|
AMBMC |
Human7T » Human7T
Human 7T cortical atlases![]() IntroductionDigital MRI atlases serve to integrate data from differing modalities, stereotactic localisation, automated region identification, automated segmentation and direct comparisons between individuals [1]. While paper atlases can provide exquisite detail of delineated structures, they are typically based upon an individual subject's histology and as such make it difficult to identify structures in novel subjects in an automated fashion. Below are a number of atlases generated via minimum deformation average (MDA) from a population of subjects based upon high resolution 7T MR imaging. MethodAll data was acquired on a 7 T whole-body Magnetom research scanner (Siemens Healthcare, Erlangen, Germany) with a gradient strength of 70 mT/m, slew rate of 200 T/m/s and 32-channel headcoil (Nova Medical, USA). A probabilistic model of all modalities was created using the method in Janke et al [2] and Grabner et al [4]. In the present case, the fitting strategy consisted of 2 linear fits to the evolving internal model followed by a hierarchical series of non-linear grid transforms. These transforms started with a step size of 32mm followed by 16mm, 12mm, 8mm, 6mm, 4mm, 2mm, and finished with 1.5mm. These fitting steps use progressively de-blurred data with a 3D kernel FWHM of half the current step size. Twenty iterations at each fitting stage were performed using the ANIMAL algorithm [5]. As the step size decreased the resolution of the evolving model to which data was being fit was increased, starting with a step size of 1.0mm and finishing with a resolution of 0.3mm. Given the multiple overlapping samples it is possible to increase the resolution to this point without suffering from a lack of information at any point. Our technique differs from Fonov et al's [3] during the intermediate model generation in that a robust averaging process is used to reduce the effect of artefacts and small handling tears in the brain. The averaging technique is a “winner takes all” approach and as such places a lower weight on data at each voxel that is greater than two standard deviations from the current model. This increases the likelihood that a single minimum is achieved for the entire model. ConclusionThe increase in resolution and signal from the modelling process means that we can now readily identify multiple thalamic and neocortical nuclei that are not visible in individual subjects. In the future, we plan to release a complete multi-modal model including segmentations and tissue density maps. Code is available as part of MINC in the volgenmodel package There are currently 4 models available. MP2RAGE - MP2RAGE T1 style model GRE/QSM - Model generated from QSM data TSE - Turbo Spin Echo Hippocampal model PETRA - PETRA model Please reference use of the model as such:Janke AL, O'Brien K, Bollmann S, Kober T, Marstaller L, Barth M. A 7T Human Brain Microstructure Atlas by Minimum Deformation Averaging at 300um. In 24th Annual ISMRM Scientific Meeting and Exhibition, Singapore. A copy of the poster can be downloaded References1. Evans AC, Janke AL, Collins DL, Baillet S. Brain templates and atlases. Neuroimage 2012 |
© 2018 The National Imaging Facility, Authorised by: Director Maintained by: andrew.janke@uq.edu.au