8,399 research outputs found
Orientation matching for diffusion tensor image registration.
This thesis develops a registration algorithm specifically for diffusion-tensor (DT) images. The proposed approach matches the tensor orientations to find the registration transformation. Early results show that local optimisation does not find the global minimum in registration of DT-MR brain images. Therefore, a global optimisation registration technique is also implemented. This thesis proposes several new similarity measures for DT registration and provides a comparison of them along with several others previously proposed in the literature. The thesis also proposes several new performance evaluation measures to assess registration quality and develops a performance evaluation framework that uses directional coherence and landmark separation. Experiments with direct optimisation demonstrate increased local minima in tensor registration objective functions over scalar registration. Using registration with global optimisation, this thesis compares the performance of scalar-derived similarity measures with those derived from the full tensor. Results suggest that similarity measures derived from the full tensor matrix do not find a more accurate registration than those based on the derived scalar indices. Affine and higher-order polynomial registration is not reliable enough to make a firm conclusion about whether diffusion tensor orientation matching improves the accuracy of registration over registration algorithms that ignore orientation. The main problem preventing a firm conclusion is that the local minima problem persists despite the use of global optimisation, causing poor registration of the regions of interest
Spatial transformations of diffusion tensor magnetic resonance images
The authors address the problem of applying spatial transformations (or “image warps”) to diffusion tensor magnetic resonance images. The orientational information that these images contain must be handled appropriately when they are transformed spatially during image registration. The authors present solutions for global transformations of three-dimensional images up to 12-parameter affine complexity and indicate how their methods can be extended for higher order transformations. Several approaches are presented and tested using synthetic data. One method, the preservation of principal direction algorithm, which takes into account shearing, stretching and rigid rotation, is shown to be the most effective. Additional registration experiments are performed on human brain data obtained from a single subject, whose head was imaged in three different orientations within the scanner. All of the authors' methods improve the consistency between registered and target images over naive warping algorithms
Diffeomorphic Metric Mapping of High Angular Resolution Diffusion Imaging based on Riemannian Structure of Orientation Distribution Functions
In this paper, we propose a novel large deformation diffeomorphic
registration algorithm to align high angular resolution diffusion images
(HARDI) characterized by orientation distribution functions (ODFs). Our
proposed algorithm seeks an optimal diffeomorphism of large deformation between
two ODF fields in a spatial volume domain and at the same time, locally
reorients an ODF in a manner such that it remains consistent with the
surrounding anatomical structure. To this end, we first review the Riemannian
manifold of ODFs. We then define the reorientation of an ODF when an affine
transformation is applied and subsequently, define the diffeomorphic group
action to be applied on the ODF based on this reorientation. We incorporate the
Riemannian metric of ODFs for quantifying the similarity of two HARDI images
into a variational problem defined under the large deformation diffeomorphic
metric mapping (LDDMM) framework. We finally derive the gradient of the cost
function in both Riemannian spaces of diffeomorphisms and the ODFs, and present
its numerical implementation. Both synthetic and real brain HARDI data are used
to illustrate the performance of our registration algorithm
Generating Diffusion MRI scalar maps from T1 weighted images using generative adversarial networks
Diffusion magnetic resonance imaging (diffusion MRI) is a non-invasive
microstructure assessment technique. Scalar measures, such as FA (fractional
anisotropy) and MD (mean diffusivity), quantifying micro-structural tissue
properties can be obtained using diffusion models and data processing
pipelines. However, it is costly and time consuming to collect high quality
diffusion data. Here, we therefore demonstrate how Generative Adversarial
Networks (GANs) can be used to generate synthetic diffusion scalar measures
from structural T1-weighted images in a single optimized step. Specifically, we
train the popular CycleGAN model to learn to map a T1 image to FA or MD, and
vice versa. As an application, we show that synthetic FA images can be used as
a target for non-linear registration, to correct for geometric distortions
common in diffusion MRI
Deep learning-based parameter mapping for joint relaxation and diffusion tensor MR Fingerprinting
Magnetic Resonance Fingerprinting (MRF) enables the simultaneous
quantification of multiple properties of biological tissues. It relies on a
pseudo-random acquisition and the matching of acquired signal evolutions to a
precomputed dictionary. However, the dictionary is not scalable to
higher-parametric spaces, limiting MRF to the simultaneous mapping of only a
small number of parameters (proton density, T1 and T2 in general). Inspired by
diffusion-weighted SSFP imaging, we present a proof-of-concept of a novel MRF
sequence with embedded diffusion-encoding gradients along all three axes to
efficiently encode orientational diffusion and T1 and T2 relaxation. We take
advantage of a convolutional neural network (CNN) to reconstruct multiple
quantitative maps from this single, highly undersampled acquisition. We bypass
expensive dictionary matching by learning the implicit physical relationships
between the spatiotemporal MRF data and the T1, T2 and diffusion tensor
parameters. The predicted parameter maps and the derived scalar diffusion
metrics agree well with state-of-the-art reference protocols. Orientational
diffusion information is captured as seen from the estimated primary diffusion
directions. In addition to this, the joint acquisition and reconstruction
framework proves capable of preserving tissue abnormalities in multiple
sclerosis lesions
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