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

Abstract excerpt

BACKGROUND: 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 entering clinical practice. Consequently, variant analysis is increasingly important to facilitate a better understanding of disease entities and prognoses. Furthermore, variant calling allows to adapt...

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