Individualized Cortical Parcellation Based on Diffusion MRI Tractography.

The spatial topological properties of cortical regions vary across individuals. Connectivity-based functional and anatomical cortical mapping in individuals will facilitate research on structure-function relationships. However, individual-specific cortical topographic properties derived from anatomical connectivity are less explored than those based on functional connectivity. We aimed to develop a novel individualized anatomical connectivity-based parcellation framework and investigate individual differences in spatial topographic features of cortical regions using diffusion magnetic resonance imaging (dMRI) tractography. Using a high-quality, repeated-session dMRI dataset (42 subjects, 2 sessions per subject), cortical parcels were derived through in vivo anatomical connectivity-based parcellation. These individual-specific parcels demonstrated good within-individual reproducibility and reflected interindividual differences in anatomical brain organization. Connectivity in these individual-specific parcels was significantly more homogeneous than that based on the group atlas. We found that the position, size, and topography of these anatomical parcels were highly variable across individuals and demonstrated nonredundant information about individual differences. Finally, we found that intersubject variability in anatomical connectivity was correlated with the diversity of anatomical connectivity patterns. Overall, we identified cortical parcels that show homogeneous anatomical connectivity patterns. These parcels displayed marked intersubject spatial variability, which may be used in future functional studies to reveal structure-function relationships in the human brain.

Sample sizes and population differences in brain template construction.

Spatial normalization or deformation to a standard brain template is routinely used as a key module in various pipelines for the processing of magnetic resonance imaging (MRI) data. Brain templates are often constructed using MRI data from a limited number of subjects. Individual brains show significant variabilities in their morphology; thus, sample sizes and population differences are two key factors that influence brain template construction. To address these influences, we employed two independent groups from the Human Connectome Project (HCP) and the Chinese Human Connectome Project (CHCP) to quantify the impacts of sample sizes and population on brain template construction. We first assessed the effect of sample size on the construction of volumetric brain templates using data subsets from the HCP and CHCP datasets. We applied a voxel-wise index of the deformation variability and a logarithmically transformed Jacobian determinant to quantify the variability associated with the template construction and modeled the brain template variability as a power function of the sample size. At the system level, the frontoparietal control network and dorsal attention network demonstrated higher deformation variability and logged Jacobian determinants, whereas other primary networks showed lower variability. To investigate the population differences, we constructed Caucasian and Chinese standard brain atlases (namely, US200 and CN200). The two demographically matched templates, particularly the language-related areas, exhibited dramatic bilaterally in supramarginal gyri and inferior frontal gyri differences in their deformation variability and logged Jacobian determinant. Using independent data from the HCP and CHCP, we examined the segmentation and registration accuracy and observed significant reduction in the performance of the brain segmentation and registration when the population-mismatched templates were used in the spatial normalization. Our findings provide evidence to support the use of population-matched templates in human brain mapping studies. The US200 and CN200 templates have been released on the Neuroimage Informatics Tools and Resources Clearinghouse (NITRC) website (https://www.nitrc.org/projects/us200_cn200/).

Increasing diversity in connectomics with the Chinese Human Connectome Project.

Cultural differences and biological diversity play important roles in shaping human brain structure and function. To date, most large-scale multimodal neuroimaging datasets have been obtained primarily from people living in Western countries, omitting the crucial contrast with populations living in other regions. The Chinese Human Connectome Project (CHCP) aims to address these resource and knowledge gaps by acquiring imaging, genetic and behavioral data from a large sample of participants living in an Eastern culture. The CHCP collected multimodal neuroimaging data from healthy Chinese adults using a protocol comparable to that of the Human Connectome Project. Comparisons between the CHCP and Human Connectome Project revealed both commonalities and distinctions in brain structure, function and connectivity. The corresponding large-scale brain parcellations were highly reproducible across the two datasets, with the language processing task showing the largest differences. The CHCP dataset is publicly available in an effort to facilitate transcultural and cross-ethnic brain-mind studies.

Designs of multipass optical configurations based on the use of a cube corner retroreflector in the interferometer.

We describe designs of the multipass optical configurations of an interferometer with high spectral resolution with respect to 6, 12, and 24 times more optical passes than the conventional Michelson interferometer. In each design, a movable cube corner retroreflector is combined with a folding reflector group (FRG) as the interferometer's moving combination to implement the multipass optical configuration with the characteristic of surface division. Analyses reveal that when there are 12 or more optical passes, the net effect of the ray's angular deviation of the entire moving combination amounts to only the alignment error of one of the reflectors in the FRG, demonstrating the self-aligning property of the interferometer.