This package provides functions to support data cleaning, evaluation, and description, developed for integration with Maelstrom Research software tools. madshapR provides functions primarily to evaluate and manipulate datasets and data dictionaries in preparation for data harmonization with the package Rmonize and to facilitate integration and transfer between RStudio servers and secure Opal environments. madshapR functions can be used independently but are optimized in conjunction with â Rmonizeâ functions for streamlined and coherent harmonization processing.

Facilitate frequentist and Bayesian meta-analysis of diagnosis and prognosis research studies. It includes functions to summarize multiple estimates of prediction model discrimination and calibration performance (Debray et al., 2019) <doi:10.1177/0962280218785504>. It also includes functions to evaluate funnel plot asymmetry (Debray et al., 2018) <doi:10.1002/jrsm.1266>. Finally, the package provides functions for developing multivariable prediction models from datasets with clustering (de Jong et al., 2021) <doi:10.1002/sim.8981>.

Speeds up the process of loading raw data from MBA (Multiplex Bead Assay) examinations, performs quality control checks, and automatically normalises the data, preparing it for more advanced, downstream tasks. The main objective of the package is to create a simple environment for a user, who does not necessarily have experience with R language. The package is developed within the project of the same name - PvSTATEM', which is an international project aiming for malaria elimination.

Using matrix layout to visualize the unique, common, or individual contribution of each predictor (or matrix of predictors) towards explained variation on different models. These contributions were derived from variation partitioning (VP) and hierarchical partitioning (HP), applying the algorithm of "Lai et al. (2022) Generalizing hierarchical and variation partitioning in multiple regression and canonical analyses using the rdacca.hp R package.Methods in Ecology and Evolution, 13: 782-788 <doi:10.1111/2041-210X.13800>".

PCA done by eigenvalue decomposition of a data correlation matrix, here it automatically determines the number of factors by eigenvalue greater than 1 and it gives the uncorrelated variables based on the rotated component scores, Such that in each principal component variable which has the high variance are selected. It will be useful for non-statisticians in selection of variables. For more information, see the <http://www.ijcem.org/papers032013/ijcem_032013_06.pdf> web page.

An integrated set of functions for building, analyzing, and visualizing Analytic Hierarchy Process (AHP) models, designed to support structured decision-making in consultancy, policy analysis, and research (Bose 2022 <doi:10.1002/mcda.1784>; Bose 2023 <doi:10.1002/mcda.1821>). In addition to tools for assessing and improving the consistency of pairwise comparison matrices (PCMs), the package supports full-hierarchy weight computation, intuitive tree-based visualization, sensitivity analysis, along with convenient PCM generation from user preferences.

Biostatistical and clinical data analysis, including descriptive statistics, exploratory data analysis, sample size and power calculations, statistical inference, and data visualization. Normality tests are implemented following Mishra et al. (2019) <doi:10.4103/aca.ACA_157_18>, omnibus test procedures are based on Blanca et al. (2017) <doi:10.3758/s13428-017-0918-2> and Field et al. (2012, ISBN:9781446200469), while sample size and power calculation methods follow Chow et al. (2017) <doi:10.1201/9781315183084>.

Color palettes for all people, including those with color vision deficiency. Popular color palette series have been organized by type and have been scored on several properties such as color-blind-friendliness and fairness (i.e. do colors stand out equally?). Own palettes can also be loaded and analysed. Besides the common palette types (categorical, sequential, and diverging) it also includes cyclic and bivariate color palettes. Furthermore, a color for missing values is assigned to each palette.

This package provides functions to have visualization and clean-up of enriched gene ontologies (GO) terms, protein complexes and pathways (obtained from multiple databases) using ConsensusPathDB from gene set over-expression analysis. Performs clustering of pathway based on similarity of over-expressed gene sets and visualizations similar to Ingenuity Pathway Analysis (IPA) when up and down regulated genes are known. The methods are described in a paper currently submitted by Orecchioni et al, 2020 in Nanoscale.

Use spectrophotometry measurements performed on insects as a way to infer pathogens virulence. Insect movements cause fluctuations in fluorescence signal, and functions are provided to estimate when the insect has died as the moment when variance in autofluorescence signal drops to zero. The package provides functions to obtain this estimate together with functions to import spectrophotometry data from a Biotek microplate reader. Details of the method are given in Parthuisot et al. (2018) <doi:10.1101/297929>.

This package implements a variant of the Self-Organizing Map (SOM) algorithm designed for mixed-attribute datasets. Similarity between observations is computed using the Gower distance, and categorical prototypes are updated via heuristic strategies (weighted mode and multinomial sampling). Provides functions for model fitting, mapping, visualization (U-Matrix and component planes), and evaluation, making SOM applicable to heterogeneous real-world data. For methodological details see Sáez and Salas (2026) <doi:10.1007/s41060-025-00941-6>.

Implementation of a parametric joint model for modelling recurrent and competing event processes using generalised survival models as described in Entrop et al., (2025) <doi:10.1002/bimj.70038>. The joint model can subsequently be used to predict the mean number of events in the presence of competing risks at different time points. Comparisons of the mean number of event functions, e.g. the differences in mean number of events between two exposure groups, are also available.

