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Systematic prediction and validation of breakpoints associated with copy-number variants in the human genome
Copy-number variants (CNVs) are an abundant form of genetic variation in humans. However, approaches for determining exact CNV breakpoint sequences (physical deletion or duplication boundaries) across individuals, crucial for associating genotype to phenotype, have been lacking so far, and the vast...
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| Main Authors: | , , , , , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
National Academy of Sciences
2007
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC1891248/ https://ncbi.nlm.nih.gov/pubmed/17551006 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1073/pnas.0703834104 |
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