SeqBench: Integrated solution for the management and analysis of exome sequencing data

7Citations
Citations of this article
32Readers
Mendeley users who have this article in their library.

This article is free to access.

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.

Cite

CITATION STYLE

APA

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

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free