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Somatic cancer mutation databases | Genome annotation

High-throughput DNA sequencing has revolutionized the study of cancer genomics with numerous discoveries that are relevant to cancer diagnosis and treatment. The latest sequencing and analysis methods have successfully identified somatic alterations, including single-nucleotide variants, insertions and deletions, copy-number aberrations, structural variants and gene fusions.

Source text:
(Ding et al., 2014) Expanding the computational toolbox for mining cancer genomes. Nat Rev Genet.

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