Загрузка...
Machine learning-based reclassification of germline variants of unknown significance: The RENOVO algorithm
The increasing scope of genetic testing allowed by next-generation sequencing (NGS) dramatically increased the number of genetic variants to be interpreted as pathogenic or benign for adequate patient management. Still, the interpretation process often fails to deliver a clear classification, result...
Сохранить в:
| Опубликовано в: : | Am J Hum Genet |
|---|---|
| Главные авторы: | , , , , , , , |
| Формат: | Artigo |
| Язык: | Inglês |
| Опубликовано: |
Elsevier
2021
|
| Предметы: | |
| Online-ссылка: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8059374/ https://ncbi.nlm.nih.gov/pubmed/33761318 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.ajhg.2021.03.010 |
| Метки: |
Добавить метку
Нет меток, Требуется 1-ая метка записи!
|