The use of structured elicitation to inform decision making has grown dramatically in recent decades, however, judgements from multiple experts must be aggregated into a single estimate. Empirical evidence suggests that mathematical aggregation provides more reliable estimates than enforcing behavioural consensus on group estimates. aggreCAT provides state-of-the-art mathematical aggregation methods for elicitation data including those defined in Hanea, A. et al. (2021) <doi:10.1371/journal.pone.0256919>. The package also provides functions to visualise and evaluate the performance of your aggregated estimates on validation data.
This package provides tools for conducting epigenome-wide association studies (EWAS) and visualizing results. Users provide sample metadata and methylation matrices to run EWAS with linear models, linear mixed-effects models, or Cox models. The package supports downstream visualization, bootstrap validation, enrichment analysis, batch effect correction, and differentially methylated region (DMR) analysis with optional parallel computing. Methods are described in Wang et al. (2025) <doi:10.1093/bioadv/vbaf026>, Johnson et al. (2007) <doi:10.1093/biostatistics/kxj037>, and Peters et al. (2015) <doi:10.1186/1756-8935-8-6>.
In practical applications, the assumptions underlying generalized linear models frequently face violations, including incorrect specifications of the outcome variable's distribution or omitted predictors. These deviations can render the results of standard generalized linear models unreliable. As the sample size increases, what might initially appear as minor issues can escalate to critical concerns. To address these challenges, we adopt a permutation-based inference method tailored for generalized linear models. This approach offers robust estimations that effectively counteract the mentioned problems, and its effectiveness remains consistent regardless of the sample size.
The main function performs meta-analysis of genetic association study summary statistics that may be correlated due to cryptic relatedness or other confounders, generalizing inverse variance weighted methods. The function that estimates the correlation structure is also provided standalone. Another key innovation, the estimation of the correlation parameter from the median product of correlated standard normal variables, is provided, as well as a complete set of functions for their underlying distribution: density, cumulative, quantile, and random deviates. Described in Tu and Ochoa (2026) <doi:10.1016/j.xhgg.2026.100657>.
This package provides functions to calculate the out-of-bag learning curve for random forests for any measure that is available in the mlr package. Supported random forest packages are randomForest and ranger and trained models of these packages with the train function of mlr'. The main function is OOBCurve() that calculates the out-of-bag curve depending on the number of trees. With the OOBCurvePars() function out-of-bag curves can also be calculated for mtry', sample.fraction and min.node.size for the ranger package.
This package implements a sequential imputation framework using Bayesian Mixed-Effects Trees ('SBMTrees') for handling missing data in longitudinal studies. The package supports a variety of models, including non-linear relationships and non-normal random effects and residuals, leveraging Dirichlet Process priors for increased flexibility. Key features include handling Missing at Random (MAR) longitudinal data, imputation of both covariates and outcomes, and generating posterior predictive samples for further analysis. The methodology is designed for applications in epidemiology, biostatistics, and other fields requiring robust handling of missing data in longitudinal settings.
In the past decade, genome-scale metabolic reconstructions have widely been used to comprehend the systems biology of metabolic pathways within an organism. Different GSMs are constructed using various techniques that require distinct steps, but the input data, information conversion and software tools are neither concisely defined nor mathematically or programmatically formulated in a context-specific manner.The tool that quantitatively and qualitatively specifies each reconstruction steps and can generate a template list of reconstruction steps dynamically selected from a reconstruction step reservoir, constructed based on all available published papers.
Parametric source-filter synthesis of harmonic-noise signals, such as animal vocalizations and human voice, with control over pitch, formants, noise, amplitude modulation, nonlinear phenomena, and morphing. General signal processing tools for audio analysis and manipulation: pitch tracking, formant and vocal tract length estimation, reassigned and auditory spectrograms, modulation spectra and psychoacoustic roughness, self-similarity and surprisal, audio segmentation, pitch and formant shifting, etc. Includes four interactive web apps for audio synthesis, annotation, formant analysis, and manually correcting pitch contours. Reference: Anikin (2019) <doi:10.3758/s13428-018-1095-7>.
