arXiv subjects

Yutong Jin

Publications and source records attributed to Yutong Jin.

6 recordsLinked to original sources

arXiv2026

Security, Privacy, and Ethical Risks in OpenClaw

This paper systematically investigates the security, privacy, and ethical risks, as well as the traceability challenges of OpenClaw, a locally executable AI agent system for natural language interaction and real-world task completion. While OpenClaw shows strong potential for personal assistance, office automation, cross-platform task management, and information integration, it also raises serious security, privacy, and ethical concerns. By analyzing its system architecture, core functionalities, deployment model, and representative application scenarios, this paper aims to reveal the risks that may arise when such a highly privileged agent is integrated into personal and organizational digital environments. We focus in particular on the challenges associated with persistent local storage, tool invocation, cross-context information aggregation, multi-user interaction, and the integration of plugins and external services. We argue that these issues constitute major barriers to the trustworthy deployment and widespread adoption of this technology. Finally, we summarize the open challenges in security defenses, privacy protection, ethical governance, and traceability in agent use, and call for joint efforts from researchers, developers, deployers, and regulators to build AI agent systems that are safer, more reliable, and more trustworthy.

cs.CR↗

arXiv2026

MelShield: Robust Mel-Domain Audio Watermarking for Provenance Attribution of AI Generated Synthesized Speech

In this paper, we propose MelShield, a robust, in-generation, keyed audio watermarking framework that embeds identifiable signals into AI-generated audio for copyright protection and reliable attribution. Specifically, MelShield operates in the Mel-spectrogram domain during the generation process, targeting intermediate acoustic representations in Mel-conditioned pipelines for text-to-speech (TTS) generation. The core idea is to treat the intermediate Mel-spectrogram as the host signal and embed a short binary payload via low-energy, keyed spread-spectrum perturbations distributed across carefully selected time-frequency regions prior to waveform synthesis. By performing watermarking before vocoder inference, MelShield remains plug-and-play for Mel-conditioned TTS architectures and does not require modification or retraining of the underlying TTS generation vocoder, such as DiffWave and HiFi-GAN. Moreover, the multi-user keyed construction enables scalable user-specific attribution, while the keyed verification mechanism limits unauthorized decoding, thereby reducing the risk of large-scale extractor probing and adversarial analysis. Extensive experiments on DiffWave and HiFi-GAN demonstrate that MelShield achieves reliable watermark extraction, approaching 100\% bit accuracy, even under signal distortions, e.g., compression and additive noise, while preserving high perceptual audio quality.

cs.SD↗

arXiv2024

A class of nonparametric methods for evaluating the effect of continuous treatments on survival outcomes

In randomized trials and observational studies, it is often necessary to evaluate the extent to which an intervention affects a time-to-event outcome, which is only partially observed due to right censoring. For instance, in infectious disease studies, it is frequently of interest to characterize the relationship between risk of acquisition of infection with a pathogen and a biomarker previously measuring for an immune response against that pathogen induced by prior infection and/or vaccination. It is common to conduct inference within a causal framework, wherein we desire to make inferences about the counterfactual probability of survival through a given time point, at any given exposure level. To determine whether a causal effect is present, one can assess if this quantity differs by exposure level. Recent work shows that, under typical causal assumptions, summaries of the counterfactual survival distribution are identifiable. Moreover, when the treatment is multi-level, these summaries are also pathwise differentiable in a nonparametric probability model, making it possible to construct estimators thereof that are unbiased and approximately normal. In cases where the treatment is continuous, the target estimand is no longer pathwise differentiable, rendering it difficult to construct well-behaved estimators without strong parametric assumptions. In this work, we extend beyond the traditional setting with multilevel interventions to develop approaches to nonparametric inference with a continuous exposure. We introduce methods for testing whether the counterfactual probability of survival time by a given time-point remains constant across the range of the continuous exposure levels. The performance of our proposed methods is evaluated via numerical studies, and we apply our method to data from a recent pair of efficacy trials of an HIV monoclonal antibody.

stat.ME↗

arXiv2024

Is it the model or the metric -- On robustness measures of deeplearning models

Determining the robustness of deep learning models is an established and ongoing challenge within automated decision-making systems. With the advent and success of techniques that enable advanced deep learning (DL), these models are being used in widespread applications, including high-stake ones like healthcare, education, border-control. Therefore, it is critical to understand the limitations of these models and predict their regions of failures, in order to create the necessary guardrails for their successful and safe deployment. In this work, we revisit robustness, specifically investigating the sufficiency of robust accuracy (RA), within the context of deepfake detection. We present robust ratio (RR) as a complementary metric, that can quantify the changes to the normalized or probability outcomes under input perturbation. We present a comparison of RA and RR and demonstrate that despite similar RA between models, the models show varying RR under different tolerance (perturbation) levels.

cs.LG↗

arXiv2024

Comparing HIV Vaccine Immunogenicity across Trials with Different Populations and Study Designs

Safe and effective preventive vaccines have the potential to help stem the HIV epidemic. The efficacy of such vaccines is typically measured in randomized, double-blind phase IIb/III trials and described as a reduction in newly acquired HIV infections. However, such trials are often expensive, time-consuming, and/or logistically challenging. These challenges lead to a great interest in immune responses induced by vaccination, and in identifying which immune responses predict vaccine efficacy. These responses are termed vaccine correlates of protection. Studies of vaccine-induced immunogenicity vary in size and design, ranging from small, early phase trials, to case-control studies nested in a broader late-phase randomized trial. Moreover, trials can be conducted in geographically diverse study populations across the world. Such diversity presents a challenge for objectively comparing vaccine-induced immunogenicity. To address these practical challenges, we propose a framework that is capable of identifying appropriate causal estimands and estimators, which can be used to provide standardized comparisons of vaccine-induced immunogenicity across trials. We evaluate the performance of the proposed estimands via extensive simulation studies. Our estimators are well-behaved and enjoy robustness properties. The proposed technique is applied to compare vaccine immunogenicity using data from three recent HIV vaccine trials.

stat.ME↗

arXiv2021

Real-time tracking of COVID-19 and coronavirus research updates through text mining

The novel coronavirus (SARS-CoV-2) which causes COVID-19 is an ongoing pandemic. There are ongoing studies with up to hundreds of publications uploaded to databases daily. We are exploring the use-case of artificial intelligence and natural language processing in order to efficiently sort through these publications. We demonstrate that clinical trial information, preclinical studies, and a general topic model can be used as text mining data intelligence tools for scientists all over the world to use as a resource for their own research. To evaluate our method, several metrics are used to measure the information extraction and clustering results. In addition, we demonstrate that our workflow not only have a use-case for COVID-19, but for other disease areas as well. Overall, our system aims to allow scientists to more efficiently research coronavirus. Our automatically updating modules are available on our information portal at https://ghddi-ailab.github.io/Targeting2019-nCoV/ for public viewing.

cs.IR↗