Protein Design as Proposal-Verification Search

Protein-protein interactions underpin nearly all biological processes. Yet, designing proteins with desired interactions remains challenging due to the structural complexity governing molecular recognition. This study views protein design as a search optimization problem over a combinatorial sequence space under expensive structural evaluation. Toward this goal, we introduce a novel tree-based search framework, ProteoCraft, that employs approximate structural gradients from diffusion-based structure predictors as effective proposal policies to specify where the search should explore. Complete no-gradient inference of folding models separately assigns values to the resulting sequences, determining what is good. ProteoCraft allocates this verification budget through a coarse-to-fine paradigm: multi-site edits first explore distinct sequence basins, then verified promising states undergo strict single-site refinement. Across fourteen de novo binder-design settings spanning eight target proteins, five immune-relevant TCR-facing targets, and four localized CDR redesign tasks, ProteoCraft improves design quality and high-confidence yield. These improvements persist under independent AF2-IG and Rosetta-based interface evaluation. Prospective experimental validation further yielded an 82.9% binding hit rate for PD-L1 miniproteins, with a best measured KD of 0.879 nM, and confirmed binding of designed IFNAR2 VHH. Our code is available at https://github.com/smiles724/ProteoCraft_v1.

cs.CE↗

arXiv2026

RiboBridge: protein-conditioned de novo RNA binder structure design

Designing RNA molecules that bind to target protein structures requires generating both an RNA conformation and its bound complex geometry, without assuming a predefined binding site. Existing approaches generally model these coupled processes within a unified representation, entangling RNA conformation generation with protein-relative placement. In this work, we introduce RiboBridge, a structure-first framework that separates RNA conformational generation from protein--RNA assembly through cross-frame interaction geometry. RiboBridge first proposes multiple candidate RNA-binding interfaces on the protein surface, generates canonical RNA conformations within a pretrained RNA structural latent space (RiboSphere), and then predicts protein--RNA interaction constraints to bridge the independently defined RNA and protein coordinate frames. The resulting interaction geometry is converted into a geometrically consistent protein-relative pose through rigid placement. We evaluate RiboBridge on a temporally split, sequence-filtered, and redundancy-controlled benchmark of 124 protein--RNA complexes. Under post-hoc interface-correspondence evaluation, where native information is used only after generation to select among already generated predicted-pocket candidates, RiboBridge achieves the highest fNAT and DockQ and the lowest interface and ligand RMSDs among compared methods. Component ablations and stage-wise diagnostics further characterize the contributions of RNA conformational generation, interaction prediction, and rigid placement, identifying the main sources of complex-recovery error.

cs.LG↗

arXiv2026

RNA Design via Conditioned Flow Matching and Finite-Policy Reinforcement Learning

RNA design aims to identify sequences that fold into specified secondary structures. Existing methods formulate the task as target-specific search or conditional generation. However, natural RNA evolution proceeds through sequence variation and selection, with compensatory substitutions, whereas these methods do not explicitly model this process. To address this limitation, we propose a two-stage framework comprising RNA Inverse-Folding Flow (RNA-IFlow) and RNA-IFlow-RL. RNA-IFlow uses structure-conditioned Dirichlet Flow Matching to model coordinated variation across the sequence, while RNA-IFlow-RL maps the learned flow to a pairing-preserving finite policy and refines it with thermodynamic feedback. Our framework achieves leading performance on multiple benchmarks, reaching 85.19% Pass@1 on Rfam-27. Further analyses reveal thermodynamic gains, policy dynamics, and robustness across settings. Our work couples coordinated variation with thermodynamic selection, offering a novel paradigm for RNA design.

q-bio.BM↗

arXiv2026

MatToolBench: Benchmarking Multimodal Agents in Real-World Materials Science Workflows

