The interface package to access data from the EpiGraphDB <https://epigraphdb.org> platform. It provides easy access to the EpiGraphDB platform with functions that query the corresponding REST endpoints on the API <https://api.epigraphdb.org> and return the response data in the tibble data frame format.

This contains functions that can be used to estimate a smoothed and a non-smoothed (empirical) time-dependent receiver operating characteristic curve and the corresponding area under the receiver operating characteristic curve for correlated right-censored time-to-event data. See Beyene and Chen (2024) <doi:10.1177/09622802231220496>.

Downloads all the datasets (you can exclude the daily ones or specify a list of those you are targeting specifically) from Kenneth French's Website at <https://mba.tuck.dartmouth.edu/pages/faculty/ken.french/data_library.html>, process them and convert them to list of xts (time series).

Classical hierarchical clustering algorithms, agglomerative and divisive clustering. Algorithms are implemented as a theoretical way, step by step. It includes some detailed functions that explain each step. Every function allows options to get different results using different techniques. The package explains non expert users how hierarchical clustering algorithms work.

Support functions, data sets, and vignettes for the psych package. Contains several of the biggest data sets for the psych package as well as four vignettes. A few helper functions for file manipulation are included as well. For more information, see the <https://personality-project.org/r/> web page.

The prevalence package provides Frequentist and Bayesian methods for prevalence assessment studies. IMPORTANT: the truePrev functions in the prevalence package call on JAGS (Just Another Gibbs Sampler), which therefore has to be available on the user's system. JAGS can be downloaded from <https://mcmc-jags.sourceforge.io/>.

This package creates ggplot2'-based visualizations of smooth effects from GAM (Generalized Additive Models) fitted with mgcv and spline effects from GLM (Generalized Linear Models). Supports interaction terms and provides hazard ratio plots with histograms for survival analysis. Wood (2017, ISBN:9781498728331) provides comprehensive methodology for generalized additive models.

This package provides functions for performing common tasks when working with slippy map tile service APIs e.g. Google maps, Open Street Map, Mapbox, Stamen, among others. Functionality includes converting from latitude and longitude to tile numbers, determining tile bounding boxes, and compositing tiles to a georeferenced raster image.

Simulation methods to study the effect of management policies on efforts to restore populations back to their original genetic composition. Allows for single-scenario simulation and for optimization of specific chosen scenarios. Further information can be found in Hernandez, Janzen and Lavretsky (2023) <doi:10.1111/1755-0998.13892>.

This package provides a mathematical optimization procedure in combination with statistical bootstrap for the estimation of the latent signals (sometimes called scores) informing the global consensus ranking (often named aggregation ranking). To solve mid/large-scale problems, users should install the gurobi optimiser (available from <https://www.gurobi.com/>).

Create dense vector representation of words and documents using quanteda'. Currently implements Word2vec (Mikolov et al., 2013) <doi:10.48550/arXiv.1310.4546> and Latent Semantic Analysis (Deerwester et al., 1990) <doi:10.1002/(SICI)1097-4571(199009)41:6%3C391::AID-ASI1%3E3.0.CO;2-9>.

This package provides a set of R functions for identifying and correcting HGNC human gene symbols. In addition, you can identify MGI mouse gene symbols, which have been converted to date format by Excel, withdrawn, or aliased. It also contains functions for reversibly converting between HGNC symbols and valid R names.

Radiance is a web application environment, which is sort of like a web framework, but more general, more flexible. It should let you write personal websites and generally deployable applications easily and in such a way that they can be used on practically any setup without having to undergo special adaptations.

The package aims to facilitate Russian typesetting (based on input using MicroSoft Code Page 1251). Russian hyphenation is selected, and various mathematical commands are set up in Russian style. Furthermore all Cyrillic letters catcodes are set to letter, so that commands with Cyrillic letters in their names may be defined.

Algorithm and tools for in silico pack-TYPE transposon discovery. Filters a given genome for properties unique to DNA transposons and provides tools for the investigation of returned matches. Sequences are input in DNAString format, and ranges are returned as a dataframe (in the format returned by as.dataframe(GRanges)).

This package provides a novel feature selection algorithm for binary classification using support vector machine recursive feature elimination SVM-RFE and t-statistic. In this feature selection process, the selected features are differentially significant between the two classes and also they are good classifier with higher degree of classification accuracy.

This package provides tools for the multiscale spatial analysis of multivariate data. Several methods are based on the use of a spatial weighting matrix and its eigenvector decomposition (Moran's Eigenvectors Maps, MEM). Several approaches are described in the review Dray et al (2012) <doi:10.1890/11-1183.1>.

This package provides a helpful R6 class and methods for interacting with the Posit Connect Server API along with some meaningful utility functions for regular tasks. API documentation varies by Posit Connect installation and version, but the latest documentation is also hosted publicly at <https://docs.posit.co/connect/api/>.

Genotyping of triploid individuals from luminescence data (marker probeset A and B). Works also for diploids. Two main functions: Run_Clustering() that regroups individuals with a same genotype based on proximity and Run_Genotyping() that assigns a genotype to each cluster. For Shiny interface use: launch_GenoShiny().

This package provides tools for specifying and evaluating standard and truncated probability distributions, with support for log-space computation and joint distribution specification. It enables Bayesian computation for cognition models and includes utilities for density calculation, sampling, and visualisation, facilitating prior distribution specification and model assessment in hierarchical Bayesian frameworks.

Convenience functions for multivariate MCMC using univariate samplers including: slice sampler with stepout and shrinkage (Neal (2003) <DOI:10.1214/aos/1056562461>), adaptive rejection sampler (Gilks and Wild (1992) <DOI:10.2307/2347565>), adaptive rejection Metropolis (Gilks et al (1995) <DOI:10.2307/2986138>), and univariate Metropolis with Gaussian proposal.

Uses the outputs of a logistic regression model, from caret <https://CRAN.R-project.org/package=caret>, to build an odds plot. This allows for the rapid visualisation of odds plot ratios and works best with the outputs of CARET's GLM model class, by returning the final trained model.

Implementation of the scregclust algorithm described in Larsson, Held, et al. (2024) <doi:10.1038/s41467-024-53954-3> which reconstructs regulatory programs of target genes in scRNA-seq data. Target genes are clustered into modules and each module is associated with a linear model describing the regulatory program.

The Gene Ontology (GO) Consortium <https://geneontology.org/> organizes genes into hierarchical categories based on biological process (BP), molecular function (MF) and cellular component (CC, i.e., subcellular localization). Tools such as GoMiner (see Zeeberg, B.R., Feng, W., Wang, G. et al. (2003) <doi:10.1186/gb-2003-4-4-r28>) can leverage GO to perform ontological analysis of microarray and proteomics studies, typically generating a list of significant functional categories. The significance is traditionally determined by randomizing the input gene list to computing the false discovery rate (FDR) of the enrichment p-value for each category. We explore here the novel alternative of randomizing the GO database rather than the gene list.