detect.ic {ccid} | R Documentation |
Multiple change-point detection in the cross-covariance structure of multivariate high-dimensional time series using a model selection criterion optimisation
Description
This function detects multiple change-points in the cross-covariance structure of a multivariate time series using a model selection criterion optimisation.
Usage
detect.ic(
X,
approach = c("euclidean", "infinity"),
th_max = 2.1,
th_sum = 0.5,
pointsgen = 10,
scales = -1,
alpha_gen = 0.1,
preaverage_gen = FALSE,
scal_gen = 3,
min_dist = 1
)
Arguments
X |
A numerical matrix representing the multivariate time series, with the columns representing its components. |
approach |
A character string, which defines the metric to be used in
order to detect the change-points. If approach = “euclidean”, which is
also the default value, then the |
th_max |
A positive real number with default value equal to 2.1. It is
used to define the threshold for the change-point overestimation step if
the |
th_sum |
A positive real number with default value equal to 0.5. It is
used to define the threshold for the change-point overestimation step if
the |
pointsgen |
A positive integer with default value equal to 10. It defines the distance between two consecutive end- or start-points of the right- or left-expanding intervals, respectively; see Details for more information. |
scales |
Negative integers for wavelet scales, with a small negative integer representing a fine scale. The default value is equal to -1. |
alpha_gen |
A positive real number with default value equal to 0.1. It is used to define how strict the user wants to be with the penalty used. |
preaverage_gen |
A logical variable with default value equal to
|
scal_gen |
A positive integer number with default value equal to 3.
It is used to define the way we pre-average the given data sequence
only if |
min_dist |
A positive integer number with default value equal to 1. It is used in order to provide the minimum distance acceptable between detected change-points if such restrictions apply. |
Details
The time series X_t
is of dimensionality p
and we are
looking for changes in the cross-covariance structure between the
different time series components
X_{t}^{(1)}, X_{t}^{(2)}, ..., X_{t}^{(p)}
. We first use a
wavelet-based approach for the various given scales in scales
in
order to transform the given time series X_t
to a multiplicative
model Y_{t}^{(k)} = \sigma^{(k)}_t (Z_t^{(k)})^2; t=1,2,\ldots,T; k = 1,2,\ldots,d,
where Z_t^{(k)}
is a sequence of standard normal random variables,
E(Y_t^{(k)}) = \sigma_t^{(k)}
, and d
is the new
dimensionality, which depends on the value given in scales
.
The function has been extensively tested on fMRI data, hence, its parameters
have been tuned for this data type. The function might not work well in other
structures, such as time series that are negatively serially correlated.
Value
A list with the following components:
changepoints | The locations of the detected change-points. |
no.of.cpts | The number of the detected change-points. |
sol_path | A vector containing the solution path. |
ic_curve | A vector with values of the information criterion for different number of change-points. |
If the minimum distance between the detected change-points is less than
the value given in min_dist
, then only the number and the locations of the
“pruned” change-points are returned.
Author(s)
Andreas Anastasiou, anastasiou.andreas@ucy.ac.cy
References
“Cross-covariance isolate detect: a new change-point method for estimating dynamic functional connectivity”, Anastasiou et al (2020), preprint <doi:10.1101/2020.12.20.423696>.
See Also
Examples
set.seed(11)
A <- matrix(rnorm(10*200), nrow = 200) ## No change-point
M1 <- detect.ic(A, approach = 'euclidean', scales = -1)
M2 <- detect.ic(A, approach = 'infinity', scales = -1)
M1$changepoints
M2$changepoints
set.seed(1)
num.nodes <- 30 # number of nodes
etaA.1 <- 0.95
etaA.2 <- 0.05
pcor1 <- GeneNet::ggm.simulate.pcor(num.nodes, etaA = etaA.1)
pcor2 <- GeneNet::ggm.simulate.pcor(num.nodes, etaA = etaA.2)
n <- 50
data1 <- GeneNet::ggm.simulate.data(n, pcor1)
data2 <- GeneNet::ggm.simulate.data(n, pcor2)
X1 <- rbind(data1, data2, data1, data2) ## change-points at 50, 100, 150
N1 <- detect.ic(X1, approach = 'euclidean', scales = -1)
N2 <- detect.ic(X1, approach = 'infinity', scales = -1)
N1$changepoints
N2$changepoints
N1$no.of.cpts
N2$no.of.cpts
N1$sol_path
N2$sol_path