PhD in Rare Variant Genomics to Decode Musculoskeletal Disease
Listed on 2026-11-02
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Research/Development
Genetics / Genomics, Research Scientist, Biomedical Science
University of Exeter in collaboration with the University of Oxford invites applications for a funded PhD studentship focused on rare genetic variants driving musculoskeletal disorders. The project combines health data science, statistical genomics, and molecular genetics to uncover causal genes and mechanisms.
Phase 1 is computational analysis using large datasets;
Phase 2 moves to laboratory validation in tissue models, CRISPR editing, and functional genomics to define disease pathways and
This is a great position to take on the PhD in Rare Variant Genomics to Decode Musculoskeletal Disease role at University of Exeter.
We are seeking a motivated PhD in Rare Variant Genomics to Decode Musculoskeletal Disease to join University of Exeter in Exeter, England, United Kingdom.
Consider building your career as a PhD in Rare Variant Genomics to Decode Musculoskeletal Disease at University of Exeter.
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