This package provides a tool for multiply imputing missing data using MIDAS', a deep learning method based on denoising autoencoder neural networks (see Lall and Robinson, 2022; <doi:10.1017/pan.2020.49>). This algorithm offers significant accuracy and efficiency advantages over other multiple imputation strategies, particularly when applied to large datasets with complex features. Alongside interfacing with Python to run the core algorithm, this package contains functions for processing data before and after model training, running imputation model diagnostics, generating multiple completed datasets, and estimating regression models on these datasets. For more information see Lall and Robinson (2023) <doi:10.18637/jss.v107.i09>. This package is deprecated in favor of rMIDAS2'; it remains available for existing workflows but will receive only compatibility and documentation updates.

Mixed Treatment Comparison is a methodology to compare directly and/or indirectly health strategies (drugs, treatments, devices). This package provides an Rcmdr plugin to perform Mixed Treatment Comparison for binary outcome using BUGS code from Bristol University (Lu and Ades).

This package provides functions for performing spatial microsimulation ('raking') in R.

This package contains logic for sample-level variable set scoring using randomized reduced rank reconstruction error. Frost, H. Robert (2023) "Reconstruction Set Test (RESET): a computationally efficient method for single sample gene set testing based on randomized reduced rank reconstruction error" <doi:10.1101/2023.04.03.535366>.

This package performs Random Subspace Method (RSM) for high-dimensional linear regression to obtain variable importance measures. The final model is chosen based on validation set or Generalized Information Criterion.

This package implements a robust multivariate control-chart methodology for batch-based industrial processes with multiple correlated variables using the Dual STATIS (Structuration des Tableaux A Trois Indices de la Statistique) framework. A robust compromise covariance matrix is constructed from Phase I batches with the Minimum Covariance Determinant (MCD) estimator, and a Hotelling-type T² statistic is applied for anomaly detection in Phase II. The package includes functions to simulate clean and contaminated batches, to compute both robust and classical Hotelling T² control charts, to visualize results via robust biplots, and to launch an interactive shiny dashboard. An internal dataset (pharma_data) is provided for reproducibility. See Lavit, Escoufier, Sabatier and Traissac (1994) <doi:10.1016/0167-9473(94)90134-1> for the original STATIS methodology, and Rousseeuw and Van Driessen (1999) <doi:10.1080/00401706.1999.10485670> for the MCD estimator.

Adaptation of the Matlab tsEVA toolbox developed by Lorenzo Mentaschi available here: <https://github.com/menta78/tsEva>. It contains an implementation of the Transformed-Stationary (TS) methodology for non-stationary extreme value Analysis (EVA) as described in Mentaschi et al. (2016) <doi:10.5194/hess-20-3527-2016>. In synthesis this approach consists in: (i) transforming a non-stationary time series into a stationary one to which the stationary extreme value theory can be applied; and (ii) reverse-transforming the result into a non-stationary extreme value distribution. RtsEva offers several options for trend estimation (mean, extremes, seasonal) and contains multiple plotting functions displaying different aspects of the non-stationarity of extremes.

This package provides utilities for the design and analysis of replication studies. Features both traditional methods based on statistical significance and more recent methods such as the sceptical p-value; Held L. (2020) <doi:10.1111/rssa.12493>, Held et al. (2022) <doi:10.1214/21-AOAS1502>, Micheloud et al. (2023) <doi:10.1111/stan.12312>. Also provides related methods including the harmonic mean chi-squared test; Held, L. (2020) <doi:10.1111/rssc.12410>, and intrinsic credibility; Held, L. (2019) <doi:10.1098/rsos.181534>. Contains datasets from five large-scale replication projects.

This package provides methods for multiway data analysis by means of Parafac and Tucker 3 models. Robust versions (Engelen and Hubert (2011) <doi:10.1016/j.aca.2011.04.043>) and versions for compositional data are also provided (Gallo (2015) <doi:10.1080/03610926.2013.798664>, Di Palma et al. (2018) <doi:10.1080/02664763.2017.1381669>). Several optimization methods alternative to ALS are available (Simonacci and Gallo (2019) <doi:10.1016/j.chemolab.2019.103822>, Simonacci and Gallo (2020) <doi:10.1007/s00500-019-04320-9>).

Calculation of ratios between two data sets containing environmental data like element concentrations by different methods. Additionally plant element concentrations can be corrected for adhering particles (soil, airborne dust).

Conduct simulations of the Response Adaptive Block Randomization (RABR) design to evaluate its type I error rate, power and operating characteristics for binary and continuous endpoints. For more details of the proposed method, please refer to Zhan et al. (2021) <doi:10.1002/sim.9104>.

