Abstract descriptions of (yet) unobserved variables.

This package provides a suite of analytical functionalities to process and analyze visual meteor observations from the Visual Meteor Database of the International Meteor Organization <https://www.imo.net/>.

Estimates the type of variables in non-quality controlled data. The prediction is based on a random forest model, trained on over 5000 medical variables with accuracy of 99%. The accuracy can hardy depend on type and coding style of data.

Calibrates population-level cause-specific mortality fractions (CSMFs) that are derived using computer-coded verbal autopsy (CCVA) algorithms. Leveraging the data collected in the Child Health and Mortality Prevention Surveillance (CHAMPS;<https://champshealth.org/>) project, the package stores misclassification matrix estimates of three CCVA algorithms (EAVA, InSilicoVA, and InterVA) and two age groups (neonates aged 0-27 days, and children aged 1-59 months) across countries (specific estimates for Bangladesh, Ethiopia, Kenya, Mali, Mozambique, Sierra Leone, and South Africa, and a combined estimate for all other countries), enabling global calibration. These estimates are obtained using the framework proposed in Pramanik et al. (2025;<doi:10.1214/24-AOAS2006>) and are analyzed in Pramanik et al. (2026;<doi:10.1136/bmjgh-2025-021747>). Given VA-only data for an age group, CCVA algorithm, and country, the package utilizes the corresponding misclassification matrix estimate in the modular VA-Calibration framework (Pramanik et al.,2025;<doi:10.1214/24-AOAS2006>) and produces calibrated estimates of CSMFs. The package also supports ensemble calibration to accommodate multiple algorithms. More generally, this allows calibration of population-level prevalence derived from single-class predictions of discrete classifiers. For this, users need to provide fixed or uncertainty-quantified misclassification matrices. This work is supported by the Eunice Kennedy Shriver National Institute of Child Health K99 NIH Pathway to Independence Award (1K99HD114884-01A1), the Bill and Melinda Gates Foundation (INV-034842), and the Johns Hopkins Data Science and AI Institute.

Visual contour and 2D point and contour plots for binary classification modeling under algorithms such as glm', rf', gbm', nnet and svm', presented over two dimensions generated by famd and mca methods. Package FactoMineR for multivariate reduction functions and package MBA for interpolation functions are used. The package can be used to visualize the discriminant power of input variables and algorithmic modeling, explore outliers, compare algorithm behaviour, etc. It has been created initially for teaching purposes, but it has also many practical uses under the XAI paradigm.

R Codes and Datasets for Duchateau, L. and Janssen, P. and Rowlands, G. J. (1998). Linear Mixed Models. An Introduction with applications in Veterinary Research. International Livestock Research Institute.

Calculate and plot Venn diagrams in 2D and 3D.

Visualize Variance is an intuitive shiny applications tailored for agricultural research data analysis, including one-way and two-way analysis of variance, correlation, and other essential statistical tools. Users can easily upload their datasets, perform analyses, and download the results as a well-formatted document, streamlining the process of data analysis and reporting in agricultural research.The experimental design methods are based on classical work by Fisher (1925) and Scheffe (1959). The correlation visualization approaches follow methods developed by Wei & Simko (2021) and Friendly (2002) <doi:10.1198/000313002533>.

This package provides templates and functions to simplify the production and maintenance of curriculum vitae.

Full model selection (detection of the relevant features and estimation of the number of clusters) for model-based clustering (see reference here <doi:10.1007/s11222-016-9670-1>). Data to analyze can be continuous, categorical, integer or mixed. Moreover, missing values can occur and do not necessitate any pre-processing. Shiny application permits an easy interpretation of the results.

Identifies the optimal confidence level to represent the results of a set of pairwise tests as suggested by Armstrong and Poirier (2025) <doi:10.1017/pan.2024.24>.

The vcfpp.h (<https://github.com/Zilong-Li/vcfpp>) provides an easy-to-use C++ API of htslib', offering full functionality for manipulating Variant Call Format (VCF) files. The vcfppR package serves as the R bindings of the vcfpp.h library, enabling rapid processing of both compressed and uncompressed VCF files. Explore a range of powerful features for efficient VCF data manipulation.

Trading Strategies for high Option Volatility environment are represented here through their Graphs. The graphic indicators, strategies, calculations, functions and all the discussions are for academic, research, and educational purposes only and should not be construed as investment advice and come with absolutely no Liability. Guy Cohen (â The Bible of Options Strategies (2nd ed.)â , 2015, ISBN: 9780133964028). Zura Kakushadze, Juan A. Serur (â 151 Trading Strategiesâ , 2018, ISBN: 9783030027919). John C. Hull (â Options, Futures, and Other Derivatives (11th ed.)â , 2022, ISBN: 9780136939979).

