GenoArmory: A Unified Evaluation Framework for Adversarial Attacks on Genomic Foundation Models
Haozheng Luo, Chenghao Qiu, Yimin Wang, Shang Wu, Jiahao Yu, Zhenyu Pan, Weian Mao, Haoyang Fang, Hao Xu, Han Liu, Binghui Wang, Yan Chen
TL;DR
GenoArmory tackles the safety and robustness of Genomic Foundation Models by delivering a unified benchmark that standardizes adversarial attacks and defenses across multiple GFMs. It introduces GenoAdv as a representative adversarial dataset, provides robust pipelines for red-teaming and defense evaluation, and delivers a reproducible framework with visualization to interpret perturbation effects in genomic sequences. Key findings show that generative GFMs (e.g., GenomeOcean) are more vulnerable than classification-focused GFMs, and that tokenization strategy (e.g., BPE vs. k-mer) and quantization materially influence attack efficacy and defense performance. The work significantly impacts the safe deployment of GFMs by enabling systematic assessment, fostering defense development, and promoting transparent, reproducible genomic AI research.
Abstract
We propose the first unified adversarial attack benchmark for Genomic Foundation Models (GFMs), named GenoArmory. Unlike existing GFM benchmarks, GenoArmory offers the first comprehensive evaluation framework to systematically assess the vulnerability of GFMs to adversarial attacks. Methodologically, we evaluate the adversarial robustness of five state-of-the-art GFMs using four widely adopted attack algorithms and three defense strategies. Importantly, our benchmark provides an accessible and comprehensive framework to analyze GFM vulnerabilities with respect to model architecture, quantization schemes, and training datasets. Additionally, we introduce GenoAdv, a new adversarial sample dataset designed to improve GFM safety. Empirically, classification models exhibit greater robustness to adversarial perturbations compared to generative models, highlighting the impact of task type on model vulnerability. Moreover, adversarial attacks frequently target biologically significant genomic regions, suggesting that these models effectively capture meaningful sequence features.
