Abstract
Background: The rapid development of next generation sequencing technologies, including the recently introduced benchtop sequencers, made sequencing affordable for smaller research institutions. A widely applied method to identify causing mutations of diseases is exome sequencing, which proved to be cost-effective and time-saving. Findings. SeqBench, a web-based application, combines management and analysis of exome sequencing data into one solution. It provides a user friendly data acquisition module to facilitate comprehensive and intuitive data handling. SeqBench provides direct access to the analysis pipeline SIMPLEX, which can be configured to run locally, on a cluster, or in the cloud. Identified genomic variants are presented along with several functional annotations and can be interpreted in a family context. Conclusions: The web-based application SeqBench supports the management and analysis of exome sequencing data, is open-source and available at. © 2014 Dander et al.; licensee BioMed Central Ltd.
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Dander, A., Pabinger, S., Sperk, M., Fischer, M., Stocker, G., & Trajanoski, Z. (2014). SeqBench: Integrated solution for the management and analysis of exome sequencing data. BMC Research Notes, 7(1). https://doi.org/10.1186/1756-0500-7-43
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