A rich set of applications and workflows for translational research

BaseSpace Sequence Hub for Translational Research

BaseSpace Sequence Hub is the Illumina genomics computing environment for next-generation sequencing (NGS) data analysis. It offers a deep and continually growing set of applications for translational research.

The environment facilitates collaboration and sharing of data with fellow researchers, which is a cornerstone of translational research. Applications are authored by Illumina or peer researchers at leading academic, medical, and commercial institutions. This flexible solution is available in both cloud and onsite packages.

BaseSpace Hub offers ready-to-use applications (apps) for human whole-genome sequencing, targeted resequencing, copy number variation analysis, and transcriptome analysis, to name a few. There are apps to support research and analysis whether you’re a scientist at a pharmaceutical company or a practicing clinician.

BaseSpace Hub also includes applications and workflows for annotation and effect prediction. These tools are useful for researchers focusing on model organisms commonly studied in translational research (such as rat and mouse), as well as human samples.

Learn more about BaseSpace Hub