Full employer posting
Mayo Clinic in Jacksonville, Florida, is seeking a postdoctoral research fellow in human genetics, computational genomics, or bioinformatics to work with Dr. Joseph Cheung on an emerging research program at the intersection of genetics, sleep, and autism . Mayo Clinic is a world-class health care organization, with cutting-edge research programs.
The program investigates genetic contributions to neurodevelopmental conditions and sleep phenotypes, including individuals with unresolved genetic etiologies. The fellow will analyze whole-exome and whole-genome sequencing data , develop reproducible analytical workflows, and integrate genomic findings with clinical phenotypes. Projects may include rare-variant prioritization, family-based analyses, reanalysis of unresolved cases, and genotype–phenotype studies.
The position offers opportunities to develop independent research questions, lead manuscripts, and contribute to grant applications.
include a Ph. D. degree in human genetics, genomics, bioinformatics, computational biology, statistical genetics, neuroscience or with appropriate computational genomics research experience. Demonstrated experience analyzing human germline WES and/or WGS data, including copy-number and structural variants, quality control, variant annotation, filtering, and phenotype-driven variant prioritization; a strong understanding of inheritance and genotype–phenotype relationships.
Excellent written and oral communication skills are required. Prior experience in sleep research is not required. Strong human genetics candidates interested in developing expertise in autism and sleep are encouraged to apply.
The position is available immediately and is 2-3 years in duration, with the possibility of extension. Questions should be directed to Dr. Joseph Cheung: Cheung.joseph@mayo.edu.
- Full time Benefits
- Medical: Multiple plan options
- Dental: Delta Dental or reimbursement account for flexible coverage
- Vision: Affordable plan with national network
- Pre-Tax Savings: HSA and FSAs for eligible expenses
- Retirement: Competitive retirement package to secure your future
About the role
The fellow will analyze whole-exome and whole-genome sequencing data , develop reproducible analytical workflows, and integrate genomic findings with clinical phenotypes. Projects may include rare-variant prioritization, family-based analyses, reanalysis of unresolved cases, and genotype–phenotype studies.