The Human Genetics Department is a deeply collaborative and interdisciplinary group dedicated to leveraging public and internal genetic data to elucidate causal biological mechanisms driving human disease for the purpose of drug discovery and development. By utilizing large-scale genetic analyses in ancestrally diverse populations and biobank-scale datasets (such as UK Biobank and All Of Us), the department drives target and biomarker discovery for prioritized diseases and therapies. Research ranges from computational methods development to targeted analyses of disease-relevant phenotypes. Integrating genetic, genomic, transcriptomic, and proteomic information with rich clinical data, we characterize the relationships between genetic variation, molecular phenotypes, and clinical outcomes. This internship position is located in South San Francisco, on-site. Methods for Understanding Immune-Associated Genetic Variation: Genetic association studies have resulted in important insights into disease risk and progression. Most have focused on simple genetic variants, such as single nucleotide polymorphisms. Much genetic variation is complex, in that it may have high levels of allelic diversity or may be variable in copy number. The project will focus on developing methods for better understanding such complex variation, focusing on immune-associated genetic variants and their associations to disease. The Major Histocompatibility Complex (MHC), which includes the Human Leukocyte Antigen (HLA) genes, and the Killer Immunoglobulin-like Receptor (KIR) genes will be the main interest.
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Job Type
Full-time
Career Level
Intern
Education Level
Ph.D. or professional degree