arXiv subjects

Daniel Mackner

Publications and source records attributed to Daniel Mackner.

4 recordsLinked to original sources

arXiv2026

BART Online Open-Source Sequence Toolbox for Computational MRI

Purpose In advanced computational MRI techniques, acquisition and reconstruction techniques are jointly designed. For reproducibility, it is therefore important to provide an open implementation of both. At the same time, any use in a clinical environment usually requires a close integration with the MRI scanner. Ensuring long-time reproducibility and maintenance then poses additional challenges. In this work, we aim to provide a fully integrated open-source framework that can meet these demands. Methods A software framework to develop pulse sequences is added to the BART toolbox. In addition, a vendor-specific driver sequence is developed that can be used to run the sequence on a clinical MRI scanner enabling online adjustment of all relevant sequence parameters. Using the Pulseq format, the exact same sequence can also be reproduced offline. As proof-of-concept, quantitative MRI methods for T1 and joint water/fat R2*, B0 mapping using radial FLASH and model-based reconstruction are implemented in the proposed framework. Consistency between online and offline acquisition is validated in phantom and in vivo experiments. Results Quantitative MRI methods consisting of acquisition and reconstruction were successfully implemented in BART. Acquisition parameters and FOV can be adapted online on a clinical MRI system. Quantitative parameter maps from model-based reconstruction agree for online and offline regenerated Pulseq acquisitions. Conclusion This work enables reproducibility of advanced computational MRI methods within a comprehensive end-to-end open-source framework.

physics.med-ph↗

arXiv2025

Dynamic transitions for fast joint acquisition and reconstruction of CEST-Rex and T1

Purpose: This work proposes a method for the simultaneous estimation of the exchange-dependent relaxation rate Rex and the longitudinal relaxation time T1 from a single acquisition. Methods: A novel acquisition scheme was developed that combines CEST saturation with an inversion pulse and a Look-Locker readout to capture the magnetization evolution starting from the inverse transient Z-spectrum. The corresponding signal model, derived from the Bloch-McConnell equations, describes both the transient Z-spectrum and the Look-Locker dynamics. A model-based reconstruction approach is employed to jointly estimate Rex and T1. The proposed method was validated using a numerical phantom and benchmarked against conventional CEST and Look-Locker T1 mapping in phantom and in vivo on a clinical 3T scanner. Results: The joint estimation approach demonstrated strong agreement with ground truth and conventional methods across a wide range of T1 and CEST parameters. The acquisition time was reduced by 20-30% compared to standard CEST protocols, while providing higher signal-to-noise ratio (SNR) in parameter maps. Conclusion: The proposed technique enables robust and efficient simultaneous quantification of CEST Rex and T1 in a single acquisition. It improves parameter map quality and reduces scan time, making it suitable for both phantom and in vivo imaging across a wide range of physiological conditions.

physics.med-ph↗

arXiv2024

Model-Based Reconstruction for Joint Estimation of $T_{1}$, $R_{2}^{*}$ and $B_{0}$ Field Maps Using Single-Shot Inversion-Recovery Multi-Echo Radial FLASH

Purpose: To develop a model-based nonlinear reconstruction for simultaneous water-specific $T_{1}$, $R_{2}^{*}$, $B_{0}$ field and/or fat fraction (FF) mapping using single-shot inversion-recovery (IR) multi-echo radial FLASH. Methods: The proposed model-based reconstruction jointly estimates water-specific $T_{1}$, $R_{2}^{*}$, $B_{0}$ field and/or FF maps, as well as a set of coil sensitivities directly from $k$-space obtained with a single-shot IR multi-echo radial FLASH sequence using blip gradients across echoes. Joint sparsity constraints are exploited on multiple quantitative maps to improve precision. Validations are performed on numerical and NIST phantoms and with in vivo studies of the human brain and liver at 3 T. Results: Numerical phantom studies demonstrate the effects of fat signals in $T_{1}$ estimation and confirm good quantitative accuracy of the proposed method for all parameter maps. NIST phantom results confirm good quantitative $T_{1}$ and $R_{2}^{*}$ accuracy in comparison to Cartesian references. Apart from good quantitative accuracy and precision for multiple parameter maps, in vivo studies show improved image details utilizing the proposed joint estimation. The proposed method can achieve simultaneous water-specific $T_{1}$, $R_{2}^{*}$, $B_{0}$ field and/or FF mapping for brain (0.81 $\times$ 0.81 $\times$ 5 mm$^{3}$) and liver (1.6 $\times$ 1.6 $\times$ 6 mm$^{3}$) imaging within four seconds. Conclusion: The proposed model-based nonlinear reconstruction, in combination with a single-shot IR multi-echo radial FLASH acquisition, enables joint estimation of accurate water-specific $T_{1}$, $R_{2}^{*}$, $B_{0}$ field and/or FF maps within four seconds. The present work is of potential value for specific clinical applications.

physics.med-ph↗

arXiv2024

Rational Approximation of Golden Angles: Accelerated Reconstructions for Radial MRI

Purpose: To develop a generic radial sampling scheme that combines the advantages of golden ratio sampling with simplicity of equidistant angular patterns. The irrational angle between consecutive spokes in golden ratio based sampling schemes enables a flexible retrospective choice of temporal resolution, while preserving good coverage of k-space for each individual bin. Nevertheless, irrational increments prohibit precomputation of the point-spread function (PSF), can lead to numerical problems, and require more complex processing steps. To avoid these problems, a new sampling scheme based on a rational approximation of golden angles (RAGA) is developed. Methods: The theoretical properties of RAGA sampling are mathematically derived. Sidelobe-to-peak ratios (SPR) are numerically computed and compared to the corresponding golden ratio sampling schemes. The sampling scheme is implemented in the BART toolbox and in a radial gradient-echo sequence. Feasibility is shown for quantitative imaging in a phantom and a cardiac scan of a healthy volunteer. Results: RAGA sampling can accurately approximate golden ratio sampling and has almost identical PSF and SPR. In contrast to golden ratio sampling, each frame can be reconstructed with the same equidistant trajectory using different sampling masks, and the angle of each acquired spoke can be encoded as a small index, which simplifies processing of the acquired data. Conclusion: RAGA sampling provides the advantages of golden ratio sampling while simplifying data processing, rendering it a valuable tool for dynamic and quantitative MRI.

physics.med-ph↗