Evidence map›Paper›PMID 38416785›Full record

ArticlePLoS computational biology2024

STGIC: A graph and image convolution-based method for spatial transcriptomic clustering.

Chen Zhang, Junhui Gao, Hong-Yu Chen, Lingxin Kong, Guangshuo Cao, Xiangyu Guo, Wei Liu, Bin Ren, Dong-Qing Wei

Open access · goldAbstract read
In one paragraph

Article in PLoS computational biology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
1.4field-weighted citation impact, top 20% of its field
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

3 citing papers in PubMed, 6 citations in OpenAlex.

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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

9 authors at 5 institutions in 2 countries.

Chen ZhangSchool of Life Sciences and Biotechnology, Shanghai Jiao Tong University, Shanghai, China.ORCID 0009-0005-8396-9398
Junhui GaoDepartment of Computer Science and Engineering, Shanghai Jiao Tong University, Shanghai, China.
Hong-Yu ChenCollege of Life Science and Technology, Huazhong University of Science and Technology, Wuhan, China.
Lingxin KongSchool of Life Sciences and Biotechnology, Shanghai Jiao Tong University, Shanghai, China.
Guangshuo CaoState Key Laboratory of Public Big Data, College of Computer Science and Technology, Guizhou University, Guiyang.
Xiangyu GuoSmart-Health Initiative, King Abdullah University of Science and Technology, Jeddah, Saudi Arabia.ORCID 0000-0001-5835-490X
Wei LiuMarine Science and Technology College, Zhejiang Ocean University, Zhoushan, China.
Bin RenSchool of Life Sciences and Biotechnology, Shanghai Jiao Tong University, Shanghai, China.
Dong-Qing WeiSchool of Life Sciences and Biotechnology, Shanghai Jiao Tong University, Shanghai, China.ORCID 0000-0003-4200-7502
Shanghai Jiao Tong University · CNGuizhou University · CNHuazhong University of Science and Technology · CNKing Abdullah University of Science and Technology · SAZhejiang Ocean University · CN

Funding

National Natural Science Foundation of China
6 · The paper itself

Abstract

Spatial transcriptomic (ST) clustering employs spatial and transcription information to group spots spatially coherent and transcriptionally similar together into the same spatial domain. Graph convolution network (GCN) and graph attention network (GAT), fed with spatial coordinates derived adjacency and transcription profile derived feature matrix are often used to solve the problem. Our proposed method STGIC (spatial transcriptomic clustering with graph and image convolution) is designed for techniques with regular lattices on chips. It utilizes an adaptive graph convolution (AGC) to get high quality pseudo-labels and then resorts to dilated convolution framework (DCF) for virtual image converted from gene expression information and spatial coordinates of spots. The dilation rates and kernel sizes are set appropriately and updating of weight values in the kernels is made to be subject to the spatial distance from the position of corresponding elements to kernel centers so that feature extraction of each spot is better guided by spatial distance to neighbor spots. Self-supervision realized by Kullback-Leibler (KL) divergence, spatial continuity loss and cross entropy calculated among spots with high confidence pseudo-labels make up the training objective of DCF. STGIC attains state-of-the-art (SOTA) clustering performance on the benchmark dataset of 10x Visium human dorsolateral prefrontal cortex (DLPFC). Besides, it's capable of depicting fine structures of other tissues from other species as well as guiding the identification of marker genes. Also, STGIC is expandable to Stereo-seq data with high spatial resolution.

Indexed as

Gene Expression ProfilingTranscriptomeBenchmarkingCluster AnalysisEntropyHumans

Identifiers

PMID38416785
PMCPMC10927115
OpenAlexW4392230499

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.