Thalassemia genetic testing has long been complex and time-consuming, requiring multiple assays and extensive hands-on work. Devyser Thalassemia v2 is designed to change that. This next-generation sequencing (NGS) solution simplifies genetic profiling by integrating alpha and beta thalassemia detection—including SNV and CNV analysis, and beta modifiers—into a single, efficient assay. 

Watch and learn how Devyser Thalassemia v2 can help your laboratory:

1. Reduce workflow complexity with a streamlined NGS protocol
2. Achieve rapid, comprehensive genetic results in a single test 
3. Detect structural variants with superior CNV analysis
4. Minimize hands-on time and eliminate the need for bioinformatics expertise