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Supporting Freebayes, to Serve Our Customers and the Community

Freebayes is a variant calling tool for short-read sequencing by Erik Garrison, Gabor Marth, and others, which played a significant role in the 1000 Genomes Project. It’s widely appreciated for its quality results, cost-effective performance, and permissive open-source license. At DNAnexus, many of our customers have come to rely on it in their sequencing pipelines. But, like many software tools in genome informatics, its development might have stopped at the conclusion of its (hugely successful) sponsor project.

We listened to our customers, and heard clearly that freebayes is too valuable to let that happen. A few months ago, we began working with Erik on a roadmap for ongoing development and maintenance with our support. Through our collaboration, Erik recently delivered a capability to generate gVCF output files, a significant feature both for individual genome interpretation and for aggregate analysis of vast cohorts. We’re continuing to refine that feature, and we have many more queued up to ensure freebayes remains a tool of choice for both research and clinical sequencing pipelines.

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Importantly, freebayes and our collective contributions to it will remain free for all to use and build upon, under the MIT license. Furthermore, best efforts will be made to assist all its users through public forums. We’d love to hear about your use cases and ideas to further improve freebayes – reach us on GitHub or Gitter, or send us a tweet. Erik remains in his day job, realizing a totally new paradigm in genome informatics, and we’re delighted he can also work with us to make freebayes endure as a tool the community can count on. So to all the genome hackers out there: please hack on freebayes too!

Because no single tool can possibly serve all applications, DNAnexus continues to work with numerous collaborators toward advancing methods in genome informatics, both free and commercially licensed. We also continue to wholeheartedly support our customers’ choice of methodologies to deploy on our platform, whether sourced from our partner network or elsewhere. We’re delighted by this opportunity to both deliver value to our customers and give back to the broader community. To the genome hackers again: we’re on the lookout for more of these opportunities! (We’re hiring, too!)

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About DNAnexus

DNAnexus the leader in biomedical informatics and data management, has created the global network for genomics and other biomedical data, operating in 33 countries including North America, Europe, China, Australia, South America, and Africa. The secure, scalable, and collaborative DNAnexus Platform helps thousands of researchers across a spectrum of industries — biopharmaceutical, bioagricultural, sequencing services, clinical diagnostics, government, and research consortia — accelerate their genomics programs.

The DNAnexus team is made up of experts in computational biology and cloud computing who work with organizations to tackle some of the most exciting opportunities in human health, making it easier—and in many cases feasible—to work with genomic data. With DNAnexus, organizations can stay a step ahead in leveraging genomics to achieve their goals. The future of human health is in genomics. DNAnexus brings it all together.