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Zhongkun Zuo

dblp:426/4514 · DBLP profile ↗
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1ranked-venue papers
0as first author
1since 2021 · last 2024
—ORCID · unresolved

Domains — the database's venue-derived domains; a paper can count in several

Applied, interdisciplinary, general and emerging computing · 1 · 1 since 2021

Expertise — from the expertise taxonomy: the topics of the expert's papers under the CCF categories. A weight counts papers with recency: 1 for a paper about the topic, 0.3 when the topic is its context, halved every five years.

Interdisciplinary, comprehensive, and emerging computing
1 paper
Bioinformatics and computational biology · 100%

Topics — the 4 heaviest of 4, each with the papers that count most for it

TopicWeightPapersLastEvidence papers
Bioinformatics and computational biology › genomics
computational genomics
0.812024
A signal-diffusion-based unsupervised contrastive representation learning for spatial transcriptomics analysis · Bioinform. 2024
Bioinformatics and computational biology
contrastive learning
0.812024
A signal-diffusion-based unsupervised contrastive representation learning for spatial transcriptomics analysis · Bioinform. 2024
Bioinformatics and computational biology › transcriptomics › spatial transcriptomics
spatial domain identification
0.812024
A signal-diffusion-based unsupervised contrastive representation learning for spatial transcriptomics analysis · Bioinform. 2024
Bioinformatics and computational biology › transcriptomics › spatial transcriptomics
spatial transcriptomics analysis
0.812024
A signal-diffusion-based unsupervised contrastive representation learning for spatial transcriptomics analysis · Bioinform. 2024

Methods — techniques the papers use, named apart from their topics

unsupervised contrastive learning · 0.8signal diffusion · 0.8mutual information maximization · 0.8
YearPublicationVenuePosition
2024 A signal-diffusion-based unsupervised contrastive representation learning for spatial transcriptomics analysis
abstract
MOTIVATION: Spatial transcriptomics allows for the measurement of high-throughput gene expression data while preserving the spatial structure of tissues and histological images. Integrating gene expression, spatial information, and image data to learn discriminative low-dimensional representations is critical for dissecting tissue heterogeneity and analyzing biological functions. However, most existing methods have limitations in effectively utilizing spatial information and high-resolution histological images. We propose a signal-diffusion-based unsupervised contrast learning method (SDUCL) for learning low-dimensional latent embeddings of cells/spots. RESULTS: SDUCL integrates image features, spatial relationships, and gene expression information. We designed a signal diffusion microenvironment discovery algorithm, which effectively captures and integrates interaction information within the cellular microenvironment by simulating the biological signal diffusion process. By maximizing the mutual information between the local representation and the microenvironment representation of cells/spots, SDUCL learns more discriminative representations. SDUCL was employed to analyze spatial transcriptomics datasets from multiple species, encompassing both normal and tumor tissues. SDUCL performed well in downstream tasks such as clustering, visualization, trajectory inference, and differential gene analysis, thereby enhancing our understanding of tissue structure and tumor microenvironments. AVAILABILITY AND IMPLEMENTATION: https://github.com/WeiMin-Li-visual/SDUCL.
Weimin Li 0001, Fangfang Liu 0008, Yin Luo, Zhongkun Zuo
Bioinform.6