Simultaneous identification of clinically relevant single nucleotide variants, copy number alterations and gene fusions in solid tumors by targeted next-generation sequencing

In this study, we have set-up a routine pipeline to evaluate the clinical application of Oncomine™ Focus Assay, a panel that allows the simultaneous detection of single nucleotide hotspot mutations in 35 genes, copy number alterations (CNAs) in 19 genes and gene fusions involving 23 genes in cancer...

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Detalles Bibliográficos
Autores principales: Oliveira, Duarte Mendes, Mirante, Teresa, Mignogna, Chiara, Scrima, Marianna, Migliozzi, Simona, Rocco, Gaetano, Franco, Renato, Corcione, Francesco, Viglietto, Giuseppe, Malanga, Donatella, Rizzuto, Antonia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2018
Materias:
Research Paper
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5978263/
https://www.ncbi.nlm.nih.gov/pubmed/29854313
http://dx.doi.org/10.18632/oncotarget.25229

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5978263/
https://www.ncbi.nlm.nih.gov/pubmed/29854313
http://dx.doi.org/10.18632/oncotarget.25229

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