Author

Nerses Bebek

Istanbul UniversityORCID 0000-0002-4749-1471Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 1 Genomics· 1

Signature Assays, Organisms & Methods

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

Frequent Co-Authors

Ahmad A. BeydouniD· 1 shared Alica M. GoldmaniD· 1 shared Alison AndersoniD· 1 shared Andrew J. ColeiD· 1 shared Annika B. FauconiD· 1 shared Antonio GambardellaiD· 1 shared Barbara CastellottiiD· 1 shared Barış SalmaniD· 1 shared

Activity by Year

2024-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 36 mutual co-author links

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1 shared paperGenetic & Genomic Medicine

Ahmad A. BeydounORCID

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2 papers

Recent·Most cited

GenomicsBioinformatics AdvancesPeer-reviewedJan 1, 2026

XhetRel: A Pipeline for X Heterozygosity and Relatedness Analysis in Sequencing Data

Barış Salman, Nerses Bebek, Sibel Uğur İşeri

XhetRel analyzes X heterozygosity and relatedness in sequencing data to improve quality control and identify sources of error in variant calling.

DOI 10.1093/bioadv/vbag002

whole-genome sequencingstatistical model

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Genetic & Genomic MedicineNature NeurosciencePeer-reviewedOct 1, 2024

Exome sequencing of 20,979 individuals with epilepsy reveals shared and distinct ultra-rare genetic risk across disorder subtypes

Epi25 Collaborative, Siwei Chen, Bassel W Abou-Khalil…·Alica M. Goldman

This study identifies shared and distinct ultra-rare genetic risk factors for epilepsy subtypes using whole-exome sequencing of 20,979 patients and 33,444 controls.

72 citationstop 1%

humanwhole-exome sequencing

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