58 research outputs found
Liver segmentation using 3D CT scans.
Master of Science in Computer Science. University of KwaZulu-Natal, Durban, 2018.Abstract available in PDF file
SVRDA: A Web-based Dataset Annotation Tool for Slice-to-Volume Registration
Background and Objective: The lack of benchmark datasets has impeded the
development of slice-to-volume registration algorithms. Such datasets are
difficult to annotate, primarily due to the dimensional difference within data
and the dearth of task-specific software. We aim to develop a user-friendly
tool to streamline dataset annotation for slice-to-volume registration.
Methods: The proposed tool, named SVRDA, is an installation-free web
application for platform-agnostic collaborative dataset annotation. It enables
efficient transformation manipulation via keyboard shortcuts and smooth case
transitions with auto-saving. SVRDA supports configuration-based data loading
and adheres to the separation of concerns, offering great flexibility and
extensibility for future research. Various supplementary features have been
implemented to facilitate slice-to-volume registration.
Results: We validated the effectiveness of SVRDA by indirectly evaluating the
post-registration segmentation quality on UK Biobank data, observing a dramatic
overall improvement (24.02% in the Dice Similarity Coefficient and 48.93% in
the 95th percentile Hausdorff distance, respectively) supported by highly
statistically significant evidence ().We further showcased the
clinical usage of SVRDA by integrating it into test-retest T1 quantification on
in-house magnetic resonance images, leading to more consistent results after
registration.
Conclusions: SVRDA can facilitate collaborative annotation of benchmark
datasets while being potentially applicable to other pipelines incorporating
slice-to-volume registration. Full source code and documentation are available
at https://github.com/Roldbach/SVRDAComment: 18 pages, 11 figures, In submission to Computer Methods and Programs
in Biomedicin
Computerized Analysis of Magnetic Resonance Images to Study Cerebral Anatomy in Developing Neonates
The study of cerebral anatomy in developing neonates is of great importance for
the understanding of brain development during the early period of life. This
dissertation therefore focuses on three challenges in the modelling of cerebral
anatomy in neonates during brain development. The methods that have been
developed all use Magnetic Resonance Images (MRI) as source data.
To facilitate study of vascular development in the neonatal period, a set of image
analysis algorithms are developed to automatically extract and model cerebral
vessel trees. The whole process consists of cerebral vessel tracking from
automatically placed seed points, vessel tree generation, and vasculature
registration and matching. These algorithms have been tested on clinical Time-of-
Flight (TOF) MR angiographic datasets.
To facilitate study of the neonatal cortex a complete cerebral cortex segmentation
and reconstruction pipeline has been developed. Segmentation of the neonatal
cortex is not effectively done by existing algorithms designed for the adult brain
because the contrast between grey and white matter is reversed. This causes pixels
containing tissue mixtures to be incorrectly labelled by conventional methods. The
neonatal cortical segmentation method that has been developed is based on a novel
expectation-maximization (EM) method with explicit correction for mislabelled
partial volume voxels. Based on the resulting cortical segmentation, an implicit
surface evolution technique is adopted for the reconstruction of the cortex in
neonates. The performance of the method is investigated by performing a detailed
landmark study.
To facilitate study of cortical development, a cortical surface registration algorithm
for aligning the cortical surface is developed. The method first inflates extracted
cortical surfaces and then performs a non-rigid surface registration using free-form
deformations (FFDs) to remove residual alignment. Validation experiments using
data labelled by an expert observer demonstrate that the method can capture local
changes and follow the growth of specific sulcus
Studying neuroanatomy using MRI
The study of neuroanatomy using imaging enables key insights into how our brains function, are shaped by genes and environment, and change with development, aging, and disease. Developments in MRI acquisition, image processing, and data modelling have been key to these advances. However, MRI provides an indirect measurement of the biological signals we aim to investigate. Thus, artifacts and key questions of correct interpretation can confound the readouts provided by anatomical MRI. In this review we provide an overview of the methods for measuring macro- and mesoscopic structure and inferring microstructural properties; we also describe key artefacts and confounds that can lead to incorrect conclusions. Ultimately, we believe that, though methods need to improve and caution is required in its interpretation, structural MRI continues to have great promise in furthering our understanding of how the brain works
Foetal echocardiographic segmentation
Congenital heart disease affects just under one percentage of all live births [1].
