For single tensor data, any matrix factorization method can be specified the matricised tensor in each dimension by Multi-way Component Analysis (MWCA). An originally extended MWCA is also implemented to specify and decompose multiple matrices and tensors simultaneously (CoupledMWCA). See the reference section of GitHub README.md <https://github.com/rikenbit/mwTensor>, for details of the methods.

Developed for model-based clustering using the finite mixtures of skewed sub-Gaussian stable distributions developed by Teimouri (2022) <arXiv:2205.14067> and estimating parameters of the symmetric stable distribution within the Bayesian framework.

Gibbs sampler for fitting multivariate Bayesian linear regression with shrinkage priors (MBSP), using the three parameter beta normal family. The method is described in Bai and Ghosh (2018) <doi:10.1016/j.jmva.2018.04.010>.

The inference in multi-state models is traditionally performed under a Markov assumption that claims that past and future of the process are independent given the present state. In this package, we consider tests of the Markov assumption that are applicable to general multi-state models. Three approaches using existing methodology are considered: a simple method based on including covariates depending on the history in Cox models for the transition intensities; methods based on measuring the discrepancy of the non-Markov estimators of the transition probabilities to the Markov Aalen-Johansen estimators; and, finally, methods that were developed by considering summaries from families of log-rank statistics where patients are grouped by the state occupied of the process at a particular time point (see Soutinho G, Meira-Machado L (2021) <doi:10.1007/s00180-021-01139-7> and Titman AC, Putter H (2020) <doi:10.1093/biostatistics/kxaa030>).

Bayesian variable selection methods for data with multivariate responses and multiple covariates. The package contains implementations of multivariate Bayesian variable selection methods for continuous data (Lee et al., Biometrics, 2017 <doi:10.1111/biom.12557>) and zero-inflated count data (Lee et al., Biostatistics, 2020 <doi:10.1093/biostatistics/kxy067>).

Create native charts for Microsoft PowerPoint', Microsoft Excel and Microsoft Word documents. The resulting charts can then be edited and annotated in the host application. It provides functions to create charts and to modify their content and formatting. The chart's underlying data is automatically saved within the Word', Excel or PowerPoint file. It extends the officer package, which does not provide native Microsoft chart production.

This package provides methods for quality control and robust pre-processing and analysis of MALDI mass spectrometry data (Palarea-Albaladejo et al. (2018) <doi:10.1093/bioinformatics/btx628>).

This package implements a semi-parametric estimation framework combined with a boosting algorithm to marginally estimate the conditional cumulative distribution function of survival times given informative covariates. It then utilizes the graphical lasso method to reconstruct network structures among multivariate time-to-event variables, accommodating both multivariate outcomes measured within a single dataset and survival times integrated from heterogeneous (multi-source) datasets..

Providing C implementation for the computing of monotonic spline bases, including M-splines, I-splines, and C-splines, denoted by MIC splines. The definitions of the spline bases are described in Meyer (2008) <doi: 10.1214/08-AOAS167>. The package also provides the computing of constrained least-squares estimates when a subset of or all of the regression coefficients are constrained to be non-negative.

This package provides functions are provided for calculating efficiency using multiplier DEA (Data Envelopment Analysis): Measuring the efficiency of decision making units (Charnes et al., 1978 <doi:10.1016/0377-2217(78)90138-8>) and cross efficiency using single and two-phase approach. In addition, it includes some datasets for calculating efficiency and cross efficiency.

Plotting functions for mutational signatures and mutational spectra, including single base substitutions (SBS), doublet base substitutions (DBS), and small insertions and deletions (indels). Generates plots similar to those used previously in Alexandrov et al. (2020)<doi:10.1038/s41586-020-1943-3> and Rozen et al. (2026)<doi:10.5281/zenodo.18451842>.

Calculates the Most Probable Number (MPN) to quantify the concentration (density) of microbes in serial dilutions of a laboratory sample (described in Jarvis, 2010 <doi:10.1111/j.1365-2672.2010.04792.x>). Also calculates the Aerobic Plate Count (APC) for similar microbial enumeration experiments.

Modular implementation of Multiobjective Evolutionary Algorithms based on Decomposition (MOEA/D) [Zhang and Li (2007), <DOI:10.1109/TEVC.2007.892759>] for quick assembling and testing of new algorithmic components, as well as easy replication of published MOEA/D proposals. The full framework is documented in a paper published in the Journal of Statistical Software [<doi:10.18637/jss.v092.i06>].

Estimates monotone regression and variance functions in a nonparametric model, based on Dette, Holger, Neumeyer, and Pilz (2006) <doi:10.3150/bj/1151525131>.

The maybe type represents the possibility of some value or nothing. It is often used instead of throwing an error or returning `NULL`. The advantage of using a maybe type over `NULL` is that it is both composable and requires the developer to explicitly acknowledge the potential absence of a value, helping to avoid the existence of unexpected behaviour.

