Extension to the spatstat package, enabling the user to fit point process models to point pattern data by local composite likelihood ('geographically weighted regression').

This package performs the permutation test using difference in the restricted mean survival time (RMST) between groups as a summary measure of the survival time distribution. When the sample size is less than 50 per group, it has been shown that there is non-negligible inflation of the type I error rate in the commonly used asymptotic test for the RMST comparison. Generally, permutation tests can be useful in such a situation. However, when we apply the permutation test for the RMST comparison, particularly in small sample situations, there are some cases where the survival function in either group cannot be defined due to censoring in the permutation process. Horiguchi and Uno (2020) <doi:10.1002/sim.8565> have examined six workable solutions to handle this numerical issue. It performs permutation tests with implementation of the six methods outlined in the paper when the numerical issue arises during the permutation process. The result of the asymptotic test is also provided for a reference.

Proposes a torch implementation of Graph Net architecture allowing different options for message passing and feature embedding.

This package provides computational tools for estimating inverse regions and constructing the corresponding simultaneous outer and inner confidence regions. Acceptable input includes both one-dimensional and two-dimensional data for linear, logistic, functional, and spatial generalized least squares regression models. Functions are also available for constructing simultaneous confidence bands (SCBs) for these models. The definition of simultaneous confidence regions (SCRs) follows Sommerfeld et al. (2018) <doi:10.1080/01621459.2017.1341838>. Methods for estimating inverse regions, SCRs, and the nonparametric bootstrap are based on Ren et al. (2024) <doi:10.1093/jrsssc/qlae027>. Methods for constructing SCBs are described in Crainiceanu et al. (2024) <doi:10.1201/9781003278726> and Telschow et al. (2022) <doi:10.1016/j.jspi.2021.05.008>.

Calculates performance criteria measures and associated Monte Carlo standard errors for simulation results. Includes functions to help run simulation studies, following a general simulation workflow that closely aligns with the approach described by Morris, White, and Crowther (2019) <DOI:10.1002/sim.8086>. Also includes functions for calculating bootstrap confidence intervals (including normal, basic, studentized, percentile, bias-corrected, and bias-corrected-and-accelerated) with tidy output, as well as for extrapolating confidence interval coverage rates and hypothesis test rejection rates following techniques suggested by Boos and Zhang (2000) <DOI:10.1080/01621459.2000.10474226>.

This package provides a tool for bootstrapping new packages with useful defaults, including a test suite outline that passes checks and helpers for running tests, checking test coverage, building vignettes, and more. Package skeletons it creates are set up for pushing your package to GitHub and using other hosted services for building and test automation.

Add significance marks to any R Boxplot, including a given significance niveau.

Regularized version of partial least square approaches providing sparse, group, and sparse group versions of partial least square regression models (Liquet, B., Lafaye de Micheaux, P., Hejblum B., Thiebaut, R. (2016) <doi:10.1093/bioinformatics/btv535>). Version of PLS Discriminant analysis is also provided.

Building predictive models with stacking which is a type of ensemble learning. Learners can be specified from those implemented in caret'. For more information of the package, see Nukui and Onogi (2023) <doi:10.1101/2023.06.06.543970>.

Quickly and flexibly calculates weights for survey data, in order to correct for survey non-response or other sampling issues. Uses rake weighting, a common technique also know as rim weighting or iterative proportional fitting. This technique allows for weighting on multiple variables, even when the interlocked distribution of the two variables is not known. Interacts with Thomas Lumley's survey package, as described in Lumley, Thomas (2011, ISBN:978-1-118-21093-2). Adds additional functionality, more adaptable syntax, and error-checking to the base weighting functionality in survey.'.

This package provides a programmatic interface to <http://sp2000.org.cn>, re-written based on an accompanying Species 2000 API. Access tables describing catalogue of the Chinese known species of animals, plants, fungi, micro-organisms, and more. This package also supports access to catalogue of life global <http://catalogueoflife.org>, China animal scientific database <http://zoology.especies.cn> and catalogue of life Taiwan <https://taibnet.sinica.edu.tw/home_eng.php>. The development of SP2000 package were supported by Biodiversity Survey and Assessment Project of the Ministry of Ecology and Environment, China <2019HJ2096001006>,Yunnan University's "Double First Class" Project <C176240405> and Yunnan University's Research Innovation Fund for Graduate Students <2019227>.

