In this work, we present SynesLM, an unified model which can perform three multimodal language understanding tasks: audio-visual automatic speech recognition(AV-ASR) and visual-aided speech/machine translation(VST/VMT). Unlike previous research that focused on lip motion as visual cues for speech signals, our work explores more general visual information within entire frames, such as objects and actions. Additionally, we use synthetic image data to enhance the correlation between image and speech data. We benchmark SynesLM against the How2 dataset, demonstrating performance on par with state-of-the-art (SOTA) models dedicated to AV-ASR while maintaining our multitasking framework. Remarkably, for zero-shot AV-ASR, SynesLM achieved SOTA performance by lowering the Word Error Rate (WER) from 43.4% to 39.4% on the VisSpeech Dataset. Furthermore, our results in VST and VMT outperform the previous results, improving the BLEU score to 43.5 from 37.2 for VST, and to 54.8 from 54.4 for VMT.

Sepsis is a lethal syndrome of organ dysfunction that is triggered by an infection and claims 11 million lives per year globally. Prognostic algorithms based on deep learning have shown promise in detecting the onset of sepsis hours before the actual event but use a large number of bio-markers, including vital signs and laboratory tests. The latter makes the deployment of such systems outside hospitals or in resource-limited environments extremely challenging. This paper introduces SepAl, an energy-efficient and lightweight neural network, using only data from low-power wearable sensors, such as photoplethysmography (PPG), inertial measurement units (IMU), and body temperature sensors, designed to deliver alerts in real-time. SepAl leverages only six digitally acquirable vital signs and tiny machine learning algorithms, enabling on-device real-time sepsis prediction. SepAl uses a lightweight temporal convolution neural network capable of providing sepsis alerts with a median predicted time to sepsis of 9.8 hours. The model has been fully quantized, being able to be deployed on any low-power processors, and evaluated on an ARM Cortex-M33 core. Experimental evaluations show an inference efficiency of 0.11MAC/Cycle and a latency of 143ms, with an energy per inference of 2.68mJ. This work aims at paving the way toward accurate disease prediction, deployable in a long-lasting multi-vital sign wearable device, suitable for providing sepsis onset alerts at the point of care. The code used in this work has been open-sourced and is available at https://github.com/mgiordy/sepsis-prediction

The early and accurate diagnosis of sepsis is critical for enhancing patient outcomes. This study aims to use heart rate variability (HRV) features to develop an effective predictive model for sepsis detection. Critical HRV features are identified through feature engineering methods, including statistical bootstrapping and the Boruta algorithm, after which XGBoost and Random Forest classifiers are trained with differential hyperparameter settings. In addition, ensemble models are constructed to pool the prediction probabilities of high-recall and high-precision classifiers and improve model performance. Finally, a neural network model is trained on the HRV features, achieving an F1 score of 0.805, a precision of 0.851, and a recall of 0.763. The best-performing machine learning model is compared to this neural network through an interpretability analysis, where Local Interpretable Model-agnostic Explanations are implemented to determine decision-making criterion based on numerical ranges and thresholds for specific features. This study not only highlights the efficacy of HRV in automated sepsis diagnosis but also increases the transparency of black box outputs, maximizing clinical applicability.

The rapid integration of machine learning methodologies in healthcare has ignited innovative strategies for disease prediction, particularly with the vast repositories of Electronic Health Records (EHR) data. This article delves into the realm of multi-disease prediction, presenting a comprehensive study that introduces a pioneering ensemble feature selection model. This model, designed to optimize learning systems, combines statistical, deep, and optimally selected features through the innovative Stabilized Energy Valley Optimization with Enhanced Bounds (SEV-EB) algorithm. The objective is to achieve unparalleled accuracy and stability in predicting various disorders. This work proposes an advanced ensemble model that synergistically integrates statistical, deep, and optimally selected features. This combination aims to enhance the predictive power of the model by capturing diverse aspects of the health data. At the heart of the proposed model lies the SEV-EB algorithm, a novel approach to optimal feature selection. The algorithm introduces enhanced bounds and stabilization techniques, contributing to the robustness and accuracy of the overall prediction model. To further elevate the predictive capabilities, an HSC-AttentionNet is introduced. This network architecture combines deep temporal convolution capabilities with LSTM, allowing the model to capture both short-term patterns and long-term dependencies in health data. Rigorous evaluations showcase the remarkable performance of the proposed model. Achieving a 95% accuracy and 94% F1-score in predicting various disorders, the model surpasses traditional methods, signifying a significant advancement in disease prediction accuracy. The implications of this research extend beyond the confines of academia.

Generative Pre-Trained Transformer models have been shown to be surprisingly effective at a variety of natural language processing tasks -- including generating computer code. We evaluate the effectiveness of open source GPT models for the task of automatic identification of the presence of vulnerable code syntax (specifically targeting C and C++ source code). This task is evaluated on a selection of 36 source code examples from the NIST SARD dataset, which are specifically curated to not contain natural English that indicates the presence, or lack thereof, of a particular vulnerability. The NIST SARD source code dataset contains identified vulnerable lines of source code that are examples of one out of the 839 distinct Common Weakness Enumerations (CWE), allowing for exact quantification of the GPT output classification error rate. A total of 5 GPT models are evaluated, using 10 different inference temperatures and 100 repetitions at each setting, resulting in 5,000 GPT queries per vulnerable source code analyzed. Ultimately, we find that the GPT models that we evaluated are not suitable for fully automated vulnerability scanning because the false positive and false negative rates are too high to likely be useful in practice. However, we do find that the GPT models perform surprisingly well at automated vulnerability detection for some of the test cases, in particular surpassing random sampling, and being able to identify the exact lines of code that are vulnerable albeit at a low success rate. The best performing GPT model result found was Llama-2-70b-chat-hf with inference temperature of 0.1 applied to NIST SARD test case 149165 (which is an example of a buffer overflow vulnerability), which had a binary classification recall score of 1.0 and a precision of 1.0 for correctly and uniquely identifying the vulnerable line of code and the correct CWE number.

