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Field
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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
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molecular biology expertise in mammalian cell culture, and genome editing techniques strong analytical and problem-solving skills preferably skills in next generation sequencing-based methods and
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extraction, qPCR, cloning etc.), biochemistry (eg, metabolomics using LC-MS, extraction and purification of plant metabolites), bioinformatics (amplicon sequencing/metagenomics). Strong interest in tree
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validation, and regulatory reporter assays. Learn more about the group here . YOUR MISSION: Investigate how genetic variants affect male reproductive function Perform single-nucleus and bulk RNA sequencing