An R implementation of the python program Metabolomics Peak Analysis Computational Tool ('MPACT') (Robert M. Samples, Sara P. Puckett, and Marcy J. Balunas (2023) <doi:10.1021/acs.analchem.2c04632>). Filters in the package serve to address common errors in tandem mass spectrometry preprocessing, including: (1) isotopic patterns that are incorrectly split during preprocessing, (2) features present in solvent blanks due to carryover between samples, (3) features whose abundance is greater than user-defined abundance threshold in a specific group of samples, for example media blanks, (4) ions that are inconsistent between technical replicates, and (5) in-source fragment ions created during ionization before fragmentation in the tandem mass spectrometry workflow.

This package provides flexible dictionary-based cleaning that allows users to specify implicit and explicit missing data, regular expressions for both data and columns, and global matches, while respecting ordering of factors. This package is part of the RECON (<https://www.repidemicsconsortium.org/>) toolkit for outbreak analysis.

This package provides tools to help convert credit risk data at two timepoints into traditional credit state migration (aka, "transition") matrices. At a higher level, migrate is intended to help an analyst understand how risk moved in their credit portfolio over a time interval. References to this methodology include: 1. Schuermann, T. (2008) <doi:10.1002/9780470061596.risk0409>. 2. Perederiy, V. (2017) <doi:10.48550/arXiv.1708.00062>.

This package provides a flexible framework for fitting multivariate ordinal regression models with composite likelihood methods. Methodological details are given in Hirk, Hornik, Vana (2020) <doi:10.18637/jss.v093.i04>.

This package provides a comprehensive framework for calculating unbiased distances in datasets containing mixed-type variables (numerical and categorical). The package implements a general formulation that ensures multivariate additivity and commensurability, meaning that variables contribute equally to the overall distance regardless of their type, scale, or distribution. Supports multiple distance measures including Gower's distance, Euclidean distance, Manhattan distance, and various categorical variable distances such as simple matching, Eskin, occurrence frequency, and association-based distances. Provides tools for variable scaling (standard deviation, range, robust range, and principal component scaling), and handles both independent and association-based category dissimilarities. Implements methods to correct for biases that typically arise from different variable types, distributions, and number of categories. Particularly useful for cluster analysis, data visualization, and other distance-based methods when working with mixed data. Methods based on van de Velden et al. (2024) <doi:10.48550/arXiv.2411.00429> "Unbiased mixed variables distance".

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/>.

Easy implementation of the MABAC multi-criteria decision method, that was introduced by PamuÄ ar and Ä iroviÄ in the work entitled: "The selection of transport and handling resources in logistics centers using Multi-Attributive Border Approximation area Comparison (MABAC)" - <doi:10.1016/j.eswa.2014.11.057> - which aimed to choose implements for logistics centers. This package receives data, preferably in a spreadsheet, reads it and applies the mathematical algorithms inherent to the MABAC method to generate a ranking with the optimal solution according to the established criteria, weights and type of criteria. The data will be normalized, weighted by the weights, the border area will be determined, the distances to this border area will be calculated and finally a ranking with the optimal option will be generated.

R functions for the estimation and eigen-decomposition of multivariate autoregressive models.

This package provides utilities for estimation for the multivariate inverse Gaussian distribution of Minami (2003) <doi:10.1081/STA-120025379>, including random vector generation and explicit estimators of the location vector and scale matrix. The package implements kernel density estimators discussed in Belzile, Desgagnes, Genest and Ouimet (2024) <doi:10.48550/arXiv.2209.04757> for smoothing multivariate data on half-spaces.

Implementation of the MarkerPen algorithm, short for marker gene detection via penalized principal component analysis, described in the paper by Qiu, Wang, Lei, and Roeder (2021, <doi:10.1093/bioinformatics/btab257>). MarkerPen is a semi-supervised algorithm for detecting marker genes by combining prior marker information with bulk transcriptome data.

Used for general multiple mediation analysis. The analysis method is described in Yu and Li (2022) (ISBN: 9780367365479) "Statistical Methods for Mediation, Confounding and Moderation Analysis Using R and SAS", published by Chapman and Hall/CRC; and Yu et al.(2017) <DOI:10.1016/j.sste.2017.02.001> "Exploring racial disparity in obesity: a mediation analysis considering geo-coded environmental factors", published on Spatial and Spatio-temporal Epidemiology, 21, 13-23.

This package creates modules inline or from a file. Modules can contain any R object and be nested. Each module have their own scope and package "search path" that does not interfere with one another or the user's working environment.

Multi-Dimensional Analysis (MDA) is an adaptation of factor analysis developed by Douglas Biber (1992) <doi:10.1007/BF00136979>. Its most common use is to describe language as it varies by genre, register, and use. This package contains functions for carrying out the calculations needed to describe and plot MDA results: dimension scores, dimension means, and factor loadings.

Computing the Mann-Whitney effect based on copula models. Estimation of the association parameter in survival copula models. A description of the underlying methods is described in Nakazono et al. (2024) <doi:10.3390/math12101453> and Nakazono et al. (accepted for publication in Statistical Papers).

