Derives prediction rule ensembles (PREs). Largely follows the procedure for deriving PREs as described in Friedman & Popescu (2008; <DOI:10.1214/07-AOAS148>), with adjustments and improvements described in Fokkema (2020; <DOI:10.18637/jss.v092.i12>) and Fokkema & Strobl (2020; <DOI:10.1037/met0000256>). The main function pre() derives prediction rule ensembles consisting of rules and/or linear terms for continuous, binary, count, multinomial, survival and multivariate continuous responses. Function gpe() derives generalized prediction ensembles, consisting of rules, hinge and linear functions of the predictor variables.

This package implements the Single Transferable Vote (STV) electoral system, with clear explanatory graphics. The core function stv() uses Meek's method, the purest expression of the simple principles of STV, but which requires electronic counting. It can handle votes expressing equal preferences for subsets of the candidates. A function stv.wig() implementing the Weighted Inclusive Gregory method, as used in Scottish council elections, is also provided, and with the same options, as described in the manual. The required vote data format is as an R list: a function pref.data() is provided to transform some commonly used data formats into this format. References for methodology: Hill, Wichmann and Woodall (1987) <doi:10.1093/comjnl/30.3.277>, Hill, David (2006) <https://www.votingmatters.org.uk/ISSUE22/I22P2.pdf>, Mollison, Denis (2023) <arXiv:2303.15310>, (see also the package manual pref_pkg_manual.pdf).

Package for the position related analysis of quantitative functional genomics data.

Spatial estimation of a prevalence surface or a relative risks surface, using data from a Demographic and Health Survey (DHS) or an analog survey, see Larmarange et al. (2011) <doi:10.4000/cybergeo.24606>.

The prebs package aims at making RNA-sequencing (RNA-seq) data more comparable to microarray data. The comparability is achieved by summarizing sequencing-based expressions of probe regions using a modified version of RMA algorithm. The pipeline takes mapped reads in BAM format as an input and produces either gene expressions or original microarray probe set expressions as an output.

This package performs a fast Wilcoxon rank sum test and auROC analysis.

This package provides a collection of templates to author preregistration documents for scientific studies in PDF format.

Allows users to derive multi-objective weights from pairwise comparisons, which research shows is more repeatable, transparent, and intuitive other techniques. These weights can be rank existing alternatives or to define a multi-objective utility function for optimization.

Convenient structures for creating, sourcing, reading, writing and manipulating ordinal preference data. Methods for writing to/from PrefLib formats. See Nicholas Mattei and Toby Walsh "PrefLib: A Library of Preference Data" (2013) <doi:10.1007/978-3-642-41575-3_20>.

This package performs genomic prediction of hybrid performance using eight statistical methods including GBLUP, BayesB, RKHS, PLS, LASSO, EN, LightGBM and XGBoost along with additive and additive-dominance models. Users are able to incorporate parental phenotypic information in all methods based on their specific needs. (Xu S et al(2017) <doi:10.1534/g3.116.038059>; Xu Y et al (2021) <doi: 10.1111/pbi.13458>).

Drop-in replacements for standard base graphics functions. The replacements are prettier versions of the originals.

This package provides tools for accurate calculations and visualization of precision-recall and ROC (Receiver Operator Characteristics) curves.

This package provides a database containing the names of the babies born in Quebec between 1980 and 2020.

This package provides functions for conventionally formatting descriptive stats, reshaping data frames and formatting R output as HTML.

An implementation of prediction intervals for overdispersed count data, for overdispersed binomial data and for linear random effects models.

This repository contains the codes for using the predictive accuracy comparison tests developed in Pitarakis, J. (2023) <doi:10.1017/S0266466623000154>.

This package provides a set of tools to implement the non-parametric bounds and Bayesian methods for assessing post-treatment bias developed in Blackwell, Brown, Hill, Imai, and Yamamoto (2025) <doi:10.1017/pan.2025.3>.

An open-access tool/framework to download, validate, visualize, and analyze multi-source precipitation data. More information and an example of implementation can be found in Vargas Godoy and Markonis (2023, <doi:10.1016/j.envsoft.2023.105711>).

Makes output files from select PreSens Fiber Optic Oxygen Transmitters easier to work with in R. See <http://www.presens.de> for more information about PreSens (Precision Sensing GmbH). Note: this package is neither created nor maintained by PreSens.

This package provides a doubly robust precision medicine approach to fit, cross-validate and visualize prediction models for the conditional average treatment effect (CATE). It implements doubly robust estimation and semiparametric modeling approach of treatment-covariate interactions as proposed by Yadlowsky et al. (2020) <doi:10.1080/01621459.2020.1772080>.

Bland (2009) <doi:10.1136/bmj.b3985> recommended to base study sizes on the width of the confidence interval rather the power of a statistical test. The goal of presize is to provide functions for such precision based sample size calculations. For a given sample size, the functions will return the precision (width of the confidence interval), and vice versa.

An efficient data integration method is provided for multiple spatial transcriptomics data with non-cluster-relevant effects such as the complex batch effects. It unifies spatial factor analysis simultaneously with spatial clustering and embedding alignment, requiring only partially shared cell/domain clusters across datasets. More details can be referred to Wei Liu, et al. (2023) <doi:10.1038/s41467-023-35947-w>.

Generates design matrix for analysing real paired comparisons and derived paired comparison data (Likert type items/ratings or rankings) using a loglinear approach. Fits loglinear Bradley-Terry model (LLBT) exploiting an eliminate feature. Computes pattern models for paired comparisons, rankings, and ratings. Some treatment of missing values (MCAR and MNAR). Fits latent class (mixture) models for paired comparison, rating and ranking patterns using a non-parametric ML approach.

This package can be used to predict the r-species accumulation curve (r-SAC), which is the number of species represented at least r times as a function of the sampling effort. When r = 1, the curve is known as the species accumulation curve, or the library complexity curve in high-throughput genomic sequencing. The package includes both parametric and nonparametric methods, as described by Deng C, et al. (2018).