This package provides functions that calculate appropriate sample sizes for one-sample t-tests, two-sample t-tests, and F-tests for microarray experiments based on desired power while controlling for false discovery rates. For all tests, the standard deviations (variances) among genes can be assumed fixed or random. This is also true for effect sizes among genes in one-sample and two sample experiments. Functions also output a chart of power versus sample size, a table of power at different sample sizes, and a table of critical test values at different sample sizes.

Save the state of applications built with shiny', the web application framework by Chang et al. (2026) <doi:10.32614/CRAN.package.shiny>. Users can share their work and continue it in another session. Input values and selected values held by the server are saved in JSON (JavaScript Object Notation) files that can be read and edited by hand. Saved state can be restored without reloading the page or setting up bookmarking. Restoration waits for inputs that appear as the page changes and reports which values were restored, missing, or could not be applied.

In order to make it easy to use variance reduction algorithms for any simulation, this framework can help you. We propose user friendly and easy to extend framework. Antithetic Variates, Inner Control Variates, Outer Control Variates and Importance Sampling algorithms are available in the framework. User can write its own simulation function and use the Variance Reduction techniques in this package to obtain more efficient simulations. An implementation of Asian Option simulation is already available within the package. See Kemal Dinçer Dingeç & Wolfgang Hörmann (2012) <doi:10.1016/j.ejor.2012.03.046>.

This package enables you to create interactive cluster heatmaps that can be saved as a stand-alone HTML file, embedded in R Markdown documents or in a Shiny app, and made available in the RStudio viewer pane. Hover the mouse pointer over a cell to show details or drag a rectangle to zoom. A heatmap is a popular graphical method for visualizing high-dimensional data, in which a table of numbers is encoded as a grid of colored cells. The rows and columns of the matrix are ordered to highlight patterns and are often accompanied by dendrograms.

This package implements unit root tests for bounded time series following Cavaliere and Xu (2014) <doi:10.1016/j.jeconom.2013.08.026>. Standard unit root tests (ADF, Phillips-Perron) have non-standard limiting distributions when the time series is bounded. This package provides modified ADF and M-type tests (MZ-alpha, MZ-t, MSB) with p-values computed via Monte Carlo simulation of bounded Brownian motion. Supports one-sided (lower bound only) and two-sided bounds, with automatic lag selection using the MAIC criterion of Ng and Perron (2001) <doi:10.1111/1468-0262.00256>.

This package provides a curated collection of biodiversity and species-related datasets (birds, plants, reptiles, turtles, mammals, bees, marine data and related biological measurements), together with small utilities to load and explore them. The package gathers data sourced from public repositories (including Kaggle and well-known ecological/biological R packages) and standardizes access for researchers, educators, and data analysts working on biodiversity, biogeography, ecology and comparative biology. It aims to simplify reproducible workflows by packaging commonly used example datasets and metadata so they can be easily inspected, visualized, and used for teaching, testing, and prototyping analyses.

Supervised learning on tabular data with blockwise missing patterns, using the Blockwise Reduced Modeling (BRM) method of Srinivasan, Currim, and Ram (2025) <doi:10.1287/ijds.2022.9016>. BRM partitions the training data into overlapping subsets based on per-row feature-missing patterns, fits one user-supplied learner per subset with minimal imputation, and at prediction time routes each test instance to the best-matching subset model. The interface is learner-agnostic: any fit-and-predict pair can be plugged in, and convenience specifications are provided for linear models, tree models, random forests, and gradient boosting.

After using this, a publication-ready correlation table with p-values indicated will be created. The input can be a full data frame; any string and Boolean terms will be dropped as part of functionality. Correlations and p-values are calculated using the Hmisc framework. Output of the correlation_matrix() function is a table of strings; this gets saved out to a .csv2 with the save_correlation_matrix() function for easy insertion into a paper. For more details about the process, consult <https://paulvanderlaken.com/2020/07/28/publication-ready-correlation-matrix-significance-r/>.

