annoFuse: an R Package to annotate, prioritize, and interactively explore putative oncogenic RNA fusions

BACKGROUND: Gene fusion events are significant sources of somatic variation across adult and pediatric cancers and are some of the most clinically-effective therapeutic targets, yet low consensus of RNA-Seq fusion prediction algorithms makes therapeutic prioritization difficult. In addition, events...

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Detalles Bibliográficos
Autores principales: Gaonkar, Krutika S., Marini, Federico, Rathi, Komal S., Jain, Payal, Zhu, Yuankun, Chimicles, Nicholas A., Brown, Miguel A., Naqvi, Ammar S., Zhang, Bo, Storm, Phillip B., Maris, John M., Raman, Pichai, Resnick, Adam C., Strauch, Konstantin, Taroni, Jaclyn N., Rokita, Jo Lynne
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Software
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7737294/
https://www.ncbi.nlm.nih.gov/pubmed/33317447
http://dx.doi.org/10.1186/s12859-020-03922-7

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7737294/
https://www.ncbi.nlm.nih.gov/pubmed/33317447
http://dx.doi.org/10.1186/s12859-020-03922-7

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