Multimodal GUI agents have achieved impressive results on general software benchmarks, yet their ability to operate professional scientific software remains largely unexplored. In materials science, sparse domain-specific web data, specialized interfaces, and tacit workflow conventions create blind spots that general-purpose pretraining cannot readily bridge. We present MatToolBench, the first real-environment benchmark for evaluating multimodal GUI agents on professional materials science software, comprising 204 tasks across 10 tools in three modalities: GUI operation, OriginPro scripting, and code-based database queries, all executed inside a Windows 11 VM. Each task is decomposed into fine-grained sub-criteria by domain experts, enabling interpretable partial-credit scoring; the GUI component of our multi-level evaluation pipeline achieves an average F1 of 0.98. For OriginPro figure-generation tasks, we further conduct a human-LLM agreement study to validate the use of a multimodal judge for secondary aesthetic assessment. Our experiments show that strong performance on general benchmarks does not transfer to professional scientific workflows, and that this gap is not a visual-grounding problem alone: failures arise from domain-specific operational knowledge, sparse pretraining coverage of scientific software, weak cross-tool artifact handoff, and critical states exposed only visually. Even the best model reaches only 25% success rate on GUI tasks and 45% on code tasks. MatToolBench therefore serves as a challenging diagnostic benchmark and real-environment testbed for data-scarce, knowledge-intensive scientific workflows.

cs.AI↗

arXiv2026

Feedback-Calibrated Protein Optimization with Batch-Aligned Tail Arbitration

Protein optimization aims to discover high-fitness sequences under a limited experimental budget. Existing machine-learning methods use task-specific predictors, biological priors, or ranking-aware objectives to guide which variants are tested in the next experimental round. However, these methods cannot adapt to shifts in the reliability of predictive evidence as measurements accumulate and ensure the correct ranking of key high-fitness candidates. To address these challenges, we propose Batch-Aligned Tail Arbitration (BATA), which uses experimental feedback to adaptively combine prior-informed and task-specific rankings for next-batch selection, with calibration focused on the batch-aligned high-fitness region. Across measured GB1, PABP, and TrpB landscapes, BATA achieves the best mean task rank (1.67) in final best fitness after 480 measurements. Controlled comparisons further show task-dependent gains from high-fitness calibration and batch alignment. Our work introduces feedback-calibrated predictor arbitration, where experimental feedback dynamically determines how predictive evidence guides next-batch selection, opening a new direction for protein optimization.

cs.LG↗

arXiv2026

Equivariant Neural Primal-Dual Assignment for Maximum Common Edge Subgraphs

Maximum common edge subgraph (MCES) matching finds a partial vertex correspondence between two labeled graphs that preserves as many labeled edges as possible. Molecular similarity search requires matching many graph pairs, making the cost of repeated queries important. The strongest baseline attains accurate MCES solutions but trains a separate network for each pair. We introduce Equivariant Neural Primal-Dual Assignment (ENPDA), which learns a shared matching policy and applies it to new pairs without further training, answering queries roughly three orders of magnitude faster and recovering its training cost after a few dozen queries. The policy recomputes exact objective marginals for candidate matches and learns corrections and step sizes that update their scores. Target prices respond to competition when several source vertices favor the same target. Four update rounds and a Hungarian projection produce a partial one-to-one matching. We prove per-pair guarantees that hold for any network parameters. In exact arithmetic, reordering either graph permutes the assignment and price states, the projected matching is one-to-one, and repaired prices give a valid MCES upper bound. Subtracting the preserved-edge count bounds the optimality gap; combined with structural caps, these certificates prove global optimality for 60 of 291 native test pairs. On three molecular benchmarks with disjoint train/validation/test splits, ENPDA improves over an analytic counterpart with the same update and projection budget by 7.4-8.6 accuracy points; after one second of refinement search, 2.5-3 points of the gain remain. Transferred without fine-tuning to edge-deletion tasks from social and protein graphs, the policy gains 9.1-17.6 points over the analytic counterpart. When output matchings must keep aromatic rings intact, ENPDA recovers more reference bonds than the baselines on all three datasets.

cs.LG↗

arXiv2026

ChemMLLM: Chemical Multimodal Large Language Model

Recent years have seen rapid progress in multimodal large language models (MLLMs) in the field of chemistry. However, chemical MLLMs that can handle cross-modal understanding and generation remain underexplored. To fill this gap, we propose ChemMLLM, a unified chemical multimodal large language model for molecule understanding and generation. In this work, we design five types of multimodal tasks across text, molecular SMILES strings and images, and curate the datasets. We benchmark ChemMLLM against a range of general leading MLLMs, Chemical LLMs and specialized models on these tasks. Experimental results show that ChemMLLM achieves superior performance among general-purpose MLLMs and close performance to specialized models across all evaluated tasks. Our work extends the capabilities of chemical multimodal large language models to the realm of image generation, demonstrating the feasibility of unifying multiple cross-modal chemical tasks within a single foundation model and enabling more intuitive, visual human-AI interaction.

