SearcharxivSearch

arXiv subjects

Brian J. Soher

Publications and source records attributed to Brian J. Soher.

2 recordsLinked to original sources

The 2024 MRSI Data Processing and Quantification Challenge Synthetic Dataset

Synthetic data is central to magnetic resonance spectroscopy method development because they provide ground truths for software validation, reproducible benchmarking, and machine- and deep-learning training. In MRSI, synthetic data must capture spatially varying anatomy, field inhomogeneity, nuisance signals, and measurement effects. The 2024 MRSI Data Processing and Quantification Challenge Synthetic Dataset is a simulated 3T brain FID-MRSI resource with ground-truth metabolite maps developed as a controlled testbed for MRSI processing and quantification methods. Subject-specific simulations used anatomical images and field maps from Human Connectome Project subjects. Tissue masks, quantum-mechanically simulated metabolite basis functions, in vivo-derived macromolecular components, Bloch-simulated post-WET residual water, registered in vivo lipid signals, spectral baseline, $B_0$-dependent frequency shifts, Voigt lineshape variations, and complex Gaussian noise were combined in a forward model. Water and lipid signals were synthesized on a high-resolution grid and Fourier-truncated to the final echo-planar spectroscopic imaging grid to model the finite spatial point spread function. This resource has 24 training and 8 testing datasets containing contaminated FID-MRSI data, anatomical images, $B_0$ maps, metadata, and ground-truth metabolite and component signals. Forward-model parameters are documented, including tissue-specific metabolite concentrations and relaxation times, macromolecular amplitude ratios, the water model, noise, and field-inhomogeneity ranges. This synthetic benchmark supports development and comparison of MRSI processing, nuisance-signal removal, and metabolite-quantification methods, while enabling method evaluation. It illustrates how characterized synthetic data can support rigorous evaluation when ground truth is difficult or impossible to obtain.

physics.med-ph

Automatic deep learning-based normalization of breast dynamic contrast-enhanced magnetic resonance images

Objective: To develop an automatic image normalization algorithm for intensity correction of images from breast dynamic contrast-enhanced magnetic resonance imaging (DCE-MRI) acquired by different MRI scanners with various imaging parameters, using only image information. Methods: DCE-MR images of 460 subjects with breast cancer acquired by different scanners were used in this study. Each subject had one T1-weighted pre-contrast image and three T1-weighted post-contrast images available. Our normalization algorithm operated under the assumption that the same type of tissue in different patients should be represented by the same voxel value. We used four tissue/material types as the anchors for the normalization: 1) air, 2) fat tissue, 3) dense tissue, and 4) heart. The algorithm proceeded in the following two steps: First, a state-of-the-art deep learning-based algorithm was applied to perform tissue segmentation accurately and efficiently. Then, based on the segmentation results, a subject-specific piecewise linear mapping function was applied between the anchor points to normalize the same type of tissue in different patients into the same intensity ranges. We evaluated the algorithm with 300 subjects used for training and the rest used for testing. Results: The application of our algorithm to images with different scanning parameters resulted in highly improved consistency in pixel values and extracted radiomics features. Conclusion: The proposed image normalization strategy based on tissue segmentation can perform intensity correction fully automatically, without the knowledge of the scanner parameters. Significance: We have thoroughly tested our algorithm and showed that it successfully normalizes the intensity of DCE-MR images. We made our software publicly available for others to apply in their analyses.

cs.CV