The base tools union() intersect(), etc., follow the algebraic definition that each element of a set must be unique. Since it's often helpful to compare all elements of two vectors, this toolset treats every element as unique for counting purposes. For ease of use, all functions in vecsets have an argument multiple which, when set to FALSE, reverts them to the base::sets (alias for all the items) tools functionality.

This package performs variable selection/feature reduction under a clustering or classification framework. In particular, it can be used in an automated fashion using mixture model-based methods ('teigen and mclust are currently supported). Can account for mixtures of non-Gaussian distributions via Manly transform (via ManlyMix'). See Andrews and McNicholas (2014) <doi:10.1007/s00357-013-9139-2> and Neal and McNicholas (2023) <doi:10.48550/arXiv.2305.16464>.

This package provides new classes for (rotated) BB1, BB6, BB7, BB8, and Tawn copulas, extends the existing Gumbel and Clayton families with rotations, and allows to set up a vine copula model using the copula API. Corresponding objects from the VineCopula API can easily be converted.

Identification of Latent Patient Phenotype from Electronic Health Records (EHR) Data using Variational Bayes Gaussian Mixture Model for Latent Class Analysis and Variational Bayes regression for Biomarker level shifts, both implemented by Coordinate Ascent Variational Inference algorithms. Variational methods are used to enable Bayesian analysis of very large Electronic Health Records data. For VB GMM details see Bishop (2006,ISBN:9780-387-31073-2). For Logistic VB see Jaakkola and Jordan (2000) <doi:10.1023/A:1008932416310>. Please see preprint of JSS-submitted paper <doi:10.48550/arXiv.2512.14272>.

Computes the Gaussian variational approximation of the Bayesian empirical likelihood posterior. This is an implementation of the function found in Yu, W., & Bondell, H. D. (2023) <doi:10.1080/01621459.2023.2169701>.

Alternative splicing produces a variety of different protein products from a given gene. VALERIE enables visualisation of alternative splicing events from high-throughput single-cell RNA-sequencing experiments. VALERIE computes percent spliced-in (PSI) values for user-specified genomic coordinates corresponding to alternative splicing events. PSI is the proportion of sequencing reads supporting the included exon/intron as defined by Shiozawa (2018) <doi:10.1038/s41467-018-06063-x>. PSI are inferred from sequencing reads data based on specialised infrastructures for representing and computing annotated genomic ranges by Lawrence (2013) <doi:10.1371/journal.pcbi.1003118>. Computed PSI for each single cell are subsequently presented in the form of a heatmap implemented using the pheatmap package by Kolde (2010) <https://CRAN.R-project.org/package=pheatmap>. Board overview of the mean PSI difference and associated p-values across different user-defined groups of single cells are presented in the form of a line graph using the ggplot2 package by Wickham (2007) <https://CRAN.R-project.org/package=ggplot2>.

This package provides a set of basic tools to transform functions into functions with input validation checks, in a manner suitable for both programmatic and interactive use.

This package provides tools to explore and visualize transitions between clusters in multivariate data. The package generates pseudo-samples by interpolating between cluster medoids, enabling the study of gradual changes in feature space. It also computes k-nearest neighbors (KNN)-based statistics to relate pseudo-samples to real data and summarize variable behavior using mean, median, or standard deviation. Finally, the package offers interactive visualizations of variable trajectories along cluster transitions, including both direct trajectory plots and bootstrap-based interactive plots with confidence intervals to assess variability and uncertainty across the transition path.

Variance function estimation for models proposed by W. Sadler in his variance function program ('VFP', www.aacb.asn.au/AACB/Resources/Variance-Function-Program). Here, the idea is to fit multiple variance functions to a data set and consequently assess which function reflects the relationship Var ~ Mean best. For in-vitro diagnostic ('IVD') assays modeling this relationship is of great importance when individual test-results are used for defining follow-up treatment of patients.

This package provides statistical methods for analytical method comparison and validation studies. Implements Bland-Altman analysis for assessing agreement between measurement methods (Bland & Altman (1986) <doi:10.1016/S0140-6736(86)90837-8>), Passing-Bablok regression for non-parametric method comparison (Passing & Bablok (1983) <doi:10.1515/cclm.1983.21.11.709>), and Deming regression accounting for measurement error in both variables (Linnet (1993) <doi:10.1093/clinchem/39.3.424>). Also includes tools for setting quality goals based on biological variation (Fraser & Petersen (1993) <doi:10.1093/clinchem/39.7.1447>) and calculating Six Sigma metrics, precision experiments with variance component analysis, precision profiles for functional sensitivity estimation (Kroll & Emancipator (1993) <https://pubmed.ncbi.nlm.nih.gov/8448849/>). Commonly used in clinical laboratory method validation. Provides publication-ready plots and comprehensive statistical summaries.

This package provides an easy to calculate local variable importance measure based on Ceteris Paribus profile and global variable importance measure based on Partial Dependence Profiles.