cs.LG↗

arXiv2026

ClinicalReTrial: Clinical Trial Redesign with Self-Evolving Agents

Clinical trials constitute a critical yet exceptionally challenging and costly stage of drug development (\$2.6B per drug), where protocols are encoded as complex natural language documents, motivating the use of AI systems beyond manual analysis. Existing AI methods accurately predict trial failure, but do not provide actionable remedies. To fill this gap, this paper proposes ClinicalReTrial, a multi-agent system that formulates clinical trial optimization as an iterative redesign problem on textual protocols. Our method integrates failure diagnosis, safety-aware modifications, and candidate evaluation in a closed-loop, reward-driven optimization framework. Serving the outcome prediction model as a simulation environment, ClinicalReTrial enables low-cost evaluation and dense reward signals for continuous self-improvement. We further propose a hierarchical memory that captures iteration-level feedback within trials and distills transferable redesign patterns across trials. Empirically, ClinicalReTrial turns 56.7% of failed protocols into predicted successes under the simulation environment, with a mean success probability gain of 7.4% at negligible cost (\$0.156 per trial). Extensive retrospective case studies further show that ClinicalReTrial recovers clinically meaningful modification patterns that align with real-world expert-driven protocol changes.

cs.AI↗

arXiv2026

Compute Allocation for Self-Evolving LLMs: From Depth-Breadth to Multi-Armed Bandits

LLM-guided evolutionary search (Evolve systems) has reached state-of-the-art results on mathematical and combinatorial tasks, yet most existing systems report only the best of many runs and leave the run-to-run distribution undocumented. We ask how a fixed budget of LLM calls should be allocated, and how reliably a single run reaches the reported numbers. Sweeping the depth-breadth grid over five models and three tasks, we identify two empirical regularities: a fitness-compute envelope along which capability ordering largely collapses when measured in effective FLOPs, and a bilinear depth-breadth fit with task-specific interaction; both are gated by model-task capability. Motivated by these regularities, we propose BaSE (Bandit-based Self-Evolving), a multi-armed bandit that allocates LLM calls across parallel trajectories. Without changing the model, prompt, or evaluator, BaSE improves mean fitness by 12.3% over the strongest island-protocol baseline across 8 (model, task) cells, with the largest gains on high-variance settings: a reliability gain from allocation alone.

cs.CL↗

arXiv2026

AgentFold: Closed-Loop Agentic Search for Protein Folding Model Design

Scientific LLM agents have shown promise in literature reasoning, tool use, and experiment planning, but it remains unclear whether they can autonomously improve large, tightly coupled scientific machine-learning systems through executable code changes and computationally expensive validation. We study this question in protein folding, where progress requires coordinated architectural modifications, multi-objective evaluation, and domain-aware interpretation. We present AgentFold, a multi-agent framework that formulates folding-model development as a closed-loop search over executable code variants. Starting from ESMFold, AgentFold proposes hypotheses, implements and debugs code-level modifications, evaluates model variants, analyzes experimental outcomes, and stores both successful and failed interventions in structured memory. An MCTS-style policy allocates computational resources across high-scoring search branches. On an engineering-scale protein-folding codebase comprising more than 2,000 lines of code, AgentFold explores approximately 80 model variants using approximately 5,000 GPU-hours and 170 million LLM tokens. Under a matched computational budget, AgentFold improves the best lDDT by 7.5% over independent Codex proposals and outperforms a random-search control. Beyond model improvement, the resulting intervention traces reveal recurring empirical design patterns: stable gains tend to arise from early, soft, learnable priors and gated refinement, whereas direct geometric perturbations and geometry-conditioned feedback often destabilize training. The code and experimental resources are publicly available at https://github.com/lmqfly/AgentFold.

