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Data

Clinicogenomics for greater data insights

Better understand diseases and drug development opportunities with our genomics solution.

Unlock the potential of genomic data

The information within the human genome can help us diagnose rare diseases, identify individuals at risk of developing certain conditions and create effective treatment regimens. But today’s genomic data sets often come with limitations for researchers. They’re noisy, not representative, and lack information on the patient journey, limiting their value.

Optum Life Sciences combines the rich depth of genomic sequencing data with our world-class clinical and claims assets to offer researchers a new frontier in their search for life-changing treatments, vaccines and cures.

Accelerate time to market for targeted therapies

Our research-ready, de-identified clinicogenomics data sets link genomic and other -omic data with the longitudinal health record. This allows for:

  • Genotypic and phenotypic research across all stages of therapy development and use in the real world
  • Comparison of clinical trial data to real-world data (RWD)
  • Development of companion diagnostics
  • Understanding the genetic testing landscape

With these real-world data, your teams can spend less time on unproductive research and development, and accelerate the time to market for innovative, targeted therapies.

Key benefits

Clinicogenomics data sets should reflect real-life populations. Ours are built to be representative and depict real clinical care.

High-quality RWD foundation

More than 115 million lives of de-identified clinical data allow for more detailed patient journeys from the start.

Data for all therapeutic areas  

Beyond our 117,000 individual oncology patients linked with genomic data, our data spans thousands of conditions, including rare diseases.

Real-world populations reflected

For some therapeutic areas, you can design cohorts that are 100% non-Caucasian to analyze specific demographic trends.

Full patient journeys uncovered

Because tumor biology changes over time, our oncology data include sequential sequencing for over 15% of individuals.

Raw sequencing files

Our genomic data comes from raw sequencing files, rather than PDFs or other EMR-based reports.

Research across product lifecycles

From biomarker discovery, to market access, to creating external control arms, our diversified data sets help answer a variety of questions.

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Product information and resources

  • PDF

     

    Fact sheet

    Cardiology and metabolic conditions

    Optum can focus a customized cohort on individuals who are diverse with unique combinations of comorbid profiles.

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  • PDF

     

    Fact sheet

    Oncology

    Enable precision medicine, reveal the patient journey both before and after diagnosis, and help uncover new information about cancer types.

    Learn more
  • PDF

     

    Fact sheet

    Autoimmune and inflammatory conditions

    Explore the clinical and genomic pillars that reveal which patient populations should receive targeted treatments.

    Learn more

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