IDS aims to protect computer networks from security threats by detecting, notifying, and taking appropriate action to prevent illegal access and protect confidential information. As the globe becomes increasingly dependent on technology and automated processes, ensuring secured systems, applications, and networks has become one of the most significant problems of this era. The global web and digital technology have significantly accelerated the evolution of the modern world, necessitating the use of telecommunications and data transfer platforms. Researchers are enhancing the effectiveness of IDS by incorporating popular datasets into machine learning algorithms. IDS, equipped with machine learning classifiers, enhances security attack detection accuracy by identifying normal or abnormal network traffic. This paper explores the methods of capturing and reviewing intrusion detection systems (IDS) and evaluates the challenges existing datasets face. A deluge of research on machine learning (ML) and deep learning (DL) architecture-based intrusion detection techniques has been conducted in the past ten years on various cybersecurity datasets, including KDDCUP'99, NSL-KDD, UNSW-NB15, CICIDS-2017, and CSE-CIC-IDS2018. We conducted a literature review and presented an in-depth analysis of various intrusion detection methods that use SVM, KNN, DT, LR, NB, RF, XGBOOST, Adaboost, and ANN. We provide an overview of each technique, explaining the role of the classifiers and algorithms used. A detailed tabular analysis highlights the datasets used, classifiers employed, attacks detected, evaluation metrics, and conclusions drawn. This article offers a thorough review for future IDS research.

The field of health informatics has been profoundly influenced by the development of random forest models, which have led to significant advances in the interpretability of feature interactions. These models are characterized by their robustness to overfitting and parallelization, making them particularly useful in this domain. However, the increasing number of features and estimators in random forests can prevent domain experts from accurately interpreting global feature interactions, thereby compromising trust and regulatory compliance. A method called the surrogate interpretability graph has been developed to address this issue. It uses graphs and mixed-integer linear programming to analyze and visualize feature interactions. This improves their interpretability by visualizing the feature usage per decision-feature-interaction table and the most dominant hierarchical decision feature interactions for predictions. The implementation of a surrogate interpretable graph enhances global interpretability, which is critical for such a high-stakes domain.

Weaknesses: The main concern I have with the paper is in the argument that the estimator does in fact converge to MCR and MCR- for random forests. Section 4.1 provides an argument that, as the number of trees goes to infinity, each tree will be replaced with one from its Rashomon set that is maximally dependent on X1 (when doing the MCR procedure). In finite samples, and with a finite number of trees, there are reasons to doubt whether this method provides consistent estimation of MCR for the random forest as a whole. The favorable generalization properties of random forests are known to be derived from the diversity of trees in the ensemble: a well known result of Breiman is that the generalization error decreases as the correlation of the residuals from the trees decreases. While the predictions of a tree and its surrogate may be identical for a given dataset, replacing a tree with the surrogate seems that it may decrease the expected generalization error of the tree as a whole.

The COVID-19 pandemic response relied heavily on statistical and machine learning models to predict key outcomes such as case prevalence and fatality rates. These predictions were instrumental in enabling timely public health interventions that helped break transmission cycles. While most existing models are grounded in traditional epidemiological data, the potential of alternative datasets, such as those derived from genomic information and human behavior, remains underexplored. In the current study, we investigated the usefulness of diverse modalities of feature sets in predicting case surges. Our results highlight the relative effectiveness of biological (e.g., mutations), public health (e.g., case counts, policy interventions) and human behavioral features (e.g., mobility and social media conversations) in predicting country-level case surges. Importantly, we uncover considerable heterogeneity in predictive performance across countries and feature modalities, suggesting that surge prediction models may need to be tailored to specific national contexts and pandemic phases. Overall, our work highlights the value of integrating alternative data sources into existing disease surveillance frameworks to enhance the prediction of pandemic dynamics.

