JAFFAL: detecting fusion genes with long-read transcriptome sequencing
Details
Publication Year 2022-01-06,Volume 23,Issue #1,Page 10
Journal Title
Genome Biology
Abstract
In cancer, fusions are important diagnostic markers and targets for therapy. Long-read transcriptome sequencing allows the discovery of fusions with their full-length isoform structure. However, due to higher sequencing error rates, fusion finding algorithms designed for short reads do not work. Here we present JAFFAL, to identify fusions from long-read transcriptome sequencing. We validate JAFFAL using simulations, cell lines, and patient data from Nanopore and PacBio. We apply JAFFAL to single-cell data and find fusions spanning three genes demonstrating transcripts detected from complex rearrangements. JAFFAL is available at https://github.com/Oshlack/JAFFA/wiki .
Publisher
BMC
Keywords
Fusions; Long reads; Nanopore; PacBio; RNA sequencing; Translocations
Research Division(s)
Blood Cells And Blood Cancer
PubMed ID
34991664
Open Access at Publisher's Site
https://doi.org/10.1186/s13059-021-02588-5
Terms of Use/Rights Notice
Refer to copyright notice on published article.


Creation Date: 2022-02-18 11:36:34
Last Modified: 2022-02-18 01:15:38
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