Author

Benjamin Huremagic

KU LeuvenORCID 0009-0001-5198-1318Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Bioinformatics· 1 Genetic & Genomic Medicine· 1

Signature Assays, Organisms & Methods

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Research Focus:differential expression· 2 Organism:human· 2 Research Focus:variant calling· 2 Assay:whole-genome sequencing· 2 Approach:experimental assay· 1 Approach:statistical model· 1

Frequent Co-Authors

Joris Robert VermeeschiD· 2 shared Amin ArdeshirdavaniiD· 1 shared Erika L. SoucheiD· 1 shared Geert VandeweyeriD· 1 shared Griet Van BuggenhoutiD· 1 shared Haleh ChizariiD· 1 shared Hilde PeetersiD· 1 shared Hilde Van EschiD· 1 shared

Activity by Year

2022-2024 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 27 mutual co-author links

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2 shared papersGenetic & Genomic Medicine

Joris Robert VermeeschORCID

Mutual co-authors in cluster

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2 papers

Recent·Most cited

Genetic & Genomic MedicinemedRxivPreprintApr 19, 2024

Nanopore sequencing-based episignature detection

Mathilde Geysens, Benjamin Huremagic, Erika L. Souche…·Joris Robert Vermeesch

This study demonstrates that nanopore sequencing can detect episignatures in developmental disorders, matching microarray results and identifying pathogenic variants.

3 citations

humanwhole-genome sequencing

𝕏 PostBluesky

BioinformaticsbioRxivPreprintJun 23, 2022

WiNGS: Widely integrated NGS platform for federated genome analysis

Haleh Chizari, Nishkala Sattanathan, Amin Ardeshirdavani…·Geert Vandeweyer

WiNGS enables federated analysis of omics data across a consortium without centralized storage, supporting variant interpretation for rare disease diagnosis.

2 citations

humanwhole-genome sequencing

𝕏 PostBluesky