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imaging-driven quantitative Mass Spectrometry-based omics methods, both at bulk population and single-cell levels, for this project. You will work closely with experts in cellular signalling, proteomics
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state-of-the art methods. Extensive experience in Heterogeneous Catalysis research area as evidenced through peer-reviewed journal publications. Applicants are encouraged to add their three best
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generation of scientists with the skills and knowledge from multiple disciplines to become leaders in childhood hematological malignancy research. The program provides an enriched training experience
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Postdoctoral Research Associate - Training in Pediatric Cancer Survivorship Outcomes and Interventio
devoted solely to children. Successful applicants will have excellent communications skills and a PhD, MD, DO, or PharmD in a relevant field. Multiple positions are available, funded through a new T32
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Postdoctoral Research Associate- Training in the Design & Development of Infectious Disease Therapeu
. Multiple positions are available, funded through a new T32 training grant from the National Institute for Allergies and Infectious Diseases or our institutional budget. Applicants to positions funded by
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, single-cell transcriptomics, proteomics, metabolomics, and network reconstruction. Former trainees of the Chi lab have been principal investigators in multiple academic institutions. Please also see the
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supported by the lab's infrastructure, which includes a wet-lab component. Postdocs have considerable flexibility and freedom to develop their research programs. St. Jude provides a highly interactive and
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funding, and deliver on multiple projects carried out in one of the most dynamic groups in food science at Aahrus University. You will have many opportunities to connect with other research partners, and
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experience in machine learning methods, tools, and platforms. Proficiency in Python, with demonstrated software development experience. Hands-on experience in MLOps, including the design and deployment
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pediatric cancers. In prior work, we have developed tools and methods to map the cellular diversity of pediatric tumors by adapting single-cell sequencing techniques to archival frozen tumors. In that work