The plotcli package provides terminal-based plotting in R. It supports colored scatter plots, line plots, bar plots, boxplots, histograms, density plots, and more. The ggplotcli() function is a universal converter that renders any ggplot2 plot in the terminal using Unicode Braille characters or ASCII. Features include support for 15+ geom types, faceting (facet_wrap/facet_grid), automatic theme detection, legends, optimized color mapping, and multiple canvas types.

Portable /proc/self/maps as a data frame. Determine which library or other region is mapped to a specific address of a process. -- R packages can contain native code, compiled to shared libraries at build or installation time. When loaded, each shared library occupies a portion of the address space of the main process. When only a machine instruction pointer is available (e.g. from a backtrace during error inspection or profiling), the address space map determines which library this instruction pointer corresponds to.

Calculate and optimize dynamic performance ratings of association football teams competing in matches, in accordance with the method used in the research paper "Determining the level of ability of football teams by dynamic ratings based on the relative discrepancies in scores between adversaries", by Constantinou and Fenton (2013) <doi:10.1515/jqas-2012-0036> This dynamic rating system has proven to provide superior results for predicting association football outcomes.

Provide summary table of daily physical activity and per-person/grouped heat map for accelerometer data from SenseWear Armband. See <https://templehealthcare.wordpress.com/the-sensewear-armband/> for more information about SenseWear Armband.

Eco-phylogenetic and community phylogenetic analyses. Keeps community ecological and phylogenetic data matched up and comparable using comparative.comm objects. Wrappers for common community phylogenetic indices ('pez.shape', pez.evenness', pez.dispersion', and pez.dissimilarity metrics). Implementation of Cavender-Bares (2004) correlation of phylogenetic and ecological matrices ('fingerprint.regression'). Phylogenetic Generalised Linear Mixed Models (PGLMMs; pglmm') following Ives & Helmus (2011) and Rafferty & Ives (2013). Simulation of null assemblages, traits, and phylogenies ('scape', sim.meta.comm').

Extends ggplot2 to help replace points in a scatter plot with pie-chart glyphs showing the relative proportions of different categories. The pie glyphs are independent of the axes and plot dimensions, to prevent distortions when the plot dimensions are changed.

Estimating Non-Simplified Vine Copulas Using Penalized Splines.

Set of tools to automatize extraction of data on pests from EPPO Data Services and EPPO Global Database and to put them into tables with human readable format. Those function use EPPO database API', thus you first need to register on <https://data.eppo.int> (free of charge). Additional helpers allow to download, check and connect to SQLite EPPO database'.

This package implements a set of methodological tools that enable researchers to apply matching methods to time-series cross-sectional data. Imai, Kim, and Wang (2023) <http://web.mit.edu/insong/www/pdf/tscs.pdf> proposes a nonparametric generalization of the difference-in-differences estimator, which does not rely on the linearity assumption as often done in practice. Researchers first select a method of matching each treated observation for a given unit in a particular time period with control observations from other units in the same time period that have a similar treatment and covariate history. These methods include standard matching methods based on propensity score and Mahalanobis distance, as well as weighting methods. Once matching and refinement is done, treatment effects can be estimated with standard errors. The package also offers diagnostics for researchers to assess the quality of their results.

This package provides data set and function for exploration of Multiple Indicator Cluster Survey 2014 Household Listing questionnaire data for Punjab, Pakistan.

Calculates profile repeatability for replicate stress response curves, or similar time-series data. Profile repeatability is an individual repeatability metric that uses the variances at each timepoint, the maximum variance, the number of crossings (lines that cross over each other), and the number of replicates to compute the repeatability score. For more information see Reed et al. (2019) <doi:10.1016/j.ygcen.2018.09.015>.

This package provides tools for calculating statistical power for experiments analyzed using linear mixed models. It supports standard designs, including randomized block, split-plot, and Latin Square designs, while offering flexibility to accommodate a variety of other complex study designs.

This package provides a collection of functions to process digital images, depict greenness index trajectories and extract relevant phenological stages.

Permutation based non-parametric analysis of CRISPR screen data. Details about this algorithm are published in the following paper published on BMC genomics, Jia et al. (2017) <doi:10.1186/s12864-017-3938-5>: A permutation-based non-parametric analysis of CRISPR screen data. Please cite this paper if you use this algorithm for your paper.

