We investigate the use of generalized anisotropy profiles (GAPs) for delineating boundaries between subcortical gray and white matter in vivo. Replicating results from a previous ex vivo study, we show that GAPs, which are computed from the diffusion propagator, provide more informative contrasts than T1- and T2-weighted images or conventional diffusion metrics. An undersampled Cartesian-grid sampling of q-space can be used to obtain these profiles with a reasonable scan time. Thus, GAPs show promise as a multi-channel contrast that could be used in the future to improve structural segmentation.
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