Evidence map›Paper›PMID 39614161›Full record

ArticleBMC genomics2024

Deciphering spatial domains from spatially resolved transcriptomics through spatially regularized deep graph networks.

Daoliang Zhang, Na Yu, Xue Sun, Haoyang Li, Wenjing Zhang, Xu Qiao, Wei Zhang, Rui Gao

Abstract read
In one paragraph

Article in BMC genomics, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Daoliang Zhang *Center of Intelligent Medicine, School of Control Science and Engineering, Shandong University, Jinan, Shandong, 250061, China.
Na Yu *Center of Intelligent Medicine, School of Control Science and Engineering, Shandong University, Jinan, Shandong, 250061, China.
Xue SunCenter of Intelligent Medicine, School of Control Science and Engineering, Shandong University, Jinan, Shandong, 250061, China.
Haoyang LiCenter of Intelligent Medicine, School of Control Science and Engineering, Shandong University, Jinan, Shandong, 250061, China.
Wenjing ZhangCenter of Intelligent Medicine, School of Control Science and Engineering, Shandong University, Jinan, Shandong, 250061, China.
Xu QiaoCenter of Intelligent Medicine, School of Control Science and Engineering, Shandong University, Jinan, Shandong, 250061, China. qiaoxu@sdu.edu.cn.
Wei ZhangCenter of Intelligent Medicine, School of Control Science and Engineering, Shandong University, Jinan, Shandong, 250061, China. zw@sdu.edu.cn.
Rui GaoCenter of Intelligent Medicine, School of Control Science and Engineering, Shandong University, Jinan, Shandong, 250061, China. gaorui@sdu.edu.cn.

Funding

National Natural Science Foundation of China 62303271National Natural Science Foundation of China U1806202Natural Science Foundation of Shandong Province ZR2023QF081
6 · The paper itself

Abstract

backgroundRecent advancements in spatially resolved transcriptomics (SRT) have opened up unprecedented opportunities to explore gene expression patterns within spatial contexts. Deciphering spatial domains is a critical task in spatial transcriptomic data analysis, aiding in the elucidation of tissue structural heterogeneity and biological functions. However, existing spatial domain detection methods ignore the consistency of expression patterns and spatial arrangements between spots, as well as the severe gene dropout phenomenon present in SRT data, resulting in suboptimal performance in identifying tissue spatial heterogeneity.

resultsIn this paper, we introduce a novel framework, spatially regularized deep graph networks (SR-DGN), which integrates gene expression profiles with spatial information to learn spatially-consistent and informative spot representations. Specifically, SR-DGN employs graph attention networks (GAT) to adaptively aggregate gene expression information from neighboring spots, considering local expression patterns between spots. In addition, the spatial regularization constraint ensures the consistency of neighborhood relationships between physical and embedded spaces in an end-to-end manner. SR-DGN also employs cross-entropy (CE) loss to model gene expression states, effectively mitigating the impact of noisy gene dropouts.

conclusionsExperimental results demonstrate that SR-DGN outperforms state-of-the-art methods in spatial domain identification across SRT data from different sequencing platforms. Moreover, SR-DGN is capable of recovering known microanatomical structures, yielding clearer low-dimensional visualizations and more accurate spatial trajectory inferences.

Indexed as

Gene Expression ProfilingAlgorithmsComputational BiologyHumansTranscriptomeCross-entropy lossGraph attention networkSpatial domainsSpatial regularization constraintSpatial resolved transcriptomics

Identifiers

PMID39614161
PMCPMC11607964

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

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.