The base apply function and its variants, as well as the related functions in the plyr package, typically apply user-defined functions to a single argument (or a list of vectorized arguments in the case of mapply). The multiApply package extends this paradigm with its only function, Apply, which efficiently applies functions taking one or a list of multiple unidimensional or multidimensional arrays (or combinations thereof) as input. The input arrays can have different numbers of dimensions as well as different dimension lengths, and the applied function can return one or a list of unidimensional or multidimensional arrays as output. This saves development time by preventing the R user from writing often error-prone and memory-inefficient loops dealing with multiple complex arrays. Also, a remarkable feature of Apply is the transparent use of multi-core through its parameter ncores'. In contrast to the base apply function, this package suggests the use of target dimensions as opposite to the margins for specifying the dimensions relevant to the function to be applied.

Random Forest Spatial Interpolation (RFSI, SekuliÄ et al. (2020) <doi:10.3390/rs12101687>) and spatio-temporal geostatistical (spatio-temporal regression Kriging (STRK)) interpolation for meteorological (Kilibarda et al. (2014) <doi:10.1002/2013JD020803>, SekuliÄ et al. (2020) <doi:10.1007/s00704-019-03077-3>) and other environmental variables. Contains global spatio-temporal models calculated using publicly available data.

Algorithms for solving various Maximum Weight Connected Subgraph Problems, including variants with budget constraints, cardinality constraints, weighted edges and signals. The package represents an R interface to high-efficient solvers based on relax-and-cut approach (Ã lvarez-Miranda E., Sinnl M. (2017) <doi:10.1016/j.cor.2017.05.015>) mixed-integer programming (Loboda A., Artyomov M., and Sergushichev A. (2016) <doi:10.1007/978-3-319-43681-4_17>) and simulated annealing.

This package provides a collection of functions for processing and analyzing metabolite data. The namesake function mrbin() converts 1D or 2D Nuclear Magnetic Resonance data into a matrix of values suitable for further data analysis and performs basic processing steps in a reproducible way. Negative values, a common issue in such data, can be replaced by positive values (<doi:10.1021/acs.jproteome.0c00684>). All used parameters are stored in a readable text file and can be restored from that file to enable exact reproduction of the data at a later time. The function fia() ranks features according to their impact on classifier models, especially artificial neural network models.

This package provides an algorithm for creating mandalas. From the perspective of classic mathematical curves and rigid movements on the plane, the package allows you to select curves and produce mandalas from the curve. The algorithm was developed based on the book by Alcoforado et. al. entitled "Art, Geometry and Mandalas with R" (2022) in press by the USP Open Books Portal.

Multivariate estimation and testing, currently a package for testing parametric data. To deal with parametric data, various multivariate normality tests and outlier detection are performed and visualized using the ggplot2 package. Homogeneity tests for covariance matrices are also possible, as well as the Hotelling's T-square test and the multivariate analysis of variance test. We are exploring additional tests and visualization techniques, such as profile analysis and randomized complete block design, to be made available in the future and making them easily accessible to users.

This package provides a lightweight, dependency-free data engine for R that provides a grammar for tabular and time-series manipulation. Built entirely on Base R, m61r offers a fluent, chainable API inspired by modern data tools while prioritizing memory efficiency and speed. It includes optimized versions of common data verbs such as filtering, mutation, grouped aggregation, and approximate temporal joins, making it an ideal choice for environments where external dependencies are restricted or where performance in pure R is required.

This package provides a set of evolutionary algorithms to solve many-objective optimization. Hybridization between the algorithms are also facilitated. Available algorithms are: SMS-EMOA <doi:10.1016/j.ejor.2006.08.008> NSGA-III <doi:10.1109/TEVC.2013.2281535> MO-CMA-ES <doi:10.1145/1830483.1830573> The following many-objective benchmark problems are also provided: DTLZ1'-'DTLZ4 from Deb, et al. (2001) <doi:10.1007/1-84628-137-7_6> and WFG4'-'WFG9 from Huband, et al. (2005) <doi:10.1109/TEVC.2005.861417>.

Mitteroecker & Gunz (2009) <doi:10.1007/s11692-009-9055-x> describe how geometric morphometric methods allow researchers to quantify the size and shape of physical biological structures. We provide tools to extend geometric morphometric principles to the study of non-physical structures, hormone profiles, as outlined in Ehrlich et al (2021) <doi:10.1002/ajpa.24514>. Easily transform daily measures into multivariate landmark-based data. Includes custom functions to apply multivariate methods for data exploration as well as hypothesis testing. Also includes shiny web app to streamline data exploration. Developed to study menstrual cycle hormones but functions have been generalized and should be applicable to any biomarker over any time period.