11,463 research outputs found
MRI Super-Resolution using Multi-Channel Total Variation
This paper presents a generative model for super-resolution in routine
clinical magnetic resonance images (MRI), of arbitrary orientation and
contrast. The model recasts the recovery of high resolution images as an
inverse problem, in which a forward model simulates the slice-select profile of
the MR scanner. The paper introduces a prior based on multi-channel total
variation for MRI super-resolution. Bias-variance trade-off is handled by
estimating hyper-parameters from the low resolution input scans. The model was
validated on a large database of brain images. The validation showed that the
model can improve brain segmentation, that it can recover anatomical
information between images of different MR contrasts, and that it generalises
well to the large variability present in MR images of different subjects. The
implementation is freely available at https://github.com/brudfors/spm_superre
MRI super-resolution using multi-channel total variation
This paper presents a generative model for super-resolution in routine clinical magnetic resonance images (MRI), of arbitrary orientation and contrast. The model recasts the recovery of high resolution images as an inverse problem, in which a forward model simulates the slice-select profile of the MR scanner. The paper introduces a prior based on multi-channel total variation for MRI super-resolution. Bias-variance trade-off is handled by estimating hyper-parameters from the low resolution input scans. The model was validated on a large database of brain images. The validation showed that the model can improve brain segmentation, that it can recover anatomical information between images of different MR contrasts, and that it generalises well to the large variability present in MR images of different subjects
Joint Total Variation ESTATICS for Robust Multi-Parameter Mapping
Quantitative magnetic resonance imaging (qMRI) derives tissue-specific
parameters -- such as the apparent transverse relaxation rate R2*, the
longitudinal relaxation rate R1 and the magnetisation transfer saturation --
that can be compared across sites and scanners and carry important information
about the underlying microstructure. The multi-parameter mapping (MPM) protocol
takes advantage of multi-echo acquisitions with variable flip angles to extract
these parameters in a clinically acceptable scan time. In this context,
ESTATICS performs a joint loglinear fit of multiple echo series to extract R2*
and multiple extrapolated intercepts, thereby improving robustness to motion
and decreasing the variance of the estimators. In this paper, we extend this
model in two ways: (1) by introducing a joint total variation (JTV) prior on
the intercepts and decay, and (2) by deriving a nonlinear maximum \emph{a
posteriori} estimate. We evaluated the proposed algorithm by predicting
left-out echoes in a rich single-subject dataset. In this validation, we
outperformed other state-of-the-art methods and additionally showed that the
proposed approach greatly reduces the variance of the estimated maps, without
introducing bias.Comment: 11 pages, 2 figures, 1 table, conference paper, accepted at MICCAI
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Voxel-wise comparisons of cellular microstructure and diffusion-MRI in mouse hippocampus using 3D Bridging of Optically-clear histology with Neuroimaging Data (3D-BOND)
A key challenge in medical imaging is determining a precise correspondence between image properties and tissue microstructure. This comparison is hindered by disparate scales and resolutions between medical imaging and histology. We present a new technique, 3D Bridging of Optically-clear histology with Neuroimaging Data (3D-BOND), for registering medical images with 3D histology to overcome these limitations. Ex vivo 120 × 120 × 200 μm resolution diffusion-MRI (dMRI) data was acquired at 7 T from adult C57Bl/6 mouse hippocampus. Tissue was then optically cleared using CLARITY and stained with cellular markers and confocal microscopy used to produce high-resolution images of the 3D-tissue microstructure. For each sample, a dense array of hippocampal landmarks was used to drive registration between upsampled dMRI data and the corresponding confocal images. The cell population in each MRI voxel was determined within hippocampal subregions and compared to MRI-derived metrics. 3D-BOND provided robust voxel-wise, cellular correlates of dMRI data. CA1 pyramidal and dentate gyrus granular layers had significantly different mean diffusivity (p > 0.001), which was related to microstructural features. Overall, mean and radial diffusivity correlated with cell and axon density and fractional anisotropy with astrocyte density, while apparent fibre density correlated negatively with axon density. Astrocytes, axons and blood vessels correlated to tensor orientation
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