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preferably bioinformatics. Experience in next-generation sequencing technologies and computational analysis, such as those related with spatial transcriptomics, epigenomics (e.g., ATAC- seq), and/or single
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lentiviral barcoding, will be employed to reconstruct lineage trees and uncover cell fate dynamics. The candidate will use existing bioinformatic pipelines to resolve embryonic lineages based on embryonic
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Ph.D. in a relevant field. Given the scope of the research, a range of different backgrounds could be appropriate, including bioanalytical chemistry, mass spectrometry, spatial biology, or bioinformatics
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written proficiency in English Experience with comparative genomic methods (e.g. genome alignments, CAFE analyses) Documented skills in bioinformatics (published articles, github repositories, etc
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affect offspring health by developmental programming. We use mouse model, human cohort samples and state-of-the-art techniques including single-cell sequencing, organoids-on-a-chip, and bioinformatics to
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Postdoctoral studies in the immunology of the peripheral neuro-immune microenvironment (scholarship)
analysis, bioinformatics, and vascular biology and access to core facilities, including cell sorting, and animal facilities. We have dedicated instruments for neurophysiology, optogenetics and nerve
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knowledge in bioinformatics (Phyton and/or R programming for statistical computing and graphics) is an asset. What do we offer? A creative and inspiring environment with wide-ranging expertise and interests
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Disease group at the University of Helsinki Your mission We aim to recruit a highly motivated postdoctoral researcher with a strong research background in clinical genetics and bioinformatics. The aim
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. Additional resources include platforms for tissue analysis, bioinformatics, and vascular biology and access to core facilities, including cell sorting, and animal facilities. We have dedicated instruments
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clinical genetics and bioinformatics. The aim of the project is to identify new genetic causes for skeletal disorders with osteoporosis and abnormal mineral homeostasis, and to characterize the molecular