Abstract:We present a new toolbox and library of standardised tractography protocols devised for the robust automated extraction of white matter tracts both in the human and the macaque brain. Using in vivo data from the Human Connectome Project (HCP) and the UK Biobank and ex vivo data for the macaque brain datasets, we obtain white matter atlases, as well as atlases for tract endpoints on the white-grey matter boundary, for both species. We illustrate that our protocols are robust against data quality, generalisable … Show more
“…All tractography protocols except for those of the cross-hemispheric structures use the sagittal midline as an exclusion mask to prevent streamline propagation into the contralateral hemisphere. These tract protocols allow for reproducible tractography of pigs registered to the common PNI50 space and are compatible with the recently released XTRACT package 21 . The repository we present here provides all 27 tractography protocols, the nal tracts used to construct the connectivity blueprint, and the corresponding data-driven ICAs for each tract 18,27 .…”
Section: Resultsmentioning
confidence: 99%
“…The volumetric and surface template les are included in the data and code release (https://github.com/neurabenn/pig_connectivity_bp_preprint), opening our data-driven and protocolbased tractography methods to be used by other researchers. All protocols were de ned in the PNI50 and form part of an open resource for pig researchers compatible with FSL's Xtract and autoPtx 20,21 .…”
Section: Discussionmentioning
confidence: 99%
“…Using anatomical and diffusion-weighted imaging (DWI), we then characterize the white matter structural organization in a subgroup of six pigs in an exploratory data-driven analysis ( Figure 1A) 18,19 . Our exploratory analysis overcomes the scarcity of knowledge regarding the pig's white matter architecture and was used to guide the de nition of hand-drawn tractography protocols in the PNI50 space for automated tractography in FSL autoPTX and Xtract 20,21 . We delineated 27 tracts to include in our WM atlas of the pig, including the projection, cross-hemispheric, association, and limbic tracts.…”
The characterization and definition of homology in the cerebral cortex needed for a species to be adopted as a translational model in neuroscience is a unique challenge given the diverse array of cortical morphology present in the mammalian lineage. Using the domestic pig as an example, we provide a roadmap of how leveraging Magnetic Resonance Imaging of the brain and data-driven tractography can overcome these obstacles and facilitate cortical alignment between distantly related species. In doing so, we created a full platform of neuroimaging tools to be used in the pig, including volumetric and surface templates, a structural white matter atlas, and the establishment of a common connectivity space to facilitate pig-human cortical alignment. Releasing our data and code and our pig-human cortical alignment, we permit researchers already working with the pig to accentuate the clinical relevance and translational capacity of their work. By sharing the intermediate outputs and scripts used to construct our pig-human cortical alignment, we also provide a roadmap to expand the current repertoire of animal models used in neuroscience.
“…All tractography protocols except for those of the cross-hemispheric structures use the sagittal midline as an exclusion mask to prevent streamline propagation into the contralateral hemisphere. These tract protocols allow for reproducible tractography of pigs registered to the common PNI50 space and are compatible with the recently released XTRACT package 21 . The repository we present here provides all 27 tractography protocols, the nal tracts used to construct the connectivity blueprint, and the corresponding data-driven ICAs for each tract 18,27 .…”
Section: Resultsmentioning
confidence: 99%
“…The volumetric and surface template les are included in the data and code release (https://github.com/neurabenn/pig_connectivity_bp_preprint), opening our data-driven and protocolbased tractography methods to be used by other researchers. All protocols were de ned in the PNI50 and form part of an open resource for pig researchers compatible with FSL's Xtract and autoPtx 20,21 .…”
Section: Discussionmentioning
confidence: 99%
“…Using anatomical and diffusion-weighted imaging (DWI), we then characterize the white matter structural organization in a subgroup of six pigs in an exploratory data-driven analysis ( Figure 1A) 18,19 . Our exploratory analysis overcomes the scarcity of knowledge regarding the pig's white matter architecture and was used to guide the de nition of hand-drawn tractography protocols in the PNI50 space for automated tractography in FSL autoPTX and Xtract 20,21 . We delineated 27 tracts to include in our WM atlas of the pig, including the projection, cross-hemispheric, association, and limbic tracts.…”
The characterization and definition of homology in the cerebral cortex needed for a species to be adopted as a translational model in neuroscience is a unique challenge given the diverse array of cortical morphology present in the mammalian lineage. Using the domestic pig as an example, we provide a roadmap of how leveraging Magnetic Resonance Imaging of the brain and data-driven tractography can overcome these obstacles and facilitate cortical alignment between distantly related species. In doing so, we created a full platform of neuroimaging tools to be used in the pig, including volumetric and surface templates, a structural white matter atlas, and the establishment of a common connectivity space to facilitate pig-human cortical alignment. Releasing our data and code and our pig-human cortical alignment, we permit researchers already working with the pig to accentuate the clinical relevance and translational capacity of their work. By sharing the intermediate outputs and scripts used to construct our pig-human cortical alignment, we also provide a roadmap to expand the current repertoire of animal models used in neuroscience.
