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Single-molecule PCR: an artifact-free PCR approach for the analysis of somatic mutations.

机译:单分子PCR:一种无人工产物的PCR方法,用于分析体细胞突变。

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摘要

A critical review of the clone-by-clone approach to the analysis of complex spectra of somatic mutations is presented. The study of a priori unknown somatic mutations requires painstaking analysis of complex mixtures of multiple mutant and non-mutant DNA molecules. If mutant fractions are sufficiently high, these mixtures can be dissected by the cloning of individual DNA molecules and scanning of the individual clones for mutations (e.g., by sequencing). Currently, the majority of such cloning is performed using PCR fragments. However, post-PCR cloning may result in various PCR artifacts - PCR errors and jumping PCR - and preferential amplification of certain mutations. This review argues that single-molecule PCR is a simple alternative that promises to evade the disadvantages inherent to post-PCR cloning and enhance mutational analysis in the future.
机译:提出了对克隆的体细胞突变的复杂光谱分析方法的严格审查。对先验未知的体细胞突变的研究需要对多个突变和非突变DNA分子的复杂混合物进行艰苦的分析。如果突变部分足够高,则可以通过克隆单个DNA分子并扫描单个克隆的突变(例如,通过测序)来解剖这些混合物。目前,大多数此类克隆是使用PCR片段进行的。但是,PCR后克隆可能会导致各种PCR伪像-PCR错误和PCR跳跃-以及某些突变的优先扩增。这篇评论认为单分子PCR是一种简单的选择,有望避免PCR后克隆固有的缺点,并在将来增强突变分析。

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