This package provides a suite of tools to allow you to download all publicly available parasite rate survey points, mosquito occurrence points and raster surfaces from the Malaria Atlas Project <https://malariaatlas.org/> servers as well as utility functions for plotting the downloaded data.

Different examples and methods for testing (including different proposals described in Ameijeiras-Alonso et al., 2019 <DOI:10.1007/s11749-018-0611-5>) and exploring (including the mode tree, mode forest and SiZer) the number of modes using nonparametric techniques <DOI:10.18637/jss.v097.i09>.

Allows practitioners and researchers a wholesale approach for deriving magnitude-based inferences from raw data. A major goal of mbir is to programmatically detect appropriate statistical tests to run in lieu of relying on practitioners to determine correct stepwise procedures independently.

Matrix-Based Flexible Project Planning. This package models, plans, and schedules flexible, such as agile, extreme, and hybrid project plans. The package contains project planning, scheduling, and risk assessment functions. Kosztyan (2022) <doi:10.1016/j.softx.2022.100973>.

Facilitate tasks typically encountered during metabolomics data analysis including data import, filtering, missing value imputation (Stacklies et al. (2007) <doi:10.1093/bioinformatics/btm069>, Stekhoven et al. (2012) <doi:10.1093/bioinformatics/btr597>, Tibshirani et al. (2017) <doi:10.18129/B9.BIOC.IMPUTE>, Troyanskaya et al. (2001) <doi:10.1093/bioinformatics/17.6.520>), normalization (Bolstad et al. (2003) <doi:10.1093/bioinformatics/19.2.185>, Dieterle et al. (2006) <doi:10.1021/ac051632c>, Zhao et al. (2020) <doi:10.1038/s41598-020-72664-6>) transformation, centering and scaling (Van Den Berg et al. (2006) <doi:10.1186/1471-2164-7-142>) as well as statistical tests and plotting. metamorphr introduces a tidy (Wickham et al. (2019) <doi:10.21105/joss.01686>) format for metabolomics data and is designed to make it easier to build elaborate analysis workflows and to integrate them with tidyverse packages including dplyr and ggplot2'.

Easily import the MI-SUVI data sets. The user can import data sets with full metrics, percentiles, Z-scores, or rankings. Data is available at both the County and Zip Code Tabulation Area (ZCTA) levels. This package also includes a function to import shape files for easy mapping and a function to access the full technical documentation. All data is sourced from the Michigan Department of Health and Human Services.

An interactive document on the topic of multidimensional scaling and principal component analysis using rmarkdown and shiny packages. Runtime examples are provided in the package function as well as at <https://kartikeyabolar.shinyapps.io/MDS_PCAShiny/>.

This package provides functions to estimate start and duration of moult from moult data, based on models developed in Underhill and Zucchini (1988, 1990).

This package provides a set of functions to calculate solar irradiance and insolation on Mars horizontal and inclined surfaces. Based on NASA Technical Memoranda 102299, 103623, 105216, 106321, and 106700, i.e. the canonical Mars solar radiation papers.

This package provides the function mixor for fitting a mixed-effects ordinal and binary response models and associated methods for printing, summarizing, extracting estimated coefficients and variance-covariance matrix, and estimating contrasts for the fitted models.

Apply tests of multiple comparisons based on studentized midrange and range distributions. The tests are: Tukey Midrange ('TM test), Student-Newman-Keuls Midrange ('SNKM test), Means Grouping Midrange ('MGM test) and Means Grouping Range ('MGR test). The first two tests were published by Batista and Ferreira (2020) <doi:10.1590/1413-7054202044008020>. The last two were published by Batista and Ferreira (2023) <doi:10.28951/bjb.v41i4.640>.

Fits single-component and finite-mixture Kronecker-structured matrix-normal models and imputes incomplete matrix-variate data using matrix partial expectation-maximization. General MPEM handles arbitrary missingness, while Rect-MPEM exploits rectangular structural missingness. The methods are described in Lu, Andrews and Browne (2026) "An Efficient EM Algorithm for Both Element-Wise and Structural Missingness in Matrix-Variate Normal Mixture Models" <doi:10.48550/arXiv.2609.00616>.

Collection of functions to perform fixed and random-effects multivariate and univariate meta-analysis and meta-regression.