Computes classical epidemiological measures and returns the complete worked derivation alongside the result: every intermediate quantity, the formula, and the formula with the observed numbers substituted in. Intended for teaching, for checking hand calculations, and for generating worked solutions in course materials. Scope is deliberately limited to methods a student can compute by hand on paper. Methods follow Mantel and Haenszel (1959) <doi:10.1093/jnci/22.4.719>, Greenland and Robins (1985, Biometrics 41, 55-68), Robins, Breslow and Greenland (1986, Biometrics 42, 311-323), and Breslow and Day (1980, IARC Scientific Publications No. 32).

This package provides functional control charts for statistical process monitoring of functional data, using the methods of Capezza et al. (2020) <doi:10.1002/asmb.2507>, Centofanti et al. (2021) <doi:10.1080/00401706.2020.1753581>, Capezza et al. (2024) <doi:10.1080/00224065.2024.2383674>, Capezza et al. (2024) <doi:10.1080/00401706.2024.2327346>, Centofanti et al. (2025) <doi:10.1080/00224065.2024.2430978>, Capezza et al. (2025) <doi:10.48550/arXiv.2410.20138>. The package is thoroughly illustrated in the paper of Capezza et al (2023) <doi:10.1080/00224065.2023.2219012>.

The purpose is to account for the random displacements (jittering) of true survey household cluster center coordinates in geostatistical analyses of Demographic and Health Surveys program (DHS) data. Adjustment for jittering can be implemented either in the spatial random effect, or in the raster/distance based covariates, or in both. Detailed information about the methods behind the package functionality can be found in our two papers. Umut Altay, John Paige, Andrea Riebler, Geir-Arne Fuglstad (2024) <doi:10.32614/RJ-2024-027>. Umut Altay, John Paige, Andrea Riebler, Geir-Arne Fuglstad (2023) <doi:10.1177/1471082X231219847>.

This package provides generalized univariate and multivariate Gelman-Rubin convergence diagnostics, effective sample size ('ESS') estimates, and principled termination thresholds for Markov chain Monte Carlo ('MCMC') simulations, based on Vats and Knudson (2021) <doi:10.1214/20-STS812>. The package incorporates replicated lugsail batch means variance estimators to construct stable convergence statistics for single and multiple chains. Additionally, it offers comprehensive tools for evaluating MCMC output generated from user-supplied probability density functions ('PDF') or log-likelihoods, including implementations for censored data models under right, left, interval, Type-I', Type-II', progressive, and hybrid censoring schemes.

Takes a .state file generated by IQ-TREE as an input and, for each ancestral node present in the file, generates a FASTA-formatted maximum likelihood (ML) sequence as well as an âAltAllâ sequence in which uncertain sites, determined by the two parameters thres_1 and thres_2, have the maximum likelihood state swapped with the next most likely state as described in Geeta N. Eick, Jamie T. Bridgham, Douglas P. Anderson, Michael J. Harms, and Joseph W. Thornton (2017), "Robustness of Reconstructed Ancestral Protein Functions to Statistical Uncertainty" <doi:10.1093/molbev/msw223>.

This package provides a single unified interface for computing a wide variety of classical and modern correlation and association measures. Continuous methods include classical correlations (Pearson, Spearman, Kendall), modern dependence measures (distance correlation, maximal information coefficient, Hilbert-Schmidt independence criterion, Chatterjee's xi, Hoeffding's D, mutual information), robust correlations (biweight midcorrelation, percentage bend, Winsorized), ordinal correlations (polychoric, tetrachoric), partial and semi-partial correlations, and nonparametric measures (ball correlation, Bergsma-Dassios tau*). Categorical association measures (Cramer's V, phi coefficient, Goodman-Kruskal gamma, Somers D, contingency coefficient, Tschuprow's T) are available via moderncor_cat().

This package provides interface to the Spectator Earth API <https://api.spectator.earth/>, mainly for obtaining the acquisition plans and satellite overpasses for Sentinel-1, Sentinel-2, Landsat-8 and Landsat-9 satellites. Current position and trajectory can also be obtained for a much larger set of satellites. It is also possible to search the archive for available images over the area of interest for a given (past) period, get the URL links to download the whole image tiles, or alternatively to download the image for just the area of interest based on selected spectral bands.

