Jiazhou Chen

Jiazhou Chen, Guoqiang Han, Hongmin Cai et al.

Converging evidence shows that disease-relevant brain alterations do not appear in random brain locations, instead, its spatial pattern follows large scale brain networks. In this context, a powerful network analysis approach with a mathematical foundation is indispensable to understand the mechanism of neuropathological events spreading throughout the brain. Indeed, the topology of each brain network is governed by its native harmonic waves, which are a set of orthogonal bases derived from the Eigen-system of the underlying Laplacian matrix. To that end, we propose a novel connectome harmonic analysis framework to provide enhanced mathematical insights by detecting frequency-based alterations relevant to brain disorders. The backbone of our framework is a novel manifold algebra appropriate for inference across harmonic waves that overcomes the limitations of using classic Euclidean operations on irregular data structures. The individual harmonic difference is measured by a set of common harmonic waves learned from a population of individual Eigen systems, where each native Eigen-system is regarded as a sample drawn from the Stiefel manifold. Specifically, a manifold optimization scheme is tailored to find the common harmonic waves which reside at the center of Stiefel manifold. To that end, the common harmonic waves constitute the new neuro-biological bases to understand disease progression. Each harmonic wave exhibits a unique propagation pattern of neuro-pathological burdens spreading across brain networks. The statistical power of our novel connectome harmonic analysis approach is evaluated by identifying frequency-based alterations relevant to Alzheimer's disease, where our learning-based manifold approach discovers more significant and reproducible network dysfunction patterns compared to Euclidian methods.

Hong Peng, Yu Hu, Jiazhou Chen et al.

The performance of most the clustering methods hinges on the used pairwise affinity, which is usually denoted by a similarity matrix. However, the pairwise similarity is notoriously known for its vulnerability of noise contamination or the imbalance in samples or features, and thus hinders accurate clustering. To tackle this issue, we propose to use information among samples to boost the clustering performance. We proved that a simplified similarity for pairs, denoted by a fourth order tensor, equals to the Kronecker product of pairwise similarity matrices under decomposable assumption, or provide complementary information for which the pairwise similarity missed under indecomposable assumption. Then a high order similarity matrix is obtained from the tensor similarity via eigenvalue decomposition. The high order similarity capturing spatial information serves as a robust complement for the pairwise similarity. It is further integrated with the popular pairwise similarity, named by IPS2, to boost the clustering performance. Extensive experiments demonstrated that the proposed IPS2 significantly outperformed previous similarity-based methods on real-world datasets and it was capable of handling the clustering task over under-sampled and noisy datasets.