GRNFormer: A Biologically-Guided Framework for Integrating Gene Regulatory Networks into RNA Foundation Models

Foundation models for single-cell RNA sequencing (scRNA-seq) have shown promising capabilities in capturing gene expression patterns. However, current approaches face critical limitations: they ignore biological prior knowledge encoded in gene regulatory relationships and fail to leverage multi-omics signals that could provide complementary regulatory insights. In this paper, we propose GRNFormer, a new framework that systematically integrates multi-scale Gene Regulatory Networks (GRNs) inferred from multi-omics data into RNA foundation model training. Our framework introduces two key innovations. First, we introduce a pipeline for constructing hierarchical GRNs that capture regulatory relationships at both cell-type-specific and cell-specific resolutions. Second, we design a structure-aware integration framework that addresses the information asymmetry in GRNs through two technical advances: (1) A graph topological adapter using multi-head cross-attention to weight regulatory relationships dynamically, and (2) a novel edge perturbation strategy that perturb GRNs with biologically-informed co-expression links to augment graph neural network training. Comprehensive experiments have been conducted on three representative downstream tasks across multiple model architectures to demonstrate the effectiveness of GRNFormer. It achieves consistent improvements over state-of-the-art (SoTA) baselines: $3.6\%$ increase in drug response prediction correlation, $9.6\%$ improvement in single-cell drug classification AUC, and $1.1\%$ average gain in gene perturbation prediction accuracy.

Symbiotic Cooperation for Web Agents: Harnessing Complementary Strengths of Large and Small LLMs

Web browsing agents powered by large language models (LLMs) have shown tremendous potential in automating complex web-based tasks. Existing approaches typically rely on large LLMs (e.g., GPT-4o) to explore web environments and generate trajectory data, which is then used either for demonstration retrieval (for large LLMs) or to distill small LLMs (e.g., Llama3) in a process that remains decoupled from the exploration. In this paper, we propose AgentSymbiotic, an iterative framework that couples data synthesis with task-performance, yielding a "symbiotic improvement" for both large and small LLMs. Our study uncovers a complementary dynamic between LLM types: while large LLMs excel at generating high-quality trajectories for distillation, the distilled small LLMs-owing to their distinct reasoning capabilities-often choose actions that diverge from those of their larger counterparts. This divergence drives the exploration of novel trajectories, thereby enriching the synthesized data. However, we also observe that the performance of small LLMs becomes a bottleneck in this iterative enhancement process. To address this, we propose two innovations in LLM distillation: a speculative data synthesis strategy that mitigates off-policy bias, and a multi-task learning approach designed to boost the reasoning capabilities of the student LLM. Furthermore, we introduce a Hybrid Mode for Privacy Preservation to address user privacy concerns. Evaluated on the WEBARENA benchmark, AgentSymbiotic achieves SOTA performance with both LLM types. Our best Large LLM agent reaches 52%, surpassing the previous best of 45%, while our 8B distilled model demonstrates a competitive 49%, exceeding the prior best of 28%. Code will be released upon acceptance.