Solutions

Key to Health and Wellbeing

Genetic testing plays a growing role in everyone’s health and wellbeing. Working closely with clinicians, more patients are making informed, proactive health decisions based on insights generated by Genoox.

Genoox Research Applications

An end-to-end approach to population genomics

Faster screening, faster reporting

Robust cohort research

An end-to-end approach to population genomics

Genoox helps health systems and research institutions across the globe accelerate the integration of genomics into clinical care - facilitating novel genetic discoveries and improving patient care.

Faster screening, faster reporting

Genoox facilities more rapid screening and reporting of risk-associated variants – helping clinicians inform and guide their patients more accurately.

Robust cohort research

Genoox enables research on patient cohorts, helping identify new risk-associated variants and impacting health policies,

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
classification

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

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