Enter the query into the form above. You can look for specific version of a package by using @ symbol like this: gcc@10.
API method:
GET /api/packages?search=hello&page=1&limit=20
where search is your query, page is a page number and limit is a number of items on a single page. Pagination information (such as a number of pages and etc) is returned
in response headers.
If you'd like to join our channel search send a patch to ~whereiseveryone/toys@lists.sr.ht adding your channel as an entry in channels.scm.
This package provides drop-in replacements for functions from the stringr package, with the same user interface. These functions have no external dependencies and can be copied directly into your package code using the staticimports package.
Efficient coordinate ascent algorithm for fitting regularization paths for linear models penalized by Spike-and-Slab LASSO of Rockova and George (2018) <doi:10.1080/01621459.2016.1260469>.
Processor for selected ion flow tube mass spectrometer (SIFT-MS) output file from breath analysis. It allows the filtering of the SIFT output file (i.e., variation over time of the target analyte concentration) and the following analysis for the determination of: maximum, average, and standard deviation value of target concentration measured at each exhalation, and the respiratory rate over the measurement. Additionally, it is possible to align the SIFT-MS data with other on-line techniques such as cardio pulmonary exercise test (CPET) for a comprehensive characterization of breath samples.
Generates data from R or JAGS code for use in simulation studies. The data are returned as an nlist::nlists object and/or saved to file as individual .rds files. Parallelization is implemented using the future package. Progress is reported using the progressr package.
Complex machine learning models are often hard to interpret. However, in many situations it is crucial to understand and explain why a model made a specific prediction. Shapley values is the only method for such prediction explanation framework with a solid theoretical foundation. Previously known methods for estimating the Shapley values do, however, assume feature independence. This package implements methods which accounts for any feature dependence, and thereby produces more accurate estimates of the true Shapley values. An accompanying Python wrapper ('shaprpy') is available through PyPI.
An implementation of semi-supervised regression methods including self-learning and co-training by committee based on Hady, M. F. A., Schwenker, F., & Palm, G. (2009) <doi:10.1007/978-3-642-04274-4_13>. Users can define which set of regressors to use as base models from the caret package, other packages, or custom functions.
Tool for statistical simulations that have two components. One component generates the data and the other one analyzes the data. The main aims of the package are the reduction of the administrative source code (mainly loops and management code for the results) and a simple applicability of the package that allows the user to quickly learn how to work with it. Parallel computing is also supported. Finally, convenient functions are provided to summarize the simulation results.
This package provides functions to take samples of data, sample size estimation and getting useful estimators such as total, mean, proportion about its population using simple random, stratified, systematic and cluster sampling.
This package provides a set of functions used in teaching STATS 201/208 Data Analysis at the University of Auckland. The functions are designed to make parts of R more accessible to a large undergraduate population who are mostly not statistics majors.
This package provides functions for performing stochastic search variable selection (SSVS) for binary and continuous outcomes and visualizing the results. SSVS is a Bayesian variable selection method used to estimate the probability that individual predictors should be included in a regression model. Using MCMC estimation, the method samples thousands of regression models in order to characterize the model uncertainty regarding both the predictor set and the regression parameters. For details see Bainter, McCauley, Wager, and Losin (2020) Improving practices for selecting a subset of important predictors in psychology: An application to predicting pain, Advances in Methods and Practices in Psychological Science 3(1), 66-80 <DOI:10.1177/2515245919885617>.
Datasets used in "Statistical Methods for the Social Sciences" (SMSS) by Alan Agresti and Barbara Finlay.
Estimates a covariance matrix using Stein's isotonized covariance estimator, or a related estimator suggested by Haff.
