A substantial fraction of the human genome displays high sequence similarity with at least one other genomic sequence, posing a challenge for the identification of somatic mutations from short-read sequencing data. Here we annotate genomic variants in 2,658 cancers from the Pan-Cancer Analysis of Whole Genomes (PCAWG) cohort with links to similar sites across the human genome. We train a machine learning model to use signals distributed over multiple genomic sites to call somatic events in non-unique regions and validate the data against linked-read sequencing in an independent dataset. Using this approach, we uncover previously hidden mutations in ~1,700 coding sequences and in thousands of regulatory elements, including in known cancer genes, immunoglobulins and highly mutated gene families. Mutations in non-unique regions are consistent with mutations in unique regions in terms of mutation burden and substitution profiles. The analysis provides a systematic summary of the mutation events in non-unique regions at a genome-wide scale across multiple human cancers.
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PanCancer analysis of somatic mutations in repetitive regions reveals recurrent mutations in snRNA U2
npj Genomic Medicine Open Access 14 March 2022
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This work is supported by The Francis Crick Institute, which receives its core funding from Cancer Research UK (FC001202), the UK Medical Research Council (FC001202) and the Wellcome Trust (FC001202). M.T. was supported as a postdoctoral fellow by the European Union’s Horizon 2020 research and innovation program (Marie Skłodowska-Curie grant agreement 747852-SIOMICS) and is a postdoctoral researcher of the F.R.S.-FNRS. J.D. is a postdoctoral fellow of the Research Foundation, Flanders (FWO). A.M.F. is an NIHR senior investigator and is supported by the National Institute for Health Research, UCLH Biomedical Research Centre and the CRUK Experimental Cancer Centre. P.V.L. is a Winton Group Leader in recognition of the Winton Charitable Foundation’s support toward the establishment of The Francis Crick Institute. T.K. would like to thank D. Smedley. This project was enabled through the Crick Scientific Computing STP and through access to the MRC eMedLab Medical Bioinformatics infrastructure, supported by the UK Medical Research Council (grant number MR/L016311/1). The Bone Cancer Research Trust funded sample biobanking.
The authors declare no competing interests.
Peer review information Nature Biotechnology thanks the anonymous reviewers for their contribution to the peer review of this work.
Publisher’s note Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Supplementary Figs. 1–28.
Summary of z-scores and histology specificity for all genomic regions. The table contains summary statistics for all genes in the annotation set. Counts, z-scores and entropy scores are provided based on non-hypermutated samples.
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Tarabichi, M., Demeulemeester, J., Verfaillie, A. et al. A pan-cancer landscape of somatic mutations in non-unique regions of the human genome. Nat Biotechnol 39, 1589–1596 (2021). https://doi.org/10.1038/s41587-021-00971-y
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PanCancer analysis of somatic mutations in repetitive regions reveals recurrent mutations in snRNA U2
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