This package creates geographic map tiles from geospatial map files or non-geographic map tiles from simple image files. This package provides a tile generator function for creating map tile sets for use with packages such as leaflet'. In addition to generating map tiles based on a common raster layer source, it also handles the non-geographic edge case, producing map tiles from arbitrary images. These map tiles, which have a non-geographic, simple coordinate reference system (CRS), can also be used with leaflet when applying the simple CRS option. Map tiles can be created from an input file with any of the following extensions: tif, grd and nc for spatial maps and png, jpg and bmp for basic images. This package requires Python and the gdal library for Python'. Windows users are recommended to install OSGeo4W (<https://trac.osgeo.org/osgeo4w/>) as an easy way to obtain the required gdal support for Python'.

The genetic algorithm can be used directly to find the similarity of users and more effectively to increase the efficiency of the collaborative filtering method. By identifying the nearest neighbors to the active user, before the genetic algorithm, and by identifying suitable starting points, an effective method for user-based collaborative filtering method has been developed. This package uses an optimization algorithm (continuous genetic algorithm) to directly find the optimal similarities between active users (users for whom current recommendations are made) and others. First, by determining the nearest neighbor and their number, the number of genes in a chromosome is determined. Each gene represents the neighbor's similarity to the active user. By estimating the starting points of the genetic algorithm, it quickly converges to the optimal solutions. The positive point is the independence of the genetic algorithm on the number of data that for big data is an effective help in solving the problem.

This package provides tools to conduct Bayesian multivariate network meta-analysis providing - the single correlation coefficient model by Efthimiou et al. (2015) <doi:10.1093/biostatistics/kxu030>; - per-outcome consistency checks using the node-splitting method (Dias et al., 2010) <doi:10.1002/sim.3767>; - per-outcome treatment hierarchies using the surface under the cumulative ranking curve (SUCRA), the probability of best value, or median (or mean) ranks (Salanti et al., 2011) <doi:10.1016/j.jclinepi.2010.03.016>; - across-outcomes benefit-risk assessment using the ViÅ¡eKriterijumska Optimizacija I Kompromisno ReÅ¡enje (VIKOR) method (Opricovic & Tzeng, 2004) <doi:10.1016/S0377-2217(03)00020-1>; - convergence checks using trace plots, density plots, or the R-hat statistic; - forest plots of treatment estimates and consistency checks, scatter plots of per-outcome rankings, Hasse diagrams (Carlsen & Bruggemann, 2014) <doi:10.1002/cem.2569> to visualize the partial order of the treatments across all outcomes.

Annotates single-cell and spatial-transcriptomic (ST) data using context-matching marker datasets. It creates a unified marker list (`Markers_list`) from multiple sources: built-in curated databases ('Cellmarker2', PanglaoDB', ScType', CellTypist', scIBD', TCellSI', PCTIT', PCTAM'), Seurat objects with cell labels, or user-provided Excel tables. SlimR first uses adaptive machine learning for parameter optimization, and then offers two automated annotation approaches: cluster-based and per-cell'. Cluster-based annotation assigns one label per cluster, expression-based probability calculation, and AUC validation. Per-cell annotation assigns labels to individual cells using three scoring methods with adaptive thresholds and ratio-based confidence filtering, plus optional UMAP spatial smoothing, making it ideal for heterogeneous clusters and rare cell types. The package also supports semi-automated workflows with heatmaps, feature plots, and combined visualizations for manual annotation. For more information, see the package documentation at <https://github.com/zhaoqing-wang/SlimR>.

This package provides a simulation-based tool made to help researchers to become familiar with multilevel variations, and to build up sampling designs for their study. This tool has two main objectives: First, it provides an educational tool useful for students, teachers and researchers who want to learn to use mixed-effects models. Users can experience how the mixed-effects model framework can be used to understand distinct biological phenomena by interactively exploring simulated multilevel data. Second, it offers research opportunities to those who are already familiar with mixed-effects models, as it enables the generation of data sets that users may download and use for a range of simulation-based statistical analyses such as power and sensitivity analysis of multilevel and multivariate data [Allegue, H., Araya-Ajoy, Y.G., Dingemanse, N.J., Dochtermann N.A., Garamszegi, L.Z., Nakagawa, S., Reale, D., Schielzeth, H. and Westneat, D.F. (2016) <doi: 10.1111/2041-210X.12659>].

