A fully-automated integrative workflow to streamline NGS-based analyses within Molecular Tumour Boards
Maria Giulia Carta, Miriam Angeloni, Lars Tögel, Christoph Schubart, Annett Hölsken, Robert Stoehr, Simona Vatrano, Davide Rizzi, Paolo Magni, Filippo Fraggetta, Arndt Hartmann, Florian Haller, Fulvia Ferrazzi
This paper develops a fully-automated workflow to streamline NGS-based analyses in Molecular Tumour Boards by integrating variant interpretation and biomarker estimation.
medRxiv · Dec 15, 2025 · PreprintGenetic & Genomic Medicine