“…Despite the large potential of diffusion imaging for exploring early developmental stages of the brain, current analysis techniques follow the paradigms that have been established for the adult brain. For instance, dMRI tractography protocols for identifying specific white matter bundles typically rely on delineation of regions of interest (ROIs) that provide a priori anatomical knowledge on the route of the tract; and these ROIs can be defined relative to a template for automated delineation de Groot et al, 2013;Warrington et al, 2019).…”
Mapping connections in the neonatal brain can provide insight into the crucial early stages of neurodevelopment that shape brain organisation and lay the foundations for cognition and behaviour. Diffusion MRI and tractography provide unique opportunities for such explorations, through estimation of white matter bundles and brain connectivity. Atlas-based tractography protocols, i.e. a priori defined sets of masks and logical operations in a template space, have been commonly used in the adult brain to drive such explorations. However, rapid growth and maturation of the brain during early development make it challenging to ensure correspondence and validity of such atlas-based tractography approaches in the developing brain. An alternative can be provided by data-driven methods, which do not depend on predefined regions of interest. Here, we develop a novel data-driven framework to extract white matter bundles and their associated grey matter networks from neonatal tractography data, based on non-negative matrix factorisation that is inherently suited to the non-negative nature of structural connectivity data. We also develop a non-negative dual regression framework to map group-level components to individual subjects. Using in-silico simulations, we evaluate the accuracy of our approach in extracting connectivity components and compare with an alternative data-driven method, independent component analysis. We apply non-negative matrix factorisation to whole-brain connectivity obtained from publicly available datasets from the Developing Human Connectome Project, yielding grey matter components and their corresponding white matter bundles. We assess the validity and interpretability of these components against traditional tractography results and grey matter networks obtained from resting-state fMRI in the same subjects. We subsequently use them to generate a parcellation of the neonatal cortex using data from 323 new-born babies and we assess the robustness and reproducibility of this connectivity-driven parcellation.
“…Six methods for tractography and virtual bundle dissection were employed on all diffusion datasets in native space (Figure 2, Subjectlevel processing). These included (1) TractSeg [50], (2) Recobundles [45], (3) Tracula [33], (4) XTract [51], (5) Automatic Fibertract Quantification (AFQ) [52], and (6) post-processing of AFQ where only the stem of the bundle was retained, which we call AFQ-clipped.…”
Brain atlases have proven to be valuable neuroscience tools for localizing regions of interest and performing statistical inferences on populations. Although many human brain atlases exist, most do not contain information about white matter structures, often neglecting them completely or labelling all white matter as a single homogenous substrate. While few white matter atlases do exist based on diffusion MRI fiber tractography, they are often limited to descriptions of white matter as spatially separate "regions" rather than as white matter "bundles" or fascicles, which are well-known to overlap throughout the brain. Additional limitations include small sample sizes, few white matter pathways, and the use of outdated diffusion models and techniques. Here, we present a new population-based collection of white matter atlases represented in both volumetric and surface coordinates in a standard space. These atlases are based on 2443 subjects, and include 216 white matter bundles derived from 6 different state-of-the-art tractography techniques. This atlas is freely available and will be a useful resource for parcellation and segmentation.
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