Evidence map›Paper›PMID 40543050›Full record

ArticleG3 (Bethesda, Md.)2025

Minimizing detection bias of somatic mutations in a highly heterozygous oak genome.

Wenfei Xian, Pablo Carbonell-Bejerano, Fernando A Rabanal, Ilja Bezrukov, Philippe Reymond, Detlef Weigel

Abstract read
In one paragraph

Article in G3 (Bethesda, Md.), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing 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

8 citing papers in PubMed.

  1. Genome degradation in plant tissue culture.Proceedings of the National Academy of Sciences of the United States of America · 2026
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  8. Nanorate sequencing reveals theProceedings of the National Academy of Sciences of the United States of America · 2025
    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

6 authors.

Wenfei XianDepartment of Molecular Biology, Max Planck Institute for Biology Tübingen, Tübingen 72076, Germany.
Pablo Carbonell-BejeranoDepartment of Molecular Biology, Max Planck Institute for Biology Tübingen, Tübingen 72076, Germany.ORCID 0000-0002-7266-9665
Fernando A RabanalDepartment of Molecular Biology, Max Planck Institute for Biology Tübingen, Tübingen 72076, Germany.ORCID 0000-0003-1538-9752
Ilja BezrukovDepartment of Molecular Biology, Max Planck Institute for Biology Tübingen, Tübingen 72076, Germany.
Philippe ReymondDepartment of Plant Molecular Biology, University of Lausanne, Lausanne 1015, Switzerland.ORCID 0000-0002-3341-6200
Detlef WeigelDepartment of Molecular Biology, Max Planck Institute for Biology Tübingen, Tübingen 72076, Germany.ORCID 0000-0002-2114-7963

Funding

Max Planck SocietyNovozymes Prize of the Novo Nordisk Foundation
6 · The paper itself

Abstract

Somatic mutations are particularly relevant for long-lived organisms. Sources of somatic mutations include imperfect DNA repair, replication errors, and exogenous damage such as ultraviolet radiation. A previous study estimated a surprisingly low number of somatic mutations in a 234-year-old individual of the pedunculate oak (Quercus robur), known as the Napoleon Oak. It has been suggested that the true number of somatic mutations was underestimated due to gaps in the reference genome and too conservative filtering of potential mutations. We therefore generated new high-fidelity long-read data for the Napoleon Oak (n = 12) to produce both a pseudo-haploid genome assembly and a partially phased diploid assembly. The high heterozygosity allowed for complete reconstruction of phased and gapless centromeres for 22 of the 24 chromosomes. On the other hand, the high heterozygosity posed challenges for short-read alignments. Use of only the pseudo-haploid assembly as a reference led to potential misalignments, while use of only the diploid assembly reduced variant detection sensitivity. Since most somatic mutations are layer-specific, the fraction of reads covering a specific somatic mutation is expected to be relatively low, even where all cells in a single layer contain a specific mutation. To address this challenge, we employed a read assignment strategy, selecting the appropriate reference sequence (pseudo-haploid or diploid) based on alignment score and mapping quality. Ultimately, we identified 198 high-confidence somatic mutations, compared with 17 somatic mutations identified before with the same set of short reads. Our approach thus increased the total estimated annual mutation rate by a factor of 5.

Indexed as

Genome, PlantHeterozygoteMutationQuercusHiFi assemblyQuercus roburSomatic mutations

Identifiers

PMID40543050
PMCPMC12341919

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.