Evidence map›Paper›PMID 40610627›Full record

ArticleNature genetics2025

Detecting and quantifying clonal selection in somatic stem cells.

Verena Körber, Niels Asger Jakobsen, Naser Ansari-Pour, Rachel Moore, Nina Claudino, Marlen Metzner, Eva Thielecke, Franziska Esau, Batchimeg Usukhbayar, Mirian Angulo Salazar and 13 more

Abstract read
In one paragraph

Article in Nature genetics, 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. Clonal selection of somatic mutations shapes NK cell memory.bioRxiv : the preprint server for biology · 2026
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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

23 authors.

Verena KörberDivision of Theoretical Systems Biology, German Cancer Research Center (DKFZ), Heidelberg, Germany. verena.korber@ndcls.ox.ac.uk.ORCID http://orcid.org/0009-0005-3888-2648
Niels Asger JakobsenMRC Molecular Haematology Unit, Oxford Biomedical Research Center, Hematology Theme, Oxford Centre for Haematology, Weatherall Institute of Molecular Medicine, Radcliffe Department of Medicine, University of Oxford, Oxford, UK.ORCID http://orcid.org/0000-0002-5776-5085
Naser Ansari-PourMRC Molecular Haematology Unit, Oxford Biomedical Research Center, Hematology Theme, Oxford Centre for Haematology, Weatherall Institute of Molecular Medicine, Radcliffe Department of Medicine, University of Oxford, Oxford, UK.
Rachel MooreMRC Molecular Haematology Unit, Oxford Biomedical Research Center, Hematology Theme, Oxford Centre for Haematology, Weatherall Institute of Molecular Medicine, Radcliffe Department of Medicine, University of Oxford, Oxford, UK.
Nina ClaudinoDivision of Theoretical Systems Biology, German Cancer Research Center (DKFZ), Heidelberg, Germany.
Marlen MetznerMRC Molecular Haematology Unit, Oxford Biomedical Research Center, Hematology Theme, Oxford Centre for Haematology, Weatherall Institute of Molecular Medicine, Radcliffe Department of Medicine, University of Oxford, Oxford, UK.
Eva ThieleckeDivision of Theoretical Systems Biology, German Cancer Research Center (DKFZ), Heidelberg, Germany.ORCID http://orcid.org/0009-0001-3997-4297
Franziska EsauDivision of Theoretical Systems Biology, German Cancer Research Center (DKFZ), Heidelberg, Germany.
Batchimeg UsukhbayarMRC Molecular Haematology Unit, Oxford Biomedical Research Center, Hematology Theme, Oxford Centre for Haematology, Weatherall Institute of Molecular Medicine, Radcliffe Department of Medicine, University of Oxford, Oxford, UK.
Mirian Angulo SalazarMRC Molecular Haematology Unit, Oxford Biomedical Research Center, Hematology Theme, Oxford Centre for Haematology, Weatherall Institute of Molecular Medicine, Radcliffe Department of Medicine, University of Oxford, Oxford, UK.
Simon NewmanNuffield Department of Orthopaedics, Rheumatology and Musculoskeletal Sciences, Botnar Research Centre, University of Oxford, Oxford, UK.
Benjamin J L KendrickNuffield Department of Orthopaedics, Rheumatology and Musculoskeletal Sciences, Botnar Research Centre, University of Oxford, Oxford, UK.
Adrian H TaylorNuffield Department of Orthopaedics, Rheumatology and Musculoskeletal Sciences, Botnar Research Centre, University of Oxford, Oxford, UK.
Rasheed Afinowi-LuitzNuffield Orthopaedic Centre, Oxford University Hospitals NHS Foundation Trust, Oxford, UK.
Roger GundleNuffield Department of Orthopaedics, Rheumatology and Musculoskeletal Sciences, Botnar Research Centre, University of Oxford, Oxford, UK.
Bridget WatkinsNuffield Department of Orthopaedics, Rheumatology and Musculoskeletal Sciences, Botnar Research Centre, University of Oxford, Oxford, UK.
Kim WhewayNuffield Department of Orthopaedics, Rheumatology and Musculoskeletal Sciences, Botnar Research Centre, University of Oxford, Oxford, UK.
Debra BeazleyNuffield Department of Orthopaedics, Rheumatology and Musculoskeletal Sciences, Botnar Research Centre, University of Oxford, Oxford, UK.
Stephanie G DakinNuffield Department of Orthopaedics, Rheumatology and Musculoskeletal Sciences, Botnar Research Centre, University of Oxford, Oxford, UK.
Antony PalmerNuffield Department of Orthopaedics, Rheumatology and Musculoskeletal Sciences, Botnar Research Centre, University of Oxford, Oxford, UK.
Andrew J CarrNuffield Department of Orthopaedics, Rheumatology and Musculoskeletal Sciences, Botnar Research Centre, University of Oxford, Oxford, UK.
Paresh Vyas *MRC Molecular Haematology Unit, Oxford Biomedical Research Center, Hematology Theme, Oxford Centre for Haematology, Weatherall Institute of Molecular Medicine, Radcliffe Department of Medicine, University of Oxford, Oxford, UK. paresh.vyas@imm.ox.ac.uk.ORCID http://orcid.org/0000-0003-3931-0914
Thomas Höfer *Division of Theoretical Systems Biology, German Cancer Research Center (DKFZ), Heidelberg, Germany. t.hoefer@dkfz.de.ORCID http://orcid.org/0000-0003-3560-8780

Funding

Bundesministerium für Bildung und Forschung (Federal Ministry of Education and Research) 01KD2206BDeutsche Forschungsgemeinschaft (German Research Foundation) 497777320Deutsche Forschungsgemeinschaft (German Research Foundation) 526169089Gordon and Betty Moore Foundation (Gordon E. and Betty I. Moore Foundation) 2919.02National Science Foundation (NSF) PHY-2309135
6 · The paper itself

Abstract

As DNA variants accumulate in somatic stem cells, become selected or evolve neutrally, they may ultimately alter tissue function. When, and how, selection occurs in homeostatic tissues is incompletely understood. Here, we introduce SCIFER, a scalable method that identifies selection in an individual tissue, without requiring knowledge of the driver event. SCIFER also infers self-renewal and mutation dynamics of the tissue's stem cells, and the size and age of selected clones. Probing bulk whole-genome sequencing data of nonmalignant human bone marrow and brain, we detected pervasive selection in both tissues. Selected clones in hematopoiesis, with or without known drivers, were initiated uniformly across life. In the brain, we found pre-malignant clones with glioma-initiating mutations and clones without known drivers. In contrast to hematopoiesis, selected clones in the brain originated preferentially from childhood to young adulthood. SCIFER is broadly applicable to renewing somatic tissues to detect and quantify selection.

Indexed as

Stem CellsAdultBrainChildClonal EvolutionClone CellsGliomaHematopoiesisHumansMutationSelection, GeneticWhole Genome Sequencing

Identifiers

PMID40610627
PMCPMC12283403

What Socratic holds

Textmetadata
LicenceCC BY
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Registered trials

None linked

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 Socratic graph.