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

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

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_b17c2203e9b546a2b0b10ad745481e80

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

About this item

Full title

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

Publisher

England: BioMed Central Ltd

Journal title

BMC bioinformatics, 2020-12, Vol.21 (1), p.577-21, Article 577

Language

English

Formats

Publication information

Publisher

England: BioMed Central Ltd

More information

Scope and Contents

Contents

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 such as polymerase read-throughs, mis-mapping due to gene homo...

Alternative Titles

Full title

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

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_doaj_primary_oai_doaj_org_article_b17c2203e9b546a2b0b10ad745481e80

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_b17c2203e9b546a2b0b10ad745481e80

Other Identifiers

ISSN

1471-2105

E-ISSN

1471-2105

DOI

10.1186/s12859-020-03922-7

How to access this item