Obtains lists of files of remote sensing collections for Southern Ocean surface properties. Commonly used data sources of sea surface temperature, sea ice concentration, and altimetry products such as sea surface height and sea surface currents are cached in object storage on the Pawsey Supercomputing Research Centre facility. Patterns of working to retrieve data from these object storage catalogues are described. The catalogues include complete collections of datasets Reynolds et al. (2008) "NOAA Optimum Interpolation Sea Surface Temperature (OISST) Analysis, Version 2.1" <doi:10.7289/V5SQ8XB5>, Spreen et al. (2008) "Artist Advanced Microwave Scanning Radiometer for Earth Observing System (AMSR-E) sea ice concentration" <doi:10.1029/2005JC003384>. In future releases helpers will be added to identify particular data collections and target specific dates for earth observation data for reading, as well as helpers to retrieve data set citation and provenance details. This work was supported by resources provided by the Pawsey Supercomputing Research Centre with funding from the Australian Government and the Government of Western Australia. This software was developed by the Integrated Digital East Antarctica program of the Australian Antarctic Division.

Add-on for the scan package that creates plots from single-case data frames ('scdf'). It includes functions for styling single-case plots, adding phase-based lines to indicate various statistical parameters, and predefined themes for presentations and publications. More information and in depth examples can be found in the online book "Analyzing Single-Case Data with R and scan" Jürgen Wilbert (2026) <https://jazznbass.github.io/scan-Book/>.

Nonparametric estimation of Spearman's rank correlation with bivariate survival (right-censored) data as described in Eden, S.K., Li, C., Shepherd B.E. (2021), Nonparametric Estimation of Spearman's Rank Correlation with Bivariate Survival Data, Biometrics (under revision). The package also provides functions that visualize bivariate survival data and bivariate probability mass function.

Instrumental variable analysis methods for causal inference on survival data based on the Cox model allowing for various treatment and effect types, including orthogonality method-of-moments instrumental variable estimation for the Cox model, two-stage residual inclusion Cox estimation with frailty, sequential trial emulation, sequential Cox analyses, and sequential two-stage residual inclusion Cox analyses. Methodological background includes MacKenzie et al. (2014) <doi:10.1007/s10742-014-0117-x>, Martinez-Camblor et al. (2019) <doi:10.1093/biostatistics/kxx062>, Martinez-Camblor et al. (2019) <doi:10.1111/rssc.12341>, Gran et al. (2010) <doi:10.1002/sim.4048>, and Keogh et al. (2023) <doi:10.1002/sim.9718>.

Adjusts model-based small area estimates so that their weighted aggregate agrees with the weighted aggregate of the direct estimates, using the difference, ratio, and optimum benchmarking methods described in Rao and Molina (2015, ISBN:978-1-118-73578-7) and Wang, Fuller and Qu (2008). The mean squared error (MSE) of the benchmarked empirical best linear unbiased predictor (EBLUP) under the Fay-Herriot model is estimated with the second-order approximation or the parametric bootstrap of Steorts and Ghosh (2013) <doi:10.5705/ss.2012.053>. The posterior MSE of the benchmarked hierarchical Bayes (HB) estimator follows Datta, Ghosh, Steorts and Maples (2011) <doi:10.1007/s11749-010-0218-y>.

Code and data for modelling and simulation of stochastic kinetic biochemical network models. It contains the code and data associated with the second and third editions of the book Stochastic Modelling for Systems Biology, published by Chapman & Hall/CRC Press.

This package implements the following approaches for multidimensional scaling (MDS) based on stress minimization using majorization (smacof): ratio/interval/ordinal/spline MDS on symmetric dissimilarity matrices, MDS with external constraints on the configuration, individual differences scaling (idioscal, indscal), MDS with spherical restrictions, and ratio/interval/ordinal/spline unfolding (circular restrictions, row-conditional). Various tools and extensions like jackknife MDS, bootstrap MDS, permutation tests, MDS biplots, gravity models, unidimensional scaling, drift vectors (asymmetric MDS), classical scaling, and Procrustes are implemented as well.

This is a collection of various kinds of data with broad uses for teaching. My students, and academics like me who teach the same topics I teach, should find this useful if their teaching workflow is also built around the R programming language. The applications are multiple but mostly cluster on topics of statistical methodology, international relations, and political economy.

This package provides functions for the collection of 3D points and curves using a stereo camera setup.

This package provides a powerful and flexible tool for visualizing proportional data across spatially resolved contexts. By combining the concepts of scatter plots and stacked bar charts, scatterbar allows users to create scattered bar chart plots, which effectively display the proportions of different categories at each (x, y) location. This visualization is particularly useful for applications where understanding the distribution of categories across spatial coordinates is essential. This package features automatic determination of optimal scaling factors based on data, customizable scaling and padding options for both x and y axes, flexibility to specify custom colors for each category, options to customize the legend title, and integration with ggplot2 for robust and high-quality visualizations. For more details, see Velazquez et al. (2024) <doi:10.1101/2024.08.14.606810>.

This package provides tools for the simultaneous improvement of multiple traits in plant breeding. Building upon the classical selection index (Smith 1937 <doi:10.1111/j.1469-1809.1936.tb02143.x>) and modern quantitative genetics (Kang 2020 <doi:10.1007/978-3-319-91223-3>), this package calculates classical phenotypic, genomic, marker-assisted, restricted/constrained, and eigen selection indices. It also incorporates multi-stage selection evaluation and stochastic simulations to estimate genetic advance based on economic weights, heritability, and genetic correlations.

