The estimation of average treatment effects (ATEs), defined as the difference in expected outcomes between treatment and control groups, is a central topic in causal inference. This study develops semiparametric efficient estimators for ATE estimation in a setting where only a treatment group and an unknown group-comprising units for which it is unclear whether they received the treatment or control-are observable. This scenario represents a variant of learning from positive and unlabeled data (PU learning) and can be regarded as a special case of ATE estimation with missing data. For this setting, we derive semiparametric efficiency bounds, which provide lower bounds on the asymptotic variance of regular estimators. We then propose semiparametric efficient ATE estimators whose asymptotic variance aligns with these efficiency bounds. Our findings contribute to causal inference with missing data and weakly supervised learning.

Lung cancer is a major issue in worldwide public health, requiring early diagnosis using stable techniques. This work begins a thorough investigation of the use of machine learning (ML) methods for precise classification of lung cancer stages. A cautious analysis is performed to overcome overfitting issues in model performance, taking into account minimum child weight and learning rate. A set of machine learning (ML) models including XGBoost (XGB), LGBM, Adaboost, Logistic Regression (LR), Decision Tree (DT), Random Forest (RF), CatBoost, and k-Nearest Neighbor (k-NN) are run methodically and contrasted. Furthermore, the correlation between features and targets is examined using the deep neural network (DNN) model and thus their capability in detecting complex patternsis established. It is argued that several ML models can be capable of classifying lung cancer stages with great accuracy. In spite of the complexity of DNN architectures, traditional ML models like XGBoost, LGBM, and Logistic Regression excel with superior performance. The models perform better than the others in lung cancer prediction on the complete set of comparative metrics like accuracy, precision, recall, and F-1 score

We propose a novel redaction methodology that can be used to sanitize natural text data. Our new technique provides better privacy benefits than other state of the art techniques while maintaining lower redaction levels.

Antibiotics are often grouped by their mechanisms of action, such as blocking protein synthesis, disrupting folate biosynthesis, changing cell wall construction, compromising the cell membrane integrity and affecting DNA replication [93, 25]. These antibiotics, whether created in labs or found in nature, serve as the primary defence against bacterial infections. However, bacteria employ a series of strategies in response to resist these antibiotics, including inactivating antibiotics through enzymatic degradation, altering the antibiotic target, modifying cell membrane permeability, and using efflux pumps to maintain intracellular antibiotic concentrations of antibiotics below inhibitory levels [25]. Moreover, the gene transfer of antibiotic-resistant bacteria (ARB) further aggravates this challenge [92].

Machine learning models are increasingly used to produce predictions that serve as input data in subsequent statistical analyses. For example, computer vision predictions of economic and environmental indicators based on satellite imagery are used in downstream regressions; similarly, language models are widely used to approximate human ratings and opinions in social science research. However, failure to properly account for errors in the machine learning predictions renders standard statistical procedures invalid. Prior work uses what we call the Predict-Then-Debias estimator to give valid confidence intervals when machine learning algorithms impute missing variables, assuming a small complete sample from the population of interest. We expand the scope by introducing bootstrap confidence intervals that apply when the complete data is a nonuniform (i.e., weighted, stratified, or clustered) sample and to settings where an arbitrary subset of features is imputed. Importantly, the method can be applied to many settings without requiring additional calculations. We prove that these confidence intervals are valid under no assumptions on the quality of the machine learning model and are no wider than the intervals obtained by methods that do not use machine learning predictions.

The search for symbolic regression models with genetic programming (GP) has a tendency of revisiting expressions in their original or equivalent forms. Repeatedly evaluating equivalent expressions is inefficient, as it does not immediately lead to better solutions. However, evolutionary algorithms require diversity and should allow the accumulation of inactive building blocks that can play an important role at a later point. The equality graph is a data structure capable of compactly storing expressions and their equivalent forms allowing an efficient verification of whether an expression has been visited in any of their stored equivalent forms. We exploit the e-graph to adapt the subtree operators to reduce the chances of revisiting expressions. Our adaptation, called eggp, stores every visited expression in the e-graph, allowing us to filter out from the available selection of subtrees all the combinations that would create already visited expressions. Results show that, for small expressions, this approach improves the performance of a simple GP algorithm to compete with PySR and Operon without increasing computational cost. As a highlight, eggp was capable of reliably delivering short and at the same time accurate models for a selected set of benchmarks from SRBench and a set of real-world datasets.

