GENOOX Solutions for Research & Pharma

Providing software, services and support to simplify complex genomic challenges

pharmaceutical & research applications

GWAS studies - GENOMIC DATA

DRUG DISCOVERY

DRUG DISCOVERY

HOW CAN WE HELP?

Easily identify variants that are significant drivers of disease, potentially impacting toxicity and efficacy on a personalized basis, including complex family pedigrees and advanced prediction of disease progression
clinical trial - GENOMIC DATA

CLINICAL TRIALS

CLINICAL TRIALS

HOW CAN WE HELP?

Optimize clinical trials from a design, planning, and enrolment perspective. Segment participants based on genomic profiles and observed therapeutic response using specific gene panels as well as whole exome or genome sequencing
drug repositioning - GENOMIC DATA

CASE CONTROL STUDIES

CASE CONTROL STUDIES

HOW CAN WE HELP?

Enable pharmaceutical companies and clinicians to screen patients for marketed and in-development targeted therapies by examining complex correlations in and between analysis groups comprising diverse patients/samples
pharmagenomics testing - GENOMIC DATA

COUNTRYWIDE GENOME PROGRAMS

COUNTRYWIDE GENOME PROGRAMS

HOW CAN WE HELP?

Apply sophisticated genome-wide association studies (GWAS) analysis tools to investigate genetic variants on a wide scale in large population studies and countrywide genome projects

Enhancing research with robust genomic analytics

Collaborate with Genoox to simplify complex sequencing data and make impactful discoveries using the most advanced genetic tools and applications
  • Apply advanced AI algorithms to uncover disease-driving variants
  • Perform deep statistical analyses using both public and private data
  • Stay up to date with all curated/uncurated publications
  • Comprehensively view population-speci c genetics
  • Create a durable searchable genomic patient data repository

the genoox advantage

 
Create a fully customizable pipeline for biological research
Utilizing a wholly modular system from which you select the 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 draws from diverse sources to increase detection of structural variants and SNP mutations
 
 
Reach all available data
Aggregating and frequently updating information from published research, new and existing archives, and curated and uncurated databases
 
 
Use only relevant data
Prioritizing using an advanced collective metrics and scoring methods to filter out ‘noise’ and highlight evidence crucial to decision making
 
 
Optimize your historical data
Developing a durable genomic data repository that can be queried against variant statistics, subjected to linkage assessment, and analyzed for ongoing disease studies and clinical trial recruitment
 

Check out one of our success stories

THE GENE BEHIND THE DISEASE


The Genoox platform was used by Teva as part of cohort analysis looking for a genetically-validated drug target for the treatment of pain phenotypes.
Put Genoox to work for you

SIMPLY RESOLVE COMPLEX GENOMIC CHALLENGES

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