The fxl Charting package is used to prepare and design single case design figures that are typically prepared in spreadsheet software. With fxl', there is no need to leave the R environment to prepare these works and many of the more unique conventions in single case experimental designs can be performed without the need for physically constructing features of plots (e.g., drawing annotations across plots). Support is provided for various different plotting arrangements (e.g., multiple baseline), annotations (e.g., brackets, arrows), and output formats (e.g., svg, rasters).

This package provides a collection of user-friendly functions for assessing and visualizing fragility of individual studies (Walsh et al., 2014 <doi:10.1016/j.jclinepi.2013.10.019>; Lin, 2021 <doi:10.1111/jep.13428>), conventional pairwise meta-analyses (Atal et al., 2019 <doi:10.1016/j.jclinepi.2019.03.012>), and network meta-analyses of multiple treatments with binary outcomes (Xing et al., 2020 <doi:10.1016/j.jclinepi.2020.07.003>). The included functions are designed to: 1) calculate the fragility index (i.e., the minimal event status modifications that can alter the significance or non-significance of the original result) and fragility quotient (i.e., fragility index divided by sample size) at a specific significance level; 2) give the cases of event status modifications for altering the result's significance or non-significance and visualize these cases; 3) visualize the trend of statistical significance as event status is modified; 4) efficiently derive fragility indexes and fragility quotients at multiple significance levels, and visualize the relationship between these fragility measures against the significance levels; and 5) calculate fragility indexes and fragility quotients of multiple datasets (e.g., a collection of clinical trials or meta-analyses) and produce plots of their overall distributions. The outputs from these functions may inform the robustness of clinical results in terms of statistical significance and aid the interpretation of fragility measures. The usage of this package is illustrated in Lin et al. (2023 <doi:10.1016/j.ajog.2022.08.053>) and detailed in Lin and Chu (2022 <doi:10.1371/journal.pone.0268754>).

It implements the Nelson-Siegel and the Nelson-Siegel-Svensson term structures.

The goal of forstringr is to enable complex string manipulation in R especially to those more familiar with LEFT(), RIGHT(), and MID() functions in Microsoft Excel. The package combines the power of stringr with other manipulation packages such as dplyr and tidyr'.

Robust estimation methods for the mean vector, scatter matrix, and covariance matrix (if it exists) from data (possibly containing NAs) under multivariate heavy-tailed distributions such as angular Gaussian (via Tyler's method), Cauchy, and Student's t distributions. Additionally, a factor model structure can be specified for the covariance matrix. The latest revision also includes the multivariate skewed t distribution. The package is based on the papers: Sun, Babu, and Palomar (2014); Sun, Babu, and Palomar (2015); Liu and Rubin (1995); Zhou, Liu, Kumar, and Palomar (2019); Pascal, Ollila, and Palomar (2021).

Access data from the Federal Register API <https://www.federalregister.gov/developers/api/v1>.

The proximate composition analysis is the quantification of main components that constitutes nutritional profile of any food and food products including fish, shellfish, fish feed and their ingredients. Understanding this composition is essential for evaluating their nutritional value and for making informed dietary choices. The primary components typically analyzed include; moisture/ water in foods, crude protein, crude fat/ lipid, total ash, fiber and carbohydrates AOAC(2005,ISBN:0-935584-77-3). In case of fish, shellfish and its products, the proximate composition consists of four primary constituents - water, protein, fat, and ash (mostly minerals). Fish exhibit significant variation in their chemical makeup based on age, sex, environment, and season, both within the same species and between individual fish. There is minimal fluctuation in the content of ash and protein. The lipid concentration varies remarkably and is inversely correlated with the water content. In case of fish, carbohydrates are present in minor quantity so that are quantified by subtracting total of other components from 100 to get percentage of carbohydrates.

Play or simulate games of "Four in a Row" in the R console. This package is designed for educational purposes, encouraging users to write their own functions to play the game automatically. It contains a collection of built-in functions that play the game at various skill levels, for users to test their own functions against.

Package for parametric relative survival analyses. It allows to model non-linear and non-proportional effects and both non proportional and non linear effects, using splines (B-spline and truncated power basis), Weighted Cumulative Index of Exposure effect, with correction model for the life table. Both non proportional and non linear effects are described in Remontet, L. et al. (2007) <doi:10.1002/sim.2656> and Mahboubi, A. et al. (2011) <doi:10.1002/sim.4208>.

