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Isamu Isozaki

Publications and source records attributed to Isamu Isozaki.

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Billion-Scale Nearest-Neighbor Search under Fully Homomorphic Encryption on a Single GPU, Balancing Leakage and Cost

We build a system that answers "which database vectors are most similar to my query?" without the server ever seeing the query. The query is encrypted with fully homomorphic en- cryption (FHE); the server does all its scoring on ciphertexts and returns encrypted results that only the client can read. The challenge is speed: at a billion vectors, scoring every row under encryption is far too slow, so we combine two ideas - rank reduction (shrink each vector's dimen- sion) and a hierarchy (route to a small candidate set instead of scanning everything) - executed under encryption on a single GPU. We evaluate on three corpora at very different scales: a face corpus of 222 049 centroids clustered from ~10 M face images (512-dim), DataComp-1B (1.39 x 10^9 vectors, 512-dim CLIP), and Deep1B (10^9 vectors, 96-dim). On DataComp-1B we reach a recall@10 of 0.90 against the single labeled answer, or 0.95 when a near-duplicate im- age in the top-10 also counts as correct (the data is web-scraped and full of duplicates), at ~6 s per encrypted query on a GPU; a lighter configuration reaches 0.78/0.83 at ~1.8 s. These are warm (deployable) server-side latencies - client decryption and network transfer are excluded. On Deep1B we reach recall@10 0.90 under all-levels FHE (0.9045 measured over 2000 FHE queries, matching the 0.906 plaintext routing - the 96 -> 128 zero-pad is exact, correlation 1.0) at 2.3 s warm per query. We describe the full client-server protocol in enough detail to repro- duce it, and report accuracy and latency for every configuration. We also measure what this speed costs: the hierarchy's access pattern leaks the database geometry (an observer recovers 72% of the coarse-cell neighbor graph from access patterns alone), and we show that seeded (fixed-group) padding cuts this leak by ~35x (to ~2%), where naive padding is defeated by a repeated-query attack.

cs.CR

Towards Automated Penetration Testing: Introducing LLM Benchmark, Analysis, and Improvements

Hacking poses a significant threat to cybersecurity, inflicting billions of dollars in damages annually. To mitigate these risks, ethical hacking, or penetration testing, is employed to identify vulnerabilities in systems and networks. Recent advancements in large language models (LLMs) have shown potential across various domains, including cybersecurity. However, there is currently no comprehensive, open, automated, end-to-end penetration testing benchmark to drive progress and evaluate the capabilities of these models in security contexts. This paper introduces a novel open benchmark for LLM-based automated penetration testing, addressing this critical gap. We first evaluate the performance of LLMs, including GPT-4o and LLama 3.1-405B, using the state-of-the-art PentestGPT tool. Our findings reveal that while LLama 3.1 demonstrates an edge over GPT-4o, both models currently fall short of performing end-to-end penetration testing even with some minimal human assistance. Next, we advance the state-of-the-art and present ablation studies that provide insights into improving the PentestGPT tool. Our research illuminates the challenges LLMs face in each aspect of Pentesting, e.g. enumeration, exploitation, and privilege escalation. This work contributes to the growing body of knowledge on AI-assisted cybersecurity and lays the foundation for future research in automated penetration testing using large language models.

cs.CR

Generative Artificial Intelligence Reproducibility and Consensus

We performed a billion locality sensitive hash comparisons between artificially generated data samples to answer the critical question - can we reproduce the results of generative AI models? Reproducibility is one of the pillars of scientific research for verifiability, benchmarking, trust, and transparency. Futhermore, we take this research to the next level by verifying the "correctness" of generative AI output in a non-deterministic, trustless, decentralized network. We generate millions of data samples from a variety of open source diffusion and large language models and describe the procedures and trade-offs between generating more verses less deterministic output. Additionally, we analyze the outputs to provide empirical evidence of different parameterizations of tolerance and error bounds for verification. For our results, we show that with a majority vote between three independent verifiers, we can detect image generated perceptual collisions in generated AI with over 99.89% probability and less than 0.0267% chance of intra-class collision. For large language models (LLMs), we are able to gain 100% consensus using greedy methods or n-way beam searches to generate consensus demonstrated on different LLMs. In the context of generative AI training, we pinpoint and minimize the major sources of stochasticity and present gossip and synchronization training techniques for verifiability. Thus, this work provides a practical, solid foundation for AI verification, reproducibility, and consensus for generative AI applications.

cs.DC

Functional Protein Structure Annotation Using a Deep Convolutional Generative Adversarial Network

Identifying novel functional protein structures is at the heart of molecular engineering and molecular biology, requiring an often computationally exhaustive search. We introduce the use of a Deep Convolutional Generative Adversarial Network (DCGAN) to classify protein structures based on their functionality by encoding each sample in a grid object structure using three features in each object: the generic atom type, the position atom type, and its occupancy relative to a given atom. We train DCGAN on 3-dimensional (3D) decoy and native protein structures in order to generate and discriminate 3D protein structures. At the end of our training, loss converges to a local minimum and our DCGAN can annotate functional proteins robustly against adversarial protein samples. In the future we hope to extend the novel structures we found from the generator in our DCGAN with more samples to explore more granular functionality with varying functions. We hope that our effort will advance the field of protein structure prediction.

q-bio.BM