Targeted adaptive long-read sequencing for discovery of complex phased variants in inherited retinal disease patients
Abstract Inherited retinal degenerations (IRDs) are a heterogeneous group of predominantly monogenic disorders with over 300 causative genes identified. Short-read exome sequencing is commonly used to genotypically diagnose patients with clinical features of IRDs, however, in up to 30% of patients w...
| Published in: | Scientific Reports |
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| Main Authors: | , , , |
| Format: | Article |
| Language: | English |
| Published: |
Nature Portfolio
2023-05-01
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| Online Access: | https://doi.org/10.1038/s41598-023-35791-4 |