Easily calculate precession and obliquity from an orbital solution (defaults to ZB18a from Zeebe and Lourens (2019) <doi:10.1126/science.aax0612>) and assumed or reconstructed values for tidal dissipation (Td) and dynamical ellipticity (Ed). This is a translation and adaptation of the C'-code in the supplementary material to Zeebe and Lourens (2022) <doi:10.1029/2021PA004349>, with further details on the methodology described in Zeebe (2022) <doi:10.3847/1538-3881/ac80f8>. The name of the C'-routine is snvec', which refers to the key units of computation: spin vector s and orbit normal vector n.

Toolbox containing a variety of spectral clustering tools functions. Among the tools available are the hierarchical spectral clustering algorithm, the Shi and Malik clustering algorithm, the Perona and Freeman algorithm, the non-normalized clustering, the Von Luxburg algorithm, the Partition Around Medoids clustering algorithm, a multi-level clustering algorithm, recursive clustering and the fast method for all clustering algorithm. As well as other tools needed to run these algorithms or useful for unsupervised spectral clustering. This toolbox aims to gather the main tools for unsupervised spectral classification. See <http://mawenzi.univ-littoral.fr/> for more information and documentation.

MetNet contains functionality to infer metabolic network topologies from quantitative data and high-resolution mass/charge information. Using statistical models (including correlation, mutual information, regression and Bayes statistics) and quantitative data (intensity values of features) adjacency matrices are inferred that can be combined to a consensus matrix. Mass differences calculated between mass/charge values of features will be matched against a data frame of supplied mass/charge differences referring to transformations of enzymatic activities. In a third step, the two levels of information are combined to form a adjacency matrix inferred from both quantitative and structure information.

This package implements several basic algorithms for estimating regression parameters for semiparametric accelerated failure time (AFT) model. The main methods are: Jin rank-based method (Jin (2003) <doi:10.1093/biomet/90.2.341>), Hellerâ s estimating method (Heller (2012) <doi:10.1198/016214506000001257>), Polynomial smoothed Gehan function method (Chung (2013) <doi:10.1007/s11222-012-9333-9>), Buckley-James method (Buckley (1979) <doi:10.2307/2335161>) and Jin`s improved least squares method (Jin (2006) <doi:10.1093/biomet/93.1.147>). This package can be used for modeling right-censored data and for comparing different estimation algorithms.

This package performs Bayesian posterior inference for heteroskedastic Gaussian processes. Models are trained through MCMC including elliptical slice sampling (ESS) of latent noise processes and Metropolis-Hastings sampling of kernel hyperparameters. Replicates are handled efficientyly through a Woodbury formulation of the joint likelihood for the mean and noise process (Binois, M., Gramacy, R., Ludkovski, M. (2018) <doi:10.1080/10618600.2018.1458625>) For large data, Vecchia-approximation for faster computation is leveraged (Sauer, A., Cooper, A., and Gramacy, R., (2023), <doi:10.1080/10618600.2022.2129662>). Incorporates OpenMP and SNOW parallelization and utilizes C'/'C++ under the hood.

Real-time quantitative polymerase chain reaction (qPCR) data sets by Batsch et al. (2008) <doi:10.1186/1471-2105-9-95>. This package provides five data sets, one for each PCR target: (i) rat SLC6A14, (ii) human SLC22A13, (iii) pig EMT, (iv) chicken ETT, and (v) human GAPDH. Each data set comprises a five-point, four-fold dilution series. For each concentration there are three replicates. Each amplification curve is 45 cycles long. Original raw data file: <https://static-content.springer.com/esm/art%3A10.1186%2F1471-2105-9-95/MediaObjects/12859_2007_2080_MOESM5_ESM.xls>.

This package provides classes (S4) of commonly used elliptical, Archimedean, extreme-value and other copula families, as well as their rotations, mixtures and asymmetrizations. Nested Archimedean copulas, related tools and special functions. Methods for density, distribution, random number generation, bivariate dependence measures, Rosenblatt transform, Kendall distribution function, perspective and contour plots. Fitting of copula models with potentially partly fixed parameters, including standard errors. Serial independence tests, copula specification tests (independence, exchangeability, radial symmetry, extreme-value dependence, goodness-of-fit) and model selection based on cross-validation. Empirical copula, smoothed versions, and non-parametric estimators of the Pickands dependence function.

