Data input/output functions for data that conform to the Digital Imaging and Communications in Medicine (DICOM) standard, part of the Rigorous Analytics bundle.

An extension to the Regression Modeling Strategies package that facilitates plotting ordinal regression model predictions together with confidence intervals for each dependent variable level. It also adds a functionality to plot the model summary as a modifiable object.

High-performance implementation of 37 optimal binning algorithms (16 categorical, 21 numerical) for Weight of Evidence ('WoE') transformation, credit scoring, and risk modeling. Includes advanced methods such as Mixed Integer Linear Programming ('MILP'), Genetic Algorithms, Simulated Annealing, and Monotonic Regression. Features automatic method selection based on Information Value ('IV') maximization, strict monotonicity enforcement, and efficient handling of large datasets via Rcpp'. Provides automated variable screening by Information Value strength and bin ordering, and generation of the equivalent SQL CASE expressions for in-database scoring. Fully integrated with the tidymodels ecosystem for building robust machine learning pipelines. Based on methods described in Siddiqi (2006) <doi:10.1002/9781119201731> and Navas-Palencia (2020) <doi:10.48550/arXiv.2001.08025>.

The ordered panel methodology (Zezulinski et al 2025 <doi:10.1159/000545366>) provides a structured framework for identifying and organizing sets of biomarkers, such as genetic variants, that distinguish between positive and negative subjects in a study when only a training cohort is available. This approach is particularly useful in situations where an independent validation cohort does not yet exist, rendering conventional performance metrics such as the receiver operating characteristic (ROC) curve and area under the ROC curve (AUC) inappropriate or potentially misleading. The methodology emphasizes transparent construction and evaluation of ordered signatures of biomarkers, allowing investigators to examine operating characteristics without establishing predictive performance.

Enables the usage of the OpenDota API from <https://www.opendota.com/>, get game lists, and download JSON's of parsed replays from the OpenDota API. Also has functionality to execute own code to extract the specific parts of the JSON file.

This package implements the Univariate Bootstrap and the Traditional (Naive) Bootstrap for resampling multivariate data while preserving covariance structure. Also provides functions for DeFries-Fulker behavioral genetics models, including the Rodgers-Kohler formulation with robust standard errors.

Two-part system for first collecting then managing direct observation data, as described by Hibbing PR, Ellingson LD, Dixon PM, & Welk GJ (2018) <doi:10.1249/MSS.0000000000001486>.

Tetra-allele cross often referred as four-way cross or double cross or four-line cross are those type of mating designs in which every cross is obtained by mating amongst four inbred lines. A tetra-allele cross can be obtained by crossing the resultant of two unrelated diallel crosses. A common triallel cross involving four inbred lines A, B, C and D can be symbolically represented as (A X B) X (C X D) or (A, B, C, D) or (A B C D) etc. Tetra-allele cross can be broadly categorized as Complete Tetra-allele Cross (CTaC) and Partial Tetra-allele Crosses (PTaC). Rawlings and Cockerham (1962)<doi:10.2307/2527461> firstly introduced and gave the method of analysis for tetra-allele cross hybrids using the analysis method of single cross hybrids under the assumption of no linkage. The set of all possible four-way mating between several genotypes (individuals, clones, homozygous lines, etc.) leads to a CTaC. If there are N number of inbred lines involved in a CTaC, the the total number of crosses, T = N*(N-1)*(N-2)*(N-3)/8. When more number of lines are to be considered, the total number of crosses in CTaC also increases. Thus, it is almost impossible for the investigator to carry out the experimentation with limited available resource material. This situation lies in taking a fraction of CTaC with certain underlying properties, known as PTaC.

When people make decisions, they may do so using a wide variety of decision rules. The package allows users to easily create obfuscation games to test the obfuscation hypothesis. It provides an easy to use interface and multiple options designed to vary the difficulty of the game and tailor it to the user's needs. For more detail: Chorus et al., 2021, Obfuscation maximization-based decision-making: Theory, methodology and first empirical evidence, Mathematical Social Sciences, 109, 28-44, <doi:10.1016/j.mathsocsci.2020.10.002>.

