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., molecular cloning); cell biology approaches (e.g., immunofluorescence, RNA/DNA fluorescence in situ hybridization); routine chromatin techniques and sequencing-based technologies (e.g., RNA-seq, ATAC-seq, CUT
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long-read sequencing data (PacBio HiFi, Oxford Nanopore) Working with large-scale genomic, epigenomic (DNA methylation, chromatin accessibility), and transcriptomic datasets Contributing to genome
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members to examine how stress-inducible epigenetic changes at biosynthetic genes alter root exudation chemistry. By linking stress-induced changes in DNA methylation and chromatin accessibility to shifts in
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characterization of genetically modified mice using spatial transcriptomics and gene targeting *Bioinformatic analysis of whole genome DNA methylation and expression data *Conduct chromatin profiling and analysis
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option for extension Appointment Start Date: start date flexible / rolling Group or Departmental Website: http://cfna.stanford.edu (link is external) How to Submit Application Materials: Email: weigu