Author

Nadja Brait

Medical University of ViennaORCID 0000-0002-9289-3453Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Signature Assays, Organisms & Methods

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Research Focus:variant calling· 2 Assay:whole-genome sequencing· 2 Assay:DNA methylation· 1 Approach:experimental assay· 1 Organism:human· 1 Approach:statistical model· 1 Research Focus:variant effect prediction· 1

Frequent Co-Authors

Büşra KülekçiiD· 1 shared Irene Goerzer· 1 shared Sébastian LequimeiD· 1 shared Thomas HackliD· 1 shared

Activity by Year

2022-2025 · peak 1/yr

Co-Author Collaboration Network

4 top collaborators · 2 mutual co-author links

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1 shared paperGenomics

Büşra KülekçiORCID

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2 papers

Recent·Most cited

BioinformaticsMolecular Ecology ResourcesPeer-reviewedFeb 12, 2025

detectEVE: fast, sensitive and precise detection of endogenous viral elements in genomic data

Nadja Brait, Thomas Hackl, Sébastian Lequime

detectEVE identifies non-retroviral endogenous viral elements in genomic data with high sensitivity and specificity, offering a faster and more accurate alternative to existing tools.

4 citations

whole-genome sequencingstatistical model

𝕏 PostBluesky

GenomicsBMC GenomicsPeer-reviewedJan 6, 2022

Long Range PCR-based deep sequencing for haplotype determination in mixed HCMV infections

Nadja Brait, Büşra Külekçi, Irene Goerzer

This paper introduces a long amplicon sequencing method to accurately determine haplotypes in mixed HCMV infections, showing improved resolution compared to short-read sequencing.

14 citations

humanDNA methylation

𝕏 PostBluesky