The package solves linear system of equations Ax=b by using Preconditioned Conjugate Gradient Algorithm where A is real symmetric positive definite matrix. A suitable preconditioner matrix may be provided by user. This can also be used to minimize quadratic function (x'Ax)/2-bx for unknown x.

This package performs smoothed (and non-smoothed) principal/independent components analysis of functional data. Various functional pre-whitening approaches are implemented as discussed in Vidal and Aguilera (2022) â Novel whitening approaches in functional settings", <doi:10.1002/sta4.516>. Further whitening representations of functional data can be derived in terms of a few principal components, providing an avenue to explore hidden structures in low dimensional settings: see Vidal, Rosso and Aguilera (2021) â Bi-smoothed functional independent component analysis for EEG artifact removalâ , <doi:10.3390/math9111243>.

Fit linear splines to species time series to detect population growth scenarios based on Hyndman, R J and Mesgaran, M B and Cousens, R D (2015) <doi:10.1007/s10530-015-0962-8>.

Computes partial eta-squared effect sizes for fixed effects in linear mixed models fitted with the lme4 package. Supports crossed, nested, and mixed (crossed-and-nested) random effects structures with any number of grouping factors. Mixed designs handle cases where grouping factors are simultaneously crossed with some variables and nested within others (e.g., photos nested within models, but both crossed with participants). Factor predictors are supported directly, and a single factor-level (omnibus) effect size can be obtained for a multi-level factor or multi-df interaction. Random slope variances are translated to the outcome scale using a variance decomposition approach, correctly accounting for predictor scaling and interaction terms. Both general and operative effect sizes are provided, with optional parametric bootstrap confidence intervals. For correlated predictors, per-predictor effect sizes use unique (semipartial) variance by default. Methods are based on Correll, Mellinger, McClelland, and Judd (2020) <doi:10.1016/j.tics.2019.12.009>, Correll, Mellinger, and Pedersen (2022) <doi:10.3758/s13428-021-01687-2>, and Rights and Sterba (2019) <doi:10.1037/met0000184>.

PHATE is a tool for visualizing high dimensional single-cell data with natural progressions or trajectories. PHATE uses a novel conceptual framework for learning and visualizing the manifold inherent to biological systems in which smooth transitions mark the progressions of cells from one state to another. To see how PHATE can be applied to single-cell RNA-seq datasets from hematopoietic stem cells, human embryonic stem cells, and bone marrow samples, check out our publication in Nature Biotechnology at <doi:10.1038/s41587-019-0336-3>.

Set of functions for analysis of Principal Coordinates of Phylogenetic Structure (PCPS).

This R package provides power calculations via internal simulation methods. The package also provides a frontend to the now abandoned PBAT program (developed by Christoph Lange), and reads in the corresponding output and displays results and figures when appropriate. The license of this R package itself is GPL. However, to have the program interact with the PBAT program for some functionality of the R package, users must additionally obtain the PBAT program from Christoph Lange, and accept his license. Both the data analysis and power calculations have command line and graphical interfaces using tcltk.

This package contains functions to fit proportional hazards (PH) model to partly interval-censored (PIC) data (Pan et al. (2020) <doi:10.1177/0962280220921552>), PH model with spatial frailty to spatially dependent PIC data (Pan and Cai (2021) <doi:10.1080/03610918.2020.1839497>), and mixed effects PH model to clustered PIC data. Each random intercept/random effect can follow both a normal prior and a Dirichlet process mixture prior. It also includes the corresponding functions for general interval-censored data.

This package provides tools to compute unbiased pleiotropic heritability estimates of complex diseases from genome-wide association studies (GWAS) summary statistics. We estimate pleiotropic heritability from GWAS summary statistics by estimating the proportion of variance explained from an estimated genetic correlation matrix (Bulik-Sullivan et al. 2015 <doi:10.1038/ng.3406>) and employing a Monte-Carlo bias correction procedure to account for sampling noise in genetic correlation estimates.

