R interface to POSIX mmap and Window's MapViewOfFile.

Check concordance of a vector of mutation impacts with standard dictionaries such as Sequence Ontology (SO) <http://www.sequenceontology.org/>, Mutation Annotation Format (MAF) <https://docs.gdc.cancer.gov/Encyclopedia/pages/Mutation_Annotation_Format_TCGAv2/> or Prediction and Annotation of Variant Effects (PAVE) <https://github.com/hartwigmedical/hmftools/tree/master/pave>. It enables conversion between SO/PAVE and MAF terms and selection of the most severe consequence where multiple ampersand (&) delimited impacts are given.

This package provides a system for Analysis of RBD when there is one missing observation. Methods for this process is described in A.M.Gun,M.K.Gupta,B.Dasgupta(2019,ISBN:81-87567-81-3).

High-dimensional data integration is a critical but difficult problem in genomics research because of potential biases from high-throughput experiments. We present MANCIE, a computational method for integrating two genomic data sets with homogenous dimensions from different sources based on a PCA procedure as an approximation to a Bayesian approach.

This package provides a set of functions to investigate raw data from (metabol)omics experiments intended to be used on a raw data matrix, i.e. following peak picking and signal deconvolution. Functions can be used to normalize data, detect biomarkers and perform sample classification. A detailed description of best practice usage may be found in the publication <doi:10.1007/978-1-4939-7819-9_20>.

Generates blocked designs for mixed-level factorial experiments for a given block size. Internally, it uses finite-field based, collapsed, and heuristic methods to construct block structures that minimize confounding between block effects and factorial effects. The package creates the full treatment combination table, partitions runs into blocks, and computes detailed confounding diagnostics for main effects and two-factor interactions. It also checks orthogonal factorial structure (OFS) and computes efficiencies of factorial effects using the methods of Nair and Rao (1948) <doi:10.1111/j.2517-6161.1948.tb00005.x>. When OFS is not satisfied but the design has equal treatment replications and equal block sizes, a general method based on the C-matrix and custom contrast vectors is used to compute efficiencies. The output includes the generated design, finite-field metadata, confounding summaries, OFS diagnostics, and efficiency results.

This package provides the ability to perform "Marginal Mediation"--mediation wherein the indirect and direct effects are in terms of the average marginal effects (Bartus, 2005, <https://EconPapers.repec.org/RePEc:tsj:stataj:v:5:y:2005:i:3:p:309-329>). The style of the average marginal effects stems from Thomas Leeper's work on the "margins" package. This framework allows the use of categorical mediators and outcomes with little change in interpretation from the continuous mediators/outcomes. See <doi:10.13140/RG.2.2.18465.92001> for more details on the method.

We implement functions allowing for mediation analysis to be performed in cases where the mediator is a count variable with excess zeroes. First a function is provided allowing users to perform analysis for zero-inflated count variables using the marginalized zero-inflated Poisson (MZIP) model (Long et al. 2014 <DOI:10.1002/sim.6293>). Using the counterfactual approach to mediation and MZIP we can obtain natural direct and indirect effects for the overall population. Using delta method processes variance estimation can be performed instantaneously. Alternatively, bootstrap standard errors can be used. We also provide functions for cases with exposure-mediator interactions with four-way decomposition of total effect.

Information of the centroids and geographical limits of the regions, departments, provinces and districts of Peru.

Implemented are the one-sided and two-sided multiple-direction logrank test for two-sample right censored data. In addition to the statistics p-values are calculated: 1. For the one-sided testing problem one p-value based on a wild bootstrap approach is determined. 2. In the two-sided case one p-value based on a chi-squared approximation and a second p-values based on a permutation approach are calculated. Ditzhaus, M. and Friedrich, S. (2018) <arXiv:1807.05504>. Ditzhaus, M. and Pauly, M. (2018) <arXiv:1808.05627>.

This package provides an extension of the shadow-test approach to computerized adaptive testing (CAT) implemented in the TestDesign package for the assessment framework involving multiple tests administered periodically throughout the year. This framework is referred to as the Multiple Administrations Adaptive Testing (MAAT) and supports multiple item pools vertically scaled and multiple phases (stages) of CAT within each test. Between phases and tests, transitioning from one item pool (and associated constraints) to another is allowed as deemed necessary to enhance the quality of measurement.

Multivariate Surrogate Synchrony ('mvSUSY') estimates the synchrony within datasets that contain more than two time series. mvSUSY was developed from Surrogate Synchrony ('SUSY') with respect to implementing surrogate controls, and extends synchrony estimation to multivariate data. mvSUSY works as described in Meier & Tschacher (2021).

