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Detection of recurrent rearrangement breakpoints from copy number data
BACKGROUND: Copy number variants (CNVs), including deletions, amplifications, and other rearrangements, are common in human and cancer genomes. Copy number data from array comparative genome hybridization (aCGH) and next-generation DNA sequencing is widely used to measure copy number variants. Compa...
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| Main Authors: | , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BioMed Central
2011
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3112242/ https://ncbi.nlm.nih.gov/pubmed/21510904 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2105-12-114 |
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