GENOOX Solutions for Clinical Genetics

Streamlining the path from DNA sample to clinical report

clinical Applications

hereditary and clinical genetics

Hereditary Genetics

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Advanced Hereditary Genetics

How Can We Help?

- Conduct single genome, trio, and family analyses for assessing germline variants found in rare disease
- Detect causative genomic alterations in hereditary and pediatric disorders with WGS, WES and gene panel-specific analysis platforms
- Rapidly and confidently identify and classify relevant pathogenic variants according to ACMG guidelines
cancer risk assessment

cancer risk assessment

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Advanced Cancer Risk Assessment

How Can We Help?

- Streamline the workflow for utilizing molecular data in a clinical setting
- Enable use of complex genomic data in novel ways to refine oncology patient treatment strategies and improve outcomes
pharmagenomics testing - GENOMIC DATA -clinical genetics

PHARMAGENOMICS TESTING

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Advanced Pharmacogenetics Testing

How Can We Help?

- Predict drug exposure-response relationships
- Better understand a patient's unique genetic makeup and select therapies with fewer side effects, optimize drug dosing and assess personal disease risk
carrier screening - clinical genetics

Carrier screening

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Advanced Carrier Screening

How Can We Help?

- Simplify laboratory processes for provision of high precision, preconception screening and family planning utilizing the GENOOX fully automated platform
- Choose from comprehensive WES screening or more limited panels for the most common hereditary disorders depending on specific needs of the clinic
- Expedite care of children exhibiting dysmorphic features at birth with early and actionable results from newborn screening applications

Clinical insights through quality data

Utilizing a cloud-based advanced AI framework that encompasses purpose-built applications, users can easily manage the entire genetic sequencing process and create virtual genetic test modules allowing plug- and-play for the delivery of clinically actionable insights and disease diagnoses

our customers

 
carrier screening - clinical genetics
Health Systems
carrier screening - clinical genetics
Children’s Hospitals
carrier screening - clinical genetics
Academic Medical Centers
carrier screening - clinical genetics
Cancer Centers
carrier screening - clinical genetics
Commercial Labs
 

the genoox advantage

 
Select the right tools to empower your pipeline
Offering a wholly modular platform from which you select the relevant tools critical to maximizing the efficiency and accuracy of your NGS pipeline
 
 
Access the next level of alignment processes
Applying proprietary ultra-sensitive statistical modeling drawn from diverse sources to increase detection of structural variants and SNP mutations
 
 
Retrieve the ACMG-AMP clinical evidence for your variant of interest
Delivering fully transparent ACMG-based variant classi cation, and providing the clinical tools you need to make the call, via your evidence-weighting modi cations - all in a fraction of the time required by manual or older methodologies
 
 
Reach all available data and use only what is relevant
Prioritizing aggregated and frequently updated information from published research, new and existing archives, and curated and uncurated databases to filter out ‘noise’ and highlight evidence crucial to decision making
 
 
Optimize your historical data
Generating a durable genomic data repository that can be queried against variant statistics and maximizing linkage and assessment for comprehensive clinical classification and reporting using stored historical sample data
 

Check out one of our success stories

END THE DIAGNOSTIC ODYSSEY: RESOLVING OLD CASES IN MINUTES WITH GENOOX


Organizations are using Genoox to resolve old cases which were not possible to date, resulting in a confident, actionable diagnosis for patients.
Put Genoox to work for you

SIMPLY RESOLVE COMPLEX GENOMIC CHALLENGES

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