TensorFlow SIG Addons <https://www.tensorflow.org/addons> is a repository of community contributions that conform to well-established API patterns, but implement new functionality not available in core TensorFlow'. TensorFlow natively supports a large number of operators, layers, metrics, losses, optimizers, and more. However, in a fast moving field like Machine Learning, there are many interesting new developments that cannot be integrated into core TensorFlow (because their broad applicability is not yet clear, or it is mostly used by a smaller subset of the community).
The United Nations Sustainable Development Goals (SDGs) have become an important guideline for organisations to monitor and plan their contributions to social, economic, and environmental transformations. The text2sdg package is an open-source analysis package that identifies SDGs in text using scientifically developed query systems, opening up the opportunity to monitor any type of text-based data, such as scientific output or corporate publications. For more information see Meier, Mata & Wulff (2025) <doi:10.32614/RJ-2024-005> and Wulff, Meier & Mata (2024) <doi:10.1007/s11625-024-01516-3>.
Make it easy to deal with multiple cross-tables in data exploration, by creating them, manipulating them, and adding color helpers to highlight deviations (differences from totals, comparisons between lines or columns, contributions to variance, odds ratios, etc.) and significance (confidence intervals, stars, etc.). Create the same kind of tables for regression models, with a framework to compare model effects with their crude/observed counterpart systematically. All functions render data frames which can be easily manipulated. All tables can be exported with formats and colors to Excel', html and markdown.
The purpose of this package is to identify traits in a dataset that can separate groups. This is done on two levels. First, clustering is performed, using an implementation of sparse K-means. Secondly, the generated clusters are used to predict outcomes of groups of individuals based on their distribution of observations in the different clusters. As certain clusters with separating information will be identified, and these clusters are defined by a sparse number of variables, this method can reduce the complexity of data, to only emphasize the data that actually matters.
Circular layout is an efficient way to visualise huge amounts of information. This package provides an implementation of circular layout generation in R as well as an enhancement of available software. Its flexibility is based on the usage of low-level graphics functions such that self-defined high-level graphics can be easily implemented by users for specific purposes. Together with the seamless connection between the powerful computational and visual environment in R, it gives users more convenience and freedom to design figures for better understanding complex patterns behind multi-dimensional data.
This package implements Competitive Adaptive Reweighted Sampling (CARS) algorithm for variable selection from high-dimensional dataset using Partial Least Squares (PLS) regression models. CARS algorithm iteratively applies the Monte Carlo sub-sampling and exponential variable elimination techniques to identify/select the most informative variables/features subjected to minimal cross-validated RMSE score. The implementation of CARS algorithm is inspired from the work of Li et al. (2009) <doi:10.1016/j.aca.2009.06.046>. This algorithm is widely applied in near-infrared (NIR), mid-infrared (MIR), hyperspectral chemometrics areas, etc.
This package provides a novel framework for detecting, quantifying, and analyzing dormant patterns in multivariate data. Dormant patterns are statistical relationships that exist in data but remain inactive until specific trigger conditions emerge. This concept, inspired by biological dormancy (seeds, pathogens) and geological phenomena (dormant faults), provides tools to identify latent risks, hidden correlations, and potential phase transitions in complex systems. The package introduces methods for quantifying dormancy depth, trigger sensitivity, and awakening risk - enabling analysts to discover patterns that conventional methods miss because they focus only on currently active relationships.
Analysis of agreement for nominal data between two raters using the Delta model. This model is proposed as an alternative to the widespread measure Cohen kappa coefficient, which performs poorly when the marginal distributions are very asymmetric (Martin-Andres and Femia-Marzo (2004), <doi:10.1348/000711004849268>; Martin-Andres and Femia-Marzo (2008) <doi:10.1080/03610920701669884>). The package also contains a function to perform a massive analysis of multiple raters against a gold standard. A shiny app is also provided to obtain the measures of nominal agreement between two raters.
