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                Leibniz-Institute for Plant Genetics and Crop Plant Research | Neu Seeland, Brandenburg | Germany | 2 months ago
architecture of important crop traits like grain yield heterosis. In the era of large population size and dense genomic data such as whole-genome sequencing, new algorithms are needed to remove the bottleneck
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gene expression studies in real-time PCR RNA sequencing and transcriptome analysis with corresponding bioinformatic evaluations You will document your work, analyze and interpret the measured values
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technique. If successful, this could pave the way to nano-optical read and write heads for future data storage as well as to direct sequencing of nucleic acid and protein sequences by scanning-probe Raman
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expertise and supervision of experienced researchers from multiple institutes at Forschungszentrum Jülich. As one of Europe’s largest and most multidisciplinary research centers, Forschungszentrum Jülich
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taxonomically identify the strains carry out whole genome sequencing for selected strains analyse sequence data concerning safety and dye production characteristics confirm involvement of genes in biogenic dye
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Description A PhD position is immediately available to study microbiota - B cell crosstalk. The Rollenske lab uses single B cell receptor sequencing and repertoire analysis, monoclonal antibody
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Collaborative Doctoral Project (PhD Position) - AI-guided design of scaffold-free DNA nanostructures
-based digital twin, which can predict the assortment and sequence of two-dimensional all-DNA motifs required for the engineering desired tessellation patterns at the nanometer scale. We will use available
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the era of large population size and dense genomic data such as whole-genome sequencing, new algorithms are needed to remove the bottleneck of computational load for such a development. In the frame of a
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single cell sequencing, chromatin and pan-omics analyses are available for innovative transdisciplinary cancer research. Your academic qualifications: Completed scientific university studies in natural
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at diagnosis and relapse, and compare them to healthy hematopoietic specimens using nanopore-based direct tRNA sequencing. Complementary transcriptomic, proteomic, and metabolomic profiling will be performed