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characterize novel photoreceptors in marine Synechococcus using CRISPR and protein biochemistry approaches. This project is funded by the NSF Systems and Synthetic Biology Program and builds on our successful
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Appointment Term: 1 year Appointment Start Date: June 1st, 2026 Group or Departmental Website: https://cepikalab.figma.site/ (link is external) How to Submit Application Materials: To apply, please submit
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-specific promoters and the human TET1 DNA demethylase, as well as CRISPR-based vectors that target ROS1/TET1 activity to specific genomic regions. TRAINING AND SKILLS This project offers comprehensive
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assays is highly desirable. Expertise in CRISPR-Cas9 genome editing (knockout and correction) and in NGS workflows—such as ChIP-seq, RNA-seq, miRNA-seq, single-cell RNA-seq preparation, and CUT&RUN—is
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photoreceptors in marine Synechococcus using CRISPR and protein biochemistry approaches. This project is funded by the NSF Systems and Synthetic Biology Program and builds on our successful initial studies of Type
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situ hybridization. Help with lab jobs, as needed. Make CRISPR mutants. Maintain lab notebook. Other duties and responsibilities as assigned Qualifications Bachelor of Science and 0 to 1 year of
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machinery and permit functional characterisation. Cell cycle inhibitors may be employed to investigate cell cycle checkpoints, and molecular approaches (e.g. fluorescent tagging, RNAi, CRISPR/Cas9 etc) will
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using CRISPR-based in vivo perturbational approaches developed within the lab. You will be embedded both within an experimental and computational team, providing a unique atmosphere where there is
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this, we integrate mouse genetics & in vivo imaging, CRISPR gene editing, single-cell and spatial transcriptomics, high-content imaging & bioinformatics, electrophysiology & disease modeling Our lab culture
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biochemistry, bioinformatics, single cell genomics, epigenetics, pharmacology and pathology. The Nelson laboratory website provides additional information: https://research.fhcrc.org/peternelson/en.html