This package provides tools for creating and working with survey replicate weights, extending functionality of the survey package from Lumley (2004) <doi:10.18637/jss.v009.i08>. Implements bootstrap methods for complex surveys, including the generalized survey bootstrap as described by Beaumont and Patak (2012) <doi:10.1111/j.1751-5823.2011.00166.x>. Methods are provided for applying nonresponse adjustments to both full-sample and replicate weights as described by Rust and Rao (1996) <doi:10.1177/096228029600500305>. Implements methods for sample-based calibration described by Opsomer and Erciulescu (2021) <https://www150.statcan.gc.ca/n1/pub/12-001-x/2021002/article/00006-eng.htm>. Diagnostic functions are included to compare weights and weighted estimates from different sets of replicate weights.
The Swiss Ephemeris (version 2.10.03) is a high precision ephemeris based upon the DE431 ephemerides from NASA's JPL. It covers the time range 13201 BCE to 17191 CE. This package uses the semi-analytic theory by Steve Moshier. For faster and more accurate calculations, the compressed Swiss Ephemeris data is available in the swephRdata package. To access this data package, run install.packages("swephRdata", repos = "https://rstub.r-universe.dev", type = "source")'. The size of the swephRdata package is approximately 115 MB. The user can also use the original JPL DE431 data.
The synchrosqueezed wavelet transform is implemented. The package is a translation of MATLAB Synchrosqueezing Toolbox, version 1.1 originally developed by Eugene Brevdo (2012). The C code for curve_ext was authored by Jianfeng Lu, and translated to Fortran by Dongik Jang. Synchrosqueezing is based on the papers: [1] Daubechies, I., Lu, J. and Wu, H. T. (2011) Synchrosqueezed wavelet transforms: An empirical mode decomposition-like tool. Applied and Computational Harmonic Analysis, 30. 243-261. [2] Thakur, G., Brevdo, E., Fukar, N. S. and Wu, H-T. (2013) The Synchrosqueezing algorithm for time-varying spectral analysis: Robustness properties and new paleoclimate applications. Signal Processing, 93, 1079-1094.
Estimate morphometric and gonadal size at sexual maturity for organisms, usually fish and invertebrates. It includes methods for classification based on relative growth (using principal components analysis, hierarchical clustering, discriminant analysis), logistic regression (Frequentist or Bayes), parameters estimation and some basic plots. Optional ggplot-style graphics are available for selected plot methods.
Fitting a smooth path to a given set of noisy spherical data observed at known time points. It implements a piecewise geodesic curve fitting method on the unit sphere based on a velocity-based penalization scheme. The proposed approach is implemented using the Riemannian block coordinate descent algorithm. To understand the method and algorithm, one can refer to Bak, K. Y., Shin, J. K., & Koo, J. Y. (2023) <doi:10.1080/02664763.2022.2054962> for the case of order 1. Additionally, this package includes various functions necessary for handling spherical data.
This package implements a Super Learner framework for right-censored survival data. The package fits convex combinations of parametric, semiparametric, and machine learning survival learners by minimizing cross-validated risk using inverse probability of censoring weighting (IPCW). It provides tools for automated hyperparameter grid search, high-dimensional variable screening, and evaluation of prediction performance using metrics such as the Brier score, Uno's C-index, and time-dependent area under the curve (AUC). Additional utilities support model interpretation for survival ensembles, including Shapley additive explanations (SHAP), and estimation of covariate-adjusted restricted mean survival time (RMST) contrasts. The methodology is related to treatment-specific survival curve estimation using machine learning described by Westling et al. (2024) <doi:10.1080/01621459.2023.2205060>, and the unified ensemble framework described in Lyu et al. (2026) <doi:10.64898/2026.03.11.711010>.
This package provides estimates for the bivariate and trivariate distribution functions and bivariate and trivariate survival functions for censored gap times. Two approaches, using existing methodologies, are considered: (i) the Lin's estimator, which is based on the extension the Kaplan-Meier estimator of the distribution function for the first event time and the Inverse Probability of Censoring Weights for the second time (Lin DY, Sun W, Ying Z (1999) <doi:10.1093/biomet/86.1.59> and (ii) another estimator based on Kaplan-Meier weights (Una-Alvarez J, Meira-Machado L (2008) <https://w3.math.uminho.pt/~lmachado/Biometria_conference.pdf>). The proposed methods are the landmark estimators based on subsampling approach, and the estimator based on weighted cumulative hazard estimator. The package also provides nonparametric estimator conditional to a given continuous covariate. All these methods have been submitted to be published.
