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Field
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professionals. Under the guidance of a CDC mentor, you may: Analyze respiratory virus sequence data and associated surveillance metadata; Gain experience preparing routine and ad hoc genomic surveillance reports
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and cell biology, chemical biology, immunology, functional genomics, CRIPSR screening, signal transduction, single-cell sequencing, spatial sequencing, metabolism, drug development, structural biology
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sequencing and study of genotoxic stress markers. This project is funded through a four-year US Ovarian Cancer Research Program grant. This is an on-site position located at Vancouver Hospital Campus. Key
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biology, genomics, epigenomics, microbiome science, proteomics, and clinical research. The position will focus on the development and evaluation of low-input whole genome sequencing and study of genotoxic
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at NTU are looking for a Research Fellow (RF) to carry out research in probabilistic machine learning and GenAI, by exploring cutting-edge approaches such as sequence model design, continual learning
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and human HFpEF using multi-omics approaches. Perform bioinformatics analyses of sequencing datasets, including data processing, quality control, integration, and biological interpretation. Integrate
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of diverse PRRSV strains causing extreme pathogenesis and disease. Transcriptomics datasets have been generated via bulk and single-cell RNA sequencing from blood and disease-affected tissues and will be
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laboratory work, bioinformatic processing of Next Generation Sequencing data, and population genomic analyses, including demographic inference. The purpose of the fellowship is research training leading
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Office of Women's Health Grant Program (OWH GP) | Jefferson, Arkansas | United States | about 4 hours ago
while developing skills in cell culture, next-generation sequencing, assay development, and bioinformatics. Enhance your communication skills by participating in the writing of reports and publishable
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related discipline. · Demonstrated expertise in next-generation sequencing technologies, including long-read, short-read, and single-cell sequencing data generation and analysis. · Extensive