Fit multiclass Classification version of Bayesian Adaptive Smoothing Splines (CBASS) to data using reversible jump MCMC. The multiclass classification problem consists of a response variable that takes on unordered categorical values with at least three levels, and a set of inputs for each response variable. The CBASS model consists of a latent multivariate probit formulation, and the means of the latent Gaussian random variables are specified using adaptive regression splines. The MCMC alternates updates of the latent Gaussian variables and the spline parameters. All the spline parameters (variables, signs, knots, number of interactions), including the number of basis functions used to model each latent mean, are inferred. Functions are provided to process inputs, initialize the chain, run the chain, and make predictions. Predictions are made on a probabilistic basis, where, for a given input, the probabilities of each categorical value are produced. See Marrs and Francom (2023) "Multiclass classification using Bayesian multivariate adaptive regression splines" Under review.

Reads and writes clinical-trial datasets losslessly across SAS XPORT (XPT), Clinical Data Interchange Standards Consortium (CDISC) Dataset-JSON, and Apache Parquet', applying a specification to produce submission-ready Study Data Tabulation Model (SDTM) and Analysis Data Model (ADaM) datasets. A single canonical metadata model carries labels, CDISC data types, lengths, SAS display formats, controlled-terminology references, and sort keys identically across every format, so conversion between any two formats is lossless by construction. Pure R and lightweight, with no external SAS or Java runtime. Reads and writes CDISC Define-XML, the specification document that accompanies a submission, and renders it as HTML through the bundled Define-XML stylesheet. Implements the published format specifications for CDISC Dataset-JSON (<https://cdisc-org.github.io/DataExchange-DatasetJson/doc/dataset-json1-1.html>), CDISC Define-XML (<https://www.cdisc.org/standards/data-exchange/define-xml>), and SAS XPORT (<https://www.loc.gov/preservation/digital/formats/fdd/fdd000466.shtml>).

Joint and Individual Variation Explained (JIVE) is a method for decomposing multiple datasets obtained on the same subjects into shared structure, structure unique to each dataset, and noise. The two most common implementations are R.JIVE, an iterative approach, and AJIVE, which uses principal angle analysis. JIVE estimates subspaces but interpreting these subspaces can be challenging with AJIVE or R.JIVE. We expand upon insights into AJIVE as a canonical correlation analysis (CCA) of principal component scores. This reformulation, which we call CJIVE, 1) provides an ordering of joint components by the degree of correlation between corresponding canonical variables; 2) uses a computationally efficient permutation test for the number of joint components, which provides a p-value for each component; and 3) can be used to predict subject scores for out-of-sample observations. Please cite the following article when utilizing this package: Murden, R., Zhang, Z., Guo, Y., & Risk, B. (2022) <doi:10.3389/fnins.2022.969510>.

An R interface to FLINT <https://flintlib.org/>, a C library for number theory. FLINT extends GNU MPFR <https://www.mpfr.org/> and GNU MP <https://gmplib.org/> with support for operations on standard rings (the integers, the integers modulo n, finite fields, the rational, p-adic, real, and complex numbers) as well as matrices and polynomials over rings. FLINT implements midpoint-radius interval arithmetic, also known as ball arithmetic, in the real and complex numbers, enabling computation in arbitrary precision with rigorous propagation of rounding and other errors; see Johansson (2017) <doi:10.1109/TC.2017.2690633>. Finally, FLINT provides ball arithmetic implementations of many special mathematical functions, with high coverage of reference works such as the NIST Digital Library of Mathematical Functions <https://dlmf.nist.gov/>. The R interface defines S4 classes, generic functions, and methods for representation and basic operations as well as plain R functions mirroring and vectorizing entry points in the C library.

Constructs and analyzes optimal row-column designs for mixed-level factorial experiments under square and rectangular field layouts. For square field layouts, the package implements direct common-factor constructions by first forming two component treatment arrays, one for each factor or super-factor, and then combining them through a symbolic cell-wise product following Gopinath, Parsad and Mandal (2018) <doi:10.1080/03610926.2017.1376091>. For rectangular field layouts, the package constructs designs by extracting a balanced principal block from a mixed-level block design, treating it as the principal column, taking the complete treatment set as the principal row, and generating the full row-column design by cyclic modular development. The package also includes repair utilities for improving disconnected or partially connected row-column designs through bounded treatment-swap searches while preserving the row-column layout structure. The package provides diagnostic tools for connectedness, orthogonal factorial structure, balance, estimability, and selected optimality criteria for row-column designs.

