DEEPGEN<sup>TM</sup>—A Novel Variant Calling Assay for Low Frequency Variants

Detection of genetic variants in clinically relevant genomic hot-spot regions has become a promising application of next-generation sequencing technology in precision oncology. Effective personalized diagnostics requires the detection of variants with often very low frequencies. This can be achieved...

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Bibliographic Details
Main Authors: Bernd Timo Hermann, Sebastian Pfeil, Nicole Groenke, Samuel Schaible, Robert Kunze, Frédéric Ris, Monika Elisabeth Hagen, Johannes Bhakdi
Format: Article
Language:English
Published: MDPI AG 2021-03-01
Series:Genes
Subjects:
NGS
Online Access:https://www.mdpi.com/2073-4425/12/4/507