Demonstration venue · read-only. Every page can be browsed; the buttons that would change it are switched off. Create an account to run TaxoReview on your own data. A simulation from public publication records: the people listed were not invited and did not agree to review.
? Tutorial for this page

Yongwang Wang

dblp:426/0995 · DBLP profile ↗
← Back
1ranked-venue papers
0as first author
1since 2021 · last 2024
—ORCID · none

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 3 heaviest of 3, each with the papers that count most for it

TopicWeightPapersLastEvidence papers
Bioinformatics and computational biology › transcriptomics › spatial transcriptomics
spatial domain identification
0.812024
A multi-modality and multi-granularity collaborative learning framework for identifying spatial domains and spatially variable genes · Bioinform. 2024
Bioinformatics and computational biology › transcriptomics › spatial transcriptomics
spatially variable gene detection
0.812024
A multi-modality and multi-granularity collaborative learning framework for identifying spatial domains and spatially variable genes · Bioinform. 2024
Bioinformatics and computational biology › transcriptomics
spatial transcriptomics
0.812024
A multi-modality and multi-granularity collaborative learning framework for identifying spatial domains and spatially variable genes · Bioinform. 2024

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

multi-modality fusion · 0.8graph self-supervised learning · 0.8graph convolutional network · 0.8
YearPublicationVenuePosition
2024 A multi-modality and multi-granularity collaborative learning framework for identifying spatial domains and spatially variable genes
abstract
MOTIVATION: Recent advances in spatial transcriptomics technologies have provided multi-modality data integrating gene expression, spatial context, and histological images. Accurately identifying spatial domains and spatially variable genes is crucial for understanding tissue structures and biological functions. However, effectively combining multi-modality data to identify spatial domains and determining SVGs closely related to these spatial domains remains a challenge. RESULTS: In this study, we propose spatial transcriptomics multi-modality and multi-granularity collaborative learning (spaMMCL). For detecting spatial domains, spaMMCL mitigates the adverse effects of modality bias by masking portions of gene expression data, integrates gene and image features using a shared graph convolutional network, and employs graph self-supervised learning to deal with noise from feature fusion. Simultaneously, based on the identified spatial domains, spaMMCL integrates various strategies to detect potential SVGs at different granularities, enhancing their reliability and biological significance. Experimental results demonstrate that spaMMCL substantially improves the identification of spatial domains and SVGs. AVAILABILITY AND IMPLEMENTATION: The code and data of spaMMCL are available on Github: Https://github.com/liangxiao-cs/spaMMCL.
Baiyun Chen, Wei Liu 0296, Wanwan Shi, Yongwang Wang, Xiangtao Chen, Jiawei Luo 0001
Bioinform.7