Miscellaneous printing of numeric or statistical results in R Markdown or Quarto documents according to guidelines of the "Publication Manual" of the American Psychological Association (2020, ISBN: 978-1-4338-3215-4). These guidelines are usually referred to as APA style (<https://apastyle.apa.org/>) and include specific rules on the formatting of numbers and statistical test results. APA style has to be implemented when submitting scientific reports in a wide range of research fields, especially in the social sciences. The default output of numbers in the R console or R Markdown and Quarto documents does not meet the APA style requirements, and reformatting results manually can be cumbersome and error-prone. This package covers the automatic conversion of R objects to textual representations that meet the APA style requirements, which can be included in R Markdown or Quarto documents. It covers some basic statistical tests (t-test, ANOVA, correlation, chi-squared test, Wilcoxon test) as well as some basic number printing manipulations (formatting p-values, removing leading zeros for numbers that cannot be greater than one, and others). Other packages exist for formatting numbers and tests according to the APA style guidelines, such as papaja (<https://cran.r-project.org/package=papaja>) and apa (<https://cran.r-project.org/package=apa>), but they do not offer all convenience functionality included in prmisc'. The vignette has an overview of most of the functions included in the package.

This package provides methods to calculate and present PHENTHAUproc', an early warning and decision support system for hazard assessment and control of oak processionary moth (OPM) using local and spatial temperature data. It was created by Halbig et al. 2024 (<doi:10.1016/j.foreco.2023.121525>) at FVA (<https://www.fva-bw.de/en/homepage/>) Forest Research Institute Baden-Wuerttemberg, Germany and at BOKU - University of Natural Ressources and Life Sciences, Vienna, Austria.

Function to read PX-Web data into R via API. The example code reads data from the three national statistical institutes, Statistics Norway, Statistics Sweden and Statistics Finland.

Data sets and functions used in the polish book "Przewodnik po pakiecie R" (The Hitchhiker's Guide to the R). See more at <http://biecek.pl/R>. Among others you will find here data about housing prices, cancer patients, running times and many others.

Retrieves a pluscode by inputting latitude and longitude. Includes additional functions to retrieve neighbouring pluscodes'.

Handles and formats author information in scientific writing in R Markdown and Quarto'. plume provides easy-to-use and flexible tools for inserting author data in YAML as well as generating author and contribution lists (among others) as strings from tabular data.

Reverse depends for a given package are queued such that multiple workers can run the reverse-dependency tests in parallel.

Tailoring the optimal biomarker(s) for disease screening or diagnosis based on subjects individual characteristics.

This is an implementation of model-based trees with global model parameters (PALM trees). The PALM tree algorithm is an extension to the MOB algorithm (implemented in the partykit package), where some parameters are fixed across all groups. Details about the method can be found in Seibold, Hothorn, Zeileis (2016) <arXiv:1612.07498>. The package offers coef(), logLik(), plot(), and predict() functions for PALM trees.

This package provides a multiple testing procedure for testing several groups of hypotheses is implemented. Linear dependency among the hypotheses within the same group is modeled by using hidden Markov Models. It is noted that a smaller p value does not necessarily imply more significance due to the dependency. A typical application is to analyze genome wide association studies datasets, where SNPs from the same chromosome are treated as a group and exhibit strong linear genomic dependency. See Wei Z, Sun W, Wang K, Hakonarson H (2009) <doi:10.1093/bioinformatics/btp476> for more details.

This package implements permutation tests for any test statistic and randomization scheme and constructs associated confidence intervals as described in Glazer and Stark (2024) <doi:10.48550/arXiv.2405.05238>.

Fits the Poisson-Tweedie generalized linear mixed model described in Signorelli et al. (2021, <doi:10.1177/1471082X20936017>). Likelihood approximation based on adaptive Gauss Hermite quadrature rule.

Algorithms to speed up the Bayesian Lasso Cox model (Lee et al., Int J Biostat, 2011 <doi:10.2202/1557-4679.1301>) and the Bayesian Lasso Cox with mandatory variables (Zucknick et al. Biometrical J, 2015 <doi:10.1002/bimj.201400160>).

Partial Least Squares Path Modeling (PLS-PM), Tenenhaus, Esposito Vinzi, Chatelin, Lauro (2005) <doi:10.1016/j.csda.2004.03.005>, analysis for both metric and non-metric data, as well as REBUS analysis, Esposito Vinzi, Trinchera, Squillacciotti, and Tenenhaus (2008) <doi:10.1002/asmb.728>.

R functions to access provenance information collected by rdt or rdtLite'. The information is stored inside a ProvInfo object and can be accessed through a collection of functions that will return the requested data. The exact format of the JSON created by rdt and rdtLite is described in <https://github.com/End-to-end-provenance/ExtendedProvJson>.