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of neurodegeneration, totaling to over 1,500 human brain samples. Using an array of -omics techniques, e.g. long read DNA sequencing, single nuclei transcriptomics and multi-modal proteomics, the team aims to identify
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: Gene silencing and cell targeting properties of DNA nanostructures Systematically evaluate the cellular uptake and gene silencing of DNA (in vitro and in vivo) Conference presentation Mentoring
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less than 5 years since PhD completion are strongly encouraged to apply. Mandatory keywords for selection: DNA cloning using viral vectors; mammalian cell transduction. Highly valued keywords: synthetic
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cancer and developing innovative biomarkers for early detection and patient stratification. ⸻ Required Qualifications • PhD in a relevant field (e.g., Molecular Biology, Genetics, Bioinformatics
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Max Planck Institute of Molecular Cell Biology and Genetics, Dresden | Dresden, Sachsen | Germany | 5 days ago
Stability. The research group of Nagaraja Chappidi investigates how macromolecular assemblies and compartment-like structures contribute to accurate DNA replication and DNA repair. The research combines
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at Harvard Medical School (Boston – USA) and Institut Gustave Roussy (Paris – France). Profile: The candidate should have a PhD in molecular biology or related field and must be familiar with the field of DNA
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recognise yourself in the following: A PhD completed by the time of the appointment in (palaeo)genomics, archaeology, ecology, or related field, including demonstrable experience with DNA analysis
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enthusiastic motivated recently graduated PhD with a strong expertise in DNA nanotechnology, Biophysics, Biochemistry, or Structural Biology, and a strong interest in applying this knowledge to biology
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be focused primarily on the development and application of novel computational algorithms to analyze and integrate diverse omics datasets, including bulk and single-cell RNA-seq, ADT-seq, ATAC-seq, DNA
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the lab of Professor Sten Eirik W. Jacobsen . The research project(s) will be focused on genetic fate mapping of normal mouse and human hematopoietic stem cells (HSCs), using DNA mutations for HSC clonal