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on studying genetic variation and determining how different variants co-occur on the same paternal or maternal haplotype, a process known as haplotype phasing. We have previously developed methods for haplotype
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employing a combination of genetics, molecular biology, including Ribo-Seq, RNA pull-down and mass spectrometry, reporter assays in cells and tissues, and computational sequence analyses. This implies to work
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, the interplay between genetic variation and human phenotypes, and the development of AI-driven approaches to better understand human biology and disease and to translate these insights into data-driven strategies
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the genetic material, and how it interacts with various kinds of micro-organisms. Using this knowledge, we try to elucidate the causes of diseases, and find new ways to diagnose and treat them. The Institute is
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Uppsala University, Department of Ecology and Genetics PhD position in evolutionary genomics Would you like to conduct research on the evolution of sex chromosomes and sex ratio, supported by
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computational methods with a particular focus on deep learning and image analysis. The project relies on a close collaboration with researchers at the Department of Immunology, Genetics and Pathology (IGP
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, genetics or a related subject. Additional requirements are: Demonstrated, hands-on experience in molecular biology techniques, particularly nucleic acid work and sequencing library preparation Experience in