VertexWiseR can be installed and loaded using the following code in R:
install.packages('VertexWiseR')
library(VertexWiseR)
##Alternatively
#install.packages("devtools")
#devtools::install_github("CogBrainHealthLab/VertexWiseR")VertexWiseR imports and makes use of the R package reticulate.
reticulate is a package that allows R to borrow or
translate python functions into R. Using reticulate, the package calls
functions from the BrainStat Python
module. Brainstat also comes with a number of fsaverage templates that
need to be downloaded for use with VertexWiseR cortical analyses.
For reticulate to work properly with VertexWiseR, the latest version
of Miniconda needs to be installed with it — Miniconda is a
lightweight version of Python, specifically for use within RStudio.
Alternatively, a suitable version of Python must be installed.
A function can be run to download and install all the system requirements (Miniconda, brainstat, BrainStat’s fsaverage/parcellation templates) if they are not installed yet:
VWRfirstrun()Note: A pop-up/prompt from reticulate asking ‘Would you like to create a default Python environment for the reticulate package?’ may appear. Clicking Yes will let reticulate install Python in a virtual environment. This is entirely optional. Simply click No/Cancel to ignore.
Alternatively, advanced users may specify a pre-installed python environment using reticulate’s use_python() or use_virtualenv() functions.
For this example, we use Spreng and colleagues’ neurocognitive aging openneuro dataset ds003592:
demodata = readRDS(system.file('demo_data/SPRENG_behdata_site1.rds', package = 'VertexWiseR'))The dataset T1 weighted images were preprocessed using the recon-all FreeSurfer pipeline. This tutorial will not reiterate these steps. For a detailed guide about surface extraction (from FreeSurfer, fMRIprep, HPC and HippUnfold outputs), see the Extracting surface data in VertexWiseR article.
Here, we explain how, from a given FreeSurfer subject directory, VertexWiseR extracts surface-based measures and synthesizes the whole-sample data into a compact matrix object (.rds) for later analyses.
SURFvextract() gives the opportunity to extract surface-based measures including ‘thickness’, ‘curv’, ‘sulc’, and ‘area’. Here, we are interested in cortical thickness:
SURFvextract(sdirpath = "MY_SUBJECTS_DIR/", filename = "SPRENG_CTv.rds", measure = "thickness") A cortical thickness (CT) matrix object extracted from the Spreng dataset is included in the VertexWiseR git repository and can be loaded with the following code:
SPRENG_CTv=readRDS(file=url("https://github.com/CogBrainHealthLab/VertexWiseR/blob/main/inst/demo_data/SPRENG_CTv_site1.rds?raw=TRUE"))VertexWiseR gives the option to smooth the surface data with a desired full width at half maximum (FWHM) value. It can also optionally directly be done as an option for RFT_vertex_analysis() which will be discussed below. Here, we smooth it before the analysis at 10 mm:
SPRENG_CTv = smooth_surf(SPRENG_CTv, 10)The vertex-wise analysis model works as a multiple regression model
where the Dependent Variable/outcome is the CT at each vertex, and you
will decide which Independent Variables/predictors to enter into the
model to predict the vertices’ CT. In this example, we shall use
age and sex to predict CT. Among these IVs, we
are mostly interested in age, sex being entered into the model to
control for its confounding influence on CT. We thus select those two
variables and save them into a new data.frame called
all_pred.
all_pred=demodata[,c("sex","age")]
head(all_pred)## sex age
## 1 F 21
## 2 F 73
## 3 F 77
## 4 M 68
## 5 F 60
## 6 F 71The next code chunk runs the analysis. There is an optional
p parameter for the RFT_vertex_analysis()
function to specify the p threshold; default p is set to 0.05. The atlas
with which to label the significant clusters can also be set
(1=aparc/Desikan-Killiany-70 (default), 2=Schaefer-100, 3=Schaefer-200,
4=Glasser-360, 5=Destrieux-148).
