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the identification and translation of biosynthetic gene clusters into chemicals useful in human health or other applications from marine organisms. Expertise in genome assembly from metagenomic data is
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. Summarizes data analyses results in the form suitable as the basis for the first draft of written reports, and makes preliminary interpretations of the data. Assists with assembly, annotation, meta-genomic
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The Ismagilov Lab at the California Institute of Technology is looking for a Research Scientist, Bioinformatics to join a fast-paced ~20-person interdisciplinary laboratory team. The research agenda
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bioinformatics, systems biology, imaging, and multi-omics technologies in the priority areas of Health and Life Sciences and Science for Sustainability.The research group in UNIBO has been active for almost 20
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, we are making major contributions in the application of genomics to understand the fundamentals of biology and to improve human health and wellbeing. Genome Sciences boasts a collaborative, integrated
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Experience with microbial bioinformatics. Computational experience analyzing samples to identify microbial (bacteria, fungi, and virus) taxonomy, metagenomic assembled genomes (MAGs), and functional gene
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of London (QMUL), and EMBL-European Bioinformatics Institute (EBI). Our collaborative human functional genomics cluster aims to advance our understanding of the genetic basis of rare diseases and end
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of London (QMUL), and EMBL-European Bioinformatics Institute (EBI). Our collaborative human functional genomics cluster aims to advance our understanding of the genetic basis of rare diseases and end
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Bioinformatician, Sr. Analyst – Duchossois Family Institute, The University of Chicago, 3 months agoDepartment BSD DFI - Bioinformatics About the Department The Duchossois Family Institute (DFI) focuses on the role of commensal bacteria in enhancing disease resistance and is using genomic and
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of London (QMUL), and EMBL-European Bioinformatics Institute (EBI). Our collaborative human functional genomics cluster aims to advance our understanding of the genetic basis of rare diseases and end