A fast detection of fusion genes from paired-end RNA-seq data

BACKGROUND: Fusion genes are known to be drivers of many common cancers, so they are potential markers for diagnosis, prognosis or therapy response. The advent of paired-end RNA sequencing enhances our ability to discover fusion genes. While there are available methods, routine analyses of large num...

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Detalles Bibliográficos
Autores principales: Vu, Trung Nghia, Deng, Wenjiang, Trac, Quang Thinh, Calza, Stefano, Hwang, Woochang, Pawitan, Yudi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Methodology Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6211471/
https://www.ncbi.nlm.nih.gov/pubmed/30382840
http://dx.doi.org/10.1186/s12864-018-5156-1

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6211471/
https://www.ncbi.nlm.nih.gov/pubmed/30382840
http://dx.doi.org/10.1186/s12864-018-5156-1

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