The DOI matches its Crossref record; 43 of the 43 references it cites were found in a registry or an index.
Substitution mutational signatures in whole-genome–sequenced cancers in the UK population
Open accessAbstract
Whole-genome sequencing (WGS) permits comprehensive cancer genome analyses, revealing mutational signatures, imprints of DNA damage, and repair processes that have arisen in each patient’s cancer. We performed mutational signature analyses on 12,222 whole-genome–sequenced tumor-normal matched pairs from patients recruited via the UK National Health Service (NHS). We contrasted our results with two independent cancer WGS datasets—from the International Cancer Genome Consortium (ICGC) and the Hartwig Medical Foundation (HMF)—involving 18,640 whole-genome–sequenced cancers in total. Our analyses add 40 single and 18 double substitution signatures to the current mutational signature tally. We show for each organ that cancers have a limited number of common signatures and a long tail of rare signatures, and we provide a practical solution for applying this concept of common versus rare signatures to future analyses.
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Coorens, T. H. H., Collord, G., Jung, H., Wang, Y., Moore, L., Hooks, Y., Mahbubani, K., Law, S. Y. K., Yan, H. H. N., Yuen, S. T., et al. (2025) · Nature · doi:10.1038/s41586-025-08708-6 · Cited by 57
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Metadata
- Authors
- Degasperi, A., Zou, X., Dias Amarante, T., Martinez-Martinez, A., Koh, G. C. C., Dias, J. M. L., Heskin, L., Chmelova, L., Rinaldi, G., Wang, V. Y. W., Nanda, A. S., Bernstein, A., Momen, S. E., Young, J., Perez-Gil, D., Memari, Y., Badja, C., Shooter, S., Czarnecki, J., Brown, M. A., Davies, H. R., Genomics England Research Consortium†, Nik-Zainal, S., Ambrose, J. C., Arumugam, P., Bevers, R., Bleda, M., Boardman-Pretty, F., Boustred, C. R., Brittain, H., Caulfield, M. J., Chan, G. C., Fowler, T., Giess, A., Hamblin, A., Henderson, S., Hubbard, T. J. P., Jackson, R., Jones, L. J., Kasperaviciute, D., Kayikci, M., Kousathanas, A., Lahnstein, L., Leigh, S. E. A., Leong, I. U. S., Lopez, F. J., Maleady-Crowe, F., McEntagart, M., Minneci, F., Moutsianas, L., Mueller, M., Murugaesu, N., Need, A. C., O‘Donovan, P., Odhams, C. A., Patch, C., Perez-Gil, D., Pereira, M. B., Pullinger, J., Rahim, T., Rendon, A., Rogers, T., Savage, K., Sawant, K., Scott, R. H., Siddiq, A., Sieghart, A., Smith, S. C., Sosinsky, A., Stuckey, A., Tanguy, M., Taylor Tavares, A. L., Thomas, E. R. A., Thompson, S. R., Tucci, A., Welland, M. J., Williams, E., Witkowska, K., & Wood, S. M.
- Venue
- Science
- Published
- 2022-04-22
- Volume
- 376
- Issue
- 6591
- ISSN
- 0036-8075 (ISSN-L)
- 1095-9203
- OpenAlex
- W4224263489
- Cited by
- 280
- References
- 43
- FWCI
- 19.67
- Type
- journal article
- Language
- en
- Open access
- green
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- Degasperi, A., Zou, X., Dias Amarante, T., Martinez-Martinez, A., Koh, G. C. C., Dias, J. M. L., Heskin, L., Chmelova, L., Rinaldi, G., Wang, V. Y. W., Nanda, A. S., Bernstein, A., Momen, S. E., Young, J., Perez-Gil, D., Memari, Y., Badja, C., Shooter, S., Czarnecki, J., . . . Wood, S. M. (2022). Substitution mutational signatures in whole-genome–sequenced cancers in the UK population. Science. https://doi.org/10.1126/science.abl9283
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