Profiling KRAS mutations in whole blood by error-corrected maximum depth sequencing
Abstract Clinical use of circulating tumor DNA (ctDNA) sequencing is rapidly increasing, but performance is limited by the sensitivity of next generation sequencing and relies on specialized sample collection. Here we describe sequencing the most frequently mutated oncogene K RAS by adapting error-c...
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| Principais autores: | , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Nature Portfolio
2026-04-01
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| Colecção: | npj Precision Oncology |
| Acesso em linha: | https://doi.org/10.1038/s41698-026-01399-w |
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