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sequencing (scRNA-seq) and proteomics datasets. • Design and execute experiments investigating retinal degeneration mechanisms using cell culture and animal models. • Perform molecular and cell biology
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work progress, questions, timelines, and feedback Excellent analytical and organizational skills and ability to manage multiple tasks, especially complex projects with multiple due dates Demonstrated
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plasmid purification, sequencing, transfection by electroporation, transduction of viral supernatants into cell lines, and using standard software (such as Image J, BioRad, SnapGene, etc) to facilitate
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supports the goals and purposes of Stanford Medicine, including a significant focus on securing resources to realize the aspirations of the medical enterprise in alignment with the Stanford University-wide
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, single cell and multi-omics data analysis, and a high-performance computing environment (Unix/Linux) is highly preferred. An individual with Next generation sequencing experience is preferred. A good
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new knowledge across areas of research that are crucial for advancing the long-term prosperity of the planet and people; Institutes bridge scholarship at Stanford and beyond, bringing multiple
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-based assays), including defining controls, acceptance criteria, and documentation/SOPs. Experience supporting long-read sequencing workflows for repeat expansion disorders, including preparation and QC
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isolation, library preparation, and analysis and interpretation of genomic data. A deep understanding of bulk and single-cell sequencing assays is highly desirable. Familiarity with brain development, brain
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leaders, HR Business Partners and Operations, and facilitators, both internal and external to identify skill gaps, develop talent end-to-end programming, and implement impactful learning solutions aligned
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, DNA sequencing, RNA analysis and qRT-PCR. Experience in additional molecular biology techniques is a plus * Preferred to have some experience or literacy with bioinformatics analysis EDUCATION