This package performs Non-negative Matrix Factorization (NMF) with Kernel Covariates. Given an observation matrix and kernel covariates, it optimizes both a basis matrix and a parameter matrix. Notably, if the kernel matrix is an identity matrix, the method simplifies to standard NMF. Also provides NMF with Random Effects (NMF-RE) via nmfre(), which estimates a mixed-effects model combining covariate-driven scores with unit-specific random effects together with wild bootstrap inference, and NMF-based Structural Equation Modeling (NMF-SEM) via nmf.sem(), which fits a two-block input-output model for blind source separation and path analysis. References: Satoh (2025) <doi:10.48550/arXiv.2403.05359>; Satoh (2026) <doi:10.1007/s42081-026-00349-x>; Satoh (2025) <doi:10.48550/arXiv.2512.18250>; Satoh (2026) <doi:10.48550/arXiv.2603.01468>; Satoh and Tokuda (2026) <doi:10.48550/arXiv.2607.27474>; Satoh (2026) <doi:10.1007/s42081-025-00314-0>.

Toolbox for different kinds of spatio-temporal analyses to be performed on observed point patterns, following the growing stream of literature on point process theory. This R package implements functions to perform different kinds of analyses on point processes, proposed in the papers (Siino, Adelfio, and Mateu 2018<doi:10.1007/s00477-018-1579-0>; Siino et al. 2018<doi:10.1002/env.2463>; Adelfio et al. 2020<doi:10.1007/s00477-019-01748-1>; Dâ Angelo, Adelfio, and Mateu 2021<doi:10.1016/j.spasta.2021.100534>; Dâ Angelo, Adelfio, and Mateu 2022<doi:10.1007/s00362-022-01338-4>; Dâ Angelo, Adelfio, and Mateu 2023<doi:10.1016/j.csda.2022.107679>). The main topics include modeling, statistical inference, and simulation issues on spatio-temporal point processes on Euclidean space and linear networks. Version 1.0.0 has been updated for accompanying the journal publication D Angelo and Adelfio 2025 <doi:10.18637/jss.v113.i10>.

This package provides tools for differentially private principal component analysis (PCA) visualization. It includes functions for estimating private principal component directions, constructing private scree and proportion of variance explained summaries, and visualizing two-dimensional PCA score summaries using additive and sparse histogram mechanisms. Group-wise score visualizations and an interactive shiny app are also provided. Private principal component directions are based on Kim and Jung (2025) <doi:10.1002/sam.70053>. Private scree summaries use mechanisms motivated by Dwork and Roth (2014) <doi:10.1561/0400000042>, Ramsay and Spicker (2025) <doi:10.48550/arXiv.2501.14095>, and Yu, Ren and Zhou (2024) <doi:10.3150/23-BEJ1706>. Private score plot frames use smooth sensitivity quantiles from Nissim, Raskhodnikova and Smith (2007) <doi:10.1145/1250790.1250803>. Private score histograms use additive and sparse histogram ideas from Wasserman and Zhou (2010) <doi:10.1198/jasa.2009.tm08651> and Karwa and Vadhan (2018) <doi:10.4230/LIPIcs.ITCS.2018.44>.

This package contains a mixture of statistical methods including the MCMC methods to analyze normal mixtures. Additionally, model based clustering methods are implemented to perform classification based on (multivariate) longitudinal (or otherwise correlated) data. The basis for such clustering is a mixture of multivariate generalized linear mixed models. The package is primarily related to the publications Komárek (2009, Comp. Stat. and Data Anal.) <doi:10.1016/j.csda.2009.05.006> and Komárek and Komárková (2014, J. of Stat. Soft.) <doi:10.18637/jss.v059.i12>. It also implements methods published in Komárek and Komárková (2013, Ann. of Appl. Stat.) <doi:10.1214/12-AOAS580>, Hughes, Komárek, Bonnett, Czanner, Garcà a-Fiñana (2017, Stat. in Med.) <doi:10.1002/sim.7397>, Jaspers, Komárek, Aerts (2018, Biom. J.) <doi:10.1002/bimj.201600253> and Hughes, Komárek, Czanner, Garcà a-Fiñana (2018, Stat. Meth. in Med. Res) <doi:10.1177/0962280216674496>.

