This package provides half-normal plots, reference plots, and Pareto plots of effects from an unreplicated experiment, along with various pseudo-standard-error measures, simulated reference distributions, and other tools. Many of these methods are described in Daniel C. (1959) <doi:10.1080/00401706.1959.10489866> and/or Lenth R.V. (1989) <doi:10.1080/00401706.1989.10488595>, but some new approaches are added and integrated in one package.

This package provides tools for analyzing sequencing data containing unique molecular identifiers generated by UMIErrorCorrect (<https://github.com/stahlberggroup/umierrorcorrect>).

Calculates the Urban Centrality Index (UCI) as in Pereira et al., (2013) <doi:10.1111/gean.12002>. The UCI measures the extent to which the spatial organization of a city or region varies from extreme polycentric to extreme monocentric in a continuous scale from 0 to 1. Values closer to 0 indicate more polycentric patterns and values closer to 1 indicate a more monocentric urban form.

Does uniformly most powerful (UMP) and uniformly most powerful unbiased (UMPU) tests. At present only distribution implemented is binomial distribution. Also does fuzzy tests and confidence intervals (following Geyer and Meeden, 2005, <doi:10.1214/088342305000000340>) for the binomial distribution (one-tailed procedures based on UMP test and two-tailed procedures based on UMPU test).

This package provides a tool for checking how much information is disclosed when reporting summary statistics.

Construct and plot objective hierarchies and associated value and utility functions. Evaluate the values and utilities and visualize the results as colored objective hierarchies or tables. Visualize uncertainty by plotting median and quantile intervals within the nodes of objective hierarchies. Get numerical results of the evaluations in standard R data types for further processing.

This package provides a suite of utilities for working with the UK Biobank <https://www.ukbiobank.ac.uk/> Nuclear Magnetic Resonance spectroscopy (NMR) metabolomics data <https://biobank.ndph.ox.ac.uk/showcase/label.cgi?id=220>. Includes functions for extracting biomarkers from decoded UK Biobank field data, removing unwanted technical variation from biomarker concentrations, computing an extended set of lipid, fatty acid, and cholesterol fractions, and for re-deriving composite biomarkers and ratios after adjusting data for unwanted biological variation. For further details on methods see Ritchie SC et al. Sci Data (2023) <doi:10.1038/s41597-023-01949-y>.

This program realizes a universal estimation approach that accommodates multi-category variables and effect scales, making up for the deficiencies of the existing approaches when dealing with non-binary exposures and complex models. The estimation via bootstrapping can simultaneously provide results of causal mediation on risk difference (RD), odds ratio (OR) and risk ratio (RR) scales with tests of the effects difference. The estimation is also applicable to many other settings, e.g., moderated mediation, inconsistent covariates, panel data, etc. The high flexibility and compatibility make it possible to apply for any type of model, greatly meeting the needs of current empirical researches.

Fetch United States Congressional Records from their API <https://api.govinfo.gov/docs/> such as congressional speeches, speaker names, and metadata about congressional sessions, and detailed granule records. Optional parameters allow users to specify congressional sessions, and the maximum number of speeches to retrieve. Data is parsed, cleaned, and returned in a structured dataframe for analysis.

We propose a new procedure, called model uncertainty variance, which can quantify the uncertainty of model selection on Autoregressive Moving Average models. The model uncertainty variance not pay attention to the accuracy of prediction, but focus on model selection uncertainty and providing more information of the model selection results. And to estimate the model measures, we propose an simplify and faster algorithm based on bootstrap method, which is proven to be effective and feasible by Monte-Carlo simulation. At the same time, we also made some optimizations and adjustments to the Model Confidence Bounds algorithm, so that it can be applied to the time series model selection method. The consistency of the algorithm result is also verified by Monte-Carlo simulation. We propose a new procedure, called model uncertainty variance, which can quantify the uncertainty of model selection on Autoregressive Moving Average models. The model uncertainty variance focuses on model selection uncertainty and providing more information of the model selection results. To estimate the model uncertainty variance, we propose an simplified and faster algorithm based on bootstrap method, which is proven to be effective and feasible by Monte-Carlo simulation. At the same time, we also made some optimizations and adjustments to the Model Confidence Bounds algorithm, so that it can be applied to the time series model selection method. The consistency of the algorithm result is also verified by Monte-Carlo simulation. Please see Li,Y., Luo,Y., Ferrari,D., Hu,X. and Qin,Y. (2019) Model Confidence Bounds for Variable Selection. Biometrics, 75:392-403.<DOI:10.1111/biom.13024> for more information.

