Basepair is a SaaS platform for genomic data analysis and interactive visualization that can be used for multitude of application areas across epigenetics, genomics, transcriptomics and others.

Bioinformaticians can leverage the powerful CLI or APIs to deploy, orchestrate and scale their custom tools and pipelines built in any workflow language. The platform comes with advanced enterprise features that abstract away the DevOps, accelerating the migration and deployment of Next Generation Sequencing (NGS) workflows to the cloud, freeing you up to focus on the science.

Meanwhile, bench scientists can then use the point-and-click GUI to drag and drop their files to upload their raw data and run either those same custom workflows, or choose from a number of industry standard, peer reviewed tools and pipelines to analyze their data. Instead of just providing the resulting flat files and static html pages, Basepair's reports and project sharing hierarchy streamline interactive exploration of the resulting data and collaboration with bioinformatics teams to validate observations.

Pay-as-you-go per sample pricing includes unlimited users and re-analysis of data, with annual licenses scaling cost effectively to deliver much lower prices per sample.

Minimal configuration allows the platform to: a) leverage the storage AND compute resources in your own cloud account to benefit from existing pricing agreements and economies of scale with AWS b) be white labeled to look and feel like your own web portal c) utilize back end coupon technology to facilitate bundling of analysis with the sale of another product (eg kit, assay, service etc)

Please contact us directly should you be interested in any of these options or additional prepaid pricing schemes.