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cytogenetic and molecular techniques, including chromosome analysis, fluorescence in situ hybridization (FISH), chromosomal microarray (CMA), and exome sequencing for diagnosis or treatment in cancer and
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molecular biology and biochemical techniques such as cloning, in vitro transcription, nucleic acid purification, PCR, next generation sequencing library preparation and immunoblotting. Help prepare data
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-aligned services. • Develop research projects that address key challenges in carbohydrate chemistry, including structure-function relationships, molecular weight analysis, and substitution patterns and
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Institute, Stanford University), our lab has access to one of the largest iPSC biobanks in the United States, which give us access to multiple cell lineages carrying mutation in multiple genes key
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energetic costs in experimentally evolved populations. The ideal candidate should have prior experience and/or a strong interest in conducting genome and transcriptome sequencing and analysis, ribosome
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, all with the goal of improving human health. Aligned with Rutgers University–New Brunswick and collaborating university wide, RBHS includes eight schools, a behavioral health network, and five centers
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syndromes. Dr. Stamberger is part of the Weckhuysen team which performs leading edge research in gene discovery in epilepsy syndromes using different omics approaches such as short and long-read sequencing
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depending on the project and assigned research/scholarly functions, or other creative aspects. Preferred Qualifications Salary Commensurate with experience. Number of Vacancies Multiple Desired Start Date 09
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(high-throughput TCR sequencing, nanostring analysis, single cell RNAseq, multispectral labeling and imaging of tissue, spatial profiling, and laser capture microscopy). We work with both human specimens
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responsible for establishing standard omics techniques for the lab, such as qRT-PCR, RNA and DNA sequencing, and various quality control validation assays to ensure the high integrity of samples and rigorous