Accurate isoform discovery with IsoQuant using long reads
University of Helsinki · St Petersburg University · +6 more institutions
Abstract
Annotating newly sequenced genomes and determining alternative isoforms from long-read RNA data are complex and incompletely solved problems. Here we present IsoQuant-a computational tool using intron graphs that accurately reconstructs transcripts both with and without reference genome annotation. For novel transcript discovery, IsoQuant reduces the false-positive rate fivefold and 2.5-fold for Oxford Nanopore reference-based or reference-free mode, respectively. IsoQuant also improves performance for Pacific Biosciences data.
Citation impact
- FWCI
- 46.89
- Percentile
- 100%
- References
- 35
Authors
7- ADAndrey D. PrjibelskiCorresponding
University of Helsinki, St Petersburg University
- AMAlla Mikheenko
St Petersburg University
- AJAnoushka Joglekar
Cornell University, MIND Research Institute, Tri-Institutional PhD Program in Chemical Biology, Center for Neuro-Oncology, Weill Cornell Medicine
- ASAlexander Smetanin
Bioinformatics Institute
- JJJulien Jarroux
Cornell University, MIND Research Institute, Center for Neuro-Oncology, Weill Cornell Medicine
Topics & keywords
- Gene isoform
- Computational biology
- Focus (optics)
- Biology
- Genetics
- Gene
- Life below water