Evidence map›Paper›PMID 39763408›Full record

ArticleSmall methods2025

UCS: A Unified Approach to Cell Segmentation for Subcellular Spatial Transcriptomics.

Yuheng Chen, Xin Xu, Xiaomeng Wan, Jiashun Xiao, Can Yang

Abstract read
In one paragraph

Article in Small methods, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing 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

9 citing papers in PubMed.

  1. Review
  2. Article
  3. Review
  4. Artificial Intelligence Revolution in Transcriptomics: From Single Cells to Spatial Atlases.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
    Review
  5. Article
  6. AI/ML-Assisted Detection ofInternational journal of molecular sciences · 2025
    Article
  7. A unified framework for identification of cell-type-specific spatially variable genes in spatial transcriptomic studies.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  8. Article
  9. 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

5 authors.

Yuheng ChenDepartment of Mathematics, The Hong Kong University of Science and Technology, Hong Kong SAR, 999077, China.
Xin XuDepartment of Mathematics, The Hong Kong University of Science and Technology, Hong Kong SAR, 999077, China.
Xiaomeng WanDepartment of Mathematics, The Hong Kong University of Science and Technology, Hong Kong SAR, 999077, China.
Jiashun XiaoShenzhen Research Institute of Big Data, ShenZhen, 518100, China.
Can YangDepartment of Mathematics, The Hong Kong University of Science and Technology, Hong Kong SAR, 999077, China.ORCID 0009-0004-7365-6323

Funding

Hong Kong University of Science and Technology 16301419Hong Kong University of Science and Technology 16302823Hong Kong University of Science and Technology 16307221Hong Kong University of Science and Technology 16307322Hong Kong University of Science and Technology 16308120Hong Kong University of Science and Technology R9405Hong Kong University of Science and Technology Z0428Innovation and Technology Commission ITCPD/17-9NSFC 12401384Shenzhen Science and Technology Program RCBS20231211090613024
6 · The paper itself

Abstract

Subcellular Spatial Transcriptomics (SST) represents an innovative technology enabling researchers to investigate gene expression at the subcellular level within tissues. To comprehend the spatial architecture of a given tissue, cell segmentation plays a crucial role in attributing the measured transcripts to individual cells. However, existing cell segmentation methods for SST datasets still face challenges in accurately distinguishing cell boundaries due to the varying characteristics of SST technologies. In this study, a unified approach is proposed to cell segmentation (UCS) specifically designed for SST data obtained from diverse platforms, including 10X Xenium, NanoString CosMx, MERSCOPE, and Stereo-seq. UCS leverages deep learning techniques to achieve high accuracy in cell segmentation by integrating nuclei segmentation from nuclei staining and transcript data. Compared to current methods, UCS not only provides more precise transcript assignment to individual cells but also offers computational advantages for large-scale SST data analysis. The analysis output of UCS further supports versatile downstream analyses, such as subcellular gene classification and missing cell detection. By employing UCS, researchers gain the ability to characterize gene expression patterns at both the cellular and subcellular levels, leading to a deeper understanding of tissue architecture and function.

Indexed as

Gene Expression ProfilingTranscriptomeAnimalsCell NucleusComputational BiologyDeep LearningHumansSingle-Cell Analysiscell segmentationdeep learningsubcellular spatial transcriptomics

Identifiers

PMID39763408
PMCPMC12103228

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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.