Power analysis and sample size calculation for Welch and Hsu (Hedderich and Sachs (2018), ISBN:978-3-662-56657-2) t-tests including Monte-Carlo simulations of empirical power and type-I-error. Power and sample size calculation for Wilcoxon rank sum and signed rank tests via Monte-Carlo simulations. Power and sample size required for the evaluation of a diagnostic test(-system) (Flahault et al. (2005), <doi:10.1016/j.jclinepi.2004.12.009>; Dobbin and Simon (2007), <doi:10.1093/biostatistics/kxj036>) as well as for a single proportion (Fleiss et al. (2003), ISBN:978-0-471-52629-2; Piegorsch (2004), <doi:10.1016/j.csda.2003.10.002>; Thulin (2014), <doi:10.1214/14-ejs909>), comparing two negative binomial rates (Zhu and Lakkis (2014), <doi:10.1002/sim.5947>), ANCOVA (Shieh (2020), <doi:10.1007/s11336-019-09692-3>), reference ranges (Jennen-Steinmetz and Wellek (2005), <doi:10.1002/sim.2177>), multiple primary endpoints (Sozu et al. (2015), ISBN:978-3-319-22005-5), and AUC (Hanley and McNeil (1982), <doi:10.1148/radiology.143.1.7063747>).

This package performs multi-omic differential network analysis by revealing differential interactions between molecular entities (genes, proteins, transcription factors, or other biomolecules) across the omic datasets provided. For each omic dataset, a differential network is constructed where links represent statistically significant differential interactions between entities. These networks are then integrated into a comprehensive visualization using distinct colors to distinguish interactions from different omic layers. This unified display allows interactive exploration of cross-omic patterns, such as differential interactions present at both transcript and protein levels. For each link, users can access differential statistical significance metrics (p values or adjusted p values, calculated via robust or traditional linear regression with interaction term) and differential regression plots. The methods implemented in this package are described in Sciacca et al. (2023) <doi:10.1093/bioinformatics/btad192>.

Flexible and informed regression with Multiple Change Points. mcp can infer change points in means, variances, autocorrelation structure, and any combination of these, as well as the parameters of the segments in between. All parameters are estimated with uncertainty and prediction intervals are supported - also near the change points. mcp supports hypothesis testing via Savage-Dickey density ratio, posterior contrasts, and cross-validation. mcp is described in Lindeløv (submitted) <doi:10.31219/osf.io/fzqxv> and generalizes the approach described in Carlin, Gelfand, & Smith (1992) <doi:10.2307/2347570> and Stephens (1994) <doi:10.2307/2986119>.

This package provides a comprehensive suite for assessing multivariate normality using six statistical tests (Mardia, Henzeâ Zirkler, Henzeâ Wagner, Royston, Doornikâ Hansen, Energy). Also includes univariate diagnostics, bivariate density visualization, robust outlier detection, power transformations (e.g., Boxâ Cox, Yeoâ Johnson), and imputation strategies ("mean", "median", "mice") for handling missing data. Bootstrap resampling is supported for selected tests to improve p-value accuracy in small samples. Diagnostic plots are available via both ggplot2 and interactive plotly visualizations. See Korkmaz et al. (2014) <https://journal.r-project.org/articles/RJ-2014-031/RJ-2014-031.pdf>.

Fits probabilistic principal components analysis, probabilistic principal components and covariates analysis and mixtures of probabilistic principal components models to metabolomic spectral data.

The mFilter package implements several time series filters useful for smoothing and extracting trend and cyclical components of a time series. The routines are commonly used in economics and finance, however they should also be interest to other areas. Currently, Christiano-Fitzgerald, Baxter-King, Hodrick-Prescott, Butterworth, and trigonometric regression filters are included in the package.

Tool for exploring DNA and amino acid variation and inferring the presence of target lineages from microbial high-throughput genomic DNA samples that potentially contain mixtures of variants/lineages. MixviR was originally created to help analyze environmental SARS-CoV-2/Covid-19 samples from environmental sources such as wastewater or dust, but can be applied to any microbial group. Inputs include reference genome information in commonly-used file formats (fasta, bed) and one or more variant call format (VCF) files, which can be generated with programs such as Illumina's DRAGEN, the Genome Analysis Toolkit, or bcftools. See DePristo et al (2011) <doi:10.1038/ng.806> and Danecek et al (2021) <doi:10.1093/gigascience/giab008> for these tools, respectively. Available outputs include a table of mutations observed in the sample(s), estimates of proportions of target lineages in the sample(s), and an R Shiny dashboard to interactively explore the data.

This package provides a set of functions for weather and climate data manipulation, and other helper functions, to support dynamic ecological modeling, particularly crop and crop disease modeling.

This package implements random number generation, plotting, and estimation algorithms for the two-parameter one-sided and two-sided M-Wright (Mainardi-Wright) family. The M-Wright distributions naturally generalize the widely used one-sided (Airy and half-normal or half-Gaussian) and symmetric (Airy and Gaussian or normal) models. These are widely studied in time-fractional differential equations. References: Cahoy and Minkabo (2017) <doi:10.3233/MAS-170388>; Cahoy (2012) <doi:10.1007/s00180-011-0269-x>; Cahoy (2012) <doi:10.1080/03610926.2010.543299>; Cahoy (2011); Mainardi, Mura, and Pagnini (2010) <doi:10.1155/2010/104505>.

An interface to build machine learning models for classification and regression problems. mikropml implements the ML pipeline described by TopçuoÄ lu et al. (2020) <doi:10.1128/mBio.00434-20> with reasonable default options for data preprocessing, hyperparameter tuning, cross-validation, testing, model evaluation, and interpretation steps. See the website <https://www.schlosslab.org/mikropml/> for more information, documentation, and examples.