MINTIE: identifying novel structural and splice variants in transcriptomes using RNA-seq data

Abstract Calling fusion genes from RNA-seq data is well established, but other transcriptional variants are difficult to detect using existing approaches. To identify all types of variants in transcriptomes we developed MINTIE, an integrated pipeline for RNA-seq data. We take a reference-free approa...

Full description

Bibliographic Details
Main Authors: Marek Cmero, Breon Schmidt, Ian J. Majewski, Paul G. Ekert, Alicia Oshlack, Nadia M. Davidson
Format: Article
Language:English
Published: BMC 2021-10-01
Series:Genome Biology
Online Access:https://doi.org/10.1186/s13059-021-02507-8