Random sampling from distributions with user-specified population covariance matrix. Marginal information may be fully specified, for which the package implements the VITA (VIne-To-Anything) algorithm Grønneberg and Foldnes (2017) <doi:10.1007/s11336-017-9569-6>. See also Grønneberg, Foldnes and Marcoulides (2022) <doi:10.18637/jss.v102.i03>. Alternatively, marginal skewness and kurtosis may be specified, for which the package implements the IG (independent generator) and PLSIM (piecewise linear) algorithms, see Foldnes and Olsson (2016) <doi:10.1080/00273171.2015.1133274> and Foldnes and Grønneberg (2021) <doi:10.1080/10705511.2021.1949323>, respectively.

This project provides a group of new functions to calculate the outputs of the two main components of the Canadian Forest Fire Danger Rating System (CFFDRS) Van Wagner and Pickett (1985) <https://ostrnrcan-dostrncan.canada.ca/entities/publication/29706108-2891-4e5d-a59a-a77c96bc507c>) at various time scales: the Fire Weather Index (FWI) System Wan Wagner (1985) <https://ostrnrcan-dostrncan.canada.ca/entities/publication/d96e56aa-e836-4394-ba29-3afe91c3aa6c> and the Fire Behaviour Prediction (FBP) System Forestry Canada Fire Danger Group (1992) <https://cfs.nrcan.gc.ca/pubwarehouse/pdfs/10068.pdf>. Some functions have two versions, table and raster based.

This package implements a generalized linear model approach for detecting differentially expressed genes across treatment groups in count data. The package supports both quasi-Poisson and negative binomial models to handle over-dispersion, ensuring robust identification of differential expression. It allows for the inclusion of treatment effects and gene-wise covariates, as well as normalization factors for accurate scaling across samples. Additionally, it incorporates statistical significance testing with options for p-value adjustment and log2 fold range thresholds, making it suitable for RNA-seq analysis as described in by Xu et al., (2024) <doi:10.1371/journal.pone.0300565>.

The EXPOS model uses a digital elevation model (DEM) to estimate exposed and protected areas for a given hurricane wind direction and inflection angle. The resulting topographic exposure maps can be combined with output from the HURRECON model to estimate hurricane wind damage across a region. For details on the original version of the EXPOS model written in Borland Pascal', see: Boose, Foster, and Fluet (1994) <doi:10.2307/2937142>, Boose, Chamberlin, and Foster (2001) <doi:10.1890/0012-9615(2001)071[0027:LARIOH]2.0.CO;2>, and Boose, Serrano, and Foster (2004) <doi:10.1890/02-4057>.

The geomod does spatial prediction of the Geotechnical soil properties. It predicts the spatial distribution of Geotechnical properties of soil e.g. shear strength, permeability, plasticity index, Standard Penetration Test (SPT) counts, etc. The output of the prediction takes the form of a map or a series of maps. It uses the interpolation technique where a single or statistically â bestâ estimate of spatial occurrence soil property is determined. The interpolation is based on both the sampled data and a variogram model for the spatial correlation of the sampled data. The single estimate is produced by a Kriging technique.

Base R's default setting for stringsAsFactors within data.frame() and as.data.frame() is supposedly the most often complained about piece of code in the R infrastructure. The hellno package provides an explicit solution without changing R itself or having to mess around with options. It tries to solve this problem by providing alternative data.frame() and as.data.frame() functions that are in fact simple wrappers around base R's data.frame() and as.data.frame() with stringsAsFactors option set to HELLNO ( which in turn equals FALSE ) by default.

This package provides a set of tools for estimating hierarchical linear models and effect sizes based on data from single-case designs. Functions are provided for calculating standardized mean difference effect sizes that are directly comparable to standardized mean differences estimated from between-subjects randomized experiments, as described in Hedges, Pustejovsky, and Shadish (2012) <DOI:10.1002/jrsm.1052>; Hedges, Pustejovsky, and Shadish (2013) <DOI:10.1002/jrsm.1086>; Pustejovsky, Hedges, and Shadish (2014) <DOI:10.3102/1076998614547577>; and Chen, Pustejovsky, Klingbeil, and Van Norman (2023) <DOI:10.1016/j.jsp.2023.02.002>. Includes an interactive web interface.

