Stiller Mathias
Department of Biology, The Pennsylvania State University, 320 Mueller Laboratory, University Park, PA 16802, USA.
Methods Mol Biol. 2012;840:171-6. doi: 10.1007/978-1-61779-516-9_20.
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.
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。