An Approach to Ultrasensitive Detection and Quantification of Copy Number Variations (CNVs) and Mutations

In this webinar we will introduce Quantitative Amplicon Sequencing (QASeq): a highly sensitive and robust NGS-based method for the detection and quantification of low frequency Copy Number Variations (CNVs) and Single Nucleotide Variants (SNVs) in a wide range of sample types including fresh frozen, FFPE, and cell-free DNA. We will demonstrate that QASeq can accurately detect CNVs down to 5% heterozygous single copy gain or loss (ploidy=2.05/1.95). Additionally, we will introduce NuProbe’s custom assay development program.

 

Learning Objectives

 

By the end of the webinar, the attendees will be able to:

Disclaimer: Products are for research use only, not for use in diagnostic procedures.