University of Cincinnati

USA
1 Scholarships 196 Programs 3 Degree levels
Masters

Master's in Genetics

Offered at University of Cincinnati, USA
DegreeMasters
FieldGenetics.
C

Cost & earnings at University of Cincinnati What students borrow here, and what they go on to earn

You borrow $21,250 median federal debt
You repay $242/mo over 10 years
Graduates earn $54,810 10 yrs after entry
Debt clears in 1.4 yrs of the salary premium
US Department of Education figures See the full breakdown →

The Master of Science in Genetics with a focus on Mitochondrial Genetics at the University of Cincinnati is a research-led programme that combines advanced coursework in mitochondrial biology with hands-on laboratory training and bioinformatics. It suits students with a strong undergraduate background in biological sciences who want to pursue research, diagnostics or translational careers addressing mitochondrial disease, ageing and metabolic disorders.

What you'll study

This master's emphasises the molecular and cellular biology of mitochondria and their roles in health and disease. Core topics include mitochondrial genetics and genomics, mitochondrial DNA replication and repair, oxidative phosphorylation and bioenergetics, and mechanisms of mitochondrial quality control (mitophagy and dynamics). Students also study disease mechanisms in mitochondrial disorders, mitochondrial contributions to neurodegeneration and ageing, and the role of mitochondria in metabolic disease and cancer.

  • Advanced molecular genetics and genomics of mitochondria
  • Techniques in mitochondrial biology: cell culture, mitochondrial isolation, proteomics and metabolomics
  • Next-generation sequencing and bioinformatic analysis of mtDNA variation and heteroplasmy
  • Genome editing approaches relevant to mitochondrial research and model systems
  • Quantitative methods: statistics for genomics, experimental design and reproducibility
  • Seminars, journal clubs and research ethics with emphasis on clinical and translational work

The programme typically combines taught modules with practical laboratory rotations or a lab-based research project leading to a substantive dissertation. Students are trained in core techniques such as high-throughput sequencing, image-based mitochondrial assays, respirometry, mass spectrometry for mitochondrial proteomics, and computational pipelines for analyzing mtDNA heteroplasmy and copy number. Interdisciplinary electives may cover population genetics, pharmacology, or clinical genetics, allowing projects that bridge basic science and patient-oriented research.

Entry requirements

Applicants are normally expected to hold a bachelor’s degree in biology, genetics, biochemistry, molecular biology, biomedical sciences or a closely related discipline. Successful candidates typically demonstrate strong performance in undergraduate coursework in genetics, cell biology and biochemistry, and have laboratory experience.

  • Academic transcripts showing a relevant undergraduate degree
  • Curriculum vitae or résumé detailing laboratory experience and research projects
  • Personal statement describing research interests and fit with mitochondrial genetics
  • Two or three academic references who can comment on research potential
  • International applicants must meet the University of Cincinnati’s English language proficiency requirements

Standardised test requirements (such as the GRE) may vary by programme and application cycle; prospective applicants should consult the department for current guidance. Prior hands-on research experience in molecular biology or genomics is strongly recommended for admission and will strengthen an application.

Career prospects

Graduates of this specialised master's are prepared for a variety of roles in research, healthcare and industry. Typical career paths include:

  • Laboratory-based research positions in academic laboratories studying mitochondrial biology, ageing or metabolic disease
  • Roles in biotech and pharmaceutical companies focused on mitochondrial-targeted therapeutics, biomarkers and drug discovery
  • Clinical and diagnostic laboratory positions analysing mitochondrial DNA and metabolic function in patient samples
  • Bioinformatics and genomic data analysis roles working with mtDNA sequencing, heteroplasmy detection and multi-omic datasets
  • Further study at the doctoral level (PhD) or transition to clinically oriented training such as genetic counselling or clinical laboratory science

The programme’s emphasis on both wet-lab and computational skills is intended to make graduates adaptable to translational projects and interdisciplinary teams in academic medical centres, industry, and government laboratories.

Why study at University of Cincinnati

The University of Cincinnati offers a research-intensive environment with interdisciplinary links to regional medical and research centres. Students benefit from collaborative opportunities with clinical research groups, access to core facilities for genomics, proteomics and high-resolution imaging, and mentorship from faculty whose research spans basic mitochondrial biology to translational studies of mitochondrial disease.

  • Hands-on training in well-equipped core facilities that support next-generation sequencing, mass spectrometry and advanced microscopy
  • Opportunities to work alongside clinician-scientists and researchers engaged in patient-oriented mitochondrial research and translational projects
  • A curriculum designed to balance theoretical understanding with practical techniques and computational analysis, preparing students for diverse career pathways
  • Access to professional development resources, internships and networking within a city that hosts regional biotechnology and healthcare employers

Prospective students are encouraged to contact faculty in the relevant genetics and molecular biology groups to discuss research fit and potential supervisors before applying.

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Programme details are indicative and may change — always verify current information with the official university website before applying.