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Mutation spectrum revealed by breakpoint sequencing of human germline CNVs
Precisely characterizing the breakpoints of copy number variants (CNVs) is crucial for assessing their functional impact. However, fewer than 0% of known germline CNVs have been mapped to the single-nucleotide level. We characterized the sequence breakpoints from a dataset of all CNVs detected in th...
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| Autors principals: | , , , , , , , |
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| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
2010
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3428939/ https://ncbi.nlm.nih.gov/pubmed/20364136 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/ng.564 |
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