{"title":"Identification of Mutations in Zebrafish Using Next-Generation Sequencing","authors":"Katrin Henke, Margot E. Bowen, Matthew P. Harris","doi":"10.1002/0471142727.mb0713s104","DOIUrl":null,"url":null,"abstract":"<p>Whole-genome sequencing (WGS) has been used in many invertebrate model organisms as an efficient tool for mapping and identification of mutations affecting particular morphological or physiological processes. However, the application of WGS in highly polymorphic, larger genomes of vertebrates has required new experimental and analytical approaches. As a consequence, a wealth of different analytical tools has been developed. As the generation and analysis of data stemming from WGS can be unwieldy and daunting to researchers not accustomed to many common bioinformatic analyses and Unix-based computational tools, we focus on how to manage and analyze next-generation sequencing datasets without an extensive computational infrastructure and in-depth bioinformatic knowledge. Here we describe methods for the analysis of WGS for use in mapping and identification of mutations in the zebrafish. We stress key elements of the experimental design and the analytical approach that allow the use of this method across different sequencing platforms and in different model organisms with annotated genomes. <i>Curr. Protoc. Mol. Biol</i>. 104:7.13.1-7.13.33. © 2013 by John Wiley & Sons, Inc.</p>","PeriodicalId":10734,"journal":{"name":"Current Protocols in Molecular Biology","volume":"104 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2018-02-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1002/0471142727.mb0713s104","citationCount":"7","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Current Protocols in Molecular Biology","FirstCategoryId":"1085","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/0471142727.mb0713s104","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"Biochemistry, Genetics and Molecular Biology","Score":null,"Total":0}
引用次数: 7
Abstract
Whole-genome sequencing (WGS) has been used in many invertebrate model organisms as an efficient tool for mapping and identification of mutations affecting particular morphological or physiological processes. However, the application of WGS in highly polymorphic, larger genomes of vertebrates has required new experimental and analytical approaches. As a consequence, a wealth of different analytical tools has been developed. As the generation and analysis of data stemming from WGS can be unwieldy and daunting to researchers not accustomed to many common bioinformatic analyses and Unix-based computational tools, we focus on how to manage and analyze next-generation sequencing datasets without an extensive computational infrastructure and in-depth bioinformatic knowledge. Here we describe methods for the analysis of WGS for use in mapping and identification of mutations in the zebrafish. We stress key elements of the experimental design and the analytical approach that allow the use of this method across different sequencing platforms and in different model organisms with annotated genomes. Curr. Protoc. Mol. Biol. 104:7.13.1-7.13.33. © 2013 by John Wiley & Sons, Inc.
利用新一代测序技术鉴定斑马鱼的突变
全基因组测序(WGS)已被用于许多无脊椎模式生物中,作为一种有效的工具,用于绘制和鉴定影响特定形态或生理过程的突变。然而,将WGS应用于高度多态性、较大基因组的脊椎动物需要新的实验和分析方法。因此,大量不同的分析工具被开发出来。由于WGS数据的生成和分析对于不习惯许多常见生物信息学分析和基于unix的计算工具的研究人员来说可能是笨拙和令人生畏的,我们专注于如何在没有广泛的计算基础设施和深入的生物信息学知识的情况下管理和分析下一代测序数据集。在这里,我们描述了用于绘制和鉴定斑马鱼突变的WGS分析方法。我们强调实验设计和分析方法的关键要素,允许在不同的测序平台和不同的模式生物中使用这种方法。咕咕叫。Protoc。摩尔。生物。104:7.13.1-7.13.33。©2013 by John Wiley &儿子,Inc。
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