This package provides data set and function for exploration of Multiple Indicator Cluster Survey (MICS) 2017-18 data for Punjab, Pakistan. The results of the present survey are critically important for the purposes of SDG monitoring, as the survey produces information on 32 global SDG indicators. The data was collected from 53,840 households selected at the second stage with systematic random sampling out of a sample of 2,692 clusters selected using Probability Proportional to size sampling. Six questionnaires were used in the survey: (1) a household questionnaire to collect basic demographic information on all de jure household members (usual residents), the household, and the dwelling; (2) a water quality testing questionnaire administered in three households in each cluster of the sample; (3) a questionnaire for individual women administered in each household to all women age 15-49 years; (4) a questionnaire for individual men administered in every second household to all men age 15-49 years; (5) an under-5 questionnaire, administered to mothers (or caretakers) of all children under 5 living in the household; and (6) a questionnaire for children age 5-17 years, administered to the mother (or caretaker) of one randomly selected child age 5-17 years living in the household.

This package performs genomic prediction of hybrid performance using eight GS methods including GBLUP, BayesB, RKHS, PLS, LASSO, Elastic net, XGBoost and LightGBM. GBLUP: genomic best liner unbiased prediction, RKHS: reproducing kernel Hilbert space, PLS: partial least squares regression, LASSO: least absolute shrinkage and selection operator, XGBoost: extreme gradient boosting, LightGBM: light gradient boosting machine. It also provides fast cross-validation and mating design scheme for training population (Xu S et al (2016) <doi:10.1111/tpj.13242>; Xu S (2017) <doi:10.1534/g3.116.038059>). A complete manual for this package is provided in the manual folder of the package installation directory. You can locate the manual by running the following command in R: system.file("manual", package = "predhy.GUI").

Compute standard Non-Compartmental Analysis (NCA) parameters for typical pharmacokinetic analyses and summarize them.

Data are partitioned (clustered) into k clusters "around medoids", which is a more robust version of K-means implemented in the function pam() in the cluster package. The PAM algorithm is described in Kaufman and Rousseeuw (1990) <doi:10.1002/9780470316801>. Please refer to the pam() function documentation for more references. Clustered data is plotted as a split heatmap allowing visualisation of representative "group-clusters" (medoids) in the data as separated fractions of the graph while those "sub-clusters" are visualised as a traditional heatmap based on hierarchical clustering.

The portmanteau local feature discriminant approach first identifies the local discriminant features and their differential structures, then constructs the discriminant rule by pooling the identified local features together. This method is applicable to high-dimensional matrix-variate data. See the paper by Xu, Luo and Chen (2023, <doi:10.1007/s13171-021-00255-2>).

For a data matrix with m rows and n columns (m>=n), the power method is used to compute, simultaneously, the eigendecomposition of a square symmetric matrix. This result is used to obtain the singular value decomposition (SVD) and the principal component analysis (PCA) results. Compared to the classical SVD method, the first r singular values can be computed.

Recent years have seen an increased interest in novel methods for analyzing quantitative data from experimental psychology. Currently, however, they lack an established and accessible software framework. Many existing implementations provide no guidelines, consisting of small code snippets, or sets of packages. In addition, the use of existing packages often requires advanced programming experience. PredPsych is a user-friendly toolbox based on machine learning predictive algorithms. It comprises of multiple functionalities for multivariate analyses of quantitative behavioral data based on machine learning models.

Perform permutation-based hypothesis testing for randomized experiments as suggested in Ludbrook & Dudley (1998) <doi:10.2307/2685470> and Ernst (2004) <doi:10.1214/088342304000000396>, introduced in Pham et al. (2022) <doi:10.1016/j.chemosphere.2022.136736>.

Facilitates analysis of paleontological sequences of trait values. Functions are provided to fit, using maximum likelihood, simple evolutionary models (including unbiased random walks, directional evolution,stasis, Ornstein-Uhlenbeck, covariate-tracking) and complex models (punctuation, mode shifts).

Sensitivity and power analysis, for calculating statistics describing pedigrees from wild populations, and for visualizing pedigrees. This is a reboot of the methods developed by Morrissey and Wilson (2010) <doi: 10.1111/j.1755-0998.2009.02817.x>.

