Evidence map›Paper›PMID 41614193›Full record

ArticleJACS Au2026

Nanobody-Tethered Transposition for Dual Profiling of Histone Modification and DNA Methylation.

Jizhou Liu, Jindi Zhou, Ziang Lu, Guorun Tang, Zhiying Wang, Yelin Lan, Xiang Zhou, Guanzheng Luo, Yafen Wang, Xiaocheng Weng

Abstract read
In one paragraph

Article in JACS Au, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

10 authors.

Jizhou LiuDepartment of Neurosurgery, Zhongnan Hospital of Wuhan University, Wuhan 430071, China.
Jindi ZhouState Key Laboratory of Metabolism and Regulation in Complex Organisms, College of Chemistry and Molecular Sciences, Taikang Center for Life and Medical Sciences, Wuhan University, Wuhan 430072, China.
Ziang LuState Key Laboratory of Metabolism and Regulation in Complex Organisms, College of Chemistry and Molecular Sciences, Taikang Center for Life and Medical Sciences, Wuhan University, Wuhan 430072, China.
Guorun TangSchool of Life Sciences, MOE Key Laboratory of Gene Function and Regulation, Sun Yat-sen University, Guangzhou 510275, China.
Zhiying WangState Key Laboratory of Metabolism and Regulation in Complex Organisms, College of Chemistry and Molecular Sciences, Taikang Center for Life and Medical Sciences, Wuhan University, Wuhan 430072, China.
Yelin LanSchool of Life Sciences, MOE Key Laboratory of Gene Function and Regulation, Sun Yat-sen University, Guangzhou 510275, China.
Xiang ZhouState Key Laboratory of Metabolism and Regulation in Complex Organisms, College of Chemistry and Molecular Sciences, Taikang Center for Life and Medical Sciences, Wuhan University, Wuhan 430072, China.ORCID https://orcid.org/0000-0002-1829-9368
Guanzheng LuoSchool of Life Sciences, MOE Key Laboratory of Gene Function and Regulation, Sun Yat-sen University, Guangzhou 510275, China.
Yafen WangSchool of Public Health, Wuhan University, Wuhan 430072, China.ORCID https://orcid.org/0000-0003-2281-1763
Xiaocheng WengDepartment of Neurosurgery, Zhongnan Hospital of Wuhan University, Wuhan 430071, China.ORCID https://orcid.org/0000-0002-0605-8495

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

DNA methylation and histone modifications are critical epigenetic regulators that orchestrate gene expression and modulate various physiological and pathological processes. However, existing methodologies for simultaneous profiling of these epigenetic marks often require high cell input and suffer from data loss due to bisulfite conversion. In this study, we present advanced multimodal chromatin profiling methods, MethylTag and Multi-MethylTag, that address these challenges by integrating Tn5 transposase with methylated adaptors and optimizing postbisulfite library preparation. These methods enable high-resolution, multidimensional chromatin profiling with reduced cell input and improved data integrity. We validated these techniques in various human and mouse cell lines, revealing complex interactions between DNA methylation and histone modifications. Our findings highlight the utility of these approaches in enhancing epigenetic research and deepening our understanding of the regulatory mechanisms underlying gene expression.

Indexed as

CUT&tagDNA methylationhistone modificationmultimodal chromatin profiling

Identifiers

PMID41614193
PMCPMC12848732

What OpenQuestion holds

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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.