bioRxivBioinformaticsPreprint
A dedicated caller for DUX4 rearrangements from whole-genome sequencing data
Pascal GrobeckeriD, Stefano BerriiD, John F. Peden, Kai-Jie Chow, Claire FieldingiD, Ivana Armogida, Helen Northen, David J. McBrideiD, Peter J. CampbelliD, Jennifer Becq, Sarra L. RyaniD, David Bentley, Christine J. HarrisoniD, Anthony V. MoormaniD, Mark T. RossiD, Martina Mijušković
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.
- organism: human
- assay: whole-genome sequencing
- research focus: variant calling
- approach: statistical model
- Citations
- 1
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