This package provides functions to retrieve the location of R scripts loaded through the source() function or run from the command line using the Rscript command. This functionality is analogous to the Bash shell's $BASH_SOURCE[0]. Users can first set the project root's path relative to the script path and then all subsequent paths relative to the root. This system ensures that all paths lead to the same location regardless of where any script is executed/loaded from without resorting to the use of setwd() at the top of the scripts.

This package implements the algorithm described in Barron, M., and Li, J. (Not yet published). This algorithm clusters samples from multiple ordered populations, links the clusters across the conditions and identifies marker genes for these changes. The package was designed for scRNA-Seq data but is also applicable to many other data types, just replace cells with samples and genes with variables. The package also contains functions for estimating the parameters for SparseMDC as outlined in the paper. We recommend that users further select their marker genes using the magnitude of the cluster centers.

This package provides methods for handling the missing values outliers are introduced in this package. The recognized missing values and outliers are replaced using a model-based approach. The model may consist of both autoregressive components and external regressors. The methods work robust and efficient, and they are fully tunable. The primary motivation for writing the package was preprocessing of the energy systems data, e.g. power plant production time series, but the package could be used with any time series data. For details, see Narajewski et al. (2021) <doi:10.1016/j.softx.2021.100809>.

This package provides functions for Estimating a (c)DCC-GARCH Model in large dimensions based on a publication by Engle et,al (2017) <doi:10.1080/07350015.2017.1345683> and Nakagawa et,al (2018) <doi:10.3390/ijfs6020052>. This estimation method is consist of composite likelihood method by Pakel et al. (2014) <http://paneldataconference2015.ceu.hu/Program/Cavit-Pakel.pdf> and (Non-)linear shrinkage estimation of covariance matrices by Ledoit and Wolf (2004,2015,2016). (<doi:10.1016/S0047-259X(03)00096-4>, <doi:10.1214/12-AOS989>, <doi:10.1016/j.jmva.2015.04.006>).

Some R functions, such as optim(), require a function of its gradient passed as separate arguments. When these are expensive to calculate it may be much faster to calculate the function (fn) and gradient (gr) together since they often share many calculations (chain rule). This package allows the user to pass in a single function that returns both the function and gradient, then splits (hence splitfngr) them so the results can be accessed separately. The functions provided allow this to be done with any number of functions/values, not just for functions and gradients.

Algebraic procedures for analyses of multiple social networks are delivered with this package. multiplex makes possible, among other things, to create and manipulate multiplex, multimode, and multilevel network data with different formats. Effective ways are available to treat multiple networks with routines that combine algebraic systems like the partially ordered semigroup with decomposition procedures or semiring structures with the relational bundles occurring in different types of multivariate networks. multiplex provides also an algebraic approach for affiliation networks through Galois derivations between families of the pairs of subsets in the two domains of the network with visualization options.

This package provides an automatic aggregation tool to manage point data privacy, intended to be helpful for the production of official spatial data and for researchers. The package pursues the data accuracy at the smallest possible areas preventing individual information disclosure. The methodology, based on hierarchical geographic data structures performs aggregation and local suppression of point data to ensure privacy as described in Lagonigro, R., Oller, R., Martori J.C. (2017) <doi:10.2436/20.8080.02.55>. The data structures are created following the guidelines for grid datasets from the European Forum for Geography and Statistics.

This package provides a novel interpretable machine learning-based framework to automate the development of a clinical scoring model for predefined outcomes. Our novel framework consists of six modules: variable ranking with machine learning, variable transformation, score derivation, model selection, domain knowledge-based score fine-tuning, and performance evaluation.The details are described in our research paper<doi:10.2196/21798>. Users or clinicians could seamlessly generate parsimonious sparse-score risk models (i.e., risk scores), which can be easily implemented and validated in clinical practice. We hope to see its application in various medical case studies.

Estimate the Å estákâ Berggren kinetic model (degradation model) from experimental data. A closed-form (analytic) solution to the degradation model is implemented as a non-linear fit, allowing for the extrapolation of the degradation of a drug product - both in time and temperature. Parametric bootstrap, with kinetic parameters drawn from the multivariate t-distribution, and analytical formulae (the delta method) are available options to calculate the confidence and prediction intervals. The results (modelling, extrapolations and statistical intervals) can be visualised with multiple plots. The examples illustrate the accelerated stability modelling in drugs and vaccines development.