Evidence map›Paper›PMID 40000710›Full record

ArticleScientific data2025

Single-cell assay for transposase-accessible chromatin sequencing of human clear cell renal cell carcinoma.

Wenhao Lu, Yixuan Liu, Jiaping Li, Shengzhu Huang, Zheng Wen, Cheng Su, Zheng Lu, Zengnan Mo, Zhenyuan Yu

Abstract read
In one paragraph

Article in Scientific data, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Review
  2. Review
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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.

Wenhao Lu *Department of Urology, The First Affiliated Hospital of Guangxi Medical University, Nanning, 530021, Guangxi, China.
Yixuan Liu *Department of Urology, The First Affiliated Hospital of Guangxi Medical University, Nanning, 530021, Guangxi, China.
Jiaping Li *Guangxi Key Laboratory of Precision Medicine in Cardio-Cerebrovascular Diseases Control and Prevention, The First Affiliated Hospital of Guangxi Medical University, Nanning, 530021, Guangxi, China.
Shengzhu HuangCenter for Genomic and Personalized Medicine, Guangxi key Laboratory for Genomic and Personalized Medicine, Guangxi Collaborative Innovation Center for Genomic and Personalized Medicine, Guangxi Medical University, Nanning, 530021, Guangxi, China.
Zheng WenCenter for Genomic and Personalized Medicine, Guangxi key Laboratory for Genomic and Personalized Medicine, Guangxi Collaborative Innovation Center for Genomic and Personalized Medicine, Guangxi Medical University, Nanning, 530021, Guangxi, China.
Cheng SuCenter for Genomic and Personalized Medicine, Guangxi key Laboratory for Genomic and Personalized Medicine, Guangxi Collaborative Innovation Center for Genomic and Personalized Medicine, Guangxi Medical University, Nanning, 530021, Guangxi, China.
Zheng LuDepartment of Urology, The First Affiliated Hospital of Guangxi Medical University, Nanning, 530021, Guangxi, China. lzz134@163.com.
Zengnan MoDepartment of Urology, The First Affiliated Hospital of Guangxi Medical University, Nanning, 530021, Guangxi, China. mozengnan@gxmu.edu.cn.ORCID http://orcid.org/0000-0002-3047-3138
Zhenyuan YuDepartment of Urology, The First Affiliated Hospital of Guangxi Medical University, Nanning, 530021, Guangxi, China. yuzhenyuan@gxmu.edu.cn.ORCID http://orcid.org/0000-0002-3848-5504

Funding

Natural Science Foundation of Guangxi Province (Guangxi Natural Science Foundation) 2018GXNSFAA138192Natural Science Foundation of Guangxi Province (Guangxi Natural Science Foundation) 2024GXNSFBA010055
6 · The paper itself

Abstract

Regulating the occurrence and progression of tumor cells at the epigenetic level is a new insight of clear cell renal cell carcinoma (ccRCC). Chromatin accessibility is an important pathway of epigenetic regulation, which may explain the mystery of tumor occurrence. Assay for transposase-accessible chromatin sequencing (ATAC-seq) provides insight into the epigenetic regulatory features of ccRCC, especially at the single-cell level. In this study, we performed scATAC-seq of 3 ccRCC samples and captured a total of 18,703 high-quality cell nuclei and 104,818 unique peaks. Our protocol for nuclear extraction was reliable and stable, which can be used to deal with fresh and frozen single-cell suspensions. We presented basic methods for scATAC-seq data analysis, such as cell clustering, gene activity scoring, cell subtype specific peaks, transcription factors, motif and motif footprinting analysis. Taken together, our data indicated the valuable epigenetic features of ccRCC, which will provide more references for the study of ccRCC.

Indexed as

Carcinoma, Renal CellChromatinKidney NeoplasmsSingle-Cell AnalysisTransposasesEpigenesis, GeneticHumansChromatinTransposases

Identifiers

PMID40000710
PMCPMC11861977

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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.