Cargando…
A novel molecular diagnostics platform for somatic and germline precision oncology
BACKGROUND: Next‐generation sequencing (NGS) opens new options in clinical oncology, from therapy selection to genetic counseling. However, realization of this potential not only requires succeeding in the bioinformatics and interpretation of the results, but also in their integration into the clini...
Autores principales: | Cabanillas, Rubén, Diñeiro, Marta, Castillo, David, Pruneda, Patricia C., Penas, Cristina, Cifuentes, Guadalupe A., de Vicente, Álvaro, Durán, Noelia S., Álvarez, Rebeca, Ordóñez, Gonzalo R., Cadiñanos, Juan |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2017
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5511795/ https://www.ncbi.nlm.nih.gov/pubmed/28717660 http://dx.doi.org/10.1002/mgg3.291 |
Ejemplares similares
-
Sequencing results from multiple individuals of different ethnicities strongly question the existence of the KCNE1B pseudogene
por: Diñeiro, Marta, et al.
Publicado: (2019) -
Comprehensive genomic diagnosis of inherited retinal and optical nerve disorders reveals hidden syndromes and personalized therapeutic options
por: Diñeiro, Marta, et al.
Publicado: (2020) -
Comprehensive genomic diagnosis of non-syndromic and syndromic hereditary hearing loss in Spanish patients
por: Cabanillas, Rubén, et al.
Publicado: (2018) -
Clinical utility of liquid biopsy and integrative genomic profiling in early-stage and oligometastatic cancer patients treated with radiotherapy
por: Cifuentes, Guadalupe A., et al.
Publicado: (2022) -
Establishing a Framework for the Clinical Translation of Germline Findings in Precision Oncology
por: Dixon, Katherine, et al.
Publicado: (2020)