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MRzero sequence generation using analytic signal equations as forward model and neural network reconstruction for efficient auto-encoding
Simon Weinmüller1, Hoai Nam Dang1, Alexander Loktyushin2,3, Felix Glang2, Arnd Doerfler1, Andreas Maier4, Bernhard Schölkopf3, Klaus Scheffler2,5, and Moritz Zaiss1,2
1Neuroradiology, University Clinic Erlangen, Friedrich-Alexander Universität Erlangen-Nürnberg (FAU), Erlangen, Germany, 2Max-Planck Institute for Biological Cybernetics, Magnetic Resonance Center, Tübingen, Germany, 3Max-Planck Institute for Intelligent Systems, Empirical Inference, Tübingen, Germany, 4Pattern Recognition Lab Friedrich-Alexander-University Erlangen-Nürnberg, Erlangen, Germany, 5Department of Biomedical Magnetic Resonance, Eberhard Karls University Tübingen, Tübingen, Germany
Using analytic signal equations combined with neural network reconstruction allows fast, fully differentiable supervised learning of MRI sequences. This forms a fast alternative to the full Bloch-equation-based MRzero framework in certain cases.
Figure 1: Schematic of the MRzero framework. Topmost part: An MR image is simulated for given sequence parameters and Bloch parameters (PD, B1 and T1) with an analytic signal equation. The evolution of the signals are mapped pixelwise to B1 and T1 values with a NN. The output is compared to the target (B1 and T1 value) and gradient descent optimization is performed to update sequence parameters TI, Trec, TR, $$$\alpha_{gre}$$$, $$$\alpha_{prep}$$$ and NN parameters.
Figure 4: Pixelwise evaluation of the NN-predicted B1 (A) and T1 (B) maps for the optimized sequence (first column) and the inversion recovery (second column). B1 map from the WASABI measurement as reference (third column). Correlation between WASABI and optimized sequence with correlation coefficient R=0.88 and correlation between WASABI and inversion recovery with correlation coefficient R=0.90 (C). Comparison of obtained T1 values for different tissue ROIs with literature values (D).