FUCHS - Towards full circular RNA characterization using RNAseq

Max-Planck Institute for Biology of Ageing, 50931 Cologne, Germany
Max-Planck-Genome-Centre Cologne, 50829 Cologne, Germany
Department of Internal Medicine III, Klaus Tschira Institute for Integrative Computational Cardiology, 69120 Heidelberg, Germany
Partner site Heidelberg/Mannheim, German Centre for Cardiovascular Research (DZHK), 69120 Heidelberg, Germany
DOI
10.7287/peerj.preprints.2418v1
Subject Areas
Bioinformatics, Computational Biology, Genomics, Molecular Biology
Keywords
Circular RNA, Alternative-splicing, Transcriptomics
Copyright
© 2016 Metge et al.
Licence
This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, reproduction and adaptation in any medium and for any purpose provided that it is properly attributed. For attribution, the original author(s), title, publication source (PeerJ Preprints) and either DOI or URL of the article must be cited.
Cite this article
Metge F, Czaja-Hasse LF, Reinhardt R, Dieterich C. 2016. FUCHS - Towards full circular RNA characterization using RNAseq. PeerJ Preprints 4:e2418v1

Abstract

Circular RNAs (circRNAs) belong to a recently re-discovered species of RNA that emerge during RNA maturation through a process called back-splicing. A downstream 5’ splice site is linked to an upstream 3’ splice site to form a circular transcript instead of a canonical linear transcript. Recent advances in next-generation sequencing (NGS) have brought circRNAs back into the focus of many scientists. Since then, several studies reported that circRNAs are differentially expressed across tissue types and developmental stages, implying that they are actively regulated and not merely a by-product of splicing. Though functional studies have shown that some circRNAs could act as miRNA-sponges, the function of most circRNAs remains unknown. To expand our understanding of possible roles of circular RNAs, we propose a new pipeline that could fully characterizes candidate circRNA structure from RNAseq data – FUCHS: FUll CHaracterization of circular RNA using RNA- Sequencing.

Currently, most computational prediction pipelines use back-spliced reads to identify circular RNAs. FUCHS extends this concept by considering all RNA-seq information from long reads (typically > 150 bp) to learn more about the exon coverage, the number of double break point fragments, the different circular isoforms arising from one host-gene, and the alternatively spliced exons within the same circRNA boundaries.

This new knowledge will enable the user to carry out differential-motif enrichment and miRNA-seed analysis to determine potential regulators during circRNA biogenesis. FUCHS is an easy-to-use Python based pipeline that contributes a new aspect to the circRNA research.

The pipeline is available as git repository: https://github.com/dieterich-lab/FUCHS

Author Comment

This is an article which has been accepted for the "GCB 2016 Conference"