29 multiple-sequence-alignment Postdoctoral positions at The Ohio State University in United States
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include analyzing whole-genome sequencing data, conducting genome assembly and gene annotation, performing variant calling and population genetic analyses, presenting research findings at national and
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education to contribute to research broadly aligned with the aims of the DoD Child Development Virtual Laboratory School project at The Ohio State University around supporting the development and well-being
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include DNA sequence data curation, processing, and analysis using high performance computing; excellent verbal and written communication skills; and a collaborative mentality towards research and mentoring
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passion for scientific discovery and bold initiatives that seek to break barriers and maximize clinical impact. Applicants should have experience with MRI pulse sequence and/or reconstruction method
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will have a passion for scientific discovery and bold initiatives that seek to break barriers and maximize clinical impact. Applicants should have experience with MRI pulse sequence and/or reconstruction
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Cancer-Free World Begins Here. The OSUCCC – James is the only cancer program in the United States that features a National Cancer Institute (NCI)-designated comprehensive cancer center aligned with a
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experiments in protein engineering, molecular biology, biochemistry, and next-generation sequencing (NGS). The ideal candidate will have experience with computational tools for protein modeling and design—such
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cytometry, scRNA-sequencing, bioinformatics, and confocal microscopy; develops, adopts and implements new laboratory methods; performs routine procedures on lab animals including surgical procedures and/or
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and executes advanced microbiology and immunology techniques, including flow cytometry, scRNA-sequencing, bioinformatics, and confocal microscopy; develops, adopts and implements new laboratory methods
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QUALIFICATIONS AND EDUCATION (List all desired skills/qualifications) Knowledge of evolutionary theory and use of genomic data to infer epidemic patterns Experience using next-generation sequencing to study within