An enterprise-targeted scalable and UI-standardized shiny framework including a variety of developer convenience functions with the goal of both streamlining robust application development while assisting with creating a consistent user experience regardless of application or developer.

Utilize the Bayesian prior and posterior predictive checking approach to provide a statistical assessment of replication success and failure. The package is based on the methods proposed in Zhao,Y., Wen X.(2021) <arXiv:2105.03993>.

This package provides tools for estimating the statistical power of Interrupted Time Series (ITS) designs, with a focus on healthcare applications. The package supports prospective power calculations before a study begins, and retrospective assessments of whether a completed study was adequately powered. It includes functions to estimate nuisance parameters (baseline, residual standard deviation, autocorrelation) from data observed before the intervention, and to estimate power via Monte Carlo simulation for single-site and multi-site designs. Utility functions for design optimisation sweeps and publication- ready plots are also provided.

Download press freedom index data from Reporters Without Borders (RSF) with period-aware encoding handling. Data are downloaded from the RSF website (<https://rsf.org/en/index>). Provides infrastructure for data cleaning and ISO 3166 standardization in downstream phases.

Improves genotype inference and downstream Adaptive Immune Receptor Repertoire Sequence data analysis. Inference of allele similarity clusters, an alternative naming scheme and genotype inference for immunoglobulin heavy chain repertoires. The main tools are allele similarity clusters, and allele based genotype. The first tool is designed to reduce the ambiguity within the immunoglobulin heavy chain V alleles. The ambiguity is caused by duplicated or similar alleles which are shared among different genes. The second tool is an allele based genotype, that determined the presence of an allele based on a threshold derived from a naive population. See Peres et al. (2023) <doi:10.1093/nar/gkad603>.

Facilitates population-level analysis of ligand-receptor (LR) interactions using large-scale single-cell transcriptomic data. Identifies significant LR pairs and quantifies their interactions through correlation-based filtering and projection score computations. Designed for large-sample single-cell studies, the package employs statistical modeling, including linear regression, to investigate LR relationships between cell types. It provides a systematic framework for understanding cell-cell communication, uncovering regulatory interactions and signaling mechanisms. Offers tools for LR pair-level, sample-level, and differential interaction analyses, with comprehensive visualization support to aid biological interpretation. The methodology is described in a manuscript currently under review and will be referenced here once published or publicly available.

Computing Average and TPX Power under various BHFDR type sequential procedures. All of these procedures involve control of some summary of the distribution of the FDP, e.g. the proportion of discoveries which are false in a given experiment. The most widely known of these, the BH-FDR procedure, controls the FDR which is the mean of the FDP. A lesser known procedure, due to Lehmann and Romano, controls the FDX, or probability that the FDP exceeds a user provided threshold. This is less conservative than FWE control procedures but much more conservative than the BH-FDR proceudre. This package and the references supporting it introduce a new procedure for controlling the FDX which we call the BH-FDX procedure. This procedure iteratively identifies, given alpha and lower threshold delta, an alpha* less than alpha at which BH-FDR guarantees FDX control. This uses asymptotic approximation and is only slightly more conservative than the BH-FDR procedure. Likewise, we can think of the power in multiple testing experiments in terms of a summary of the distribution of the True Positive Proportion (TPP), the portion of tests truly non-null distributed that are called significant. The package will compute power, sample size or any other missing parameter required for power defined as (i) the mean of the TPP (average power) or (ii) the probability that the TPP exceeds a given value, lambda, (TPX power) via asymptotic approximation. All supplied theoretical results are also obtainable via simulation. The suggested approach is to narrow in on a design via the theoretical approaches and then make final adjustments/verify the results by simulation. The theoretical results are described in Izmirlian, G (2020) Statistics and Probability letters, "<doi:10.1016/j.spl.2020.108713>", and an applied paper describing the methodology with a simulation study is in preparation. See citation("pwrFDR").

Multi-group (dynamical) structural equation models in combination with confirmatory network models from cross-sectional, time-series and panel data <doi:10.31234/osf.io/8ha93>. Allows for confirmatory testing and fit as well as exploratory model search.

Figures rendered on graphics devices are usually rescaled to fit pre-determined device dimensions. plotscale implements the reverse: desired plot dimensions are specified and device dimensions are calculated to accommodate marginal material, giving consistent proportions for plot elements. Default methods support grid graphics such as lattice and ggplot. See "example('devsize')" and "vignette('plotscale')".

This package provides a broad-view perspective on data via linear mapping of data onto a radial coordinate system. The package contains functions to visualize the residual values of linear regression and Cartesian data in the defined radial scheme. See the pacviz documentation page for more information: <https://pacviz.sriley.dev/>.

