Abstract
So far, fingerprinting studies have focused on identifying features from single-modality MRI data, which capture individual characteristics in terms of brain structure, function, or white matter microstructure. However, due to the lack of a framework for comparing across multiple modalities, studies based on multi-modal data remain elusive. This paper presents a multi-modal analysis of genetically-related subjects to compare and contrast the information provided by various MRI modalities. The proposed framework represents MRI scans as bags of SIFT features, and uses these features in a nearest-neighbor graph to measure subject similarity. Experiments using the T1/T2-weighted MRI and diffusion MRI data of 861 Human Connectome Project subjects demonstrate strong links between the proposed similarity measure and genetic proximity.
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Acknowledgements
Data were provided in part by the Human Connectome Project, WU-Minn Consortium (Principal Investigators: David Van Essen and Kamil Ugurbil; 1U54MH091657) funded by the 16 NIH Institutes and Centers that support the NIH Blueprint for Neuroscience Research; and by the McDonnell Center for Systems Neuroscience at Washington University.
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Kumar, K., Chauvin, L., Toews, M., Colliot, O., Desrosiers, C. (2018). Multi-Modal Analysis of Genetically-Related Subjects Using SIFT Descriptors in Brain MRI. In: Kaden, E., Grussu, F., Ning, L., Tax, C., Veraart, J. (eds) Computational Diffusion MRI. Mathematics and Visualization. Springer, Cham. https://doi.org/10.1007/978-3-319-73839-0_17
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DOI: https://doi.org/10.1007/978-3-319-73839-0_17
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