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, an understanding of computational data analysis is highly encouraged and supported. Research activities may include: Culture and maintenance of mammalian cancer cell lines and our established pre-clinical platform
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). Maintain rigorous experimental documentation, data management practices, and reproducible analysis pipelines. Present results at lab meetings, departmental seminars, and scientific conferences; contribute
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histological and multiomic analysis of MS brain tissue to elucidate cellular and molecular mechanisms underlying demyelination and neurodegeneration. The laboratory is embedded within a highly collaborative
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analysis, kinetic modeling, data analysis, and results dissemination. Qualifications: The ideal candidate will have some prior hands-on experience in preclinical PET/CT or PET/MR imaging, image processing
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projects. The research associate will develop expertise in retinal imaging, experimental design, data analysis, scientific writing, manuscript preparation, and presentation of research findings, supporting
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cultures and brain organoids. Molecular and cellular biology approaches, including gene-expression analysis and characterization of cellular phenotypes. Genetic and genomic approaches, including gene editing
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and PBWT-based algorithms (RaPID, RAFFI, FiMAP, ROH analysis, local ancestry inference), now extending into GBWT/RLBWT-based pangenome indexing, efficient pangenome graph construction and query, cross
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impactful scientific projects and manuscripts. The successful candidate will contribute to multi-center projects that integrate population science, molecular epidemiology, and large-scale cohort analysis
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, comparative genomics, machine learning, and evolutionary analysis to address fundamental questions in molecular biology and human disease. Responsibilities Develop computational pipelines for the discovery
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analysis of cerebrovascular genetics and multiomic studies. The laboratories jointly investigate the genetic basis of cerebrovascular disorders, including intracranial aneurysms, cavernous malformations, and