AI Article Synopsis

  • This study addresses the challenges of manual brain tissue segmentation in MRI data analysis and highlights the limitations of existing automated methods, especially CNNs, in achieving reliable results.
  • The authors introduce a new hybrid CNN-Transformer architecture that enhances performance for 3D medical image segmentation, demonstrating its effectiveness on diverse T1-weighted MRI datasets.
  • The model's robustness is validated across multiple sites and conditions, showing superior generality and reliability, making it a promising tool for brain research and available for public access via GitHub.

Article Abstract

Brain tissue segmentation has demonstrated great utility in quantifying MRI data by serving as a precursor to further post-processing analysis. However, manual segmentation is highly labor-intensive, and automated approaches, including convolutional neural networks (CNNs), have struggled to generalize well due to properties inherent to MRI acquisition, leaving a great need for an effective segmentation tool. This study introduces a novel CNN-Transformer hybrid architecture designed to improve brain tissue segmentation by taking advantage of the increased performance and generality conferred by Transformers for 3D medical image segmentation tasks. We first demonstrate the superior performance of our model on various T1w MRI datasets. Then, we rigorously validate our model's generality applied across four multi-site T1w MRI datasets, covering different vendors, field strengths, scan parameters, and neuropsychiatric conditions. Finally, we highlight the reliability of our model on test-retest scans taken in different time points. In all situations, our model achieved the greatest generality and reliability compared to the benchmarks. As such, our method is inherently robust and can serve as a valuable tool for brain related T1w MRI studies. The code for the TABS network is available at: https://github.com/raovish6/TABS.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10406272PMC
http://dx.doi.org/10.3389/fnimg.2022.1023481DOI Listing

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