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单细胞全基因组扩增技术会影响 SNP 微阵列基因分型和拷贝数分析的准确性。

Single-cell whole-genome amplification technique impacts the accuracy of SNP microarray-based genotyping and copy number analyses.

机构信息

Reproductive Medicine Associates of New Jersey, Morristown, NJ 07960, USA.

出版信息

Mol Hum Reprod. 2011 Jun;17(6):335-43. doi: 10.1093/molehr/gaq103. Epub 2010 Dec 21.

Abstract

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.

摘要

单细胞综合微阵列非整倍体筛查方法正在迅速涌现。全基因组扩增(WGA)仍然是这些方法成功的关键组成部分。一些商业上可用的 WGA 试剂盒已在以前的单细胞微阵列研究中独立使用。然而,它们在单细胞上的性能尚未进行直接比较。本研究表明,在以前发表的方法中,与基于 REPLI-g 或 GenomiPhi 的方案相比,单细胞 GenomePlex WGA 方案在单核苷酸多态性微阵列拷贝数(CN)分析方面提供了最佳的速度和准确性组合。另一方面,对于没有周转时间限制且针对准确基因分型而不是 CN 分配的应用,基于 REPLI-g 的方案可能是最佳解决方案。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a9c7/3097071/0be6d848a2f2/gaq10301.jpg

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