BioDiscovery White Papers

Topic: Copy Number

Comparison of the BAM (multiscale reference) algorithm to other methods for CNV detection from NGS

Learn more about the various methods that have been proposed to detect CNVs from NGS data in tumor-normal matched paired colon adenocarcinoma samples.

Analyzing NGS Data For Copy Number Events

Next-generation sequencing (NGS) is mainly used to obtain sequence variants (SNVs). However, getting copy number variants (CNVs) from NGS has gained momentum in both research and clinical applications.