We provide functions to perform taxometric analyses. This package contains 46 functions, but only 5 should be called directly by users. CheckData() should be run prior to any taxometric analysis to ensure that the data are appropriate for taxometric analysis. RunTaxometrics() performs taxometric analyses for a sample of data. RunCCFIProfile() performs a series of taxometric analyses to generate a CCFI profile. CreateData() generates a sample of categorical or dimensional data. ClassifyCases() assigns cases to groups using the base-rate classification method.

Presentation-ready results tables for epidemiologists in an automated, reproducible fashion. The user provides the final analytical dataset and specifies the design of the table, with rows and/or columns defined by exposure(s), effect modifier(s), and estimands as desired, allowing to show descriptors and inferential estimates in one table -- bridging the rift between epidemiologists and their data, one table at a time. See Rothman (2017) <doi:10.1007/s10654-017-0314-3>.

This package implements the algorithm by Pourahmadi and Wang (2015) <doi:10.1016/j.spl.2015.06.015> for generating a random p x p correlation matrix. Briefly, the idea is to represent the correlation matrix using Cholesky factorization and p(p-1)/2 hyperspherical coordinates (i.e., angles), sample the angles from a particular distribution and then convert to the standard correlation matrix form. The angles are sampled from a distribution with pdf proportional to sin^k(theta) (0 < theta < pi, k >= 1) using the efficient sampling algorithm described in Enes Makalic and Daniel F. Schmidt (2018) <arXiv:1809.05212>.

Offers a handful of useful wrapper functions which streamline the reading, analyzing, and visualizing of variant call format (vcf) files in R. This package was designed to facilitate an explicit pipeline for optimizing Stacks (Rochette et al., 2019) (<doi:10.1111/mec.15253>) parameters during de novo (without a reference genome) assembly and variant calling of restriction-enzyme associated DNA sequence (RADseq) data. The pipeline implemented here is based on the 2017 paper "Lost in Parameter Space" (Paris et al., 2017) (<doi:10.1111/2041-210X.12775>) which establishes clear recommendations for optimizing the parameters m', M', and n', during the process of assembling loci.

This package provides functions for conducting robust variance estimation (RVE) meta-regression using both large and small sample RVE estimators under various weighting schemes. These methods are distribution free and provide valid point estimates, standard errors and hypothesis tests even when the degree and structure of dependence between effect sizes is unknown. Also included are functions for conducting sensitivity analyses under correlated effects weighting and producing RVE-based forest plots.

Gene annotation of rice (Oryza Sativa L.spp.japonica). The package is based on the annotation file from the website <http://plants.ensembl.org/Oryza_sativa/Info/Index>. Input gene's name then return some information, including the from position, the end position, the position type and the chromosome number.

Ray Shooting Depth functions are provided for bivariate analysis. This mainly includes functions for computing the bivariate depth as well as RS median. Drawing functions for depth bags are also provided.

This package implements efficient simulation procedures to estimate tail loss probabilities and conditional excess for a stock portfolio. The log-returns are assumed to follow a t-copula model with generalized hyperbolic or t marginals.

This package implements diversification analyses using the phylogenetic birth-death-shift model. It leverages belief propagation techniques to calculate branch-specific diversification rates, see Kopperud & Hoehna (2025) <doi:10.1093/sysbio/syaf041>.

Utilities for reading, writing, and managing RCDF files, including encryption and decryption support. It offers a flexible interface for handling data stored in encrypted Parquet format, along with metadata extraction, key management, and secure operations using AES and RSA encryptions.

This package provides a set of functions to simplify reading data from files. The main function, reader(), should read most common R datafile types without needing any parameters except the filename. Other functions provide simple ways of handling file paths and extensions, and automatically detecting file format and structure.

This package provides tools for response surface analysis, using a comparative framework that identifies best-fitting solutions across 37 families of polynomials. Many of these tools are based upon and extend the RSA package, by testing a larger scope of polynomials (+27 families), more diverse response surface probing techniques (+acceleration points), more plots (+line of congruence, +line of incongruence, both with extrema), and other useful functions for exporting results.

Risk-related information (like the prevalence of conditions, the sensitivity and specificity of diagnostic tests, or the effectiveness of interventions or treatments) can be expressed in terms of frequencies or probabilities. By providing a toolbox of corresponding metrics and representations, riskyr computes, translates, and visualizes risk-related information in a variety of ways. Adopting multiple complementary perspectives provides insights into the interplay between key parameters and renders teaching and training programs on risk literacy more transparent (see <doi:10.3389/fpsyg.2020.567817>, for details).