Bina's inherited disease pipeline gives you the complete picture. With structural variants and SNVs in a single pipeline, you get a better understanding of potential disease markers, how multiple genes work together to affect disease, and more.
Our 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.
Bina's germline analysis pipeline offers the highest throughput in the industry at 6 whole genomes and 50 whole exomes per day.
Over 140 annotions from public and private databases including: 1000 Genomes, HGMD, PGMD, dbSNP, SnpEff.
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