Author

Alberte Aspaas Lundquist

Statens Serum InstitutORCID 0000-0002-8574-9824Unclaimed 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 calling· 1 Assay:whole-genome sequencing· 1

Frequent Co-Authors

Allan Meldgaard LundiD· 1 shared Anna ByrjalseniD· 1 shared Caroline M. Junker MentzeliD· 1 shared Christian ErikstrupiD· 1 shared Christian M. HageniD· 1 shared Erik Soerensen· 1 shared Henrik HjalgrimiD· 1 shared J Tfelt-Hansen· 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

Allan Meldgaard LundORCID

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1 paper

Recent·Most cited

Genetic & Genomic MedicinemedRxivPreprintJul 10, 2026

Low-cost rare variant detection for population scale genetic screening

Mads Cort Nielsen, Caroline M. Junker Mentzel, Ulrik Kristoffer Stoltze…·Simon Rasmussen

This paper introduces DoBSeq, a low-cost framework for detecting rare variants in population-scale genetic screening, achieving 95% variant detection and recovering all clinically relevant pathogenic variants in ACMG genes.

DOI 10.64898/2026.07.07.26357001

humanwhole-genome sequencing