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Common coordinate-based workflows involving processed chromatin loop and genomic element data are considered and packaged into appropriate customizable functions. Includes methods for linking element sets via chromatin loops and creating consensus loop datasets.
Print vectors (and data frames) of floating point numbers using a non-scientific format optimized for human readers. Vectors of numbers are rounded using significant digits, aligned at the decimal point, and all zeros trailing the decimal point are dropped. See: Wright (2016). Lucid: An R Package for Pretty-Printing Floating Point Numbers. In JSM Proceedings, Statistical Computing Section. Alexandria, VA: American Statistical Association. 2270-2279.
This package implements novel nonparametric approaches to address biases and confounding when comparing treatments or exposures in observational studies of outcomes. While designed and appropriate for use in studies involving medicine and the life sciences, the package can be used in other situations involving outcomes with multiple confounders. The package implements a family of methods for non-parametric bias correction when comparing treatments in observational studies, including survival analysis settings, where competing risks and/or censoring may be present. The approach extends to bias-corrected personalized predictions of treatment outcome differences, and analysis of heterogeneity of treatment effect-sizes across patient subgroups. For further details, please see: Lauve NR, Nelson SJ, Young SS, Obenchain RL, Lambert CG. LocalControl: An R Package for Comparative Safety and Effectiveness Research. Journal of Statistical Software. 2020. p. 1â 32. Available from <doi:10.18637/jss.v096.i04>.
The Lorentz transform in special relativity; also the gyrogroup structure of three-velocities. Performs active and passive transforms and has the ability to use units in which the speed of light is not unity. Includes some experimental functionality for celerity and rapidity. For general relativity, see the schwarzschild package.
Estimate the slope and intercept of a bivariate linear relationship by calculating a posterior density that is invariant to interchange and scaling of the coordinates.
Estimation of latent class models with individual covariates for capture-recapture data. See Bartolucci, F. and Forcina, A. (2022), Estimating the size of a closed population by modeling latent and observed heterogeneity, Biometrics, 80(2), ujae017.
Classical tests of goodness-of-fit aim to validate the conformity of a postulated model to the data under study. In their standard formulation, however, they do not allow exploring how the hypothesized model deviates from the truth nor do they provide any insight into how the rejected model could be improved to better fit the data. To overcome these shortcomings, we establish a comprehensive framework for goodness-of-fit which naturally integrates modeling, estimation, inference and graphics. In this package, the deviance tests and comparison density plots are performed to conduct the LP smoothed inference, where the letter L denotes nonparametric methods based on quantiles and P stands for polynomials. Simulations methods are used to perform variance estimation, inference and post-selection adjustments. Algeri S. and Zhang X. (2020) <arXiv:2005.13011>.
This package provides a graphical user interface with an integrated diagrammer for latent variable models from the lavaan package. It offers two core functions: first, lavaangui() launches a web application that allows users to specify models by drawing path diagrams, fitting them, assessing model fit, and more; second, plot_lavaan() creates interactive path diagrams from models specified in lavaan'. After customizing a diagram interactively, export_plot() saves it to a file, enabling reproducible scripts without sacrificing fine-grained control over appearance. Karch (2024) <doi: 10.1080/10705511.2024.2420678> contains a tutorial.
Offers a convenient pipeline to test and compare various missing data imputation algorithms on simulated and real data. These include simpler methods, such as mean and median imputation and random replacement, but also include more sophisticated algorithms already implemented in popular R packages, such as mi', described by Su et al. (2011) <doi:10.18637/jss.v045.i02>; mice', described by van Buuren and Groothuis-Oudshoorn (2011) <doi:10.18637/jss.v045.i03>; missForest', described by Stekhoven and Buhlmann (2012) <doi:10.1093/bioinformatics/btr597>; missMDA', described by Josse and Husson (2016) <doi:10.18637/jss.v070.i01>; and pcaMethods', described by Stacklies et al. (2007) <doi:10.1093/bioinformatics/btm069>. The central assumption behind missCompare is that structurally different datasets (e.g. larger datasets with a large number of correlated variables vs. smaller datasets with non correlated variables) will benefit differently from different missing data imputation algorithms. missCompare takes measurements of your dataset and sets up a sandbox to try a curated list of standard and sophisticated missing data imputation algorithms and compares them assuming custom missingness patterns. missCompare will also impute your real-life dataset for you after the selection of the best performing algorithm in the simulations. The package also provides various post-imputation diagnostics and visualizations to help you assess imputation performance.
Straightforward and detailed evaluation of machine learning models. MLeval can produce receiver operating characteristic (ROC) curves, precision-recall (PR) curves, calibration curves, and PR gain curves. MLeval accepts a data frame of class probabilities and ground truth labels, or, it can automatically interpret the Caret train function results from repeated cross validation, then select the best model and analyse the results. MLeval produces a range of evaluation metrics with confidence intervals.
This package provides estimation and leave-one-cluster-out jackknife standard errors for four longitudinal cluster-randomized trial estimands: horizontal individual average treatment effect (h-iATE), horizontal cluster average treatment effect (h-cATE), vertical individual average treatment effect (v-iATE), and vertical cluster-period average treatment effect (v-cATE), using unadjusted and augmented (model-robust standardization) estimators. The working model may be fit using linear mixed models for continuous outcomes or generalized estimating equations and generalized linear mixed models for binary outcomes. Period inclusion for aggregation is determined automatically: only periods with both treated and control clusters are included in the construction of the marginal means and treatment effect contrasts. See Fang et al. (2025) <doi:10.48550/arXiv.2507.17190>.
