Over the past decade, NGS focused gene panels, clinical and whole exome have emerged as reliable and cost-effective solutions to diagnose and characterize rare, inherited diseases and tumors. Genoox helps laboratories enhance their brand with personalized medicine – enabling any lab to design, validate, and run its own NGS panel tests. Our user-friendly, cost-effective and advanced analytical tools manage the computational demands of data processing, variant classification, and clinical reporting - getting your test up and running, fast.

Workflow for Any Need

Rare & Inherited Diseases

Reproductive Health

Hereditary Panels


Rare & Inherited Diseases

Genoox conducts single genome, trio and family analyses for assessing germline variants found in rare diseases. The platform prioritizes potential causative genomic alterations in hereditary and pediatric disorders from WGS, WES and gene-panel specific analysis platforms. It does this by rapidly and confidently identifying and classifying pathogenic variants according to ACMG guidelines, and matching clinical evidence with patient phenotypes.

Reproductive Health

Genoox simplifies laboratory processes, facilitating the use of high-precision preconception screening and family planning. We work with various vendors on a variety of gene panels and provide full solutions that cover the entire spectrum - from carrier screening through newborn genetic testing.

Hereditary Panels

Genoox delivers clinically actionable recommendations by identifying and reporting rare mutations. We do this using a dedicated workflow that encompasses a large database of known disease-associated genetic abnormalities from single or heterogenetic backgrounds linked to cardiomyopathies.


Genoox streamlines workflows for utilizing molecular data in a clinical setting, and enables use of complex genomic data in novel ways to refine oncology patient treatment strategies and improve outcomes

Why Genoox?

Created for professionals,
by professionals

Genoox is the creator of the world’s first open genomic community. Our users leverage our vendor-neutral, workflow-agnostic platform to create accurate data insights across the genomic value chain.

The right tools to
empower your pipeline

Genoox is a fully modular platform that enables
selection of relevant tools to maximize the efficiency
and accuracy of your NGS pipeline.

AI-based variant

Our AI engine provides the best classifier based on any publicly available data source. It suggests relevant evidence, refines metrics and addresses gene-specific recommendations - delivering a fully-transparent ACMG\AMP-based variant classification.

Reach all available data,
use only what is relevant

Genoox prioritizes and aggregates frequently-updated information from published research, new and existing archives, and curated and uncurated databases. We filter out ‘noise’ and highlight evidence crucial to your decision making.

Harness your
genetic data

Genoox generates a durable genomic data repository that can be queried against variant statistics - maximizing linkage and assessment for comprehensive clinical classification and reporting using curated information and historical sample data.

Contact Us

If you’d like to chat about Genoox in more detail, complete this form
and we’ll get back to you.