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CNV Workshop: an integrated platform for high-throughput copy number variation discovery and clinical diagnostics
BACKGROUND: Recent studies have shown that copy number variations (CNVs) are frequent in higher eukaryotes and associated with a substantial portion of inherited and acquired risk for various human diseases. The increasing availability of high-resolution genome surveillance platforms provides opport...
| Autores principales: | , , , , , , , , , |
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| Formato: | Texto |
| Lenguaje: | English |
| Publicado: |
BioMed Central
2010
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2827374/ https://www.ncbi.nlm.nih.gov/pubmed/20132550 http://dx.doi.org/10.1186/1471-2105-11-74 |