Detection of recurrent rearrangement breakpoints from copy number data
<p>Abstract</p> <p>Background</p> <p>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 co...
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| Principais autores: | , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
BMC
2011-04-01
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| Series: | BMC Bioinformatics |
| Acceso en liña: | http://www.biomedcentral.com/1471-2105/12/114 |
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