Streamlines exploratory data analysis by providing a turnkey approach to visualising n-dimensional data which graphically reveals correlative or associative relationships between 2 or more features. Represents all dataset features as distinct, vertically aligned bar or tile plots, with plot types auto-selected based on whether variables are categorical or numeric.

Interact with Google Cloud Storage <https://cloud.google.com/storage/> API in R. Part of the cloudyr <https://cloudyr.github.io/> project.

This package implements the generalized propensity score cumulative distribution function proposed by Greene (2017) <https://digitalcommons.library.tmc.edu/dissertations/AAI10681743/>. A single scalar balancing score is calculated for any generalized propensity score vector with three or more treatments. This balancing score is used for propensity score matching and stratification in outcome analyses when analyzing either ordinal or multinomial treatments.

Supports image files and graphic objects to be visualized in ggplot2 graphic system.

This package provides a group of sample points are evaluated against a user-defined expression, the sample points are lists of parameters with values that may be substituted into that expression. The genetic algorithm attempts to make the result of the expression as low as possible (usually this would be the sum of residuals squared).

Design of group sequential trials, including non-binding futility analysis at multiple time points (Gallo, Mao, and Shih, 2014, <doi:10.1080/10543406.2014.932285>).

This package provides functions for implementing the Generalized Bayesian Optimal Phase II (G-BOP2) design using various Particle Swarm Optimization (PSO) algorithms, including: - PSO-Default, based on Kennedy and Eberhart (1995) <doi:10.1109/ICNN.1995.488968>, "Particle Swarm Optimization"; - PSO-Quantum, based on Sun, Xu, and Feng (2004) <doi:10.1109/ICCIS.2004.1460396>, "A Global Search Strategy of Quantum-Behaved Particle Swarm Optimization"; - PSO-Dexp, based on Stehlà k et al. (2024) <doi:10.1016/j.asoc.2024.111913>, "A Double Exponential Particle Swarm Optimization with Non-Uniform Variates as Stochastic Tuning and Guaranteed Convergence to a Global Optimum with Sample Applications to Finding Optimal Exact Designs in Biostatistics"; - and PSO-GO.

This package provides a collection of sampling formulas for the unified neutral model of biogeography and biodiversity. Alongside the sampling formulas, it includes methods to perform maximum likelihood optimization of the sampling formulas, methods to generate data given the neutral model, and methods to estimate the expected species abundance distribution. Sampling formulas included in the GUILDS package are the Etienne Sampling Formula (Etienne 2005), the guild sampling formula, where guilds are assumed to differ in dispersal ability (Janzen et al. 2015), and the guilds sampling formula conditioned on guild size (Janzen et al. 2015).

Computes the probability density, survival function, the hazard rate functions and generates random samples from the GTDL distribution given by Mackenzie, G. (1996) <doi:10.2307/2348408>. The likelihood estimates, the randomized quantile (Louzada, F., et al. (2020) <doi:10.1109/ACCESS.2020.3040525>) residuals and the normally transformed randomized survival probability (Li,L., et al. (2021) <doi:10.1002/sim.8852>) residuals are obtained for the GTDL model.

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.

Perform gene set enrichment analyses using the Gene set Ordinal Association Test (GOAT) algorithm and visualize your results. Koopmans, F. (2024) <doi:10.1038/s42003-024-06454-5>.

Server implementation of GraphQL <http://graphql.github.io/graphql-spec/>, a query language originally created by Facebook for describing data requirements on complex application data models. Visit <http://graphql.org> to learn more about GraphQL'.

The risk plot may be one of the most commonly used figures in tumor genetic data analysis. We can conclude the following two points: Comparing the prediction results of the model with the real survival situation to see whether the survival rate of the high-risk group is lower than that of the low-level group, and whether the survival time of the high-risk group is shorter than that of the low-risk group. The other is to compare the heat map and scatter plot to see the correlation between the predictors and the outcome.

Group Bayesian Networks: This package implements the inference of group Bayesian networks based on hierarchical feature clustering, and the adaptive refinement of the grouping regarding an outcome of interest, as described in Becker et. al (2021) <doi: 10.1371/journal.pcbi.1008735>.

This package provides classes and methods for handling networks or graphs whose nodes are geographical (i.e. locations in the globe). The functionality includes the creation of objects of class geonetwork as a graph with node coordinates, the computation of network measures, the support of spatial operations (projection to different Coordinate Reference Systems, handling of bounding boxes, etc.) and the plotting of the geonetwork object combined with supplementary cartography for spatial representation.

Facilitates efficient visualization of Relative Synonymous Codon Usage patterns across species. Based on analytical outputs from codonW', MEGA', and Phylosuite', it supports multi-species RSCU comparisons and allows users to explore visual analysis of structurally similar datasets.

This package provides a coherent interface and implementation for creating grouped date classes.

Toolset to create perpendicular profile graphs and swath profiles. Method are based on coordinate rotation algorithm by Schaeben et al. (2024) <doi:10.1002/mma.9823>.

Generalized Mann-Whitney type tests based on probabilistic indices and new diagnostic plots, for the underlying manuscript see Fischer, Oja (2015) <doi:10.18637/jss.v065.i09>.

Trace plots and convergence diagnostics for Markov Chain Monte Carlo (MCMC) algorithms on highly multivariate or unordered spaces. Methods outlined in a forthcoming paper.

Gene-Ranking Analysis of Pathway Expression (GRAPE) is a tool for summarizing the consensus behavior of biological pathways in the form of a template, and for quantifying the extent to which individual samples deviate from the template. GRAPE templates are based only on the relative rankings of the genes within the pathway and can be used for classification of tissue types or disease subtypes. GRAPE can be used to represent gene-expression samples as vectors of pathway scores, where each pathway score indicates the departure from a given collection of reference samples. The resulting pathway- space representation can be used as the feature set for various applications, including survival analysis and drug-response prediction. Users of GRAPE should use the following citation: Klein MI, Stern DF, and Zhao H. GRAPE: A pathway template method to characterize tissue-specific functionality from gene expression profiles. BMC Bioinformatics, 18:317 (June 2017).

Utility functions to read, manipulate, analyse and write transit feeds in the General Transit Feed Specification (GTFS) data format.

Sankey and alluvial diagrams visualise flows of quantities across stages in stacked bars. This package makes it easy to create such diagrams using ggplot2'.

This package provides an expectation-maximization (EM) algorithm using the approach introduced in Warasi (2023) <doi:10.1080/03610918.2021.2009867>. The EM algorithm can be used to estimate the prevalence (overall proportion) of a disease and to estimate a binary regression model from among the class of generalized linear models based on group testing data. The estimation framework we consider offers a flexible and general approach; i.e., its application is not limited to any specific group testing protocol. Consequently, the EM algorithm can model data arising from simple pooling as well as advanced pooling such as hierarchical testing, array testing, and quality control pooling. Also, provided are functions that can be used to conduct the Wald tests described in Buse (1982) <doi:10.1080/00031305.1982.10482817> and to simulate the group testing data described in Kim et al. (2007) <doi:10.1111/j.1541-0420.2007.00817.x>. We offer a function to compute relative efficiency measures, which can be used to optimize the maximum likelihood estimator of disease prevalence.