Next-generation sequencing has helped scientists make significant breakthroughs in cancer research. Bina's cancer genomics workflows provide researchers with fast, accurate and reliable NGS tools in the industry to further pursue their research.
Bina's robust workflows include sensitive alignment and detection (including SNP, Indel and Structural Variant), so your results are not only complete, but highly accurate
Traditionally, it takes 130 hours for a cancer sample to move through the entire analysis workflow. With Bina Enterprise, it’s done in 5 hours.
Automatic updates ensure that you have the latest and greatest tools at your fingertips. Be modern forever.
Over 140 annotions from database sources including: COSMIC, ClinVar, Cancer Gene Census, HGMD, PGMD
Providing an infrastructure for analyzing terabytes of data on a daily basis is no simple task. Bina’s architecture allows you to scale out as much as you need with minimal external infrastructure needs.
Automation via REST API
Smart Software Updates
Robust User Management
Reports & Auditability