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Responsibilities: · Design and conduct independent research projects in placental biology or in utero gene editing. · Develop and optimize CRISPR-Cas9 base editing strategies, including plasmid and
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well as associated structural birth defects, such as spina bifida, or defects affecting the heart/blood/bone/kidney. We are further interested in how the axial mesoderm develops into the intervertebral discs, and
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lab employs an integrative research strategy that combines structural biology, biochemistry, and molecular biology to investigate complex biological systems central to disease progression. We focus
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extended to 2 years. The primary focus of this research will be focused on optimization of multimodal treatment of pancreatic cancer (clinical outcome research). In this role, you will be expected to work
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– Requisition #:37228 Job Summary: This position is responsible for conducting mechanistic studies into the impact of SMARCB1 structure/function on iPSC differentiation and defining how SMARCB1 loss and BMI1
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structured and unstructured biomedical data, including EHR data, wearable sensor time-series data, or clinical annotations. Demonstrated ability to build interactive or web-based systems using frameworks with
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transcription factors and chromatin structure Prior experience with analyses of “omics” data. Knowledge, Skills and Abilities: Documented training and experience in molecular/cell biology and/or animal models
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populations and synaptic inputs Large-scale extracellular electrophysiology (Neuropixels) Biophysical modeling and construction of ML-based models Statistical analysis of single-cell and population-level