Previous investigations of the genome of Wilms tumour have demonstrated surprisingly few driver mutations and low tumour mutational burden. Integrating duplex sequencing and use of laser-captured specimens and tumour organoids unveiled a fourfold increased tumour mutational burden and a new vision of clonal architecture in infant Wilms tumour.
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Hong, A.L., Mullen, E.A. Finding a brush when you expect a broom: a novel model of paediatric Wilms tumour evolution. Nat Rev Urol (2025). https://doi.org/10.1038/s41585-025-01082-y
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DOI: https://doi.org/10.1038/s41585-025-01082-y