Evidence map›Paper›PMID 37640936›Full record

ArticleNature methods2023

scNanoHi-C: a single-cell long-read concatemer sequencing method to reveal high-order chromatin structures within individual cells.

Wen Li, Jiansen Lu, Ping Lu, Yun Gao, Yichen Bai, Kexuan Chen, Xinjie Su, Mengyao Li, Jun'e Liu, Yijun Chen and 2 more

Abstract read
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In one paragraph

Article in Nature methods, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers.

0numbers the graph read from it
0cells of the map it votes in
39citing 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

39 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
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  5. Article
  6. Article
  7. Enhancer Dynamics for Gene Regulation in the Cardiovascular System.Arteriosclerosis, thrombosis, and vascular biology · 2026
    Review
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  9. Article
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  11. Review
  12. Review
  13. Article
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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

12 authors.

Wen Li *School of Life Sciences, Biomedical Pioneering Innovative Center, Peking University, Beijing, China.ORCID http://orcid.org/0000-0002-6873-0283
Jiansen Lu *School of Life Sciences, Biomedical Pioneering Innovative Center, Peking University, Beijing, China.ORCID http://orcid.org/0000-0002-8320-1435
Ping LuSchool of Life Sciences, Biomedical Pioneering Innovative Center, Peking University, Beijing, China.ORCID http://orcid.org/0000-0002-4340-2670
Yun GaoSchool of Life Sciences, Biomedical Pioneering Innovative Center, Peking University, Beijing, China.ORCID http://orcid.org/0000-0003-3530-7259
Yichen BaiSchool of Life Sciences, Biomedical Pioneering Innovative Center, Peking University, Beijing, China.
Kexuan ChenSchool of Life Sciences, Biomedical Pioneering Innovative Center, Peking University, Beijing, China.ORCID http://orcid.org/0000-0002-7236-6402
Xinjie SuSchool of Life Sciences, Biomedical Pioneering Innovative Center, Peking University, Beijing, China.ORCID http://orcid.org/0009-0006-9486-1128
Mengyao LiSchool of Life Sciences, Biomedical Pioneering Innovative Center, Peking University, Beijing, China.ORCID http://orcid.org/0000-0003-0739-4236
Jun'e LiuSchool of Life Sciences, Biomedical Pioneering Innovative Center, Peking University, Beijing, China.
Yijun ChenPeking-Tsinghua Center for Life Sciences, Academy for Advanced Interdisciplinary Studies, Peking University, Beijing, China.ORCID http://orcid.org/0000-0001-6122-6271
Lu WenSchool of Life Sciences, Biomedical Pioneering Innovative Center, Peking University, Beijing, China.ORCID http://orcid.org/0000-0002-1773-1876
Fuchou TangSchool of Life Sciences, Biomedical Pioneering Innovative Center, Peking University, Beijing, China. tangfuchou@pku.edu.cn.ORCID http://orcid.org/0000-0002-8625-7717

Funding

National Natural Science Foundation of China (National Science Foundation of China) 32288102
6 · The paper itself

Abstract

The high-order three-dimensional (3D) organization of regulatory genomic elements provides a topological basis for gene regulation, but it remains unclear how multiple regulatory elements across the mammalian genome interact within an individual cell. To address this, herein, we developed scNanoHi-C, which applies Nanopore long-read sequencing to explore genome-wide proximal high-order chromatin contacts within individual cells. We show that scNanoHi-C can reliably and effectively profile 3D chromatin structures and distinguish structure subtypes among individual cells. This method could also be used to detect genomic variations, including copy-number variations and structural variations, as well as to scaffold the de novo assembly of single-cell genomes. Notably, our results suggest that extensive high-order chromatin structures exist in active chromatin regions across the genome, and multiway interactions between enhancers and their target promoters were systematically identified within individual cells. Altogether, scNanoHi-C offers new opportunities to investigate high-order 3D genome structures at the single-cell level.

Indexed as

ChromatinNanopore SequencingSequence Analysis, DNASingle-Cell AnalysisAnimalsDNA Copy Number VariationsHigh-Throughput Nucleotide SequencingHumansMicePromoter Regions, GeneticChromatin

Identifiers

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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.