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Devyser Thalassemia NGS a complete thalassemia testing in a single tube
Reduce turnaround time and simplify laboratory workflow with a single-assay thalassemia DNA screening solution that eliminates multiple parallel test protocols.
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A simple NGS method for the detection of sequence variants causing thalassemia
This whitepaper by Mehmet Uzunel Ph.D., Devyser, Stockholm, Sweden, demonstrates an amplicon-based NGS method using only ONE oligo-mix to detect virtually all known variants for alpha and beta thalassemia.
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The Cyprus Institute of Neurology and Genetics transforms testing with NGS
In this case study, Dr. Papasavva describes her laboratory’s journey from traditional thalassemia testing to state-of-the-art NGS technology and what a difference this has made in their daily work.