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connections to clinicians, patients, and European initiatives such as ERDERA. What sets us apart is our unique position at the interface of bioinformatics, clinical genetics, and patient care. This ensures
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will be doing In adult mammals, including humans, fibrosis is the predominant response to many forms of tissue injury, unlike many lower vertebrates and invertebrates, where complete tissue repair is the
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-ON-BRAIN) that connects different countries with the overarching aim to develop cutting-edge human in vitro and in silico biomedical tools to better understand the biology of brain disease/disorders. You
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candidate genes that regulate somatic embryogenesis who’s function will be further confirmed by functional analyses. Your research involves: Using different types of microscopy to describe the development
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) that connects different countries with the overarching aim to develop cutting-edge human in vitro and in silico biomedical tools to better understand the biology of brain disease/disorders. You will employ
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. Your research involves: Using different types of microscopy to describe the development progression of somatic embryogenesis in different ecotypes; Mapping QTL, eQTL (RNA-seq) and pQTL (mass-spectrometry
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-derived neurons that generalize over different patients. To test candidate intervention strategies that normalize these phenotypes. In addition to these core activities, you will perform bioinformatic
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optimizations tailored to different environments. The optimizations range from algebraic optimizations (e.g., term rewriting) to algorithmic optimizations (e.g., group level algorithms), and to hardware
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work will focus on identifying the mathematical knowledge and properties to guide hardware optimizations tailored to different environments. The optimizations range from algebraic optimizations (e.g
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. Your work will focus on identifying the mathematical knowledge and properties to guide hardware optimizations tailored to different environments. The optimizations range from algebraic optimizations (e.g