This package provides data set and function for exploration of Multiple Indicator Cluster Survey 2014 Women (age 15-49 years) questionnaire data for Punjab, Pakistan.

This package provides a tidyverse'-style interface to the Brazilian Central Bank (<https://www.bcb.gov.br>) PIX Open Data API <https://olinda.bcb.gov.br/olinda/servico/Pix_DadosAbertos/versao/v1/aplicacao#!/recursos>. Retrieve statistics on PIX keys, transactions by municipality, and monthly transaction summaries. All functions return tibbles and support OData query parameters for filtering, selecting, and ordering data.

Plots with high flexibility and easy handling, including informative regression diagnostics for many models.

Kappa, ICC, reliability coefficient, parallel analysis, multi-traits multi-methods, spherical representation of a correlation matrix.

This package provides a project infrastructure with a focus on manuscript creation. Creates a project folder with a single command, containing subdirectories for specific components, templates for manuscripts, and so on.

Hybridization probes for target sequences can be made based on melting temperature value calculated by R package TmCalculator <https://CRAN.R-project.org/package=TmCalculator> and methods extended from Beliveau, B. J.,(2018) <doi:10.1073/pnas.1714530115>, and those hybridization probes can be used to capture specific target regions in fluorescence in situ hybridization and next generation sequence experiments.

An application to calculate a patient's pretest probability (PTP) for obstructive Coronary Artery Disease (CAD) from a collection of guidelines or studies. Guidelines usually comes from the American Heart Association (AHA), American College of Cardiology (ACC) or European Society of Cardiology (ESC). Examples of PTP scores that comes from studies are the 2020 Winther et al. basic, Risk Factor-weighted Clinical Likelihood (RF-CL) and Coronary Artery Calcium Score-weighted Clinical Likelihood (CACS-CL) models <doi:10.1016/j.jacc.2020.09.585>, 2019 Reeh et al. basic and clinical models <doi:10.1093/eurheartj/ehy806> and 2017 Fordyce et al. PROMISE Minimal-Risk Tool <doi:10.1001/jamacardio.2016.5501>. As diagnosis of CAD involves a costly and invasive coronary angiography procedure for patients, having a reliable PTP for CAD helps doctors to make better decisions during patient management. This ensures high risk patients can be diagnosed and treated early for CAD while avoiding unnecessary testing for low risk patients.

Density, distribution function, quantile function and random generation for the family of power and reversal power distributions.

Model-implied simulation-based power estimation (MSPE) for nonlinear (and linear) SEM, path analysis and regression analysis. A theoretical framework is used to approximate the relation between power and sample size for given type I error rates and effect sizes. The package offers an adaptive search algorithm to find the optimal N for given effect sizes and type I error rates. Plots can be used to visualize the power relation to N for different parameters of interest (POI). Theoretical justifications are given in Irmer et al. (2024a) <doi:10.31219/osf.io/pe5bj> and detailed description are given in Irmer et al. (2024b) <doi:10.3758/s13428-024-02476-3>.

The pharmaverse is a set of packages that compose multiple pathways through clinical data generation and reporting in the pharmaceutical industry. This package is designed to guide users to our work-spaces on GitHub', Slack and LinkedIn as well as our website and examples. Learn more about the pharmaverse at <https://pharmaverse.org>.

This package contains model fitting functions for linear and non-linear adsorption kinetic and diffusion models. Adsorption kinetics is used for characterizing the rate of solute adsorption and the time necessary for the adsorption process. Adsorption kinetics offers vital information on adsorption rate, adsorbent performance in response time, and mass transfer processes. In addition, diffusion models are included in the package as solute diffusion affects the adsorption kinetic experiments. This package consists of 20 adsorption and diffusion models, including Pseudo First Order (PFO), Pseudo Second Order (PSO), Elovich, and Weber-Morris model (commonly called the intraparticle model) stated by Plazinski et al. (2009) <doi:10.1016/j.cis.2009.07.009>. This package also contains a summary function where the statistical errors of each model are ranked for a more straightforward determination of the best fit model.

Price volatility refers to the degree of variation in series over a certain period of time. This volatility is especially noticeable in agricultural commodities, adding uncertainty for farmers, traders, and others in the agricultural supply chain. Commonly and popularly used four volatility models viz, GARCH, Glosten Jagannatan Runkle-GARCH (GJR-GARCH) model, exponentially weighted moving average (EWMA) model and Multiplicative Error Model (MEM) are selected and implemented. PWAVE, weighted ensemble model based on particle swarm optimization (PSO) is proposed to combine the forecast obtained from all the candidate models. This package has been developed using algorithm of Paul et al. <doi:10.1007/s40009-023-01218-x> and Yeasin and Paul (2024) <doi:10.1007/s11227-023-05542-3>.

