Master of Science in Medical Genetics (MSc)
The UBC Department of Medical Genetics is an inspiring and productive community of scholars of genetics and genomics; an outstanding provider of knowledge, technical expertise, and compassionate care for our patients. The Department is composed of dozens of faculty members at the forefront of their fields who use cutting edge genetic, epigenetic, genomic, and bioinformatic methodologies to gain insight into diseases such as cancer, diabetes, obesity, neurodegenerative and neurological disorders, and other genetic diseases. Research is highly interactive and often involves local, national, and international collaborations which further enrich the research experience.
Individual labs conduct clinical and/or translational research and basic experimental research engaging a wide variety of approaches including the use of model organisms such as mice, flies (D. melanogaster), worms (C. elegans), and yeast (S. cerevisiae).
What makes the program unique?
The mission of the Department of Medical Genetics is to pursue basic and clinical research for diagnosis, prevention and treatment of genetic disease. Our goal is to be a world leader in the research, clinical practice and teaching of Genetic Medicine.
Research in the Department of Medical Genetics covers the study of human genetics with areas of focus in mammalian development, regulation of gene expression, genetic diseases due to single gene or complex inheritance, birth defects, reproduction, cancer, immunology, genomics, bioinformatics, ethics and population health.
Developmental Genetics & Birth Defects;
Epigenetics & Chromosome Transmission;
Genomics & Bioinformatics;
Genetic Epidemiology & Human Gene Mapping;
Neurogenetics & Immunogenetics;
Stem Cells & Gene Therapy;
Clinical Genetics, Genetic Counselling and Ethics & Policy.
TOEFL (ibT) Overall Score Requirement
IELTS Overall Score Requirement
Supervisor commitment required prior to application?
Prerequisites / Course Requirements
Recent, advanced-level courses in: genetics; biochemistry; and statistics (biometrics)
Relevant laboratory research experience; excellent references with assessment of applicant's research expertise and aptitude.
Stipend Amount and Duration: The recommended minimum yearly stipend for a full time Medical Genetics (MEDG) graduate student is $22,000. The student is expected to pay tuition from their stipend. This stipend may come from an independent studentship award and/or from the Research Supervisor's research grant. Admission to the Medical Genetics Graduate Program normally includes a commitment from the Supervisor to ensure that each student is supported to the recommended funding level. Exceptions to this policy may be granted under unusual circumstances. Financial support from personal resources is not acceptable as “funding” for incoming students in the Medical Genetics Graduate Program.
The duration of the annual stipend is normally two years for a MSc student and four years for a PhD student. After the two-year MSc and four-year PhD point, continued funding is at the discretion of the Supervisor. The Supervisor should inform their student in writing (with a copy to the Medical Genetics Graduate Program office) at least six months prior to the end-date of the student's stipend.
Funding depends both on satisfactory academic and research progress, as determined by the Student’s Advisory Committee, and on the Research Supervisor's continued grant support. Termination of funding for other justifiable reasons must be approved by a majority of the Medical Genetics Graduate Advisory Committee.
Tuition / Program Costs
|Fees||Canadian Citizen / Permanent Resident / Refugee / Diplomat||International|
|Installments per year||3||3|
|Tuition per installment||$1,632.61||$2,868.22|
|Tuition per year||$4,897.83||$8,604.66|
|Int. Tuition Award (ITA) per year (if eligible)||$3,200.00 (-)|
|Other Fees and Costs|
|Student Fees (yearly)||$923.38 (approx.)|
|Costs of living (yearly)||starting at $16,884.10 (check cost calculator)|
All fees for the year are subject to adjustment and UBC reserves the right to change any fees without notice at any time, including tuition and student fees. In case of a discrepancy between this webpage and the UBC Calendar, the UBC Calendar entry will be held to be correct.
Completion Rates & Times
This list shows faculty members with full supervisory privileges who are affiliated with this program. It is not a comprehensive list of all potential supervisors as faculty from other programs or faculty members without full supervisory privileges can request approvals to supervise graduate students in this program.
Aparicio, Samuel (Breast cancer, genome sequencing )
Arbour, Laura (northern and aboriginal health issues as they pertain to genetics)
Austin, Jehannine (Genetics, genomics, genetic counseling, psychiatric illness, mental illness, mental health, psychiatry, schizophrenia, bipolar disorder, depression, postpartum depression, perinatal mental health, Mood & Anxiety Disorders, Schizophrenia)
Birol, Inanc (bioinformatics, computational biology, genomics, transcriptome analysis, next generation sequencing, cancer, Bioinformatics, sequence assembly, transcriptomics, gene regulation networks, high throughput informatics for big data)
Brinkman, Ryan (Bioinformatics, flow cytometry, high throughput data analysis, data standars, GvHD biomarker identification, cluster identification)
Brooks-Wilson, Angela (human genetics, cancer genetics, cancer families, longevity, Super seniors, genetic susceptibility)
Brown, Carolyn Janet (Epigenetic control of gene expression, X-chromosome inactivation, Long non-coding RNAs, XIST RNA, Genes escaping X-chromosome inactivation, DNA methylation)
Burgess, Michael (Philosophy and social sciences, ethics and social policy in the areas of genomics, genetics and biotechnology (health, agriculture and environment))
Carleton, Bruce (Pharmacogenomics, Adverse drug reactions (ADRs), Drug safety and effectiveness, Clinical pharmacology, Pharmacovigilance)
Clarke, Lorne (Lysosomal storage disease, disorders or sulfate transport, mucopolysaccharidosis, phenylketonuria)
Conibear, Elizabeth (Molecular pathways, cellular transportation, Alzheimer's, lysomsomal storage diseases, yeast genetics)
Eaves, Constance Jean (Normal and leukemic stem cells, normal and malignant breast stem cells)
Farrer, Matthew (Parkinson's disease, Dementia, Epilepsy)
Friedman, Jan Marshall (Application of whole genome sequencing to diagnose genetic disease, Clinical genomics, Neurofibromatosis, Birth defects epidemiology)
Gibson, William (Childhood Diseases; Weaver syndrome - mutation detection and new therapies; Cohen-Gibson syndrome - mutation detection and new therapies; Appetite regulation; Energy expenditure; Body composition; Monogenic human obesity disorders; Familial Brain Aneurysms)
Goldowitz, Daniel (Genetic basis of brain disease, neurobiology of autism, Huntingtong's gene, mouse/mice epigenetics, gene regulatory network)
Hayden, Michael (Huntington disease, Disease progression, Diabetes)
Hieter, Philip (Molecular biology of eukaryotic chromosome transmission )
Holt, Robert (Immunogenetics, Metagenomics - Infectious agents in Cancer, Cancer Genomes, Neurobiology, DNA Sequencing)
Hoodless, Pamela (Embryology, Transcriptional regulation, Epigenetics, Heart valve formation, Liver development)
Humphries, Richard Keith (Genetic control and manipulation of hemopoiesis. Stem Cell Regulation. Retroviral Gene Transfer. Transgenic Mice.)
Huntsman, David (hereditary cancer, molecular pathology, cancer biomarkers, Pancreas centre)
Jefferies, Wilfred Arthur (Iron transport molecules)
Jiang, Xiaoyan (Basic and translational leukemia research, Leukemic stem cell biology , Gene regulation , Drug resistance , Proteomics)
Jones, Steven J (Bioinformatics, genome science, mutations, cancer progression)