Author

Annett Hölsken

Friedrich-Alexander-Universität Erlangen-NürnbergORCID 0000-0002-0826-6300Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 2

Signature Assays, Organisms & Methods

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Organism:human· 2 Approach:statistical model· 2 Research Focus:variant effect prediction· 2 Assay:whole-exome sequencing· 2 Research Focus:benchmarking· 1 Research Focus:variant calling· 1

Frequent Co-Authors

Arndt HartmanniD· 2 shared Christoph SchubartiD· 2 shared Florian HalleriD· 2 shared Fulvia FerrazziiD· 2 shared Lars TögeliD· 2 shared Maria Giulia CartaiD· 2 shared Paolo MagniiD· 2 shared Robert StoehriD· 2 shared

Activity by Year

2025-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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2 shared papersGenetic & Genomic Medicine

Arndt HartmannORCID

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2 papers

Recent·Most cited

Oncogenicity Variant Interpreter (OncoVI): oncogenicity guidelines implementation to support somatic variants interpretation in precision oncology

Maria Giulia Carta, Lars Tögel, Annett Hölsken, Christoph Schubart, Heinrich Sticht, Robert Stoehr, Silvia Spoerl, Norbert Meidenbauer, Arndt Hartmann, Paolo Magni, Florian Haller, Fulvia Ferrazzi

OncoVI is a Python-based tool that automates oncogenicity classification of somatic variants using guidelines, achieving 80% accuracy on test data and 79% agreement with expert assessments.

Journal of Molecular Diagnostics · Apr 3, 2026Peer-reviewedGenetic & Genomic Medicine

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