The American Association Research (AACR) Project Genomics Evidence Neoplasia Information Exchange (GENIE) BioPharma Collaborative represents a multi-year, multi-institution effort to build a pan-cancer repository of linked clinico-genomic data. The genomic and clinical data are provided in multiple releases (separate releases for each cancer cohort with updates following data corrections), which are stored on the data sharing platform Synapse <https://www.synapse.org/>. The genieBPC package provides a seamless way to obtain the data corresponding to each release from Synapse and to prepare datasets for analysis.
We provide an efficient implementation for two-step multi-source transfer learning algorithms in high-dimensional generalized linear models (GLMs). The elastic-net penalized GLM with three popular families, including linear, logistic and Poisson regression models, can be fitted. To avoid negative transfer, a transferable source detection algorithm is proposed. We also provides visualization for the transferable source detection results. The details of methods can be found in "Tian, Y., & Feng, Y. (2023). Transfer learning under high-dimensional generalized linear models. Journal of the American Statistical Association, 118(544), 2684-2697.".
Data sets related to the Islas Malvinas /// Sets de datos relacionados a las Islas Malvinas - La Nación Argentina ratifica su legà tima e imprescriptible soberanà a sobre las islas Malvinas, Georgias del Sur y Sándwich del Sur y los espacios marà timos e insulares correspondientes, por ser parte integrante del territorio nacional. La recuperación de dichos territorios y el ejercicio pleno de la soberanà a, respetando el modo de vida de sus habitantes y conforme a los principios del Derecho Internacional, constituyen un objetivo permanente e irrenunciable del pueblo argentino.
Modelling Multivariate Binary Data with Blocks of Specific One-Factor Distribution. Variables are grouped into independent blocks. Each variable is described by two continuous parameters (its marginal probability and its dependency strength with the other block variables), and one binary parameter (positive or negative dependency). Model selection consists in the estimation of the repartition of the variables into blocks. It is carried out by the maximization of the BIC criterion by a deterministic (faster) algorithm or by a stochastic (more time consuming but optimal) algorithm. Tool functions facilitate the model interpretation.
This package provides a collection of data structures and methods for handling volumetric brain imaging data, with a focus on functional magnetic resonance imaging (fMRI). Provides efficient representations for three-dimensional and four-dimensional neuroimaging data through sparse and dense array implementations, memory-mapped file access for large datasets, and spatial transformation capabilities. Implements methods for image resampling, spatial filtering, region of interest analysis, and connected component labeling. General introduction to fMRI analysis can be found in Poldrack et al. (2024, "Handbook of functional MRI data analysis", <ISBN:9781108795760>).
Pharmacometric tools for common data analytical tasks; closed-form solutions for calculating concentrations at given times after dosing based on compartmental PK models (1-compartment, 2-compartment and 3-compartment, covering infusions, zero- and first-order absorption, and lag times, after single doses and at steady state, per Bertrand & Mentre (2008) <https://www.facm.ucl.ac.be/cooperation/Vietnam/WBI-Vietnam-October-2011/Modelling/Monolix32_PKPD_library.pdf>); parametric simulation from NONMEM-generated parameter estimates and other output; and parsing, tabulating and plotting results generated by Perl-speaks-NONMEM (PsN).
The use of overparameterization is proposed with combinatorial analysis to test a broader spectrum of possible ARIMA models. In the selection of ARIMA models, the most traditional methods such as correlograms or others, do not usually cover many alternatives to define the number of coefficients to be estimated in the model, which represents an estimation method that is not the best. The popstudy package contains several tools for statistical analysis in demography and time series based in Shryock research (Shryock et. al. (1980) <https://books.google.co.cr/books?id=8Oo6AQAAMAAJ>).
Detects variable types (continuous, count, binary, ordinal, categorical) and selects the appropriate correlation method for each pair. Supports Pearson, Spearman, Kendall's tau, point-biserial, rank-biserial, phi, tetrachoric, polychoric, polyserial, Cramer's V, Tschuprow's T, Theil's U, Yule's Q, and Goodman-Kruskal's gamma, each with a confidence interval and p-value. Explains the selection rationale in the output, follows tidy data principles, and works in both interactive and scripted workflows. The methodology is described in Harshvardhan and Ranjan (2026) <doi:10.48550/arXiv.2607.22285>.