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A dedicated caller for DUX4 rearrangements from whole-genome sequencing data.

Authors :
Grobecker, Pascal
Berri, Stefano
Peden, John F.
Chow, Kai-Jie
Fielding, Claire
Armogida, Ivana
Northen, Helen
McBride, David J.
Campbell, Peter J.
Becq, Jennifer
Ryan, Sarra L.
Bentley, David R.
Harrison, Christine J.
Moorman, Anthony V.
Ross, Mark T.
Mijuskovic, Martina
Source :
BMC Medical Genomics; 1/30/2025, Vol. 18 Issue 1, p1-11, 11p
Publication Year :
2025

Abstract

Rearrangements involving the DUX4 gene (DUX4-r) define a subtype of paediatric and adult acute lymphoblastic leukaemia (ALL) with a favourable outcome. Currently, there is no 'standard of care' diagnostic method for their confident identification. Here, we present an open-source software tool designed to detect DUX4-r from short-read, whole-genome sequencing (WGS) data. Evaluation on a cohort of 210 paediatric ALL cases showed that our method detects all known, as well as previously unidentified, cases of IGH::DUX4 and rearrangements with other partner genes. These findings demonstrate the possibility of robustly detecting DUX4-r using WGS in the routine clinical setting. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
17558794
Volume :
18
Issue :
1
Database :
Complementary Index
Journal :
BMC Medical Genomics
Publication Type :
Academic Journal
Accession number :
182565217
Full Text :
https://doi.org/10.1186/s12920-024-02069-1