Microdroplet-based PCR enrichment for large-scale targeted sequencing.

Microdroplet-based PCR enrichment for large-scale targeted sequencing.
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DOI:
10.1038/nbt.1583
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发表时间:
2009-11
影响因子:
46.9
通讯作者:
Frazer, Kelly A.
Frazer, Kelly A.
中科院分区:
工程技术1区
文献类型:
--
作者:
Tewhey, Ryan;Warner, Jason B.;Nakano, Masakazu;Libby, Brian;Medkova, Martina;David, Patricia H.;Kotsopoulos, Steve K.;Samuels, Michael L.;Hutchison, J. Brian;Larson, Jonathan W.;Topol, Eric J.;Weiner, Michael P.;Harismendy, Olivier;Olson, Jeff;Link, Darren R.;Frazer, Kelly A.

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人类基因组特定位点的靶向测序是最大化第二代测序技术用于基于人群的遗传变异研究的效率的有前途的方法。在这里,我们描述了微滴PCR,它执行150万个单独的扩增平行,作为一种方法,在人类基因组中富集靶序列。我们最初设计了47个基因的435个外显子的引物,这些基因被选择为具有广泛的序列特征。使用该引物组,我们通过微滴和传统的单重PCR扩增了相同的六个样品,并使用Illumina GAII对产物进行测序,这表明两种方法都产生了类似的高质量数据; 84%的唯一映射读段落在靶序列内,约90%的靶碱基的均匀覆盖,序列变体调用的准确度大于99%,不同样品间的重现性高(r2=0.9)。接下来,我们将微滴PCR扩展到3976个扩增子,总计1.49 Mb的序列,在Illumina GAII和Roche 454平台上对所得样品进行测序,并获得具有同样高的特异性和灵敏度质量的数据。我们的研究结果表明,微滴技术非常适合于处理DNA,用于大规模平行扩增人类基因组的特定子集,以进行靶向测序。
Targeted sequencing of specific loci of the human genome is a promising approach for maximizing the efficiency of second-generation sequencing technologies for population-based studies of genetic variation. Here we describe microdroplet PCR, which performs 1.5 million separate amplifications in parallel, as an approach for enriching targeted sequences in the human genome. We initially designed primers to 435 exons of 47 genes that were selected for having a broad spectrum of sequence characteristics. Using this primer set we amplified the same six samples by both microdroplet and traditional singleplex PCR and sequenced the products using the Illumina GAII demonstrating that both methods generate similarly high quality data; 84% of the uniquely mapping reads fell within the targeted sequences, uniform coverage of ~90% of the targeted bases, greater than 99% accuracy in sequence variant calls, and high reproducibility between different samples (r2=0.9). We next scaled the microdroplet PCR to 3976 amplicons totaling 1.49 Mb of sequence, sequenced the resulting sample on both the Illumina GAII and Roche 454 platforms, and obtained data with equally high specificity and sensitivity quality. Our results demonstrate that microdroplet technology is well suited for processing DNA for massively parallel amplification of specific subsets of the human genome for targeted sequencing.
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发表时间: 2009-09-10
期刊: Nature
影响因子: 64.8
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期刊: GENOME RESEARCH
影响因子: 7
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发表时间: 2008-11-06
期刊: NATURE
影响因子: 64.8
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发表时间: 2008-10-23
期刊: NATURE
影响因子: 64.8
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影响因子: 11.1
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通讯作者: Davis, Ronald