TY - JOUR
T1 - Denoise magnitude diffusion magnetic resonance images via variance-stabilizing transformation and optimal singular-value manipulation
AU - Ma, Xiaodong
AU - Uğurbil, Kâmil
AU - Wu, Xiaoping
N1 - Publisher Copyright:
© 2020 The Authors
PY - 2020/7/15
Y1 - 2020/7/15
N2 - Although shown to have a great utility for a wide range of neuroscientific and clinical applications, diffusion-weighted magnetic resonance imaging (dMRI) faces a major challenge of low signal-to-noise ratio (SNR), especially when pushing the spatial resolution for improved delineation of brain's fine structure or increasing the diffusion weighting for increased angular contrast or both. Here, we introduce a comprehensive denoising framework for denoising magnitude dMRI. The framework synergistically combines the variance stabilizing transform (VST) with optimal singular value manipulation. The purpose of VST is to transform the Rician data to Gaussian-like data so that an asymptotically optimal singular value manipulation strategy tailored for Gaussian data can be used. The output of the framework is the estimated underlying diffusion signal for each voxel in the image domain. The usefulness of the proposed framework for denoising magnitude dMRI is demonstrated using both simulation and real-data experiments. Our results show that the proposed denoising framework can significantly improve SNR across the entire brain, leading to substantially enhanced performances for estimating diffusion tensor related indices and for resolving crossing fibers when compared to another competing method. More encouragingly, the proposed method when used to denoise a single average of 7 Tesla Human Connectome Project-style diffusion acquisition provided comparable performances relative to those achievable with ten averages for resolving multiple fiber populations across the brain. As such, the proposed denoising method is expected to have a great utility for high-quality, high-resolution whole-brain dMRI, desirable for many neuroscientific and clinical applications.
AB - Although shown to have a great utility for a wide range of neuroscientific and clinical applications, diffusion-weighted magnetic resonance imaging (dMRI) faces a major challenge of low signal-to-noise ratio (SNR), especially when pushing the spatial resolution for improved delineation of brain's fine structure or increasing the diffusion weighting for increased angular contrast or both. Here, we introduce a comprehensive denoising framework for denoising magnitude dMRI. The framework synergistically combines the variance stabilizing transform (VST) with optimal singular value manipulation. The purpose of VST is to transform the Rician data to Gaussian-like data so that an asymptotically optimal singular value manipulation strategy tailored for Gaussian data can be used. The output of the framework is the estimated underlying diffusion signal for each voxel in the image domain. The usefulness of the proposed framework for denoising magnitude dMRI is demonstrated using both simulation and real-data experiments. Our results show that the proposed denoising framework can significantly improve SNR across the entire brain, leading to substantially enhanced performances for estimating diffusion tensor related indices and for resolving crossing fibers when compared to another competing method. More encouragingly, the proposed method when used to denoise a single average of 7 Tesla Human Connectome Project-style diffusion acquisition provided comparable performances relative to those achievable with ten averages for resolving multiple fiber populations across the brain. As such, the proposed denoising method is expected to have a great utility for high-quality, high-resolution whole-brain dMRI, desirable for many neuroscientific and clinical applications.
KW - Denoising
KW - Diffusion MRI
KW - High field MRI
KW - Human connectome project
KW - Simultaneous multi-slice
KW - Singular value decomposition
KW - Variance stabilizing transformation
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U2 - 10.1016/j.neuroimage.2020.116852
DO - 10.1016/j.neuroimage.2020.116852
M3 - Article
C2 - 32305566
AN - SCOPUS:85083592902
SN - 1053-8119
VL - 215
JO - NeuroImage
JF - NeuroImage
M1 - 116852
ER -