The second line displays the results.
results=RFT_vertex_analysis(model = all_pred, contrast =all_pred$age, surf_data = SPRENG_CTv, atlas = 1)
print(results$cluster_level_results)## $`Positive contrast`
## clusid nverts P X Y Z tstat region
## 1 1 142 0.015 -22.8 11.5 -42 6.45 lh-temporalpole
## $`Negative contrast`
## clusid nverts P X Y Z tstat region
## 1 1 8039 <0.001 47 4.0 -16.6 -12.64 rh-superiortemporal
## 2 2 7660 <0.001 -34 -25.7 16.2 -14.23 lh-insulaIn the above results, the clusters that appear under the
Positive contrast section are clusters of vertices which
correlate positively with your contrast variable,
vice-versa for the Negative contrast.
nverts: number of vertices in the cluster
P: p-value of the cluster
X, Y and Z: MNI coordinates of the vertex with the
highest t-stat in the cluster
tstat: t statistic of the vertex with the highest
t-stat in the cluster
region: the region this highest t-stat vertex is
located in. Here, it is determined/labelled using the Desikan
atlas
plot_surf(surf_data = results$thresholded_tstat_map, filename = 'sigcluster.png', surface = 'inflated', cmap = 'seismic')surf_data: A numeric vector (length of V) or a
matrix (N rows x V columns), where N is the number of subplots, and V is
the number of vertices. It can be the output from SURFvextract(),
FSLRvextract(), HIPvextract() as well as masks or vertex-wise results
outputted by analyses functions.
filename: A string object containing the desired
name of the output .png. Default is ‘plot.png’ in the R temporary
directory (tempdir()).Only filenames with a .png extension are
allowed.
cmap (optional) : A string object specifying the
name of an existing colormap or a vector of hexadecimal color codes to
be used as a custom colormap. The names of existing colormaps are listed
in the .
Default cmap is set to "Reds" for positive values,
"Blues_r" for negative values and "RdBu" when
both positive and negative values exist.
title (optional) : A string object for setting the
title in the plot. Default is none. For titles that too long to be fully
displayed within the plot, we recommend splitting them into multiple
lines by inserting “\n”.
surface (optional) : A string object containing the
name of the type of cortical surface background rendered. Possible
options include "white",
"smoothwm","pial" and "inflated"
(default). The surface parameter is ignored for hippocampal surface
data.
If you want to carry out some follow-up analyses (e.g., mediation),
you might want to extract, for each subject in the dataset, the mean CT
in the significant clusters colored in red (positive clusters). You can
simply do a matrix multiplication (operator for matrix multiplication
:%*%) between the CT data SPRENG_CTv and the
positive mask results$pos_mask . A mask in the context of
brain images refers to a vector of 1s and 0s. In this case, the vertices
which are within the significant clusters are coded as 1s, vertices
outside these significant clusters are coded as 0s.
sum(results$pos_mask) gives you the sum of all the 1s,
which essentially is the number of significant vertices.
Thus, the SPRENG_CTv %*% results$pos_mask is divided by
sum(results$pos_mask) to obtain an average CT value. Here,
this average CT is saved into a new variable sig_avCT
within the demodata dataframe.
demodata$sig_avCT=SPRENG_CTv %*% results$pos_mask/sum(results$pos_mask)
head(demodata$sig_avCT)## [,1]
##[1,] 2.769453
##[2,] 3.003829
##[3,] 2.586192
##[4,] 2.851196
##[5,] 3.199390
##[6,] 3.050331As a sanity check, these mean CT values should correlate with
age
cor.test(demodata$sig_avCT,demodata$age)##
##Pearson's product-moment correlation
##
##data: demodata$sig_avCT and demodata$age
##t = 4.826, df = 236, p-value = 2.502e-06
##alternative hypothesis: true correlation is not equal to 0
##95 percent confidence interval:
## 0.1793792 0.4111954
##sample estimates:
## cor
##0.2997047 After running the whole-brain vertex-wise analyses, you may be able
to identify regions in the brain in which cortical thickness (CT) values
are significantly different between groups or these CT values predict a
certain IV significantly. How do we make sense of these regions? We can
plot out the results using the plot_surf() function, but
still, it may be difficult to interpret the results in terms of the
functional relevance of the regions identified. Here we present a tool
that you can use to facilitate such interpretations.
