The Scientist

Uncovering the Meaning in Your NGS Data: Tackling the Biological Analysis and Interpretation of Sequence Variation

Next generation sequencing has revealed a lot about genetic variations such as single nucleotide polymorphisms (SNPs), single nucleotide variations (SNVs), copy number variations (CNVs), insertions ...
GEN

Target Enrichment Technology Optimized for Analysis of SNPs, Mutations, and Copy Number Changes in 509 Cancer Gene Targets

Targeted resequencing of DNA allows researchers to focus on genes of interest for cost-effective analysis of genetic variations. Typically, to analyze single nucleotide mutations and copy number ...
Labroots

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 ...
GEN

Copy Number Variation Probes Inform Diverse Applications

The evolution of the MUC7 gene, which encodes a saliva protein, was studied by scientists at the University at Buffalo. To capture the gene’s proline-, threonine-, and serine-rich tandem repeat copy ...