We develop new algorithms to analyze and exploit the joint subspace structure of a set of related images to facilitate the process of concurrent segmentation of a large set of images. Most existing approaches for this problem are either limited to extracting a single similar object across the given image set or do not scale well to a large number of images containing multiple objects varying at different scales. One of the goals of this paper is to show that various desirable properties of such an algorithm (ability to handle images with objects showing scale variations) can be cast elegantly using simple constructs from linear algebra: this significantly extends the operating range of such methods. While intuitive, this formulation leads to a hard optimization problem where one must perform the image segmentation task together with appropriate constraints which enforce desired algebraic regularity (e.g., common subspace structure). We propose efficient iterative algorithms (with small computational requirements) whose key steps reduce to objective functions solvable by and/or nearly . We study the qualitative, theoretical, and empirical properties of the method, and present results on benchmark datasets.
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http://dx.doi.org/10.1007/978-3-642-33765-9_10 | DOI Listing |
Biological memory networks are thought to store information by experience-dependent changes in the synaptic connectivity between assemblies of neurons. Recent models suggest that these assemblies contain both excitatory and inhibitory neurons (E/I assemblies), resulting in co-tuning and precise balance of excitation and inhibition. To understand computational consequences of E/I assemblies under biologically realistic constraints we built a spiking network model based on experimental data from telencephalic area Dp of adult zebrafish, a precisely balanced recurrent network homologous to piriform cortex.
View Article and Find Full Text PDFGigascience
January 2025
School of Computer Science, Hunan University of Technology, Zhuzhou 412007, Hunan, China.
Background: The accurate deciphering of spatial domains, along with the identification of differentially expressed genes and the inference of cellular trajectory based on spatial transcriptomic (ST) data, holds significant potential for enhancing our understanding of tissue organization and biological functions. However, most of spatial clustering methods can neither decipher complex structures in ST data nor entirely employ features embedded in different layers.
Results: This article introduces STMSGAL, a novel framework for analyzing ST data by incorporating graph attention autoencoder and multiscale deep subspace clustering.
Physiol Meas
January 2025
Academy of Military Science of the People's Liberation Army, Beijing, 100073, CHINA.
Objective: Humanity faces many health challenges, among which respiratory diseases are one of the leading causes of human death. Existing AI-driven pre-diagnosis approaches can enhance the efficiency of diagnosis but still face challenges. For example, single-modal data suffer from information redundancy or loss, difficulty in learning relationships between features, and revealing the obscure characteristics of complex diseases.
View Article and Find Full Text PDFBioinformatics
January 2025
The Shmunis School of Biomedicine and Cancer Research, George S. Wise Faculty of Life Sciences, Tel Aviv University, Tel Aviv 69978, Israel.
Phys Rev Lett
December 2024
Institute for Advanced Study, Tsinghua University, Beijing 100084, China.
The nonintegrable higher spin Kitaev honeycomb model has an exact Z_{2} gauge structure, which exclusively identifies quantum spin liquid in the half-integer spin Kitaev model. But its constraints for the integer-spin Kitaev model are much limited, and even trivially gapped insulators cannot be excluded. The physical implications of exact Z_{2} gauge structure, especially Z_{2} fluxes, in integer-spin models remain largely unexplored.
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