An implementation of optimal weight exchange algorithm Yang(2013) <doi:10.1080/01621459.2013.806268> for three models. They are Crossover model with subject dropout, crossover model with proportional first order residual effects and interference model. You can use it to find either A-opt or D-opt approximate designs. Exact designs can be automatically rounded from approximate designs and relative efficiency is provided as well.

This package implements a tree-based method specifically designed for personalized medicine applications. By using genomic and mutational data, ODT efficiently identifies optimal drug recommendations tailored to individual patient profiles. The ODT algorithm constructs decision trees that bifurcate at each node, selecting the most relevant markers (discrete or continuous) and corresponding treatments, thus ensuring that recommendations are both personalized and statistically robust. This iterative approach enhances therapeutic decision-making by refining treatment suggestions until a predefined group size is achieved. Moreover, the simplicity and interpretability of the resulting trees make the method accessible to healthcare professionals. Includes functions for training the decision tree, making predictions on new samples or patients, and visualizing the resulting tree. For detailed insights into the methodology, please refer to Gimeno et al. (2023) <doi:10.1093/bib/bbad200>.

This package provides a tool for visualizing numerical data (e.g., gene expression, protein abundance) on predefined anatomical maps of human/mouse organs and subcellular organelles. It supports customization of color schemes, filtering by organ systems (for organisms) or organelle types, and generation of optional bar charts for quantitative comparison. The package integrates coordinate data for organs and organelles to plot anatomical/subcellular contours, mapping data values to specific structures for intuitive visualization of biological data distribution.The underlying method was described in the preprint by Zhou et al. (2022) <doi:10.1101/2022.09.07.506938>.

The openMSE package is designed for building operating models, doing simulation modelling and management strategy evaluation for fisheries. openMSE is an umbrella package for the MSEtool (Management Strategy Evaluation toolkit), DLMtool (Data-Limited Methods toolkit), and SAMtool (Stock Assessment Methods toolkit) packages. By loading and installing openMSE', users have access to the full functionality contained within these packages. Learn more about openMSE at <https://openmse.com/>.

This package provides functions for creating ensembles of optimal trees for regression, classification (Khan, Z., Gul, A., Perperoglou, A., Miftahuddin, M., Mahmoud, O., Adler, W., & Lausen, B. (2019). (2019) <doi:10.1007/s11634-019-00364-9>) and class membership probability estimation (Khan, Z, Gul, A, Mahmoud, O, Miftahuddin, M, Perperoglou, A, Adler, W & Lausen, B (2016) <doi:10.1007/978-3-319-25226-1_34>) are given. A few trees are selected from an initial set of trees grown by random forest for the ensemble on the basis of their individual and collective performance. Three different methods of tree selection for the case of classification are given. The prediction functions return estimates of the test responses and their class membership probabilities. Unexplained variations, error rates, confusion matrix, Brier scores, etc. are also returned for the test data.

This package provides functions for optimal policy learning in socioeconomic applications helping users to learn the most effective policies based on data in order to maximize empirical welfare. Specifically, OPL allows to find "treatment assignment rules" that maximize the overall welfare, defined as the sum of the policy effects estimated over all the policy beneficiaries. Documentation about OPL is provided by several international articles via Athey et al (2021, <doi:10.3982/ECTA15732>), Kitagawa et al (2018, <doi:10.3982/ECTA13288>), Cerulli (2022, <doi:10.1080/13504851.2022.2032577>), the paper by Cerulli (2021, <doi:10.1080/13504851.2020.1820939>) and the book by Gareth et al (2013, <doi:10.1007/978-1-4614-7138-7>).

The comprehensive knowledge of epigenetic modifications in plants, encompassing histone modifications in regulating gene expression, is not completely ingrained. It is noteworthy that histone deacetylation and histone H3 lysine 27 trimethylation (H3K27me3) play a role in repressing transcription in eukaryotes. In contrast, histone acetylation (H3K9ac) and H3K4me3 have been inevitably linked to the stimulation of gene expression, which significantly influences plant development and plays a role in plant responses to biotic and abiotic stresses. To our knowledge this the first multiclass classifier for predicting histone modification in plants. <doi:10.1186/s12864-019-5489-4>.

