The enormous diversity of life forms thriving in drastically different environmental milieus involves a complex interplay among constituent proteins interacting with each other. However, the organizational principles characterizing the evolution of protein interaction networks (PINs) across the tree of life are largely unknown. Here we study 4,738 PINs belonging to 16 phyla to discover phyla-specific architectural features and examine if there are some evolutionary constraints imposed on the networks' topologies. We utilized positional information of a network's nodes by normalizing the frequencies of automorphism orbits appearing in graphlets of sizes 2-5. We report that orbit usage profiles (OUPs) of networks belonging to the three domains of life are contrastingly different not only at the domain level but also at the scale of phyla. Integrating the information related to protein families, domains, subcellular location, gene ontology, and pathways, our results indicate that wiring patterns of PINs in different phyla are not randomly generated rather they are shaped by evolutionary constraints imposed on them. There exist subtle but substantial variations in the wiring patterns of PINs that enable OUPs to differentiate among different superfamilies. A deep neural network was trained on differentially expressed orbits resulting in a prediction accuracy of 85%.

Designing more efficient, reliable, and explainable neural network architectures is critical to studies that are based on artificial intelligence (AI) techniques. Previous studies, by post-hoc analysis, have found that the best-performing ANNs surprisingly resemble biological neural networks (BNN), which indicates that ANNs and BNNs may share some common principles to achieve optimal performance in either machine learning or cognitive/behavior tasks. Inspired by this phenomenon, we proactively instill organizational principles of BNNs to guide the redesign of ANNs. We leverage the Core-Periphery (CP) organization, which is widely found in human brain networks, to guide the information communication mechanism in the self-attention of vision transformer (ViT) and name this novel framework as CP-ViT. In CP-ViT, the attention operation between nodes is defined by a sparse graph with a Core-Periphery structure (CP graph), where the core nodes are redesigned and reorganized to play an integrative role and serve as a center for other periphery nodes to exchange information. We evaluated the proposed CP-ViT on multiple public datasets, including medical image datasets (INbreast) and natural image datasets. Interestingly, by incorporating the BNN-derived principle (CP structure) into the redesign of ViT, our CP-ViT outperforms other state-of-the-art ANNs. In general, our work advances the state of the art in three aspects: 1) This work provides novel insights for brain-inspired AI: we can utilize the principles found in BNNs to guide and improve our ANN architecture design; 2) We show that there exist sweet spots of CP graphs that lead to CP-ViTs with significantly improved performance; and 3) The core nodes in CP-ViT correspond to task-related meaningful and important image patches, which can significantly enhance the interpretability of the trained deep model.

The evolution of convolutional neural networks (CNNs) can be largely attributed to the design of its architecture, i.e., the network wiring pattern. Neural architecture search (NAS) advances this by automating the search for the optimal network architecture, but the resulting network instance may not generalize well in different tasks. To overcome this, exploring network design principles that are generalizable across tasks is a more practical solution. In this study, We explore a novel brain-inspired design principle based on the core-periphery property of the human brain network to guide the design of CNNs. Our work draws inspiration from recent studies suggesting that artificial and biological neural networks may have common principles in optimizing network architecture. We implement the core-periphery principle in the design of network wiring patterns and the sparsification of the convolution operation. The resulting core-periphery principle guided CNNs (CP-CNNs) are evaluated on three different datasets. The experiments demonstrate the effectiveness and superiority compared to CNNs and ViT-based methods. Overall, our work contributes to the growing field of brain-inspired AI by incorporating insights from the human brain into the design of neural networks.

In-vivo examination of the physical connectivity of axonal projections through the white matter of the human brain is made possible by diffusion weighted magnetic resonance imaging (dMRI) Analysis of dMRI commonly considers derived scalar metrics such as fractional anisotrophy as proxies for "white matter integrity," and differences of such measures have been observed as significantly correlating with various neurological diagnosis and clinical measures such as executive function, presence of multiple sclerosis, and genetic similarity. The analysis of such voxel measures is confounded in areas of more complicated fiber wiring due to crossing, kissing, and dispersing fibers. Recently, Volz et al. introduced a simple probabilistic measure of the count of distinct fiber populations within a voxel, which was shown to reduce variance in group comparisons. We propose a complementary measure that considers the complexity of a voxel in context of its local region, with an aim to quantify the localized wiring complexity of every part of white matter. This allows, for example, identification of particularly ambiguous regions of the brain for tractographic approaches of modeling global wiring connectivity. Our method builds on recent advances in image inpainting, in which the task is to plausibly fill in a missing region of an image. Our proposed method builds on a Bayesian estimate of heteroscedastic aleatoric uncertainty of a region of white matter by inpainting it from its context. We define the localized wiring complexity of white matter as how accurately and confidently a well-trained model can predict the missing patch. In our results, we observe low aleatoric uncertainty along major neuronal pathways which increases at junctions and towards cortex boundaries. This directly quantifies the difficulty of lesion inpainting of dMRI images at all parts of white matter.