This package implements an Integer Programming-based method for optimising genetic gain in polyclonal selection, where the goal is to select a group of genotypes that jointly meet multi-trait selection criteria. The method uses predictors of genotypic effects obtained from the fitting of mixed models. Its application is demonstrated with grapevine data, but is applicable to other species and breeding contexts. For more details see Surgy et al. (2025) <doi:10.1007/s00122-025-04885-0>.

Build your own universe of packages similar to the tidyverse package <https://tidyverse.org/> with this meta-package creator. Create a package-verse, or meta package, by supplying a custom name for the collection of packages and the vector of desired package names to includeâ and optionally supply a destination directory, an indicator of whether to keep the created package directory, and/or a vector of verbs implement via the usethis <http://usethis.r-lib.org/> package.

This package provides a lightweight yet powerful framework for building robust data analysis pipelines. With pipeflow', you initialize a pipeline with your dataset and construct workflows step by step by adding R functions. You can modify, remove, or insert steps and parameters at any stage, while pipeflow ensures the pipeline's integrity. Overall, this package offers a beginner-friendly framework that simplifies and streamlines the development of data analysis pipelines by making them modular, intuitive, and adaptable.

It aggregates protein panel data and metadata for protein quantitative trait locus (pQTL) analysis using pQTLtools (<https://jinghuazhao.github.io/pQTLtools/>). The package includes data from affinity-based panels such as Olink (<https://olink.com/>) and SomaScan (<https://somalogic.com/>), as well as mass spectrometry-based panels from CellCarta (<https://cellcarta.com/>), Seer (<https://seer.bio/>) and SWATH-MS (<doi:10.15252/msb.20178126>). The metadata encompasses updated annotations and publication details.

Easy-to-use interface to X-13-ARIMA-SEATS, the seasonal adjustment software by the US Census Bureau. It offers full access to almost all options and outputs of X-13, including X-11 and SEATS, automatic ARIMA model search, outlier detection and support for user defined holiday variables, such as Chinese New Year or Indian Diwali. A graphical user interface can be used through the seasonalview package. Uses the X-13-binaries from the x13binary package.

Efficient implementation of sparse group lasso with optional bound constraints on the coefficients; see <doi:10.18637/jss.v110.i06>. It supports the use of a sparse design matrix as well as returning coefficient estimates in a sparse matrix. Furthermore, it correctly calculates the degrees of freedom to allow for information criteria rather than cross-validation with very large data. Finally, the interface to compiled code avoids unnecessary copies and allows for the use of long integers.

Visualizes sulcal morphometry data derived from BrainVisa <https://brainvisa.info/> including width, depth, surface area, and length. The package enables mapping of statistical group results or subject-level values onto cortical surface maps, with options to focus on all sulci or only selected regions of interest. Users can display all four measures simultaneously or restrict plots to chosen measures, creating composite, publication-quality brain visualizations in R to support the analysis and interpretation of sulcal morphology.

This package provides a template dashboard system with AI agent integrated. Comes with default themes that can be customized. Developers can upload modified templates on Github', and users can easily download templates with RStudio project wizard. The key features of the default template include light and dark theme switcher, resizing graphs, synchronizing inputs across sessions, new notification system, fancy progress bars, and card-like flip panels with back sides, as well as various of HTML tool widgets.

This package provides tools for constructing conditional two-dimensional reference regions in continuous data, particularly suited for clinical, biological, or epidemiological studies requiring robust multivariate assessment. The implemented methodology combines directional quantiles with medianâ based partial correlation models to produce reliable and interpretable reference regions even in the presence of outliers. Key features include robust conditional modeling for two responses conditioned on covariates, directional quantile regions, crossâ validation of coverage, visualization tools, and flexible formulaâ based inputs.

Transfer learning for generalized factor models with support for continuous, count (Poisson), and binary data types. The package provides functions for single and multiple source transfer learning, source detection to identify positive and negative transfer sources, factor decomposition using Maximum Likelihood Estimation (MLE), and information criteria ('IC1 and IC2') for rank selection. The methods are particularly useful for high-dimensional data analysis where auxiliary information from related source datasets can improve estimation efficiency in the target domain.

A slightly modified version of rivertile layout generator for river.

Compared to rivertile, rivercarro adds:

1. Monocle layout, views will takes all the usable area on the screen.

2. Gaps instead of padding around views or layout area.

3. Modify gaps size at runtime.

4. Smart gaps, if there is only one view, gaps will be disable.

5. Limit the width of the usable area of the screen.

6. Per tag configurations.

7. Cycle through layout

Perform large scale genomic data retrieval and functional annotation retrieval. This package aims to provide users with a standardized way to automate genome, proteome, RNA, coding sequence (CDS), GFF, and metagenome retrieval from NCBI RefSeq, NCBI Genbank, ENSEMBL, and UniProt databases. Furthermore, an interface to the BioMart database allows users to retrieve functional annotation for genomic loci. In addition, users can download entire databases such as NCBI RefSeq, NCBI nr, NCBI nt, NCBI Genbank, etc with only one command.