Comparison of TCGA and GENIE genomic datasets for the detection of clinically actionable alterations in breast cancer

Whole exome sequencing (WES), targeted gene panel sequencing and single nucleotide polymorphism (SNP) arrays are increasingly used for the identification of actionable alterations that are critical to cancer care. Here, we compared The Cancer Genome Atlas (TCGA) and the Genomics Evidence Neoplasia I...

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Detalles Bibliográficos
Autores principales: Kaur, Pushpinder, Porras, Tania B., Ring, Alexander, Carpten, John D., Lang, Julie E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6365517/
https://www.ncbi.nlm.nih.gov/pubmed/30728399
http://dx.doi.org/10.1038/s41598-018-37574-8

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6365517/
https://www.ncbi.nlm.nih.gov/pubmed/30728399
http://dx.doi.org/10.1038/s41598-018-37574-8

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