We provide comprehensive draft data for major professional sports leagues, including the National Football League (NFL), National Basketball Association (NBA), and National Hockey League (NHL). It offers access to both historical and current draft data, allowing for detailed analysis and research on player biases and player performance. The package is useful for sports fans and researchers interested in identifying biases and trends within scouting reports. Created by web scraping data from leading websites that cover professional sports player scouting reports, the package allows users to filter and summarize data for analytical purposes. For further details on the methods used, please refer to Wickham (2022) "rvest: Easily Harvest (Scrape) Web Pages" <https://CRAN.R-project.org/package=rvest> and Harrison (2023) "RSelenium: R Bindings for Selenium WebDriver" <https://CRAN.R-project.org/package=RSelenium>.

Market odds from from Pinnacle, an online sports betting bookmaker (see <https://www.pinnacle.com> for more information). Included are datasets for the Major League Baseball (MLB) 2016 season and the USA election 2016. These datasets can be used to build models and compare statistical information with the information from prediction markets.The Major League Baseball (MLB) 2016 dataset can be used for sabermetrics analysis and also can be used in conjunction with other popular Major League Baseball (MLB) datasets such as Retrosheets or the Lahman package by merging by GameID.

This package provides functions for calculating and analyzing the proliferative index (PI) from an RNA-seq dataset. As described in Ramaker & Lasseigne, et al. bioRxiv, 2016 <doi:10.1101/063057>.

This package provides a Shiny application for calculating phytosanitary inspection plans based on risks. It generates a diagram of pallets in a lot, highlights the units to be sampled, and documents them based on the selected sampling method (simple random or systematic sampling).

Executes simple parametric models for right-censored survival data. Functionality emulates capabilities in Minitab', including fitting right-censored data, assessing fit, plotting survival functions, and summary statistics and probabilities.

This package provides a tool which aims to help evaluate the effect of external borrowing using an integrated approach described in Lewis et al., (2019) <doi:10.1080/19466315.2018.1497533> that combines propensity score and Bayesian dynamic borrowing methods.

NOTE: PARAMLINK HAS BEEN SUPERSEDED BY THE PEDSUITE PACKAGES (<https://magnusdv.github.io/pedsuite/>). PARAMLINK IS MAINTAINED ONLY FOR LEGACY PURPOSES AND SHOULD NOT BE USED IN NEW PROJECTS. A suite of tools for analysing pedigrees with marker data, including parametric linkage analysis, forensic computations, relatedness analysis and marker simulations. The core of the package is an implementation of the Elston-Stewart algorithm for pedigree likelihoods, extended to allow mutations as well as complex inbreeding. Features for linkage analysis include singlepoint LOD scores, power analysis, and multipoint analysis (the latter through a wrapper to the MERLIN software). Forensic applications include exclusion probabilities, genotype distributions and conditional simulations. Data from the Familias software can be imported and analysed in paramlink'. Finally, paramlink offers many utility functions for creating, manipulating and plotting pedigrees with or without marker data (the actual plotting is done by the kinship2 package).

Priority-ElasticNet extends the Priority-LASSO method (Klau et al. (2018) <doi:10.1186/s12859-018-2344-6>) by incorporating the ElasticNet penalty, allowing for both L1 and L2 regularization. This approach fits successive ElasticNet models for several blocks of (omics) data with different priorities, using the predicted values from each block as an offset for the subsequent block. It also offers robust options to handle block-wise missingness in multi-omics data, improving the flexibility and applicability of the model in the presence of incomplete datasets.

Use the paged media properties in CSS and the JavaScript library paged.js to split the content of an HTML document into discrete pages. Each page can have its page size, page numbers, margin boxes, and running headers, etc. Applications of this package include books, letters, reports, papers, business cards, resumes, and posters.

This package provides a power analysis tool for jointly testing the cause-1 cause-specific hazard and the any-cause hazard with competing risks data.

This package provides a suite of non-parametric, visual tools for assessing differences in data structures for two datasets that contain different observations of the same variables. These tools are all based on Principal Component Analysis (PCA) and thus effectively address differences in the structures of the covariance matrices of the two datasets. The PCASDC tools consist of easy-to-use, intuitive plots that each focus on different aspects of the PCA decompositions. The cumulative eigenvalue (CE) plot describes differences in the variance components (eigenvalues) of the deconstructed covariance matrices. The angle plot presents the information loss when moving from the PCA decomposition of one dataset to the PCA decomposition of the other. The chroma plot describes the loading patterns of the two datasets, thereby presenting the relative weighting and importance of the variables from the original dataset.

Includes functions and data used in the book "Presenting Statistical Results Effectively", Andersen and Armstrong (2022, ISBN: 978-1446269800). Several functions aid in data visualization - creating compact letter displays for simple slopes, kernel density estimates with normal density overlay. Other functions aid in post-model evaluation heatmap fit statistics for binary predictors, several variable importance measures, compact letter displays and simple-slope calculation. Finally, the package makes available the example datasets used in the book.

This package provides functions to get prediction intervals and prediction points of future observations from mixture distributions like gamma, beta, Weibull and normal.

Set of tools to automatize extraction of data on pests from EPPO Data Services and EPPO Global Database and to put them into tables with human readable format. Those function use EPPO database API', thus you first need to register on <https://data.eppo.int> (free of charge). Additional helpers allow to download, check and connect to SQLite EPPO database'.