Those defects that manifest themselves as changes to the cardiac chamber volumes
are the motivation for the research presented in this thesis.
Blood volume measurements in vivo require delineation of the cardiac chambers and
manual tracing of foetal cardiac chambers is very time consuming and operator
dependent. This thesis presents a multi region based level set snake deformable
model applied in both 2D and 3D which can automatically adapt to some extent
towards ultrasound noise such as attenuation, speckle and partial occlusion artefacts.
The algorithm presented is named Mumford Shah Sarti Collision Detection (MSSCD).
The level set methods presented in this thesis have an optional shape prior term for
constraining the segmentation by a template registered to the image in the presence
of shadowing and heavy noise.
When applied to real data in the absence of the template the MSSCD algorithm is
initialised from seed primitives placed at the centre of each cardiac chamber. The
voxel statistics inside the chamber is determined before evolution. The MSSCD stops
at open boundaries between two chambers as the two approaching level set fronts
meet. This has significance when determining volumes for all cardiac compartments
since cardiac indices assume that each chamber is treated in isolation. Comparison
of the segmentation results from the implemented snakes including a previous level
set method in the foetal cardiac literature show that in both 2D and 3D on both real
and synthetic data, the MSSCD formulation is better suited to these types of data.
All the algorithms tested in this thesis are within 2mm error to manually traced
segmentation of the foetal cardiac datasets. This corresponds to less than 10% of
the length of a foetal heart. In addition to comparison with manual tracings all the
amorphous deformable model segmentations in this thesis are validated using a
physical phantom. The volume estimation of the phantom by the MSSCD
segmentation is to within 13% of the physically determined volume
Connectomics across development:towards mapping brain structure from birth to childhood
The brain is probably the most complex system of the human body, composed of numerous neural units interconnected at dierent scales. This highly structured architecture provides the ability to communicate, synthesize information and perform the analytical tasks of human beings. Its development starts during the transition between the embryonic and fetal periods, from a simple tubular to a highly complex folded structure. It is globally organized as early as birth. This developing process is highly vulnerable to antenatal adverse conditions. Indeed, extreme prematurity and intra uterine growth restriction are major risk factors for long-term morbidities, including developmental ailments such as cerebral palsy, mental retardation and a wide spectrum of learning disabilities and behavior disorders. In this context, the characterization of the brainâs normative wiring pattern is crucial for our understanding of its architecture and workings, as the origin of many neurological and neurobehavioral disorders is found in early structural brain development. Diusion magnetic resonance imaging (dMRI) allows the in vivo assessment of biological tissues at the microstructural level. It has emerged as a powerful tool to study brain connectivity and analyse the underlying substrate of the human brain, comprising its structurally integrated and functionally specialized architecture. dMRI has been widely used in adult studies. Nevertheless, due to technical constraints, this mapping at earlier stages of development has not yet been accomplished. Yet, this time period is of extreme importance to comprehend the structural and functional integrity of the brain. This thesis is motivated by this shortfall, and intends to fill the gap between the clinical and neuroscience demands and the methodological developments needed to fulfill them. In our work, we comprehensibly study the brain structural connectivity of children born extremely prematurely and/or with additional prenatal restriction at school-age. We provide evidence that brain systems that mature early in development are the most vulnerable to antenatal insults. Interestingly, the alterations highlighted in these systems correlate with the neurobehavioral and cognitive impairments seen in these children at school-age. The overall brain organization appear also altered after preterm birth and prenatal restriction. Indeed, these children show dierent brain network modular topology, with a reduction in the overall network capacity. What remains unclear is whether the alterations seen at school age are already present at birth and, if yes, to what extent. In this thesis we set the technical basis to enable the connectome analysis as early as at birth. This task is challenging when dealing with neonatal data. Indeed, most of the assumptions used in adult data processing methods do not hold, due to the inverted image contrast and other MRI artefacts such as motion, partial volume and intensity inhomogeneities. Here, we propose a novel technique for surface reconstruction, and provide a fully-automatic procedure to delineate the newborn cortical surface, opening the way to establish the newborn connectome
