The diagnostic application of RNA sequencing in patients with thyroid cancer: an analysis of 851 variants and 133 fusions in 524 genes

BACKGROUND: Thyroid carcinomas are known to harbor oncogenic driver mutations and advances in sequencing technology now allow the detection of these in fine needle aspiration biopsies (FNA). Recent work by The Cancer Genome Atlas (TCGA) Research Network has expanded the number of genetic alterations...

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Detalhes bibliográficos
Publicado no:BMC Bioinformatics
Main Authors: Pagan, Moraima, Kloos, Richard T., Lin, Chu-Fang, Travers, Kevin J., Matsuzaki, Hajime, Tom, Ed Y., Kim, Su Yeon, Wong, Mei G., Stewart, Andrew C., Huang, Jing, Walsh, P. Sean, Monroe, Robert J., Kennedy, Giulia C.
Formato: Artigo
Idioma:Inglês
Publicado em: BioMed Central 2016
Assuntos:
Proceedings
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4895782/
https://ncbi.nlm.nih.gov/pubmed/26818556
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12859-015-0849-9
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