cs.AI↗

arXiv2026

CAi Copilot: Reducing Operational Workload in Molecular Design through Intent-Driven Agentic Workflows

Early-stage molecular design is an iterative process, not just a task of generating molecules. Researchers turn broad goals into design strategies, refine candidates, assess many properties, and gather evidence before synthesis and tests. AI methods can generate molecules, optimize several goals, predict properties, dock compounds, and account for synthesis. Yet these functions are spread across specialized tools. Experts must still coordinate each step, judge interim results, and integrate evidence. The central challenge is thus to turn research intent into adaptive, traceable runs grounded in scientific tools. We cast this challenge as intent-to-evidence molecular design workflow execution and present CAi Copilot, an expert-oriented agent with three linked layers. The Research Interface Layer turns intent into an executable plan. The Agent Reasoning Layer uses interim results to guide each run. The Execution Substrate supplies molecular tools, metrics, reusable utilities, and backend services. Across 45 tasks, CAi achieves the strongest overall performance, with an outcome score of 84.59, exceeding the next-best result by 18.07 points. Additional benchmarks test how CAi coordinates generation, screening, and multi-criteria evaluation, while exposing limits in long-horizon execution. These results show that CAi turns broad molecular-design intent into transparent, traceable workflows that connect interim decisions to candidate-level evidence.

cs.AI↗

arXiv2026

RiboSphere: Learning Unified and Efficient Representations of RNA Structures

Accurate RNA structure modeling remains difficult because RNA backbones are highly flexible, non-canonical interactions are prevalent, and experimentally determined 3D structures are comparatively scarce. We introduce RiboSphere, a framework that learns discrete geometric representations of RNA by combining vector quantization with flow matching. Our design is motivated by the modular organization of RNA architecture: complex folds are composed from recurring structural motifs. RiboSphere uses a geometric transformer encoder trained using mean-centered coordinates and random rotation augmentation to produce geometry-aware features, which are discretized with finite scalar quantization (FSQ) into a finite vocabulary of latent codes. Conditioned on these discrete codes, a flow-matching decoder reconstructs atomic coordinates, enabling high-fidelity structure generation. We find that the learned code indices are enriched for specific RNA motifs, suggesting that the model captures motif-level compositional structure rather than acting as a purely compressive bottleneck. Across benchmarks, RiboSphere achieves strong performance in structure reconstruction (RMSD 1.25,Å, TM-score 0.84), and its pretrained discrete representations transfer effectively to inverse folding and RNA--ligand binding prediction, with robust generalization in data-scarce regimes. Code is available at https://github.com/Zhangz312/RiboSphere.

cs.LG↗

arXiv2026

Data-DPO: Direct Preference Optimization for Target Model Data Selection in LLM Post-Training

Data selection in supervised fine-tuning aims to select a small set of effective samples from large-scale candidate data, reducing training cost while preserving model performance. However, existing methods usually treat data value as a relatively static property, and pay limited attention to the compatibility between data and the capability distribution of the target model. To address this issue, we propose Data-DPO, a target model-oriented SFT data selection method. Data-DPO observes the local training feedback of the target model on different samples through one-step probing, transforms activation differences among samples into pairwise data preferences, and trains a lightweight reward model to learn target-model-aware data preferences. In the final selection stage, Data-DPO further combines target model preference, external quality scores, and marginal diversity to construct a more stable and effective training subset. Experimental results on Vision-Flan and LLaVA-CoT show that Data-DPO consistently outperforms existing data selection baselines under multiple data budgets and stably surpasses full data training performance.

cs.LG↗

arXiv2026

Hierarchical Data Selection via Manifold Coverage and Sparse Feature Coverage in LLM Post-training

As supervised fine-tuning data continues to scale, selecting high-value subsets from large candidate pools is crucial for reducing training cost and improving model performance. Existing methods often measure diversity directly in the original embedding space, where geometric metrics entangle dominant semantic directions, fine-grained supervision differences, and local noise. We address this limitation by formulating data selection as a coarse-to-fine hierarchical coverage problem and propose MASS. MASS learns low-dimensional principal manifold coordinates with a dense autoencoder for coarse semantic grouping, and then performs quality-aware sparse feature coverage within each group using a TopK sparse autoencoder. Experiments on Vision Flan and LLaVA-CoT show that MASS consistently outperforms strong data selection baselines across multiple budgets, and in several settings matches or surpasses full data training with only a small subset of data.

