Evidence map›Paper›PMID 41953641›Full record

ReviewMedComm2026

Single-Cell and Spatial Omics: Methods and Applications.

Xiaoping Cen, Xiaolan Huang, Enjin Deng, Xue Gong, Na Tan, Jifeng Ye, Yin Wang, Roland Eils, Qun Luo, Yixue Li and 1 more

Abstract readReview
In one paragraph

Review in MedComm, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Review
  5. Review
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

11 authors.

Xiaoping CenGuangzhou National Laboratory, Guangzhou International Bio Island Guangzhou Guangdong Province China.ORCID https://orcid.org/0000-0002-4848-4302
Xiaolan HuangGuangzhou National Laboratory, Guangzhou International Bio Island Guangzhou Guangdong Province China.
Enjin DengGuangzhou National Laboratory, Guangzhou International Bio Island Guangzhou Guangdong Province China.
Xue GongGMU-GIBH Joint School of Life Sciences Guangdong Provincial Key Laboratory of Protein Modification and Disease The Guangdong-Hong Kong-Macao Joint Laboratory for Cell Fate Regulation and Diseases Guangzhou Medical University Guangzhou China.
Na TanDepartment of Biomedical Engineering School of Intelligent Medicine China Medical University Shenyang Liaoning China.
Jifeng YeGMU-GIBH Joint School of Life Sciences Guangdong Provincial Key Laboratory of Protein Modification and Disease The Guangdong-Hong Kong-Macao Joint Laboratory for Cell Fate Regulation and Diseases Guangzhou Medical University Guangzhou China.
Yin WangDepartment of Biomedical Engineering School of Intelligent Medicine China Medical University Shenyang Liaoning China.ORCID https://orcid.org/0000-0003-3120-8579
Roland EilsDigital Health Center Berlin Institute of Health (BIH) Charité - Universitätsmedizin Berlin Berlin Germany.
Qun LuoGuangzhou National Laboratory, Guangzhou International Bio Island Guangzhou Guangdong Province China.
Yixue LiGuangzhou National Laboratory, Guangzhou International Bio Island Guangzhou Guangdong Province China.
Fangfang QuGuangzhou National Laboratory, Guangzhou International Bio Island Guangzhou Guangdong Province China.ORCID https://orcid.org/0000-0001-5193-0644

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Single-cell and spatial omics have revolutionized biomedical research by enabling high-resolution molecular profiling across cells and tissues, thereby overcoming key limitations of bulk sequencing and revealing unprecedented cellular heterogeneity and spatial organization central to development, homeostasis, and disease. Specifically, advances in high-throughput, subcellular, and multiomics profiling are promoting the field toward deeper insights. In parallel, computational progress, including generative artificial intelligence (AI) and foundation models, is developing rapidly for manipulating multimodal multiomics data. These advancements have been applied to diverse diseases and biological systems, facilitating innovative biomedical findings. However, a significant gap persists between rapid methodological advances and their systematic application for deciphering human biology and pathology. This review synthesizes recent breakthroughs in single-cell and spatial technologies and surveys computational methods, including AI-driven approaches, foundation models, and multi-omics integration algorithms for both single-cell and spatial analyses. We then summarize representative applications across major human organ systems in health and disease, highlighting opportunities for biomarker discovery, therapeutic target identification, and precision medicine. Finally, we discuss current challenges and future directions for bridging technological innovation with robust biomedical discovery and translational impact. This review provides a vital guide for researchers in the field, offering critical insights for accelerating the translation of single-cell and spatial omics.

Indexed as

artificial intelligencefoundation modelsmulti‐omics integrationprecision medicinesingle‐cell omicsspatial omics

Identifiers

PMID41953641
PMCPMC13053676

What OpenQuestion holds

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LicenceCC BY
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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.