Accurate diabetes risk prediction relies on identifying key features from complex health datasets, but conventional methods like mutual information (MI) filters and genetic algorithms (GAs) often overlook extreme dependencies critical for high-risk subpopulations. In this study we introduce a feature-selection framework using the upper-tail dependence coefficient (λU) of the novel A2 copula, which quantifies how often extreme higher values of a predictor co-occur with diabetes diagnoses (target variable). Applied to the CDC Diabetes Health Indicators dataset (n=253,680), our method prioritizes five predictors (self-reported general health, high blood pressure, body mass index, mobility limitations, and high cholesterol levels) based on upper tail dependencies. These features match or outperform MI and GA selected subsets across four classifiers (Random Forest, XGBoost, Logistic Regression, Gradient Boosting), achieving accuracy up to 86.5% (XGBoost) and AUC up to 0.806 (Gradient Boosting), rivaling the full 21-feature model. Permutation importance confirms clinical relevance, with BMI and general health driving accuracy. To our knowledge, this is the first work to apply a copula's upper-tail dependence for supervised feature selection, bridging extreme-value theory and machine learning to deliver a practical toolkit for diabetes prevention.

We propose a principled method for autoencoding with random forests. Our strategy builds on foundational results from nonparametric statistics and spectral graph theory to learn a low-dimensional embedding of the model that optimally represents relationships in the data. We provide exact and approximate solutions to the decoding problem via constrained optimization, split relabeling, and nearest neighbors regression. These methods effectively invert the compression pipeline, establishing a map from the embedding space back to the input space using splits learned by the ensemble's constituent trees. The resulting decoders are universally consistent under common regularity assumptions. The procedure works with supervised or unsupervised models, providing a window into conditional or joint distributions. We demonstrate various applications of this autoencoder, including powerful new tools for visualization, compression, clustering, and denoising. Experiments illustrate the ease and utility of our method in a wide range of settings, including tabular, image, and genomic data.

The Rashomon effect is a mixed blessing in responsible machine learning. It enhances the prospects of finding models that perform well in accuracy while adhering to ethical standards, such as fairness or interpretability. Conversely, it poses a risk to the credibility of machine decisions through predictive multiplicity. While recent studies have explored the Rashomon effect across various machine learning algorithms, its impact on gradient boosting---an algorithm widely applied to tabular datasets---remains unclear. We provide rigorous theoretical derivations to examine the Rashomon effect in the context of gradient boosting and offer an information-theoretic characterization of the Rashomon set.

Gradient boosting is a sequential ensemble method that fits a new weaker learner to pseudo residuals at each iteration. We propose Wasserstein gradient boosting, a novel extension of gradient boosting, which fits a new weak learner to alternative pseudo residuals that are Wasserstein gradients of loss functionals of probability distributions assigned at each input. It solves distribution-valued supervised learning, where the output values of the training dataset are probability distributions. In classification and regression, a model typically returns, for each input, a point estimate of a parameter of a noise distribution specified for a response variable, such as the class probability parameter of a categorical distribution specified for a response label. A main application of Wasserstein gradient boosting in this paper is tree-based evidential learning, which returns a distributional estimate of the response parameter for each input.

Automated machine learning (AutoML) can produce complex model ensembles by stacking, bagging, and boosting many individual models like trees, deep networks, and nearest neighbor estimators. While highly accurate, the resulting predictors are large, slow, and opaque as compared to their constituents. To improve the deployment of AutoML on tabular data, we propose FAST-DAD to distill arbitrarily-complex ensemble predictors into individual models like boosted trees, random forests, and deep networks. At the heart of our approach is a data augmentation strategy based on Gibbs sampling from a self-attention pseudolikelihood estimator. Across 30 datasets spanning regression and binary/multiclass classification tasks, FAST-DAD distillation produces significantly better individual models than one obtains through standard training on the original data.

Sparse autoencoders (SAEs) are used to decompose neural network activations into human-interpretable features. Typically, features learned by a single SAE are used for downstream applications. However, it has recently been shown that SAEs trained with different initial weights can learn different features, demonstrating that a single SAE captures only a limited subset of features that can be extracted from the activation space. Motivated by this limitation, we propose to ensemble multiple SAEs through naive bagging and boosting. Specifically, SAEs trained with different weight initializations are ensembled in naive bagging, whereas SAEs sequentially trained to minimize the residual error are ensembled in boosting. We evaluate our ensemble approaches with three settings of language models and SAE architectures. Our empirical results demonstrate that ensembling SAEs can improve the reconstruction of language model activations, diversity of features, and SAE stability. Furthermore, ensembling SAEs performs better than applying a single SAE on downstream tasks such as concept detection and spurious correlation removal, showing improved practical utility.