26 research outputs found

    Anatomo-functional correspondence in the superior temporal sulcus

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    The superior temporal sulcus (STS) is an intriguing region both for its complex anatomy and for the multiple functions that it hosts. Unfortunately, most studies explored either the functional organization or the anatomy of the STS only. Here, we link these two aspects by investigating anatomo-functional correspondences between the voice-sensitive cortex (Temporal Voice Areas) and the STS depth. To do so, anatomical and functional scans of 116 subjects were processed such as to generate individual surface maps on which both depth and functional voice activity can be analyzed. Individual depth profiles of manually drawn STS and functional profiles from a voice localizer (voice > non-voice) maps were extracted and compared to assess anatomo-functional correspondences. Three major results were obtained: first, the STS exhibits a highly significant rightward depth asymmetry in its middle part. Second, there is an anatomo-functional correspondence between the location of the voice-sensitive peak and the deepest point inside this asymmetrical region bilaterally. Finally, we showed that this correspondence was independent of the gender and, using a machine learning approach, that it existed at the individual level. These findings offer new perspectives for the understanding of anatomo-functional correspondences in this complex cortical region

    Distance Metric Learning using Graph Convolutional Networks: Application to Functional Brain Networks

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    Evaluating similarity between graphs is of major importance in several computer vision and pattern recognition problems, where graph representations are often used to model objects or interactions between elements. The choice of a distance or similarity metric is, however, not trivial and can be highly dependent on the application at hand. In this work, we propose a novel metric learning method to evaluate distance between graphs that leverages the power of convolutional neural networks, while exploiting concepts from spectral graph theory to allow these operations on irregular graphs. We demonstrate the potential of our method in the field of connectomics, where neuronal pathways or functional connections between brain regions are commonly modelled as graphs. In this problem, the definition of an appropriate graph similarity function is critical to unveil patterns of disruptions associated with certain brain disorders. Experimental results on the ABIDE dataset show that our method can learn a graph similarity metric tailored for a clinical application, improving the performance of a simple k-nn classifier by 11.9% compared to a traditional distance metric.Comment: International Conference on Medical Image Computing and Computer-Assisted Interventions (MICCAI) 201

    Independent Component Analysis of spatially distributed patterns of brain activation measured by fMRI

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    Ces dernières années, l'Analyse en Composantes Indépendantes (ICA) a été utilisée avec succès pour détecter l'activité cérébrale lors d'expériences d'Imagerie par Résonance Magnétique fonctionnelle (IRMf). Depuis, la précision des résultats obtenus a été étudiée en utilisant comme critères la localisation des zones d'activités, ou leur évolution temporelle, à la fois sur des données simulées et réelles. D'autres travaux récents ont démontré l'importance de la distribution spatiale de l'intensité de l'activité à l'intérieur d'une région d'intérêt de grande taille. Nous présentons dans cet article des résultats prouvant que ICA peut estimer avec précision ces « figures d'activité distribuée », en examinant des données IRMf simulées et réelles

    Atypical sulcal anatomy in young children with autism spectrum disorder

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    AbstractAutism spectrum disorder is associated with an altered early brain development. However, the specific cortical structure abnormalities underlying this disorder remain largely unknown. Nonetheless, atypical cortical folding provides lingering evidence of early disruptions in neurodevelopmental processes and identifying changes in the geometry of cortical sulci is of primary interest for characterizing these structural abnormalities in autism and their evolution over the first stages of brain development. Here, we applied state-of-the-art sulcus-based morphometry methods to a large highly-selective cohort of 73 young male children of age spanning from 18 to 108 months. Moreover, such large cohort was selected through extensive behavioral assessments and stringent inclusion criteria for the group of 59 children with autism. After manual labeling of 59 different sulci in each hemisphere, we computed multiple shape descriptors for each single sulcus element, hereby separating the folding measurement into distinct factors such as the length and depth of the sulcus. We demonstrated that the central, intraparietal and frontal medial sulci showed a significant and consistent pattern of abnormalities across our different geometrical indices. We also found that autistic and control children exhibited strikingly different relationships between age and structural changes in brain morphology. Lastly, the different measures of sulcus shapes were correlated with the CARS and ADOS scores that are specific to the autistic pathology and indices of symptom severity. Inherently, these structural abnormalities are confined to regions that are functionally relevant with respect to cognitive disorders in ASD. In contrast to those previously reported in adults, it is very unlikely that these abnormalities originate from general compensatory mechanisms unrelated to the primary pathology. Rather, they most probably reflect an early disruption on developmental trajectory that could be part of the primary pathology

