5,146 research outputs found
Coupled non-parametric shape and moment-based inter-shape pose priors for multiple basal ganglia structure segmentation
This paper presents a new active contour-based, statistical method for simultaneous volumetric segmentation of multiple subcortical structures in the brain. In biological tissues, such as the human brain, neighboring structures exhibit co-dependencies which can aid in segmentation, if properly analyzed and modeled. Motivated by this observation, we formulate the segmentation problem as a maximum a posteriori estimation problem, in which we incorporate statistical prior models on the shapes and inter-shape (relative) poses of the structures of interest. This provides a principled mechanism to bring high level information about the shapes and the relationships of anatomical structures into the segmentation problem. For learning the prior densities we use a nonparametric multivariate kernel density estimation framework. We combine these priors with data in a variational framework and develop an active contour-based iterative segmentation algorithm.
We test our method on the problem of volumetric segmentation of basal ganglia structures in magnetic resonance (MR) images.
We present a set of 2D and 3D experiments as well as a quantitative performance analysis. In addition, we perform a comparison to several existent segmentation methods and demonstrate the improvements provided by our approach in terms of segmentation accuracy
The ENIGMA Stroke Recovery Working Group: Big data neuroimaging to study brainâbehavior relationships after stroke
The goal of the Enhancing Neuroimaging Genetics through MetaâAnalysis (ENIGMA) Stroke Recovery working group is to understand brain and behavior relationships using wellâpowered metaâ and megaâanalytic approaches. ENIGMA Stroke Recovery has data from over 2,100 stroke patients collected across 39 research studies and 10 countries around the world, comprising the largest multisite retrospective stroke data collaboration to date. This article outlines the efforts taken by the ENIGMA Stroke Recovery working group to develop neuroinformatics protocols and methods to manage multisite stroke brain magnetic resonance imaging, behavioral and demographics data. Specifically, the processes for scalable data intake and preprocessing, multisite data harmonization, and largeâscale stroke lesion analysis are described, and challenges unique to this type of big data collaboration in stroke research are discussed. Finally, future directions and limitations, as well as recommendations for improved data harmonization through prospective data collection and data management, are provided
Investigating microstructural variation in the human hippocampus using non-negative matrix factorization
In this work we use non-negative matrix factorization to identify patterns of microstructural variance in the human hippocampus. We utilize high-resolution structural and diffusion magnetic resonance imaging data from the Human Connectome Project to query hippocampus microstructure on a multivariate, voxelwise basis. Application of non-negative matrix factorization identifies spatial components (clusters of voxels sharing similar covariance patterns), as well as subject weightings (individual variance across hippocampus microstructure). By assessing the stability of spatial components as well as the accuracy of factorization, we identified 4 distinct microstructural components. Furthermore, we quantified the benefit of using multiple microstructural metrics by demonstrating that using three microstructural metrics (T1-weighted/T2-weighted signal, mean diffusivity and fractional anisotropy) produced more stable spatial components than when assessing metrics individually. Finally, we related individual subject weightings to demographic and behavioural measures using a partial least squares analysis. Through this approach we identified interpretable relationships between hippocampus microstructure and demographic and behavioural measures. Taken together, our work suggests non-negative matrix factorization as a spatially specific analytical approach for neuroimaging studies and advocates for the use of multiple metrics for data-driven component analyses
Segmentation of brain MRI during early childhood
The objective of this thesis is the development of automatic methods to measure the changes in
volume and growth of brain structures in prematurely born infants. Automatic tools for accurate
tissue quantification from magnetic resonance images can provide means for understanding
how the neurodevelopmental effects of the premature birth, such as cognitive, neurological or
behavioural impairment, are related to underlying changes in brain anatomy. Understanding
these changes forms a basis for development of suitable treatments to improve the outcomes of
premature birth.
In this thesis we focus on the segmentation of brain structures from magnetic resonance images
during early childhood. Most of the current brain segmentation techniques have been focused
on the segmentation of adult or neonatal brains. As a result of rapid development, the brain
anatomy during early childhood differs from anatomy of both adult and neonatal brains and
therefore requires adaptations of available techniques to produce good results.
To address the issue of anatomical differences of the brain during early childhood compared
to other age-groups, population-specific deformable and probabilistic atlases are introduced. A
method for generation of population-specific prior information in form of a probabilistic atlas
is proposed and used to enhance existing segmentation algorithms.
The evaluation of registration-based and intensity-based approaches shows the techniques to
be complementary in the quality of automatic segmentation in different parts of the brain. We
propose a novel robust segmentation method combining the advantages of both approaches. The
method is based on multiple label propagation using B-spline non-rigid registration followed by
EM segmentation.
Intensity inhomogeneity is a shading artefact resulting from the acquisition process, which
significantly affects modern high resolution MR data acquired at higher magnetic field strengths.
A novel template based method focused on correcting the intensity inhomogeneity in data
acquired at higher magnetic field strengths is therefore proposed.
The proposed segmentation method combined with proposed intensity inhomogeneity correction
method offers a robust tool for quantification of volumes and growth of brain structures during
early childhood. The tool have been applied to 67 T1-weigted images of subject at one and two years of age
Simultaneous lesion and neuroanatomy segmentation in Multiple Sclerosis using deep neural networks
Segmentation of both white matter lesions and deep grey matter structures is
an important task in the quantification of magnetic resonance imaging in
multiple sclerosis. Typically these tasks are performed separately: in this
paper we present a single segmentation solution based on convolutional neural
networks (CNNs) for providing fast, reliable segmentations of multimodal
magnetic resonance images into lesion classes and normal-appearing grey- and
white-matter structures. We show substantial, statistically significant
improvements in both Dice coefficient and in lesion-wise specificity and
sensitivity, compared to previous approaches, and agreement with individual
human raters in the range of human inter-rater variability. The method is
trained on data gathered from a single centre: nonetheless, it performs well on
data from centres, scanners and field-strengths not represented in the training
dataset. A retrospective study found that the classifier successfully
identified lesions missed by the human raters.
Lesion labels were provided by human raters, while weak labels for other
brain structures (including CSF, cortical grey matter, cortical white matter,
cerebellum, amygdala, hippocampus, subcortical GM structures and choroid
plexus) were provided by Freesurfer 5.3. The segmentations of these structures
compared well, not only with Freesurfer 5.3, but also with FSL-First and
Freesurfer 6.0
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