The Collins Genomics Lab (https://labs.dana-farber.org/collins-genomics) at Dana-Farber Cancer Institute seeks a POSTDOCTORAL COMPUTATIONAL BIOLOGIST FELLOW to lead cutting-edge studies of genetic risk for cancer using large-scale multimodal sequencing datasets across tens of thousands of individuals. The main objective of these studies is to define how inherited variation influences gene regulation, tumor evolution, and clinical cancer phenotypes towards the ultimate goal of earlier cancer detection and improved prevention strategies. The ideal candidate will have expertise in cancer genomics and/or functional genomics, paired with strong computational and statistical training, and will be excited to lead independent projects at the interface of germline genetics and tumor biology. The Collins Genomics Lab offers a highly collaborative environment for this work by facilitating close collaborations with other investigators at Dana-Farber, the Broad Institute, and other institutions on cancer risk, tumorigenesis, early detection, prevention, and patient outcomes. Located in Boston and the surrounding communities, Dana-Farber Cancer Institute is a leader in life changing breakthroughs in cancer research and patient care. We are united in our mission of conquering cancer, HIV/AIDS, and related diseases. We strive to create an inclusive, diverse, and equitable environment where we provide compassionate and comprehensive care to patients of all backgrounds, and design programs to promote public health particularly among high-risk and underserved populations. We conduct groundbreaking research that advances treatment, we educate tomorrow's physician/researchers, and we work with amazing partners, including other Harvard Medical School-affiliated hospitals. The successful candidate will integrate large-scale germline genome sequencing with functional genomic assays (e.g., RNA-seq, chromatin profiling, single-cell multiomics) from cancer patients and controls to identify genetic mechanisms of cancer predisposition and progression. We are particularly interested in statistically rigorous approaches that connect inherited variation to gene expression, cell state-specific regulatory programs, and clinical outcomes. Related projects will include: Develop and apply statistical or machine learning approaches to model the effects of common and rare germline variants (including structural variants) on gene expression and cancer phenotypes in large, clinically annotated cohorts Integrate germline and somatic genomics with bulk and single-cell functional genomic datasets to define how inherited variation shapes cell state-specific gene regulation, somatic driver selection, and tumor evolution Perform population-scale genetic association and outcome analyses to identify coding and regulatory risk factors for early-onset, aggressive, and/or hereditary cancers The successful candidate will lead projects from conceptualization through publication, including analytical design, implementation, manuscript preparation, and presentation of findings. They will contribute to shared computational infrastructure, maintain well-documented and reproducible code, and collaborate closely with clinical and laboratory investigators. This role offers flexibility to pursue both methodological innovation and biologically driven discovery.
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Job Type
Full-time
Career Level
Mid Level
Education Level
Ph.D. or professional degree