This package provides an interface to the FORCIS database (Chaabane et al. (2024) <doi:10.5281/zenodo.7390791>) on global foraminifera distribution. This package allows to download and to handle FORCIS data. It is part of the FRB-CESAB working group FORCIS. <https://www.fondationbiodiversite.fr/en/the-frb-in-action/programs-and-projects/le-cesab/forcis/>.

This method is a new class of model selection strategies, for mixed model selection, which includes linear and generalized linear mixed models. The idea involves a procedure to isolate a subgroup of what are known as correct models (of which the optimal model is a member). This is accomplished by constructing a statistical fence, or barrier, to carefully eliminate incorrect models. Once the fence is constructed, the optimal model is selected from among those within the fence according to a criterion which can be made flexible. References: 1. Jiang J., Rao J.S., Gu Z., Nguyen T. (2008), Fence Methods for Mixed Model Selection. The Annals of Statistics, 36(4): 1669-1692. <DOI:10.1214/07-AOS517> <https://projecteuclid.org/euclid.aos/1216237296>. 2. Jiang J., Nguyen T., Rao J.S. (2009), A Simplified Adaptive Fence Procedure. Statistics and Probability Letters, 79, 625-629. <DOI:10.1016/j.spl.2008.10.014> <https://www.researchgate.net/publication/23991417_A_simplified_adaptive_fence_procedure> 3. Jiang J., Nguyen T., Rao J.S. (2010), Fence Method for Nonparametric Small Area Estimation. Survey Methodology, 36(1), 3-11. <http://publications.gc.ca/collections/collection_2010/statcan/12-001-X/12-001-x2010001-eng.pdf>. 4. Jiming Jiang, Thuan Nguyen and J. Sunil Rao (2011), Invisible fence methods and the identification of differentially expressed gene sets. Statistics and Its Interface, Volume 4, 403-415. <http://www.intlpress.com/site/pub/files/_fulltext/journals/sii/2011/0004/0003/SII-2011-0004-0003-a014.pdf>. 5. Thuan Nguyen & Jiming Jiang (2012), Restricted fence method for covariate selection in longitudinal data analysis. Biostatistics, 13(2), 303-314. <DOI:10.1093/biostatistics/kxr046> <https://academic.oup.com/biostatistics/article/13/2/303/263903/Restricted-fence-method-for-covariate-selection-in>. 6. Thuan Nguyen, Jie Peng, Jiming Jiang (2014), Fence Methods for Backcross Experiments. Statistical Computation and Simulation, 84(3), 644-662. <DOI:10.1080/00949655.2012.721885> <https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3891925/>. 7. Jiang, J. (2014), The fence methods, in Advances in Statistics, Hindawi Publishing Corp., Cairo. <DOI:10.1155/2014/830821>. 8. Jiming Jiang and Thuan Nguyen (2015), The Fence Methods, World Scientific, Singapore. <https://www.abebooks.com/9789814596060/Fence-Methods-Jiming-Jiang-981459606X/plp>.

Estimates heterogeneous effects in factorial (and conjoint) models. The methodology employs a Bayesian finite mixture of regularized logistic regressions, where moderators can affect each observation's probability of group membership and a sparsity-inducing prior fuses together levels of each factor while respecting ANOVA-style sum-to-zero constraints. Goplerud, Imai, and Pashley (2024) <doi:10.48550/ARXIV.2201.01357> provide further details.

The fusion learning method uses a model selection algorithm to learn from multiple data sets across different experimental platforms through group penalization. The responses of interest may include a mix of discrete and continuous variables. The responses may share the same set of predictors, however, the models and parameters differ across different platforms. Integrating information from different data sets can enhance the power of model selection. Package is based on Xin Gao, Raymond J. Carroll (2017) <arXiv:1610.00667v1>.

Brings a set of tools to help and automatically realise the description of principal component analyses (from FactoMineR functions). Detection of existing outliers, identification of the informative components, graphical views and dimensions description are performed threw dedicated functions. The Investigate() function performs all these functions in one, and returns the result as a report document (Word, PDF or HTML).

