Read examples with interlinear glosses from files or from text and print them in a way compatible with both Latex and HTML outputs.

This is an add-on package to gamlss'. The purpose of this package is to allow users to fit GAMLSS (Generalised Additive Models for Location Scale and Shape) models when the response variable is defined either in the intervals [0,1), (0,1] and [0,1] (inflated at zero and/or one distributions), or in the positive real line including zero (zero-adjusted distributions). The mass points at zero and/or one are treated as extra parameters with the possibility to include a linear predictor for both. The package also allows transformed or truncated distributions from the GAMLSS family to be used for the continuous part of the distribution. Standard methods and GAMLSS diagnostics can be used with the resulting fitted object.

Wrappers for functions in the gRain package to emulate some RHugin functionality, allowing the building of Bayesian networks consisting on discrete chance nodes incrementally, through adding nodes, edges and conditional probability tables, the setting of evidence, both hard (boolean) or soft (likelihoods), querying marginal probabilities and normalizing constants, and generating sets of high-probability configurations. Computations will typically not be so fast as they are with RHugin', but this package should assist users without access to Hugin to use code written to use RHugin'.

This package provides tools to assist planning and monitoring of time-to-event trials under complicated censoring assumptions and/or non-proportional hazards. There are three main components: The first is analytic calculation of predicted time-to-event trial properties, providing estimates of expected hazard ratio, event numbers and power under different analysis methods. The second is simulation, allowing stochastic estimation of these same properties. Thirdly, it provides parametric event prediction using blinded trial data, including creation of prediction intervals. Methods are based upon numerical integration and a flexible object-orientated structure for defining event, censoring and recruitment distributions (Curves).

This package provides tools for fitting sparse generalised linear mixed models with l0 regularisation. Selects fixed and random effects under the hierarchy constraint that fixed effects must precede random effects. Uses coordinate descent and local search algorithms to rapidly deliver near-optimal estimates. Gaussian and binomial response families are currently supported. For more details see Thompson, Wand, and Wang (2025) <doi:10.48550/arXiv.2506.20425>.

Gene and Region Counting of Mutations (GARCOM) package computes mutation (or alleles) counts per gene per individuals based on gene annotation or genomic base pair boundaries. It comes with features to accept data formats in plink(.raw) and VCF. It provides users flexibility to extract and filter individuals, mutations and genes of interest.

Robust Estimation of Multivariate Location and Scatter in the Presence of Cellwise and Casewise Contamination and Missing Data.

It implements a hybrid spatial model for improved spatial prediction by combining the variable selection capability of LASSO (Least Absolute Shrinkage and Selection Operator) with the Geographically Weighted Regression (GWR) model that captures the spatially varying relationship efficiently. For method details see, Wheeler, D.C.(2009).<DOI:10.1068/a40256>. The developed hybrid model efficiently selects the relevant variables by using LASSO as the first step; these selected variables are then incorporated into the GWR framework, allowing the estimation of spatially varying regression coefficients at unknown locations and finally predicting the values of the response variable at unknown test locations while taking into account the spatial heterogeneity of the data. Integrating the LASSO and GWR models enhances prediction accuracy by considering spatial heterogeneity and capturing the local relationships between the predictors and the response variable. The developed hybrid spatial model can be useful for spatial modeling, especially in scenarios involving complex spatial patterns and large datasets with multiple predictor variables.

Automated General-to-Specific (GETS) modelling of the mean and variance of a regression, and indicator saturation methods for detecting and testing for structural breaks in the mean, see Pretis, Reade and Sucarrat (2018) <doi:10.18637/jss.v086.i03> for an overview of the package. In advanced use, the estimator and diagnostics tests can be fully user-specified, see Sucarrat (2021) <doi:10.32614/RJ-2021-024>.

Triangular and trapezoidal fuzzy numbers are used to study fuzzy logic, fuzzy reasoning and approximating, fuzzy regression models, etc. This package builds the generating function for triangular and trapezoidal fuzzy numbers based on Souliotis et al. (2022)<doi:10.3390/math10183350>. They proposed a method for the construction of fuzzy numbers via a cumulative distribution function based on the possibility theory.

We define generalized multipartite networks as the joint observation of several networks implying some common pre-specified groups of individuals. The aim is to fit an adapted version of the popular stochastic block model to multipartite networks, as described in Bar-hen, Barbillon and Donnet (2020) <arXiv:1807.10138>.

Reproducible, programmatic retrieval of datasets from the GESIS Data Archive. The GESIS Data Archive <https://search.gesis.org> makes available thousands of invaluable datasets, but researchers using these datasets are caught in a bind. The archive's terms and conditions bar dissemination of downloaded datasets to third parties, but to ensure that one's work can be reproduced, assessed, and built upon by others, one must provide access to the raw data one has employed. The gesisdata package cuts this knot by providing registered users with programmatic, reproducible access to GESIS datasets from within R'.