Canonical correlation analysis (CCA) via reduced-rank regression with support for regularization and cross-validation. Several methods for estimating CCA in high-dimensional settings are implemented. The first set of methods, cca_rrr() (and variants: cca_group_rrr() and cca_graph_rrr()), assumes that one dataset is high-dimensional and the other is low-dimensional, while the second, ecca() (for Efficient CCA) assumes that both datasets are high-dimensional. For both methods, standard l1 regularization as well as group-lasso regularization are available. cca_graph_rrr further supports total variation regularization when there is a known graph structure among the variables of the high-dimensional dataset. In this case, the loadings of the canonical directions of the high-dimensional dataset are assumed to be smooth on the graph. For more details see Donnat and Tuzhilina (2024) <doi:10.48550/arXiv.2405.19539> and Wu, Tuzhilina and Donnat (2025) <doi:10.48550/arXiv.2507.11160>.

The debar sequence processing pipeline is designed for denoising high throughput sequencing data for the animal DNA barcode marker cytochrome c oxidase I (COI). The package is designed to detect and correct insertion and deletion errors within sequencer outputs. This is accomplished through comparison of input sequences against a profile hidden Markov model (PHMM) using the Viterbi algorithm (for algorithm details see Durbin et al. 1998, ISBN: 9780521629713). Inserted base pairs are removed and deleted base pairs are accounted for through the introduction of a placeholder character. Since the PHMM is a probabilistic representation of the COI barcode, corrections are not always perfect. For this reason debar censors base pairs adjacent to reported indel sites, turning them into placeholder characters (default is 7 base pairs in either direction, this feature can be disabled). Testing has shown that this censorship results in the correct sequence length being restored, and erroneous base pairs being masked the vast majority of the time (>95%).

This package provides a layered grammar of graphics that compiles plots to a resolution-independent scene description and renders it through two back-ends: a self-contained SVG writer with embedded JavaScript for interactive figures (tooltips, hover highlighting, zoom, pan and legend toggling) and R's own graphics devices for publication-quality output at any resolution. Geographic layers are first class: a simplified world polygon dataset ships with the package and can be drawn with several map projections, including Robinson, Equal Earth and an orthographic globe. The layered grammar follows Wickham (2010) <doi:10.1198/jcgs.2009.07098>; projections follow Snyder (1987) <doi:10.3133/pp1395> and, for Equal Earth, Savric, Patterson and Jenny (2019) <doi:10.1080/13658816.2018.1504949>; line simplification uses Douglas and Peucker (1973) <doi:10.3138/FM57-6770-U75U-7727>; the default colour scales follow the guidance on perceptually uniform palettes of Crameri, Shephard and Heron (2020) <doi:10.1038/s41467-020-19160-7>.

This package provides a tool for inferring kinase activity changes from phosphoproteomics data. pKSEA uses kinase-substrate prediction scores to weight observed changes in phosphopeptide abundance to calculate a phosphopeptide-level contribution score, then sums up these contribution scores by kinase to obtain a phosphoproteome-level kinase activity change score (KAC score). pKSEA then assesses the significance of changes in predicted substrate abundances for each kinase using permutation testing. This results in a permutation score (pKSEA significance score) reflecting the likelihood of a similarly high or low KAC from random chance, which can then be interpreted in an analogous manner to an empirically calculated p-value. pKSEA contains default databases of kinase-substrate predictions from NetworKIN (NetworKINPred_db) <http://networkin.info> Horn, et. al (2014) <doi:10.1038/nmeth.2968> and of known kinase-substrate links from PhosphoSitePlus (KSEAdb) <https://www.phosphosite.org/> Hornbeck PV, et. al (2015) <doi:10.1093/nar/gku1267>.

This package provides functions for analyzing citizens bicycle usage pattern and predicting rental amount on specific conditions. Functions on this package interacts with data on tashudata package, a drat repository. tashudata package contains rental/return history on public bicycle system('Tashu'), weather for 3 years and bicycle station information. To install this data package, see the instructions at <https://github.com/zeee1/Tashu_Rpackage>. top10_stations(), top10_paths() function visualizes image showing the most used top 10 stations and paths. daily_bike_rental() and monthly_bike_rental() shows daily, monthly amount of bicycle rental. create_train_dataset(), create_test_dataset() is data processing function for prediction. Bicycle rental history from 2013 to 2014 is used to create training dataset and that on 2015 is for test dataset. Users can make random-forest prediction model by using create_train_model() and predict amount of bicycle rental in 2015 by using predict_bike_rental().

