Evidence map›Paper›PMID 40539696›Full record

ArticleAdvanced science (Weinheim, Baden-Wurttemberg, Germany)2025

SGCD: High-Resolution Spatial Domain Characterization via Data Interpolation and Cell-Type Deconvolution.

Tianjiao Zhang, Shenghe Li, Ruolan Zhang, Hongfei Zhang, Zhongqian Zhao, Hao Sun, Zhenao Wu, Guohua Wang

Abstract read
In one paragraph

Article in Advanced science (Weinheim, Baden-Wurttemberg, Germany), 2025. 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
–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

3 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
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.

Tianjiao ZhangCollege of Computer and Control Engineering, Northeast Forestry University, No. 26 Hexing Road, Xiangfang District, Harbin, 150040, China.ORCID https://orcid.org/0000-0001-9807-8620
Shenghe LiCollege of Computer and Control Engineering, Northeast Forestry University, No. 26 Hexing Road, Xiangfang District, Harbin, 150040, China.ORCID https://orcid.org/0009-0009-7622-1743
Ruolan ZhangCollege of Computer and Control Engineering, Northeast Forestry University, No. 26 Hexing Road, Xiangfang District, Harbin, 150040, China.ORCID https://orcid.org/0009-0009-3846-8286
Hongfei ZhangCollege of Computer and Control Engineering, Northeast Forestry University, No. 26 Hexing Road, Xiangfang District, Harbin, 150040, China.ORCID https://orcid.org/0009-0002-4643-9716
Zhongqian ZhaoCollege of Computer and Control Engineering, Northeast Forestry University, No. 26 Hexing Road, Xiangfang District, Harbin, 150040, China.ORCID https://orcid.org/0009-0006-6754-7109
Hao SunCollege of Computer and Control Engineering, Northeast Forestry University, No. 26 Hexing Road, Xiangfang District, Harbin, 150040, China.ORCID https://orcid.org/0009-0009-6935-2905
Zhenao WuCollege of Computer and Control Engineering, Northeast Forestry University, No. 26 Hexing Road, Xiangfang District, Harbin, 150040, China.ORCID https://orcid.org/0009-0007-3774-8660
Guohua WangCollege of Computer and Control Engineering, Northeast Forestry University, No. 26 Hexing Road, Xiangfang District, Harbin, 150040, China.ORCID https://orcid.org/0000-0001-7381-2374

Funding

National Key Research and Development Program of China 2024YFF1206603National Natural Science Foundation of China 62473094National Science Foundation for Distinguished Young Scholars of China 62225109Natural Science Foundation of Heilongjiang Province, China LH2024F003
6 · The paper itself

Abstract

The rapid advancement of spatial transcriptomics has provided a critical data foundation for the high-resolution characterization of tissue spatial domains. Traditional methods for spatial domain identification primarily rely on gene expression data from sampled spots in low-resolution spatial transcriptomic data, often overlooking valuable information between spots that can be crucial for domain identification. Furthermore, these methods are limited by their focus on gene expression data from neighboring spots, without fully integrating prior knowledge of cell types within the tissue's spatial structure. To address these challenges, SGCD, a novel method for tissue spatial domain identification based on data interpolation and cell type deconvolution is proposed. SGCD utilizes interpolation techniques to estimate gene expression data for cells in the gaps between spots and applies deconvolution to extract cell type information from both spots and interstitial regions. By integrating gene expression, cell type, and spatial location data, SGCD achieves accurate delineation of complex spatial domains through graph contrastive learning. Evaluations on various publicly available datasets, including the human dorsolateral prefrontal cortex, mouse brain, pancreatic ductal adenocarcinoma, and breast cancer, demonstrate that SGCD significantly outperforms existing methods in both accuracy and detail, offering strong support for advancing the understanding of tissue functions and disease mechanisms.

Indexed as

Gene Expression ProfilingTranscriptomeAlgorithmsAnimalsBrainBreast NeoplasmsCarcinoma, Pancreatic DuctalFemaleHumansMicePrefrontal Cortexcell type deconvolutiondata interpolationspatial domain recognitionsspatial transcriptomics

Identifiers

PMID40539696
PMCPMC12442644

What Socratic holds

Textmetadata
LicenceCC BY
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 Socratic graph.