cs.LG↗

arXiv2026

Reachability Is Not Realization: Tracing the Sources of LLM Benchmark Gains

Benchmark gains are often treated as evidence of greater LLM capability. Yet the same gain can reflect different changes in model behavior. A model may reach new answers, or produce answers that were already within reach. Aggregate scores do not distinguish these changes question by question. We establish a question-level audit under fixed budgets, temperatures, and answer formats. A question is realized when the default deployment procedure produces the correct answer. A question is reachable when a specified probe finds that answer within a fixed budget. We first test whether inference-time layer routing can expand reachability. Under a matched budget, random routes match or exceed structured search in all 43 model and task settings. Answer-blind procedures retain almost none of this gain, which instead requires access to the correct answer. We then ask why reachable answers sometimes fail to appear. Across six cases spanning 0.5B to 31B, silencing one identified MLP block repairs 68 to 92 percent of a predefined failure set. We next test whether training closes the gap by expanding reachability. In five of six matched evaluations, deployed performance rises while the reachable ceiling remains flat or falls. For DAPO, the deployed score rises by 14.7 points while the reachable ceiling falls by 13.3 points. Across the settings we audit, realization and reachability therefore do not always change together. Claims of capability expansion should report both realized performance and reachability under matched evaluation conditions. Code is available at https://github.com/LiZaiyuan0619/reachability-not-realization

cs.AI↗

arXiv2026

Disagree to Accelerate: Closing the Loop on Diffusion Feature Forecasts

Training-free feature forecasting accelerates diffusion sampling by predicting features at skipped denoising steps. Recent work has mainly focused on designing stronger forecasters. Yet forecast error varies sharply across steps, and open-loop caches trust the forecast in full at every skipped step. This fixed trust is what breaks as acceleration turns aggressive. The missing question is not only how to forecast better, but when and how much to trust a forecast. We show that reliability can be observed from the cache itself. Two forecasts agree where the feature trajectory is smooth, and they diverge where prediction turns hard. Their disagreement is a cheap runtime signal, and it costs no extra denoiser evaluation. Based on this signal, we introduce RACER, a training-free closed-loop controller with two responses. It continuously shrinks uncertain forecasts toward the last computed feature. At the riskiest steps, RACER refreshes the feature and repays the added evaluation by skipping a later scheduled one. We derive a deterministic error bound for the shrinkage and empirically evaluate its validity and tightness across acceleration regimes. At the same number of denoiser evaluations, RACER improves the strongest open-loop baseline across SD3.5-Large, FLUX.1-dev, Wan2.1-14B, and HunyuanVideo on DrawBench, VBench, and COCO. On SD3.5, we further show that RACER samples faster at equal quality. RACER generalizes across forecasting designs as well. For example, it recovers much of the quality lost on a Taylor base. These results show that reliable diffusion acceleration also depends on how forecasts are used. Code is available at https://github.com/LiZaiyuan0619/RACER

cs.LG↗

arXiv2026

ABOPD: Antibody CDR Design via On-Policy Distillation

Antibodies are essential therapeutic molecules, and their complementarity-determining regions (CDRs) form the primary antigen-recognition interface. Recent protein generative models have demonstrated broad capabilities in biomolecular design, yet post-training strategies for downstream objectives remain limited. Standard denoising training operates on noisy states obtained by perturbing native structures, whereas recursive generation proceeds through model-generated intermediate states. For flexible antibody CDR loops such as CDR-H3, this mismatch can allow backbone deviations to accumulate along the denoising trajectory and compromise antigen-facing loop geometry. We introduce ABOPD, an antibody design framework based on on-policy distillation that leverages privileged native geometry during training to supervise states visited along the model's own denoising trajectories. With this fine-grained structural supervision, ABOPD substantially improves structural recovery on RAbD CDR-H3 generation, reducing RMSD by 0.42 Å (from 2.37 Å to 1.95 Å) and outperforming supervised fine-tuning and offline distillation controls, offering a path to higher-fidelity protein design.

cs.LG↗