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Mixed Model Association Test for GEne-Environment Interaction
Use a 'glmmkin' class object (GMMAT package) from the null model to perform generalized linear mixed model-based single-variant and variant set main effect tests, gene-environment interaction tests, and joint tests for association, as proposed in Wang et al. (2020)
Estimate (Generalized) Linear Mixed Models with Factor Structures
Utilizes the 'lme4' and 'optimx' packages (previously the optim()
function from 'stats') to estimate (generalized) linear mixed models (GLMM)
with factor structures using a profile likelihood approach, as outlined in
Jeon and Rabe-Hesketh (2012)
Robust Bayesian Longitudinal Regularized Semiparametric Mixed Models
Our recently developed fully robust Bayesian semiparametric mixed-effect model for high-dimensional longitudinal studies with heterogeneous observations can be implemented through this package. This model can distinguish between time-varying interactions and constant-effect-only cases to avoid model misspecifications. Facilitated by spike-and-slab priors, this model leads to superior performance in estimation, identification and statistical inference. In particular, robust Bayesian inferences in terms of valid Bayesian credible intervals on both parametric and nonparametric effects can be validated on finite samples. The Markov chain Monte Carlo algorithms of the proposed and alternative models are efficiently implemented in 'C++'.
Generalized Fiducial Inference for Normal Linear Mixed Models
Simulation of the generalized fiducial distribution for
normal linear mixed models with interval data. Fiducial inference is
somehow similar to Bayesian inference, in the sense that it is based
on a distribution that represents the uncertainty about the
parameters, like the posterior distribution in Bayesian statistics. It
does not require a prior distribution, and it yields results close to
frequentist results. Reference: Cisewski and Hannig (2012)
Variable Selection in Linear Mixed Models for SNP Data
Fit penalized multivariable linear mixed models with a single
random effect to control for population structure in genetic association
studies. The goal is to simultaneously fit many genetic variants at the
same time, in order to select markers that are independently associated
with the response. Can also handle prior annotation information,
for example, rare variants, in the form of variable weights. For more
information, see the website below and the accompanying paper:
Bhatnagar et al., "Simultaneous SNP selection and adjustment for
population structure in high dimensional prediction models", 2020,
Tables and Graphs for Mixed Models for Repeated Measures (MMRM)
Mixed models for repeated measures (MMRM) are a popular
choice for analyzing longitudinal continuous outcomes in randomized
clinical trials and beyond; see for example Cnaan, Laird and Slasor
(1997)
Bayesian Robust Generalized Mixed Models for Longitudinal Data
To perform model estimation using MCMC algorithms with Bayesian methods for incomplete longitudinal studies on binary and ordinal outcomes that are measured repeatedly on subjects over time with drop-outs. Details about the method can be found in the vignette or < https://sites.google.com/view/kuojunglee/r-packages/bayesrgmm>.
Fit a Cosinor Model Using a Generalized Mixed Modeling Framework
Allows users to fit a cosinor model using the 'glmmTMB' framework.
This extends on existing cosinor modeling packages, including 'cosinor'
and 'circacompare', by including a wide range of available link functions
and the capability to fit mixed models. The cosinor model is described by
Cornelissen (2014)
Partial Eta-Squared for Crossed, Nested, and Mixed Linear Mixed Models
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). 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. Methods are based on Correll, Mellinger, McClelland, and Judd
(2020)
Nonlinear Mixed Effects Models in Population PK/PD
Fit and compare nonlinear mixed-effects models in differential
equations with flexible dosing information commonly seen in pharmacokinetics
and pharmacodynamics (Almquist, Leander, and Jirstrand 2015