Companion package of Carrion-i-Silvestre & Sansó (2026): "Testing for Constant Unconditional Variance in Heavy-Tailed Time Series". It implements the Modified Iterative Cumulative Sum of Squares Algorithm, which is an extension of the Iterative Cumulative Sum of Squares (ICSS) Algorithm of Inclan and Tiao (1994), and it checks for changes in the unconditional variance of a time series controlling for the tail index of the underlying distribution. The fourth order moment is estimated non-parametrically to avoid the size problems when the innovations are non-Gaussian (see, Sansó et al., 2004). Critical values and p-values are generated using a Generalized Extreme Value distribution approach. References Carrion-i-Silvestre J.J & Sansó A (2026) <doi:10.1080/03610918.2026.2615207>. Inclan C & Tiao G.C (1994) <doi:10.1080/01621459.1994.10476824>, Sansó A & Aragó V & Carrion-i-Silvestre J.L (2004) <https://dspace.uib.es/xmlui/bitstream/handle/11201/152078/524035.pdf>.

An R-Shiny module containing a "markdownInput". This input allows the user to write some markdown code and to preview the result. This input has been inspired by the "comment" window of <https://github.com/>.

Impute the covariance matrix of incomplete data so that factor analysis can be performed. Imputations are made using multiple imputation by Multivariate Imputation with Chained Equations (MICE) and combined with Rubin's rules. Parametric Fieller confidence intervals and nonparametric bootstrap confidence intervals can be obtained for the variance explained by different numbers of principal components. The method is described in Nassiri et al. (2018) <doi:10.3758/s13428-017-1013-4>.

The iterative procedure estimates structural changes in the success probability of Bernoulli variables. It estimates the number and location of the breakpoints as well as the success probability of the different sequences between the breakpoints. In addition, it provides a graphical illustration of the result.

Estimates membership for the Mandelbrot set.

This package provides tools for estimation and prediction using Maximum Agreement Linear Predictors (MALPs). MALPs provide an alternative to least squares linear predictors when agreement between predicted and observed values, as measured by Lin's Concordance Correlation Coefficient (CCC), is of primary interest. Applications include missing value imputation and calibration studies. The package includes functions for model estimation, prediction, statistical inference, cross-validation, and model diagnostics. The implemented methodology is described in Kim et al. (2026) <doi:10.1214/26-EJS2550>.

This package provides tools to create a layout for figures made of multiple panels, and to fill the panels with base, lattice', ggplot2 and ComplexHeatmap plots, grobs, as well as content from all image formats supported by ImageMagick (accessed through magick').

This package provides a declarative language for specifying multilevel models, solving for population parameters based on specified variance-explained effect size measures, generating data, and conducting power analyses to determine sample size recommendations. The specification allows for any number of within-cluster effects, between-cluster effects, covariate effects at either level, and random coefficients. Moreover, the models do not assume orthogonal effects, and predictors can correlate at either level and accommodate models with multiple interaction effects.

Estimation of treatment hierarchies in network meta-analysis using a novel frequentist approach based on treatment choice criteria (TCC) and probabilistic ranking models, as described by Evrenoglou et al. (2024) <DOI:10.48550/arXiv.2406.10612>. The TCC are defined using a rule based on the smallest worthwhile difference (SWD). Using the defined TCC, the NMA estimates (i.e., treatment effects and standard errors) are first transformed into treatment preferences, indicating either a treatment preference (e.g., treatment A > treatment B) or a tie (treatment A = treatment B). These treatment preferences are then synthesized using a probabilistic ranking model, which estimates the latent ability parameter of each treatment and produces the final treatment hierarchy. This parameter represents each treatments ability to outperform all the other competing treatments in the network. Here the terms ability to outperform indicates the propensity of each treatment to yield clinically important and beneficial effects when compared to all the other treatments in the network. Consequently, larger ability estimates indicate higher positions in the ranking list.

Fits fixed-, random-, or mixed-effects multivariate meta-analysis models using dynamic model estimates from each individual building on and extending Lee and Gates (2023) <doi:10.1080/00273171.2023.2229310>.

An approach to identifies metabolic biomarker signature for metabolic data by discovering predictive metabolite for predicting survival and classifying patients into risk groups. Classifiers are constructed as a linear combination of predictive/important metabolites, prognostic factors and treatment effects if necessary. Several methods were implemented to reduce the metabolomics matrix such as the principle component analysis of Wold Svante et al. (1987) <doi:10.1016/0169-7439(87)80084-9> , the LASSO method by Robert Tibshirani (1998) <doi:10.1002/(SICI)1097-0258(19970228)16:4%3C385::AID-SIM380%3E3.0.CO;2-3>, the elastic net approach by Hui Zou and Trevor Hastie (2005) <doi:10.1111/j.1467-9868.2005.00503.x>. Sensitivity analysis on the quantile used for the classification can also be accessed to check the deviation of the classification group based on the quantile specified. Large scale cross validation can be performed in order to investigate the mostly selected predictive metabolites and for internal validation. During the evaluation process, validation is accessed using the hazard ratios (HR) distribution of the test set and inference is mainly based on resampling and permutations technique.