Formatting of population and case data, calculation of Standardized Incidence Ratios, and fitting the BYM model using INLA'. For details see Brown (2015) <doi:10.18637/jss.v063.i12>.

Diagnostic classification models are psychometric models used to categorically estimate respondents mastery, or proficiency, on a set of predefined skills (Bradshaw, 2016, <doi:10.1002/9781118956588.ch13>). Diagnostic models can be estimated with Stan'; however, the necessary scripts can be long and complicated. This package automates the creation of Stan scripts for diagnostic classification models. Specify different types of diagnostic models, define prior distributions, and automatically generate the necessary Stan code for estimating the model.

Extends the algebraic.dist distribution algebra to random variables with internal structure: coherent reliability systems decomposed into components arranged by a structure function (series, parallel, k-out-of-n, bridge, and arbitrary topologies via minimal path sets). Every dist_structure object is a dist', so the full distribution algebra (mean, vcov, sampler, surv, cdf) works automatically via default methods that compose component-level distributions through the topology. Adds structural queries: structure function evaluation, minimal path and cut sets, system signature, critical states, dual, Birnbaum structural importance, and system reliability. Topology shortcut constructors (series_dist, parallel_dist, kofn_dist, bridge_dist) produce ready-to-use dists from component dists and a chosen structure.

Transform newswire and earnings call transcripts as PDF obtained from Nexis Uni to R data frames. Various newswires and FairDisclosure earnings call formats are supported. Further, users can apply several pre-defined dictionaries on the data based on Graffin et al. (2016)<doi:10.5465/amj.2013.0288> and Gamache et al. (2015)<doi:10.5465/amj.2013.0377>.

This package provides a series of functions which aid in both simulating and determining the properties of finite, discrete-time, discrete state markov chains. Two functions (DTMC, MultDTMC) produce n iterations of a Markov Chain(s) based on transition probabilities and an initial distribution. The function FPTime determines the first passage time into each state. The function statdistr determines the stationary distribution of a Markov Chain.

Track and document dplyr data pipelines. As you filter, mutate, and join your way through a data set, dtrackr seamlessly keeps track of your data flow and makes publication ready documentation of a data pipeline simple.

Collection of functions for distributed lag linear and non-linear models.

Prepare prescription data (such as from the Clinical Practice Research Datalink) into an analysis-ready format, with start and stop dates for each patient's prescriptions. Based on Pye et al (2018) <doi:10.1002/pds.4440>.

DEploid (Zhu et.al. 2018 <doi:10.1093/bioinformatics/btx530>) is designed for deconvoluting mixed genomes with unknown proportions. Traditional phasing programs are limited to diploid organisms. Our method modifies Li and Stephenâ s algorithm with Markov chain Monte Carlo (MCMC) approaches, and builds a generic framework that allows haloptype searches in a multiple infection setting. This package provides R functions to support data analysis and results interpretation.

Seasonal- and calendar adjustment of time series with daily frequency using the DSA approach developed by Ollech, Daniel (2018): Seasonal adjustment of daily time series. Bundesbank Discussion Paper 41/2018.

This package provides a set of functions for inferring, visualizing, and analyzing B cell phylogenetic trees. Provides methods to 1) reconstruct unmutated ancestral sequences, 2) build B cell phylogenetic trees using multiple methods, 3) visualize trees with metadata at the tips, 4) reconstruct intermediate sequences, 5) detect biased ancestor-descendant relationships among metadata types Workflow examples available at documentation site (see URL). Citations: Hoehn et al (2022) <doi:10.1371/journal.pcbi.1009885>, Hoehn et al (2021) <doi:10.1101/2021.01.06.425648>.

Joint dimension reduction and spatial clustering is conducted for Single-cell RNA sequencing and spatial transcriptomics data, and more details can be referred to Wei Liu, Xu Liao, Yi Yang, Huazhen Lin, Joe Yeong, Xiang Zhou, Xingjie Shi and Jin Liu. (2022) <doi:10.1093/nar/gkac219>. It is not only computationally efficient and scalable to the sample size increment, but also is capable of choosing the smoothness parameter and the number of clusters as well.