This package provides functions and example datasets for phytosociological analysis, forest inventory, biomass and carbon estimation, and visualization of vegetation data. Includes functions to compute structural parameters [phytoparam(), summary.param(), stats()], estimate above-ground biomass and carbon [AGB()], stratify wood volume by diameter at breast height (DBH) classes [stratvol()], generate collector and rarefaction curves [collector.curve(), rarefaction()], and visualize basal areas on quadrat maps [BAplot(), including rectangular plots and individual coordinates]. Several example datasets are provided to demonstrate the functionality of these tools. For more details see FAO (1981, ISBN:92-5-101132-X) "Manual of forest inventory", IBGE (2012, ISBN:9788524042720) "Manual técnico da vegetação brasileira" and Heringer et al. (2020) "Phytosociology in R: A routine to estimate phytosociological parameters" <doi:10.22533/at.ed.3552009033>.

Defines functions to describe regression models using only pre-computed summary statistics (i.e. means, variances, and covariances) in place of individual participant data. Possible models include linear models for linear combinations, products, and logical combinations of phenotypes. Implements methods presented in Wolf et al. (2021) <doi:10.3389/fgene.2021.745901> Wolf et al. (2020) <doi:10.1142/9789811215636_0063> and Gasdaska et al. (2019) <doi:10.1142/9789813279827_0036>.

This package provides a variety of tools relevant to the analysis of marine soundscape data. There are tools for downloading AIS (automatic identification system) data from Marine Cadastre <https://hub.marinecadastre.gov>, connecting AIS data to GPS coordinates, plotting summaries of various soundscape measurements, and downloading relevant environmental variables (wind, swell height) from the National Center for Atmospheric Research data server <https://gdex.ucar.edu/datasets/d084001/>. Most tools were developed to work well with output from Triton software, but can be adapted to work with any similar measurements.

It creates a lattice plot to visualize panel or longitudinal data. The observed values are plotted as dots and the fitted values as lines, both against time. The plot is customizable and easy to edit, even if you do not know how to construct a lattice plot from scratch.

In causal mediation analysis with multiple causally ordered mediators, a set of path-specific effects are identified under standard ignorability assumptions. This package implements an imputation approach to estimating these effects along with a set of bias formulas for conducting sensitivity analysis (Zhou and Yamamoto <doi:10.31235/osf.io/2rx6p>). It contains two main functions: paths() for estimating path-specific effects and sens() for conducting sensitivity analysis. Estimation uncertainty is quantified using the nonparametric bootstrap.

Makes it easy to push data to Power BI using R and the Power BI REST APIs (see <https://docs.microsoft.com/en-us/rest/api/power-bi/>). A set of functions for turning data frames into Power BI datasets and refreshing these datasets are provided. Administrative tasks such as monitoring refresh statuses and pulling metadata about workspaces and users are also supported.

Use phenotype risk scores based on linked clinical and genetic data to study Mendelian disease and rare genetic variants. See Bastarache et al. 2018 <doi:10.1126/science.aal4043>.

In short, this package is a locator for cool, refreshing beverages. It will find and return the nearest location where you can get a cold one.

Given k populations (can be in thousands), what is the probability that a given subset of size t contains the true top t populations? This package finds this probability and offers three tuning parameters (G, d, L) to relax the definition.

Easy and efficient access to the API provided by Prevedere', an industry insights and predictive analytics company. Query and download indicators, models and workbenches built with Prevedere for further analysis and reporting <https://www.prevedere.com/>.

This package provides tools for anonymizing sensitive patient and research data. Helps protect privacy while keeping data useful for analysis. Anonymizes IDs, names, dates, locations, and ages while maintaining referential integrity. Methods based on: Sweeney (2002) <doi:10.1142/S0218488502001648>, Dwork et al. (2006) <doi:10.1007/11681878_14>, El Emam et al. (2011) <doi:10.1371/journal.pone.0028071>, Fung et al. (2010) <doi:10.1145/1749603.1749605>.

Calculates multivariate analysis of variance based on permutations and some associated pictorial representations. The pictorial representation is based on the principal coordinates of the group means. There are some original results that will be published soon.

This package implements a phylogeny-aware Bayesian graphical modeling framework for microbial network inference using a shrinkage precision estimator guided by a phylogenetic kernel, with optional hyperparameter-ensemble edge reliability analysis.

The purpose of PH1XBAR is to build a Phase I Shewhart control chart for the basic Shewhart, the variance components and the ARMA models in R for subgrouped and individual data. More details can be found: Yao and Chakraborti (2020) <doi: 10.1002/qre.2793>, Yao and Chakraborti (2021) <doi: 10.1080/08982112.2021.1878220>, and Yao et al. (2023) <doi: 10.1080/00224065.2022.2139783>.