Evidence map›Paper›PMID 41107232›Full record

ArticleNature communications2025

Systematic benchmarking of high-throughput subcellular spatial transcriptomics platforms across human tumors.

Pengfei Ren, Rui Zhang, Yunfeng Wang, Peng Zhang, Ce Luo, Suyan Wang, Xiaohong Li, Zongxu Zhang, Yanping Zhao, Yufeng He and 9 more

Abstract read
In one paragraph

Article in Nature communications, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 56 papers.

0numbers the graph read from it
0cells of the map it votes in
56citing 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

56 citing papers in PubMed.

  1. Article
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  11. Multi-omics characterization of a GPRC5AJournal of translational medicine · 2026
    Article
  12. Review
  13. Review
  14. Article
  15. Article
  16. Article
  17. Article
  18. Review
  19. Article
  20. CD4Science (New York, N.Y.) · 2026
    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

19 authors.

Pengfei Ren *Peking-Tsinghua Center for Life Sciences, Academy for Advanced Interdisciplinary Studies, Peking University, Beijing, China.
Rui Zhang *Peking-Tsinghua Center for Life Sciences, Academy for Advanced Interdisciplinary Studies, Peking University, Beijing, China.
Yunfeng WangPeking-Tsinghua Center for Life Sciences, Academy for Advanced Interdisciplinary Studies, Peking University, Beijing, China.
Peng ZhangCenter for Quantitative Biology, Academy for Advanced Interdisciplinary Studies, Peking University, Beijing, China.
Ce LuoCenter for Quantitative Biology, Academy for Advanced Interdisciplinary Studies, Peking University, Beijing, China.ORCID http://orcid.org/0000-0001-8024-6753
Suyan WangPeking University Chengdu Academy for Advanced Interdisciplinary Biotechnologies, Chengdu, Sichuan, China.
Xiaohong LiCenter for Quantitative Biology, Academy for Advanced Interdisciplinary Studies, Peking University, Beijing, China.
Zongxu ZhangCenter for Quantitative Biology, Academy for Advanced Interdisciplinary Studies, Peking University, Beijing, China.ORCID http://orcid.org/0009-0006-2909-5842
Yanping ZhaoTsinghua-Peking Center for Life Sciences, School of Life Sciences, Tsinghua University, Beijing, China.
Yufeng HePeking-Tsinghua Center for Life Sciences, Academy for Advanced Interdisciplinary Studies, Peking University, Beijing, China.ORCID http://orcid.org/0009-0000-3978-4103
Haorui ZhangPeking-Tsinghua Center for Life Sciences, Academy for Advanced Interdisciplinary Studies, Peking University, Beijing, China.
Yufeng LiDepartment of Obstetrics and Gynecology, Chinese PLA Medical School, Beijing, China.
Zhidong GaoDepartment of Gastroenterological Surgery, Peking University People's Hospital, Beijing, China.ORCID http://orcid.org/0000-0002-8415-7587
Xiuping ZhangFaculty of Hepato-Biliary-Pancreatic Surgery, the First Medical Center of Chinese People's Liberation Army (PLA) General Hospital, Chinese PLA Medical School, Beijing, China.
Yahui ZhaoState Key Laboratory of Molecular Oncology, National Cancer Center, National Clinical Research Center for Cancer, Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.
Zhihua LiuState Key Laboratory of Molecular Oncology, National Cancer Center, National Clinical Research Center for Cancer, Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.ORCID http://orcid.org/0000-0003-4242-033X
Yuanguang MengDepartment of Obstetrics and Gynecology, Seventh Medical Center of Chinese PLA General Hospital, Beijing, China. meng6512@sina.vip.com.
Zhe ZhangDepartment of Obstetrics and Gynecology, Seventh Medical Center of Chinese PLA General Hospital, Beijing, China. tj.zhe.zhang@gmail.com.
Zexian ZengPeking-Tsinghua Center for Life Sciences, Academy for Advanced Interdisciplinary Studies, Peking University, Beijing, China. zexianzeng@pku.edu.cn.ORCID http://orcid.org/0000-0002-3905-3244

Funding

National Natural Science Foundation of China (National Science Foundation of China) 92374116, 32470664, 82404094, and T2321001Natural Science Foundation of Beijing Municipality (Beijing Natural Science Foundation) L248043
6 · The paper itself

Abstract

Recent advancements in spatial transcriptomics technologies have significantly enhanced resolution and throughput, underscoring an urgent need for systematic benchmarking. Here, we generate serial tissue sections from colon adenocarcinoma, hepatocellular carcinoma, and ovarian cancer samples for systematic evaluation. Using these uniformly processed samples, we generate spatial transcriptomics data across four high-throughput platforms with subcellular resolution: Stereo-seq v1.3, Visium HD FFPE, CosMx 6K, and Xenium 5K. To establish ground truth datasets, we profile proteins on tissue sections adjacent to all platforms using CODEX and perform single-cell RNA sequencing on the same samples. Leveraging manual nuclear segmentation and detailed annotations, we systematically assess each platform's performance across capture sensitivity, specificity, diffusion control, cell segmentation, cell annotation, spatial clustering, and concordance with adjacent CODEX. The uniformly generated and processed multi-omics dataset could advance computational method development and biological discoveries. The dataset is accessible via SPATCH, a user-friendly web server for visualization and download.

Indexed as

Gene Expression ProfilingNeoplasmsTranscriptomeBenchmarkingCarcinoma, HepatocellularColonic NeoplasmsFemaleHigh-Throughput Nucleotide SequencingHumansLiver NeoplasmsOvarian NeoplasmsSingle-Cell Analysis

Identifiers

PMID41107232
PMCPMC12534522

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.