Author

Sabine Oesterle

SIB Swiss Institute of BioinformaticsORCID 0000-0003-3248-7899Unclaimed 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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Research Focus:benchmarking· 1 Research Focus:software / tool· 1 Assay:whole-genome sequencing· 1

Frequent Co-Authors

Ali SaadatiD· 1 shared D. Sean FroeseiD· 1 shared David Hans-Ulrich Haerry· 1 shared Dylan LawlessiD· 1 shared Jacques FellayiD· 1 shared Jan Armida· 1 shared Luregn Jan SchlapbachiD· 1 shared Mariam Ait OumellouliD· 1 shared

Activity by Year

2026-2026 · peak 1/yr

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10 top collaborators · 45 mutual co-author links

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1 shared paperGenetic & Genomic Medicine

Ali SaadatORCID

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1 paper

Recent·Most cited

Genetic & Genomic MedicineBioinformaticsPeer-reviewedJan 21, 2026

Application of qualifying variants for genomic analysis

Dylan Lawless, Ali Saadat, Mariam Ait Oumelloul…·Jacques Fellay

The paper introduces a framework for defining and reusing qualifying variants (QVs) in genomic analysis to improve transparency, reproducibility, and interoperability across pipelines.

DOI 10.1093/bioinformatics/btaf676

whole-genome sequencingbenchmarking

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