This package provides a toolbox for constructing potential landscapes for dynamical systems using Monte Carlo simulation. The method is based on the potential landscape definition by Wang et al. (2008) <doi:10.1073/pnas.0800579105> (also see Zhou & Li, 2016 <doi:10.1063/1.4943096> for further mathematical discussions) and can be used for a large variety of models.

Non-proportional hazard (NPH) is commonly observed in immuno-oncology studies, where the survival curves of the treatment and control groups show delayed separation. To properly account for NPH, several statistical methods have been developed. One such method is Max-Combo test, which is a straightforward and flexible hypothesis testing method that can simultaneously test for constant, early, middle, and late treatment effects. However, the majority of the Max-Combo test performed in clinical studies are unstratified, ignoring the important prognostic stratification factors. To fill this gap, we have developed an R package for stratified Max-Combo testing that accounts for stratified baseline factors. Our package explores various methods for calculating combined test statistics, estimating joint distributions, and determining the p-values.

Given a list of substance compositions, a list of substances involved in a process, and a list of constraints in addition to mass conservation of elementary constituents, the package contains functions to build the substance composition matrix, to analyze the uniqueness of process stoichiometry, and to calculate stoichiometric coefficients if process stoichiometry is unique. (See Reichert, P. and Schuwirth, N., A generic framework for deriving process stoichiometry in enviromental models, Environmental Modelling and Software 25, 1241-1251, 2010 for more details.).

This package provides a set of functions for generating SPSS syntax files from the R environment.

Fits linear regression models on datasets residing in SQL databases without pulling data into R memory. Computes sufficient statistics inside the database engine via a single aggregation query and solves the normal equations in R.

This package provides a flexible moving average algorithm for modeling drug exposure in pharmacoepidemiology studies as presented in the article: Ouchi, D., Giner-Soriano, M., Gómez-Lumbreras, A., Vedia Urgell, C.,Torres, F., & Morros, R. (2022). "Automatic Estimation of the Most Likely Drug Combination in Electronic Health Records Using the Smooth Algorithm : Development and Validation Study." JMIR medical informatics, 10(11), e37976. <doi:10.2196/37976>.

This package provides standard load profiles (SLPs) for electricity and gas published by the German Association of Energy and Water Industries (BDEW Bundesverband der Energie- und Wasserwirtschaft e.V.) in a tidy format. The electricity profiles cover the 1999 profiles â households (H0), commercial (G0â G6), and agriculture (L0â L2) â and the updated 2025 profiles (H25, G25, L25, P25, S25), which additionally represent households with photovoltaic systems and battery storage. An interface generates an electricity load profile over a user-defined date range. A second interface generates daily standard load profiles for gas using the synthetic SigLinDe method. More information on the data and methodology for electricity is described in "Standardlastprofile Strom", <https://www.bdew.de/energie/standardlastprofile-strom/>, and for gas in "Standardlastprofile Gas", <https://www.bdew.de/energie/standardlastprofile-gas/>.

An R interface to the Python sqlfluff SQL linter and formatter via the reticulate package. Enables linting, fixing, and parsing of SQL queries with support for multiple dialects. Includes special handling for glue SQL syntax with curly-brace placeholders.

This package provides tools for analyzing spatial cell-cell interactions based on ligand-receptor pairs, including functions for local, regional, and global analysis using spatial transcriptomics data. Integrates with databases like CellChat <https://github.com/jinworks/CellChat>, CellPhoneDB <https://www.cellphonedb.org/>, Cellinker <https://www.rna-society.org/cellinker/>, ICELLNET <https://github.com/soumelis-lab/ICELLNET>, and ConnectomeDB <https://humanconnectome.org/software/connectomedb/> to identify ligand-receptor pairs, visualize interactions through heatmaps, chord diagrams, and infer interactions on different spatial scales.

This package implements the "shrinkage t" statistic introduced in Opgen-Rhein and Strimmer (2007) <DOI:10.2202/1544-6115.1252> and a shrinkage estimate of the "correlation-adjusted t-score" (CAT score) described in Zuber and Strimmer (2009) <DOI:10.1093/bioinformatics/btp460>. It also offers a convenient interface to a number of other regularized t-statistics commonly employed in high-dimensional case-control studies.

Inferring causation from spatial cross-sectional data through empirical dynamic modeling (EDM), with methodological extensions including geographical convergent cross mapping from Gao et al. (2023) <doi:10.1038/s41467-023-41619-6>, geographical cross mapping cardinality as introduced by Lyu et al. (2026) <doi:10.1080/13658816.2026.2687121>, as well as the spatial causality test following the approach of Herrera et al. (2016) <doi:10.1111/pirs.12144>, together with geographical pattern causality proposed in Zhang & Wang (2025) <doi:10.1080/13658816.2025.2581207>.

This package provides a simple function that anonymises a list of variables in a consistent way: anonymised factors are not recycled and the same original levels receive the same anonymised factor even if located in different datasets.

Generates random values from a univariate and multivariate continuous distribution by using kernel density estimation based on a sample. Duong (2017) <doi:10.18637/jss.v021.i07>, Christian P. Robert and George Casella (2010 ISBN:978-1-4419-1575-7) <doi:10.1007/978-1-4419-1576-4>.