Evidence map›Paper›PMID 39413798›Full record

ArticleBriefings in bioinformatics2024

SELF-Former: multi-scale gene filtration transformer for single-cell spatial reconstruction.

Tianyi Chen, Xindian Wei, Lianxin Xie, Yunfei Zhang, Cheng Liu, Wenjun Shen, Si Wu, Hau-San Wong

Abstract read
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Article in Briefings in bioinformatics, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

6 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

8 authors.

Tianyi ChenDepartment of Computer Science, City University of Hong Kong, Kowloon 999077, Hong Kong.
Xindian WeiDepartment of Computer Science, City University of Hong Kong, Kowloon 999077, Hong Kong.
Lianxin XieSchool of Computer Science and Engineering, South China University of Technology, Guangdong 510006, China.
Yunfei ZhangSchool of Future Technology, South China University of Technology, Guangdong 511442, China.
Cheng LiuDepartment of Computer Science, Shantou University, Shantou 515063, China.
Wenjun ShenDepartment of Bioinformatics, Shantou University Medical College, Shantou 515041, China.
Si WuSchool of Computer Science and Engineering, South China University of Technology, Guangdong 510006, China.
Hau-San WongDepartment of Computer Science, City University of Hong Kong, Kowloon 999077, Hong Kong.

Funding

City University of Hong Kong 7005986Guangdong Basic and Applied Basic Research Foundation 2022A1515011160National Natural Science Foundation of China 62072189Research Grants Council of the Hong Kong Special Administration Region 11206622TCL Science and Technology Innovation Fund 20231752
6 · The paper itself

Abstract

The spatial reconstruction of single-cell RNA sequencing (scRNA-seq) data into spatial transcriptomics (ST) is a rapidly evolving field that addresses the significant challenge of aligning gene expression profiles to their spatial origins within tissues. This task is complicated by the inherent batch effects and the need for precise gene expression characterization to accurately reflect spatial information. To address these challenges, we developed SELF-Former, a transformer-based framework that utilizes multi-scale structures to learn gene representations, while designing spatial correlation constraints for the reconstruction of corresponding ST data. SELF-Former excels in recovering the spatial information of ST data and effectively mitigates batch effects between scRNA-seq and ST data. A novel aspect of SELF-Former is the introduction of a gene filtration module, which significantly enhances the spatial reconstruction task by selecting genes that are crucial for accurate spatial positioning and reconstruction. The superior performance and effectiveness of SELF-Former's modules have been validated across four benchmark datasets, establishing it as a robust and effective method for spatial reconstruction tasks. SELF-Former demonstrates its capability to extract meaningful gene expression information from scRNA-seq data and accurately map it to the spatial context of real ST data. Our method represents a significant advancement in the field, offering a reliable approach for spatial reconstruction.

Indexed as

Single-Cell AnalysisAlgorithmsComputational BiologyGene Expression ProfilingHumansSequence Analysis, RNASoftwareTranscriptomegene filtrationmulti-scalesingle-cell RNA sequencespatial transcriptomicstransformer

Identifiers

PMID39413798
PMCPMC11483138

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.