47 multiple-sequence-alignment Postdoctoral positions at Stanford University in United States
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stakeholders, ensuring the research remains impactful and aligned with real-world needs. Finally, the postdoc will participate in disseminating research findings through presentations, talks, and publications
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cell fate decisions, particularly during early neural development or during the epithelial-to-mesenchymal transition (EMT) in cancer. Our recent work reveals that coding sequences (CDS) and their cognate
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our team. We are looking for postdoc candidates to develop and apply cutting-edge technologies in spatial transcriptomics, single-cell sequencing, machine learning, and functional genomics
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scholars appointed through the Office of Postdoctoral Affairs. The FY25 minimum is $73,800. We are seeking a highly motivated postdoctoral researcher with expertise in genomic sequencing and viral vector
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sequence: Curriculum Vitae: including list of publications, presentations and other research products, teaching experience, and service (related to research, education or outreach) inside and outside your
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), among others. Required Qualifications: Have acquired formal training in genomics and sequencing. Have acquired formal training in developmental biology and molecular biology. Have acquired in quantitative
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, molecular biology, and in vivo models. Analyze and interpret data, integrating experimental and computational findings. Utilize bioinformatics tools and techniques to analyze high-throughput sequencing data
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, aligning academic research to practical challenges in education. Our mission is to inspire a virtuous cycle between research and practice, supporting equity in education through the open dissemination
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core facility; (4) testing compounds of interest in iPSC-derived neurons and (5) collaborating with multiple labs to coordinate further in vitro and in vivo testing of select compounds in preclinical
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the use of R and/or Python Basic understanding of statistical modeling, and machine learning Understanding of high-throughput sequencing techniques including whole genome, whole exome, targeted capture, RNA