Evidence map›Paper›PMID 41676327›Full record

ArticleQuantitative biology (Beijing, China)2026

DNA methylation meets lineage tracing: History, recent progress, and future directions.

Ruijiang Fu, Mengyang Chen, Shou-Wen Wang

Abstract read
In one paragraph

Article in Quantitative biology (Beijing, China), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Review
  2. 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

3 authors.

Ruijiang FuWestlake Laboratory of Life Sciences and Biomedicine Hangzhou Zhejiang China.
Mengyang ChenWestlake Laboratory of Life Sciences and Biomedicine Hangzhou Zhejiang China.
Shou-Wen WangWestlake Laboratory of Life Sciences and Biomedicine Hangzhou Zhejiang China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Lineage tracing techniques have been developed rapidly in the past decades by employing new genetic engineering tools. However, due to their invasive nature, these are difficult to apply to humans. Although endogenous DNA mutations can be used for in vivo lineage tracing in humans, their extremely low mutation rate presents substantial technical challenges. Epimutations on DNA methylation happen at a rate of about 0.001 per CpG site per division. Such rich and stable information enables high-resolution, noninvasive lineage tracing in humans, as recently achieved with both MethylTree and EPI-Clone. MethylTree is a computational innovation that accurately predicts cell lineages from single-cell DNA methylation data, be it genome-wide or targeted. EPI-Clone is a targeted approach that requires careful CpG panel selection for specific tissues, which has been validated in blood. In this review, we present an overview of related historical studies, discuss the development of both MethylTree and EPI-Clone, and compare these two approaches. Although EPI-Clone is more scalable and cheaper, MethylTree has a higher resolution and works directly across different tissues. We demonstrate here that MethylTree also works well with EPI-Clone data, thus providing a unified solution for epimutation-based lineage tracing. Finally, we highlight the advantages of epimutation-based lineage tracing, discuss future directions for tool development, and touch on considerations in biological applications. Epimutation-based lineage tracing opens up an exciting avenue for noninvasive lineage tracing in humans across many biological processes.

Indexed as

DNA methylationlineage tracingsingle‐cell multi‐omics

Identifiers

PMID41676327
PMCPMC12806027

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.