Author

Simona Vatrano

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

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Genetic & Genomic Medicine· 1

Signature Assays, Organisms & Methods

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Research Focus:benchmarking· 1 Organism:human· 1 Approach:statistical model· 1 Research Focus:variant calling· 1 Research Focus:variant effect prediction· 1 Assay:whole-exome sequencing· 1

Frequent Co-Authors

Annett HölskeniD· 1 shared Arndt HartmanniD· 1 shared Christoph SchubartiD· 1 shared Davide Rizzi· 1 shared Filippo Fraggetta· 1 shared Florian HalleriD· 1 shared Fulvia FerrazziiD· 1 shared Lars TögeliD· 1 shared

Activity by Year

2025-2025 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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1 shared paperGenetic & Genomic Medicine

Annett HölskenORCID

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1 paper

Recent·Most cited

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