Author

Volha Skrahina

University of RostockORCID 0000-0001-8476-8508Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Signature Assays, Organisms & Methods

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

Frequent Co-Authors

Aliaksandr SkrahiniD· 2 shared Afërdita TakoiD· 1 shared Agim GjikopulliiD· 1 shared Arndt Rolfs· 1 shared Avenida P. H. RolfsiD· 1 shared Erjon TrojaiD· 1 shared Ermira DervishiiD· 1 shared Gabriela E. OpreaiD· 1 shared

Activity by Year

2023-2025 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 27 mutual co-author links

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2 shared papersGenetic & Genomic Medicine

Aliaksandr SkrahinORCID

Mutual co-authors in cluster

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2 papers

Recent·Most cited

Genetic & Genomic MedicinemedRxivPreprintJul 24, 2025

Comparative analysis of WGS and WES for genetic diagnosis in a pediatric Albanian population.

Paskal Cullufi, Mirela Tabaku, Aliaksandr Skrahin…·Avenida P. H. Rolfs

This study compares whole-genome sequencing (WGS) and whole-exome sequencing (WES) in a pediatric Albanian population, finding WGS more effective in diagnosing rare genetic disorders and identifying complex variants.

DOI 10.1101/2025.07.24.25332056

humanwhole-genome sequencing

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Genetic & Genomic MedicineLife Science AlliancePeer-reviewedJan 12, 2023

Secondary findings in a large Pakistani cohort tested with whole genome sequencing

Aliaksandr Skrahin, Huma Arshad Cheema, Maqbool Hussain…·Volha Skrahina

The paper analyzes secondary findings in a Pakistani cohort using whole genome sequencing, identifying rates and types of actionable genetic variants.

9 citations

humanwhole-genome sequencing

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