Studying the Genetic Origins of Disease
At Sanford Research, we study how all the genes in your body – the genome – work in concert to promote healthy cellular function. We focus on studying origins of disease at the level of people, organs, or even one individual cell at a time.
Harnessing the power of bioinformatics and big data, we work to generate more personalized medicines and individualized treatments.
The Genetics and Genomics Group focuses on:
- Understanding cellular identity and what leads to disease progression
- Using genomic sequencing and bioinformatics to understand cell development
- Developing personalized therapies and treatments
We use this information to integrate clinical genetics into everyday primary care. Providers can then make better decisions on prescribing medications and screening for risk of chronic disorders.
The Genetics and Genomics Group supports:
Primary Faculty
Secondary Faculty
Sanford Health News
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National cancer study aims to reach Midwestern patients
Enrolling in NCI research can help scientists find better ways to prevent cancer
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Research path runs from rural South to South Dakota
Doctoral student finds new community in colleagues at Sanford Research
Classes & Events
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Teen Science Café
Tue 04/02/24 5:30 PM - Tue 04/02/24 7:00 PM
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PROMISE Summer Programs
Mon 06/03/24 8:30 AM - Mon 06/03/24 3:00 PM
Sanford PROMISE Community Lab