“…While this technique can be used to separate the sub‐voxel signal contributions from WM, GM, and CSF, it still assumes a single kernel for all voxels of a given tissue type, which needs to be calibrated a priori (Tax, Jeurissen, Vos, Viergever, & Leemans, 2014). Inaccuracies of the calibrated kernels can further bias the estimated fractions and fibre ODFs (Guo et al, 2019; Parker et al, 2013). Alternatively, the voxel‐wise kernel can be estimated by first factoring out the ODF through the computation of rotational invariants, and then fitting the data to signal models that set a pre‐defined number of microscopic environments with potentially constrained diffusion properties (Kaden, Kelm, Carson, Does, & Alexander, 2016; Novikov et al, 2019; Novikov, Veraart, Jelescu, & Fieremans, 2018).…”