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Flow cytometry-based DNA hybridization and polymorphism analysis

机译:基于流式细胞术的DNA杂交和多态性分析

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Functional analysis of the human genome, including the quantification of differential gene expression and the identification of polymorphic sites and disease genes, is an important element of the Human Genome Project. Current methods of analysis are mainly gel-based assays that are not well-suited to rapid genome-scale analyses. To analyze DNA sequence on a large scale, robust and high throughput assays are needed. We are developing a suite of microsphere-based approaches employing fluorescence detection to screen and analyze genomic sequence. Our approaches include competitive DNA hybridization to measure DNA or RNA targets in unknown samples, and oligo ligation or extension assays to analyze single-nucleotide polymorphisms. Apart from the advantages of sensitivity, simplicity, and low sample consumption, these flow cytometric approaches have the potential for high throughput multiplexed analysis using multicolored microspheres and automated sample handling.
机译:人类基因组的功能分析,包括定量差异基因表达和多态性位点和疾病基因的鉴定,是人类基因组项目的重要因素。目前的分析方法主要是基于凝胶的测定,其不适合于快速基因组级分析。为了分析大规模的DNA序列,需要稳健和高通量测定。我们正在开发一种使用荧光检测的基于微球的方法套件,以筛选和分析基因组序列。我们的方法包括竞争性DNA杂交,以测量未知样品中的DNA或RNA靶标,寡核苷酸结扎或延伸测定以分析单核苷酸多态性。除了灵敏度,简单性和低样品消耗的优点之外,这些流式细胞识别方法具有使用多色微球和自动样品处理的高通量复用分析的可能性。

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