What this tool does is correlate your input image (cortical surface maps obtained from an earlier vertex-wise analysis, currently supporting fsaverage5 surface space) with images from a large database of task-based fMRI and voxel-based morphometric studies. Each of these images in the database is tagged with a few keywords, describing the task and/or sample characteristics. The correlations that are carried out essentially measure how similar your input image is to each of the images in the database. Higher correlations would mean that your input image looks very similar to a certain image in the database, thus the keywords associated with that image in the database would be highly relevant to your input image.
In this example, we will first run a whole-brain vertex-wise analysis to compare the cortical thickness between males and females in the young adult population of the SPRENG dataset. The thresholded cortical surface maps obtained from this analysis will then be fed into an image-decoding procedure to identify keywords that are relevant to our results
The NiMARE python module is needed in order for the imaging decoding to work. It is similarly imported by VertexWiseR via reticulate in the decode_surf_data() function.
#filter out old participants
dat_beh=demodata[demodata$agegroup=="Y",]
dat_CT=SPRENG_CTv[demodata$agegroup=="Y",]
all_pred=dat_beh[,c("site","age","sex")]
head(all_pred)## site age sex
## 1 1 21 F
## 15 1 32 M
## 16 1 20 M
## 17 1 21 M
## 18 1 24 M
## 19 1 20 Mresults=RFT_vertex_analysis(model = all_pred, contrast =all_pred$sex, surf_data = dat_CT)
results$cluster_level_results## The binary variable 'sex' will be recoded with F=0 and M=1 for the analysis
##
## smooth_FWHM argument was not given. surf_data will not be smoothed here.
##
## $`Positive contrast`
## clusid nverts P X Y Z tstat region
## 1 1 301 <0.001 -40.7 -13.0 16.5 5.06 lh-postcentral
## 2 2 181 0.002 56.3 12.1 -10.1 4.43 rh-superiortemporal
## 3 3 150 0.003 21.9 -51.6 -1.2 4.41 rh-lingual
##
## $`Negative contrast`
## [1] "No significant clusters"plot_surf(surf_data = results$thresholded_tstat_map,filename = "sexdiff.png")
According to these results, since the female sex is coded as 0 and males as 1 (this can be done manually beforehand), the regions colored in red are thicker in males.
Now, let’s enter the thresholded_tstat_map into the
decode_img() function. The previous results only contained
positive clusters. But in case of bidirectionality, the function
requires to choose one direction with the contrast option. In this
instance, we simply decode the positive clusters, by setting
contrast="positive".
If you are running this for the first time, a ~7.5 MB file
neurosynth_dataset.pkl.gz needs to be downloaded to your
current directory for the decoding to work. This file will contain the
images from the Neurosynth
database that will be correlated with your input image. Run
VWRfirstrun(requirement=‘neurosynth’) to assist you with the data’s
installation.
keywords=decode_surf_data(surf_data=results$thresholded_tstat_map, contrast = "positive")##Converting and interpolating the surface data ...
##✓
## Correlating input image with images in the neurosynth database. This may take a while ...
##
##✓ print(keywords[1:10,])## keyword r
##449 pain 0.099
##50 auditory 0.098
##648 temporal 0.093
##617 speech 0.092
##334 listening 0.089
##607 sounds 0.070
##450 painful 0.068
##4 acoustic 0.062
##397 music 0.062
##398 musical 0.062The above procedure will display the top 10 keywords from images in
the database that are the most correlated with your input image.
According to these results, you can see that the positive clusters
(which are thicker in males) are typically found to be associated with
pain and auditory processing. If you simply run keyword
without specifying the index within the square brackets
[1:10,]. All 715 keywords will be displayed.
In your presentation slides or results section of your paper, you might want to illustrate these keywords using the wordcloud and paletteer packages. You can set the size of the keyword to vary according to its r value:
#install.packages("wordcloud","paletteer")
library(wordcloud)
library(paletteer)
wordcloud(words = keywords$keyword, ##keyword input
freq = keywords$r, ##setting the size of the keyword to vary with its r value
min.freq = 0.05, ##minimum r value in order for the keyword to be displayed
colors=paletteer_c("grDevices::Temps", 10) ##color scheme
,scale=c(1,2)
)
par(mar = rep(0, 4))
These keywords may not be very accurate but they should give a rough idea for interpreting your results. Take note that these keywords are specific to the positive clusters.