From uncertain to certain—how to proceed with variants of uncertain significance
Abstract With the increased next generation sequencing (NGS) based genetic diagnosis due to technological boon, the biomedical world is getting a substantial number of single nucleotide variations (SNVs) every day along with other genetic variations. The detected SNVs may or may not have clinical si...
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| Asıl Yazarlar: | , , , |
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| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
SpringerOpen
2024-08-01
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| Seri Bilgileri: | Middle East Fertility Society Journal |
| Konular: | |
| Online Erişim: | https://doi.org/10.1186/s43043-024-00202-9 |
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