An output-only black-box attack on Evo 2 is presented that selects convergent groups of repeated generations without gradients, token likelihoods, or training-corpus access during candidate selection, establishing convergence among repeated nucleotide generations as a practical output-only signal for recovering long training-sequence segments.
Abstract
Genomic language models generate long nucleotide continuations from short prefixes, exposing a direct route for studying training-sequence extraction through the generation interface. We present an output-only black-box attack on Evo 2 that selects convergent groups of repeated generations without gradients, token likelihoods, or training-corpus access during candidate selection. Recovered content is then scored by an evaluator combining aligned length, nucleotide identity, match multiplicity, and sequence complexity. Across 304 runs on Evo 2 7B with bacteriophage and plasmid prefixes, the attack yields 888 candidate clusters, of which 85 match training segments of at least 500 bp, giving a cluster-level attack success rate of 9.57%. Final filtering retains 22 uniquely matched extraction events at the 500-bp threshold and 15 at 1,000 bp, covering 14 and 7 distinct training-sequence regions, respectively. Within-category source-homology screening retains 11 of the 22 events at a 99% exclusion threshold and four at 98%, with the latter mapping to two reference regions. The results establish convergence among repeated nucleotide generations as a practical output-only signal for recovering long training-sequence segments and characterize how recovery depends on prefix length, cluster size, perplexity, early stopping, and sequence domains.
Protein foundation models increasingly support the generation of novel biological sequences, yet their reliance on large public datasets creates opportunities for adversarial manipulation of the material they learn from and retrieve. We investigate two data-only poisoning attacks against protein design systems, targeti...
Charalampos Koilakos, K. Provatas, Michail Patsakis et al.· 0 citations
This work introduces ZEST (Zoned Encoding of Sequence Traits), an evolution-informed vocabulary derived from conserved regions of multiple sequence alignments that demonstrates that evolution-informed tokenization can substitute for massive parameter scaling, opening a new direction for efficient, biologically-grounded...
Biswajit Banerjee, Claudia A. Carreno, Anton S. Petrov· 0 citations
The genome holds the blueprint that governs the biological properties of the cell. Consequently, advancing our knowledge of genomic function is crucial both for a broader understanding of biology and for continued biomedical advances. The success of large language models on natural language and protein sequences has mo...
F. I. Marin, Panagiotis Antoniadis, Dionysia Danai Brilli et al.· 0 citations
PHACTn (Phylogeny-Aware Computing of Tolerance for nucleotide variants), a training-free, parameter-minimal method that infers nucleotide variant tolerability by traversing the mammalian phylogenetic tree and explicitly modeling the evolutionary independence of observed substitutions and their distance from the query s...
Ceren Yıldırım, Nurdan Kuru, Ogun Adebali· bioRxiv· 0 citations
An open-source, end-to-end pipeline is built to simulate LLM performance in a hypothetical scenario where they were available to inform COVID-19 models developed during the first four months of 2020, and shows that current models can extract transmission parameters from unstructured literature accurately enough to info...
X. Yang, C. Y. Lee, B. Quilty et al.· medRxiv· 0 citations
Base editors install single-nucleotide substitutions without a double-strand break or donor template, but editing at multiple susceptible positions can generate bystander alleles. Predicting the frequency of an intended outcome therefore requires both editing efficiency and the composition of edited products. Here we p...
F. Özden, Peter Minary· bioRxiv· 0 citations
We use cookies to run the site and, with your consent, for analytics and to show ads.
See our Cookie Policy.