This package provides equations commonly used in clinical pharmacokinetics and clinical pharmacology, such as equations for dose individualization, compartmental pharmacokinetics, drug exposure, anthropomorphic calculations, clinical chemistry, and conversion of common clinical parameters. Where possible and relevant, it provides multiple published and peer-reviewed equations within the respective R function.

Perform variable selection for Cox regression model with interval-censored data. Can deal with both low-dimensional and high-dimensional data. Case-cohort design can be incorporated. Two sets of covariates scenario can also be considered. The references are listed in the URL below.

Calculate a set of corrected test statistics for cases when samples are not independent, such as when classification accuracy values are obtained over resamples or through k-fold cross-validation, as proposed by Nadeau and Bengio (2003) <doi:10.1023/A:1024068626366> and presented in Bouckaert and Frank (2004) <doi:10.1007/978-3-540-24775-3_3>.

Find the location of the code for an R package based on the package's name or string representation. Checks on CRAN based on information in the URL field or BioConductor and GitHub based on constructing a URL, and verifies all paths via testing for a successful response. This can be useful when automating static code analysis based on a list of package names, and similar tasks.

This package provides a convenient R wrapper to the Comet API, which is a cloud platform allowing you to track, compare, explain and optimize machine learning experiments and models. Experiments can be viewed on the Comet online dashboard at <https://www.comet.com>.

This package provides a suite of functions for rapid and flexible analysis of codon usage bias. It provides in-depth analysis at the codon level, including relative synonymous codon usage (RSCU), tRNA weight calculations, machine learning predictions for optimal or preferred codons, and visualization of codon-anticodon pairing. Additionally, it can calculate various gene- specific codon indices such as codon adaptation index (CAI), effective number of codons (ENC), fraction of optimal codons (Fop), tRNA adaptation index (tAI), mean codon stabilization coefficients (CSCg), and GC contents (GC/GC3s/GC4d). It also supports both standard and non-standard genetic code tables found in NCBI, as well as custom genetic code tables.

Merging data from multiple sources is a relevant approach for comprehensively evaluating complex systems. However, the inherent problems encountered when analyzing single tables are amplified with the generation of multi-block datasets, and finding the relationships between data layers of increasing complexity constitutes a challenging task. For that purpose, a generic methodology is proposed by combining the strength of established data analysis strategies, i.e. multi-block approaches and the Orthogonal Partial Least Squares (OPLS) framework to provide an efficient tool for the fusion of data obtained from multiple sources. The package enables quick and efficient implementation of the consensus OPLS model for any horizontal multi-block data structures (observation-based matching). Moreover, it offers an interesting range of metrics and graphics to help to determine the optimal number of components and check the validity of the model through permutation tests. Interpretation tools include score and loading plots, Variable Importance in Projection (VIP), functionality predict for SHAP computing, and performance coefficients such as R2, Q2, and DQ2 coefficients. J. Boccard and D.N. Rutledge (2013) <doi:10.1016/j.aca.2013.01.022>.

Includes climate data from Japan Meteorological Agency ('JMA') <https://www.jma.go.jp/jma/indexe.html>. Can download climate data from JMA'.

Citation File Format ('CFF') version 1.2.0 <doi:10.5281/zenodo.5171937> is a human- and machine-readable file format for software citation metadata. Core utilities generate, read, write and validate Citation File Format metadata for R packages.

Software which provides numerous functionalities for detecting and removing group-level effects from high-dimensional scientific data which, when combined with additional assumptions, allow for causal conclusions, as-described in our manuscripts Bridgeford et al. (2024) <doi:10.1101/2021.09.03.458920> and Bridgeford et al. (2023) <doi:10.48550/arXiv.2307.13868>. Also provides a number of useful utilities for generating simulations and balancing covariates across multiple groups/batches of data via matching and propensity trimming for more than two groups.

This package provides functionality for computing support intervals for univariate parameters based on confidence intervals or parameter estimates with standard errors (Pawel et al., 2022) <doi:10.48550/arXiv.2206.12290>.

Fast C++'-backed tools for computing conspecific and total neighborhood basal area in mapped forest plots. Includes unweighted and distance-weighted neighborhoods, multiple radii, decay kernels, and basic edge correction. Outputs are model-ready covariates for forest competition, growth, and survival models, following neighborhood modeling workflows commonly used in spatial ecology (e.g., Hülsmann et al. 2024 <doi:10.1038/s41586-024-07118-4>).

Directory reads and summaries are provided for one or more of the subdirectories of the <https://cran.r-project.org/incoming/> directory, and a compact summary object is returned. The package name is a contraption of CRAN Incoming Watcher'.

This package provides a comprehensive framework for batch effect diagnostics, harmonization, and post-harmonization downstream analysis. Features include interactive visualization tools, robust statistical tests, and a range of harmonization techniques. Additionally, ComBatFamQC enables the creation of life-span age trend plots with estimated age-adjusted centiles and facilitates the generation of covariate-corrected residuals for analytical purposes. Methods for harmonization are based on approaches described in Johnson et al., (2007) <doi:10.1093/biostatistics/kxj037>, Beer et al., (2020) <doi:10.1016/j.neuroimage.2020.117129>, Pomponio et al., (2020) <doi:10.1016/j.neuroimage.2019.116450>, and Chen et al., (2021) <doi:10.1002/hbm.25688>.

