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Section: Partnerships and Cooperations

International Initiatives

Inria Associate Teams Not Involved in an Inria International Labs

MetaMRI
  • Title: Machine learning for meta-analysis of functional neuroimaging data

  • International Partner (Institution - Laboratory - Researcher):

    • Stanford (United States) - Department of Psychology - Russ Poldrack

  • Start year: 2015

  • See also: https://team.inria.fr/metamri

  • Neuroimaging produces huge amounts of complex data that are used to better understand the relations between brain structure and function. Observing that the neuroimaging community is still largely missing appropriate tools to store and organize the knowledge related to the data, Parietal team and Poldrack's lab, have decided to join forces to set up a framework for functional brain image meta-analysis, i.e. a framework in which several datasets can be jointly analyzed in order to accumulate information on the functional specialization of brain regions. MetaMRI will build upon Poldrack's lab expertise in handling, sharing and analyzing multi-protocol data and Parietal's recent developments of machine learning libraries to develop a new generation of meta-analytic tools.

LargeBrainNets
  • Title: Characterizing Large-scale Brain Networks Using Novel Computational Methods for dMRI and fMRI-based Connectivity

  • International Partner (Institution - Laboratory - Researcher):

    • Stanford (United States) - Stanford Cognitive and Systems Neuroscience Laboratory - Vinod Menon

  • Start year: 2016

  • See also: http://www-sop.inria.fr/members/Demian.Wassermann/large-brain-nets.html

  • In the past two decades, brain imaging of neurotypical individuals and clinical populations has primarily focused on localization of function and structures in the brain, revealing activation in specific brain regions during performance of cognitive tasks through modalities such as functional MRI. In parallel, technologies to identify white matter structures have been developed using diffusion MRI. More recently, interest has shifted towards developing a deeper understanding of the brain's intrinsic architecture and its influence on cognitive and affective information processing. Using for this resting state fMRI and diffusion MRI to build the functional and structural networks of the human brain.

    The human brain is a complex patchwork of interconnected regions, and graph-theoretical approaches have become increasingly useful for understanding how functionally connected systems engender, and constrain, cognitive functions. The functional nodes of the human brain and their structural inter-connectivity, collectively the "connectome", are, however, poorly understood. Critically, there is a dearth of computational methods for reliably identifying functional nodes of the brain and their structural inter-connectivity in vivo, despite an abundance of high-quality data from the Human Connectome Project (HCP). Devising and validating methods for investigating the human connectome has therefore taken added significance.

    The first major goal of this project is to develop and validate appropriate sophisticated computational and mathematical tools for identifying functional nodes at the whole-brain level and measuring structural and functional connectivity between them, using state-of-the-art human brain imaging techniques and open-source HCP data. To this end, we will first develop and validate novel computational tools for (1) identifying stable functional nodes of the human brain using resting-state functional MRI and (2) measuring structural connectivity between functional nodes of the brain using multi-shell high-angular diffusion MRI. Due to the complementarity of the two imaging techniques fMRI and dMRI, our novel computational methods methods, the synergy between the two laboratories of this associate team will allow us to reveal in unprecedented detail the structural and functional connectivity of the human brain.

    The second major goal of this project is to use our newly developed computational tools to characterize normal structural and functional brain networks in neurotypical adults.