数字聚合酶链反应
拷贝数变化
拷贝数分析
计算生物学
低拷贝数
生物
序列(生物学)
遗传学
基因组
聚合酶链反应
基因
作者
Avery Davis Bell,Christina L. Usher,Steven A. McCarroll
出处
期刊:Methods in molecular biology
日期:2018-01-01
卷期号:: 143-160
被引量:24
标识
DOI:10.1007/978-1-4939-7778-9_9
摘要
Many genomic segments vary in copy number among individuals of the same species, or between cancer and normal cells within the same person. Correctly measuring this copy number variation is critical for studying its genetic properties, its distribution in populations and its relationship to phenotypes. Droplet digital PCR (ddPCR) enables accurate measurement of copy number by partitioning a PCR reaction into thousands of nanoliter-scale droplets, so that a genomic sequence of interest-whose presence or absence in a droplet is determined by end-point fluorescence-can be digitally counted. Here, we describe how we analyze copy number variants using ddPCR and review the design of effective assays, the performance of ddPCR with those assays, the optimization of reactions, and the interpretation of data.
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