Model Selection Based on Combined Penalties. This package implements a stepwise forward variable selection algorithm based on a penalized likelihood criterion that combines the L0 with L2 or L1 norms.

Latent repeated measures ANOVA (L-RM-ANOVA) is a structural equation modeling based alternative to traditional repeated measures ANOVA. L-RM-ANOVA extends the latent growth components approach by Mayer et al. (2012) <doi:10.1080/10705511.2012.713242> and introduces latent variables to repeated measures analysis.

This package implements the S-type estimators, novel robust estimators for general linear regression models, addressing challenges such as outlier contamination and leverage points. This package introduces robust regression techniques to provide a robust alternative to classical methods and includes diagnostic tools for assessing model fit and performance. The methodology is based on the study, "Comparison of the Robust Methods in the General Linear Regression Model" by Sazak and Mutlu (2023). This package is designed for statisticians and applied researchers seeking advanced tools for robust regression analysis.

Interact with the Smartsheet platform through the Smartsheet API 2.0. <https://smartsheet.redoc.ly/>. API is an acronym for application programming interface; the Smartsheet API allows users to interact with Smartsheet sheets directly within R.

This package provides the hyphenation algorithm used for TeX'/'LaTeX and similar software, as proposed by Liang (1983, <https://tug.org/docs/liang/>). Mainly contains the function hyphen() to be used for hyphenation/syllable counting of text objects. It was originally developed for and part of the koRpus package, but later released as a separate package so it's lighter to have this particular functionality available for other packages. Support for various languages needs be added on-the-fly or by plugin packages (<https://undocumeantit.github.io/repos/>); this package does not include any language specific data. Due to some restrictions on CRAN, the full package sources are only available from the project homepage. To ask for help, report bugs, request features, or discuss the development of the package, please subscribe to the koRpus-dev mailing list (<http://korpusml.reaktanz.de>).

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>.

Spatial components offer tools for dimension reduction and spatially variable gene detection for high dimensional spatial transcriptomics data. Construction of a projection onto low-dimensional feature space of spatially dependent metagenes offers pre-processing to clustering, testing for spatial variability and denoising of spatial expression patterns. For more details, see Koehler et al. (2026) <doi:10.1093/bioinformatics/btag052>.

Identify 17 Sustainable Development Goals and associated 169 targets in text.

Because your linear models deserve better than console output. A sleek color palette and kable styling to make your regression results look sharper than they are. Includes support for Partial Least Squares (PLS) regression via both the SVD and NIPALS algorithms, along with a unified interface for model fitting and fabulous LaTeX and console output formatting. See the package website at <https://finitesample.space/snazzier>.

This package performs inference for C of risk prediction models with censored survival data, using the method proposed by Uno et al. (2011) <doi:10.1002/sim.4154>. Inference for the difference in C between two competing prediction models is also implemented.

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.

The methods discussed in this package are new non-parametric methods based on sequential normal scores SNS (Conover et al (2017) <doi:10.1080/07474946.2017.1360091>), designed for sequences of observations, usually time series data, which may occur singly or in batches, and may be univariate or multivariate. These methods are designed to detect changes in the process, which may occur as changes in location (mean or median), changes in scale (standard deviation, or variance), or other changes of interest in the distribution of the observations, over the time observed. They usually apply to large data sets, so computations need to be simple enough to be done in a reasonable time on a computer, and easily updated as each new observation (or batch of observations) becomes available. Some examples and more detail in SNS is presented in the work by Conover et al (2019) <arXiv:1901.04443>.

Understand human performance from the perspective of sampling, both looking at how people generate samples and how people use the samples they have generated. A longer overview and other resources can be found at <https://sampling.warwick.ac.uk>.