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group focuses on developing and applying multi-omics technologies (transcriptomics, epigenomics, and proteomics), and combine them with powerful fly genetic tools to study development, aging and age
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of neurodevelopmental and neuropsychiatric conditions using cutting-edge proximity proteomics, protein engineering, CRISPR genome engineering, computational structural biology, and high-throughput electrophysiological
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cancer and their survival, development of improved technology to identity extracellular platelet phosphatase in the tumor microenvironment and large-scale analysis and validation of platelet phosphatase in
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the immune response to lung cancer and their survival, development of improved technology to identity extracellular platelet phosphatase in the tumor microenvironment and large-scale analysis and validation
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to interpreting variability in NMDA receptor antagonism as it relates to ketamine treatment outcome. The objective of the fellowship is for the trainee to develop a strong portfolio of scientific work that will
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processing and analyzing data from the next-generation sequencing and single-cell technologies (e.g., scRNA-seq, scATAC-seq, scTR-seq, and/or spatial transcriptomics). Previous experience in both
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or Ph.D. in Basic Science, Health Science, or a related field. No experience required. Preferred Qualifications It is preferred that candidates demonstrate scientific productivity with peer-reviewed
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and optimizes protocols for the lab and implements new technologies for specific research projects. This individual will train others in the lab on these new technologies. Mines, analyzes and interprets
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of rare disease funded by the National Human Genome Research Institute (NHGRI) and as a sequence technology core for the Texas Medical Center Genomic Center for Infectious Disease (GCID) established by
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of the fourth most populous city in America. It is within walking distance of numerous educational and biomedical research institutions (e.g. Rice University & MD Anderson Cancer Center) as well as parks