| Literature DB >> 28069593 |
Maximilian Hastreiter1, Tim Jeske1, Jonathan Hoser1, Michael Kluge1, Kaarin Ahomaa1, Marie-Sophie Friedl1, Sebastian J Kopetzky1, Jan-Dominik Quell1, H-Werner Mewes1, Robert Küffner1.
Abstract
Summary: Analysis of Next Generation Sequencing (NGS) data requires the processing of large datasets by chaining various tools with complex input and output formats. In order to automate data analysis, we propose to standardize NGS tasks into modular workflows. This simplifies reliable handling and processing of NGS data, and corresponding solutions become substantially more reproducible and easier to maintain. Here, we present a documented, linux-based, toolbox of 42 processing modules that are combined to construct workflows facilitating a variety of tasks such as DNAseq and RNAseq analysis. We also describe important technical extensions. The high throughput executor (HTE) helps to increase the reliability and to reduce manual interventions when processing complex datasets. We also provide a dedicated binary manager that assists users in obtaining the modules' executables and keeping them up to date. As basis for this actively developed toolbox we use the workflow management software KNIME. Availability and Implementation: See http://ibisngs.github.io/knime4ngs for nodes and user manual (GPLv3 license). Contact: robert.kueffner@helmholtz-muenchen.de. Supplementary information: Supplementary data are available at Bioinformatics online.Mesh:
Year: 2017 PMID: 28069593 DOI: 10.1093/bioinformatics/btx003
Source DB: PubMed Journal: Bioinformatics ISSN: 1367-4803 Impact factor: 6.937