The rapid advancement of Large Language Models (LLMs) has ushered in an era where AI-generated text is increasingly indistinguishable from human-generated content. Detecting AI-generated text has become imperative to combat misinformation, ensure content authenticity, and safeguard against malicious uses of AI. In this paper, we propose a novel hybrid approach that combines traditional TF-IDF techniques with advanced machine learning models, including Bayesian classifiers, Stochastic Gradient Descent (SGD), Categorical Gradient Boosting (CatBoost), and 12 instances of Deberta-v3-large models. Our approach aims to address the challenges associated with detecting AI-generated text by leveraging the strengths of both traditional feature extraction methods and state-of-the-art deep learning models. Through extensive experiments on a comprehensive dataset, we demonstrate the effectiveness of our proposed method in accurately distinguishing between human and AI-generated text. Our approach achieves superior performance compared to existing methods. This research contributes to the advancement of AI-generated text detection techniques and lays the foundation for developing robust solutions to mitigate the challenges posed by AI-generated content.

We propose a root-causing procedure for accelerating system-level debug using rule-based techniques. We describe the procedure and how it provides high quality debug hints for reducing the debug effort. This includes the heuristics for engineering features from logs of many tests, and the data analytics techniques for generating powerful debug hints. As a case study, we used these techniques for root-causing failures of the Power Management (PM) design feature Package-C8 and showed their effectiveness. Furthermore, we propose an approach for mining the root-causing experience and results for reuse, to accelerate future debug activities and reduce dependency on validation experts. We believe that these techniques are beneficial also for other validation activities at different levels of abstraction, for complex hardware, software and firmware systems, both pre-silicon and post-silicon.

Data-driven Artificial Intelligence (AI) systems trained using Machine Learning (ML) are shaping an ever-increasing (in size and importance) portion of our lives, including, but not limited to, recommendation systems, autonomous driving technologies, healthcare diagnostics, financial services, and personalized marketing. On the one hand, the outsized influence of these systems imposes a high standard of quality, particularly in the data used to train them. On the other hand, establishing and maintaining standards of Data Quality (DQ) becomes more challenging due to the proliferation of Edge Computing and Internet of Things devices, along with their increasing adoption for training and deploying ML models. The nature of the edge environment -- characterized by limited resources, decentralized data storage, and processing -- exacerbates data-related issues, making them more frequent, severe, and difficult to detect and mitigate. From these observations, it follows that DQ research for edge ML is a critical and urgent exploration track for the safety and robust usefulness of present and future AI systems. Despite this fact, DQ research for edge ML is still in its infancy. The literature on this subject remains fragmented and scattered across different research communities, with no comprehensive survey to date. Hence, this paper aims to fill this gap by providing a global view of the existing literature from multiple disciplines that can be grouped under the umbrella of DQ for edge ML. Specifically, we present a tentative definition of data quality in Edge computing, which we use to establish a set of DQ dimensions. We explore each dimension in detail, including existing solutions for mitigation.

The newly deployed service -- one kind of change service, could lead to a new type of minority fault. Existing state-of-the-art methods for fault localization rarely consider the imbalanced fault classification in change service. This paper proposes a novel method that utilizes decision rule sets to deal with highly imbalanced data by optimizing the F1 score subject to cardinality constraints. The proposed method greedily generates the rule with maximal marginal gain and uses an efficient minorize-maximization (MM) approach to select rules iteratively, maximizing a non-monotone submodular lower bound. Compared with existing fault localization algorithms, our algorithm can adapt to the imbalanced fault scenario of change service, and provide interpretable fault causes which are easy to understand and verify. Our method can also be deployed in the online training setting, with only about 15% training overhead compared to the current SOTA methods. Empirical studies showcase that our algorithm outperforms existing fault localization algorithms in both accuracy and model interpretability.

Given the proliferation of deep learning over the last decade or so [5], uncertainty or confidence estimation of these models has been an active research area [4]. Predicting accurate confidences in the generations produced by a large language model (LLM) are crucial for eliciting trust in the model and is also helpful for benchmarking and ranking competing models [37]. Moreover, LLM hallucination detection and mitigation, which is one of the most pressing problems in artificial intelligence research today [33], can also benefit significantly from accurate confidence estimation as it would serve as a strong indicator of the faithfulness of a LLM response. This applies to even settings where strategies such as retrieval augmented generation (RAG) are used [3] to mitigate hallucinations. Methods for confidence estimation in LLMs assuming just black-box or query access have been explored only recently [14, 19] and this area of research is still largely in its infancy. However, effective solutions here could have significant impact given their low requirement (i.e.

Cell-penetrating peptides (CPPs) are powerful vectors for the intracellular delivery of a diverse array of therapeutic molecules. Despite their potential, the rational design of CPPs remains a challenging task that often requires extensive experimental efforts and iterations. In this study, we introduce an innovative approach for the de novo design of CPPs, leveraging the strengths of machine learning (ML) and optimization algorithms. Our strategy, named LightCPPgen, integrates a LightGBM-based predictive model with a genetic algorithm (GA), enabling the systematic generation and optimization of CPP sequences. At the core of our methodology is the development of an accurate, efficient, and interpretable predictive model, which utilizes 20 explainable features to shed light on the critical factors influencing CPP translocation capacity. The CPP predictive model works synergistically with an optimization algorithm, which is tuned to enhance computational efficiency while maintaining optimization performance. The GA solutions specifically target the candidate sequences' penetrability score, while trying to maximize similarity with the original non-penetrating peptide in order to retain its original biological and physicochemical properties. By prioritizing the synthesis of only the most promising CPP candidates, LightCPPgen can drastically reduce the time and cost associated with wet lab experiments. In summary, our research makes a substantial contribution to the field of CPP design, offering a robust framework that combines ML and optimization techniques to facilitate the rational design of penetrating peptides, by enhancing the explainability and interpretability of the design process.

