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案例研究:通过直接多重PCR测序(DMPS)对灭绝洞熊的线粒体基因组进行靶向高通量测序。

Case study: targeted high-throughput sequencing of mitochondrial genomes from extinct cave bears via direct multiplex PCR sequencing (DMPS).

作者信息

Stiller Mathias

机构信息

Department of Biology, The Pennsylvania State University, 320 Mueller Laboratory, University Park, PA 16802, USA.

出版信息

Methods Mol Biol. 2012;840:171-6. doi: 10.1007/978-1-61779-516-9_20.

Abstract

Here I describe the use of a recently developed technique for targeted high-throughput sequencing of highly degraded DNA by direct multiplex PCR sequencing (DMPS) that was used to amplify 31 near-complete mitochondrial genomes of the extinct cave bear (Ursus spelaeus). DMPS couples multiplex PCR with the generation of barcoded sequencing libraries to be sequenced in parallel on a high-throughput sequencing platform. DMPS makes it possible to generate large amounts of targeted DNA sequence data simultaneously from multiple degraded samples such as fossil remains. In this chapter, I describe an experiment that uses DMPS with different primer sets and on both modern and ancient DNA templates.

摘要

在此,我描述了一种最近开发的技术——直接多重PCR测序(DMPS),用于对高度降解的DNA进行靶向高通量测序。该技术被用于扩增已灭绝的洞熊( Ursus spelaeus)的31个近乎完整的线粒体基因组。DMPS将多重PCR与带条形码的测序文库的生成相结合,以便在高通量测序平台上进行并行测序。DMPS使得能够同时从多个降解样本(如化石残骸)中生成大量靶向DNA序列数据。在本章中,我描述了一个实验,该实验使用不同引物组的DMPS,对现代和古代DNA模板进行操作。

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