Echocardiography
The book "Echocardiography - New Techniques" brings worldwide contributions from highly acclaimed clinical and imaging science investigators, and representatives from academic medical centers. Each chapter is designed and written to be accessible to those with a basic knowledge of echocardiography. Additionally, the chapters are meant to be stimulating and educational to the experts and investigators in the field of echocardiography. This book is aimed primarily at cardiology fellows on their basic echocardiography rotation, fellows in general internal medicine, radiology and emergency medicine, and experts in the arena of echocardiography. Over the last few decades, the rate of technological advancements has developed dramatically, resulting in new techniques and improved echocardiographic imaging. The authors of this book focused on presenting the most advanced techniques useful in today's research and in daily clinical practice. These advanced techniques are utilized in the detection of different cardiac pathologies in patients, in contributing to their clinical decision, as well as follow-up and outcome predictions. In addition to the advanced techniques covered, this book expounds upon several special pathologies with respect to the functions of echocardiography
Proceedings of the First International Workshop on Mathematical Foundations of Computational Anatomy (MFCA'06) - Geometrical and Statistical Methods for Modelling Biological Shape Variability
International audienceNon-linear registration and shape analysis are well developed research topic in the medical image analysis community. There is nowadays a growing number of methods that can faithfully deal with the underlying biomechanical behaviour of intra-subject shape deformations. However, it is more difficult to relate the anatomical shape of different subjects. The goal of computational anatomy is to analyse and to statistically model this specific type of geometrical information. In the absence of any justified physical model, a natural attitude is to explore very general mathematical methods, for instance diffeomorphisms. However, working with such infinite dimensional space raises some deep computational and mathematical problems. In particular, one of the key problem is to do statistics. Likewise, modelling the variability of surfaces leads to rely on shape spaces that are much more complex than for curves. To cope with these, different methodological and computational frameworks have been proposed. The goal of the workshop was to foster interactions between researchers investigating the combination of geometry and statistics for modelling biological shape variability from image and surfaces. A special emphasis was put on theoretical developments, applications and results being welcomed as illustrations. Contributions were solicited in the following areas: * Riemannian and group theoretical methods on non-linear transformation spaces * Advanced statistics on deformations and shapes * Metrics for computational anatomy * Geometry and statistics of surfaces 26 submissions of very high quality were recieved and were reviewed by two members of the programm committee. 12 papers were finally selected for oral presentations and 8 for poster presentations. 16 of these papers are published in these proceedings, and 4 papers are published in the proceedings of MICCAI'06 (for copyright reasons, only extended abstracts are provided here)
Studying neuroanatomy using MRI
The study of neuroanatomy using imaging enables key insights into how our brains function, are shaped by genes and environment, and change with development, aging, and disease. Developments in MRI acquisition, image processing, and data modelling have been key to these advances. However, MRI provides an indirect measurement of the biological signals we aim to investigate. Thus, artifacts and key questions of correct interpretation can confound the readouts provided by anatomical MRI. In this review we provide an overview of the methods for measuring macro- and mesoscopic structure and inferring microstructural properties; we also describe key artefacts and confounds that can lead to incorrect conclusions. Ultimately, we believe that, though methods need to improve and caution is required in its interpretation, structural MRI continues to have great promise in furthering our understanding of how the brain works
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