Recent years have witnessed remarkable progress in multi-view diffusion models for 3D content creation. However, there remains a significant gap in image quality and prompt-following ability compared to 2D diffusion models. A critical bottleneck is the scarcity of high-quality 3D assets with detailed captions. To address this challenge, we propose Bootstrap3D, a novel framework that automatically generates an arbitrary quantity of multi-view images to assist in training multi-view diffusion models. Specifically, we introduce a data generation pipeline that employs (1) 2D and video diffusion models to generate multi-view images based on constructed text prompts, and (2) our fine-tuned 3D-aware MV-LLaVA for filtering high-quality data and rewriting inaccurate captions. Leveraging this pipeline, we have generated 1 million high-quality synthetic multi-view images with dense descriptive captions to address the shortage of high-quality 3D data. Furthermore, we present a Training Timestep Reschedule (TTR) strategy that leverages the denoising process to learn multi-view consistency while maintaining the original 2D diffusion prior. Extensive experiments demonstrate that Bootstrap3D can generate high-quality multi-view images with superior aesthetic quality, image-text alignment, and maintained view consistency.

In the healthcare sector, a consciousness surrounding data privacy and corresponding data protection regulations, as well as heterogeneous and non-harmonized data, pose huge challenges to large-scale data analysis. Moreover, clinical data often involves partially overlapping features, as some observations may be missing due to various reasons, such as differences in procedures, diagnostic tests, or other recorded patient history information across hospitals or institutes. To address the challenges posed by partially overlapping features and incomplete data in clinical datasets, a comprehensive approach is required. Particularly in the domain of medical data, promising outcomes are achieved by federated random forests whenever features align. However, for most standard algorithms, like random forest, it is essential that all data sets have identical parameters. Therefore, in this work the concept of federated random forest is adapted to a setting with partially overlapping features. Moreover, our research assesses the effectiveness of the newly developed federated random forest models for partially overlapping clinical data. For aggregating the federated, globally optimized model, only features available locally at each site can be used. We tackled two issues in federation: (i) the quantity of involved parties, (ii) the varying overlap of features. This evaluation was conducted across three clinical datasets. The federated random forest model even in cases where only a subset of features overlaps consistently demonstrates superior performance compared to its local counterpart. This holds true across various scenarios, including datasets with imbalanced classes. Consequently, federated random forests for partially overlapped data offer a promising solution to transcend barriers in collaborative research and corporate cooperation.

Clinical variant classification of pathogenic versus benign genetic variants remains a challenge in clinical genetics. Recently, the proposition of genomic foundation models has improved the generic variant effect prediction (VEP) accuracy via weakly-supervised or unsupervised training. However, these VEPs are not diseasespecific, limiting their adaptation at the point of care. To address this problem, we propose DYNA: Disease-specificity fine-tuning via a Siamese neural network broadly applicable to all genomic foundation models for more effective variant effect predictions in disease-specific contexts. We evaluate DYNA in two distinct diseaserelevant tasks. For coding VEPs, we focus on various cardiovascular diseases, where gene-disease relationships of loss-of-function vs. gain-of-function dictate disease-specific VEP. For non-coding VEPs, we apply DYNA to an essential posttranscriptional regulatory axis of RNA splicing, the most common non-coding pathogenic mechanism in established clinical VEP guidelines. The DYNA fine-tuned models show superior performance in the held-out rare variant testing set and are further replicated in large, clinically-relevant variant annotations in ClinVAR. Thus, DYNA offers a potent disease-specific variant effect prediction method, excelling in intra-gene generalization and generalization to unseen genetic variants, making it particularly valuable for disease associations and clinical applicability. Clinical variant interpretation is transforming precision medicine, yet limitations exist that prevent its further adaptations and utilities [1]. Following a disease diagnosis, the identification and classification of pathogenic vs benign genetic variant has important clinical implications. The outcome of clinical variant interpretation provides a basis for clinical screening [2, 3] and genetic testing of first-degree family members [4], and may serve as a prognostic marker for the affected patient [5, 6]. Currently, the utility of genetic testing is limited by the fact that a substantial proportion (30-50%) of yielded variants are classified as variant of uncertain significance (VUS) according to the ACMG guidelines [7].

We prove that the combination of a target network and over-parameterized linear function approximation establishes a weaker convergence condition for bootstrapped value estimation in certain cases, even with off-policy data. Our condition is naturally satisfied for expected updates over the entire state-action space or learning with a batch of complete trajectories from episodic Markov decision processes. Notably, using only a target network or an over-parameterized model does not provide such a convergence guarantee. Additionally, we extend our results to learning with truncated trajectories, showing that convergence is achievable for all tasks with minor modifications, akin to value truncation for the final states in trajectories. Our primary result focuses on temporal difference estimation for prediction, providing high-probability value estimation error bounds and empirical analysis on Baird's counterexample and a Four-room task. Furthermore, we explore the control setting, demonstrating that similar convergence conditions apply to Q-learning.