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Copy number variation detection and genotyping from exome sequence data
While exome sequencing is readily amenable to single-nucleotide variant discovery, the sparse and nonuniform nature of the exome capture reaction has hindered exome-based detection and characterization of genic copy number variation. We developed a novel method using singular value decomposition (SV...
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| Main Authors: | , , , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Cold Spring Harbor Laboratory Press
2012
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3409265/ https://ncbi.nlm.nih.gov/pubmed/22585873 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1101/gr.138115.112 |
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