首页> 外文期刊>The American Journal of Human Genetics >Pulling out the 1%: Whole-Genome capture for the targeted enrichment of ancient dna sequencing libraries
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Pulling out the 1%: Whole-Genome capture for the targeted enrichment of ancient dna sequencing libraries

机译:抽出1%:全基因组捕获以有针对性地丰富古代dna测序文库

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摘要

Most ancient specimens contain very low levels of endogenous DNA, precluding the shotgun sequencing of many interesting samples because of cost. Ancient DNA (aDNA) libraries often contain <1% endogenous DNA, with the majority of sequencing capacity taken up by environmental DNA. Here we present a capture-based method for enriching the endogenous component of aDNA sequencing libraries. By using biotinylated RNA baits transcribed from genomic DNA libraries, we are able to capture DNA fragments from across the human genome. We demonstrate this method on libraries created from four Iron Age and Bronze Age human teeth from Bulgaria, as well as bone samples from seven Peruvian mummies and a Bronze Age hair sample from Denmark. Prior to capture, shotgun sequencing of these libraries yielded an average of 1.2% of reads mapping to the human genome (including duplicates). After capture, this fraction increased substantially, with up to 59% of reads mapped to human and enrichment ranging from 6- to 159-fold. Furthermore, we maintained coverage of the majority of regions sequenced in the precapture library. Intersection with the 1000 Genomes Project reference panel yielded an average of 50,723 SNPs (range 3,062-147,243) for the postcapture libraries sequenced with 1 million reads, compared with 13,280 SNPs (range 217-73,266) for the precapture libraries, increasing resolution in population genetic analyses. Our whole-genome capture approach makes it less costly to sequence aDNA from specimens containing very low levels of endogenous DNA, enabling the analysis of larger numbers of samples.
机译:大多数古代标本中内源性DNA的含量非常低,由于成本原因,许多特有的标本不能进行the弹枪测序。古代DNA(aDNA)库通常包含<1%的内源DNA,大多数测序能力被环境DNA占用。在这里,我们提出了一种基于捕获的方法来丰富aDNA测序文库的内源性成分。通过使用从基因组DNA库转录的生物素化RNA诱饵,我们能够捕获整个人类基因组中的DNA片段。我们在从保加利亚的四个铁器时代和青铜时代的人类牙齿以及七个丹麦木乃伊的骨头样本和丹麦的一个青铜时代的头发样本创建的库中证明了该方法。在捕获之前,这些文库的shot弹枪测序产生了平均1.2%的读图,映射到人类基因组(包括重复序列)。捕获后,该部分显着增加,多达59%的读数定位于人,并且富集范围为6到159倍。此外,我们保持了对捕获前文库中测序的大多数区域的覆盖率。与1000个基因组计划参考小组的相交,捕获后测序的库具有100万个读数,平均产生50,723个SNP(范围为3,062-147,243),而捕获前捕获的文库平均为13,280个SNP(范围为217-73,266),从而提高了群体遗传学的分辨率分析。我们的全基因组捕获方法使从内源DNA含量极低的标本中测序aDNA的成本降低,从而能够分析大量样品。

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