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Assessing Chromosomal Aberrations from Limiting Input of Cells Using Affymetrix Copy Number and SNP Arrays

机译:评估使用Affymetrix拷贝数和SNP阵列限制细胞输入的染色体畸变

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Measurements generated from traditional RNA/DNA profiling methods typically represent an amalgam of signals compiled from tens to thousands or even millions of cells within a multi-cellular population. These approaches require a bulk amount of test material and assume that there is minimal heterogeneity among seemingly similar cells in order to draw a global conclusion. In contrast, the ability to measure signal from a single cell allows unprecedented ability to resolve genomic differences in complex mixture of individual cells, monitor circulating/rare cells often in a non-invasive manner, and allow early access to the genome during development in the form of cells taken from pre-implantation embryos.
机译:从传统的RNA / DNA分析方法产生的测量通常代表从数度到数千次甚至数百万个细胞中编制的信号的汞合金。这些方法需要大量的测试材料,并假设看似类似的细胞之间存在最小的异质性,以便利用全球结论。相反,从单个细胞测量信号的能力允许前所未有的能力解决个体细胞的复杂混合物中的基因组差异,通常以非侵入方式监测循环/稀有细胞,并在开发期间早期进入基因组从预注入胚胎中取出的细胞形式。

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