The most used functions on IPEA (Instituto de Pesquisa Economica Aplicada). Most of functions deal with brazilian names. It can guess the women single's name, extract prepositions or extract the first name.

The Ultimate Microrray Prediction, Reality and Inference Engine (UMPIRE) is a package to facilitate the simulation of realistic microarray data sets with links to associated outcomes. See Zhang and Coombes (2012) <doi:10.1186/1471-2105-13-S13-S1>. Version 2.0 adds the ability to simulate realistic mixed-typed clinical data.

In many phase I trials, the design goal is to find the dose associated with a certain target toxicity rate. In some trials, the goal can be to find the dose with a certain weighted sum of rates of various toxicity grades. For others, the goal is to find the dose with a certain mean value of a continuous response. This package provides the setup and calculations needed to run a dose-finding trial with non-binary endpoints and performs simulations to assess designâ s operating characteristics under various scenarios. Three dose finding designs are included in this package: unified phase I design (Ivanova et al. (2009) <doi:10.1111/j.1541-0420.2008.01045.x>), Quasi-CRM/Robust-Quasi-CRM (Yuan et al. (2007) <doi:10.1111/j.1541-0420.2006.00666.x>, Pan et al. (2014) <doi:10.1371/journal.pone.0098147>) and generalized BOIN design (Mu et al. (2018) <doi:10.1111/rssc.12263>). The toxicity endpoints can be handled with these functions including equivalent toxicity score (ETS), total toxicity burden (TTB), general continuous toxicity endpoints, with incorporating ordinal grade toxicity information into dose-finding procedure. These functions allow customization of design characteristics to vary sample size, cohort sizes, target dose-limiting toxicity (DLT) rates, discrete or continuous toxicity score, and incorporate safety and/or stopping rules.

This package implements mixtures of unrestricted skew-t factor analyzer models via the EM algorithm.

Predicts a smooth and continuous (individual) utility function from utility points, and computes measures of intensity for risk and higher-order risk measures (or any other measure computed with user-written function) based on this utility function and its derivatives according to the method introduced in Schneider (2017) <http://hdl.handle.net/21.11130/00-1735-0000-002E-E306-0>.

Core functions necessary for using The Globe and Mail's R data journalism template, startr', along with utilities for day-to-day data journalism tasks, such as reading and writing files, producing graphics and cleaning up datasets.

This package provides a comprehensive educational package combining clustering algorithms with detailed step-by-step explanations. Provides implementations of both traditional (hierarchical, k-means) and modern (Density-Based Spatial Clustering of Applications with Noise (DBSCAN), Gaussian Mixture Models (GMM), genetic k-means) clustering methods as described in Ezugwu et. al., (2022) <doi:10.1016/j.engappai.2022.104743>. Includes educational datasets highlighting different clustering challenges, based on scikit-learn examples (Pedregosa et al., 2011) <https://jmlr.csail.mit.edu/papers/v12/pedregosa11a.html>. Features detailed algorithm explanations, visualizations, and weighted distance calculations for enhanced learning.

Allows users to access live UK energy market information via various APIs.

By gaining the property of emergence through self-organization, the enhancement of SOMs(self organizing maps) is called Emergent SOM (ESOM). The result of the projection by ESOM is a grid of neurons which can be visualised as a three dimensional landscape in form of the Umatrix. Further details can be found in the referenced publications (see url). This package offers tools for calculating and visualising the ESOM as well as Umatrix, Pmatrix and UStarMatrix. All the functionality is also available through graphical user interfaces implemented in shiny'. Based on the recognized data structures, the method can be used to generate new data.

This package provides easy access to a curated selection of pre-processed data sets relevant to the COVID-19 outbreak in the UK for teaching and demonstration purposes.

Three functions are provided: first function changes time from local to UTC, other changes from UTC to local and third returns difference between local and UTC. %h+% operator is also provided it adds hours to a time.

Uniform sampling of Directed Acyclic Graphs (DAG) using exact enumeration by relating each DAG to a sequence of outpoints (nodes with no incoming edges) and then to a composition of integers as suggested by Kuipers, J. and Moffa, G. (2015) <doi:10.1007/s11222-013-9428-y>.

Bindings to system utilities found in most Unix systems such as POSIX functions which are not part of the Standard C Library.

This package provides a fast and simple URL parser package for R'. This package provides functions to parse URLs into their components, such as scheme, user, password, host, port, path, query, and fragment.