Construction, calculation and display of fault trees. Methods derived from Clifton A. Ericson II (2005, ISBN: 9780471739425) <DOI:10.1002/0471739421>, Antoine Rauzy (1993) <DOI:10.1016/0951-8320(93)90060-C>, Tim Bedford and Roger Cooke (2012, ISBN: 9780511813597) <DOI:10.1017/CBO9780511813597>, Nikolaos Limnios, (2007, ISBN: 9780470612484) <DOI: 10.1002/9780470612484>.

Genome-wide association study (GWAS) performed with SLOPE, short for Sorted L-One Penalized Estimation, a method for estimating the vector of coefficients in linear model. In the first step of GWAS, SNPs are clumped according to their correlations and distances. Then, SLOPE is performed on data where each clump has one representative.

Additional annotations, stats, geoms and scales for plotting "light" spectra with ggplot2', together with specializations of ggplot() and autoplot() methods for spectral data and waveband definitions stored in objects of classes defined in package photobiology'. Part of the r4photobiology suite, Aphalo P. J. (2015) <doi:10.19232/uv4pb.2015.1.14>.

The getDTeval() function facilitates the translation of the original coding statement to an optimized form for improved runtime efficiency without compromising on the programmatic coding design. The function can either provide a translation of the coding statement, directly evaluate the translation to return a coding result, or provide both of these outputs.

This package provides tools for analyzing Marshall-Olkin shock models semi-independent time. It includes interactive shiny applications for exploring copula-based dependence structures, along with functions for modeling and visualization. The methods are based on Mijanovic and Popovic (2024, submitted) "An R package for Marshall-Olkin shock models with semi-independent times.".

Two novel matching-based methods for estimating group average treatment effects (GATEs). The match_y1y0() and match_y1y0_bc() functions are used for imputing the potential outcomes based on matching and bias-corrected matching techniques, respectively. The EstGATE() function is employed to estimate the GATE after imputing the potential outcomes.

It implements the online Bayesian methods for change point analysis. It can also perform missing data imputation with methods from VIM'. The reference is Yigiter A, Chen J, An L, Danacioglu N (2015) <doi:10.1080/02664763.2014.1001330>. The link to the package is <https://CRAN.R-project.org/package=onlineBcp>.

Run simulations or other functions while easily varying parameters from one iteration to the next. Some common use cases would be grid search for machine learning algorithms, running sets of simulations (e.g., estimating statistical power for complex models), or bootstrapping under various conditions. See the paramtest documentation for more information and examples.

Nomograms are constructed to predict the cumulative incidence rate which is calculated after adjusting for competing causes to the event of interest. K-fold cross-validation is implemented to validate predictive accuracy using a competing-risk version of the concordance index. Methods are as described in: Kattan MW, Heller G, Brennan MF (2003).

This package creates some tables of clinical study. Table 1 is created by table1() to describe baseline characteristics, which is essential in every clinical study. Created by table2(), the function of Table 2 is to explore influence factors. And Table 3 created by table3() is able to make stratified analysis.

This package implements sampling, iteration, and input of FASTQ files. It includes functions for filtering and trimming reads, and for generating a quality assessment report. Data are represented as DNAStringSet-derived objects, and easily manipulated for a diversity of purposes. The package also contains legacy support for early single-end, ungapped alignment formats.

This package provides a pure data-driven gene network, WGCN(weighted gene co-expression network) could be constructed only from expression profile. Different layers in such networks may represent different time points, multiple conditions or various species. AMOUNTAIN aims to search active modules in multi-layer WGCN using a continuous optimization approach.

This package provides miscellaneous small tools and utilities. Many of them facilitate the work with matrices, e.g. inserting rows or columns, creating symmetric matrices, or checking for semidefiniteness. Other tools facilitate the work with regression models, e.g. extracting the standard errors, obtaining the number of (estimated) parameters, or calculating R-squared values.

This package provides an R implementation of an extension of the BayeScan software for codominant markers, adding the option to group individual SNPs into pre-defined blocks. A typical application of this new approach is the identification of genomic regions, genes, or gene sets containing one or more SNPs that evolved under directional selection.

This package provides tools for downloading hourly averages, daily maximums and minimums from each of the pollution, wind, and temperature measuring stations or geographic zones in the Mexico City metro area. The package also includes the locations of each of the stations and zones. See <http://aire.cdmx.gob.mx/> for more information.

Small toolbox for data analyses in environmental chemistry and ecotoxicology. Provides, for example, calibration() to calculate calibration curves and corresponding limits of detection (LODs) and limits of quantification (LOQs) according to German DIN 32645 (2008). texture() makes it easy to estimate soil particle size distributions from hydrometer measurements (ASTM D422-63, 2007).

Create local, regional, and global explanations for any machine learning model with forward marginal effects. You provide a model and data, and fmeffects computes feature effects. The package is based on the theory in: C. A. Scholbeck, G. Casalicchio, C. Molnar, B. Bischl, and C. Heumann (2022) <doi:10.48550/arXiv.2201.08837>.

Geostatistical modelling facilities using SpatRaster and SpatVector objects are provided. Non-Gaussian models are fit using INLA', and Gaussian geostatistical models use Maximum Likelihood Estimation. For details see Brown (2015) <doi:10.18637/jss.v063.i12>. The RandomFields package is available at <https://www.wim.uni-mannheim.de/schlather/publications/software>.

This package provides a quick and easy way of plotting the columns of two matrices or data frames against each other using ggplot2'. Although ggmatplot doesn't provide the same flexibility as ggplot2', it can be used as a workaround for having to wrangle wide format data into long format for plotting with ggplot2'.

This package provides a greta (Golding (2019) <doi:10.21105/joss.01601>) module that lets you use mgcv smoother functions and formula syntax to define smooth terms for use in a greta model. You can then define your own likelihood to complete the model, and fit it by Markov Chain Monte Carlo (MCMC).

An extension of ggplot2 for creating complex genomic maps. It builds on the power of ggplot2 and tidyverse adding new ggplot2'-style geoms & positions and dplyr'-style verbs to manipulate the underlying data. It implements a layout concept inspired by ggraph and introduces tracks to bring tidiness to the mess that is genomics data.

This package implements bootstrap methods for linear regression models with errors following a time-varying process, focusing on approximating the distribution of the least-squares estimator for regression models with locally stationary errors. It enables the construction of bootstrap and classical confidence intervals for regression coefficients, leveraging intensive simulation studies and real data analysis.

Solves quadratic programming problems where the Hessian is represented as the product of two matrices. Thanks to Greg Hunt for helping getting this version back on CRAN. The methods in this package are described in: Ormerod, Wand and Koch (2008) "Penalised spline support vector classifiers: computational issues" <doi:10.1007/s00180-007-0102-8>.

Implementation of the MarkerPen algorithm, short for marker gene detection via penalized principal component analysis, described in the paper by Qiu, Wang, Lei, and Roeder (2020, <doi:10.1101/2020.11.07.373043>). MarkerPen is a semi-supervised algorithm for detecting marker genes by combining prior marker information with bulk transcriptome data.