Extracts features from biological sequences. It contains most features which are presented in related work and also includes features which have never been introduced before. It extracts numerous features from nucleotide and peptide sequences. Each feature converts the input sequences to discrete numbers in order to use them as predictors in machine learning models. There are many features and information which are hidden inside a sequence. Utilizing the package, users can convert biological sequences to discrete models based on chosen properties. References: iLearn Z. Chen et al. (2019) <DOI:10.1093/bib/bbz041>. iFeature Z. Chen et al. (2018) <DOI:10.1093/bioinformatics/bty140>. <https://CRAN.R-project.org/package=rDNAse>. PseKRAAC Y. Zuo et al. PseKRAAC: a flexible web server for generating pseudo K-tuple reduced amino acids composition (2017) <DOI:10.1093/bioinformatics/btw564>. iDNA6mA-PseKNC P. Feng et al. iDNA6mA-PseKNC: Identifying DNA N6-methyladenosine sites by incorporating nucleotide physicochemical properties into PseKNC (2019) <DOI:10.1016/j.ygeno.2018.01.005>. I. Dubchak et al. Prediction of protein folding class using global description of amino acid sequence (1995) <DOI:10.1073/pnas.92.19.8700>. W. Chen et al. Identification and analysis of the N6-methyladenosine in the Saccharomyces cerevisiae transcriptome (2015) <DOI:10.1038/srep13859>.

Books are "Linear Models with R" published 1st Ed. August 2004, 2nd Ed. July 2014, 3rd Ed. February 2025 by CRC press, ISBN 9781439887332, and "Extending the Linear Model with R" published by CRC press in 1st Ed. December 2005 and 2nd Ed. March 2016, ISBN 9781584884248 and "Practical Regression and ANOVA in R" contributed documentation on CRAN (now very dated).

This package provides tools for fluctuations analysis of mutant cells counts. Main reference is A. Mazoyer, R. Drouilhet, S. Despreaux and B. Ycart (2017) <doi:10.32614/RJ-2017-029>.

Allows generating heatmap-like visualisations for data frames. Funky heatmaps can be fine-tuned by providing annotations of the columns and rows, which allows assigning multiple palettes or geometries or grouping rows and columns together in categories. Saelens et al. (2019) <doi:10.1038/s41587-019-0071-9>.

This package provides an efficient C++ code for computing an optimal segmentation model with Poisson loss, up-down constraints, and label constraints, as described by Kaufman et al. (2024) <doi:10.1080/10618600.2023.2293216>.

This package provides the function fancycut() which is like cut() except you can mix left open and right open intervals with point values, intervals that are closed on both ends and intervals that are open on both ends.

This package creates participant flow diagrams directly from a dataframe. Representing the flow of participants through each stage of a study, especially in clinical trials, is essential to assess the generalisability and validity of the results. This package provides a set of functions that can be combined with a pipe operator to create all kinds of flowcharts from a data frame in an easy way.

Random simulations of fuzzy numbers are still a challenging problem. The aim of this package is to provide the respective procedures to simulate fuzzy random variables, especially in the case of the piecewise linear fuzzy numbers (PLFNs, see Coroianua et al. (2013) <doi:10.1016/j.fss.2013.02.005> for the further details). Additionally, the special resampling algorithms known as the epistemic bootstrap are provided (see Grzegorzewski and Romaniuk (2022) <doi:10.34768/amcs-2022-0021>, Grzegorzewski and Romaniuk (2022) <doi:10.1007/978-3-031-08974-9_39>, Romaniuk et al. (2024) <doi:10.32614/RJ-2024-016>) together with the functions to apply statistical tests and estimate various characteristics based on the epistemic bootstrap. The package also includes real-life datasets of epistemic fuzzy triangular and trapezoidal numbers. The fuzzy numbers used in this package are consistent with the FuzzyNumbers package.

Scans all directories and subdirectories of a path for code snippets, R scripts, R Markdown, PDF or text files containing a specific pattern. Files found can be copied to a new folder.

Read and write PNG images with arrays, rasters, native rasters, numeric arrays, integer arrays, raw vectors and indexed values. This PNG encoder exposes configurable internal options enabling the user to select a speed-size tradeoff. For example, disabling compression can speed up writing PNG by a factor of 50. Multiple image formats are supported including raster, native rasters, and integer and numeric arrays at color depths of 1, 2, 3 or 4. 16-bit images are also supported. This implementation uses the libspng C library which is available from <https://github.com/randy408/libspng/>.