Quantitative analysis of differences in copy numbers using read depth obtained from PCR-enriched samples and controls
Quantitative analysis of differences in copy numbers using read depth obtained from PCR-enriched samples and controls
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.