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Interactive shiny application for working with Probability Distributions. Calculations and Graphs are provided.
Data sets associated with modeling examples in Craig Starbuck's book, "The Fundamentals of People Analytics: With Applications in R".
This package provides propensity score weighting methods to control for confounding in causal inference with dichotomous treatments and continuous/binary outcomes. It includes the following functional modules: (1) visualization of the propensity score distribution in both treatment groups with mirror histogram, (2) covariate balance diagnosis, (3) propensity score model specification test, (4) weighted estimation of treatment effect, and (5) augmented estimation of treatment effect with outcome regression. The weighting methods include the inverse probability weight (IPW) for estimating the average treatment effect (ATE), the IPW for average treatment effect of the treated (ATT), the IPW for the average treatment effect of the controls (ATC), the matching weight (MW), the overlap weight (OVERLAP), and the trapezoidal weight (TRAPEZOIDAL). Sandwich variance estimation is provided to adjust for the sampling variability of the estimated propensity score. These methods are discussed by Hirano et al (2003) <DOI:10.1111/1468-0262.00442>, Lunceford and Davidian (2004) <DOI:10.1002/sim.1903>, Li and Greene (2013) <DOI:10.1515/ijb-2012-0030>, and Li et al (2016) <DOI:10.1080/01621459.2016.1260466>.
This package provides a number of functions to simplify and automate the scoring, comparison, and evaluation of different ways of creating composites of data. It is particularly aimed at facilitating the creation of physiological composites of metabolic syndrome symptom score (MetSSS) and allostatic load (AL). Provides a wrapper to calculate the MetSSS on new data using the Healthy Hearts formula.
Large-scale phenotypic data processing is essential in research. Researchers need to eliminate outliers from the data in order to obtain true and reliable results. Best linear unbiased prediction (BLUP) is a standard method for estimating random effects of a mixed model. This method can be used to process phenotypic data under different conditions and is widely used in animal and plant breeding. The Phenotype can remove outliers from phenotypic data and performs the best linear unbiased prediction (BLUP), help researchers quickly complete phenotypic data analysis. H.P.Piepho. (2008) <doi:10.1007/s10681-007-9449-8>.
Perform tasks commonly encountered when preparing and analysing demographic data. Some functions are intended for end users, and others for developers. Includes functions for working with life tables.
Tabular data from statistical institutes and agencies are mostly confidential and must be protected prior to publications. The cell-key method is a post-tabular Statistical Disclosure Control perturbation technique that adds random noise to tabular data. The statistical properties of the perturbations are defined by some noise probability distributions - also referred to as perturbation tables. This tool can be used to create the perturbation tables based on a maximum entropy approach as described for example in Giessing (2016) <doi:10.1007/978-3-319-45381-1_18>. The perturbation tables created can finally be used to apply a cell-key method to frequency count or magnitude tables.
This package performs the explicit calculation -- not estimation! -- of the Rasch item parameters for dichotomous and polytomous item responses, using a pairwise comparison approach. Person parameters (WLE) are calculated according to Warm's weighted likelihood approach.
Mixtures of Poisson Generalized Linear Models for high dimensional count data clustering. The (multivariate) responses can be partitioned into set of blocks. Three different parameterizations of the linear predictor are considered. The models are estimated according to the EM algorithm with an efficient initialization scheme <doi:10.1016/j.csda.2014.07.005>.
The main attribute of PopVar is the prediction of genetic variance in bi-parental populations, from which the package derives its name. PopVar contains a set of functions that use phenotypic and genotypic data from a set of candidate parents to 1) predict the mean, genetic variance, and superior progeny value of all, or a defined set of pairwise bi-parental crosses, and 2) perform cross-validation to estimate genome-wide prediction accuracy of multiple statistical models. More details are available in Mohammadi, Tiede, and Smith (2015, <doi:10.2135/cropsci2015.01.0030>). A dataset think_barley.rda is included for reference and examples.
This package implements Profile Analysis via Multidimensional Scaling (PAMS) for the identification of population-level core response profiles from cross-sectional and longitudinal person-score data. Each person profile is decomposed into a level component (the person mean) and a pattern component (ipsatized subscores). PAMS uses nonmetric multidimensional scaling via the SMACOF algorithm to identify a small number of core profiles that represent the central response patterns in a sample of any size. Bootstrap standard errors and bias-corrected and accelerated (BCa) confidence intervals for individual core profile coordinates are estimated, enabling significance testing of coordinates that is not available in other profile analysis methods such as cluster profile analysis or latent profile analysis. Person-level weights, R-squared values, and correlations with core profiles are also estimated, allowing individual profiles to be interpreted in terms of the core profile structure. PAMS can be applied to both cross-sectional data and longitudinal data, where core trajectory profiles describe how response patterns change over time. Methods are described in Kim and Kim (2024) <doi:10.20982/tqmp.20.3.p230>, de Leeuw and Mair (2009) <doi:10.18637/jss.v031.i03>, and Kruskal (1964) <doi:10.1007/BF02289565>.
