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, or equivalent) is a strong advantage Experience with high-throughput molecular assays, particularly next-generation sequencing (NGS) data generation and/or analysis, is an advantage Experience with image
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German Cancer Research Center in the Helmholtz Association (DKFZ) | Heidelberg, Baden W rttemberg | Germany | 3 months ago
environment is highly collaborative and interdisciplinary, spanning genome biology, computational analysis, and translational cancer research. Members of the lab gain expertise in next-generation sequencing
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, pandas, scikit-learn, TensorFlow/PyTorch, or equivalent) is a strong advantage Experience with high-throughput molecular assays, particularly next-generation sequencing (NGS) data generation and/or
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single-nucleus RNA sequencing (scRNA-seq/snRNA-seq) is an advantage. Knowledge of data analysis methods, including statistical software and transcriptomic analysis pipelines is an advantage. Excellent
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experience in molecular biology after completion of their degree will also be considered. Experience in one or more of the following will be seen as assets: single cell RNA sequencing, anaerobic cultivation
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observations of successive phenological stages, collection of plant material, whole-genome DNA sequencing, genotyping using DArT-seq and RAD-seq, and molecular and bioinformatic analyses, including differential
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modifications, DNA methylation and gene regulation. Hands-on experience with molecular biology techniques, such as DNA/RNA extraction, qPCR, RT-qPCR and next-generation sequencing (NGS)-based approaches
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evolution Experience with next-generation sequencing data analysis Familiarity with bioinformatics pipelines Background in evolutionary theory and/or ecology Experience with data handling and statistical
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single-nucleus RNA sequencing (scRNA-seq/snRNA-seq) is an advantage. Knowledge of data analysis methods, including statistical software and transcriptomic analysis pipelines is an advantage. Excellent
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whether epialleles drive heritable trait variation across generations by establishing causal links between DNA methylation, gene expression, and inherited traits. It pioneers transient epigenome editing in