This package provides functions to simplify the process of preparing event and transaction for cohort analysis.

This package provides a clinical significance analysis can be used to determine if an intervention has a meaningful or practical effect for patients. You provide a tidy data set plus a few more metrics and this package will take care of it to make your results publication ready. Accompanying package to Claus et al. <doi:10.18637/jss.v111.i01>.

Map functions while capturing results, errors, warnings, messages and other output tidily, then filter and summarise data frames or lists on the basis of those side effects.

There are many estimators of false discovery rate. In this package we compute the Nonlocal False Discovery Rate (NFDR) and the estimators of local false discovery rate: Corrected False discovery Rate (CFDR), Re-ranked False Discovery rate (RFDR) and the blended estimator. Bickel, D.R., Rahal, A. (2019) <https://tinyurl.com/kkdc9rk8>.

This package provides methods for analyzing (cell) motion in two or three dimensions. Available measures include displacement, confinement ratio, autocorrelation, straightness, turning angle, and fractal dimension. Measures can be applied to entire tracks, steps, or subtracks with varying length. While the methodology has been developed for cell trajectory analysis, it is applicable to anything that moves including animals, people, or vehicles. Some of the methodology implemented in this packages was described by: Beauchemin, Dixit, and Perelson (2007) <doi:10.4049/jimmunol.178.9.5505>, Beltman, Maree, and de Boer (2009) <doi:10.1038/nri2638>, Gneiting and Schlather (2004) <doi:10.1137/S0036144501394387>, Mokhtari, Mech, Zitzmann, Hasenberg, Gunzer, and Figge (2013) <doi:10.1371/journal.pone.0080808>, Moreau, Lemaitre, Terriac, Azar, Piel, Lennon-Dumenil, and Bousso (2012) <doi:10.1016/j.immuni.2012.05.014>, Textor, Peixoto, Henrickson, Sinn, von Andrian, and Westermann (2011) <doi:10.1073/pnas.1102288108>, Textor, Sinn, and de Boer (2013) <doi:10.1186/1471-2105-14-S6-S10>, Textor, Henrickson, Mandl, von Andrian, Westermann, de Boer, and Beltman (2014) <doi:10.1371/journal.pcbi.1003752>.

Set of functions to import COVID-19 pandemic data into R. The Brazilian COVID-19 data, obtained from the official Brazilian repository at <https://covid.saude.gov.br/>, is available at the country, region, state, and city levels. The package also downloads world-level COVID-19 data from Johns Hopkins University's repository. COVID-19 data is available from the start of follow-up until to May 5, 2023, when the World Health Organization (WHO) declared an end to the Public Health Emergency of International Concern (PHEIC) for COVID-19.

Implementation of the Coarsened Exact Matching algorithm discussed along with its properties in Iacus, King, Porro (2011) <DOI:10.1198/jasa.2011.tm09599>; Iacus, King, Porro (2012) <DOI:10.1093/pan/mpr013> and Iacus, King, Porro (2019) <DOI:10.1017/pan.2018.29>.

We provide a toolbox to fit a continuous-time fractionally integrated ARMA process (CARFIMA) on univariate and irregularly spaced time series data via both frequentist and Bayesian machinery. A general-order CARFIMA(p, H, q) model for p>q is specified in Tsai and Chan (2005) <doi:10.1111/j.1467-9868.2005.00522.x> and it involves p+q+2 unknown model parameters, i.e., p AR parameters, q MA parameters, Hurst parameter H, and process uncertainty (standard deviation) sigma. Also, the model can account for heteroscedastic measurement errors, if the information about measurement error standard deviations is known. The package produces their maximum likelihood estimates and asymptotic uncertainties using a global optimizer called the differential evolution algorithm. It also produces posterior samples of the model parameters via Metropolis-Hastings within a Gibbs sampler equipped with adaptive Markov chain Monte Carlo. These fitting procedures, however, may produce numerical errors if p>2. The toolbox also contains a function to simulate discrete time series data from CARFIMA(p, H, q) process given the model parameters and observation times.

This package provides tools to extract, label, and read microdata from the 2022 National Census of Population, Households and Dwellings of Argentina stored in REDATAM databases officially distributed by INDEC. Implements a complete province-by-province extraction pipeline with efficient memory management, reconstruction of hierarchical identifiers, automatic variable labeling from official INDEC dictionaries, and integrity verification against published totals. Allows working with census data directly in R without knowledge of REDATAM syntax, and supports export to multiple formats including Parquet, CSV, SPSS and SAS. Census data must be downloaded directly from the official INDEC portal (<https://www.indec.gob.ar>). This package does not distribute census data. Duran (2026) <doi:10.5281/zenodo.19560728>.

This package implements Cramer-von Mises Statistics for testing fit to (1) fully specified discrete distributions as described in Choulakian, Lockhart and Stephens (1994) <doi:10.2307/3315828> (2) discrete distributions with unknown parameters that must be estimated from the sample data, see Spinelli & Stephens (1997) <doi:10.2307/3315735> and Lockhart, Spinelli and Stephens (2007) <doi:10.1002/cjs.5550350111> (3) grouped continuous distributions with Unknown Parameters, see Spinelli (2001) <doi:10.2307/3316040>. Maximum likelihood estimation (MLE) is used to estimate the parameters. The package computes the Cramer-von Mises Statistics, Anderson-Darling Statistics and the Watson-Stephens Statistics and their p-values.