In the situation when multiple alternative treatments or interventions available, different population groups may respond differently to different treatments. This package implements a method that discovers the population subgroups in which a certain treatment has a better effect than the other alternative treatments. This is done by first estimating the treatment effect for a given treatment and its uncertainty by computing random forests, and the resulting model is summarized by a decision tree in which the probabilities that the given treatment is best for a given subgroup is shown in the corresponding terminal node of the tree.

Simulation functions to assess or explore the power of a dataset to estimates significant random effects (intercept or slope) in a mixed model. The functions are based on the "lme4" and "lmerTest" packages.

Reads the provenance collected by the rdtLite or rdt packages, or other tools providing compatible PROV JSON output, created by the execution of a script or a console session, and provides a human-readable summary identifying the input and output files, the scripts used (if any), errors and warnings produced, and the environment in which it was executed. It can also optionally package all the files into a zip file. The exact format of the PROV JSON file created by rdtLite and rdt is described in <https://github.com/End-to-end-provenance/ExtendedProvJson>. More information about rdtLite and associated tools is available at <https://github.com/End-to-end-provenance/> and Lerner, Boose, and Perez (2018), Using Introspection to Collect Provenance in R, Informatics, <doi: 10.3390/informatics5010012>.

Analyzing genetic data obtained from pooled samples. This package can read in Fragment Analysis output files, process the data, and score peaks, as well as facilitate various analyses, including cluster analysis, calculation of genetic distances and diversity indices, as well as bootstrap resampling for statistical inference. Specifically tailored to handle genetic data efficiently, researchers can explore population structure, genetic differentiation, and genetic relatedness among samples. We updated some functions from Covarrubias-Pazaran et al. (2016) <doi:10.1186/s12863-016-0365-6> to allow for the use of new file formats and referenced the following to write our genetic analysis functions: Long et al. (2022) <doi:10.1038/s41598-022-04776-0>, Jost (2008) <doi:10.1111/j.1365-294x.2008.03887.x>, Nei (1973) <doi:10.1073/pnas.70.12.3321>, Foulley et al. (2006) <doi:10.1016/j.livprodsci.2005.10.021>, Chao et al. (2008) <doi:10.1111/j.1541-0420.2008.01010.x>.

An implementation of the Elston-Stewart algorithm for calculating pedigree likelihoods given genetic marker data (Elston and Stewart (1971) <doi:10.1159/000152448>). The standard algorithm is extended to allow inbred founders. pedprobr is part of the pedsuite', a collection of packages for pedigree analysis in R. In particular, pedprobr depends on pedtools for pedigree manipulations and pedmut for mutation modelling. For more information, see Pedigree Analysis in R (Vigeland, 2021, ISBN:9780128244302).

Permutation based non-parametric analysis of CRISPR screen data. Details about this algorithm are published in the following paper published on BMC genomics, Jia et al. (2017) <doi:10.1186/s12864-017-3938-5>: A permutation-based non-parametric analysis of CRISPR screen data. Please cite this paper if you use this algorithm for your paper.

This package implements univariate polynomial operations in R, including polynomial arithmetic, finding zeros, plotting, and some operations on lists of polynomials.

Deduplicates datasets by retaining the most complete and informative records. Identifies duplicated entries based on a specified key column, calculates completeness scores for each row, and compares values within groups. When differences between duplicates exceed a user-defined threshold, records are split into unique IDs; otherwise, they are coalesced into a single, most complete entry. Returns a list containing the original duplicates, the split entries, and the final coalesced dataset. Useful for cleaning survey or administrative data where duplicated IDs may reflect minor data entry inconsistencies.

Estimates corrected Procrustean correlation between matrices for removing overfitting effect. Coissac Eric and Gonindard-Melodelima Christelle (2019) <doi:10.1101/842070>.

Preprocess numeric data matrices into desired transformed representations. Standardization, Unitization, Cubitization and adaptive intervals are offered.

This package provides a system contains easy-to-use tools for the conditional estimation of the prevalence of an emerging or rare infectious diseases using the methods proposed in Guerrier et al. (2023) <arXiv:2012.10745>.

This package implements propensity score weighting methods for estimating counterfactual survival functions, marginal hazard ratios, and weighted Kaplan-Meier and cumulative risk curves in observational studies with time-to-event outcomes. Supports binary and multiple treatment groups with inverse probability of treatment weighting (IPW), overlap weighting (OW), and average treatment effect on the treated (ATT). Includes symmetric trimming (Crump extension) for extreme propensity scores. Variance estimation via analytical M-estimation or bootstrap. Methods based on Li et al. (2018) <doi:10.1080/01621459.2016.1260466>, Li & Li (2019) <doi:10.1214/19-AOAS1282>, and Cheng et al. (2022) <doi:10.1093/aje/kwac043>.