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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Vydáno v:BMC Bioinformatics
Hlavní autoři: 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
Médium: Artigo
Jazyk:Inglês
Vydáno: BioMed Central 2020
Témata:
Software
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC7737294/
https://ncbi.nlm.nih.gov/pubmed/33317447
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12859-020-03922-7
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