Skip to content


You're viewing the new version of our site. Please leave us feedback.

Learn more

BMC Bioinformatics

Open Access

Oqtans: a multifunctional workbench for RNA-seq data analysis

  • Vipin T Sreedharan1,
  • Sebastian J Schultheiss2,
  • Géraldine Jean2,
  • André Kahles1,
  • Regina Bohnert2,
  • Philipp Drewe1,
  • Pramod Mudrakarta2,
  • Nico Görnitz3,
  • Georg Zeller4 and
  • Gunnar Rätsch1
BMC Bioinformatics201415(Suppl 3):A7

Published: 11 February 2014


The current revolution in sequencing technologies allows us to obtain a much more detailed picture of transcriptomes via deep RNA Sequencing (RNA-Seq). In considering the full complement of RNA transcripts that comprise the transcriptome, two important analytical questions emerge: what is the abundance of RNA transcripts and which genes or transcripts are differentially expressed. In parallel with developing sequencing technologies, data analysis software is also constantly updated to improve accuracy and sensitivity while minimizing run times. The abundance of software programs, however, can be prohibitive and confusing for researchers evaluating RNA-Seq analysis pipelines.


We present an open-source workbench, Oqtans, that can be integrated into the Galaxy framework that enables researchers to set up a computational pipeline for quantitative transcriptome analysis. Its distinguishing features include a modular pipeline architecture, which facilitates comparative assessment of tool and data quality. Within Oqtans, the Galaxy’s workflow architecture enables direct comparison of several tools. Furthermore, it is straightforward to compare the performance of different programs and parameter settings on the same data and choose the best suited for the task. Oqtans analysis pipelines are easy to set up, modify, and (re-)use without significant computational skill.

Oqtans integrates more than twenty sophisticated tools that perform very well compared to the state-of-the-art for transcript identification, quantification and differential expression analysis. The toolsuite contains several tools developed in the Rätsch Laboratory, but the majority of the tools were developed by other groups. In particular, we provide tools for read alignment (bwa, STAR, TopHat, PALMapper, …), transcript prediction (cufflinks, Trinity, Scripture, …) and quantitative analyses (DESeq2, edgeR, rDiff, rQuant, …). In addition, we provide tools for alignment filtering (RNA-geeq toolbox), GFF file processing (GFF toolbox) and tools for predictive sequence analysis (EasySVM, ASP, ARTS, …). See for more details on included tools.


Oqtans is integrated into the publicly available Galaxy server which is maintained by the Rätsch Laboratory. It is also available as source code in a public GitHub repository and as a machine image (managed by Galaxy CloudMan) for the Amazon Web Service cloud environment (instructions available at Oqtans sets a new standard in terms of reproducibility and builds upon Galaxy’s features to facilitate persistent storage, exchange and documentation of intermediate results and analysis workflows.




Public Computing Server:

oqtans Demo Server:

oqtans Amazon Machine Image: ami-65376a0c

License: GPL

Authors’ Affiliations

Computational Biology Center, Memorial Sloan-Kettering Cancer Center
Friedrich Miescher Laboratory, Max Planck Society
Machine Learning/Intelligent Data Analysis Group, Technical University Berlin
Structural and Computational Biology Unit, European Molecular Biology Laboratory


© Sreedharan et al; licensee BioMed Central Ltd. 2014

This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The Creative Commons Public Domain Dedication waiver ( applies to the data made available in this article, unless otherwise stated.