Accelerated, Secured and Flexible genetic data upload and storage utilizing your existing infrastructure.
Offering a fully customizable pipeline or a selection of intuitive and ready-to-use analysis templates for routine testing of family analysis, prenatal, tumor and case control.
Generate high quality variant calls and verify genes of interest using advanced metrics techniques for variant prioritization.
From simple annotation to clinical evidence – annotate variants applying actionable clinical information accessing hundreds of data sources.
Prioritize mutations of interest applying advanced machine learning algorithms – Classify and score each mutation and its impact based on specific phenotype, disease or treatment.
Query, correlate and cross reference millions of genomic datasets with millions of medical evidences and perform genome wide association studies (GWAS).
Automated and customizable, lab-branded clinical coverage reports delivering intuitive and graphical gene-level decision support for physicians and collaborators, enabling integration for third-party downstream integration.
Enabling users to customize their organizational workflow, user permissions and process management workspaces without the need for developing new systems or disrupting existing organizational data flows.