Full characterization of unresolved structural variation through long-read sequencing and optical genome mapping

Full characterization of unresolved structural variation through long-read sequencing and optical genome mapping

Abstract Structural variants (SVs) are important contributors to human disease. Their characterization remains however difficult due to their size and association with repetitive regions. Long-read sequencing (LRS) and optical genome mapping (OGM) can aid as their molecules span multiple kilobases a...

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Bibliographic Details
Main Authors: Griet De Clercq, Lies Vantomme, Barbara Dewaele, Bert Callewaert, Olivier Vanakker, Sandra Janssens, Bart Loeys, Mojca Strazisar, Wouter De Coster, Joris Robert Vermeesch, Annelies Dheedene, Björn Menten
Format: Article
Language:English
Published: Nature Portfolio 2024-11-01
Series:Scientific Reports
Subjects:
Long-read sequencing
Optical genome mapping
Structural variation
Clinical genomics
Chromothripsis
Complex genomic rearrangements
Online Access:https://doi.org/10.1038/s41598-024-80068-z
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