Any species, any platform, any workflow: The all-purpose power tool for NGS data analysis
• Ready-to-use and flexible workflows: Over a dozen pre-built workflows to accelerate analysis of your cancer and hereditary disease data. Build your own customized analysis workflows for a wide range of both DNA and RNA sequencing data
• Intuitive interface: Interactive visualization of your data linked to a best-in-class track viewer
• Visualize and share results with the built-in Genome Viewer
• Platform independent: Supports common sequencing platforms (Illumina, Ion Torrent, PacBio, Oxford Nanopore and GeneReader) and runs on most operating systems
• Enterprise ready: Support multiple users in an intuitive way, with high-throughput analysis and automation