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从脸颊拭子到共识序列:高通量 DNA 测序完整人类线粒体基因组的 A 到 Z 方案。

From cheek swabs to consensus sequences: an A to Z protocol for high-throughput DNA sequencing of complete human mitochondrial genomes.

机构信息

Department of Anatomy, University of Otago, Dunedin, New Zealand.

出版信息

BMC Genomics. 2014 Jan 25;15:68. doi: 10.1186/1471-2164-15-68.

Abstract

BACKGROUND

Next-generation DNA sequencing (NGS) technologies have made huge impacts in many fields of biological research, but especially in evolutionary biology. One area where NGS has shown potential is for high-throughput sequencing of complete mtDNA genomes (of humans and other animals). Despite the increasing use of NGS technologies and a better appreciation of their importance in answering biological questions, there remain significant obstacles to the successful implementation of NGS-based projects, especially for new users.

RESULTS

Here we present an 'A to Z' protocol for obtaining complete human mitochondrial (mtDNA) genomes - from DNA extraction to consensus sequence. Although designed for use on humans, this protocol could also be used to sequence small, organellar genomes from other species, and also nuclear loci. This protocol includes DNA extraction, PCR amplification, fragmentation of PCR products, barcoding of fragments, sequencing using the 454 GS FLX platform, and a complete bioinformatics pipeline (primer removal, reference-based mapping, output of coverage plots and SNP calling).

CONCLUSIONS

All steps in this protocol are designed to be straightforward to implement, especially for researchers who are undertaking next-generation sequencing for the first time. The molecular steps are scalable to large numbers (hundreds) of individuals and all steps post-DNA extraction can be carried out in 96-well plate format. Also, the protocol has been assembled so that individual 'modules' can be swapped out to suit available resources.

摘要

背景

下一代 DNA 测序(NGS)技术在许多生物学研究领域都产生了巨大的影响,尤其是在进化生物学领域。NGS 显示出潜力的一个领域是高通量测序完整的线粒体 DNA 基因组(人类和其他动物)。尽管 NGS 技术的使用越来越多,人们对其在回答生物学问题中的重要性也有了更好的认识,但在成功实施基于 NGS 的项目方面仍然存在重大障碍,特别是对于新用户。

结果

本文介绍了一种从 DNA 提取到共识序列的获得完整人类线粒体(mtDNA)基因组的“从 A 到 Z”方案。虽然该方案专为人类设计,但也可用于对其他物种的小细胞器基因组和核基因座进行测序。该方案包括 DNA 提取、PCR 扩增、PCR 产物的片段化、片段的条形码标记、使用 454 GS FLX 平台进行测序以及完整的生物信息学管道(引物去除、基于参考的映射、覆盖图和 SNP 调用输出)。

结论

本方案中的所有步骤都旨在易于实施,特别是对于首次进行下一代测序的研究人员。分子步骤可扩展到大量(数百个)个体,并且 DNA 提取后的所有步骤都可以在 96 孔板格式中进行。此外,该方案已被组装,以便可以替换单个“模块”以适应可用资源。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/278d/3922791/80f3fd7166ff/1471-2164-15-68-1.jpg

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