    Microscopy-BIDS: An extension to the brain imaging data structure for microscopy data

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    The Brain Imaging Data Structure (BIDS) is a specification for organizing, sharing, and archiving neuroimaging data and metadata in a reusable way. First developed for magnetic resonance imaging (MRI) datasets, the community-led specification evolved rapidly to include other modalities such as magnetoencephalography, positron emission tomography, and quantitative MRI (qMRI). In this work, we present an extension to BIDS for microscopy imaging data, along with example datasets. Microscopy-BIDS supports common imaging methods, including 2D/3D, ex/in vivo, micro-CT, and optical and electron microscopy. Microscopy-BIDS also includes comprehensible metadata definitions for hardware, image acquisition, and sample properties. This extension will facilitate future harmonization efforts in the context of multi-modal, multi-scale imaging such as the characterization of tissue microstructure with qMRI

    Microscopy-BIDS: An Extension to the Brain Imaging Data Structure for Microscopy Data

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    The Brain Imaging Data Structure (BIDS) is a specification for organizing, sharing, and archiving neuroimaging data and metadata in a reusable way. First developed for magnetic resonance imaging (MRI) datasets, the community-led specification evolved rapidly to include other modalities such as magnetoencephalography, positron emission tomography, and quantitative MRI (qMRI). In this work, we present an extension to BIDS for microscopy imaging data, along with example datasets. Microscopy-BIDS supports common imaging methods, including 2D/3D, ex/in vivo, micro-CT, and optical and electron microscopy. Microscopy-BIDS also includes comprehensible metadata definitions for hardware, image acquisition, and sample properties. This extension will facilitate future harmonization efforts in the context of multi-modal, multi-scale imaging such as the characterization of tissue microstructure with qMRI

    On the Influence of Confounding Factors in Multisite Brain Morphometry Studies of Developmental Pathologies: Application to Autism Spectrum Disorder

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    Single-trial fMRI activation maps measured during the InterTVA event-related voice localizer. A data set ready for inter-subject pattern analysis

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    International audienceMultivariate pattern analysis (MVPA) of functional neuroimaging data has emerged as a key tool for studying the cognitive architecture of the human brain. At the group level, we have recently demonstrated the advantages of an under-exploited scheme that consists in training a machine learning model on data from a set of subjects and evaluating its generalization ability on data from unseen subjects (see Inter-subject pattern analysis: A straightforward and powerful scheme for group-level MVPA [1]). We here provide a data set that is fully ready to perform inter-subject pattern analysis, which includes 5616 single-trial brain activation maps recorded in 39 participants who were scanned using functional magnetic resonance imaging (fMRI) with a voice localizer paradigm. This data set should therefore reveal valuable for data scientists developing brain decoding algorithms as well as cognitive neuroscientists interested in voice perception

    Labelling Sulcal Graphs Across Indiviuals Using Multigraph Matching

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    International audienceThe problem of inter-individual comparison is of major importance in neuroimaging to detect patterns indicative of neurological pathology. Few works have been addressing the comparison of individual sulcal graphs in which variations across subjects manifest as changes in the number of nodes, graph topology and in the attributes that can be attached to nodes and edges. Here, we quantitatively evaluated different graph matching approaches in both the pairwise and multigraph matching frameworks, on synthetic graphs simulating the structure and attributes distributions of real data. Our results show that multigraph matching approach outperforms pairwise techniques in all simulations. The application to a set of real sulcal graphs from 134 subjects confirms this observation and demonstrates that multigraph matching approaches can scale and have a great potential in this context

    Appariement multiple de graphes avec des noyaux

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    International audienceMultigraph matching is a recent variant of the graph matching problem. In this framework, the optimization procedure considers several graphs and enforces the consistency of the matches along the graphs. This constraint can be formalized as a cycle consistency across the pairwise permutation matrices, which implies the definition of a universe of vertex~\citep{pachauri2013solving}. The label of each vertex is encoded by a sparse vector and the dimension of this space corresponds to the rank of the bulk permutation matrix, the matrix built from the aggregation of all the pairwise permutation matrices. The matching problem can then be formulated as a non-convex quadratic optimization problem (QAP) under constraints imposed on the rank and the permutations. In this paper, we introduce a novel kernelized multigraph matching technique that handles vectors of attributes on both the vertices and edges of the graphs, while maintaining a low memory usage. We solve the QAP problem using a projected power optimization approach and propose several projectors leading to improved stability of the results. We provide several experiments showing that our method is competitive against other unsupervised methods
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