The Piece-wise exponential (Additive Mixed) Model (PAMM; Bender and others (2018) <doi: 10.1177/1471082X17748083>) is a powerful model class for the analysis of survival (or time-to-event) data, based on Generalized Additive (Mixed) Models (GA(M)Ms). It offers intuitive specification and robust estimation of complex survival models with stratified baseline hazards, random effects, time-varying effects, time-dependent covariates and cumulative effects (Bender and others (2019)), as well as support for left-truncated data as well as competing risks, recurrent events and multi-state settings. pammtools provides tidy workflow for survival analysis with PAMMs, including data simulation, transformation and other functions for data preprocessing and model post-processing as well as visualization.

Toolkit for fitting point process models with sequences of LASSO penalties ("regularisation paths"), as described in Renner, I.W. and Warton, D.I. (2013) <doi:10.1111/j.1541-0420.2012.01824.x>. Regularisation paths of Poisson point process models or area-interaction models can be fitted with LASSO, adaptive LASSO or elastic net penalties. A number of criteria are available to judge the bias-variance tradeoff.

Calibrate p-values under a robust perspective using the methods developed by Sellke, Bayarri, and Berger (2001) <doi:10.1198/000313001300339950> and obtain measures of the evidence provided by the data in favor of point null hypotheses which are safer and more straightforward to interpret.

This package creates an interactive scatterplot matrix using the D3 JavaScript library. See <https://d3js.org/> for more information on D3.

This package provides a set of Analysis Data Model (ADaM) datasets constructed by modifying the ADaM datasets in the pharmaverseadam package to meet J&J Innovative Medicine's standard data structure for Clinical and Statistical Programming.

Supports analysis of aerobiological data. Available features include determination of pollen season limits, replacement of outliers (Kasprzyk and Walanus (2014) <doi:10.1007/s10453-014-9332-8>), calculation of growing degree days (Baskerville and Emin (1969) <doi:10.2307/1933912>), and determination of the base temperature for growing degree days (Yang et al. (1995) <doi:10.1016/0168-1923(94)02185-M).

Stochastic block model used for dynamic graphs represented by Poisson processes. To model recurrent interaction events in continuous time, an extension of the stochastic block model is proposed where every individual belongs to a latent group and interactions between two individuals follow a conditional inhomogeneous Poisson process with intensity driven by the individualsâ latent groups. The model is shown to be identifiable and its estimation is based on a semiparametric variational expectation-maximization algorithm. Two versions of the method are developed, using either a nonparametric histogram approach (with an adaptive choice of the partition size) or kernel intensity estimators. The number of latent groups can be selected by an integrated classification likelihood criterion. Y. Baraud and L. Birgé (2009). <doi:10.1007/s00440-007-0126-6>. C. Biernacki, G. Celeux and G. Govaert (2000). <doi:10.1109/34.865189>. M. Corneli, P. Latouche and F. Rossi (2016). <doi:10.1016/j.neucom.2016.02.031>. J.-J. Daudin, F. Picard and S. Robin (2008). <doi:10.1007/s11222-007-9046-7>. A. P. Dempster, N. M. Laird and D. B. Rubin (1977). <http://www.jstor.org/stable/2984875>. G. Grégoire (1993). <http://www.jstor.org/stable/4616289>. L. Hubert and P. Arabie (1985). <doi:10.1007/BF01908075>. M. Jordan, Z. Ghahramani, T. Jaakkola and L. Saul (1999). <doi:10.1023/A:1007665907178>. C. Matias, T. Rebafka and F. Villers (2018). <doi:10.1093/biomet/asy016>. C. Matias and S. Robin (2014). <doi:10.1051/proc/201447004>. H. Ramlau-Hansen (1983). <doi:10.1214/aos/1176346152>. P. Reynaud-Bouret (2006). <doi:10.3150/bj/1155735930>.

This package implements an n-dimensional parameter space partitioning algorithm for evaluating the global behaviour of formal computational models as described by Pitt, Kim, Navarro and Myung (2006) <doi:10.1037/0033-295X.113.1.57>.

This package provides functions are available to calibrate designs over a range of posterior and predictive thresholds, to plot the various design options, and to obtain the operating characteristics of optimal accuracy and optimal efficiency designs.

Conduct a noncompartmental analysis as closely as possible to the most widely used commercial software. Some features are 1) CDISC SDTM terms 2) Automatic slope selection with the same criterion of WinNonlin(R) 3) Supporting both linear-up linear-down and linear-up log-down method 4) Interval(partial) AUCs with linear or log interpolation method * Reference: Gabrielsson J, Weiner D. Pharmacokinetic and Pharmacodynamic Data Analysis - Concepts and Applications. 5th ed. 2016. (ISBN:9198299107).