Purpose: Diffusion-weighted imaging allows investigators to identify structural, microstructural, and connectivity-based differences between subjects, but variability due to session and scanner biases is a challenge. Methods: To investigate DWI variability, we present MASiVar, a multisite data set consisting of 319 diffusion scans acquired at 3 T from b = 1000 to 3000 s/mm 2 across 14 healthy adults, 83 healthy children (5 to 8 years), three sites, and four scanners as a publicly available, preprocessed, and de-identified data set. With the adult data, we demonstrate the capacity of MASiVar to simultaneously quantify the intrasession, intersession, interscanner, and intersubject variability of four common DWI processing approaches: (1) a tensor signal representation, (2) a multi-compartment neurite orientation dispersion and density model, (3) white-matter bundle segmentation, and (4) structural connectomics. Respectively, we evaluate region-wise fractional anisotropy, mean diffusivity, and principal eigenvector; region-wise CSF volume fraction, intracellular volume fraction, and orientation dispersion index; bundle-wise shape, | 3305 CAI et Al.
F I G U R E 8Overall trends in coefficient of variation (CoV) across DTI, NODDI, bundle segmentation, and connectomics. Visualization of median CoV across all four processing approaches on the intrasession, intersession, interscanner, and intersubject levels illustrates consistently increased variability with session, scanner, and subject effects. Statistical significance was determined with the Wilcoxon signed-rank test with and without Bonferroni correction. The outlying points correspond to the NODDI cVF approach in white matter where absolute cVF values are expected to be low.