摘要:
A method for reconstructing multiple images of a subject depicting multiple different contrast characteristics from medical image data acquired with a medical imaging system is provided. Multiple image data sets are acquired with one or more medical imaging systems and the image data sets used to estimate hyperparameters drawn from a prior distribution, such as a prior distribution of image gradient coefficients. These hyperparameters and the acquired image data sets are utilized to produce a posterior distribution, such as a posterior distribution of image gradients. From this posterior distribution, multiple images with the different contrast characteristics are reconstructed. The medical imaging system may be a magnetic resonance imaging system, an x-ray computed tomography imaging system, an ultrasound system, and so on.
摘要:
Systems and methods for reconstructing images using a hierarchically semiseparable (“HSS”) solver to compactly represent the inverse encoding matrix used in the reconstruction are provided. The reconstruction method includes solving for the actual inverse of the encoding matrix using a direct (i.e., non-iterative) HSS solver. This approach is contrary to conventional reconstruction methods that repetitively evaluate forward models (e.g., compressed sensing or parallel imaging forward models).
摘要:
Described here are systems and methods for quantitative susceptibility mapping (“QSM”) using magnetic resonance imaging (“MRI”). Susceptibility maps are reconstructed from phase images using an automatic regularization technique based in part on variable splitting. Two different regularization parameters are used, one, λ, that controls the smoothness of the final susceptibility map and one, μ, that controls the convergence speed of the reconstruction. For instance, the regularization parameters can be determined using an L-curve heuristic to find the parameters that yield the maximum curvature on the L-curve. The μ parameter can be determined based on an l2-regularization and the λ parameter can be determined based on the iterative l1-regularization used to reconstruct the susceptibility map.
摘要:
Systems and methods for reconstructing images using a hierarchically semiseparable (“HSS”) solver to compactly represent the inverse encoding matrix used in the reconstruction are provided. The reconstruction method includes solving for the actual inverse of the encoding matrix using a direct (i.e., non-iterative) HSS solver. This approach is contrary to conventional reconstruction methods that repetitively evaluate forward models (e.g., compressed sensing or parallel imaging forward models).
摘要:
A method for reconstructing multiple images of a subject depicting multiple different contrast characteristics from medical image data acquired with a medical imaging system is provided. Multiple image data sets are acquired with one or more medical imaging systems and the image data sets used to estimate hyperparameters drawn from a prior distribution, such as a prior distribution of image gradient coefficients. These hyperparameters and the acquired image data sets are utilized to produce a posterior distribution, such as a posterior distribution of image gradients. From this posterior distribution, multiple images with the different contrast characteristics are reconstructed. The medical imaging system may be a magnetic resonance imaging system, an x-ray computed tomography imaging system, an ultrasound system, and so on.
摘要:
Described here are systems and methods for quantitative susceptibility mapping (“QSM”) using magnetic resonance imaging (“MRI”). Susceptibility maps are reconstructed from phase images using an automatic regularization technique based in part on variable splitting. Two different regularization parameters are used, one, λ, that controls the smoothness of the final susceptibility map and one, μ, that controls the convergence speed of the reconstruction. For instance, the regularization parameters can be determined using an L-curve heuristic to find the parameters that yield the maximum curvature on the L-curve. The μ parameter can be determined based on an l2-regularization and the λ parameter can be determined based on the iterative l1-regularization used to reconstruct the susceptibility map.