Two arms clinical trials required sample size is calculated in the comprehensive parametric context. The calculation is based on the type of endpoints(continuous/binary/time-to-event/ordinal), design (parallel/crossover), hypothesis tests (equality/noninferiority/superiority/equivalence), trial arms noncompliance rates and expected loss of follow-up. Methods are described in: Chow SC, Shao J, Wang H, Lokhnygina Y (2017) <doi:10.1201/9781315183084>, Wittes, J (2002) <doi:10.1093/epirev/24.1.39>, Sato, T (2000) <doi:10.1002/1097-0258(20001015)19:19%3C2689::aid-sim555%3E3.0.co;2-0>, Lachin J M, Foulkes, M A (1986) <doi:10.2307/2531201>, Whitehead J(1993) <doi:10.1002/sim.4780122404>, Julious SA (2023) <doi:10.1201/9780429503658>.

This package provides functions to calculate the best linear unbiased prediction of genotype-by-environment metrics: ecovalence, environmental variance, Finlay and Wilkinson regression and Lin and Binns superiority measure, based on a multi-environment genomic prediction model.

Tests of goodness-of-fit based on a kernel smoothing of the data. References: Pavà a (2015) <doi:10.18637/jss.v066.c01>.

R provides fantastic tools for changepoint analysis, but plots generated by the tools do not have the ggplot2 style. This tool, however, combines changepoint', changepoint.np and ecp together, and uses ggplot2 to visualize changepoints. It provides a unified ggcpt S3 result class, broom'-style tidy/glance/augment methods, autoplot()', composable geoms ('geom_changepoint()', geom_cpt_segment()', geom_cpt_ci()', stat_changepoint()'), a unified cpt_detect() dispatcher with method introspection via cpt_methods()', wrappers for several optional engines (WBS, WBS2, NOT, MOSUM, FPOP, Isolate-Detect, TGUH), a method comparison module, accuracy metrics, data simulation, and canonical test signals.

Circular genomic permutation approach uses genome wide association studies (GWAS) results to establish the significance of pathway/gene-set associations whilst accounting for genomic structure. All single nucleotide polymorphisms (SNPs) in the GWAS are placed in a circular genome according to their location. Then the complete set of SNP association p-values are permuted by rotation with respect to the SNPs genomic locations. Two testing frameworks are available: permutations at the gene level, and permutations at the SNP level. The permutation at the gene level uses Fisher's combination test to calculate a single gene p-value, followed by the hypergeometric test. The SNP count methodology maps each SNP to pathways/gene-sets and calculates the proportion of SNPs for the real and the permutated datasets above a pre-defined threshold. Genomicper requires a matrix of GWAS association p-values and SNPs annotation to genes. Pathways can be obtained from within the package or can be provided by the user. Cabrera et al (2012) <doi:10.1534/g3.112.002618> .

This package provides complete detailed preprocessing of two-dimensional gas chromatogram (GCxGC) samples. Baseline correction, smoothing, peak detection, and peak alignment. Also provided are some analysis functions, such as finding extracted ion chromatograms, finding mass spectral data, targeted analysis, and nontargeted analysis with either the National Institute of Standards and Technology Mass Spectral Library or with the mass data. There are also several visualization methods provided for each step of the preprocessing and analysis.

We implement and extend the Dividing Local Gaussian Process algorithm by Lederer et al. (2020) <doi:10.48550/arXiv.2006.09446>. Its main use case is in online learning where it is used to train a network of local GPs (referred to as tree) by cleverly partitioning the input space. In contrast to a single GP, GPTreeO is able to deal with larger amounts of data. The package includes methods to create the tree and set its parameter, incorporating data points from a data stream as well as making joint predictions based on all relevant local GPs.

Multivariate time series analysis based on Generalized Space-Time Autoregressive Model by Ruchjana et al.(2012) <doi:10.1063/1.4724118>.

This package provides a genomic simulation approach for creating biologically informed individual genotypes from empirical data that 1) samples alleles from populations without replacement, 2) segregates alleles based on species-specific recombination rates. gscramble is a flexible simulation approach that allows users to create pedigrees of varying complexity in order to simulate admixed genotypes. Furthermore, it allows users to track haplotype blocks from the source populations through the pedigrees.

Data sets used in the book Marra and Radice (2025, ISBN:9781032973111) "Copula Additive Distributional Regression Using R", for illustrating the fitting of various joint (and univariate) regression models, with several types of covariate effects, in the presence of equations errors association.

Extends classical linear and quadratic discriminant analysis by incorporating permutation group symmetries into covariance matrix estimation. The package leverages methodology from the gips framework to identify and impose permutation structures that act as a form of regularization, improving stability and interpretability in settings with symmetric or exchangeable features. Several discriminant analysis variants are provided, including pooled and class-specific covariance models, as well as multi-class extensions with shared or independent symmetry structures. For more details about gips methodology see and Graczyk et al. (2022) <doi:10.1214/22-AOS2174> and Chojecki, Morgen, KoÅ odziejek (2025, <doi:10.18637/jss.v112.i07>).

The main purpose of this package is to allow fitting of mixture distributions with generalised additive models for location scale and shape models see Chapter 7 of Stasinopoulos et al. (2017) <doi:10.1201/b21973-4>.