An implementation of data analytic methods in R for analyses for data with ceiling/floor effects. The package currently includes functions for mean/variance estimation and mean comparison tests. Implemented methods are from Aitkin (1964) <doi:10.1007/BF02289723> and Liu & Wang (2021) <doi:10.3758/s13428-020-01407-2>.

Distributed Online Covariance Matrix Tests Docovt is a powerful tool designed to efficiently process and analyze distributed datasets. It enables users to perform covariance matrix tests in an online, distributed manner, making it highly suitable for large-scale data analysis. By leveraging advanced computational techniques, Docovt ensures robust and scalable solutions for statistical analysis, particularly in scenarios where data is dispersed across multiple nodes or sources. This package is ideal for researchers and practitioners working with high-dimensional data, providing a flexible and efficient framework for covariance matrix estimation and hypothesis testing. The philosophy of Docovt is described in Guo G.(2025) <doi:10.1016/j.physa.2024.130308>.

Easy access to species distribution data for 6 regions in the world, for a total of 226 anonymised species. These data are described and made available by Elith et al (2020) <doi:10.17161/bi.v15i2.13384> to compare species distribution modelling methods.

To create demographic table with simple summary statistics, with optional comparison(s) over one or more groups.

This package provides tools for estimating the Remaining Useful Life (RUL) of degrading systems using linear mixed-effects models and creating a health index. It supports both univariate and multivariate degradation signals. For multivariate inputs, the signals are merged into a univariate health index prior to modeling. Linear and exponential degradation trajectories are supported (the latter using a log transformation). Remaining Useful Life (RUL) distributions are estimated using Bayesian updating for new units, enabling on-site predictive maintenance. Based on the methodology of Liu and Huang (2016) <doi:10.1109/TASE.2014.2349733>.

Dynamic simulations and graphical depictions of autoregressive relationships.

Works as an "add-on" to packages like shiny', future', as well as rlang', and provides utility functions. Just like dipping sauce adding flavors to potato chips or pita bread, dipsaus for data analysis and visualizations adds handy functions and enhancements to popular packages. The goal is to provide simple solutions that are frequently asked for online, such as how to synchronize shiny inputs without freezing the app, or how to get memory size on Linux or MacOS system. The enhancements roughly fall into these four categories: 1. shiny input widgets; 2. high-performance computing using the future package; 3. modify R calls and convert among numbers, strings, and other objects. 4. utility functions to get system information such like CPU chip-set, memory limit, etc.

An implementation of distributional random forests as introduced in Cevid & Michel & Naf & Meinshausen & Buhlmann (2022) <doi:10.48550/arXiv.2005.14458>.

Implementation of different statistical tools for the description and analysis of gene expression data based on the concept of data depth, namely, the scale curves for visualizing the dispersion of one or various groups of samples (e.g. types of tumors), a rank test to decide whether two groups of samples come from a single distribution and two methods of supervised classification techniques, the DS and TAD methods. All these techniques are based on the Modified Band Depth, which is a recent notion of depth with a low computational cost, what renders it very appropriate for high dimensional data such as gene expression data.

This package provides methods for evaluating the probability mass function, cumulative distribution function, and generating random samples from discrete tempered stable distributions. For more details see Grabchak (2021) <doi:10.1007/s11009-021-09904-3>.

Diagnostic and prognostic models are typically evaluated with measures of accuracy that do not address clinical consequences. Decision-analytic techniques allow assessment of clinical outcomes, but often require collection of additional information may be cumbersome to apply to models that yield a continuous result. Decision curve analysis is a method for evaluating and comparing prediction models that incorporates clinical consequences, requires only the data set on which the models are tested, and can be applied to models that have either continuous or dichotomous results. See the following references for details on the methods: Vickers (2006) <doi:10.1177/0272989X06295361>, Vickers (2008) <doi:10.1186/1472-6947-8-53>, and Pfeiffer (2020) <doi:10.1002/bimj.201800240>.

An open, multi-algorithmic pipeline for easy, fast and efficient analysis of cellular sub-populations and the molecular signatures that characterize them. The pipeline consists of four successive steps: data pre-processing, cellular clustering with pseudo-temporal ordering, defining differential expressed genes and biomarker identification. More details on Ghannoum et. al. (2021) <doi:10.3390/ijms22031399>. This package implements extensions of the work published by Ghannoum et. al. (2019) <doi:10.1101/700989>.