The goal of SIHR is to provide inference procedures in the high-dimensional generalized linear regression setting for: (1) linear functionals <doi:10.48550/arXiv.1904.12891> <doi:10.48550/arXiv.2012.07133>, (2) conditional average treatment effects, (3) quadratic functionals <doi:10.48550/arXiv.1909.01503>, (4) inner product, (5) distance.
Scaffold an entire web-based report using template chunks, based on a small chapter overview and a dataset. Highly adaptable with prefixes, suffixes, translations, etc. Also contains tools for password-protecting, e.g. for each organization's report on a website. Developed for the common case of a survey across multiple organizations/sites where each organization wants to obtain results for their organization compared with everyone else. See saros (<https://CRAN.R-project.org/package=saros>) for tools used for authors in the drafted reports.
This package produces publication-ready statistical tables and figures formatted according to the 7th edition of the American Psychological Association (APA) style guidelines. Supports descriptive statistics, t-tests, z-tests, chi-square tests, Analysis of Variance (ANOVA), Analysis of Covariance (ANCOVA), two-way ANOVA with simple effects, Multivariate Analysis of Variance (MANOVA), robust and cluster-robust regression using Heteroscedasticity-Consistent (HC) standard errors, post-hoc pairwise comparisons, homoskedasticity and heteroscedasticity diagnostics including the Non-Constant Variance (NCV) test, proportion tests, and multilevel mixed-effects models with intraclass correlation coefficients (ICC) and model-comparison tables. Output can be directed to the console, Microsoft Word (via officer and flextable'), or LaTeX. For APA style guidelines see American Psychological Association (2020, ISBN:978-1-4338-3216-1).
This package provides functions to estimate kernel-smoothed spatial and spatio-temporal densities and relative risk functions, and perform subsequent inference. Methodological details can be found in the accompanying tutorial: Davies et al. (2018) <DOI:10.1002/sim.7577>.
The single cell mapper (scMappR) R package contains a suite of bioinformatic tools that provide experimentally relevant cell-type specific information to a list of differentially expressed genes (DEG). The function "scMappR_and_pathway_analysis" reranks DEGs to generate cell-type specificity scores called cell-weighted fold-changes. Users input a list of DEGs, normalized counts, and a signature matrix into this function. scMappR then re-weights bulk DEGs by cell-type specific expression from the signature matrix, cell-type proportions from RNA-seq deconvolution and the ratio of cell-type proportions between the two conditions to account for changes in cell-type proportion. With cwFold-changes calculated, scMappR uses two approaches to utilize cwFold-changes to complete cell-type specific pathway analysis. The "process_dgTMatrix_lists" function in the scMappR package contains an automated scRNA-seq processing pipeline where users input scRNA-seq count data, which is made compatible for scMappR and other R packages that analyze scRNA-seq data. We further used this to store hundreds up regularly updating signature matrices. The functions "tissue_by_celltype_enrichment", "tissue_scMappR_internal", and "tissue_scMappR_custom" combine these consistently processed scRNAseq count data with gene-set enrichment tools to allow for cell-type marker enrichment of a generic gene list (e.g. GWAS hits). Reference: Sokolowski,D.J., Faykoo-Martinez,M., Erdman,L., Hou,H., Chan,C., Zhu,H., Holmes,M.M., Goldenberg,A. and Wilson,M.D. (2021) Single-cell mapper (scMappR): using scRNA-seq to infer cell-type specificities of differentially expressed genes. NAR Genomics and Bioinformatics. 3(1). Iqab011. <doi:10.1093/nargab/lqab011>.