FusionSeq: a modular framework for finding gene fusions by analyzing paired-end RNA-sequencing data

We have developed FusionSeq to identify fusion transcripts from paired-end RNA-sequencing. FusionSeq includes filters to remove spurious candidate fusions with artifacts, such as misalignment or random pairing of transcript fragments, and it ranks candidates according to several statistics. It also...

Descripció completa

Guardat en:
Dades bibliogràfiques
Autors principals: Sboner, Andrea, Habegger, Lukas, Pflueger, Dorothee, Terry, Stephane, Chen, David Z, Rozowsky, Joel S, Tewari, Ashutosh K, Kitabayashi, Naoki, Moss, Benjamin J, Chee, Mark S, Demichelis, Francesca, Rubin, Mark A, Gerstein, Mark B
Format: Artigo
Idioma:Inglês
Publicat: BioMed Central 2010
Matèries:
Method
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC3218660/
https://ncbi.nlm.nih.gov/pubmed/20964841
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/gb-2010-11-10-r104
Etiquetes: Afegir etiqueta
Sense etiquetes, Sigues el primer a etiquetar aquest registre!

Ítems similars