MeSH (Medical Subject Headings) is the NLM controlled vocabulary used to manually index articles for MEDLINE/PubMed. MeSH terms were associated by Entrez Gene ID by three methods, gendoo, gene2pubmed and RBBH. This association is fundamental for enrichment and semantic analyses. meshes supports enrichment analysis (over-representation and gene set enrichment analysis) of gene list or whole expression profile. The semantic comparisons of MeSH terms provide quantitative ways to compute similarities between genes and gene groups. meshes implemented five methods proposed by Resnik, Schlicker, Jiang, Lin and Wang respectively and supports more than 70 species.

slalom is a scalable modelling framework for single-cell RNA-seq data that uses gene set annotations to dissect single-cell transcriptome heterogeneity, thereby allowing to identify biological drivers of cell-to-cell variability and model confounding factors. The method uses Bayesian factor analysis with a latent variable model to identify active pathways (selected by the user, e.g. KEGG pathways) that explain variation in a single-cell RNA-seq dataset. This an R/C++ implementation of the f-scLVM Python package. See the publication describing the method at https://doi.org/10.1186/s13059-017-1334-8.

Implementing the Block Coordinate Ascent with One-Step Generalized Rosen (BCA1SG) algorithm on the semiparametric models for panel count data, interval-censored survival data, and degradation data. A comprehensive description of the BCA1SG algorithm can be found in Wang et al. (2020) <https://github.com/yudongstat/BCA1SG/blob/master/BCA1SG.pdf>. For details of the semiparametric models for panel count data, interval-censored survival data, and degradation data, please see Wellner and Zhang (2007) <doi:10.1214/009053607000000181>, Huang and Wellner (1997) <ISBN:978-0-387-94992-5>, and Wang and Xu (2010) <doi:10.1198/TECH.2009.08197>, respectively.

This package infers state-recorded gender categories from first names and dates of birth using historical datasets. By using these datasets instead of lists of male and female names, this package is able to more accurately infer the gender of a name, and it is able to report the probability that a name was male or female. GUIDELINES: This method must be used cautiously and responsibly. Please be sure to see the guidelines and warnings about usage in the README or the package documentation. See Blevins and Mullen (2015) <http://www.digitalhumanities.org/dhq/vol/9/3/000223/000223.html>.

Error type I and Optimal critical values to test statistical hypothesis based on Neyman-Pearson Lemma and Likelihood ratio test based on random samples from several distributions. The families of distributions are Bernoulli, Exponential, Geometric, Inverse Normal, Normal, Gamma, Gumbel, Lognormal, Poisson, and Weibull. This package is an ideal resource to help with the teaching of Statistics. The main references for this package are Casella G. and Berger R. (2003,ISBN:0-534-24312-6 , "Statistical Inference. Second Edition", Duxbury Press) and Hogg, R., McKean, J., and Craig, A. (2019,ISBN:013468699, "Introduction to Mathematical Statistic. Eighth edition", Pearson).

Helps with the thoughtful saving, reading, and management of result files (using rds files). The core functions take a list of parameters that are used to generate a unique hash to save results under. Then, the same parameter list can be used to read those results back in. This is helpful to avoid clunky file naming when running a large number of simulations. Additionally, helper functions are available for compiling a flat file of parameters of saved results, monitoring result usage, and cleaning up unwanted or unused results. For more information, visit the indexr homepage <https://lharris421.github.io/indexr/>.

This package implements a methodology for the design and analysis of dose-response studies that combines aspects of multiple comparison procedures and modeling approaches (Bretz, Pinheiro and Branson, 2005, Biometrics 61, 738-748, <doi: 10.1111/j.1541-0420.2005.00344.x>). The package provides tools for the analysis of dose finding trials as well as a variety of tools necessary to plan a trial to be conducted with the MCP-Mod methodology. Please note: The MCPMod package will not be further developed, all future development of the MCP-Mod methodology will be done in the DoseFinding R-package.

This package provides a novel method to implement cancer subtyping and subtype specific drug targets identification via non-negative matrix tri-factorization. To improve the interpretability, we introduce orthogonal constraint to the row coefficient matrix and column coefficient matrix. To meet the prior knowledge that each subtype should be strongly associated with few gene sets, we introduce sparsity constraint to the association sub-matrix. The average residue was introduced to evaluate the row and column cluster numbers. This is part of the work "Liver Cancer Analysis via Orthogonal Sparse Non-Negative Matrix Tri- Factorization" which will be submitted to BBRC.

This package provides functionality to fit a zero-inflated estimator for small area estimation. This estimator is a combines a linear mixed effects regression model and a logistic mixed effects regression model via a two-stage modeling approach. The estimator's mean squared error is estimated via a parametric bootstrap method. Chandra and others (2012, <doi:10.1080/03610918.2011.598991>) introduce and describe this estimator and mean squared error estimator. White and others (2024+, <doi:10.48550/arXiv.2402.03263>) describe the applicability of this estimator to estimation of forest attributes and further assess the estimator's properties.

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>.