Corrects gas-chromatography peak areas for the influence of ambient air pressure on standard detectors open to the ambient atmosphere, such as the flame ionization detector, whose pressure sensitivity was characterised by Bocek, Novak and Janak (1969) <doi:10.1016/S0021-9673(00)99223-9>. Unlike the pressure compensation of Ayers and Clardy (1985) <https://patents.google.com/patent/US4512181A>, which is combined with a calibration and valid only for a single calibration period of a few days, per-cylinder peak areas are decomposed by principal components into a pressure-correlated component and per-peak drift; a common pressure-sensitivity coefficient (kappa) is estimated with a heavy-tail-robust fit on a drift-reduced signal, and slow drift plus a daily factor are removed. Returns the corrected areas together with a chi-square goodness-of-fit diagnostic. Structural-break detection (package strucchange', Zeileis and others (2002) <doi:10.18637/jss.v007.i02>) is provided for episode-level and variance breakpoint analysis.

Collection of tools to work with European basketball data. Functions available are related to friendly web scraping, data management and visualization. Data were obtained from <https://www.euroleaguebasketball.net/euroleague/>, <https://www.euroleaguebasketball.net/eurocup/> and <https://acb.com/>, following the instructions of their respectives robots.txt files, when available. Box score data are available for the three leagues. Play-by-play and spatial shooting data are also available for the Spanish league. Methods for analysis include a population pyramid, 2D plots, circular plots of players percentiles, plots of players monthly/yearly stats, team heatmaps, team shooting plots, team four factors plots, cross-tables with the results of regular season games, maps of nationalities, combinations of lineups, possessions-related variables, timeouts, performance by periods, personal fouls, offensive rebounds and different types of shooting charts. Please see Vinue (2020) <doi:10.1089/big.2018.0124>, Vinue (2024) <doi:10.1089/big.2023.0177> and Vinue (2026) <doi:10.1007/s11042-026-21930-2>.

Automates feature engineering using evolutionary algorithms inspired by genetic programming. Starting from raw input features, the package evolves candidate transformation recipes through selection, crossover, and mutation, evaluating fitness via cross-validation or train/validation splits with gradient-boosted tree models ('LightGBM or XGBoost'). Built-in transformers include arithmetic, logarithmic, and power operations, interaction terms, target encoding, quantile and log-based binning, principal component analysis, truncated singular value decomposition, Uniform Manifold Approximation and Projection (UMAP) dimensionality reduction, and minimum spanning tree (MST) graph-based clustering. The evolutionary search yields an optimised feature recipe that can be applied to new data for prediction. Methods are described in McInnes et al. (2018) <doi:10.21105/joss.00861>, Ke et al. (2017) <doi:10.48550/arXiv.1711.08789>, Chen and Guestrin (2016) <doi:10.1145/2939672.2939785>, Gagolewski (2021) <doi:10.1016/j.softx.2021.100722>, Gagolewski (2026) <doi:10.32614/CRAN.package.lumbermark>, and Gagolewski (2026) <doi:10.32614/CRAN.package.deadwood>.

The Sequence Read Archive (SRA) is the largest public repository of sequencing data from the next generation of sequencing platforms including Roche 454 GS System, Illumina Genome Analyzer, Applied Biosystems SOLiD System, Helicos Heliscope, and others. However, finding data of interest can be challenging using current tools. SRAdb is an attempt to make access to the metadata associated with submission, study, sample, experiment and run much more feasible. This is accomplished by parsing all the NCBI SRA metadata into a SQLite database that can be stored and queried locally. Fulltext search in the package make querying metadata very flexible and powerful. fastq and sra files can be downloaded for doing alignment locally. Beside ftp protocol, the SRAdb has funcitons supporting fastp protocol (ascp from Aspera Connect) for faster downloading large data files over long distance. The SQLite database is updated regularly as new data is added to SRA and can be downloaded at will for the most up-to-date metadata.

This package provides a toolkit to predict antimicrobial peptides from protein sequences on a genome-wide scale. It incorporates two support vector machine models ("precursor" and "mature") trained on publicly available antimicrobial peptide data using calculated physico-chemical and compositional sequence properties described in Meher et al. (2017) <doi:10.1038/srep42362>. In order to support genome-wide analyses, these models are designed to accept any type of protein as input and calculation of compositional properties has been optimised for high-throughput use. For best results it is important to select the model that accurately represents your sequence type: for full length proteins, it is recommended to use the default "precursor" model. The alternative, "mature", model is best suited for mature peptide sequences that represent the final antimicrobial peptide sequence after post-translational processing. For details see Fingerhut et al. (2020) <doi:10.1093/bioinformatics/btaa653>. The ampir package is also available via a Shiny based GUI at <https://ampir.marine-omics.net/>.