clme(formula, data, gfix = NULL, constraints = list(), tsf = lrt.stat, tsf.ind = w.stat.ind, mySolver = "LS", all_pair = FALSE, verbose = c(FALSE, FALSE, FALSE), levels = NULL, ncon = 1, ...)
ncon
terms will be assumed to be constrained.activeSet
).formula
that are constrained.clme
is an object of the class clme
, which is list with elements:
theta
estimates of $theta$ coefficients
theta
estimates of $theta_0$ coefficients under the null hypothesis
ssq
estimate of residual variance(s), $sigma.i^2$.
tsq
estimate of random effects variance component(s), $tau.i^2$.
cov.theta
the unconstrained covariance matrix of $theta$
ts.glb
test statistic for the global hypothesis.
ts.ind
test statistics for each of the constraints.
mySolver
the solver used for isotonization.
constraints
list containing the constraints (A
) and the contrast for the global test (B
).
dframe
data frame containing the variables in the model.
residuals
matrix containing residuals. For mixed models three types of residuals are given.
random.effects
estimates of random effects.
gfix
group sample sizes for residual variances.
gran
group sizes for random effect variance components.
gfix_group
group names for residual variances.
formula
the formula used in the model.
call
the function call.
order
list describing the specified or estimated constraints.
P1
the number of constrained parameters.
nsim
the number of bootstrap simulations used for inference.
clme_em
is run to obtain the observed values. If nsim
>0, a bootstrap test is performed
using resid_boot
.
For the argument levels
the first list element should be the column index (in data
) of the
constrained effect. The second element should be the true order of the levels.
data( rat.blood )
cons <- list(order="simple", decreasing=FALSE, node=1 )
clme.out <- clme(mcv ~ time + temp + sex + (1|id), data=rat.blood ,
constraints=cons, seed=42, nsim=10, ncon=1)
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