This package contains data from the May 2020 Occupational Employment and Wage Statistics data release from the U.S. Bureau of Labor Statistics. The dataset covers employment and wages across occupations, industries, states, and at the national level. Metropolitan data is not included.

This package provides functions for implementing different versions of the OSCV method in the kernel regression and density estimation frameworks. The package mainly supports the following articles: (1) Savchuk, O.Y., Hart, J.D. (2017). Fully robust one-sided cross-validation for regression functions. Computational Statistics, <doi:10.1007/s00180-017-0713-7> and (2) Savchuk, O.Y. (2017). One-sided cross-validation for nonsmooth density functions, <arXiv:1703.05157>.

This package provides a research-oriented statistical framework for comparing standardized biological effects across matched omics layers. It estimates layer-specific standardized effects, accounts for cross-omic dependence using matched-subject bootstrap correlations, tests multivariate omnibus evidence, synthesizes consensus effects with generalized least squares, quantifies cross-omic heterogeneity, performs practical-equivalence testing, fits covariance-aware ordered GLS effect trajectories, classifies hierarchical cross-layer effect patterns with separate confirmatory and suggestive states, supports analytic and subject-bootstrap confidence intervals for layer and consensus effects, supports empirical matched-subject permutation and centered-bootstrap calibration of omnibus and heterogeneity tests for non-Gaussian settings, and creates evidence-forest and effect-braid visualizations. The package is designed for analysis-ready bulk multi-omics data or externally estimated summary statistics. It does not perform raw sequencing or mass-spectrometry preprocessing. Methodological components draw on standardized mean-difference estimation described by Hedges (1981) <doi:10.3102/10769986006002107>, bootstrap resampling described by Efron (1979) <doi:10.1214/aos/1176344552>, and two one-sided equivalence testing described by Schuirmann (1987) <doi:10.1007/BF01068419>.

Apply unsupervised segmentation algorithms included in Orfeo ToolBox software (<https://www.orfeo-toolbox.org/>), such as mean shift or watershed segmentation.

This database contains necessary data relevant to medical costs on obesity throughout the United States. This database, in form of an R package, could output necessary data frames relevant to obesity costs, where the clients could easily manipulate the output using difference parameters, e.g. relative risks for each illnesses. This package contributes to parts of our published journal named "Modeling the Economic Cost of Obesity Risk and Its Relation to the Health Insurance Premium in the United States: A State Level Analysis". Please use the following citation for the journal: Woods Thomas, Tatjana Miljkovic (2022) "Modeling the Economic Cost of Obesity Risk and Its Relation to the Health Insurance Premium in the United States: A State Level Analysis" <doi:10.3390/risks10100197>. The database is composed of the following main tables: 1. Relative_Risks: (constant) Relative risks for a given disease group with a risk factor of obesity; 2. Disease_Cost: (obesity_cost_disease) Supplementary output with all variables related to individual disease groups in a given state and year; 3. Full_Cost: (obesity_cost_full) Complete output with all variables used to make cost calculations, as well as cost calculations in a given state and year; 4. National_Summary: (obesity_cost_national_summary) National summary cost calculations in a given year. Three functions are included to assist users in calling and adjusting the mentioned tables and they are data_load(), data_produce(), and rel_risk_fun().

Estimates optimal number of biomarkers for two-group classification based on microarray data.

This package provides lightweight R wrappers for the OKX REST API, covering endpoints for market data, trading, account management, asset balances, and copy trading. The upstream API reference is available at <https://www.okx.com/docs-v5/en/>.

This package provides a function for fitting various penalized Bayesian cumulative link ordinal response models when the number of parameters exceeds the sample size. These models have been described in Zhang and Archer (2021) <doi:10.1186/s12859-021-04432-w>.