细菌基因表达的RNA-Seq

Q4 Chemistry
Line Dahl Poulsen, Jeppe Vinther
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引用次数: 10

摘要

RNA测序(RNA-seq)已成为细菌基因表达全局定量的首选方法。随着测序技术和数据分析工具的不断进步,测序文库的制备是RNA-seq实验中劳动强度最大、成本最高的环节,也是保证测序数据质量的关键环节。在这里,我们提出了一种简单而廉价的基本方案,用于从细菌RNA中制备链特异性RNA-seq文库,以及用于测序读取数据分析的计算管道。该方案是基于Illumina平台,允许简单的样品多路复用和去除PCR重复的测序读数。©2018 by John Wiley &儿子,Inc。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
RNA-Seq for Bacterial Gene Expression

RNA sequencing (RNA-seq) has become the preferred method for global quantification of bacterial gene expression. With the continued improvements in sequencing technology and data analysis tools, the most labor-intensive and expensive part of an RNA-seq experiment is the preparation of sequencing libraries, which is also essential for the quality of the data obtained. Here, we present a straightforward and inexpensive basic protocol for preparation of strand-specific RNA-seq libraries from bacterial RNA as well as a computational pipeline for the data analysis of sequencing reads. The protocol is based on the Illumina platform and allows easy multiplexing of samples and the removal of sequencing reads that are PCR duplicates. © 2018 by John Wiley & Sons, Inc.

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来源期刊
Current Protocols in Nucleic Acid Chemistry
Current Protocols in Nucleic Acid Chemistry Chemistry-Organic Chemistry
自引率
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期刊介绍: Published in association with International Society for Nucleosides, Nucleotides & Nucleic Acids (IS3NA) , Current Protocols in Nucleic Acid Chemistry is equally valuable for biotech, pharmaceutical, and academic labs. It is the resource for designing and running successful research projects in the rapidly growing and changing field of nucleic acid, nucleotide, and nucleoside research.
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