Handling imbalanced data streams in regression tasks presents a significant challenge, as rare instances can appear anywhere in the target distribution rather than being confined to its extreme values. In this paper, we introduce novel data-level sampling strategies, \texttt{HistUS} and \texttt{HistOS}, that utilize histogram-based approaches to dynamically balance data streams. Unlike previous methods based on Chebyshev\textquotesingle s inequality, our proposed techniques identify and handle rare cases across the entire distribution effectively. We demonstrate that \texttt{HistUS} and \texttt{HistOS} outperform traditional methods through extensive experiments on synthetic and real-world datasets, leading to more accurate and robust regression models in streaming environments.

We revisit the well-studied problem of approximating a matrix product, $\mathbf{A}^T\mathbf{B}$, based on small space sketches $\mathcal{S}(\mathbf{A})$ and $\mathcal{S}(\mathbf{B})$ of $\mathbf{A} \in \R^{n \times d}$ and $\mathbf{B}\in \R^{n \times m}$. We are interested in the setting where the sketches must be computed independently of each other, except for the use of a shared random seed. We prove that, when $\mathbf{A}$ and $\mathbf{B}$ are sparse, methods based on \emph{coordinated random sampling} can outperform classical linear sketching approaches, like Johnson-Lindenstrauss Projection or CountSketch. For example, to obtain Frobenius norm error $\epsilon\|\mathbf{A}\|_F\|\mathbf{B}\|_F$, coordinated sampling requires sketches of size $O(s/\epsilon^2)$ when $\mathbf{A}$ and $\mathbf{B}$ have at most $s \leq d,m$ non-zeros per row. In contrast, linear sketching leads to sketches of size $O(d/\epsilon^2)$ and $O(m/\epsilon^2)$ for $\mathbf{A}$ and $\mathbf{B}$. We empirically evaluate our approach on two applications: 1) distributed linear regression in databases, a problem motivated by tasks like dataset discovery and augmentation, and 2) approximating attention matrices in transformer-based language models. In both cases, our sampling algorithms yield an order of magnitude improvement over linear sketching.

Regression analysis is used for prediction and to understand the effect of independent variables on dependent variables. Symbolic regression (SR) automates the search for non-linear regression models, delivering a set of hypotheses that balances accuracy with the possibility to understand the phenomena. Many SR implementations return a Pareto front allowing the choice of the best trade-off. However, this hides alternatives that are close to non-domination, limiting these choices. Equality graphs (e-graphs) allow to represent large sets of expressions compactly by efficiently handling duplicated parts occurring in multiple expressions. E-graphs allow to store and query all SR solution candidates visited in one or multiple GP runs efficiently and open the possibility to analyse much larger sets of SR solution candidates. We introduce rEGGression, a tool using e-graphs to enable the exploration of a large set of symbolic expressions which provides querying, filtering, and pattern matching features creating an interactive experience to gain insights about SR models. The main highlight is its focus in the exploration of the building blocks found during the search that can help the experts to find insights about the studied phenomena.This is possible by exploiting the pattern matching capability of the e-graph data structure.

Choosing models from a well-fitted evolved population that generalizes beyond training data is difficult. We introduce a pragmatic method to estimate model complexity using Hessian rank for post-processing selection. Complexity is approximated by averaging the model output Hessian rank across a few points (N=3), offering efficient and accurate rank estimates. This method aligns model selection with input data complexity, calculated using intrinsic dimensionality (ID) estimators. Using the StackGP system, we develop symbolic regression models for the Penn Machine Learning Benchmark and employ twelve scikit-dimension library methods to estimate ID, aligning model expressiveness with dataset ID. Our data-informed complexity metric finds the ideal complexity window, balancing model expressiveness and accuracy, enhancing generalizability without bias common in methods reliant on user-defined parameters, such as parsimony pressure in weight selection.