We are Inocras
Unlock the new era of precision health with our whole genome platform.
WHOLE GENOME SEQUENCING COMPANY
Where data, AI & care meet
Inocras is an AI-driven platform company providing whole genome insights to enable personalized care in cancer and rare diseases.
Founded in 2020 by a team of physician-scientists, geneticists, and bioinformaticians, our goal has been to improve how patients are diagnosed and treated by unlocking the full potential of genomic data. Since then, we’ve developed an IP-protected technology and proprietary whole genome insight platform while achieving operational excellence in our CLIA certified and CAP accredited lab.
We are also bringing innovation in delivery through patient-centric services that provide access to genetic counseling and clinical trial matching support.
Mission
We believe that genomic information should be accessible to everyone. By breaking down technology and cost barriers, we are paving the way for a future where genomic data drives targeted treatments and fuels healthier lives.
Values
We are fueled by our core values of patient-centricity, empowerment, innovation, and collaboration at the heart of everything we do.
What we do
For patients
When it comes to your health, or that of your loved ones, exploring all possible options is essential. Our whole genome diagnostic testing is designed to uncover broader and deeper insights that other DNA tests might miss.
- Easy-to-understand reports:
- Your detailed and easy-to-understand report will offer insights into your genome, helping you and your healthcare provider make informed decisions tailored to your unique body, and empowering you on your healthcare journey.
- Genetic counseling support:
- You will automatically have access to a genetic counselor to guide you through your sequencing results. We’ll ensure you understand the findings and potential treatment options, and that you receive the necessary support.
- Clinical trial matching support:
- We identify clinical trial matches based on your biomarkers and other criteria, and connect you with enrollment support services. Note: Clinical trial matching support is currently available only for cancer patients using CancerVision. We are working to expand it to other disease areas.
For providers
At Inocras, our goal is to help relieve your diagnostic burden so you can spend more time caring for your patients. Our whole genome platform provides you with additional data, tools, and confidence to support your best medical decision-making. Partnering with Inocras gives you cutting-edge sequencing services and genomics services to enhance human health and streamline your clinical practice.
- Actionable findings:
- Our proprietary, high-performing bioinformatics algorithm thoroughly analyzes a patient’s raw DNA data and translates it into actionable findings. Our user-friendly report is comprehensive and highlights the findings highly relevant to clinical utility.
- Clinical trial matching:
- We provide detailed clinical trial information based on each patient’s biomarkers and other pre-screening criteria, saving you time in finding the best-matched clinical trials and potential treatment options for patients (for cancer only).
- Expert support:
- You’ll have access to our in-house genomic experts on demand, while our dedicated sales and medical teams are just a phone call away. Your patient will also have access to a genetic counselor, who is also available to address any questions you may have.
For researchers
Maximize your research potential with precision DNA sequencing, curation, and interpretation.We provide our services at affordable prices thanks to high-level automation in our bioinformatics pipeline and high-throughput sequencing technology. Unlock the full potential of your research – reliably in 2 weeks. Partner with one of the leading sequencing companies to elevate your research to the next level.
- We offer end-to-end services that can be tailored to your needs, from sequencing performed with or without library prep, to world-class bioinformatics providing analytics and interpretation.
- Researchers receive expert advisory support from our team of genomic scientists (MDs and PhDs) on demand for research projects.
- Utilize our research-use and CLIA-certified, CAP-accredited clinical-use whole genome sequencing services
Our leadership team
We are a global team with a shared goal: Delivering impact to patients and the healthcare industry through actionable insights and user-centric services.
Scientific advisory board
Our investors
Our partners
