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Impact of whole genome amplification on analysis of copy number variants
Large-scale copy number variants (CNVs) have recently been recognized to play a role in human genome variation and disease. Approaches for analysis of CNVs in small samples such as microdissected tissues can be confounded by limited amounts of material. To facilitate analyses of such samples, whole...
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| Autors principals: | , , , , , , , , , |
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| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Oxford University Press
2008
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2490749/ https://ncbi.nlm.nih.gov/pubmed/18559357 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/nar/gkn378 |
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