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Next-generation teaching: a template for bringing genomic and bioinformatic tools into the classroom

机译:下一代教学:将基因组和生物信息工具带入教室的模板

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摘要

The recent increase in accessibility and scale of genetic data available through next-generation sequencing (NGS) technology has transformed biological inquiry. As a direct result, the application and analysis of NGS data has quickly become an important skill for future scientists. However, the steep learning curve for applying NGS technology to biological questions, including the complexity of sample preparation for sequencing and the analysis of large data sets, are deterrents to the integration of NGS into undergraduate education. Here, we present a course-based undergraduate research experience (CURE) designed to aid in overcoming these limitations through NGS investigations of prokaryotic diversity. Specifically, we use 16S rRNA sequencing to explore patterns of diversity stemming from student-directed hypothesis development. This CURE addresses three learning objectives: (1) it provides a forum for experimental design hypothesis generation, (2) it introduces modern genomic tools through a hands-on experience generating an NGS data-set, and (3) it provides students with an introductory experience in bioinformatics.
机译:通过下一代测序(NGS)技术可获得的遗传数据的近期可访问性和规模的增加转化了生物调查。作为直接结果,NGS数据的应用和分析很快成为未来科学家的重要技能。然而,用于将NGS技术应用于生物学问题的陡峭学习曲线,包括测序的样品制备的复杂性和大数据集的分析,是NG将NG集成到本科教育中的威慑。在这里,我们提出了一种基于课程的本科研究经验(治疗),以帮助通过NGS调查克服这些限制的原核多样性。具体而言,我们使用16S RRNA测序来探索学生指导的假设发育的多样性模式。这种治疗解决了三个学习目标:(1)它为实验设计假设发电提供了一个论坛,(2)它通过动手经验引入了现代基因组工具,生成了NGS数据集,(3)它为学生提供了一个生物信息学的介绍经验。

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