Single-cell data combined with phenotypes improves variant interpretation
Abstract Background Whole genome sequencing offers significant potential to improve the diagnosis and treatment of rare diseases by enabling the identification of thousands of rare, potentially pathogenic variants. Existing variant prioritisation tools can be complemented by approaches that incorpor...
Αποθηκεύτηκε σε:
| Κύριοι συγγραφείς: | , |
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| Μορφή: | Artigo |
| Γλώσσα: | Inglês |
| Έκδοση: |
BMC
2025-05-01
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| Σειρά: | BMC Genomics |
| Θέματα: | |
| Διαθέσιμο Online: | https://doi.org/10.1186/s12864-025-11711-w |
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