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Copy number variation detection using next generation sequencing read counts
BACKGROUND: A copy number variation (CNV) is a difference between genotypes in the number of copies of a genomic region. Next generation sequencing (NGS) technologies provide sensitive and accurate tools for detecting genomic variations that include CNVs. However, statistical approaches for CNV iden...
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| Main Authors: | , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
BioMed Central
2014
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| Assuntos: | |
| Acceso en liña: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4021345/ https://ncbi.nlm.nih.gov/pubmed/24731174 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2105-15-109 |
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