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Sensitive and accurate detection of copy number variants using read depth of coverage
Methods for the direct detection of copy number variation (CNV) genome-wide have become effective instruments for identifying genetic risk factors for disease. The application of next-generation sequencing platforms to genetic studies promises to improve sensitivity to detect CNVs as well as inversi...
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| Main Authors: | , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Cold Spring Harbor Laboratory Press
2009
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2752127/ https://ncbi.nlm.nih.gov/pubmed/19657104 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1101/gr.092981.109 |
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