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Abstract #3013

Parallelized Patch2Self & other denoising methods on 7T diffusion weighted imaging: comparisons of quality and effects on tractometry

Paul B Camacho1, Shreyas Fadnavis2, Aaron T Anderson1,3, Eleftherios Garyfallidis4, Bruce Damon3,5, Tracey M Wzsalek1,3, and Brad P Sutton1,3,6
1Beckman Institute for Advanced Science & Technology, University of Illinois at Urbana Champaign, Urbana, IL, United States, 2Johnson & Johnson, Cambridge, MA, United States, 3Carle-Illinois Advanced Imaging Center, Carle Health, Urbana, IL, United States, 4Intelligent Systems Engineering, Indiana University Bloomington, Bloomington, IN, United States, 5Stephens Family Clinical Research Institute, Carle Health, Urbana, IL, United States, 6Bioengineering, University of Illinois at Urbana Champaign, Urbana, IL, United States

Synopsis

Keywords: Data Processing, Data Processing, Denoising, Diffusion Preprocessing

Motivation: Performance of denoising methods and effects on downstream analyses for diffusion-weighted imaging at 7 Tesla are understudied.

Goal(s): Determine which denoising methods provide better performance and whether any skew tractometry outcomes.

Approach: Preliminary data acquired using two different diffusion sequences - 30 or 64 directions/shell multi-shell - were separately denoised using either Patch2Self, oversampled local-PCA, non-local means, or Marchenko-Pastur PCA before QSIPrep pre-processing and DSI Studio AutoTrack GQI.

Results: Contrast-to-noise ratios were best for Patch2Self and oversampled local-PCA, agreeing with visual assessment. Fractional anisotropy distributions were higher and mean diffusivity lower in several major bundles for non-local means than Patch2Self, especially with lower angular resolution.

Impact: The computationally-efficient parallel Patch2Self improves 7T diffusion data quality and produces lower fractional anisotropy values in tractometry of common bundles for biomarker searches than non-local means. Denoising methods should be considered in literature comparisons and image preprocessing in clinical trials.

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Keywords