AMLVaran: a software approach to implement variant analysis of targeted NGS sequencing data in an oncological care setting | BMC Medical Genomics | Full Text

AMLVaran: a software approach to implement variant analysis of targeted NGS sequencing data in an oncological care setting | BMC Medical Genomics | Full Text

AMLVaran: a software approach to implement variant analysis of targeted NGS sequencing data in an oncological care setting

Next-Generation Sequencing (NGS) enables large-scale and cost-effective sequencing of genetic samples in order to detect genetic variants. After successful use in research-oriented projects, NGS is now enterin...

Authors:Christian Wünsch, Henrik Banck, Carsten Müller-Tidow and Martin Dugas

Citation:BMC Medical Genomics 2020 13:17

Content type:Software

Published on: 4 February 2020

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