Implement Bayesian multilevel modelling for compositional data. Compute multilevel compositional data and perform log-ratio transforms at between and within-person levels, fit Bayesian multilevel models for compositional predictors and outcomes, and run post-hoc analyses such as isotemporal substitution models. References: Le, Stanford, Dumuid, and Wiley (2025) <doi:10.1037/met0000750>, Le, Dumuid, Stanford, and Wiley (2025) <doi:10.1080/00273171.2025.2565598>.

In the context of multistate models, which are popular in sociology, demography, and epidemiology, Markov chain with rewards calculations can help to refine transition timings and so obtain more accurate estimates. The package code accommodates up to nine transient states and irregular age (time) intervals. Traditional demographic life tables result as a special case. Formulas and methods involved are explained in detail in the accompanying article: Schneider / Myrskyla / van Raalte (2021): Flexible Transition Timing in Discrete-Time Multistate Life Tables Using Markov Chains with Rewards, MPIDR Working Paper WP-2021-002.

This package provides tools of Bayesian analysis framework using the method suggested by Berger (1985) <doi:10.1007/978-1-4757-4286-2> for multivariate normal (MVN) distribution and multivariate normal mixture (MixMVN) distribution: a) calculating Bayesian posteriori of (Mix)MVN distribution; b) generating random vectors of (Mix)MVN distribution; c) Markov chain Monte Carlo (MCMC) for (Mix)MVN distribution.

An implementation of the cross-validated difference in means (CVDM) test by Desmarais and Harden (2014) <doi:10.1007/s11135-013-9884-7> (see also Harden and Desmarais, 2011 <doi:10.1177/1532440011408929>) and the cross-validated median fit (CVMF) test by Desmarais and Harden (2012) <doi:10.1093/pan/mpr042>. These tests use leave-one-out cross-validated log-likelihoods to assist in selecting among model estimations. You can also utilize data from Golder (2010) <doi:10.1177/0010414009341714> and Joshi & Mason (2008) <doi:10.1177/0022343308096155> that are included to facilitate examples from real-world analysis.

Computes indirect effects, conditional effects, and conditional indirect effects in a structural equation model or path model after model fitting, with no need to define any user parameters or label any paths in the model syntax, using the approach presented in Cheung and Cheung (2024) <doi:10.3758/s13428-023-02224-z>. Can also form bootstrap confidence intervals by doing bootstrapping only once and reusing the bootstrap estimates in all subsequent computations. Supports bootstrap confidence intervals for standardized (partially or completely) indirect effects, conditional effects, and conditional indirect effects as described in Cheung (2009) <doi:10.3758/BRM.41.2.425> and Cheung, Cheung, Lau, Hui, and Vong (2022) <doi:10.1037/hea0001188>. Model fitting can be done by structural equation modeling using lavaan() or regression using lm().

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.

Tests of comparison of two or more survival curves. Allows for comparison of more than two survival curves whether the proportional hazards hypothesis is verified or not.

This package provides a set of utility functions for analysing and modelling data from continuous report short-term memory experiments using either the 2-component mixture model of Zhang and Luck (2008) <doi:10.1038/nature06860> or the 3-component mixture model of Bays et al. (2009) <doi:10.1167/9.10.7>. Users are also able to simulate from these models.

This package provides basic tools and wrapper functions for computing clusters of instances described by multiple time-to-event censored endpoints. From long-format datasets, where one instance is described by one or more dated records, the main function, `make_state_matrices()`, creates state matrices. Based on these matrices, optimised procedures using the Jaccard distance between instances enable the construction of longitudinal typologies. The package is under active development, with additional tools for graphical representation of typologies planned. For methodological details, see our accompanying paper: `Delord M, Douiri A (2025) <doi:10.1186/s12874-025-02476-7>`.

Cancer cells accumulate DNA mutations as result of DNA damage and DNA repair processes. This computational framework is aimed at deciphering DNA mutational signatures operating in cancer. The framework includes modules that support raw data import and processing, mutational signature extraction, and results interpretation and visualization. The framework accepts widely used file formats storing information about DNA variants, such as Variant Call Format files. The framework performs Non-Negative Matrix Factorization to extract mutational signatures explaining the observed set of DNA mutations. Bootstrapping is performed as part of the analysis. The framework supports parallelization and is optimized for use on multi-core systems. The software was described by Fantini D et al (2020) <doi:10.1038/s41598-020-75062-0> and is based on a custom R-based implementation of the original MATLAB WTSI framework by Alexandrov LB et al (2013) <doi:10.1016/j.celrep.2012.12.008>.

This package provides functions to perform sensitivity analysis on a model with multivariate output.

Distance between multivariate t distributions, as presented by N. Bouhlel and D. Rousseau (2023) <doi:10.1109/LSP.2023.3324594>.