Inferring structural variant cancer cell fraction.
PCAWG Evolution and Heterogeneity Working Group,
Corcoran, Niall M
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Cmero, M., Yuan, K., Ong, C. S., Schröder, J., PCAWG Evolution and Heterogeneity Working Group,, Corcoran, N. M., Papenfuss, T., et al. (2020). Inferring structural variant cancer cell fraction.. Nature communications, 11 (1), 730. https://doi.org/10.1038/s41467-020-14351-8
We present SVclone, a computational method for inferring the cancer cell fraction of structural variant (SV) breakpoints from whole-genome sequencing data. SVclone accurately determines the variant allele frequencies of both SV breakends, then simultaneously estimates the cancer cell fraction and SV copy number. We assess performance using in silico mixtures of real samples, at known proportions, created from two clonal metastases from the same patient. We find that SVclone’s performance is comparable to single nucleotide variant-based methods, despite having an order of magnitude fewer data points. As part of the Pan-Cancer Analysis of Whole Genomes (PCAWG) consortium, which aggregated whole genome sequencing data from 2,658 cancers across 38 tumour types, we use SVclone to reveal a subset of liver, ovarian and pancreatic cancers with subclonally enriched copy number neutral rearrangements that show decreased overall survival. SVclone enables improved characterisation of SV intra-tumour heterogeneity.
PCAWG Evolution and Heterogeneity Working Group, PCAWG Consortium, Humans, Neoplasms, Liver Neoplasms, Pancreatic Neoplasms, Ovarian Neoplasms, Prostatic Neoplasms, Sensitivity and Specificity, Computational Biology, Gene Frequency, Genome, Human, Algorithms, Computer Simulation, Female, Male, DNA Copy Number Variations, Whole Genome Sequencing
Cancer Research UK (15973)
Cancer Research UK (C14303_do not transfer)
Cancer Research UK (CRUK-A15973)
Embargo Lift Date
External DOI: https://doi.org/10.1038/s41467-020-14351-8
This record's URL: https://www.repository.cam.ac.uk/handle/1810/300096
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