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longitudinal clinical cohorts to perform repertoire analyses of memory B cells and antibodies from multiple compartments and time points. The overall goal is to determine whether mucosal immune responses
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description Somatic mutation accumulation and clonal evolution are central processes in cancer development. Through large-scale whole-genome sequencing and other high-throughput approaches, these processes can
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sequencing instruments into microscopes! Your mission You will join our team, a leading group in the field of DNA nanotechnology specialized in creating molecular tools for life-science research (http
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of next-generation sequencing (NGS) datasets, such as RNA-seq, ChIP-seq • Microscopy techniques, including confocal and fluorescence microscopy • RNA biology and gene expression Eligibility Doctoral
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environments, and you collaborate well with others. You are also very flexible and can complete diverse tasks within multiple projects. You have a positive attitude and are willing to assist (and be assisted by
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for this research. You will have access to a variety of techniques, such as patch-clamp electrophysiology, FIB-SEM volume imaging, tissue clearing (iDISCO), and/or single-cell sequencing. The postdoctoral researcher
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, Julia, R or C++. Have extensive experience with NGS data analysis. Have experience in sample preparation for and sequencing with NGS platforms. We value a versatile computational background; experience
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, along with strong potential to establish an independent, high-impact research program aligned with the focus areas of Molecular Biology and the MIMS organization. Applicants are expected to have completed
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pedagogical excellence, along with strong potential to establish an independent, high-impact research program aligned with the focus areas of one or several departments at Umeå University. Applicants
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on the development of innovative technologies in molecular diagnostics and determine the clinical benefits of blood analysis in cancer management. You will work with molecular methods including PCR, sequencing and