In this webinar, we introduce quantitative amplicon sequencing (QASeq): a highly-sensitive and robust NGS-based method for the detection and quantification of low frequency structural/sequence variations including Copy Number Variations (CNVs) and Single Nucleotide Variants (SNVs) in a wide range of sample types including liquid biopsy. We will demonstrate that QASeq can accurately detect CNVs down to 5% heterozygous single copy gain or loss (gene ploidy=2.05/1.95) even in a highly-multiplexed environment. Additionally, we will introduce NuProbe’s full-service custom assay development program.
