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首页> 外文期刊>Molecular human reproduction. >Single-cell whole-genome amplification technique impacts the accuracy of SNP microarray-based genotyping and copy number analyses.
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Single-cell whole-genome amplification technique impacts the accuracy of SNP microarray-based genotyping and copy number analyses.

机译:单细胞全基因组扩增技术会影响基于SNP微阵列的基因分型和拷贝数分析的准确性。

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摘要

Methods of comprehensive microarray-based aneuploidy screening in single cells are rapidly emerging. Whole-genome amplification (WGA) remains a critical component for these methods to be successful. A number of commercially available WGA kits have been independently utilized in previous single-cell microarray studies. However, direct comparison of their performance on single cells has not been conducted. The present study demonstrates that among previously published methods, a single-cell GenomePlex WGA protocol provides the best combination of speed and accuracy for single nucleotide polymorphism microarray-based copy number (CN) analysis when compared with a REPLI-g- or GenomiPhi-based protocol. Alternatively, for applications that do not have constraints on turnaround time and that are directed at accurate genotyping rather than CN assignments, a REPLI-g-based protocol may provide the best solution.
机译:在单个细胞中全面基于微阵列的非整倍性筛选的方法正在迅速兴起。全基因组扩增(WGA)仍然是这些方法获得成功的关键组成部分。在先前的单细胞微阵列研究中已独立使用了许多可商购的WGA试剂盒。但是,尚未对其电池在单个电池上的性能进行直接比较。本研究表明,在以前发布的方法中,与基于REPLI-g或GenomiPhi的单细胞GenomePlex WGA协议相比,基于单核苷酸多态性微阵列的拷贝数(CN)分析可提供速度和准确性的最佳组合协议。替代地,对于没有周转时间限制并且针对准确的基因分型而不是CN分配的应用,基于REPLI-g的协议可以提供最佳解决方案。

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