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Incidental findings from cancer next generation sequencing panels
Next-generation sequencing (NGS) technologies have facilitated multi-gene panel (MGP) testing to detect germline DNA variants in hereditary cancer patients. This sensitive technique can uncover unexpected, non-germline incidental findings indicative of mosaicism, clonal hematopoiesis (CH), or hemato...
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| Publicat a: | NPJ Genom Med |
|---|---|
| Autors principals: | , , , , , , , , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Nature Publishing Group UK
2021
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8289933/ https://ncbi.nlm.nih.gov/pubmed/34282142 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/s41525-021-00224-6 |
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