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首页> 外文期刊>Nature Communications >TruePrime is a novel method for whole-genome amplification from single cells based on TthPrimPol
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TruePrime is a novel method for whole-genome amplification from single cells based on TthPrimPol

机译:TruePrime是一种基于 Tth PrimPol从单细胞扩增全基因组的新方法

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Sequencing of a single-cell genome requires DNA amplification, a process prone to introducing bias and errors into the amplified genome. Here we introduce a novel multiple displacement amplification (MDA) method based on the unique DNA primase features of Thermus thermophilus ( Tth ) PrimPol. Tth PrimPol displays a potent primase activity preferring dNTPs as substrates unlike conventional primases. A combination of Tth PrimPol’s unique ability to synthesize DNA primers with the highly processive Phi29 DNA polymerase (Φ29DNApol) enables near-complete whole genome amplification from single cells. This novel method demonstrates superior breadth and evenness of genome coverage, high reproducibility, excellent single-nucleotide variant (SNV) detection rates with low allelic dropout (ADO) and low chimera formation as exemplified by sequencing HEK293 cells. Moreover, copy number variant (CNV) calling yields superior results compared with random primer-based MDA methods. The advantages of this method, which we named TruePrime, promise to facilitate and improve single-cell genomic analysis.
机译:单细胞基因组的测序需要DNA扩增,该过程易于将偏倚和错误引入扩增的基因组中。在这里,我们介绍一种基于嗜热栖热菌(Tth)PrimPol独特的DNA primase特性的新颖的多位移扩增(MDA)方法。 Tth PrimPol与传统的primases相比,显示出更强的primase活性,优选dNTPs作为底物。 Tth PrimPol独特的合成DNA引物的能力与高度加工的Phi29 DNA聚合酶(Φ29DNApol)结合使用,可以从单个细胞进行近乎完整的全基因组扩增。这种新方法展示了卓越的基因组覆盖范围和均匀性,高重现性,出色的单核苷酸变异(SNV)检测率,低等位基因缺失(ADO)和低嵌合体形成,如对HEK293细胞测序证明的那样。此外,与基于随机引物的MDA方法相比,拷贝数变异(CNV)调用产生了更好的结果。这种方法的优势(我们称为TruePrime)有望促进和改善单细胞基因组分析。

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