Author

Norbert Meidenbauer

Friedrich-Alexander-Universität Erlangen-NürnbergORCID 0000-0002-5438-2142Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 1

Signature Assays, Organisms & Methods

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Organism:human· 1 Approach:statistical model· 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 Florian HalleriD· 1 shared Fulvia FerrazziiD· 1 shared Heinrich StichtiD· 1 shared Lars TögeliD· 1 shared Maria Giulia CartaiD· 1 shared

Activity by Year

2026-2026 · 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

Genetic & Genomic MedicineJournal of Molecular DiagnosticsPeer-reviewedApr 3, 2026

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

Maria Giulia Carta, Lars Tögel, Annett Hölsken…·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.

3 citationstop 1%

humanwhole-exome sequencing

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