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Quantitative analysis of differences in copy numbers using read depth obtained from PCR-enriched samples and controls
BACKGROUND: Next-generation sequencing (NGS) is rapidly becoming common practice in clinical diagnostics and cancer research. In addition to the detection of single nucleotide variants (SNVs), information on copy number variants (CNVs) is of great interest. Several algorithms exist to detect CNVs by...
| Autores principales: | , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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BioMed Central
2015
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4384318/ https://www.ncbi.nlm.nih.gov/pubmed/25626454 http://dx.doi.org/10.1186/s12859-014-0428-5 |