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使用牛津纳米孔测序对遗传变异进行引导式探究调查,作为本科分子生物学实验室课程的一部分。

A guided-inquiry investigation of genetic variants using Oxford nanopore sequencing for an undergraduate molecular biology laboratory course.

机构信息

Department of Biomedical and Health Sciences, University of Vermont, Burlington, Vermont, USA.

Cellular Molecular Biomedical Sciences Program, University of Vermont, Burlington, Vermont, USA.

出版信息

Biochem Mol Biol Educ. 2021 Jul;49(4):588-597. doi: 10.1002/bmb.21514. Epub 2021 May 3.

Abstract

Next Generation Sequencing (NGS) has become an important tool in the biological sciences and has a growing number of applications across medical fields. Currently, few undergraduate programs provide training in the design and implementation of NGS applications. Here, we describe an inquiry-based laboratory exercise for a college-level molecular biology laboratory course that uses real-time MinION deep sequencing and bioinformatics to investigate characteristic genetic variants found in cancer cell-lines. The overall goal for students was to identify non-small cell lung cancer (NSCLC) cell-lines based on their unique genomic profiles. The units described in this laboratory highlight core principles in multiplex PCR primer design, real-time deep sequencing, and bioinformatics analysis for genetic variants. We found that the MinION device is an appropriate, feasible tool that provides a comprehensive, hands-on NGS experience for undergraduates. Student evaluations demonstrated increased confidence in using molecular techniques and enhanced understanding of NGS concepts. Overall, this exercise provides a pedagogical tool for incorporating NGS approaches in the teaching laboratory as way of enhancing students' comprehension of genomic sequence analysis. Further, this NGS lab module can easily be added to a variety of lab-based courses to help undergraduate students learn current DNA sequencing methods with limited effort and cost.

摘要

下一代测序(NGS)已成为生物科学领域的重要工具,并在医学领域的应用不断增加。目前,很少有本科课程提供 NGS 应用程序的设计和实施方面的培训。在这里,我们描述了一个基于探究的实验室练习,该练习适用于大学水平的分子生物学实验室课程,使用实时 MinION 深度测序和生物信息学来研究癌症细胞系中发现的特征遗传变异。学生的总体目标是根据其独特的基因组图谱鉴定非小细胞肺癌(NSCLC)细胞系。本实验室中描述的单元强调了多重 PCR 引物设计、实时深度测序和遗传变异的生物信息学分析中的核心原则。我们发现 MinION 设备是一种合适且可行的工具,可为本科生提供全面的、实践导向的 NGS 体验。学生评估表明,他们对使用分子技术的信心增强了,对 NGS 概念的理解也得到了提高。总的来说,该实验为在教学实验室中引入 NGS 方法提供了一种教学工具,有助于学生增强对基因组序列分析的理解。此外,这个 NGS 实验室模块可以轻松地添加到各种基于实验室的课程中,以帮助本科生以有限的精力和成本学习当前的 DNA 测序方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bc90/8360074/f95b29af5465/BMB-49-588-g004.jpg

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