CIFTI files contain brain imaging data in “grayordinates,” which
represent the gray matter as cortical surface vertices (left and right)
and subcortical voxels (cerebellum, basal ganglia, and other deep gray
matter). ciftiTools
provides a unified environment for
reading, writing, visualizing and manipulating CIFTI-format data. It
supports the “dscalar,” “dlabel,” and “dtseries” intents. Grayordinate
data is read in as a "xifti"
object, which is structured
for convenient access to the data and metadata, and includes support for
surface geometry files to enable spatially-dependent functionality such
as static or interactive visualizations and smoothing.
If you use ciftiTools
, please cite our paper:
Pham, D. D., Muschelli, J., & Mejia, A. F. (2022). ciftiTools: A package for reading, writing, visualizing, and manipulating CIFTI files in R. NeuroImage, 250, 118877.
You can also obtain citation information from within R like so:
citation("ciftiTools")
You can install ciftiTools
from CRAN with:
install.packages("ciftiTools")
Additionally, most of the ciftiTools
functions require
the Connectome Workbench, which can be installed from the HCP
website.
# Load the package and point to the Connectome Workbench --------
library(ciftiTools)
ciftiTools.setOption("wb_path", "path/to/workbench")
# Read and visualize a CIFTI file -------------------------------
<- ciftiTools::ciftiTools.files()$cifti["dtseries"]
cifti_fname <- ciftiTools.files()$surf["left"]
surfL_fname <- ciftiTools.files()$surf["right"]
surfR_fname
<- read_cifti(
xii
cifti_fname, surfL_fname=surfL_fname, surfR_fname=surfR_fname,
resamp_res=4000
)
view_xifti_surface(xii) # or plot(xii)
# view_xifti_volume(xii) if subcortex is present
# Access CIFTI data ---------------------------------------------
<- xii$data$cortex_left
cortexL <- xii$meta$medial_wall_mask$left
cortexL_mwall <- xii$data$cortex_right
cortexR <- xii$meta$medial_wall_mask$right
cortexR_mwall # subcortVol <- xii$data$subcort
# subcortLabs <- xii$meta$subcort$labels
# subcortMask <- xii$meta$subcort$mask
<- xii$surf$cortex_left
surfL <- xii$surf$cortex_right
surfR
# Create a `"xifti"` from data ----------------------------------
<- as.xifti(
xii2 cortexL=cortexL, cortexL_mwall=cortexL_mwall,
cortexR=cortexR, cortexR_mwall=cortexR_mwall,
#subcortVol=subcortVol, subcortLabs=subcortLabs,
#subcortMask=subcortMask,
surfL=surfL, surfR=surfR
)
# Write a CIFTI file --------------------------------------------
write_cifti(xii2, "my_cifti.dtseries.nii")
See this link to view the tutorial vignette.
Basics: reading, plotting, writing
ciftiTools.setOption
: Necessary to point to the
Connectome Workbench each time ciftiTools
is loaded.read_cifti
: Read in a CIFTI file as a
"xifti"
object.view_xifti
Plot the cortex and/or subcortex. Has many
options for controlling the visualization.write_cifti
: Write a "xifti"
object to a
CIFTI file.Manipulating CIFTI files
resample_cifti
: Resample to a different
resolution.separate_cifti
: Separate a CIFTI file into GIFTI and
NIFTI files.smooth_cifti
: Smooth the data along the surface.run_wb_cmd
to execute Connectome Workbench
commands from R)Manipulating "xifti"
objects
apply_xifti
: Similar to base::apply
.combine_xifti
: Combine "xifti"
s with
non-overlapping brain structures.convert_xifti
: Convert between dlabel, dscalar, and
dtseries.merge_xifti
: Concatenate "xifti"
s.move_from_mwall
: Convert the medial wall mask to a data
value, deleting the mask.move_to_mwall
: Mask out a particular data value.newdata_xifti
: Replace the data values.resample_xifti
: Resample to a different
resolution.scale_xifti
: Similar to base::scale
.select_xifti
: Rearrange the columns to reorder, take a
subset, or repeat them.smooth_xifti
: Smooth the data along the surface.transform_xifti
: Apply a vectorizable function.Surface gemoetry
load_surf
: Load a surface geometry included in the
package.read_surf
: Read in a GIFTI surface geometry file as a
"surf"
object.write_surf
: Write a "surf"
object to a
GIFTI surface geometry file.Parcellations
apply_parc
: Apply a function to each parcel
separately.load_parc
: Load a parcellation included in the
package.See NAMESPACE
for a full list of all exported
functions.
"xifti"
?The "xifti"
object is a general interface for not only
CIFTI files, but also GIFTI and NIFTI files. For example, we can plot a
surface GIFTI:
<- as.xifti(surfL=read_surf(ciftiTools.files()$surf["left"]))
xii plot(xii)
We can also convert metric GIFTI files and/or NIFTI files to CIFTI
files (or vice versa) using the "xifti"
object as an
intermediary.
The 3D shading may make certain plots more difficult to interpret, if
the color scale varies from light to dark: darker regions might be in a
shadow, or their values might be higher. To skip shading, use the
argument material=list(lit=FALSE)
to
view_xifti_surface
.
VoxelIndicesIJK
or the MNI coordinates for the
subcortex?For a "xifti"
object xii
with subcortical
data, the mask of data locations are saved in
xii$meta$subcort$mask
. To obtain the array coordinates of
the in-mask locations, use
which(xii$meta$subcort$mask, arr.ind=TRUE) - 1
. This matrix
has each subcortical voxel along the rows, and its I, J, and K array
coordinates along the three columns. 1 is subtracted because the
coordinates should begin with 0 rather than 1. It’s equivalent to the
original CIFTI metadata entry VoxelIndicesIJK
. To convert
array coordinates to MNI coordinates, multiply by the transformation
matrix xii$meta$subcort$trans_mat
:
VoxIJK <- which(xii$meta$subcort$mask, arr.ind=TRUE) - 1
VoxIJK <- cbind(VoxIJK, 1) # for 4th col of transform mat (translation)
VoxXYZ <- t(xii$meta$subcort$trans_mat[seq(3),] %*% t(VoxIJK)) # MNI coords
oro.nifti
,
RNifti
gifti
cifti
can read in any CIFTI file, whereas ciftiTools
provides a
user-friendly interface for CIFTI files with the dscalar, dlabel, and
dtseries intents only.fsbrain
xml2
rgl
The following data are included in the package for convenience:
Example CIFTI files provided by NITRC.
Cortical surfaces provided by the HCP, according to the Data Use Terms:
Data were provided [in part] by the Human Connectome Project, WU-Minn Consortium (Principal Investigators: David Van Essen and Kamil Ugurbil; 1U54MH091657) funded by the 16 NIH Institutes and Centers that support the NIH Blueprint for Neuroscience Research; and by the McDonnell Center for Systems Neuroscience at Washington University.
Several parcellations provided by Thomas Yeo’s Computational Brain Imaging Group (CBIG):