Spearman's rank correlation test with precomputed exact null distribution for n <= 22.
This package provides a collection of functions for modelling mutations in pedigrees with marker data, as used e.g. in likelihood computations with microsatellite data. Implemented models include equal, proportional and stepwise models, as well as random models for experimental work, and custom models allowing the user to apply any valid mutation matrix. Allele lumping is done following the lumpability criteria of Kemeny and Snell (1976), ISBN:0387901922.
Several person-fit statistics (PFSs; Meijer and Sijtsma, 2001, <doi:10.1177/01466210122031957>) are offered. These statistics allow assessing whether individual response patterns to tests or questionnaires are (im)plausible given the other respondents in the sample or given a specified item response theory model. Some PFSs apply to dichotomous data, such as the likelihood-based PFSs (lz, lz*) and the group-based PFSs (personal biserial correlation, caution index, (normed) number of Guttman errors, agreement/disagreement/dependability statistics, U3, ZU3, NCI, Ht). PFSs suitable to polytomous data include extensions of lz, U3, and (normed) number of Guttman errors.
This package provides tools for the processing, segmentation, and analysis of terrestrial laser scanning (TLS and MLS) forest point-cloud data. The package provides fast voxel-based processing, classification of point clouds into forest floor, understory, canopy, and woody components, and algorithms for single-tree analysis and structural characterization. Methods are designed to handle large and dense point-cloud datasets efficiently, supporting applications in forest structure assessment, connectivity analysis, and fire-risk evaluation. Input data are provided as .xyz', .txt', .las', or .laz point-cloud files. The circle-fitting routines used for diameter estimation are adapted, in base R, from the conicfit package (GPL-3) by Jose Gama, based on the original algorithms and code by Nikolai Chernov. For methodological details, see Ferrara and Arrizza (2025) <https://hdl.handle.net/20.500.14243/533471> and Ferrara et al. (2018) <doi:10.1016/j.agrformet.2018.04.008>.
Support Vector Machine (SVM) classification with simultaneous feature selection using penalty functions is implemented. The smoothly clipped absolute deviation (SCAD), L1-norm', Elastic Net ('L1-norm and L2-norm') and Elastic SCAD (SCAD and L2-norm') penalties are available. The tuning parameters can be found using either a fixed grid or a interval search.
This package implements multinomial CDF (P(N1<=n1, ..., Nk<=nk)) and tail probabilities (P(N1>n1, ..., Nk>nk)), as well as probabilities with both constraints (P(l1<N1<=u1, ..., lk<Nk<=uk)). Uses a method suggested by Bruce Levin (1981) <doi:10.1214/aos/1176345593>.
Population genetic analyses for hierarchical analysis of partially clonal populations built upon the architecture of the adegenet package. Originally described in Kamvar, Tabima, and Grünwald (2014) <doi:10.7717/peerj.281> with version 2.0 described in Kamvar, Brooks, and Grünwald (2015) <doi:10.3389/fgene.2015.00208>.
Manipulates invertible functions from a finite set to itself. Can transform from word form to cycle form and back. To cite the package in publications please use Hankin (2020) "Introducing the permutations R package", SoftwareX, volume 11 <doi:10.1016/j.softx.2020.100453>.
Sample size calculations for practical equivalence trial design with a time to event endpoint.
This package provides a shiny GUI that performs high dimensional cluster analysis. This tool performs data preparation, clustering and visualisation within a dynamic GUI. With interactive methods allowing the user to change settings all without having to to leave the GUI. An earlier version of this package was described in Laa and Valencia (2022) <doi:10.1140/epjp/s13360-021-02310-1>.
Interface to the Pharmpy pharmacometrics library. The Reticulate package is used to interface Python from R.
This package provides tools for extracting and processing structured annotations from R and Python source files to facilitate workflow visualization. The package scans source files for special PUT annotations that define nodes, connections, and metadata within a data processing workflow. These annotations can then be used to generate visual representations of data flows and processing steps across polyglot software environments. Builds on concepts from literate programming Knuth (1984) <doi:10.1093/comjnl/27.2.97> and utilizes directed acyclic graph (DAG) theory for workflow representation Foraita, Spallek, and Zeeb (2014) <doi:10.1007/978-0-387-09834-0_65>. Diagram generation powered by Mermaid Sveidqvist (2014) <https://mermaid.js.org/>.
This package provides functions for generating variants of curves: restricted cubic spline, periodic restricted cubic spline, periodic cubic spline. Periodic splines can be used to model data that has periodic nature / seasonality.