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Mutational concordance analysis provides supportive information for double cancer diagnosis
BACKGROUND: Mutation analysis using next-generation sequencing highlights the features of tumors with somatic alterations. However, the mutation profile of double cancer remains unclear. Here, we analyzed tumors derived from the same patient using whole exome sequencing (WES) to investigate the cohe...
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| Publicat a: | BMC Cancer |
|---|---|
| Autors principals: | , , , , , , , , , , , , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
BioMed Central
2021
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7893960/ https://ncbi.nlm.nih.gov/pubmed/33607950 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12885-021-07899-1 |
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