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Rolf F Schulte

Publications and source records attributed to Rolf F Schulte.

3 recordsLinked to original sources

Algebraic Methods and Computational Strategies for Pseudoinverse-Based MR Image Reconstruction (Pinv-Recon)

Image reconstruction in Magnetic Resonance Imaging (MRI) is fundamentally a linear inverse problem, such that the image can be recovered via explicit pseudoinversion of the encoding matrix by solving $\textbf{data} = \textbf{Encode} \times \textbf{image}$ - a method referred to here as Pinv-Recon. While the benefits of this approach were acknowledged in early studies, the field has historically favored fast Fourier transforms (FFT) and iterative techniques due to perceived computational limitations of the pseudoinversion approach. This work revisits Pinv-Recon in the context of modern hardware, software, and optimized linear algebra routines. We compare various matrix inversion strategies, assess regularization effects, and demonstrate incorporation of advanced encoding physics into a unified reconstruction framework. While hardware advances have already significantly reduced computation time compared to earlier studies, our work further demonstrates that leveraging Cholesky decomposition leads to a two-order-of-magnitude improvement in computational efficiency over previous Singular Value Decomposition-based implementations. Moreover, we demonstrate the versatility of Pinv-Recon on diverse $\textit{in vivo}$ datasets encompassing a range of encoding schemes, starting with low- to medium-resolution functional and metabolic imaging and extending to high-resolution cases. Our findings establish Pinv-Recon as a versatile and robust reconstruction framework that aligns with the increasing emphasis on open-source and reproducible MRI research.

physics.med-ph↗

Joint alignment and reconstruction of multislice dynamic MRI using variational manifold learning

Free-breathing cardiac MRI schemes are emerging as competitive alternatives to breath-held cine MRI protocols, enabling applicability to pediatric and other population groups that cannot hold their breath. Because the data from the slices are acquired sequentially, the cardiac/respiratory motion patterns may be different for each slice; current free-breathing approaches perform independent recovery of each slice. In addition to not being able to exploit the inter-slice redundancies, manual intervention or sophisticated post-processing methods are needed to align the images post-recovery for quantification. To overcome these challenges, we propose an unsupervised variational deep manifold learning scheme for the joint alignment and reconstruction of multislice dynamic MRI. The proposed scheme jointly learns the parameters of the deep network as well as the latent vectors for each slice, which capture the motion-induced dynamic variations, from the k-t space data of the specific subject. The variational framework minimizes the non-uniqueness in the representation, thus offering improved alignment and reconstructions.

eess.IV↗

Qunatification of Metabolites in MR Spectroscopic Imaging using Machine Learning

Magnetic Resonance Spectroscopic Imaging (MRSI) is a clinical imaging modality for measuring tissue metabolite levels in-vivo. An accurate estimation of spectral parameters allows for better assessment of spectral quality and metabolite concentration levels. The current gold standard quantification method is the LCModel - a commercial fitting tool. However, this fails for spectra having poor signal-to-noise ratio (SNR) or a large number of artifacts. This paper introduces a framework based on random forest regression for accurate estimation of the output parameters of a model based analysis of MR spectroscopy data. The goal of our proposed framework is to learn the spectral features from a training set comprising of different variations of both simulated and in-vivo brain spectra and then use this learning for the subsequent metabolite quantification. Experiments involve training and testing on simulated and in-vivo human brain spectra. We estimate parameters such as concentration of metabolites and compare our results with that from the LCModel.

cs.CV↗