frdHouseTest {PMCMRplus} | R Documentation |
House Test
Description
Performs House nonparametric equivalent of William's test for contrasting increasing dose levels of a treatment in a complete randomized block design.
Usage
frdHouseTest(y, ...)
## Default S3 method:
frdHouseTest(y, groups, blocks, alternative = c("greater", "less"), ...)
Arguments
y |
a numeric vector of data values, or a list of numeric data vectors. |
groups |
a vector or factor object giving the group for the
corresponding elements of |
blocks |
a vector or factor object giving the block for the
corresponding elements of |
alternative |
the alternative hypothesis. Defaults to |
... |
further arguments to be passed to or from methods. |
Details
House test is a non-parametric step-down trend test for testing several treatment levels
with a zero control. Let there be groups including the control and let
the zero dose level be indicated with
and the highest
dose level with
, then the following
m = k - 1
hypotheses are tested:
Let be a i.i.d. random variable
of at least ordinal scale. Further, let
be Friedman's average ranks and set
to be its isotonic regression estimators under the order restriction
.
The statistics is
with
and
where is the number of tied ranks.
The critical -values
as given in the tables of Williams (1972) for
(one-sided)
are looked up according to the degree of freedoms (
) and the order number of the
dose level (
).
For the comparison of the first dose level with the control, the critical
z-value from the standard normal distribution is used (
Normal
).
Value
A list with class "PMCMR"
containing the following components:
- method
a character string indicating what type of test was performed.
- data.name
a character string giving the name(s) of the data.
- statistic
lower-triangle matrix of the estimated quantiles of the pairwise test statistics.
- p.value
lower-triangle matrix of the p-values for the pairwise tests.
- alternative
a character string describing the alternative hypothesis.
- p.adjust.method
a character string describing the method for p-value adjustment.
- model
a data frame of the input data.
- dist
a string that denotes the test distribution.
References
Chen, Y.-I., 1999. Rank-Based Tests for Dose Finding in Nonmonotonic Dose–Response Settings. Biometrics 55, 1258–1262. doi:10.1111/j.0006-341X.1999.01258.x
House, D.E., 1986. A Nonparametric Version of Williams’ Test for Randomized Block Design. Biometrics 42, 187–190.
See Also
friedmanTest
, friedman.test
,
frdManyOneExactTest
, frdManyOneDemsarTest
Examples
## Sachs, 1997, p. 675
## Six persons (block) received six different diuretics
## (A to F, treatment).
## The responses are the Na-concentration (mval)
## in the urine measured 2 hours after each treatment.
## Assume A is the control.
y <- matrix(c(
3.88, 5.64, 5.76, 4.25, 5.91, 4.33, 30.58, 30.14, 16.92,
23.19, 26.74, 10.91, 25.24, 33.52, 25.45, 18.85, 20.45,
26.67, 4.44, 7.94, 4.04, 4.4, 4.23, 4.36, 29.41, 30.72,
32.92, 28.23, 23.35, 12, 38.87, 33.12, 39.15, 28.06, 38.23,
26.65),nrow=6, ncol=6,
dimnames=list(1:6, LETTERS[1:6]))
## Global Friedman test
friedmanTest(y)
## Demsar's many-one test
summary(frdManyOneDemsarTest(y=y, p.adjust = "bonferroni",
alternative = "greater"))
## Exact many-one test
summary(frdManyOneExactTest(y=y, p.adjust = "bonferroni",
alternative = "greater"))
## Nemenyi's many-one test
summary(frdManyOneNemenyiTest(y=y, alternative = "greater"))
## House test
frdHouseTest(y, alternative = "greater")