Computation and visualization of matrix correlation coefficients. The main method is the Similarity of Matrices Index, while various related measures like r1, r2, r3, r4, Yanai's GCD, RV, RV2, adjusted RV, Rozeboom's linear correlation and Coxhead's coefficient are included for comparison and flexibility.
This package implements metafrontier production function models for estimating technical efficiencies and technology gaps for firms operating under different technologies. Supports both stochastic frontier analysis (SFA) and data envelopment analysis (DEA) based metafrontiers. Includes the deterministic metafrontier of Battese, Rao, and O'Donnell (2004) <doi:10.1023/B:PROD.0000012454.06094.29>, the stochastic metafrontier of Huang, Huang, and Liu (2014) <doi:10.1007/s11123-014-0402-2>, and the metafrontier Malmquist productivity index of O'Donnell, Rao, and Battese (2008) <doi:10.1007/s00181-007-0119-4>. Additional features include panel SFA with time-varying inefficiency, bootstrap confidence intervals for technology gap ratios, latent class metafrontier estimation via the EM algorithm, Murphy-Topel corrected standard errors, and ggplot2 visualisation methods.
This package provides utilities for reading and processing microdata from Spanish official statistics with R.
Calculate the financial impact of using a churn model in terms of cost, revenue, profit and return on investment.
Identifies the optimal number of clusters by calculating the similarity between two clustering methods at the same number of clusters using the corrected indices of Rand and Jaccard as described in Albatineh and Niewiadomska-Bugaj (2011). The number of clusters at which the index attain its maximum more frequently is a candidate for being the optimal number of clusters.
This package provides tools for the calculation of effect sizes (standardised mean difference) and mean difference in pre-post controlled studies, including robust imputation of missing variances (standard deviation of changes) and correlations (Pearson correlation coefficient). The main function metacor_dual() implements several methods for imputing missing standard deviation of changes or Pearson correlation coefficient, and generates transparent imputation reports. Designed for meta-analyses with incomplete summary statistics. For details on the methods, see Higgins et al. (2023) and Fu et al. (2013).
This package provides global hypothesis tests, multiple testing procedures and simultaneous confidence intervals for multiple linear contrasts of regression coefficients in a single generalized estimating equation (GEE) model or across multiple GEE models. GEE models are fit by a modified version of the geeM package.
An R interface to version 0.3 of the ROPTLIB optimization library (see <https://www.math.fsu.edu/~whuang2/> for more information). Optimize real- valued functions over manifolds such as Stiefel, Grassmann, and Symmetric Positive Definite matrices. For details see Martin et. al. (2020) <doi:10.18637/jss.v093.i01>. Note that the optional ldr package used in some of this package's examples can be obtained from either JSS <https://www.jstatsoft.org/index.php/jss/article/view/v061i03/2886> or from the CRAN archives <https://cran.r-project.org/src/contrib/Archive/ldr/ldr_1.3.3.tar.gz>.
Three main functions about analyzing massive data (missing observations are allowed) considered from multiple layers of categories are demonstrated. Flexible and diverse applications of the function parameters make the data analyses powerful.
Estimation of models with dependent variable left-censored at zero. Null values may be caused by a selection process Cragg (1971) <doi:10.2307/1909582>, insufficient resources Tobin (1958) <doi:10.2307/1907382>, or infrequency of purchase Deaton and Irish (1984) <doi:10.1016/0047-2727(84)90067-7>.
Addressing a central challenge encountered in Mendelian randomization (MR) studies, where MR primarily focuses on discerning the effects of individual exposures on specific outcomes and establishes causal links between them. Using a network-based methodology, the intricacy involving interdependent outcomes due to numerous factors has been tackled through this routine. Based on Ni et al. (2018) <doi:10.1214/17-BA1087>, MR.RGM extends to a broader exploration of the causal landscape by leveraging on network structures and involves the construction of causal graphs that capture interactions between response variables and consequently between responses and instrument variables. The resulting Graph visually represents these causal connections, showing directed edges with effect sizes labeled. MR.RGM facilitates the navigation of various data availability scenarios effectively by accommodating three input formats, i.e., individual-level data and two types of summary-level data. The method also optionally incorporates measured covariates (when available) and allows flexible modeling of the error variance structure, including correlated errors that may reflect unmeasured confounding among responses. In the process, causal effects, adjacency matrices, and other essential parameters of the complex biological networks, are estimated. Besides, MR.RGM provides uncertainty quantification for specific network structures among response variables. Parts of the Inverse Wishart sampler are adapted from the econ722 repository by DiTraglia (GPL-2.0).
This package provides functions for testing randomness for a univariate time series with arbitrary distribution (discrete, continuous, mixture of both types) and for testing independence between random variables with arbitrary distributions. The test statistics are based on the multilinear empirical copula and multipliers are used to compute P-values. The test of independence between random variables appeared in Genest, Nešlehová, Rémillard & Murphy (2019) and the test of randomness appeared in Nasri (2022).
This function allows to generate two biological conditions synthetic microarray dataset which has similar behavior to those currently observed with common platforms. User provides a subset of parameters. Available default parameters settings can be modified.