Identification of novel transcripts in annotated genomes using RNA-Seq
Broad Institute · Harvard University · +1 more institution
Abstract
SUMMARY: We describe a new 'reference annotation based transcript assembly' problem for RNA-Seq data that involves assembling novel transcripts in the context of an existing annotation. This problem arises in the analysis of expression in model organisms, where it is desirable to leverage existing annotations for discovering novel transcripts. We present an algorithm for reference annotation-based transcript assembly and show how it can be used to rapidly investigate novel transcripts revealed by RNA-Seq in comparison with a reference annotation. AVAILABILITY: The methods described in this article are implemented in the Cufflinks suite of software for RNA-Seq, freely available from…
Citation impact
- FWCI
- 31.26
- Percentile
- 100%
- References
- 24
Authors
4- ARAdam RobertsCorresponding
Broad Institute, Harvard University, University of California, Berkeley
- HPHarold Pimentel
Broad Institute, Harvard University, University of California, Berkeley
- CTCole Trapnell
Broad Institute, Harvard University, University of California, Berkeley
- LPLior Pachter
Broad Institute, Harvard University, University of California, Berkeley
Topics & keywords
- Annotation
- Leverage (statistics)
- Software suite
- Computational biology
- Identification (biology)
- RNA-Seq
- Computer science
- Software