ArticleNucleic acids research2025
Comprehensive analysis of mutational processes across 20 000 adult and pediatric tumors.
Article in Nucleic acids research, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
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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.
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Who cites it
1 citing paper in PubMed.
- A guide to understanding tumour evolution through the lens of population genetics.Nature reviews. Cancer · 2026Review
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Authors and funding
12 authors.
Funding
Abstract
Despite being a consolidated practice in modern cancer genomics, mutational signature analysis poses various challenges. First, determining the number of signatures is a complex task and depends on heuristics. Second, several signatures lack a clear etiology, raising concerns about whether they result from computational artifacts or actual mutagenic processes. Last, approaches for signature assignment are highly influenced by the catalogue of signatures used for the analysis. To overcome these limitations, we introduce RESOLVE (Robust EStimation Of mutationaL signatures Via rEgularization), a framework designed for the efficient extraction, assignment, and confidence estimation of mutational signatures. RESOLVE enables the stratification of cancer genomes according to the active mutational processes, providing insights into those that are consistently shared among various cancer types. We applied RESOLVE to 20 000 samples from adult and pediatric cancers, providing a comprehensive characterization of subtypes associated with specific mutational processes and alterations in driver genes. Our analysis demonstrates that RESOLVE accurately fits observed mutations with a smaller set of signatures compared to existing catalogues, suggesting the existence of a limited number of dominant mutational processes in cancer genomes. Clustering analysis revealed distinct patient groups characterized by specific signatures, with significant associations between certain signatures and patient prognosis. Additionally, we identified strong associations between signatures and driver gene mutations, offering insights into cancer subtype mechanisms and evolution. Our findings highlight the efficiency of RESOLVE and its potential impact on personalized cancer treatment.
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