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Reconstructing cancer genomes from paired-end sequencing data
BACKGROUND: A cancer genome is derived from the germline genome through a series of somatic mutations. Somatic structural variants - including duplications, deletions, inversions, translocations, and other rearrangements - result in a cancer genome that is a scrambling of intervals, or "blocks&...
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| Main Authors: | , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BioMed Central
2012
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3358655/ https://ncbi.nlm.nih.gov/pubmed/22537039 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2105-13-S6-S10 |
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