A scoring system is a simple decision model that checks a set of features, adds a certain number of points to a total score for each feature that is satisfied, and finally makes a decision by comparing the total score to a threshold. Scoring systems have a long history of active use in safety-critical domains such as healthcare and justice, where they provide guidance for making objective and accurate decisions. Given their genuine interpretability, the idea of learning scoring systems from data is obviously appealing from the perspective of explainable AI. In this paper, we propose a practically motivated extension of scoring systems called probabilistic scoring lists (PSL), as well as a method for learning PSLs from data. Instead of making a deterministic decision, a PSL represents uncertainty in the form of probability distributions, or, more generally, probability intervals. Moreover, in the spirit of decision lists, a PSL evaluates features one by one and stops as soon as a decision can be made with enough confidence. To evaluate our approach, we conduct a case study in the medical domain.

The cost of errors related to machine learning classifiers, namely, false positives and false negatives, are not equal and are application dependent. For example, in cybersecurity applications, the cost of not detecting an attack is very different from marking a benign activity as an attack. Various design choices during machine learning model building, such as hyperparameter tuning and model selection, allow a data scientist to trade-off between these two errors. However, most of the commonly used metrics to evaluate model quality, such as $F_1$ score, which is defined in terms of model precision and recall, treat both these errors equally, making it difficult for users to optimize for the actual cost of these errors. In this paper, we propose a new cost-aware metric, $C_{score}$ based on precision and recall that can replace $F_1$ score for model evaluation and selection. It includes a cost ratio that takes into account the differing costs of handling false positives and false negatives. We derive and characterize the new cost metric, and compare it to $F_1$ score. Further, we use this metric for model thresholding for five cybersecurity related datasets for multiple cost ratios. The results show an average cost savings of 49%.

Anomaly detection from graph data is an important data mining task in many applications such as social networks, finance, and e-commerce. Existing efforts in graph anomaly detection typically only consider the information in a single scale (view), thus inevitably limiting their capability in capturing anomalous patterns in complex graph data. To address this limitation, we propose a novel framework, graph ANomaly dEtection framework with Multi-scale cONtrastive lEarning (ANEMONE in short). By using a graph neural network as a backbone to encode the information from multiple graph scales (views), we learn better representation for nodes in a graph. In maximizing the agreements between instances at both the patch and context levels concurrently, we estimate the anomaly score of each node with a statistical anomaly estimator according to the degree of agreement from multiple perspectives. To further exploit a handful of ground-truth anomalies (few-shot anomalies) that may be collected in real-life applications, we further propose an extended algorithm, ANEMONE-FS, to integrate valuable information in our method. We conduct extensive experiments under purely unsupervised settings and few-shot anomaly detection settings, and we demonstrate that the proposed method ANEMONE and its variant ANEMONE-FS consistently outperform state-of-the-art algorithms on six benchmark datasets.

Large Vision-Language Models (LVLMs) have achieved significant success in recent years, and they have been extended to the medical domain. Although demonstrating satisfactory performance on medical Visual Question Answering (VQA) tasks, Medical LVLMs (MLVLMs) suffer from the hallucination problem, which makes them fail to diagnose complex pathologies. Moreover, they readily fail to learn minority pathologies due to imbalanced training data. We propose two prompting strategies for MLVLMs that reduce hallucination and improve VQA performance. In the first strategy, we provide a detailed explanation of the queried pathology. In the second strategy, we fine-tune a cheap, weak learner to achieve high performance on a specific metric, and textually provide its judgment to the MLVLM. Tested on the MIMIC-CXR-JPG and Chexpert datasets, our methods significantly improve the diagnostic F1 score, with the highest increase being 0.27. We also demonstrate that our prompting strategies can be extended to general LVLM domains. Based on POPE metrics, it effectively suppresses the false negative predictions of existing LVLMs and improves Recall by approximately 0.07.

Childhood myopia constitutes a significant global health concern. It exhibits an escalating prevalence and has the potential to evolve into severe, irreversible conditions that detrimentally impact familial well-being and create substantial economic costs. Contemporary research underscores the importance of precisely predicting myopia progression to enable timely and effective interventions, thereby averting severe visual impairment in children. Such predictions predominantly rely on subjective clinical assessments, which are inherently biased and resource-intensive, thus hindering their widespread application. In this study, we introduce a novel, high-accuracy method for quantitatively predicting the myopic trajectory and myopia risk in children using only fundus images and baseline refraction data. This approach was validated through a six-year longitudinal study of 3,408 children in Henan, utilizing 16,211 fundus images and corresponding refractive data. Our method based on deep learning demonstrated predictive accuracy with an error margin of 0.311D per year and AUC scores of 0.944 and 0.995 for forecasting the risks of developing myopia and high myopia, respectively. These findings confirm the utility of our model in supporting early intervention strategies and in significantly reducing healthcare costs, particularly by obviating the need for additional metadata and repeated consultations. Furthermore, our method was designed to rely only on fundus images and refractive error data, without the need for meta data or multiple inquiries from doctors, strongly reducing the associated medical costs and facilitating large-scale screening. Our model can even provide good predictions based on only a single time measurement. Consequently, the proposed method is an important means to reduce medical inequities caused by economic disparities.