Accuracy of Next Generation Sequencing Platforms.

Edward J Fox, Kate S Reid-Bayliss, Mary J Emond, Lawrence A Loeb
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引用次数: 221

Abstract

Next-generation DNA sequencing has revolutionized genomic studies and is driving the implementation of precision diagnostics. The ability of these technologies to disentangle sequence heterogeneity, however, is limited by their relatively high error rates. A Several single molecule barcoding strategies have been propose to reduce the overall error frequency. A Duplex Sequencing additionally exploits the fact that DNA is double-strand, with one strand reciprocally encoding the sequence information of its complement, and can eliminate nearly all sequencing errors by comparing the sequence of individually tagged amplicons derived from one strand of DNA with that of its complementary strand. This method reduces errors to fewer than one per ten million nucleotides sequenced.

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下一代测序平台的准确性。
下一代DNA测序已经彻底改变了基因组研究,并正在推动精确诊断的实施。然而,这些技术解开序列异质性的能力受到其相对较高的错误率的限制。已经提出了几种单分子条形码策略来降低总体错误频率。双工测序还利用了DNA是双链的事实,其中一条链相互编码其补体的序列信息,并且可以通过比较来自一条DNA链的单独标记的扩增子序列与其互补链的扩增子序列来消除几乎所有的测序错误。这种方法将误差降低到少于1 / 1000万个核苷酸测序。
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